Cargando…

The C lostridium difficile cell wall protein CwpV confers phase‐variable phage resistance

Bacteriophages are present in virtually all ecosystems, and bacteria have developed multiple antiphage strategies to counter their attacks. C lostridium difficile is an important pathogen causing severe intestinal infections in humans and animals. Here we show that the conserved cell‐surface protein...

Descripción completa

Detalles Bibliográficos
Autores principales: Sekulovic, Ognjen, Ospina Bedoya, Maicol, Fivian‐Hughes, Amanda S., Fairweather, Neil F., Fortier, Louis‐Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737114/
https://www.ncbi.nlm.nih.gov/pubmed/26179020
http://dx.doi.org/10.1111/mmi.13121
_version_ 1782413420628279296
author Sekulovic, Ognjen
Ospina Bedoya, Maicol
Fivian‐Hughes, Amanda S.
Fairweather, Neil F.
Fortier, Louis‐Charles
author_facet Sekulovic, Ognjen
Ospina Bedoya, Maicol
Fivian‐Hughes, Amanda S.
Fairweather, Neil F.
Fortier, Louis‐Charles
author_sort Sekulovic, Ognjen
collection PubMed
description Bacteriophages are present in virtually all ecosystems, and bacteria have developed multiple antiphage strategies to counter their attacks. C lostridium difficile is an important pathogen causing severe intestinal infections in humans and animals. Here we show that the conserved cell‐surface protein CwpV provides antiphage protection in C . difficile. This protein, for which the expression is phase‐variable, is classified into five types, each differing in their repeat‐containing C‐terminal domain. When expressed constitutively from a plasmid or the chromosome of locked ‘ON’ cells of C . difficile  R20291, CwpV conferred antiphage protection. Differences in the level of phage protection were observed depending on the phage morphological group, siphophages being the most sensitive with efficiency of plaquing (EOP) values of < 5 × 10(−7) for phages ϕCD38‐2, ϕCD111 and ϕCD146. Protection against the myophages ϕMMP01 and ϕCD52 was weaker, with EOP values between 9.0 × 10(−3) and 1.1 × 10(−1). The C‐terminal domain of CwpV carries the antiphage activity and its deletion, or part of it, significantly reduced the antiphage protection. CwpV does not affect phage adsorption, but phage DNA replication is prevented, suggesting a mechanism reminiscent of superinfection exclusion systems normally encoded on prophages. CwpV thus represents a novel ubiquitous host‐encoded and phase‐variable antiphage system in C . difficile.
format Online
Article
Text
id pubmed-4737114
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-47371142016-02-11 The C lostridium difficile cell wall protein CwpV confers phase‐variable phage resistance Sekulovic, Ognjen Ospina Bedoya, Maicol Fivian‐Hughes, Amanda S. Fairweather, Neil F. Fortier, Louis‐Charles Mol Microbiol Research Articles Bacteriophages are present in virtually all ecosystems, and bacteria have developed multiple antiphage strategies to counter their attacks. C lostridium difficile is an important pathogen causing severe intestinal infections in humans and animals. Here we show that the conserved cell‐surface protein CwpV provides antiphage protection in C . difficile. This protein, for which the expression is phase‐variable, is classified into five types, each differing in their repeat‐containing C‐terminal domain. When expressed constitutively from a plasmid or the chromosome of locked ‘ON’ cells of C . difficile  R20291, CwpV conferred antiphage protection. Differences in the level of phage protection were observed depending on the phage morphological group, siphophages being the most sensitive with efficiency of plaquing (EOP) values of < 5 × 10(−7) for phages ϕCD38‐2, ϕCD111 and ϕCD146. Protection against the myophages ϕMMP01 and ϕCD52 was weaker, with EOP values between 9.0 × 10(−3) and 1.1 × 10(−1). The C‐terminal domain of CwpV carries the antiphage activity and its deletion, or part of it, significantly reduced the antiphage protection. CwpV does not affect phage adsorption, but phage DNA replication is prevented, suggesting a mechanism reminiscent of superinfection exclusion systems normally encoded on prophages. CwpV thus represents a novel ubiquitous host‐encoded and phase‐variable antiphage system in C . difficile. John Wiley and Sons Inc. 2015-08-08 2015-10 /pmc/articles/PMC4737114/ /pubmed/26179020 http://dx.doi.org/10.1111/mmi.13121 Text en © 2015 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Sekulovic, Ognjen
Ospina Bedoya, Maicol
Fivian‐Hughes, Amanda S.
Fairweather, Neil F.
Fortier, Louis‐Charles
The C lostridium difficile cell wall protein CwpV confers phase‐variable phage resistance
title The C lostridium difficile cell wall protein CwpV confers phase‐variable phage resistance
title_full The C lostridium difficile cell wall protein CwpV confers phase‐variable phage resistance
title_fullStr The C lostridium difficile cell wall protein CwpV confers phase‐variable phage resistance
title_full_unstemmed The C lostridium difficile cell wall protein CwpV confers phase‐variable phage resistance
title_short The C lostridium difficile cell wall protein CwpV confers phase‐variable phage resistance
title_sort c lostridium difficile cell wall protein cwpv confers phase‐variable phage resistance
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737114/
https://www.ncbi.nlm.nih.gov/pubmed/26179020
http://dx.doi.org/10.1111/mmi.13121
work_keys_str_mv AT sekulovicognjen theclostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance
AT ospinabedoyamaicol theclostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance
AT fivianhughesamandas theclostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance
AT fairweatherneilf theclostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance
AT fortierlouischarles theclostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance
AT sekulovicognjen clostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance
AT ospinabedoyamaicol clostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance
AT fivianhughesamandas clostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance
AT fairweatherneilf clostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance
AT fortierlouischarles clostridiumdifficilecellwallproteincwpvconfersphasevariablephageresistance