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Mutagenic analysis of six disinfection by-products in the Tk gene of mouse lymphoma cells

  • ,
  • Amadeu Creus
    ,
  • Ricard Marcos(corresponding author)
*Corresponding author for this work
  • Universitat Autonoma de Barcelona
    ,
  • Instituto de Salud Carlos III
Research Output:
Contribution to journal
Article
Peer-review

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 1045-1052 (8 pages)

Journal (Volume, Issue Number)

Journal of Hazardous Materials (Volume 190, Issue 1-3)

Publication milestones

  • Published - 15/06/2011

Publication status

Published - 15/06/2011

ISSN

0304-3894

Publication IDs

  • Scopus: 79956141971
  • PubMed: 21561708

Abstract

Drinking water must be disinfected prior to its distribution for human consumption. This water treatment process generates disinfection by-products (DBPs), formed by the interaction of the disinfectant with organic matter, anthropogenic contaminants and inorganic (bromide/iodide) matter naturally present in source water. Due to the potential genotoxic/carcinogenic risk of these DBPs, we have investigated the mutagenic potential of six of such compounds on the thymidine kinase (Tk) gene in the well-validated mouse lymphoma assay (MLA). The MLA quantifies a wide range of genetic alterations affecting the expression of this gene in L5178Y/Tk+/--3.7.2C cells. In this study we selected six emerging DBPs, corresponding to three different chemical classes: halonitromethanes (bromonitromethane and trichloronitromethane), halogenated acetaldehydes (tribromoacetaldehyde and chloral hydrate) and hydroxyfuranones (mucobromic and mucochloric acids), each class including one chlorinated and one brominated form. The results showed that after 4h of treatment, only mucobromic acid increased the frequency of mutant colonies, with a higher proportion of small colonies, which would indicate a clastogenic potential. This is the first study reporting mutagenicity data in mammalian cells for the six selected DBPs.

Funding Details

Danae Liviac was supported by a postgraduate fellowship from the Universitat Autònoma de Barcelona. This investigation was supported in part by the Spanish Ministries of Education and Science ( SAF2005-07643-00-03 ) and Environment and Rural and Marine Affairs ( A036/2007/3-14.4 ), and by the Generalitat de Catalunya ( 2009SGR-725 ).
FundersFunding numbers
Environment and Rural and Marine Affairs
A036/2007/3-14.4
Spanish Ministries of Education and Science
SAF2005-07643-00-03
Generalitat de Catalunya
2009SGR-725
UAB
-