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World News

2006 Archive
BioTech
Jan 1 - March 27
Mar 27 - April 11
BIOTECHNOLOGY
Research explores ways to improve nutritional value, productivity of rice

Colorado State University, The Institute for Genomic Research, Perlegen Sciences, Inc. and the International Rice Research Institute are joining forces to unlock the genetic secrets of rice, information that could improve rice crops and help address hunger and malnutrition for millions of people.

Rice is the world's top food crop and the principal source of nourishment for nearly half the world's population, particularly people in the poorest but fastest growing nations.

The study will focus on the genetic basis underlying important agricultural traits such as the nutritional value and disease resistance of 21 diverse lines, or varieties, of rice, by identifying and comparing differences in DNA sequences. This information will accelerate development of hardier, more productive types of rice. The U.S. Department of Agriculture's Cooperative State Research, Education and Extension Service - National Research Initiative competitive grants plant genome program provided $715,000 for the U.S. group's contribution to the collaboration. Additional funding for international collaboration will be provided by other sources.

"This collaboration will produce a powerful resource to investigate the patterns of molecular variation across the rice genome, assess evolutionary forces shaping rice and discover genes controlling important traits such as disease resistance, drought tolerance and nutritional value," said Jan Leach, the lead U.S. researcher on the study and a professor of bioagricultural sciences and pest management at Colorado State University. "In the long term, this information will be used to improve rice, and it will also help scientists better understand how to improve other crop plants."

As populations boom in countries with limited availability of productive land, the need for additional information about agriculture and crops that can improve production and nutritional values have become key in preventing hunger and malnutrition. Much of the information scientists need may reside in the genomes of wild species of rice.

DNA sequence variation accounts for many differences between individual plants and different varieties of the same plant, such as how the plant develops, how much a crop plant yields, the nutritional value and how well the plant tolerates stresses such as drought or exposure to diseases. Much of the variation in genomes is represented by single nucleotide polymorphisms, known as SNPs, which are changes at single base positions in DNA.

This collaboration will identify SNPs from across the whole genome of 21 rice strains using methodologies developed by Perlegen Sciences. Wild species of rice are a rich resource of diverse traits, and analysis of their genomic variations may provide valuable information regarding phenotypic variation between different rice strains.

SNPs are a marker of genetic variation between individuals of a species, and they allow scientists to identify regions of genetic variation that may be linked to traits. By identifying differences in SNPs among major rice varieties, the study will help uncover the genetic basis behind important agricultural traits.

"In addition to their importance in understanding genome evolution, studying the SNPs of rice is valuable for several reasons," Leach said. "First, it reveals DNA variation among different varieties of rice, which provides information for developing better varieties. It also provides the ultimate anchor to relate the study of rice and other crops."

The International Rice Research Institute is a non-profit agricultural research and training center that was established to improve the wellbeing of present and future generations of rice farmers and consumers, particularly those with low incomes. It helps farmers in developing countries produce more food on limited land, using less water, labor and chemicals. The institute has helped to develop about 1,000 modern varieties of rice, which has increased the availability of rice to populations in need and reduced the price.

Perlegen will perform the microarray experiments. Perlegen uses microarray technology to quickly assess DNA variations and compare whole genomes in an effort to identify those variations associated with human diseases and to explain and predict the efficacy and adverse effects of prescription drugs.

"Rice is an important crop for world agriculture and an excellent candidate for DNA variation study," said Kelly Frazer, vice president of genomic biology at Perlegen. "The combination of the methodologies and experience our company can provide and the initial genomic research that has been conducted by the International Rice Research Institute will give scientists the opportunity to improve the quality of one of the most critical human food sources in the world."

© 1997-2001 Colorado State University

Washington bridles at EU's urge to regulate
By George Parker and Tobias Buck

Europe is getting jittery. Soon the borders of the European Union will stretch from the Atlantic to the Black Sea, bringing the population of the world's biggest trade bloc to almost 490m - bigger than the US and Japan combined.

Seen from some European capitals, the accession of Bulgaria and Romania in 2007 or 2008 is a worrying sign of overstretch, fuelling fears that the EU is becoming too cumbersome and too diverse to have real clout in the globalised world.

In Washington there is another view. Senior officials see the latest step in the creation of a behemoth that will use its economic weight to impose European values on the rest of the world, often through excessive regulation.

According to Rockwell Schnabel, the former US ambassador to Brussels, Europe is "increasingly seeking to act as the world's economic regulator".

Little surprise then that Mr Schnabel's successor, Boyden Gray, is not a career diplomat but a top regulatory lawyer, whose mission is to minimise transatlantic friction between the world's two biggest trading partners.

Yesterday Mr Gray set out plans to improve regulatory co-operation between Europe and the US but added: "We're not interested in convergence if it would mean raising the regulatory burden in the domestic US market.

"From a US perspective, the main problem is less that our regulations differ than a general sense that Europe is overregulated and that this overregulation is stifling growth," he told the European Policy Centre think-tank.

Companies trading with Europe must comply with EU standards that are often more risk-averse than those seen in the US, manifested in new legislation on the testing of chemicals or restrictions on genetically modified food and hormone- enhanced beef.

European regulations also reflect other cultural preferences, for example in the setting of high environmental standards or the rejection of animal testing.

As Mr Schnabel notes: "The only way to make sure that EU standards do not put European industry at a competitive disadvantage is to ensure that industry around the world has to work to the same standards." Of course, it is a two-way process: US regulations such as the Sarbanes-Oxley Act imposed onerous reporting restrictions on European companies operating in America after the Enron scandal. But as Mr Schnabel notes: "Washington regulates far less than Brussels or the EU member states and, when it does regulate, it is less likely to act on the principle of ­precaution."

Not doing business with Europe is an unattractive option. The 27 members of the enlarged EU are projected by the IMF to have a gross domestic product of $14,290bn (€11,133bn, £7,584bn) in 2007, bigger than the US, at $13,943bn.

Europe's regulatory clout is particularly visible in the cars sector, where EU standards and norms are applied by countries across the world, including Japan, India, South Africa, Australia and China.

That means that European companies such as Fiat, Volkswagen and Peugeot can simply ship their cars to Japan and elsewhere without making costly tweaks to their models or getting the approval of foreign safety authorities.

US groups such as GM and Ford, on the other hand, face the administrative burden of persuading Japanese authorities that their cars meet all the requirements of domestic law.

"It is a huge advantage if you are the one setting the standards, because it is always better to make the policies rather than to follow them. That is also hugely important for our industry," says the spokesman for Günter Verheugen, the EU industry commissioner.

Mr Gray yesterday praised the campaign for "better regulation" promoted by Mr Verheugen, which aims to minimise burdens on business. The flow of new EU regulation has slowed considerably since the new European Commission took office in 2004.

But Mr Verheugen admits that a passion for regulation still resides among officials in Brussels, not to mention members of the European parliament and government ministers in member states who continue to push pet projects. Mr Schnabel concludes that his successor still has his work cut out: "It is too soon for liberals to declare victory," he says.

Mr Schnabel, who left Brussels in 2005, observes in his book, The Next Superpower?, that the Commission, the EU's executive arm, is adept at deploying economic soft power.

During a dispute over US steel tariffs in 2003, the Commission threatened trade sanctions against products from electorally sensitive states. "A market that big is why the Commission could credibly threaten to use trade sanctions to influence the 2004 US presidential election," he writes.

The EU is a regulatory machine, churning out common standards to make the bloc's single-market function effectively, allowing companies to exploit fully the economies of scale offered by a huge home market. Such rules are determined by majority voting, so the EU's expansion should not necessarily lead to legislative ­gridlock.

In developing common standards for its member states, it in effect imposes the same rules on companies wishing to trade with Europe, a fact that can give European companies a big competitive advantage.

For example, Europe's decision to adopt GSM as its standard for mobile communications gave a head start to companies such as Nokia of Finland and Eriksson of Sweden. The EU's role in opening national telecommunications markets to competition was also vital.

© Copyright The Financial Times Ltd 2006

Biotech booming, claims Ernst & Young report

The biotechnology sector is booming across the globe, with revenues of the worlds publicly traded biotech companies growing by 18 per cent in 2005.

And while the US sector is maturing, new opportunities are rapidly emerging across Asia-Pacific and elsewhere. In fact, revenues reached an all-time high last year of $63.1 billion, according to Ernst & Young.

The accountancy firm says that the European biotechnology sector has emerged from a lengthy restructuring period with double-digit revenue growth and the second-strongest financing year on record, with 3.2 billion in capital raised. The pipelines of Europes publicly traded biotech companies increased by 28 per cent, with strong growth in late-stage development.

This comes just as the World Trade Organisation confirmed a ruling against the EU in a case brought by the US and other nations against a de facto moratorium on genetically modified products.

Despite continued consumer reluctance to embrace the technology therefore, Europe is therefore moving ahead with GM technology. The EC recently adopted an overview of the state of implementation of national co-existence measures.

Simon Barber, director of the plant biotechnology unit at EuropaBio - the European association for bioindustries, said that co-existence of GM and non-GM crops is already a reality in countries such as Spain.

In Asia-Pacific meanwhile, performance of the biotechnology sector outpaces the rest of the world, with a scorching 46 per cent increase in revenues and significant progress toward profitability. Government emphasis on biotech as a strategic priority and a focus on strategic niches is helping countries competitiveness.

Indeed, foreign companies are increasingly drawn to the region with growing drug markets, economic liberalisation, and stronger intellectual property protections.

And for the third consecutive year, the US biotechnology sector is delivering strong product approvals 32 new product approvals, including 17 first-time approvals and solid financial results.

The US industry continues to approach aggregate profitability, and Canada is showing robust growth.

