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Intestinal Enterobacteriaceae that Protect Nematodes from the Effects of Benzimidazoles

The objective of this study was to investigate an interaction between nematodes and gut Enterobacteriaceae that use benzimidazoles as a carbon source. By addressing this objective, we identified an anthelmintic resistance-like mechanism for gastrointestinal nematodes. We isolated 30 gut bacteria (fa...

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Detalles Bibliográficos
Autores principales: Whittaker, John H, Robertson, Alan P, Kimber, Michael J, Day, Tim A, Carlson, Steve A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215066/
https://www.ncbi.nlm.nih.gov/pubmed/28066686
http://dx.doi.org/10.4172/2155-9597.1000294
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author Whittaker, John H
Robertson, Alan P
Kimber, Michael J
Day, Tim A
Carlson, Steve A
author_facet Whittaker, John H
Robertson, Alan P
Kimber, Michael J
Day, Tim A
Carlson, Steve A
author_sort Whittaker, John H
collection PubMed
description The objective of this study was to investigate an interaction between nematodes and gut Enterobacteriaceae that use benzimidazoles as a carbon source. By addressing this objective, we identified an anthelmintic resistance-like mechanism for gastrointestinal nematodes. We isolated 30 gut bacteria (family Enterobacteriaceae) that subsist on and putatively catabolize benzimidazole-class anthelmintics. C. elegans was protected from the effects of benzimidazoles when co-incubated with these Enterobacteriaceae that also protect adult ascarids from the effects of albendazole. This bacterial phenotype represents a novel mechanism by which gastrointestinal nematodes are potentially spared from the effects of benzimidazoles, without any apparent fitness cost to the parasite.
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spelling pubmed-52150662017-01-05 Intestinal Enterobacteriaceae that Protect Nematodes from the Effects of Benzimidazoles Whittaker, John H Robertson, Alan P Kimber, Michael J Day, Tim A Carlson, Steve A J Bacteriol Parasitol Article The objective of this study was to investigate an interaction between nematodes and gut Enterobacteriaceae that use benzimidazoles as a carbon source. By addressing this objective, we identified an anthelmintic resistance-like mechanism for gastrointestinal nematodes. We isolated 30 gut bacteria (family Enterobacteriaceae) that subsist on and putatively catabolize benzimidazole-class anthelmintics. C. elegans was protected from the effects of benzimidazoles when co-incubated with these Enterobacteriaceae that also protect adult ascarids from the effects of albendazole. This bacterial phenotype represents a novel mechanism by which gastrointestinal nematodes are potentially spared from the effects of benzimidazoles, without any apparent fitness cost to the parasite. 2016-10-31 2016-10 /pmc/articles/PMC5215066/ /pubmed/28066686 http://dx.doi.org/10.4172/2155-9597.1000294 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Whittaker, John H
Robertson, Alan P
Kimber, Michael J
Day, Tim A
Carlson, Steve A
Intestinal Enterobacteriaceae that Protect Nematodes from the Effects of Benzimidazoles
title Intestinal Enterobacteriaceae that Protect Nematodes from the Effects of Benzimidazoles
title_full Intestinal Enterobacteriaceae that Protect Nematodes from the Effects of Benzimidazoles
title_fullStr Intestinal Enterobacteriaceae that Protect Nematodes from the Effects of Benzimidazoles
title_full_unstemmed Intestinal Enterobacteriaceae that Protect Nematodes from the Effects of Benzimidazoles
title_short Intestinal Enterobacteriaceae that Protect Nematodes from the Effects of Benzimidazoles
title_sort intestinal enterobacteriaceae that protect nematodes from the effects of benzimidazoles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215066/
https://www.ncbi.nlm.nih.gov/pubmed/28066686
http://dx.doi.org/10.4172/2155-9597.1000294
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