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Mycobacteriophage-drived diversification of Mycobacterium abscessus
BACKGROUND: Mycobacterium abscessus is an emerging opportunistic pathogen which diversity was acknowledged by the recent description of two subspecies accommodating M. abscessus, Mycobacterium bolletii and Mycobacterium massiliense isolates. RESULTS: Here, genome analysis found 1–8 prophage regions...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172396/ https://www.ncbi.nlm.nih.gov/pubmed/25224692 http://dx.doi.org/10.1186/1745-6150-9-19 |
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author | Sassi, Mohamed Gouret, Philippe Chabrol, Olivier Pontarotti, Pierre Drancourt, Michel |
author_facet | Sassi, Mohamed Gouret, Philippe Chabrol, Olivier Pontarotti, Pierre Drancourt, Michel |
author_sort | Sassi, Mohamed |
collection | PubMed |
description | BACKGROUND: Mycobacterium abscessus is an emerging opportunistic pathogen which diversity was acknowledged by the recent description of two subspecies accommodating M. abscessus, Mycobacterium bolletii and Mycobacterium massiliense isolates. RESULTS: Here, genome analysis found 1–8 prophage regions in 47/48 M. abscessus genomes ranging from small prophage-like elements to complete prophages. A total of 20,304 viral and phage proteins clustered into 853 orthologous groups. Phylogenomic and phylogenetic analyses based on prophage region homology found three main clusters corresponding to M. abscessus, M. bolletii and M. massiliense. Analysing 135 annotated Tape Measure Proteins found thirteen clusters and four singletons, suggesting that at least 17 mycobacteriophages had infected M. abscessus during its evolution. The evolutionary history of phages differed from that of their mycobacterial hosts. In particular, 33 phage-related proteins have been horizontally transferred within M. abscessus genomes. They comprise of an integrase, specific mycobacteriophage proteins, hypothetical proteins and DNA replication and metabolism proteins. Gene exchanges, loss and gains which occurred in M. abscessus genomes have been driven by several mycobacteriophages. CONCLUSIONS: This analysis of phage-mycobacterium co-evolution suggests that mycobacteriophages are playing a key-role in the on-going diversification of M. abscessus. REVIEWERS: This article was reviewed by Eric Bapteste, Patrick Forterre and Eugene Koonin. |
format | Online Article Text |
id | pubmed-4172396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41723962014-09-24 Mycobacteriophage-drived diversification of Mycobacterium abscessus Sassi, Mohamed Gouret, Philippe Chabrol, Olivier Pontarotti, Pierre Drancourt, Michel Biol Direct Research BACKGROUND: Mycobacterium abscessus is an emerging opportunistic pathogen which diversity was acknowledged by the recent description of two subspecies accommodating M. abscessus, Mycobacterium bolletii and Mycobacterium massiliense isolates. RESULTS: Here, genome analysis found 1–8 prophage regions in 47/48 M. abscessus genomes ranging from small prophage-like elements to complete prophages. A total of 20,304 viral and phage proteins clustered into 853 orthologous groups. Phylogenomic and phylogenetic analyses based on prophage region homology found three main clusters corresponding to M. abscessus, M. bolletii and M. massiliense. Analysing 135 annotated Tape Measure Proteins found thirteen clusters and four singletons, suggesting that at least 17 mycobacteriophages had infected M. abscessus during its evolution. The evolutionary history of phages differed from that of their mycobacterial hosts. In particular, 33 phage-related proteins have been horizontally transferred within M. abscessus genomes. They comprise of an integrase, specific mycobacteriophage proteins, hypothetical proteins and DNA replication and metabolism proteins. Gene exchanges, loss and gains which occurred in M. abscessus genomes have been driven by several mycobacteriophages. CONCLUSIONS: This analysis of phage-mycobacterium co-evolution suggests that mycobacteriophages are playing a key-role in the on-going diversification of M. abscessus. REVIEWERS: This article was reviewed by Eric Bapteste, Patrick Forterre and Eugene Koonin. BioMed Central 2014-09-15 /pmc/articles/PMC4172396/ /pubmed/25224692 http://dx.doi.org/10.1186/1745-6150-9-19 Text en Copyright © 2014 Sassi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Sassi, Mohamed Gouret, Philippe Chabrol, Olivier Pontarotti, Pierre Drancourt, Michel Mycobacteriophage-drived diversification of Mycobacterium abscessus |
title | Mycobacteriophage-drived diversification of Mycobacterium abscessus |
title_full | Mycobacteriophage-drived diversification of Mycobacterium abscessus |
title_fullStr | Mycobacteriophage-drived diversification of Mycobacterium abscessus |
title_full_unstemmed | Mycobacteriophage-drived diversification of Mycobacterium abscessus |
title_short | Mycobacteriophage-drived diversification of Mycobacterium abscessus |
title_sort | mycobacteriophage-drived diversification of mycobacterium abscessus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172396/ https://www.ncbi.nlm.nih.gov/pubmed/25224692 http://dx.doi.org/10.1186/1745-6150-9-19 |
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