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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-6110790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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