Ernst & Young has been tracking the progress of biotechnology for two decades. Beyond Borders: Global Biotechnology Report 2006 from the group's Global Biotechnology Centre marks the 20th anniversary of the company's annual report providing data, in-depth analysis, market insights, and key trends for the biotechnology sector, and provides a special timeline charting the industrys long-term evolution.
© 2000/2006 – Decision News Media SAS

PREMIER Biosoft International releases version 5.10 of Beacon Designer with advanced support for multiplexing, crucial for diagnostic assay development.

Palo Alto - With the release of Beacon Designer Version 5.10, PREMIER Biosoft International has taken a step further in making a comprehensive, sophisticated and powerful qPCR oligo design tool available to thousands of labs all over the world," says Kay Brown, V.P. Business Development and Marketing. "We are particularly pleased with the biologist designed user interface and comprehensive support for multiplexing."

Beacon Designer can design SYBR® Green primers, TaqMan® probes, LNA spiked TaqMan® probes, FRET probes or molecular beacons for real time qRT-PCR and NASBA® assays. Beacon Designer also enables the design of compatible probes for proven SYBR® Green assays, resulting in cost saving.

The most notable feature of Beacon Designer is the use of innovative and sophisticated algorithms to ensure assay success. Primers are designed avoiding regions of significant homology, identified by automatically interpreting BLAST search results. Primer efficiency is enhanced by designing them in template-structure-free regions. For multiplexing, Beacon Designer screens millions of primer probe combinations to design primer probe sets for single tube multiplex reactions. Whether the need is to incorporate well-proven sets for some of the templates, or include reference or housekeeping genes for normalization purposes in the assay, Beacon Designer is fully equipped.
Paper looks at plants, spider silk research

Spider silk is at least five times stronger than steel, two times more elastic than nylon, waterproof, and stretchable - qualities that may make it important for the textile and construction industries.

This has led scientists to try to synthesize it in the laboratory, or to isolate the genes for spider silk and transfer them to animal cells for mass production. The former method has hitherto been unsuccessful; the latter method is expensive, and the quantity produced by animal cells is limited. In order to overcome these factors, scientists are now turning to “Transgenic Plants for Spider Silk-Like Protein Production.”

In an article in the latest issue of the Information Systems for Biotechnology Newsletter, P. S. Janaki Krishna looks at recent research on the feasibility of plant based silk-like protein (SLP) production.

One such project was reported by Jianjun Yang and co-authors, of Du Pont de Nemours & Co, USA. Scientists introduced the DP1B gene into Arabidopsis plants by an Agrobacterium-mediated floral transformation method. DP1B is a synthetic gene for spider dragline silk protein, which can be spun to form silk fiber.

After growing and evaluating transgenic plants, researchers found that: 1) transgenic plants engineered with mechanisms targeting DP1B production to the cell's endoplasmic reticulum (ER) were able to accumulate SLP in their seeds to a level greater than 15% of total soluble protein; 2) DP1B was heritable after one or two cycles of sexual reproduction; and 3) accumulation levels of the DP1B fusion protein were stable. The next step may now be to search for an industrially important crop which can support large-scale, plant-based production of DP1B SLP.

Read Paper

TRANSGENIC PLANTS FOR SPIDER SILK-LIKE PROTEIN PRODUCTION
P. S. Janaki Krishna

Spiders and insects have been able to spin silk for at least 380 million years. It has been estimated that the strength of spider silk is at least five times as strong as steel, twice as elastic as nylon, waterproof, and stretchable. Scientists have long envied the strength and elasticity of spider’s silk but have been unable to synthesize it. The dragline silk of the Golden Orb-weaving Spider is the most studied in scientific research. Dragline silk is the fiber from which spiders make the scaffolding of their webs. Of late, demonstrations of cloning and expression of silk fibroin protein, including spider dragline silk, represent an exciting scientific opportunity and technological challenge.

Spider silk is a natural polypeptide, polymeric protein and is in the scleroprotein group, which also includes collagen (in ligaments) and keratin (in nails and hair). Spider silk genes encode proteins composed of iterated peptide motifs, and the consensus sequences are multiply repeated throughout the silk proteins. Patterns of ‘Ala-rich’ blocks and ‘Gly-rich’ amorphous blocks provide both strength and elasticity, and such biomaterials might therefore be valuable for industrial and medical purposes.

Although spider silk was initially produced in animal cells, mass production from animal cells is expensive and the quantity produced is limited, mainly due to the requirement for large fermenters, sterile conditions, and expensive media. In order to overcome these factors, plants (tobacco, potato, Arabidopsis, and soy somatic cells) have been evaluated for the production of spider silk proteins. These studies demonstrated the feasibility of plant based silk-like protein (SLP) production. However, high yield and low production costs remain a challenge.

Jianjun Yang and co-authors, from Central Research Development and Crop Genetics Research, Du Pont de Nemours & Co, USA, report high yield recombinant SLP production through protein targeting in transgenic Arabidopsis. The researchers used a synthetic DP1B gene for producing SLP, achieving variable accumulation levels through protein targeting into a special cellular components.1 DP1B is a synthetic analogue of spider dragline silk protein, which can be spun to form silk fiber. An average DP1B accumulation level in plant cells below 1.5% of total soluble protein has been previously reported. However, Yang et al. showed that ER and vacuole targeting in seeds and apoplast, and ER targeting in leaves, can dramatically increase SLP accumulation. Many transgenic plants engineered with the ER targeting mechanism were able to accumulate DP1B SLP in their seeds to a level greater than 15% of total soluble protein.

A high yield of SLP was achieved by utilizing DP1B-8P, which is a plant-optimized, synthetic 8-mer DP1B gene that encodes a 64-kD DP1B SLP. Targeting of SLP to the designated cellular components was enabled by adding a 21-amino acid sporamin signal peptide, 16-amino acid sporamin propeptide, and 4-amino acid ER retention peptide to appropriate positions on the DP1B molecule. To express the resultant DP1Ba, DP1Be, and DP1Bv fusion proteins in Arabidopsis, expression plasmids pGYV501, pGYV502, and pGYV503 were introduced into Arabidopsis thaliana by an Agrobacterium-mediated floral transformation method. Healthy T1 transgenic plants were grown in soil and T2 seeds were harvested from individual T1 plants to represent independent transformation events. Later, T2 seeds were germinated on selective plates to obtain the next generation. All T2 transgenic seedlings originating from the same parents were grown together in soil. T3 seeds were collected from these plants and pooled together to represent independent transformation events. Standard molecular assays were performed to confirm transgene expression in the independent transformation events. DP1B production yield was calculated based on DP1B content and relative to total soluble protein content in the extract.

The transformation was confirmed by PCR amplification of sporamin signal peptide coding sequences from the genomic DNA. Leaf protein extract made from a pGY401 Arabidopsis plant was used to show control levels of unmodified, cytosol-accumulated 64-kD DP1B. The results of immunoblot assay showed that in leaf tissues of Arabidopsis, apoplast and ER targeting are suitable approaches for DP1B production, but the vacuole targeting is not. Results also showed that accumulation of the unmodified DP1B in leaf tissues of pGY401 plants ranged from 0.01% to 1.7% of total soluble protein (TSP), with an average yield of 0.3%, while DP1Ba accumulation in leaf tissue of pGYV501 plants was from 2.1% to 8.5% TSP, with an average yield of 4%. DP1Be accumulation in leaf tissues of pGYV502 plants was from 0.3% to 6.7% TSP with an average yield of 1.5%. Vacuole targeting did not result in accumulation of correctly-sized DP1Bv molecules. This comparison of accumulation levels between the non targeted and targeted DP1Bs revealed that DP1B productivity in leaf tissues was increased 13-fold by targeting to apoplast and 5-fold by targeting to ER lumen. Apoplast targeting is the best approach.

Characterization of seed-specific DP1B fusion proteins showed accumulation of unmodified DP1B in pGY411 seeds ranging from 1% to 1.4% TSP with an average yield of 1.2%. The accumulation of the ER-targeting DP1Be in pGYV512 seeds ranged from 1.8% to 18% TSP (avg. 9.4%), and the vacuole-targeting DP1Bv in pGYV513 seeds ranged from 4.8% to 8.2% TSP (avg. 6.5%). Thus a comparison between the targeted and non-targeted DP1Bs suggested that the ER and vacuole targeting significantly enhanced DP1B productivity in seeds by 7.8- and 5.4-fold, and at the highest levels, up to 15-fold increase was observed in ER targeting.

Importantly, DP1B transgenic plants were heritable after one and two cycles of sexual reproduction, as confirmed by transgene insertion and expression studies in T2 leaves or T3 seeds, and the accumulation level of DP1B fusion protein was stable. Thus this research demonstrates the highest level of DP1B accumulation among all protein targeting strategies. It was concluded that combining seed-specific synthesis and ER targeting is the best method of production. Though Arabidopsis is not a good candidate for commercial production, the approach may be tried in an industrially important crop that supports the large-scale plant based production of DP1B SLP.

UK research projects map out food safety hotspots
By Ahmed ElAmin

A number of food safety and nutrition research studies up for funding by the UK regulator could result in new codes of practice or regulation for the industry.

The studies are part of a programme by the UK Food Standards Agency (FSA) to increase food safety and improve nutrition throughout the country. The research studies could eventually help big and small companies improve their food safety practices.

Over recent years the FSA has been working towards a target to reduce foodborne disease by 20 per cent by the year 2006 and even further by 2010.

The FSA commissioned projects up for bid include: microbial risk management, the eggs and poultry sector, microbial surveillance, chemical contaminants from food production, a safety assessment of novel and genetically modified foods, a survey of food acceptability and choice, a survey of food choice inequalities, food authenticity, food intolerance, and research on surveillance and monitoring in Scotland.

