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When the Whole is Not Greater than the Sum of the Parts: A Critical Review of Laboratory Bioassay Effects Testing for Insecticidal Protein Interactions

机译:当整体不大于部分的总和时:杀虫蛋白相互作用的实验室生物测定效果测试的批判性回顾

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摘要

Many studies have been conducted to investigate synergism among insecticidal proteins; however, a consensus on minimal data requirements and interpretation is lacking. While some have concluded that all additive predictive-type models should be abandoned, we advocate that additivity models can remain useful as assessment tools and that an appropriately designed interaction study will never systematically underestimate the existence of synergism, irrespective of which additivity model (or none at all) may be used. To generate the most meaningful synergy assessment datasets in support of safety assessments, we highlight two beneficial steps to follow: (i) select a testing model which is the most consistent with current knowledge regarding the action of the insecticidal proteins and (ii) avoid using bioassay methods which may result in excess response heterogeneity. We also outline other experimental design elements to consider, which may be crucial for conducting future studies of this type. A contrast of underlying testing assumptions associated with the additivity models is provided, along with a comprehensive review of interaction data for Cry1, Cry2, Cry3, Cry9, and Vip3A insecticidal proteins. Our review captures four recurrent findings: i) experiments reporting synergistic interactions are a minority, ii) the degree of synergism reported is low in magnitude, iii) reported interactions are sometimes equivocal/inconclusive due to unconfirmed model assumptions or other bioassay challenges, and iv) due to biological response variation many of the reported interactions may be artefactual. A brief overview of the positioning of interaction testing data in safety assessments of GM food crops is also provided.
机译:已经进行了许多研究来研究杀虫蛋白之间的协同作用。但是,在最小数据需求和解释方面缺乏共识。尽管有些人得出结论,应该放弃所有加性预测型模型,但我们主张可加性模型可以作为评估工具继续使用,并且经过适当设计的相互作用研究永远不会系统地低估协同作用的存在,无论使用哪种可加性模型(或不考虑任何可加性模型)完全可以使用)。为了生成最有意义的协同作用评估数据集以支持安全性评估,我们着重介绍了以下两个有益步骤:(i)选择一种与当前有关杀虫蛋白作用的知识最一致的测试模型,以及(ii)避免使用生物测定方法,可能导致过度的响应异质性。我们还将概述其他要考虑的实验设计元素,这对于进行此类后续研究可能至关重要。提供了与可加性模型相关的基础测试假设的对比,以及对Cry1,Cry2,Cry3,Cry9和Vip3A杀虫蛋白相互作用数据的全面综述。我们的综述涵盖了四个复发性发现:i)报告协同相互作用的实验占少数,ii)报告的协同作用程度低,iii)由于模型假设未确认或其他生物测定挑战,报告的相互作用有时是模棱两可/不确定的,并且iv )由于生物学反应的差异,许多报道的相互作用可能是人工的。还提供了对转基因食品安全性评估中相互作用测试数据的定位的简要概述。

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