Towards a reporting guideline for developmental and reproductive toxicology testing in C. elegans and other nematodes

Author:

van der Voet Monique1,Teunis Marc2,Louter-van de Haar Johanna2,Stigter Nienke2,Bhalla Diksha3,Rooseboom Martijn4,Wever Kimberley E5,Krul Cyrille2,Pieters Raymond26,Wildwater Marjolein12,van Noort Vera37ORCID

Affiliation:

1. Vivaltes, 1704 NA, Heerhugowaard the Netherlands

2. Utrecht University of Applied Sciences, Innovative testing in Life Sciences & Chemistry, 3584 CH, Utrecht, the Netherlands

3. KU Leuven, Centre of Microbial and Plant Genetics, Faculty of Bioscience Engineering, 3001, Leuven, Belgium

4. Toxicology group Shell International B.V., 2596 HR, The Hague, the Netherlands

5. Radboud University Medical Center, Radboud Institute for Health Sciences, Department for Health Evidence, 6525 GA, Nijmegen, the Netherlands

6. Utrecht University, Institute for Risk Assessment Sciences, 3584 CM, Utrecht, the Netherlands

7. Leiden University, Institute of Biology Leiden, 2333 BE, Leiden, the Netherlands

Abstract

Abstract Implementation of reliable methodologies allowing Reduction, Refinement, and Replacement (3Rs) of animal testing is a process that takes several decades and is still not complete. Reliable methods are essential for regulatory hazard assessment of chemicals where differences in test protocol can influence the test outcomes and thus affect the confidence in the predictive value of the organisms used as an alternative for mammals. Although test guidelines are common for mammalian studies, they are scarce for non-vertebrate organisms that would allow for the 3Rs of animal testing. Here, we present a set of 30 reporting criteria as the basis for such a guideline for Developmental and Reproductive Toxicology (DART) testing in the nematode Caenorhabditis elegans. Small organisms like C. elegans are upcoming in new approach methodologies for hazard assessment; thus, reliable and robust test protocols are urgently needed. A literature assessment of the fulfilment of the reporting criteria demonstrates that although studies describe methodological details, essential information such as compound purity and lot/batch number or type of container is often not reported. The formulated set of reporting criteria for C. elegans testing can be used by (i) researchers to describe essential experimental details (ii) data scientists that aggregate information to assess data quality and include data in aggregated databases (iii) regulators to assess study data for inclusion in regulatory hazard assessment of chemicals.

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Toxicology

Reference47 articles.

1. Profiling the activity of environmental chemicals in prenatal developmental toxicity studies using the U.S. EPA’s ToxRefDB;Knudsen;Reprod Toxicol,2009

2. Can animal models of disease reliably inform human studies?;Bart van der Worp;PLoS Med,2010

3. Teratogenicity

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