dc.contributor.author | Karlsen, Christian | |
dc.contributor.author | Hjerde, Erik | |
dc.contributor.author | Klemetsen, Terje | |
dc.contributor.author | Willassen, Nils Peder | |
dc.date.accessioned | 2017-06-08T11:56:04Z | |
dc.date.available | 2017-06-08T11:56:04Z | |
dc.date.issued | 2017-04-20 | |
dc.description.abstract | 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. <p>
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.
<p>
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. | en_US |
dc.description | Source at <a href=http://dx.doi.org/10.1186/s12864-017-3693-7> http://dx.doi.org/10.1186/s12864-017-3693-7 </a> | en_US |
dc.identifier.citation | Karlsen C, Hjerde E, Klemetsen T, Willassen NP. Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa. BMC Genomics. 2017;18:313 | en_US |
dc.identifier.cristinID | FRIDAID 1469050 | |
dc.identifier.doi | 10.1186/s12864-017-3693-7 | |
dc.identifier.issn | 1471-2164 | |
dc.identifier.uri | https://hdl.handle.net/10037/11125 | |
dc.language.iso | eng | en_US |
dc.publisher | BioMed Central | en_US |
dc.relation.journal | BMC Genomics | |
dc.relation.projectID | Norges forskningsråd: 216196 | en_US |
dc.relation.projectID | Nofima AS: 11268 | en_US |
dc.relation.projectID | eu-repo/grantAgreement/RCN/HAVBRUK/216196/NORWAY/Coordinated Bacterial Virulence: Relevance in Winter Ulcer// | en_US |
dc.rights.accessRights | openAccess | en_US |
dc.subject | VDP::Landbruks- og Fiskerifag: 900::Fiskerifag: 920 | en_US |
dc.subject | VDP::Agriculture and fishery disciplines: 900::Fisheries science: 920 | en_US |
dc.title | Pan genome and CRISPR analyses of the bacterial fish pathogen Moritella viscosa | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |