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Vibrio cholerae autoinducer-1 enhances the virulence of enteropathogenic Escherichia coli
Diarrhoea is the second leading cause of death in children under the age of five. The bacterial species, Vibrio cholerae and enteropathogenic Escherichia coli (EPEC), are among the main pathogens that cause diarrhoeal diseases, which are associated with high mortality rates. These two pathogens have...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411865/ https://www.ncbi.nlm.nih.gov/pubmed/30858454 http://dx.doi.org/10.1038/s41598-019-40859-1 |
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author | Gorelik, Orna Levy, Niva Shaulov, Lihi Yegodayev, Ksenia Meijler, Michael M. Sal-Man, Neta |
author_facet | Gorelik, Orna Levy, Niva Shaulov, Lihi Yegodayev, Ksenia Meijler, Michael M. Sal-Man, Neta |
author_sort | Gorelik, Orna |
collection | PubMed |
description | Diarrhoea is the second leading cause of death in children under the age of five. The bacterial species, Vibrio cholerae and enteropathogenic Escherichia coli (EPEC), are among the main pathogens that cause diarrhoeal diseases, which are associated with high mortality rates. These two pathogens have a common infection site—the small intestine. While it is known that both pathogens utilize quorum sensing (QS) to determine their population size, it is not yet clear whether potential bacterial competitors can also use this information. In this study, we examined the ability of EPEC to determine V. cholerae population sizes and to modulate its own virulence mechanisms accordingly. We found that EPEC virulence is enhanced in response to elevated concentrations of cholera autoinducer-1 (CAI-1), even though neither a CAI-1 synthase nor CAI-1 receptors have been reported in E. coli. This CAI-1 sensing and virulence upregulation response may facilitate the ability of EPEC to coordinate successful colonization of a host co-infected with V. cholerae. To the best of our knowledge, this is the first observed example of ‘eavesdropping’ between two bacterial pathogens that is based on interspecies sensing of a QS molecule. |
format | Online Article Text |
id | pubmed-6411865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64118652019-03-13 Vibrio cholerae autoinducer-1 enhances the virulence of enteropathogenic Escherichia coli Gorelik, Orna Levy, Niva Shaulov, Lihi Yegodayev, Ksenia Meijler, Michael M. Sal-Man, Neta Sci Rep Article Diarrhoea is the second leading cause of death in children under the age of five. The bacterial species, Vibrio cholerae and enteropathogenic Escherichia coli (EPEC), are among the main pathogens that cause diarrhoeal diseases, which are associated with high mortality rates. These two pathogens have a common infection site—the small intestine. While it is known that both pathogens utilize quorum sensing (QS) to determine their population size, it is not yet clear whether potential bacterial competitors can also use this information. In this study, we examined the ability of EPEC to determine V. cholerae population sizes and to modulate its own virulence mechanisms accordingly. We found that EPEC virulence is enhanced in response to elevated concentrations of cholera autoinducer-1 (CAI-1), even though neither a CAI-1 synthase nor CAI-1 receptors have been reported in E. coli. This CAI-1 sensing and virulence upregulation response may facilitate the ability of EPEC to coordinate successful colonization of a host co-infected with V. cholerae. To the best of our knowledge, this is the first observed example of ‘eavesdropping’ between two bacterial pathogens that is based on interspecies sensing of a QS molecule. Nature Publishing Group UK 2019-03-11 /pmc/articles/PMC6411865/ /pubmed/30858454 http://dx.doi.org/10.1038/s41598-019-40859-1 Text en © The Author(s) 2019 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 Gorelik, Orna Levy, Niva Shaulov, Lihi Yegodayev, Ksenia Meijler, Michael M. Sal-Man, Neta Vibrio cholerae autoinducer-1 enhances the virulence of enteropathogenic Escherichia coli |
title | Vibrio cholerae autoinducer-1 enhances the virulence of enteropathogenic Escherichia coli |
title_full | Vibrio cholerae autoinducer-1 enhances the virulence of enteropathogenic Escherichia coli |
title_fullStr | Vibrio cholerae autoinducer-1 enhances the virulence of enteropathogenic Escherichia coli |
title_full_unstemmed | Vibrio cholerae autoinducer-1 enhances the virulence of enteropathogenic Escherichia coli |
title_short | Vibrio cholerae autoinducer-1 enhances the virulence of enteropathogenic Escherichia coli |
title_sort | vibrio cholerae autoinducer-1 enhances the virulence of enteropathogenic escherichia coli |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411865/ https://www.ncbi.nlm.nih.gov/pubmed/30858454 http://dx.doi.org/10.1038/s41598-019-40859-1 |
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