Laboratory researchers have until 19 May to put their applications to the UK regulator to receive funding for the projects.

Researchers who win the microbial risk management project will investigate the impact of different preparation and storage conditions on the growth and survival of Enterobacter sakazakii and related organisms in reconstituted powdered infant formula, follow-on formula, formula for special medical purposes and breast milk fortifiers.

The eggs and poultry project will evaluate the effectiveness of best practice recommendations to reduce the risks associated with thinning, a common practice throughout the poultry industry, where a proportion of a poultry flock is removed prior to depopulation of a broiler house.

Although it is generally accepted that this is a major risk factor for introducing Campylobacter into flocks, the majority of the UK industry sees thinning as an economic necessity, the FSA noted.

Previous research produced recommendations suitable for the production of a code of practice for the thinning process, and suggestions for suitable intervention measures.

The FSA is now funding a followup study to determine the effectiveness of the proposed recommendations and suggested interventions.

The regulator has set a new target to work with industry to achieve a 50 per cent reduction in the incidence of UK produced chicken testing positive for campylobacter by 2010.

A third project will help the regulator devise sensitive and specific examination methods for meat preparation products such as herbs, spices and injected marinates. The methods will be compared against current food testing protocols.

At present, standardised examination methods are not sufficient for the recovery of micro-organisms from raw meat preparations such as beefburgers, chicken kievs, seasoned steaks and sausages, the FSA stated in its research documentation.

"The estimation of bacterial levels may not be as accurate using current methods due to difficulties in detection or recovery," the FSA stated. "The production processes of meat preparation products can result in microorganisms being found throughout the product and not just on the surface of the food."

Micro-organisms can be present on meat cuts and some pathogens may also be introduced from ingredients such as herbs or spices. The inadequate cooking of these types of products may result in viable pathogens being present within the meat.

Another project will investigate the consumption of fish and shellfish from unmanaged UK inland waterways and if necessary, develop a sampling and analytical programme to determine the levels of environmental contaminants present.

Researchers can also apply for a project to analyse samples of milk, cheese, yoghurt, eggs and commercial seaweed for iodine. Information should be provided on other elements that may be reported as part of the analysis at no extra cost.

A project on GM organisms will help develop methods to study the modification of transgenic proteins compared with their native equivalents that can be applied in the safety assessment of such foods or ingredients.

A project to develop a sensitive test to detect gelatine in plant-based foods and beverages would be used to determine the animal source of the gelatine. The end product would be a validated standard operating procedure (SOP) for detecting the source as a means of determining whether a food or drink is vegetarian.

In a previous consumer study, consumers were the most concerned about the authenticity of foods claiming to conform to vegetarian or religious requirements.

In response to the concern, the FSA previously commissioned research to develop methods to detect meat-based ingredients in vegetarian foods.

Successful methods, which can detect animal DNA and animal based fats, were developed. There have been more recent concerns about the use of gelatine, an animal based ingredient from collagen in skin and bones, in vegetarian or halal foods.

Gelatine is used as a thickener or gelling agent, a carrier for other ingredients, and a clarifying agent in certain fruit juices, wines and beer.

"There is a need to develop a sensitive method for gelatine to be able to test vegetarian foods and beverages, which may contain gelatine at very low levels," the FSA stated.

Researchers who win project Q01R0015 will seek to apply existing methods of determining milk, egg, and fish proteins to measuring the content of animal based ingredients in composite foods. The validation of these methods will determine their accuracy and uncertainty in measuring imported products of animal origin from third countries.

The method would be used to verify whether a food consists of 50 per cent or more of an animal based ingredient.

Changes to the European Commission regulation covering veterinary checks due in 2006, will lay down more detailed rules as to which imported foods are considered products of animal origin. Products containing animal-based ingredients such as milk, eggs, fish or honey, which make up 50 per cent or more by weight of the food, will be required to be subject to veterinary checks.

Project T07R0004 will seek to determine operational thresholds for the labelling of food allergens.

All applicants will be informed of the outcome of the assessment process by 1 September 2006.

In December 2004 the FSA published its strategic plan, identifying food safety, health and choice as three key areas for research.

Canada must learn lessons from New Zealand in developing national pharmaceuticals strategy, conference told

Canadian medical and pharmacy leaders call for more consultations on
strategy to avoid pitfalls of emphasis on cost-containment

TORONTO - Canada must avoid the mistakes made with New Zealand's single-minded focus on containment of drug costs when it develops its national pharmaceuticals strategy (NPS), a conference of Canadian physicians, pharmacists and patient representatives was told by New Zealand experts here last week.

The group was brought together by Rogers Publishing Limited's Healthcare and Financial Services Group, publishers of The Medical Post and Pharmacy Post. This was the second such gathering on the NPS hosted by Rogers, the first being held in March in Ottawa. Both events were moderated by Ottawa physician Dr. Barry Dworkin.

Work on the NPS was launched by the federal and provincial health ministers nearly two years ago and although a report is due in June, little is known about what will be presented. The New Zealand model has been put forward as a potential one for Canada to follow. The group assembled by Rogers concluded with agreement on a call for the NPS "to clearly state its goals, objectives and planning strategies" and to consult healthcare professionals, pharmacists and patient advocates.

Participants were told that while New Zealand has achieved stability in its pharmaceutical costs, it has done so at a considerable price, including increased costs elsewhere in the healthcare system, in worse health outcomes for patients, and great frustration for physicians, who in many cases are unable to prescribe the best possible medicines.

New Zealand created its Pharmaceutical Management Agency, or Pharmac, in 1993, and launched its current zealous cost-containment programs in 1997, said Alex Sundakov, a leading New Zealand economist who last August produced a study of the impact of the Pharmac policies.

New Zealand drug spending as a percentage of total healthcare spending used to be above the OECD average, he said, but it is now about half, at 8 percent, compared to 17 percent in Canada. The main features of the New Zealand policy include a firm cap on the budget for pharmaceutical spending, having an all-encompassing public system with practically no private market, and a strong reliance on sole sourcing, whereby companies bid to supply the sole drug available in a particular class, the winner being the one offering the lowest price.

"Where I see rot spreading and affecting integrity," Sundakov said, "is in the effect of the system on the doctor-patient relationship." Doctors are uncomfortable discussing unfunded drugs, so ignore them. Also, because pharmaceutical companies are doing practically no marketing or education activities, New Zealand doctors "increasingly don't know what they don't know about new medications. This is seen by Pharmac as a great victory, but as an economist it makes no sense to me."

Patients forced to change medicines

Dr. Stewart Mann, Associate Professor of Cardiovascular Medicine at the Wellington School of Medicine and Health Sciences, discussed the impact of Pharmac making only one drug available in each therapeutic area and of patients have to make "overnight" changes to their medication when contracts are switched from one sole supplier to another. He asked a provocative question: "If we were doing this as a clinical trial, would we ever get ethics approval?"

He also questioned the underpinning of the sole-supplier policy, which is based on the idea that one drug in a particular class can serve all, or at least most, patients. "Assumptions about class effect may not be justified," he said, "because studies on bioequivalence are done on healthy patients, not necessarily reflecting experience in the real world with sick patients on multiple medications."

Dr. Ken Whyte of the Respiratory Medicine Service, Auckland City Hospital, discussed the challenges and frustrations of lack of access to new medicines which might be seen as expensive but are more cost-effective in the long run. He also described the problems asthma sufferers have had in getting access to newer medications. Long-acting beta antagonists (LABAs) were not funded at all for several years after they were well established elsewhere, and eventually approved but only by special authority with very restrictive criteria. "There are big problems with restrictive criteria," he said, "Pharmac has saved a lot of money, but they have also denied a lot of patients treatment. It is a good example of a good idea gone wrong and needs to be rebuilt."

Canadian scientists join war against landmines

OTTAWA - Researchers working for the Canadian and U.S. militaries, including some in Edmonton, are making progress in developing genetically modified plants that could help people avoid death and injury from landmines.

The researchers at the University of Alberta, Duke University in North Carolina and other schools are trying to develop plants that will alert people to the presence of landmines by changing colour if their roots detect compounds, such as TNT, used in mines.

"I think we're about two or three years from something that might be practical in the field," Prof. Michael Deyholos at the U of A said in an interview.

"We're a lot closer than we were."

Deyholos and others, working for the last two years, have faced a three-part problem.

They have had to develop a receptor gene that can detect TNT and be spliced into a plant's roots.

Once the TNT is detected, the plants must then be able to transmit the information to their leaves or shoots, much in the way hormones are transferred throughout the human body.

Then, more receptors are needed in the shoots or leaves to make them change colour.

Using a weed called an arabidopsis, the U of A team has solved part of the equation.

"We have had the arabidopsis roots change colour ... but we have not had the shoots change colour," Deyholos said.

Researchers at other facilities have made progress on other aspects of the project, and the goal is to have all the successful components put into one type of plant.

The seeds could be dropped from an airplane over a suspected minefield. After a few weeks of growth, soldiers and civilians could judge by the plants' colours whether the area is safe.

The plants could be a huge help to civilians who want to reclaim farmland after a war.

The United Nations estimates there are more than 110 million landmines buried around the world, with Angola alone having 10 million landmines and an amputee population of 70,000.

In a newly released research paper, Deyholos and his colleagues say landmine-detecting plants would be inexpensive and effective even in developing countries.

Deyholos is optimistic a way will be found to fill the gap between TNT-detecting roots and leaves.

"Plants naturally are able to send chemicals through their sap, so the roots can tell the leaves, 'We don't have a lot of water or we don't have a lot of nutrients, so you'd better slow down your growth.'

