Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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
_version_ 1783370346717511680
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
work_keys_str_mv AT duncanmilesc vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus
AT forbesjohnc vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus
AT nguyeny vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus
AT shulllaurenm vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus
AT gilletterebeccak vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus
AT lazinskidavidw vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus
AT aliafsar vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus
AT shanksrobertmq vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus
AT kadouridaniele vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus
AT camilliandrew vibriocholeraemotilityexertsdragforcetoimpedeattackbythebacterialpredatorbdellovibriobacteriovorus