Food/Feed and Environmental Risk Assessment of Insect-resistant and Herbicide-tolerant Genetically Modified Maize GA21 from Syngenta Seeds for Food and Feed Uses, Import and Processing under Regulation (EC) No 1829/2003 (EFSA/GMO/UK/2005/19)

A. Andreassen, P. Brandtzæg, M. Finne, A. Holck, A. Jevnaker, O. Junttila, Heidi Sjursen Konestabo, R. Meadow, A. Mikalsen, K. Nielsen, M. Sanden, V. Sipinen, R. Vikse, H. Opsahl-Sorteberg
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Opsahl-Sorteberg","doi":"10.9734/ejnfs/2020/v12i330202","DOIUrl":null,"url":null,"abstract":"In preparation for a legal implementation of EU-regulation 1829/2003, the Norwegian Scientific Committee for Food Safety (VKM) has been requested by the Norwegian Environment Agency (former Norwegian Directorate for Nature Management) and the Norwegian Food Safety Authority (NFSA) to conduct final food/feed and environmental risk assessments for all genetically modified organisms (GMOs) and products containing or consisting of GMOs that are authorized in the European Union under Directive 2001/18/EC or Regulation 1829/2003/EC. The request covers scope(s) relevant to the Gene Technology Act. The request does not cover GMOs that VKM already has conducted its final risk assessments on. However, the Agency and NFSA requests VKM to consider whether updates or other changes to earlier submitted assessments are necessary.  \n The herbicide-tolerant genetically modified maize GA21 from Syngenta Seeds (Unique Identifier MON-ØØØ21-9) is authorised for the import and placing on the market as food or feed in the EU pursuant to Regulation (EC) 1829/2003 by the Commission Decision 2008/280/EC. An application for granting consent to all uses of GA21 maize including the cultivation was submitted by Syngenta in accordance with articles 5 and 17 of the Regulation (EC) No. 1829/2003 on June 30 2008.  \n Maize GA21 has previously been assessed as food and feed by the VKM GMO Panel commissioned by the Norwegian Food Safety Authority in connection with the national finalisation of the procedure  of the notification C/ES/98/01 in 2005 (VKM 2005a). VKM also participated in the 90 days public consultation of the application for placing on the market of maize GA21 for food and feed uses, import, processing and cultivation (EFSA/GMO/UK/2008/60) in 2009, and submitted a preliminary opinion in April 2010 (VKM 2010). GA21 has also been evaluated by the VKM GMO Panel as a component of several stacked GM maize events under and Regulation (EC) 1829/2003 (VKM 2008, VKM 2009a,b,c,d, VKM 2012a,b,  VKM 2013a,b,c). Due to the publication of new scientific literature and updated guidelines for risk assessment of genetically modified plants, the VKM GMO Panel has decided to deliver an updated food/feed and environmental risk assessment of GA21. \n The updated  food/feed and environmental risk assessment of the maize GA21 is based on information provided by the applicant in the applications EFSA/GMO/UK/2005/19, EFSA/GMO/UK/2008/60 and EFSA/GMO/RX/GA21 and scientific comments from EFSA and other member states made available on the EFSA website GMO Extranet. The risk assessment also considered other peer-reviewed scientific literature as relevant.   \n The VKM GMO Panel has evaluated GA21 with reference to its intended uses in the European Economic Area (EEA), and according to the principles described in the Norwegian Food Act, the Norwegian Gene Technology Act and regulations relating to impact assessment pursuant to the Gene Technology Act, Directive 2001/18/EC on the deliberate release into the environment of genetically modified organisms, and Regulation (EC) No 1829/2003 on genetically modified food and feed. The Norwegian Scientific Committee for Food Safety has also decided to take account of the appropriate principles described in the EFSA guidelines for the risk assessment of GM plants and derived food and feed (EFSA 2011a), the environmental risk assessment of GM plants (EFSA 2010), selection of comparators for the risk assessment of GM plants (EFSA 2011b) and for the post-market environmental monitoring of GM plants (EFSA 2011c).  \n The scientific risk assessment of maize GA21 include molecular characterisation of the inserted DNA and expression of novel proteins, comparative assessment of agronomic and phenotypic characteristics, nutritional assessments, toxicology and allergenicity, unintended effects on plant fitness, potential for gene transfer, interactions between the GM plant and target and non-target organisms and effects on biogeochemical processes.  \n It is emphasized that the VKM mandate does not include assessments of contribution to sustainable development, societal utility and ethical considerations, according to the Norwegian Gene Technology Act and Regulations relating to impact assessment pursuant to the Gene Technology Act. These considerations are therefore not part of the risk assessment provided by the VKM Panel on Genetically Modified Organisms.  \n Maize GA21 expresses a modified version of 5-enolpyruvylshikimate-3-phosphate synthase (mEPSPS), which is derived from maize EPSPS, and renders maize GA21 tolerant to the herbicidal active substance glyphosate.  \n Molecular Characterization: The molecular characterisation data indicate that several copies of the GA21 construct are integrated at a single locus in the DNA, and that they are inherited as a dominant, single locus trait. Appropriate analyses of the integration site, inserted DNA sequence, flanking regions, and bioinformatics have been performed. The VKM GMO Panel considers the molecular characterisation of maize GA21 as adequate.  \n Comparative Assessment: Comparative analyses of maize event GA21 to its conventional counterpart) have been performed during multiple field trials located at representative sites and environments in North America (1997, 2004, and 2005), Europe (1996, 1997, and 2006) and Brazil (2003). With the exception of small intermittent variations, no biologically significant differences were found between maize GA21 and controls. Based on the assessment of available data, the VKM GMO Panel concludes that maize GA21 is compositionally, agronomically and phenotypically equivalent to its conventional counterpart, except for the mEPSPS protein, and that its composition fell within the range observed among nonGM varieties. \n Food and Feed Risk Assessment: Whole food feeding studies in rats, broilers and cattles have not indicated any adverse health effects of maize GA21. These studies also indicate that maize GA21 is nutritionally equivalent to conventional maize. The mEPSPS protein does not show sequence resemblance to other known toxins or IgE allergens, nor has mEPSPS been reported to cause IgE mediated allergic reactions.  \n Based on current knowledge, the VKM GMO Panel concludes that maize GA21 is nutritionally equivalent to conventional maize varieties. It is unlikely that the mESPSPS protein will introduce a toxic or allergenic potential in food or feed based on maize GA21 compared to conventional maize. \n Environmental Risk Assessment: The scope of the application EFSA/GMO/UK/2005/19 includes import and processing of maize GA21 for food and feed uses. Considering the intended uses of maize GA21, excluding cultivation, the environmental risk assessment is concerned with accidental release into the environment of viable grains during transportation and processing, and indirect exposure, mainly through manure and faeces from animals fed grains from maize GA21.  \n Maize GA21 has no altered survival, multiplication or dissemination characteristics, and there are no indications of an increased likelihood of spread and establishment of feral maize plants in the case of accidental release into the environment of seeds from maize GA21. Maize is the only representative of the genus Zea in Europe, and there are no cross-compatible wild or weedy relatives outside cultivation. The VKM GMO Panel considers the risk of gene flow from occasional feral GM maize plants to conventional maize varieties to be negligible in Norway. Considering the intended use as food and feed, interactions with the biotic and abiotic environment are not considered by the GMO Panel to be an issue. \n Overall Conclusion: Based on current knowledge, the VKM GMO Panel concludes that maize GA21 is nutritionally equivalent to conventional maize varieties. It is unlikely that the mEPSPS protein will introduce a toxic or allergenic potential in food derived from maize GA21 compared to conventional maize.  \n The VKM GMO Panel likewise concludes that maize GA21, based on current knowledge, is comparable to conventional maize varieties concerning environmental risk in Norway with the intended usage.","PeriodicalId":11994,"journal":{"name":"European Journal of Nutrition & Food Safety","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Nutrition & Food Safety","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/ejnfs/2020/v12i330202","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

In preparation for a legal implementation of EU-regulation 1829/2003, the Norwegian Scientific Committee for Food Safety (VKM) has been requested by the Norwegian Environment Agency (former Norwegian Directorate for Nature Management) and the Norwegian Food Safety Authority (NFSA) to conduct final food/feed and environmental risk assessments for all genetically modified organisms (GMOs) and products containing or consisting of GMOs that are authorized in the European Union under Directive 2001/18/EC or Regulation 1829/2003/EC. The request covers scope(s) relevant to the Gene Technology Act. The request does not cover GMOs that VKM already has conducted its final risk assessments on. However, the Agency and NFSA requests VKM to consider whether updates or other changes to earlier submitted assessments are necessary.   The herbicide-tolerant genetically modified maize GA21 from Syngenta Seeds (Unique Identifier MON-ØØØ21-9) is authorised for the import and placing on the market as food or feed in the EU pursuant to Regulation (EC) 1829/2003 by the Commission Decision 2008/280/EC. An application for granting consent to all uses of GA21 maize including the cultivation was submitted by Syngenta in accordance with articles 5 and 17 of the Regulation (EC) No. 1829/2003 on June 30 2008.   Maize GA21 has previously been assessed as food and feed by the VKM GMO Panel commissioned by the Norwegian Food Safety Authority in connection with the national finalisation of the procedure  of the notification C/ES/98/01 in 2005 (VKM 2005a). VKM also participated in the 90 days public consultation of the application for placing on the market of maize GA21 for food and feed uses, import, processing and cultivation (EFSA/GMO/UK/2008/60) in 2009, and submitted a preliminary opinion in April 2010 (VKM 2010). GA21 has also been evaluated by the VKM GMO Panel as a component of several stacked GM maize events under and Regulation (EC) 1829/2003 (VKM 2008, VKM 2009a,b,c,d, VKM 2012a,b,  VKM 2013a,b,c). Due to the publication of new scientific literature and updated guidelines for risk assessment of genetically modified plants, the VKM GMO Panel has decided to deliver an updated food/feed and environmental risk assessment of GA21.  The updated  food/feed and environmental risk assessment of the maize GA21 is based on information provided by the applicant in the applications EFSA/GMO/UK/2005/19, EFSA/GMO/UK/2008/60 and EFSA/GMO/RX/GA21 and scientific comments from EFSA and other member states made available on the EFSA website GMO Extranet. The risk assessment also considered other peer-reviewed scientific literature as relevant.    