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Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa

BACKGROUND: Winter-ulcer Moritella viscosa infections continue to be a significant burden in Atlantic salmon (Salmo salar L.) farming. M. viscosa comprises two main clusters that differ in genetic variation and phenotypes including virulence. Horizontal gene transfer through acquisition and loss of...

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Detalles Bibliográficos
Autores principales: Karlsen, Christian, Hjerde, Erik, Klemetsen, Terje, Willassen, Nils Peder
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399434/
https://www.ncbi.nlm.nih.gov/pubmed/28427330
http://dx.doi.org/10.1186/s12864-017-3693-7
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author Karlsen, Christian
Hjerde, Erik
Klemetsen, Terje
Willassen, Nils Peder
author_facet Karlsen, Christian
Hjerde, Erik
Klemetsen, Terje
Willassen, Nils Peder
author_sort Karlsen, Christian
collection PubMed
description BACKGROUND: Winter-ulcer Moritella viscosa infections continue to be a significant burden in Atlantic salmon (Salmo salar L.) farming. M. viscosa comprises two main clusters that differ in genetic variation and phenotypes including virulence. Horizontal gene transfer through acquisition and loss of mobile genetic elements (MGEs) is a major driving force of bacterial diversification. To gain insight into genomic traits that could affect sublineage evolution within this bacterium we examined the genome sequences of twelve M. viscosa strains. Matches between M. viscosa clustered, regularly interspaced, short palindromic, repeats and associated cas genes (CRISPR-Cas) were analysed to correlate CRISPR-Cas with adaptive immunity against MGEs. RESULTS: The comparative genomic analysis of M. viscosa isolates from across the North Atlantic region and from different fish species support delineation of M. viscosa into four phylogenetic lineages. The results showed that M. viscosa carries two distinct variants of the CRISPR-Cas subtype I-F systems and that CRISPR features follow the phylogenetic lineages. A subset of the spacer content match prophage and plasmid genes dispersed among the M. viscosa strains. Further analysis revealed that prophage and plasmid-like element distribution were reflected in the content of the CRISPR-spacer profiles. CONCLUSIONS: Our data suggests that CRISPR-Cas mediated interactions with MGEs impact genome properties among M. viscosa, and that patterns in spacer and MGE distributions are linked to strain relationships. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3693-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-53994342017-04-24 Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa Karlsen, Christian Hjerde, Erik Klemetsen, Terje Willassen, Nils Peder BMC Genomics Research Article BACKGROUND: Winter-ulcer Moritella viscosa infections continue to be a significant burden in Atlantic salmon (Salmo salar L.) farming. M. viscosa comprises two main clusters that differ in genetic variation and phenotypes including virulence. Horizontal gene transfer through acquisition and loss of mobile genetic elements (MGEs) is a major driving force of bacterial diversification. To gain insight into genomic traits that could affect sublineage evolution within this bacterium we examined the genome sequences of twelve M. viscosa strains. Matches between M. viscosa clustered, regularly interspaced, short palindromic, repeats and associated cas genes (CRISPR-Cas) were analysed to correlate CRISPR-Cas with adaptive immunity against MGEs. RESULTS: The comparative genomic analysis of M. viscosa isolates from across the North Atlantic region and from different fish species support delineation of M. viscosa into four phylogenetic lineages. The results showed that M. viscosa carries two distinct variants of the CRISPR-Cas subtype I-F systems and that CRISPR features follow the phylogenetic lineages. A subset of the spacer content match prophage and plasmid genes dispersed among the M. viscosa strains. Further analysis revealed that prophage and plasmid-like element distribution were reflected in the content of the CRISPR-spacer profiles. CONCLUSIONS: Our data suggests that CRISPR-Cas mediated interactions with MGEs impact genome properties among M. viscosa, and that patterns in spacer and MGE distributions are linked to strain relationships. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3693-7) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-20 /pmc/articles/PMC5399434/ /pubmed/28427330 http://dx.doi.org/10.1186/s12864-017-3693-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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 Article
Karlsen, Christian
Hjerde, Erik
Klemetsen, Terje
Willassen, Nils Peder
Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa
title Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa
title_full Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa
title_fullStr Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa
title_full_unstemmed Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa
title_short Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa
title_sort pan genome and crispr analyses of the bacterial fish pathogen moritella viscosa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399434/
https://www.ncbi.nlm.nih.gov/pubmed/28427330
http://dx.doi.org/10.1186/s12864-017-3693-7
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