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Vibrio cholerae motility exerts drag force to impede attack by the bacterial predator Bdellovibrio bacteriovorus
The bacterial predator Bdellovibrio bacteriovorus is evolved to attack and kill other bacteria, including the human intestinal pathogen Vibrio cholerae. Although B. bacteriovorus exhibit a broad prey range, little is known about the genetic determinants of prey resistance and sensitivity. Here we pe...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232129/ https://www.ncbi.nlm.nih.gov/pubmed/30420597 http://dx.doi.org/10.1038/s41467-018-07245-3 |
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author | Duncan, Miles C. Forbes, John C. Nguyen, Y Shull, Lauren M. Gillette, Rebecca K. Lazinski, David W. Ali, Afsar Shanks, Robert M. Q. Kadouri, Daniel E. Camilli, Andrew |
author_facet | Duncan, Miles C. Forbes, John C. Nguyen, Y Shull, Lauren M. Gillette, Rebecca K. Lazinski, David W. Ali, Afsar Shanks, Robert M. Q. Kadouri, Daniel E. Camilli, Andrew |
author_sort | Duncan, Miles C. |
collection | PubMed |
description | The bacterial predator Bdellovibrio bacteriovorus is evolved to attack and kill other bacteria, including the human intestinal pathogen Vibrio cholerae. Although B. bacteriovorus exhibit a broad prey range, little is known about the genetic determinants of prey resistance and sensitivity. Here we perform a genetic screen on V. cholerae and identify five pathways contributing to predation susceptibility. We find that the essential virulence regulators ToxR/S increase susceptibility to predation, as mutants of these genes are more resistant to predation. We observe by flow cytometry that lipopolysaccharide is a critical defense, as mutants lacking O-antigen are rapidly attacked by predatory B. bacteriovorus. Using polymer solutions to alter media viscosity, we find that when B. bacteriovorus attacks motile V. cholerae, increased drag forces slow its ability to prey. These results provide insights into key prey resistance mechanisms, and may be useful in the application of B. bacteriovorus in treating infections. |
format | Online Article Text |
id | pubmed-6232129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62321292018-11-14 Vibrio cholerae motility exerts drag force to impede attack by the bacterial predator Bdellovibrio bacteriovorus Duncan, Miles C. Forbes, John C. Nguyen, Y Shull, Lauren M. Gillette, Rebecca K. Lazinski, David W. Ali, Afsar Shanks, Robert M. Q. Kadouri, Daniel E. Camilli, Andrew Nat Commun Article The bacterial predator Bdellovibrio bacteriovorus is evolved to attack and kill other bacteria, including the human intestinal pathogen Vibrio cholerae. Although B. bacteriovorus exhibit a broad prey range, little is known about the genetic determinants of prey resistance and sensitivity. Here we perform a genetic screen on V. cholerae and identify five pathways contributing to predation susceptibility. We find that the essential virulence regulators ToxR/S increase susceptibility to predation, as mutants of these genes are more resistant to predation. We observe by flow cytometry that lipopolysaccharide is a critical defense, as mutants lacking O-antigen are rapidly attacked by predatory B. bacteriovorus. Using polymer solutions to alter media viscosity, we find that when B. bacteriovorus attacks motile V. cholerae, increased drag forces slow its ability to prey. These results provide insights into key prey resistance mechanisms, and may be useful in the application of B. bacteriovorus in treating infections. Nature Publishing Group UK 2018-11-12 /pmc/articles/PMC6232129/ /pubmed/30420597 http://dx.doi.org/10.1038/s41467-018-07245-3 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 Duncan, Miles C. Forbes, John C. Nguyen, Y Shull, Lauren M. Gillette, Rebecca K. Lazinski, David W. Ali, Afsar Shanks, Robert M. Q. Kadouri, Daniel E. Camilli, Andrew Vibrio cholerae motility exerts drag force to impede attack by the bacterial predator Bdellovibrio bacteriovorus |
title | Vibrio cholerae motility exerts drag force to impede attack by the bacterial predator Bdellovibrio bacteriovorus |
title_full | Vibrio cholerae motility exerts drag force to impede attack by the bacterial predator Bdellovibrio bacteriovorus |
title_fullStr | Vibrio cholerae motility exerts drag force to impede attack by the bacterial predator Bdellovibrio bacteriovorus |
title_full_unstemmed | Vibrio cholerae motility exerts drag force to impede attack by the bacterial predator Bdellovibrio bacteriovorus |
title_short | Vibrio cholerae motility exerts drag force to impede attack by the bacterial predator Bdellovibrio bacteriovorus |
title_sort | vibrio cholerae motility exerts drag force to impede attack by the bacterial predator bdellovibrio bacteriovorus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232129/ https://www.ncbi.nlm.nih.gov/pubmed/30420597 http://dx.doi.org/10.1038/s41467-018-07245-3 |
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