"So the framework is there, and now we're just looking at some different kinds of modifications we can make to those chemicals to make them work as artificial hormones."
Copyright © 2006, Canoe Inc

Ireland gives go-ahead for GMO potato trials

DUBLIN - Ireland, Europe's biggest per capita consumer of potatoes, has given the go-ahead for a German company to grow varieties of the crop that have been genetically modified to resist disease.

The Environmental Protection Agency (EPA) gave its consent to BASF Plant Science GmbH on Friday to carry out field trials on potatoes that have been modified with improved resistance to late potato blight, the disease that caused the Irish potato famine.

"This consent is for field trials only and should not be confused with the placing of GM products on the market, which requires a separate consent and approval process at EU level," the EPA said in a statement.

"Potatoes (GM or non-GM) harvested from the field trials will not be used for food or feed purposes," it added.

One million people died and two million were forced to leave Ireland in the 1840s when potato blight caused widespread famine. Today, the Irish eat some 121 kg of potatoes per person every year, or nearly 1,000 potatoes for every man, woman and child.

Previous trials of GMO foods in Ireland have been disrupted by environmentalists who pulled up crops and damaged fields.

GM-free Ireland, an organisation campaigning against genetic food engineering, invited farmers, food producers, consumers, and politicians to an emergency meeting on Friday to decide what legal steps it could take to prevent the experiment.

Irish Green Party leader Trevor Sargent said the decision threatened the country's traditional GMO-free status which he said was a key selling point for the country's food exporters.

"Life is hard enough for farmers who are seeing less and less demand for potatoes and a growing preference for ready made meals," he said. "Farmers need this GM trial like a hole in the head."

Blight-resistant GMO potatoes were first developed in 2003 after scientists discovered a species of wild potato in Mexico that is naturally resistant to the disease, then inserted the gene into commercial strains.

The field trials will be carried out at one location at County Meath and the trial site will not exceed 1 hectare (2.5 acres) in size. The experiment will last for five years from 2006 to 2010 (inclusive), with monitoring continuing until 2014

EU executive faces pressure to deal with GMO laws
by Jeremy Smith

BRUSSELS - EU countries will soon demand more clarity on rules for separating traditional, organic and biotech crops, focusing on specific plant varieties to help farmers who want to grow GMOs to be better able to do so.

The European Commission, the EU executive, issued general guidelines back in July 2003 on how farmers should separate the three crop types. The idea was for national governments to make their own laws to facilitate GMO growing if farmers wanted it.

But this was not a legal obligation and most countries have been very slow to draft and adopt laws on an area known in EU jargon as coexistence. Some have not bothered at all.

As of the end of 2005, only four EU states had coexistence laws in place, although several more have notified their plans.

The Commission has come under repeated pressure from several countries to draft an EU-wide coexistence law to cover economic liability for contamination and separation distances. In February, it disappointed many by saying this was unnecessary.

Now, following a major coexistence conference held last month in Vienna, the EU-25 is expected to instruct the Commission to come up with far more specific growing guidelines.

Later this month, EU farm ministers will vote on a paper that asks the Commission to "identify ... best practice for technical segregation measures and ... develop guidelines for crop-specific measures," according to the paper's draft text. "The conclusion from the conference was that we have to develop crop-specific guidelines, as rapeseed is different from maize, for example," a Commission official said. Privately, insiders say the guidelines are unlikely to emerge before 2007.

Last jigsaw pieces

The EU executive should also receive orders to sort out, finally, its views on how much biotech material can be tolerated in seed batches -- and end a three-year row over the EU's last major GMO law. This area has proved so controversial that even the Commission, usually united on GMO policy, cannot agree.

The Commission would "come forward as soon as possible with common labelling thresholds for seeds," the draft paper said.

"... the level of these thresholds should allow freedom of choice throughout the whole food production chain, and it should not create a disproportionate burden for any group of operators," said the document, obtained by Reuters.

Thresholds would be set so that the labelling threshold for final products at the end of the production chain, which the EU has set at 0.9 percent, can be respected.

For once, green groups and the biotech industry can agree that GMO seed thresholds are necessary and long overdue. But they differ widely on the threshold levels that should be set.

What is at stake are the percentage levels of GMO content that can reasonably be allowed in crops like maize and rapeseed before the seeds have to be labelled as biotech.

Batches of conventional seed containing genetically modified material below those thresholds would not have to be labelled.

None of this means, however, that the bloc is about to approve more GMO varieties for cultivation since "live" GMOs remain a highly controversial area for the Commission itself and the EU's 25 member states -- long divided on GMO policy.

Still, coexistence laws and seed thresholds are widely seen as the last pieces of the jigsaw in the EU's plethora of GMO laws. Some EU states say it is essential to have at least seed thresholds in place before new "live" GMOs can be contemplated.
© 2006 Reuters Limited

EPA approves controversial GM potato trials in County Meath, Ireland

The Environmental Protection Agency has approved controversial plans to grow genetically-modified potatoes in Co Meath.

The five-year trials by the German chemical firm BASF are due to take place in Arodstown, near the Teagasc research centre in Summerhill.

The potatoes will not be allowed on the market as this would require further consent and approval at EU level.

The EPA says the company will have to adhere to 10 conditions and the trials will be monitored by the agency on a continuing basis.

The EPA received dozens of submissions opposing the plan when BASF first applied for permission earlier this year.

Farmers also expressed concern about the GM potatoes contaminating their crops, while doctors said the health risks associated with GM food had still not been fully examined.

© Thomas Crosbie Media 2006.

Genetic rules - Indias foreign trade policy creates more problems than it sought to address

The conditional permission granted for the import of genetically modified foods in the new foreign trade policy, unveiled by the commerce ministry in the first week of April, has created more problems than it sought to address on this controversial issue.

Such imports will need the approval of the environment ministry's genetic engineering approval committee (GEAC), after going through cumbersome procedures and conducting time-consuming tests, besides furnishing a whole lot of information. To confound matters further, the health ministry has come out with another notification under the Prevention of Food Adulteration (PFA) Act, making it mandatory to suitably label all products, whether imported or indigenous, that are either produced through genetic modification or contain any ingredient or additive made from GM crops.

Together, these two moves have created a good deal of avoidable confusion in the processed foods and edible oil sectors. The first to get hit by these half-baked decisions has been the import of soyabean oil. Of nearly 5 million tonnes of edible oils imported annually to cover the domestic shortfall in supply, about 2 million tonnes are usually soya oil, sourced from countries like Argentina, Brazil and the US—where much of the soyabean crop happens to be genetically modified. As such, it is very difficult to get totally GM-free soya oil in the market. Ironically, even if GM soya oil is imported under a false declaration that it has no genetically modified content, it would be almost impossible to establish such a misdeclaration. That is because oil does not contain any protein, notably DNA, which alone can show whether it contains any GM inheritance or not. In any case, the damage has already been done as the uncertainty created over these imports has sent domestic soyabean oil prices soaring, especially in the futures market, where circuit breakers have had to be imposed in some cases on May soya oil contracts.

In fact, the implications of mandatory labelling of GM (and GM-derived) foods are even more far-reaching than the fairly simply matter of soya oil. Prima facie, it would seem like a good idea to most people that the consumer should be informed when something in the market is a GM product. But the sway of what has been announced by the government’s different ministries, in that these are applicable even to food additives, is so extensive that it would apply to almost all processed foods. The range here would be from wines and cheese to breads using GM yeast, and extending to traditional Indian milk products, including ghee, butter and sweets like barfi and rasagulla, if these are made from milk produced by cattle fed on GM cotton seeds and de-oiled cottonseed meal. Since GM cotton is now cultivated extensively in India, and its seeds are widely used as cattlefeed, it would be practically impossible to segregate those products requiring GM labelling from the rest.

It is also worth bearing in mind that if GM labelling is reduced to a meaningless routine—like the statutory health warning that has been on cigarette packets for decades—it would serve little purpose. Thus, the government needs to re-visit this complicated, yet significant, issue keeping in view all the problems that have cropped up. Especially because the decisions that have been taken so far are confined basically to the import and consumption of edible products and do not address the broader issue of import of non-food GMOs, including genetically modified living organisms (LMOs). What is clear is that this whole question needs to be viewed from the perspective of the Cartagena Protocol on the trans-boundary movement of GMOs. Only then will local practices on this subject conform to global norms, as required under international trade treaties.
Copyright Business Standard India

Food industry urges caution on biofuel promotion plan
By Ahmed ElAmin

A plan to increase biofuel production could lead to an increase in prices for agricultural ingredients, in particular rapeseed, the bloc's food industry association warns in a position paper.

The concern is expressed in a position paper published by the Confederation of the food and drink industries of the European Union (CIAA), which is calling for a careful monitoring of the effects of the plan on agricultural supplies and prices. The organisation also calls for biofuel production to be based on a diversified supply of agricultural products rather than just on one or two commodities.

In strategy plan adopted in February 2006, the European Commission set out measures to further increase the supply of biofuels. The strategy includes a plan to assess the impact of increasing the amount of biofuel that can be blended in petrol and diesel, an an examination of the use of certificates to ensure that the raw materials are cultivated in a sustainable way.

Biofuel is any fuel that derives from organic materials, including corn, soybeans, flaxseed and rapeseed. The food and drink industry is competing for some of the same raw materials, such as rapeseed, either for food production or for feedstock.

In its position paper the CIAA says the increase in demand for agricultural products for biofuels could decrease supply and raise prices for the food and feed sectors.

"Given the link between the different users of biomass -- food, feed, energy, and other non-food products-- the monitoring proposed by the Commission of the impact of the biofuels strategy on markets and on availability of agricultural raw materials is clearly essential for the food industry," the CIAA stated.

The Commission must also be willing to act in case of serious market imbalance through market measures. The EU should also use the measures to increase the possible feedstock supply for all markets without disrupting the food sector, the CIAA recommends.

