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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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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 |
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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 |
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