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Article Dans Une Revue Mutation Research/Mutation Research Genomics Année : 2017

Assessing the genotoxicity of two commonly occurring byproducts of water disinfection: chloral hydrate and bromal hydrate

Résumé

Water disinfection treatments result in the formation of disinfection byproducts (DBPs) that have been linked to adverse human health outcomes including higher incidence of bladder and colorectal cancer. However, data about the genotoxicity of DBPs is limited to only a small fraction of compounds. Chloral hydrate (CH) and bromal hydrate (BH) are two trihaloacetaldehydes commonly detected in disinfected waters, but little is known about their genotoxicity, especially BH. We investigated the genotoxicity of CH and BH using a test battery that includes three in vitro genotoxicity assays. We conducted the Ames test using Salmonella bacterial strains TA97a, TA98, TA100 and TA102, and the alkaline comet assay and the micronucleus test both using Chinese hamster ovary cells. We carried out the tests in the absence and presence of the metabolic fraction S9 mix. CH did not exhibit statistically significant genotoxic effects in any of the three assays. In contrast, BH exhibited mutagenic activity in the Salmonella strain TA100 and induced statistically significant DNA lesions in CHO cells as appeared in the comet assay. The genotoxic potential of BH in both assays decreased in the presence of the metabolic fraction S9 mix. BH did not induce chromosomal damage in CHO cells. Our results show that BH exhibited genotoxic activity by causing mutations and primary DNA damage while CH did not induce genotoxic effects. Our findings highlight concerns about the higher genotoxicity of brominated DBPs in comparison to their chlorinated analogues.
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Dates et versions

hal-01435494 , version 1 (19-01-2017)

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Tarek Manasfi, Michel de Méo, Carole Di Giorgio, Bruno Coulomb, Jean-Luc Boudenne. Assessing the genotoxicity of two commonly occurring byproducts of water disinfection: chloral hydrate and bromal hydrate. Mutation Research/Mutation Research Genomics, 2017, 813, pp.37-44. ⟨10.1016/j.mrgentox.2016.11.009⟩. ⟨hal-01435494⟩
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