The organisation noted that its members are already facing price increases for rapeseed oil. According to Oil World, rapeseed oil prices recently were up to 45 per cent above the five-year average to 2000. Demand for rapeseed oil within the EU is forecast to increase by 26 per cent.

"This trend can be explained by different factors, notably the development of the biodiesel industry and the total shift of food demand from soy oil into rapeseed oil because of the GMO (genetically modified organisms) issue," the CIAA stated.

Meanwhile cereals prices are forecast to increase by up to 11 per cent by the year 2010 and oilseed prices by between five to 15 per cent, the document stated.

The CIAA also called on the Commission to promote a more balanced development of biodiesel and bioethanol production. The CIAA believes that a diversification of sources for the production of biofuels will lessen the pressure on a single raw material supply.

CIAA advised the Commission to promote diversification by reviewing the biodiesel standard, as it would allow the better use of oils other than rapeseed. Sunflower oil, palm oil or soybean oil could also be promoted as the raw ingredient for biofuel production.

The CIAA urged the Commission to review of the current legal framework regarding animal fats and by-products so as to promote the use of such ingredients for biofuels production.

More authorisations of new GM rapeseed varieties for import and processing in the EU would also help reduce the supply pressure on non-GM European rapeseed used for foods.

The CIAA also stressed the need for the Commission to ensure that the byproducts derived from biofuel production comply with EU food safety standards, as these are likely to end up in the feed and food chain.

In a strategy plan published in February the Commission plans to promote increasing the use of biofuels to eight per cent of the bloc's energy requirements by 2015.

Proposed changes to U.S. patent rules would harm biotechnology companies

In January, the U.S. Patent and Trademark Office (PTO) proposed changes to patent rules that would restrict the number of claims examined in a single application and limit inventors’ rights to file continuation applications.

The Biotechnology Industry Organization (BIO) opposes these rule changes because they would have a negative impact on biotechnology companies.

“BIO believes that the PTO’s proposed rule changes will stifle biotech innovation,” BIO President & CEO Jim Greenwood stated. “It can take decades to develop a patented biotechnology invention, in part because these inventions must go through a rigorous regulatory approval process. Strong patent protections are needed to allow biotech companies to attract the investment needed to survive the long process of bringing a product to market. The changes in the PTO’s proposed rule will discourage investors from investing money in biotech innovations.”

“The PTO claims the rule changes are needed to address concerns about patent quality and to reduce the large number of backlogged patent cases. BIO believes that the proposed rules will not only lead to an increase in the number of application filings but also do nothing to address the quality concerns of the PTO. BIO recommends that the PTO hold public hearings and post advance notices of proposed rules before making such sweeping changes to patent rules,” Greenwood continued.

In comments to the PTO’s proposed rule filed yesterday, BIO recommended alternative means for reducing the backlog of patent applications, including an accelerated/deferred examination system, changes in the PTO examiner production system, increased examiner education, and improved cooperation with other patent offices.


National biotech meeting to be held at Cornell, June 12-14

ITHACA, NY - The National Agricultural Biotechnology Council (NABC) will hold its 18th annual meeting at Cornell University, on the Ithaca and Geneva campuses, June 12-14.

The meeting, entitled "Agricultural Biotechnology: Economic Development through New Products, Partnerships and Workforce Development," will address the role universities, and state and federal governments play in developing and moving research into the marketplace.

"As land grant universities seek new ways to fulfill their mission of serving society in the 21st century, they are increasingly using modern science and biotechnology, which has led to new products, economic development and job creation-main economic development themes of governments throughout the world," says Anthony Shelton, Cornell entomology professor and chairman of the NABC 18 organizing committee. "How we bridge these themes to our evolving land grant mission is a central focus of NABC 18."

The meeting revolves around four sessions: NABC member institutions' success stories, the function and role of university-based research parks in economic development, an up-close look at a local research park, and bridging the gap from lab to commercial product. It features 19 speakers, ranging from the president of the China Agricultural University to consultants and developers of products in the Netherlands, India, Brazil, Germany and Canada, to the director of an agricultural technology park, as well as many others.

NABC is a not-for-profit consortium of 36 leading agricultural research and teaching governmental agencies/institutions/universities in the U.S. and Canada. It has been hosting annual public meetings about the safe, ethical and efficacious development of agricultural biotechnology products since its formation in 1988, and is committed to providing all stakeholders the opportunity to speak, listen and learn about issues surrounding agricultural biotechnology.

A fee of $300 will apply for early bird registrants until May 10, after which the fee will increase to $350. Student registration is $200 until May 10, then $250.


Univ Saskatchewan 'Super gene' discovery holds promise of hardier crops

A University of Saskatchewan research team has discovered what it calls a "super gene" that makes crops more resistant to heat, cold and drought. lt also gets plants growing faster.

Now, plant sciences Prof. Larry Gusta and his team are wooing biotech companies to use the gene in the development of newly resilient crops, which could help farmers frustrated by drought and wacky weather.

"In a way, it is a super gene, and that's why there's several arge companies interested in licensing (it)," Gusta said.

Gusta and collaborator Albert Robertson, who is also a farmer, found a gene called Rob-5 is responsible for keeping a hardy perennial plant called brome grass tolerant to drought, heat and freezing.

When researchers treated grass cells in a dish with a hormone called abscisic acid, they found it was the Rob-5 gene that sprang into action, spurring the creation of protein to help protect the plant from harsh conditions.

Once they figured out which gene was esponsible, the team created so-called transgenic crops of canola, flax and potatoes by inserting the brome grass Rob-5 gene into those plants' genes.

When they planted the crops in fields across Manitoba, Saskatchewan and Alberta, they got a 25 to 30 per cent increase in crop yield -- and it was a dry year, Gusta added.

In laboratory chambers where they grew the crops under controlled conditions, researchers found the transgenic canola and flax had increased frost tolerance by two to four degrees Celsius, and potatoes bad another one degree leeway before they froze.

"lt's huge. lt's a huge deal," Gusta said, adding a temperature change of a few degrees can mean the difference between harvesting a crop or no crop at all for a farmer.

Other tests showed the plants were also more heat tolerant -- an important attribute for Saskatchewan crops that sometimes get baked on hot summer days.

"Two or three days with temperatures around 30 degrees and the flowers blast in canola and flax and you lose them," Gusta said.

The results are especially promising because few groups who are engineering such genes to make crops more resilient have good results from the field and the lab, Gusta said.

As a bonus, the gene got plants sprouting from seed more quickly, improving the yield and preventing the seed from rotting.

The university has a patent pending on the gene, and a large, unnamed biotech firm is in the process of inking a deal with the university to develop potential seeds for sale, Gusta said.

If it makes it to market, the product could be of huge help to farmers desperate for water who rely on pricey irrigation operations, Gusta said.

"If we could cut down water use. . . it would mean millions and millions of dollars in savings to the people who have to irrigate," he said.

The university sought a patent for the Rob-5 gene through its industry liaison office -- a university group that scours research findings for potentially marketable discoveries Doug Gill, the liaison office's managing director, said although he can't divulge specifics, the university is dose to signing a deal with a major corporation to market a product using Gusta's discovery.

The deal will mean the company should pay a licensing fee to be split 50-50 between the university and the researchers. If the product goes to market, the university can also expect to earn royalties, he said.

While nothing's inked yet, a typical agreement sees a company pay the university between 10 and 20 per cent ofthe profits, Gui said.

Thus far, the U of S has patented about 100 discoveries by university researchers and another 20 patents are pending. The university also picks up the fees for obtaining and maintaining patents. The bill for keeping up some worldwide patents sometimes runs into the hundreds of thousands of dollars, Gui said.

Still, he said the investment is worth it. Aithough it varies from year to year, the university earns between $750,000 and $1 .25 million annually from inventions it has marketed.

Gusta said the mystery company has already begun tests with his gene, and if all goes weil, more resilient seeds could be for sale within the next five years.
Copyright © Argus der Presse AG 2004

Calls for changes to laws governing gene technology in Australia largely rejected
By Anna Salleh

Calls for changes to the laws governing gene technology in Australia have been largely rejected in a new report, despite ongoing controversy over genetically modified crops.

A review of the Gene Technology Act 2000, by a government-appointed review panel, found there should only be minor changes to the Act, which it outlines in a report released this week.

The review also calls for states to end their moratoria on genetically modified (GM) crops.

"It was the issue that was raised at every forum - it was the hot issue," says review panel chair, environmental lawyer Susan Timbs.

The review rejects calls for the Act to be changed so that economic, social and marketing impacts of GM crops could be considered.

And it agrees with GM researchers and industry that GM and non-GM crops can co-exist.

The review also disagrees with some farming and consumer groups, that people releasing GM organisms (GMOs) be made strictly liable for any detrimental effects of their products.

More time to assess risky applications

But the review recommends some changes in the way the Office of the Gene Technology Regulator (OGTR) assesses applications for the release of GMOs.

The review recommends the regulator be given more time to assess applications for the commercial release of organisms deemed to be of "significant risk".

Timbs says under the proposal this would provide more time for public consultation.

But the time limit for assessing field trials would be reduced and industry and researchers conducting low risk work with GMOs would have less requirement to report their activities, Timbs says.

The review also recommends the Gene Technology Technical Advisory Committee (GTTAC), which advises the OGTR on risks, should include people with specific expertise in public health and environmental risk assessment.

Responses

Senator Stott Despoja, Australian Democrats' spokesperson on science and biotechnology, says while the review makes a few recommendations to improve the system, she disagrees with some of the findings.

"The report found a 'high level of transparency in relation to the regulatory system', which appears to be contradicted by the lack of information made available to the public on GM trials by the Office of the Gene Technology Regulator," she says.

