Assessment of the three-test genetic toxicology battery for groundwater metabolites

Author:

Fowler Paul1ORCID,Bearzatto Alessandra2,Beevers Carol3ORCID,Booth Ewan D4,Donner E Maria,Gan Lin5,Hartmann Kerstin6,Meurer Krista7,Schutte Maaike E8,Settivari Raja S9

Affiliation:

1. FStox Consulting Ltd , Raunds , United Kingdom

2. Sipcam Oxon S.p.A. , Italy

3. Corteva , Abingdon , United Kingdom

4. Syngenta Ltd. , Berkshire , UK

5. Exigent Sciences LLC , Arizona , United States

6. Bayer AG , Monheim , Germany

7. BASF SE , Limburgerhof , Germany

8. ADAMA , Leusden , Netherlands

9. Corteva , Newark , United States

Abstract

Abstract The two-test in vitro battery for genotoxicity testing (Ames and micronucleus) has in the majority of cases replaced the three-test battery (as two-test plus mammalian cell gene mutation assay) for the routine testing of chemicals, pharmaceuticals, cosmetics, and agrochemical metabolites originating from food and feed as well as from water treatment. The guidance for testing agrochemical groundwater metabolites, however, still relies on the three-test battery. Data collated in this study from 18 plant protection and related materials highlights the disparity between the often negative Ames and in vitro chromosome aberration data and frequently positive in vitro mammalian cell gene mutation assays. Sixteen of the 18 collated materials with complete datasets were Ames negative, and overall had negative outcomes in in vitro chromosome damage tests (weight of evidence from multiple tests). Mammalian cell gene mutation assays (HPRT and/or mouse lymphoma assay (MLA)) were positive in at least one test for every material with this data. Where both MLA and HPRT tests were performed on the same material, the HPRT seemed to give fewer positive responses. In vivo follow-up tests included combinations of comet assays, unscheduled DNA synthesis, and transgenic rodent gene mutation assays, all gave negative outcomes. The inclusion of mammalian cell gene mutation assays in a three-test battery for groundwater metabolites is therefore not justified and leads to unnecessary in vivo follow-up testing.

Funder

CropLife Europe Organized and Funded

Publisher

Oxford University Press (OUP)

Reference25 articles.

1. Guidance Document on the Assessment of the Relevance of Metabolites in Groundwater of Substances Regulated Under Regulation (Ec) No 1107/2009,2021

2. Evaluation of the ability of a battery of three in vitro genotoxicity tests to discriminate rodent carcinogens and non-carcinogens I Sensitivity, specificity and relative predictivity;Kirkland;Mutat Res,2005

3. Evaluation of the ability of a battery of three in vitro genotoxicity tests to discriminate rodent carcinogens and non-carcinogens II Further analysis of mammalian cell results, relative predictivity and tumour profiles;Kirkland;Mutat Res,2006

4. A core in vitro genotoxicity battery comprising the Ames test plus the in vitro micronucleus test is sufficient to detect rodent carcinogens and in vivo genotoxins;Kirkland;Mutat Res,2011

5. A core in vitro genotoxicity battery comprising the Ames test plus the mouse lymphoma assay is sufficient to detect rodent carcinogens;Moore,2011

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