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Molecular insights into Vibrio cholerae’s intra-amoebal host-pathogen interactions

Vibrio cholerae, which causes the diarrheal disease cholera, is a species of bacteria commonly found in aquatic habitats. Within such environments, the bacterium must defend itself against predatory protozoan grazers. Amoebae are prominent grazers, with Acanthamoeba castellanii being one of the best...

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Autores principales: Van der Henst, Charles, Vanhove, Audrey Sophie, Drebes Dörr, Natália Carolina, Stutzmann, Sandrine, Stoudmann, Candice, Clerc, Stéphanie, Scrignari, Tiziana, Maclachlan, Catherine, Knott, Graham, Blokesch, Melanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110790/
https://www.ncbi.nlm.nih.gov/pubmed/30150745
http://dx.doi.org/10.1038/s41467-018-05976-x
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author Van der Henst, Charles
Vanhove, Audrey Sophie
Drebes Dörr, Natália Carolina
Stutzmann, Sandrine
Stoudmann, Candice
Clerc, Stéphanie
Scrignari, Tiziana
Maclachlan, Catherine
Knott, Graham
Blokesch, Melanie
author_facet Van der Henst, Charles
Vanhove, Audrey Sophie
Drebes Dörr, Natália Carolina
Stutzmann, Sandrine
Stoudmann, Candice
Clerc, Stéphanie
Scrignari, Tiziana
Maclachlan, Catherine
Knott, Graham
Blokesch, Melanie
author_sort Van der Henst, Charles
collection PubMed
description Vibrio cholerae, which causes the diarrheal disease cholera, is a species of bacteria commonly found in aquatic habitats. Within such environments, the bacterium must defend itself against predatory protozoan grazers. Amoebae are prominent grazers, with Acanthamoeba castellanii being one of the best-studied aquatic amoebae. We previously showed that V. cholerae resists digestion by A. castellanii and establishes a replication niche within the host’s osmoregulatory organelle. In this study, we decipher the molecular mechanisms involved in the maintenance of V. cholerae’s intra-amoebal replication niche and its ultimate escape from the succumbed host. We demonstrate that minor virulence features important for disease in mammals, such as extracellular enzymes and flagellum-based motility, have a key role in the replication and transmission of V. cholerae in its aqueous environment. This work, therefore, describes new mechanisms that provide the pathogen with a fitness advantage in its primary habitat, which may have contributed to the emergence of these minor virulence factors in the species V. cholerae.
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spelling pubmed-61107902018-08-29 Molecular insights into Vibrio cholerae’s intra-amoebal host-pathogen interactions Van der Henst, Charles Vanhove, Audrey Sophie Drebes Dörr, Natália Carolina Stutzmann, Sandrine Stoudmann, Candice Clerc, Stéphanie Scrignari, Tiziana Maclachlan, Catherine Knott, Graham Blokesch, Melanie Nat Commun Article Vibrio cholerae, which causes the diarrheal disease cholera, is a species of bacteria commonly found in aquatic habitats. Within such environments, the bacterium must defend itself against predatory protozoan grazers. Amoebae are prominent grazers, with Acanthamoeba castellanii being one of the best-studied aquatic amoebae. We previously showed that V. cholerae resists digestion by A. castellanii and establishes a replication niche within the host’s osmoregulatory organelle. In this study, we decipher the molecular mechanisms involved in the maintenance of V. cholerae’s intra-amoebal replication niche and its ultimate escape from the succumbed host. We demonstrate that minor virulence features important for disease in mammals, such as extracellular enzymes and flagellum-based motility, have a key role in the replication and transmission of V. cholerae in its aqueous environment. This work, therefore, describes new mechanisms that provide the pathogen with a fitness advantage in its primary habitat, which may have contributed to the emergence of these minor virulence factors in the species V. cholerae. Nature Publishing Group UK 2018-08-27 /pmc/articles/PMC6110790/ /pubmed/30150745 http://dx.doi.org/10.1038/s41467-018-05976-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Van der Henst, Charles
Vanhove, Audrey Sophie
Drebes Dörr, Natália Carolina
Stutzmann, Sandrine
Stoudmann, Candice
Clerc, Stéphanie
Scrignari, Tiziana
Maclachlan, Catherine
Knott, Graham
Blokesch, Melanie
Molecular insights into Vibrio cholerae’s intra-amoebal host-pathogen interactions
title Molecular insights into Vibrio cholerae’s intra-amoebal host-pathogen interactions
title_full Molecular insights into Vibrio cholerae’s intra-amoebal host-pathogen interactions
title_fullStr Molecular insights into Vibrio cholerae’s intra-amoebal host-pathogen interactions
title_full_unstemmed Molecular insights into Vibrio cholerae’s intra-amoebal host-pathogen interactions
title_short Molecular insights into Vibrio cholerae’s intra-amoebal host-pathogen interactions
title_sort molecular insights into vibrio cholerae’s intra-amoebal host-pathogen interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110790/
https://www.ncbi.nlm.nih.gov/pubmed/30150745
http://dx.doi.org/10.1038/s41467-018-05976-x
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