"The report also found the states' moratoria on GM crops to have 'detrimental rather than beneficial impacts (on markets)'. Given the evidence of GM contamination of non-GM crops, and the lack of research into the impact of human consumption of GM products, the states are showing an appropriate level of caution in regard to this technology."

Professor Sue Serjeantson of the Australian Academy of Science says the Act has provided a climate of community confidence about GMO assessment.

But she says the moratoria are a disincentive for research and means the Act has failed to "capture the benefits of biotechnology for the Australian community, industry and the environment".

She says the moratoria may not be in place if the community had "access to quality information about biotechnology, the potential risks and benefits of its application".

"This highlights the necessity for the OGTR to be involved in increasing public awareness of GM technology, to assist the regulator applying the Act."

GENEREX BIOTECHNOLOGY SUBSIDIARY RECEIVES PATENT FROM EUROPEAN PATENT OFFICE

Award in Ii-Key Hybrids Technology to Regulate
Antigen Presentation by Immunoregulatory Cells

TORONTO - Generex Biotechnology Corporation announced May 1 that its wholly owned subsidiary, Antigen Express, Inc., has been granted a European patent titled “Regulation of Antigen Presentation”. The patent issued on December 21, 2005 relates to the use of Ii-Key peptides in regulating antigen presentation. It broadly covers the use of Ii-Key in potential immunotherapy treatments of cancer and infectious diseases.

Antigen Express is pursuing novel immunotherapeutics based on the antigen-specific stimulation of T helper cells. The use of Ii-Key to augment the potency of antigenic peptides constitutes one of two platform technologies being developed at the Company. The most advanced of these projects employs an Ii-Key modified peptide from the tumor-associated HER-2/neu protein. That compound has been in the clinic for a year in patients with breast cancer and has shown good activity in stimulating T helper cells to specifically recognize HER-2/neu. A similar vaccine employing Ii-Key and a fragment of the H5 protein from the H5N1 virus is being developed as a prophylactic vaccine for the potentially pandemic H5N1 avian influenza virus.

More Than 90 Percent of Growers Adhering to Bt Corn Borer Stewardship Requirements

ST. LOUIS - The National Corn Growers Association (NCGA) on April 28, 2006 announced that more than nine out of 10 growers are aware of and effectively complying with Insect Resistance Management (IRM) requirements as mandated by the Environmental Protection Agency (EPA). These findings are based on 2005 on-farm assessments along with an independent survey conducted on behalf of the Agriculture Biotechnology Stewardship Technical Committee (ABSTC).

Since 1999 Bt corn registrants - Dow AgroSciences, Monsanto, Pioneer Hi- Bred International, Inc., a subsidiary of DuPont, and Syngenta Seeds - have monitored adherence to the IRM requirements to help ensure that Bt corn borer technology remains effective against pests and is a tool readily available for all growers. This monitoring effort was expanded in 2002 with the development of the Compliance Assurance Program (CAP) which is designed to promote IRM awareness and assess implementation at the farm level.

2005 Survey Shows a Continued Positive Trend in Grower Refuge Management

The annual Bt corn borer IRM telephone survey, managed by an independent third party, shows the industry can have confidence that farmers are being good stewards and implementing refuge plans. In the 2005 survey 92 percent of U.S. Bt corn growers met or exceeded the minimum recommended refuge size. This level of adherence with the requirements is consistent with past results of 91 percent in 2004 and 86 percent in 2003. In a separate program of on- farm visits, more than 94 percent of producers assessed were found to be meeting the refuge requirements. Both large and small acreage growers are meeting refuge management requirements at similar levels.

The EPA-required Bt corn refuge obligates farmers to plant at least 20 percent refuge - that is, corn that does not contain a Bt gene for controlling corn borers. In certain cotton areas of the South, growers are required to plant at least a 50 percent refuge.

All areas of the country require that the refuge is planted within one- half mile of the Bt corn. In 2005 96 percent of growers adhered to this refuge distance requirement, an improvement over past years of 93 percent in 2004 and 89 percent in 2003.

"In 2003 the National Corn Growers Association established its online Insect Resistance Management Learning Center as a way to educate producers on the importance of IRM practices," said Martin Barbre, NCGA Biotechnology Working Group chairman. "We are pleased to see increased IRM implementation by producers, which helps ensure the Bt technology remains an available tool."

Industry Commitment to IRM Management

Growers reported the NCGA and seed companies marketing Bt hybrids are the leading sources for IRM information. Most growers surveyed recall receiving an average of four pieces of IRM literature and more than three-fourths of those surveyed noted having had an individual conversation with a seed company representative or seed dealer regarding these requirements.

U.S. Bt corn adopters have voiced their commitment to manage Bt crop technologies as 92 percent were clearly aware of the IRM and refuge requirements, and support them as an important part of preserving Bt technology for the future.

"The Biotech Working Group has engaged the technology providers and worked with the EPA to make sure NCGA is providing the correct information to its producers," Barbre said. "NCGA also works closely with its state organizations to provide information on insect resistance management. Through our online learning program, agriculture publications and printed materials, we work diligently to improve producer implementation of IRM requirements."

An element of the on-farm assessment program that reinforces how seriously Bt technology providers regard resistance management is the potential penalties for non-compliance. Failure to properly plant and manage refuges in two crop seasons can lead to a grower's inability to access technology for use on their farm in the third year.

Farmers visited in 2004 and found to be out of compliance came back into compliance in 2005, and have maintained access to corn borer protected Bt corn for this growing season.

For the small set of growers found to be non-compliant in 2005, Bt providers responded in accordance with the uniform industry standards developed to bring growers back into compliance. These standards outlined in the CAP include letters and additional IRM educational materials sent to growers as well as on-farm compliance assessments. Growers who repeatedly fail to adhere to IRM requirements risk losing access to the technology.

NCGA urges all producers to comply with IRM requirements in 2006

With the planting season starting across the United States, it is critical that growers and seed providers continue to focus on the effective implementation of IRM requirements. For assistance in managing Bt corn and refuge areas, growers are encouraged to seek information online at http://www.ncga.com/biotechnology/insectMgmtPlan/index.asp, or from their seed representative.

The Agricultural Biotechnology Stewardship Technical Committee (ABSTC) includes Bt corn registrants Dow AgroSciences; Monsanto; Pioneer Hi-Bred International, Inc., a subsidiary of DuPont, and Syngenta Seeds, Inc. The committee is working with the EPA to enforce IRM compliance. The National Corn Growers Association (NCGA) and the Biotechnology Industry Organization (BIO), along with various seed companies and universities, all support the Committee's IRM compliance efforts. For additional information on biotechnology, go to http://www.ncga.com/.


Michigan Senate approves bill on genetic modification

LANSING - The Michigan Senate signed off on legislation Thursday that aims to block local regulation of genetically modified crops.

The bill, which heads to Gov. Jennifer Granholm, would pre-empt local governments in Michigan from adopting ordinances that regulate or ban the planting of seeds, including genetically modified organisms, or GMOs.

But it includes an exception allowing for local regulation if the bipartisan state Commission of Agriculture agrees the seeds will hurt the environment or public health.

If a local government tried to ban the planting of seeds, the state Agriculture Department also would have to hold a public hearing and issue an opinion on whether environmental or public health effects will occur.

The Senate voted 24-12 to sign off on changes to the bill made by the House earlier this week.

Five California counties and cities have restricted farmers from growing genetically modified crops since 2004. Fourteen states have since passed laws barring similar measures.

Republicans have said federal regulators are better equipped to regulate GMOs than are local counties or townships, and have argued that landowners should have the right to plant what scientists have determined is safe, free from local interference.

But some Democrats have said GMOs threaten public health because its long-term effects are unknown.
Copyright © 1994-2005 South Bend Tribune

Global GM planting to rise 10% this year
By Rhea Sandique-Carlos

MANILA -The global land area used for genetically modified crops could rise by at least 10% this year from the previous year's total land area of 90 million hectares, due to growing adoption of biotech crops, the International Service For the Acquisition of Agri-Biotech Applications or ISAAA said April 25.

The ISAAA is a not-for-profit organization that delivers the benefits of new agricultural biotechnology to developing countries.

"We're optimistic it will be at least a double-digit improvement from last year," Randy Hautea, Manila-based global coordinator of ISAAA, told reporters on the sidelines of an international sugar forum in Manila.

"It will be safe and conservative to say biotech areas will increase by 10% this year," Hautea said, noting that areas planted with genetically modified crops improved by 11% to 90 million hectares in 2005, up from 81 million hectares in the previous year.

The growth will be driven mainly by expansion in genetically modified soybeans, cotton, corn and canola plantations, he said.

Worldwide, areas planted with genetically altered soybeans account for 60% of total biotech areas, cotton accounts for 28%, canola with 15% and corn crops contribute 14%.

In the Philippines, resistance to the commercial use of genetically modified corn has been steadily declining over the years since it was first introduced in 2003, Hautea said.

Areas planted with biotech corn totaled 70,000 hectares in 2005, a 34% improvement from the previous year, he said.

In the past ten years, the use of genetically altered crops has resulted in global economic benefits of around $27 billion, and reduced more than 170 million kilograms of pesticide use, Hautea said.

Genetically modified crops are also mostly herbicide resistant, he added.
Copyright ©2004 CattleNetwork.com

GMO bill hard on manufacturers
By Ross Sneyd

MONTPELIER, USA — Manufacturers of genetically engineered seeds could be liable for damages if their products drift into the fields of neighboring farmers who don't want them under a bill that won approval Tuesday April 25 in the Vermont House.