The VKM GMO Panel has evaluated GA21 with reference to its intended uses in the European Economic Area (EEA), and according to the principles described in the Norwegian Food Act, the Norwegian Gene Technology Act and regulations relating to impact assessment pursuant to the Gene Technology Act, Directive 2001/18/EC on the deliberate release into the environment of genetically modified organisms, and Regulation (EC) No 1829/2003 on genetically modified food and feed. The Norwegian Scientific Committee for Food Safety has also decided to take account of the appropriate principles described in the EFSA guidelines for the risk assessment of GM plants and derived food and feed (EFSA 2011a), the environmental risk assessment of GM plants (EFSA 2010), selection of comparators for the risk assessment of GM plants (EFSA 2011b) and for the post-market environmental monitoring of GM plants (EFSA 2011c).   The scientific risk assessment of maize GA21 include molecular characterisation of the inserted DNA and expression of novel proteins, comparative assessment of agronomic and phenotypic characteristics, nutritional assessments, toxicology and allergenicity, unintended effects on plant fitness, potential for gene transfer, interactions between the GM plant and target and non-target organisms and effects on biogeochemical processes.   It is emphasized that the VKM mandate does not include assessments of contribution to sustainable development, societal utility and ethical considerations, according to the Norwegian Gene Technology Act and Regulations relating to impact assessment pursuant to the Gene Technology Act. These considerations are therefore not part of the risk assessment provided by the VKM Panel on Genetically Modified Organisms.   Maize GA21 expresses a modified version of 5-enolpyruvylshikimate-3-phosphate synthase (mEPSPS), which is derived from maize EPSPS, and renders maize GA21 tolerant to the herbicidal active substance glyphosate.   Molecular Characterization: The molecular characterisation data indicate that several copies of the GA21 construct are integrated at a single locus in the DNA, and that they are inherited as a dominant, single locus trait. Appropriate analyses of the integration site, inserted DNA sequence, flanking regions, and bioinformatics have been performed. The VKM GMO Panel considers the molecular characterisation of maize GA21 as adequate.   Comparative Assessment: Comparative analyses of maize event GA21 to its conventional counterpart) have been performed during multiple field trials located at representative sites and environments in North America (1997, 2004, and 2005), Europe (1996, 1997, and 2006) and Brazil (2003). With the exception of small intermittent variations, no biologically significant differences were found between maize GA21 and controls. Based on the assessment of available data, the VKM GMO Panel concludes that maize GA21 is compositionally, agronomically and phenotypically equivalent to its conventional counterpart, except for the mEPSPS protein, and that its composition fell within the range observed among nonGM varieties.  Food and Feed Risk Assessment: Whole food feeding studies in rats, broilers and cattles have not indicated any adverse health effects of maize GA21. These studies also indicate that maize GA21 is nutritionally equivalent to conventional maize. The mEPSPS protein does not show sequence resemblance to other known toxins or IgE allergens, nor has mEPSPS been reported to cause IgE mediated allergic reactions.   Based on current knowledge, the VKM GMO Panel concludes that maize GA21 is nutritionally equivalent to conventional maize varieties. It is unlikely that the mESPSPS protein will introduce a toxic or allergenic potential in food or feed based on maize GA21 compared to conventional maize.  Environmental Risk Assessment: The scope of the application EFSA/GMO/UK/2005/19 includes import and processing of maize GA21 for food and feed uses. Considering the intended uses of maize GA21, excluding cultivation, the environmental risk assessment is concerned with accidental release into the environment of viable grains during transportation and processing, and indirect exposure, mainly through manure and faeces from animals fed grains from maize GA21.   