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Vibrio cholerae accessory colonisation factor AcfC: a chemotactic protein with a role in hyperinfectivity
Vibrio cholerae O1 El Tor is an aquatic Gram-negative bacterium responsible for the current seventh pandemic of the diarrheal disease, cholera. A previous whole-genome analysis on V. cholerae O1 El Tor strains from the 2010 epidemic in Pakistan showed that all strains contained the V. cholerae patho...
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/PMC5976639/ https://www.ncbi.nlm.nih.gov/pubmed/29849063 http://dx.doi.org/10.1038/s41598-018-26570-7 |
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author | Valiente, Esmeralda Davies, Cadi Mills, Dominic C. Getino, Maria Ritchie, Jennifer M. Wren, Brendan W. |
author_facet | Valiente, Esmeralda Davies, Cadi Mills, Dominic C. Getino, Maria Ritchie, Jennifer M. Wren, Brendan W. |
author_sort | Valiente, Esmeralda |
collection | PubMed |
description | Vibrio cholerae O1 El Tor is an aquatic Gram-negative bacterium responsible for the current seventh pandemic of the diarrheal disease, cholera. A previous whole-genome analysis on V. cholerae O1 El Tor strains from the 2010 epidemic in Pakistan showed that all strains contained the V. cholerae pathogenicity island-1 and the accessory colonisation gene acfC (VC_0841). Here we show that acfC possess an open reading frame of 770 bp encoding a protein with a predicted size of 28 kDa, which shares high amino acid similarity with two adhesion proteins found in other enteropathogens, including Paa in serotype O45 porcine enteropathogenic Escherichia coli and PEB3 in Campylobacter jejuni. Using a defined acfC deletion mutant, we studied the specific role of AcfC in V. cholerae O1 El Tor environmental survival, colonisation and virulence in two infection model systems (Galleria mellonella and infant rabbits). Our results indicate that AcfC might be a periplasmic sulfate-binding protein that affects chemotaxis towards mucin and bacterial infectivity in the infant rabbit model of cholera. Overall, our findings suggest that AcfC contributes to the chemotactic response of WT V. cholerae and plays an important role in defining the overall distribution of the organism within the intestine. |
format | Online Article Text |
id | pubmed-5976639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59766392018-05-31 Vibrio cholerae accessory colonisation factor AcfC: a chemotactic protein with a role in hyperinfectivity Valiente, Esmeralda Davies, Cadi Mills, Dominic C. Getino, Maria Ritchie, Jennifer M. Wren, Brendan W. Sci Rep Article Vibrio cholerae O1 El Tor is an aquatic Gram-negative bacterium responsible for the current seventh pandemic of the diarrheal disease, cholera. A previous whole-genome analysis on V. cholerae O1 El Tor strains from the 2010 epidemic in Pakistan showed that all strains contained the V. cholerae pathogenicity island-1 and the accessory colonisation gene acfC (VC_0841). Here we show that acfC possess an open reading frame of 770 bp encoding a protein with a predicted size of 28 kDa, which shares high amino acid similarity with two adhesion proteins found in other enteropathogens, including Paa in serotype O45 porcine enteropathogenic Escherichia coli and PEB3 in Campylobacter jejuni. Using a defined acfC deletion mutant, we studied the specific role of AcfC in V. cholerae O1 El Tor environmental survival, colonisation and virulence in two infection model systems (Galleria mellonella and infant rabbits). Our results indicate that AcfC might be a periplasmic sulfate-binding protein that affects chemotaxis towards mucin and bacterial infectivity in the infant rabbit model of cholera. Overall, our findings suggest that AcfC contributes to the chemotactic response of WT V. cholerae and plays an important role in defining the overall distribution of the organism within the intestine. Nature Publishing Group UK 2018-05-30 /pmc/articles/PMC5976639/ /pubmed/29849063 http://dx.doi.org/10.1038/s41598-018-26570-7 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 Valiente, Esmeralda Davies, Cadi Mills, Dominic C. Getino, Maria Ritchie, Jennifer M. Wren, Brendan W. Vibrio cholerae accessory colonisation factor AcfC: a chemotactic protein with a role in hyperinfectivity |
title | Vibrio cholerae accessory colonisation factor AcfC: a chemotactic protein with a role in hyperinfectivity |
title_full | Vibrio cholerae accessory colonisation factor AcfC: a chemotactic protein with a role in hyperinfectivity |
title_fullStr | Vibrio cholerae accessory colonisation factor AcfC: a chemotactic protein with a role in hyperinfectivity |
title_full_unstemmed | Vibrio cholerae accessory colonisation factor AcfC: a chemotactic protein with a role in hyperinfectivity |
title_short | Vibrio cholerae accessory colonisation factor AcfC: a chemotactic protein with a role in hyperinfectivity |
title_sort | vibrio cholerae accessory colonisation factor acfc: a chemotactic protein with a role in hyperinfectivity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976639/ https://www.ncbi.nlm.nih.gov/pubmed/29849063 http://dx.doi.org/10.1038/s41598-018-26570-7 |
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