The proposal could put Vermont at the forefront of a heated national debate about the wisdom of using the seeds and plants, which can be scientifically modified to resist pests or disease. Some farmers and consumers don't want such technology being used on their food. But others say it's an important way to keep food economical and to control the use of pesticides on farm fields.

That divide was starkly illustrated in the Statehouse. Supporters and opponents thronged the House chamber to witness the debate on a compromise version of the bill that's been debated in the Legislature for the past year and a half.

"As an organic farmer, my job is to make sure I'm producing a crop that's free of genetically modified (organisms)," said Leceister dairy farmer Annie Claghorn after the House voted 77-63 in favor of the bill.

But opponents were out in equal force to demonstrate to Gov. Jim Douglas, who has made pretty clear he'll veto the bill if it wins Senate approval, that they'll back him.

"We're here to show the governor he has the vote when, hopefully, he vetoes it," said St. Albans dairy farmer Mitch Montagne, standing outside the governor's office after the vote.

The issue in the legislation is fairly arcane. The bill was designed to give farmers who don't want to use modified seeds a forum to address their grievances if pollen from modified plants drift into their crops.

The bill would treat farmers as consumers and would allow them to sue a seed manufacturer, claiming the so-called drift into his or her field was a private nuisance. Such a claim could only be made if the farmer could prove that his or her total loss exceeded $3,500.

"This is a bill to protect all farmers, especially those who use genetically modified seeds," said Rep. Dexter Randall, P-Troy, the primary sponsor of the bill and a dairy farmer.

He and others said it was an attempt to give farmers a greater say over their businesses. Although manufacturers retain ownership of the genetically engineered seeds and plants and only lease them to farmers, the companies have been insulated from damage claims.

The new bill would protect a farmer using the genetically engineered seeds, making manufacturers liable for damages. Supporters said that's why they believed the bill would be good for both conventional farmers and organic farmers, who are among the leaders in opposing the use of the genetically altered seeds.

"This bill is not about dividing these farmers," said Rep. Rosemary McLaughlin, D-Royalton. "(It) is about protecting these two types of farmers."

Rep. William Johnson, R-Canaan, also a dairy farmer, argued that all the bill would do was erroneously call into question the safety of genetically modified organisms. "It's based on a false premise," he said. "It's based on the premise that there's something wrong with genetically engineered seeds or biotechnology."
Copyright © 2006 Associated Press

Argentina seed makers criticize New GMO corn rules

BUENOS AIRES, Argentina - Top seed makers have criticized an Argentine decision to encourage new companies to enter the genetically modified corn market, accusing the government of trampling intellectual property rights.

Seed companies say a government resolution passed in February paves the way for firms to seil corn containing gene technology they have obtained illegaily, and they warn the changes will send biotech crop investment plunging.

Argentina, the world's No. 2 corn exporter and the biggest grower of genetically modified crops after the United States, says the move is aimed at fostering competition and increasing the supply of corn seeds.

Last year it approved the herbicide-resistant GA21 gene developed by Switzerland's Syngenta , but it has not yet given approval for any specific GA21 corn variety containing the gene to go on the market.

Syngenta is leading criticism of the new rule, which establishes a 90-day period during which companies that want to seil corn seeds containing the approved gene can submit their applications to the government.

"Syngenta ends up losing because its intellectual property rights are being ignored. We bore the entire cost to develop (the technology)," said Hernan Pettinari, general manager of Syngenta's seed division in Argentina.

The Association of Argentine Seedmakers says the three-month period will give seed companies that have obtained the gene technology iliegally the chance to get their own corn seeds approved for sale in the lucrative Argentine market.

But Agriculture Secretary Miguel Campos has defended the controversial measure. "The exception granted is the start of a new paradigm that will facilitate the registering of (corn) varieties and hybrids that contain genes freed for commercialization," Campos said in a statement on Thursday.

EXTENSIVE TESTS

The seed makers association, known as ASA, says companies must conduct extensive tests on a new GMO variety before seeking permission to seil it on the market. And, as Syngenta was the only firm authorized to do such research, any other companies would have violated the law by doing so.

ASA -- whose members include Syngenta, U.S.-based Monsanto Co. and some 50 other seed companies -- says it will fight to the last to get the resolution overturned.

One company told Reuters it had asked the government for permission to seil GA21 corn, and local media say two other companies may have done the same.

"We made the petition (to seil GA21 corn), but we haven't committed any crime. We're within the framework of what the state requires under the country's seed law," said Ricardo Zaccardi, president of Argentina's Plusagro.

The loosening of norms to authorize the new GMO corn comes after years of increasing biotech soybean production, which has gobbled up lands often at the expense of grains such as corn.

Argentina's soy output began surging after Monsanto's Roundup Ready soybeans were approved for seeding in the mid-1990s. Monsanto engineered these soy seeds to resist its Roundup herbicide, known generically as glyphosate, and the company is locked in a battle with Argentina over how best to charge fees on them.

The Agriculture Secretariat forecasts planted soybean area at a record 15.2 million hectares this season, compared with the 3.05 million hectares seeded with corn.

Many experts think Argentina's farm sector can be sustained only if crops are rotated, and corn is particularly useful for replenishing soil nutrients that soy saps. This is another reason the government cites for promoting GA21 corn.

"As we did with soy, we need to hasten the creation of a virtuous cycle for corn as weil," Campos said.
Copyright © Argus der Presse AG 2004.

The First Decade of Genetically Engineered Crops in the United States

Ten years after the first generation of genetically engineered (GE) varieties became commercially available, adoption of these varieties by U.S. farmers is widespread for major crops.

Driven by farmers’ expectations of higher yields, savings in management time, and lower pesticide costs, the adoption of corn, soybean, and cotton GE varieties has increased rapidly. Despite the benefits, however, environmental and consumer concerns may have limited acceptance of GE crops, particularly in Europe.

This report focuses on GE crops and their adoption in the United States over the past 10 years. It examines the three major stakeholders of agricultural biotechnology and finds that:

1. The pace of R&D activity by producers of GE seed (the seed firms and technology providers) has been rapid
2. Farmers have adopted some GE varieties widely and at a rapid rate and benefited from such adoption, and 3. The level of consumer concerns about foods that contain GE ingredients varies by country, with European consumers being most concerned.

Summary

Over the past decade, developments in modern biotechnology have expanded the scope of biological innovations by providing new tools for increasing crop yields and agricultural productivity.

The role that biotechnology will play in agriculture in the United States and globally will depend on a number of factors and uncertainties. What seems certain, however, is that the ultimate contribution of agricultural biotechnology will depend on our ability to identify and measure its potential benefits and risks.

What Is the Issue?

Ten years after the first generation of genetically engineered (GE) varieties of major crops became commercially available, adoption of these varieties by U.S. farmers has become widespread. United States consumers eat many products derived from these crops--including some cornmeal, oils, sugars, and other food products--largely unaware of their GE content. Despite the rapid increase in the adoption of GE corn, soybean, and cotton varieties by U.S. farmers, questions remain regarding the impact of agricultural biotechnology. These issues range from the economic and environmental impacts to consumer acceptance.

What Did the Study Find?

This study examined the three major stakeholders in agricultural biotechnology: seed suppliers and technology providers, farmers, and consumers.

Seed suppliers/technology providers. Strengthening of intellectual property rights protection in the 1970s and 1980s increased returns to research and offered greater incentives for private companies to invest in seed development and crop biotechnology. Since 1987, seed producers have submitted nearly 11,600 applications to USDA’s Animal and Plant Health Inspection Service for field testing of GE varieties. More than 10,700 (92 percent) have been approved. Approvals peaked in 2002 with 1,190. Most approved applications involved major crops, with nearly 5,000 for corn alone, followed by soybeans, potatoes, and cotton. More than 6,600 of the approved applications included GE varieties with herbicide tolerance or insect resistance. Significant numbers of applications were approved for varieties with improved product quality, viral resistance, and enhanced agronomic proper- ties such as drought and fungal resistance.

Farmers. Adoption of GE soybeans, corn, and cotton by U.S. farmers has increased most years since these varieties became commercially available in 1996. By 2005, herbicide-tolerant soybeans accounted for 87 percent of total U.S. soybean acreage, while herbicide-tolerant cotton accounted for about 60 percent of total cotton acreage. Adoption of insect-resistant crops is concentrated in areas with high levels of pest infestation and varies across States. Insect-resistant cotton was planted on 52 percent of cotton acreage in 2005--ranging from 13 percent in California to 85 percent in Louisiana. Insect-resistant corn accounted for 35 percent of the total acreage in 2005, following the introduction of a new variety to control the corn rootworm.

The economic impact of GE crops on producers varies by crop and technology. Herbicide-tolerant cotton and corn were associated with increased returns, as were insect-resistant cotton and corn when pest infestations were more prevalent. Despite the rapid adoption of herbicide-tolerant soybeans, there was little impact on net farm returns in 1997 and 1998. However, the adoption of herbicide-tolerant soybeans is associated with increased off- farm household income, suggesting that farmers adopt this technology because the simplicity and flexibility of the technology permit them to save management time, allowing them to benefit from additional income from off-farm activities.

Genetically engineered crops also seem to have environmental benefits. Overall pesticide use is lower for adopters of GE crops, and the adoption of herbicide-tolerant soybeans may indirectly benefit the environment by encouraging the adoption of soil conservation practices.

Consumers. Most surveys and consumer studies indicate consumers have at least some concerns about foods containing GE ingredients, but these concerns have not had a large impact on the market for these foods in the United States. Despite the concerns of U.S. consumers, "GE-free" labels on foods are not widely used in the United States. Manufacturers have been active in creating a market for GE-free foods. Between 2000 and 2004, manufacturers introduced more than 3,500 products that had explicit non- GE labeling, most of them food products.