Maize GA21 has no altered survival, multiplication or dissemination characteristics, and there are no indications of an increased likelihood of spread and establishment of feral maize plants in the case of accidental release into the environment of seeds from maize GA21. Maize is the only representative of the genus Zea in Europe, and there are no cross-compatible wild or weedy relatives outside cultivation. The VKM GMO Panel considers the risk of gene flow from occasional feral GM maize plants to conventional maize varieties to be negligible in Norway. Considering the intended use as food and feed, interactions with the biotic and abiotic environment are not considered by the GMO Panel to be an issue.  Overall Conclusion: Based on current knowledge, the VKM GMO Panel concludes that maize GA21 is nutritionally equivalent to conventional maize varieties. It is unlikely that the mEPSPS protein will introduce a toxic or allergenic potential in food derived from maize GA21 compared to conventional maize.   The VKM GMO Panel likewise concludes that maize GA21, based on current knowledge, is comparable to conventional maize varieties concerning environmental risk in Norway with the intended usage.
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根据法规(EC) No 1829/2003 (EFSA/GMO/UK/2005/19)对食品和饲料用先正达种子的抗虫和耐除草剂转基因玉米GA21的进口和加工的食品/饲料和环境风险评估
为准备实施欧盟第1829/2003号条例,挪威环境局(原挪威自然管理局)和挪威食品安全局(NFSA)已要求挪威食品安全科学委员会(VKM)对欧盟根据指令2001/18/EC或法规1829/2003/EC授权的所有转基因生物(GMOs)和含有或由转基因生物组成的产品进行最终的食品/饲料和环境风险评估。该请求涵盖了与《基因技术法案》相关的范围。该请求不包括VKM已经进行了最终风险评估的转基因生物。然而,该机构和NFSA要求VKM考虑是否有必要对先前提交的评估进行更新或其他更改。先正达种子公司生产的抗除草剂转基因玉米GA21(唯一标识符MON-ØØØ21-9)已获欧盟委员会第2008/280/EC号决议授权,根据法规(EC) 1829/2003,作为食品或饲料在欧盟进口和投放市场。先正达于2008年6月30日根据欧盟第1829/2003号法规第5条和第17条提交了批准GA21玉米所有用途(包括种植)的申请。在2005年通报C/ES/98/01的国家最后定稿过程中,挪威食品安全局委托的VKM转基因生物小组对GA21玉米进行了食品和饲料评估(VKM 2005a)。VKM还于2009年参与了GA21玉米用于食品和饲料用途、进口、加工和种植的上市申请的90天公众咨询(EFSA/GMO/UK/2008/60),并于2010年4月提交了初步意见(VKM 2010)。VKM转基因生物小组还根据(EC) 1829/2003法规(VKM 2008, VKM 2009a,b,c,d, VKM 2012a,b, VKM 2013a,b,c)对GA21进行了评估,将其作为若干转基因玉米叠加事件的组成部分。由于发表了新的科学文献和更新的转基因植物风险评估指南,VKM转基因生物小组决定提供GA21的最新食品/饲料和环境风险评估。最新的GA21玉米食品/饲料和环境风险评估是基于申请人在申请EFSA/GMO/UK/2005/19、EFSA/GMO/UK/2008/60和EFSA/GMO/RX/GA21中提供的信息,以及欧洲食品安全局和其他成员国在欧洲食品安全局网站GMO Extranet上提供的科学评论。风险评估还考虑了其他同行评审的相关科学文献。VKM转基因生物专家组参照GA21在欧洲经济区(EEA)的预期用途,根据挪威食品法案、挪威基因技术法案、基因技术法案、关于转基因生物故意释放到环境中的指令2001/18/EC、转基因食品和饲料法规(EC) No 1829/2003所述原则,对GA21进行了评估。挪威食品安全科学委员会还决定考虑欧洲食品安全局转基因植物及其衍生食品和饲料风险评估指南(EFSA 2011a)、转基因植物环境风险评估指南(EFSA 2010)、转基因植物风险评估比较指标的选择(EFSA 2011b)和转基因植物上市后环境监测指南(EFSA 2011c)中所述的适当原则。玉米GA21的科学风险评估包括插入DNA的分子特征和新蛋白质的表达,农艺和表型特征的比较评估,营养评估,毒理学和过敏原性,对植物适应性的意外影响,基因转移的潜力,转基因植物与靶生物和非靶生物之间的相互作用以及对生物地球化学过程的影响。需要强调的是,根据挪威基因技术法案和与基因技术法案相关的影响评估法规,VKM任务不包括对可持续发展、社会效用和伦理考虑的贡献评估。因此,这些考虑因素不属于VKM转基因生物小组提供的风险评估的一部分。玉米GA21表达的5-烯醇丙酮酰基莽草酸-3-磷酸合成酶(mEPSPS)是由玉米EPSPS衍生而来的,使玉米GA21对除草剂活性物质草甘膦具有抗性。分子表征:分子表征数据表明,GA21结构的几个拷贝集成在DNA的单个位点上,并且它们作为显性的单位点性状遗传。对整合位点、插入DNA序列、侧翼区域和生物信息学进行了适当的分析。 VKM转基因生物小组认为玉米GA21的分子特征是充分的。比较评估:在北美(1997年、2004年和2005年)、欧洲(1996年、1997年和2006年)和巴西(2003年)的代表性地点和环境的多个田间试验中,对玉米事件GA21与常规事件进行了比较分析。除了小的间歇性变异外,在玉米GA21和对照之间没有发现显著的生物学差异。根据对现有数据的评估,VKM转基因小组得出结论,玉米GA21在组成、农艺和表型上与传统玉米相同,除了mEPSPS蛋白,其组成在non - m品种中观察到的范围内。食品和饲料风险评估:对大鼠、肉鸡和牛进行的全食物喂养研究没有表明玉米GA21对健康有任何不利影响。这些研究还表明,玉米GA21在营养上与传统玉米相当。mEPSPS蛋白没有显示出与其他已知毒素或IgE过敏原的序列相似性,也没有mEPSPS引起IgE介导的过敏反应的报道。根据目前的知识,VKM转基因专家小组得出结论,玉米GA21在营养上与传统玉米品种相当。与传统玉米相比,mESPSPS蛋白不太可能在基于玉米GA21的食品或饲料中引入毒性或致敏性。环境风险评估:EFSA/GMO/UK/2005/19申请的范围包括进口和加工用于食品和饲料用途的GA21玉米。考虑到玉米GA21的预期用途(不包括种植),环境风险评估涉及在运输和加工过程中有活性的谷物意外释放到环境中,以及间接暴露,主要是通过饲喂玉米GA21谷物的动物的粪便和粪便。玉米GA21的生存、繁殖和传播特性没有改变,并且没有迹象表明,如果玉米GA21的种子意外释放到环境中,野生玉米植物传播和建立的可能性会增加。玉米是玉米属在欧洲的唯一代表,在栽培之外没有杂交相容的野生或杂草亲缘种。VKM转基因生物小组认为,在挪威,基因从偶尔的野生转基因玉米植物流向传统玉米品种的风险可以忽略不计。考虑到作为食品和饲料的预期用途,转基因生物小组认为与生物和非生物环境的相互作用不是一个问题。总体结论:根据目前的知识,VKM转基因小组得出结论,玉米GA21在营养上与传统玉米品种相当。与传统玉米相比,mEPSPS蛋白不太可能在玉米GA21衍生食品中引入毒性或致敏性。VKM转基因生物小组同样得出结论,根据目前的知识,GA21玉米在挪威的预期用途方面与传统玉米品种的环境风险相当。
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