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Convergent evolution of pathogenicity islands in helper cos phage interference
Staphylococcus aureus pathogenicity islands (SaPIs) are phage satellites that exploit the life cycle of their helper phages for their own benefit. Most SaPIs are packaged by their helper phages using a headful (pac) packaging mechanism. These SaPIs interfere with pac phage reproduction through a var...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052747/ https://www.ncbi.nlm.nih.gov/pubmed/27672154 http://dx.doi.org/10.1098/rstb.2015.0505 |
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author | Carpena, Nuria Manning, Keith A. Dokland, Terje Marina, Alberto Penadés, José R. |
author_facet | Carpena, Nuria Manning, Keith A. Dokland, Terje Marina, Alberto Penadés, José R. |
author_sort | Carpena, Nuria |
collection | PubMed |
description | Staphylococcus aureus pathogenicity islands (SaPIs) are phage satellites that exploit the life cycle of their helper phages for their own benefit. Most SaPIs are packaged by their helper phages using a headful (pac) packaging mechanism. These SaPIs interfere with pac phage reproduction through a variety of strategies, including the redirection of phage capsid assembly to form small capsids, a process that depends on the expression of the SaPI-encoded cpmA and cpmB genes. Another SaPI subfamily is induced and packaged by cos-type phages, and although these cos SaPIs also block the life cycle of their inducing phages, the basis for this mechanism of interference remains to be deciphered. Here we have identified and characterized one mechanism by which the SaPIs interfere with cos phage reproduction. This mechanism depends on a SaPI-encoded gene, ccm, which encodes a protein involved in the production of small isometric capsids, compared with the prolate helper phage capsids. As the Ccm and CpmAB proteins are completely unrelated in sequence, this strategy represents a fascinating example of convergent evolution. Moreover, this result also indicates that the production of SaPI-sized particles is a widespread strategy of phage interference conserved during SaPI evolution. This article is part of the themed issue ‘The new bacteriology’. |
format | Online Article Text |
id | pubmed-5052747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50527472016-11-05 Convergent evolution of pathogenicity islands in helper cos phage interference Carpena, Nuria Manning, Keith A. Dokland, Terje Marina, Alberto Penadés, José R. Philos Trans R Soc Lond B Biol Sci Articles Staphylococcus aureus pathogenicity islands (SaPIs) are phage satellites that exploit the life cycle of their helper phages for their own benefit. Most SaPIs are packaged by their helper phages using a headful (pac) packaging mechanism. These SaPIs interfere with pac phage reproduction through a variety of strategies, including the redirection of phage capsid assembly to form small capsids, a process that depends on the expression of the SaPI-encoded cpmA and cpmB genes. Another SaPI subfamily is induced and packaged by cos-type phages, and although these cos SaPIs also block the life cycle of their inducing phages, the basis for this mechanism of interference remains to be deciphered. Here we have identified and characterized one mechanism by which the SaPIs interfere with cos phage reproduction. This mechanism depends on a SaPI-encoded gene, ccm, which encodes a protein involved in the production of small isometric capsids, compared with the prolate helper phage capsids. As the Ccm and CpmAB proteins are completely unrelated in sequence, this strategy represents a fascinating example of convergent evolution. Moreover, this result also indicates that the production of SaPI-sized particles is a widespread strategy of phage interference conserved during SaPI evolution. This article is part of the themed issue ‘The new bacteriology’. The Royal Society 2016-11-05 /pmc/articles/PMC5052747/ /pubmed/27672154 http://dx.doi.org/10.1098/rstb.2015.0505 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Articles Carpena, Nuria Manning, Keith A. Dokland, Terje Marina, Alberto Penadés, José R. Convergent evolution of pathogenicity islands in helper cos phage interference |
title | Convergent evolution of pathogenicity islands in helper cos phage interference |
title_full | Convergent evolution of pathogenicity islands in helper cos phage interference |
title_fullStr | Convergent evolution of pathogenicity islands in helper cos phage interference |
title_full_unstemmed | Convergent evolution of pathogenicity islands in helper cos phage interference |
title_short | Convergent evolution of pathogenicity islands in helper cos phage interference |
title_sort | convergent evolution of pathogenicity islands in helper cos phage interference |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052747/ https://www.ncbi.nlm.nih.gov/pubmed/27672154 http://dx.doi.org/10.1098/rstb.2015.0505 |
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