In the European Union and some other countries, however, consumer concerns have spurred a movement away from foods with GE ingredients. Despite the fact that some European consumers are willing to consume foods containing GE ingredients, very few of these foods are found on European grocery shelves.

Conclusion

The role that biotechnology plays in agriculture in the United States and globally depends on a number of factors and uncertainties. As the USDA Advisory Committee on Biotechnology and 21st Century Agriculture report indicates, "agricultural biotechnology sits at the crossroads of other debates on the future of American and world agriculture, on international trade rela- tions, on biological diversity and the development of international instruments related to its preservation and exploitation, on the role of the multinational corporations, and on how best to build public confidence in rapidly evolving emerging technologies in general".

One thing seems certain, however: the ultimate contribution of agricultural biotechnology will depend on our ability to identify and measure its potential benefits and its risks as well as their distribution.

Jorge Fernandez-Cornejo and Margriet Caswell,
USDA Economic Information Bulletin No. (EIB-11) 36pp, April 2006. Full report at
http://www.ers.usda.gov/publications/eib11/eib11.pdf
© 2005 AgBioWorld.

Food modification could leave us biodegraded

The global biotech industry trade show, which wrapped up last week in Chicago, featured the world's largest genetically modified indoor cornfield, compliments of Monsanto. lt attracted celebrity speakers, including former President Bill Clinton, former NBA star Magic Johnson and actor Bernie Mac.

And it hammered home the message that biotechnology, which essentially looks for innovative ways to manipulate nature, can save our overpopulated world from disease, starvation and pollution.

Here's a look at what BIO 2006 didn't include in its massive 470-page program. Maybe next year?

A breakfast plenary featuring Canadian farmer Percy Schmeiser.

Monsanto sued Schmeiser for patent infringement after genetically modified canola seeds mysteriously cropped up in his fields. Schmeiser argued the GM seeds arrived and rooted by accident, most likely blowing in from neighboring fields.

Eventually, the Supreme Court of Canada found the 75-year-old guilty of violating the patent rights ofthe powerful multinational corporation. But Schmeiser, now a leading biotech critic, didn't have to pay Monsanto because he did not profit from the canola. "Once you introduce genetically modified organisms (GMOs), there's no falling back," Schmeiser said last week during the rival Bi0ETHICS 2006 conference at Columbia College, an event held to raise awareness of the dangers of genetically modified foods. "You can't contain or coexist with GMOs. You can't control wind, movement by animals. They destroy natural crops.

Schmeiser also criticized Monsanto's patented "terminator seeds," which are engineered to die every year. Farmers become siaves to Monsanto because they are forced to buy new seeds on an annual basis, the antithesis of sustainable development, Schmeiser said.

A debate over whether genetically modified food should be labeled. By some estimates, 70 percent of the food on grocery store shelves may contain biotech ingredients, but only 25 percent of Americans think they've eaten genetically modified food. Wake up!

Biotech ingredients most often are found in cornstarch and soybean oil, but milk is bioengineered if the cows have been given recombinant bovine growth hormone (rBGH)— made only by Monsanto — to increase milk output. On the market since 1994, rBGH milk is added to cream, cheese, yogurts and baked goods.

The Food and Drug Administration, which doesn't require GMO labeling, says artificial growth hormones are safe, but they're banned in Europe and Canada. The concern is over studies that have shown injections of rBGH can increase another hormone called insulin-like growth factor-1 or IGF-1 in cow's milk. High rates of IGF-1 are Iinked with increased rates of colon, breast and prostate cancer. Europe, Japan, China, Australia and New Zealand require the labeling of foods that contain genetically engineered ingredients. lndustry maintains that labeling would unnecessarily scare people away from GMO food, which is considered safe, even though no long-term studies have been done. But labeling is important because it means people would have a choice. The only real way to avoid GMO food is to buy organic or grow your own, provided you're not downwind from a Monsanto field.

Given that organic products now can be found at Wal-Mart, it's safe to say consumers want a choice.
Copyright © Argus der Presse AG 2004.

GENEREX BIOTECHNOLOGY RECEIVES ADDITIONAL PATENT IN MEXICO

Company Expands Drug Delivery Platform Patent Portfolio

TORONTO – Generex Biotechnology Corporation announced April 23 that it has been granted a patent by the Mexico National Registry of Patents titled “Aerosol Pharmaceutical Formulation for Pulmonary and Nasal Delivery.”

The patent, an extant United States Patent registered by the Company, relates to an improved delivery system for the administration of large-molecule pharmaceuticals which may be administered by means of an aerosol into the mouth for buccal, nasal or pulmonary application.

"We are happy to further enhance the Company's existing drug delivery platform patent portfolio in the region and which emphasizes the broad application of our platform technology,” said Rose Perri, the Company’s Chief Operating Officer. “We look forward to developing and improving existing aerosol pharmaceutical formulations using the Company’s RapidMist™ system.”

The Company currently holds an aggregate of 72 patents worldwide (19 of which are United States patents) and has an aggregate of 58 patent applications pending in various jurisdictions.

Generex is engaged in the research and development of drug delivery systems and technologies. Generex has developed a proprietary platform technology for the delivery of drugs into the human body through the oral cavity (with no deposit in the lungs). The Company’s proprietary liquid formulations allow drugs typically administered by injection to be absorbed into the body by the lining of the inner mouth using the Company’s proprietary RapidMist™ device. The Company’s flagship product, oral insulin (Oral-lyn™), which has been approved for commercial sale in Ecuador for the treatment of patients with Type-1 and Type-2 diabetes, is in various stages of clinical trials around the world.

Potential of genetically engineered crops
By Mbae Lawrence

As the proponents of biotechnology have been crusading that genetically engineered crops could relieve hunger around the world, there is some evidence that biotech crops really could make a difference, at least in southern Africa.

Corn is a staple crop throughout the region, including countries like Zambia and Zimbabwe, where production has been steadily declining.

In most African countries, people rely on corn for up to 60 percent of their diet despite corn yields being terrible by world standards, not to mention US standards.

Lack of commercial fertiliser is part of the problem, but so is the lack of pesticides to control the stalk-destroying insect larvae so familiar to US growers.

Farmers in South Africa started using Bt corn, bioengineered to kill corn borers, and it is making a meaningful difference for both large, commercial farms and small-scale growers, according to a report by economists at the Agriculture Department and Rutgers, the State University of New Jersey.

Yields on large farms have increased about 11 percent with small-scale farmers also benefiting more often.

Yields for small farms shot up as much as 56 percent in two areas of the country, the report found.

Increases in four other regions varied from 7 percent to 47 percent. To put this in perspective, the average corn yield in South Africa, which has the region's most productive farmers by far, is less than three tons per hectare, or well under 50 bushels per acre.

Biotech corn only started to take off in South Africa in 2001 and 2002. Last year, farmers planted about a million acres of the crop, or about 15 percent of their production, according to Monsanto Company.

Theoretically, these increased yields should be good news to farmers in other southern African nations.

In some countries, in fact, the USDA-Rutgers study says Bt corn could reduce food shortages significantly.

In Lesotho, for example, where the average corn yield is about one-third of South Africa's, Bt corn could increase food consumption by 16 percent and that’s if Bt corn only boosted yields by 11 percent, the increase reported by South Africa's large farms. Angola, Malawi, Mozambique, Zambia and Zimbabwe also could see significant impacts.

Bt corn "can benefit Africa because it can substantially increase crop yields and reduce pesticide use," the report concluded.

Trouble is that farmers there aren't likely to be planting biotech seeds for a long time. South Africa is struggling with how to get the seeds in the hands of small-scale farmers since majority can't afford the cost.

It's tough for companies to cut their seed prices because of the cost of dealing with the thousands of small farms, the report say.

In South Africa, every farmer who buys biotech corn seed must sign a contract identifying where they are growing the crop and spelling out how they will comply with planting restrictions intended to prevent insects from becoming resistant to the plant's toxin.

The problems facing farmers in other countries are more basic with some of the countries avoiding growing biotech corn for fear they will never be able to sell their crops to Europe, where opposition to biotechnology is strong.

Zambia, Zimbabwe and Angola have either refused to take donated US corn or insisted that it be milled first while other countries have yet to take any steps towards allowing the cultivation of biotech crops.

In east Africa, Kenya is testing biotech corn and other crops whereas; Burkina Faso and Mali are moving towards production of Bt cotton in the west.

According to Calestous Juma, a native Kenyan who is an expert on biotechnology and international development at Harvard University, genetically modified seeds will ease as farmers hear about the growers' experience in South Africa and China. "You can't underestimate the power of a good example," he added.

Copyright © 2006 Times News Services Ltd

GM food - is it safe or not?
By Sheena Adams

BLOEMFONTEIN - Ground-breaking new trials using both animals and human cells to test the safety of genetically modified food products will begin soon at the country's only GM testing facility in the Free State.

Also called Frankenfoods, genetically modified organisms (GMOs) have been the subject of a raging worldwide debate for several years, with scientists divided over how safe they are to consume.

Many agree that while tests have so far failed to show conclusively that GMOs are bad for your health, no long-term tests have ever been attempted.

The project by the GMO testing facility at the University of the Free State has been described as the first "generational study", and will see scientists feeding a diet of GMO maize and soya beans to families of rats, mice and lambs over several years. The head of the facility, Professor Chris Viljoen, said this would be the first study of its kind in the world, but results would not be forthcoming for at least three years.

He added that the large-scale study was still dependent on the facility finding donors to fund the project, which he hoped to begin early next year.

"A lot of research we are funding ourselves, because the whole issue regarding GMOs is an emotional one. The fact that we are a facility that does testing means most people consider us to be anti-GM - it's actually quite ironic - and because of that, there are a number of scientists in South Africa who don't think what we are doing is important," Viljoen said.

State