Corporate Europe Observatory

Exposing the power of corporate lobbying in the EU

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Approving the GM potato: conflicts of interest, flawed science and fierce lobbying

In June 2009, experts from the European Food Safety Authority (EFSA)’s panel on genetically modified organisms (GMO panel) approved the use of an antibiotic marker gene for GMOs. This controversial decision was key for the European Commission in giving the green light in March 2010 to grow BASF’s genetically modified Amflora potato in the EU. CEO has investigated the background to this decision, including the controversial scientific advice provided by the European Food Safety Authority on the use of antibiotic resistant marker genes. CEO found that more than half of EFSA's GMO panel had conflicts of interest, as defined by the OECD. Their advice, which contravened WHO guidelines, contributed to the approval of the GM potato - and is likely to lead to the approval of similar GM crops in the near future.

Amflora is now being cultivated in open fields in Germany, Sweden and the Czech Republic, and two other GM plants (both cottons developed by Monsanto) containing the same antibiotic marker gene are in the pipeline waiting approval for cultivation.

The Amflora potato contains the nptII gene, an antibiotic resistance marker gene for neomycin and kanamycin. There are concerns that this antibiotic resistance could be transferred from the potato cells to bacteria dangerous to humans. Such a migration would reduce the effectiveness of these antibiotics in humans.

The approval of Amflora was the result of a fierce lobbying battle by BASF – which included an avalanche of letters sent to the Commission, threats to relocate outside the EU, and even legal action against the Commission.

This report by Corporate Europe Observatory (CEO) presents findings that make the EFSA June 2009 opinion even more controversial. Firstly, more than half of the GMO panel experts who signed the approval had conflicts of interest, as defined by the Organisation for Economic Co-operation and Development (OECD).

These conflicts ranged from receiving research funding from the biotech industry, being a member or collaborator in a pro-biotech industry association, to writing or reviewing industry-sponsored publications. Some conflicts revealed a conflict of scientific interests, with some panel members involved in working on the creation of transgenic plants – including potatoes – with antibiotic-resistant marker genes – including nptII.

Secondly, although none of EFSA’s GMO panel members were medical experts in the use of antibiotics in human medicine, they decided that neomycin and kanamycin were antibiotics with “no or only minor therapeutic relevance”. The World Health Organisation (WHO) classified these antibiotics as “critically important” in 2005.

This research shows that the Dutch scientist Harry Kuiper, chair of the GMO panel who had close links to the biotech industry, played a key role in the framing of this disputed key scientific advice. The opinion in fact reconfirmed an April 2004 GMO panel opinion, which itself was almost entirely a copy-paste of a “review paper” sponsored by a controversial EU-funded research project called ENTRANSFOOD, in which the biotech industry played a major role. For some reason this review paper was not credited by the GMO panel in 2004.

CEO found that (a) the authors of that review paper did not appear to have the necessary medical expertise to credibly classify some antibiotics as having “no or only minor therapeutic relevance”, (b) several authors appear to have been positively biased towards the biotech industry, and (c) all the authors were selected by Harry Kuiper, who was at that time coordinator of ENTRANSFOOD.

What is more, the original GMO panel decision appears to have been an attempt to protect GMO crops from an incoming EU directive, which sought to phase out the use of antibiotic resistance marker genes which may have adverse effects on human health and the environment.

In the light of these new findings, CEO is calling for an immediate independent reassessment of the scientific green light given to BASF’s Amflora potato and of the health and environmental risks of antibiotic resistance marker genes present in GM plants. The ongoing approval procedures for cultivation in the EU of the other GM plants containing the controversial nptII marker gene should be put on hold.

EFSA should remove members of the GMO panel that have industry ties, and should re-establish a panel made up entirely from independent scientists.

Read the full report below.

Update January 2012: Since the publication of the report, the Commission has informed us that the Monsanto GM cotton applications are only for food and feed use, and no longer for cultivation. The documents on the EU GMO Compass website however still indicate that the application is for cultivation as well.

The EC explains: “The document on MON531 which you refer to is a notification concerning cotton MON531 for cultivation, feed uses and import, submitted in 1996 by Monsanto to Spain under Directive 90/220/EC. Since the file was still pending at the adoption of Regulation (EC) 1829/2003 on GM food/feed, Monsanto was requested to submit a new file under the Regulation which they never did. As a consequence, there is no such notification anymore.”

The same goes for Monsanto's GM cotton MON1445.

Amflora is now being cultivated in open fields in Germany, Sweden and the Czech Republic, and two other GM plants (both cottons developed by Monsanto) containing the same antibiotic marker gene are in the pipeline waiting approval for cultivation.The Amflora potato contains the nptII gene, an antibiotic resistance marker gene for neomycin and kanamycin. There are concerns that this antibiotic resistance could be transferred from the potato cells to bacteria dangerous to humans. Such a migration would reduce the effectiveness of these antibiotics in humans.The approval of Amflora was the result of a fierce lobbying battle by BASF – which included an avalanche of letters sent to the Commission, threats to relocate outside the EU, and even legal action against the Commission.This report by Corporate Europe Observatory (CEO) presents findings that make the EFSA June 2009 opinion even more controversial. Firstly, more than half of the GMO panel experts who signed the approval had conflicts of interest, as defined by the Organisation for Economic Co-operation and Development (OECD).These conflicts ranged from receiving research funding from the biotech industry, being a member or collaborator in a pro-biotech industry association, to writing or reviewing industry-sponsored publications. Some conflicts revealed a conflict of scientific interests, with some panel members involved in working on the creation of transgenic plants – including potatoes – with antibiotic-resistant marker genes – including nptII.Secondly, although none of EFSA’s GMO panel members were medical experts in the use of antibiotics in human medicine, they decided that neomycin and kanamycin were antibiotics with “no or only minor therapeutic relevance”. The World Health Organisation (WHO) classified these antibiotics as “critically important” in 2005.This research shows that the Dutch scientist Harry Kuiper, chair of the GMO panel who had close links to the biotech industry, played a key role in the framing of this disputed key scientific advice. The opinion in fact reconfirmed an April 2004 GMO panel opinion, which itself was almost entirely a copy-paste of a “review paper” sponsored by a controversial EU-funded research project called ENTRANSFOOD, in which the biotech industry played a major role. For some reason this review paper was not credited by the GMO panel in 2004.CEO found that (a) the authors of that review paper did not appear to have the necessary medical expertise to credibly classify some antibiotics as having “no or only minor therapeutic relevance”, (b) several authors appear to have been positively biased towards the biotech industry, and (c) all the authors were selected by Harry Kuiper, who was at that time coordinator of ENTRANSFOOD.What is more, the original GMO panel decision appears to have been an attempt to protect GMO crops from an incoming EU directive, which sought to phase out the use of antibiotic resistance marker genes which may have adverse effects on human health and the environment.In the light of these new findings, CEO is calling for an immediate independent reassessment of the scientific green light given to BASF’s Amflora potato and of the health and environmental risks of antibiotic resistance marker genes present in GM plants. The ongoing approval procedures for cultivation in the EU of the other GM plants containing the controversial nptII marker gene should be put on hold.EFSA should remove members of the GMO panel that have industry ties, and should re-establish a panel made up entirely from independent scientists.Read the full report below.Update January 2012: Since the publication of the report, the Commission has informed us that the Monsanto GM cotton applications are only for food and feed use, and no longer for cultivation. The documents on the EU GMO Compass website however still indicate that the application is for cultivation as well.The EC explains: “The document on MON531 which you refer to is a notification concerning cotton MON531 for cultivation, feed uses and import, submitted in 1996 by Monsanto to Spain under Directive 90/220/EC. Since the file was still pending at the adoption of Regulation (EC) 1829/2003 on GM food/feed, Monsanto was requested to submit a new file under the Regulation which they never did. As a consequence, there is no such notification anymore.”The same goes for Monsanto's GM cotton MON1445.
 

The official EU assessment of glyphosate was based on unpublished studies owned by industry. Seven months later, the pesticide industry still fights disclosure and, so far, successfully. We obtained a copy of their arguments.

The European Commission proposal on scientific criteria defining endocrine disruptors (EDCs) is the latest dangerous outgrowth of a highly toxic debate. The chemical lobby, supported by certain Commission factions (notably DG SANTE and the Secretary-General) and some member states (UK and Germany), has put significant obstacles in the way of effective public health and environment regulation.

This May is dense on the EU chemicals regulation front. Crunch time for two major files: the European Commission needs to publish the identification criteria for endocrine disrupting chemicals, and together with EU States must decide how, or not, renew the market approval of glyphosate, an herbicide produced and defended by Monsanto. Last week, the Professor Alan Boobis happened to be involved in both.

Demonstrating the problematic symbiosis between corporate interests and EU institutions, the same lobbying consultancies often get hired by both.

The Commission is set to announce its proposal for a new ‘mandatory’ lobby transparency register next week. During the Summer, the Commission made public the input it received via consultation on the topic. Besides a general call from public and civil society to boost transparency systems, they also showed corporate lobby groups and trade associations’ spin, promoting transparency values while recommending limited implementation, loopholes and toothless management.

CEO's reaction to the the Bahamas leaks, which revealed ex-EU competition commissioner Neelie Kroes' offshore links.

The European Commission is about to propose a regulation on acrylamide, a dangerous contaminant formed in many starchy foods when cooked at high temperatures. But the regulation itself consists in referring to codes of best practices developed by lobby groups representing the food industry.

A new report on the Comprehensive Economic Trade Agreement (CETA) reveals how the trade deal could make EU member states vulnerable to costly lawsuits from North American investors that threaten public interest.

 
 
 
 
 
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