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dc.contributor.authorHjerde, Erik
dc.contributor.authorLorentzen, Marit Sjo
dc.contributor.authorHolden, Matthew T. G.
dc.contributor.authorSeeger, Kathy
dc.contributor.authorPaulsen, Steinar
dc.contributor.authorBason, Nathalie
dc.contributor.authorChurcher, Carol
dc.contributor.authorHarris, David
dc.contributor.authorNorbertczak, Halina
dc.contributor.authorQuail, Michael A.
dc.contributor.authorSanders, Suzanne
dc.contributor.authorThurston, Scott
dc.contributor.authorParkhill, Julian
dc.contributor.authorWillassen, Nils Peder
dc.contributor.authorThomson, Nicholas R.
dc.date.accessioned2014-04-28T15:01:33Z
dc.date.available2014-04-28T15:01:33Z
dc.date.issued2008-12-19
dc.identifier.citationHjerde , E , Lorentzen , M S , Holden , M T G , Seeger , K , Paulsen , S , Bason , N , Churcher , C , Harris , D , Norbertczak , H , Quail , M A , Sanders , S , Thurston , S , Parkhill , J , Willassen , N P & Thomson , N R 2008 , ' The genome sequence of the fish pathogen Aliivibrio salmonicida strain LFI1238 shows extensive evidence of gene decay ' BMC Genomics , vol. 9 , 616 . DOI: 10.1186/1471-2164-9-616en
dc.identifier.issn1471-2164
dc.identifier.otherPURE: 91774279
dc.identifier.otherPURE UUID: 7f4f4792-55c1-4581-8606-4da76c8c9c0c
dc.identifier.otherWOS: 000263109800001
dc.identifier.otherScopus: 59449093840
dc.identifier.urihttp://hdl.handle.net/10023/4638
dc.descriptionThis work was partly supported by grants from The Research Council of Norway and the University of Tromsø.en
dc.description.abstractBackground: The fish pathogen Aliivibrio salmonicida is the causative agent of cold-water vibriosis in marine aquaculture. The Gram-negative bacterium causes tissue degradation, hemolysis and sepsis in vivo. Results: In total, 4 286 protein coding sequences were identified, and the 4.6 Mb genome of A. salmonicida has a six partite architecture with two chromosomes and four plasmids. Sequence analysis revealed a highly fragmented genome structure caused by the insertion of an extensive number of insertion sequence (IS) elements. The IS elements can be related to important evolutionary events such as gene acquisition, gene loss and chromosomal rearrangements. New A. salmonicida functional capabilities that may have been aquired through horizontal DNA transfer include genes involved in iron-acquisition, and protein secretion and play potential roles in pathogenicity. On the other hand, the degeneration of 370 genes and consequent loss of specific functions suggest that A. salmonicida has a reduced metabolic and physiological capacity in comparison to related Vibrionaceae species. Conclusion: Most prominent is the loss of several genes involved in the utilisation of the polysaccharide chitin. In particular, the disruption of three extracellular chitinases responsible for enzymatic breakdown of chitin makes A. salmonicida unable to grow on the polymer form of chitin. These, and other losses could restrict the variety of carrier organisms A. salmonicida can attach to, and associate with. Gene acquisition and gene loss may be related to the emergence of A. salmonicida as a fish pathogen.en
dc.format.extent14en
dc.language.isoeng
dc.relation.ispartofBMC Genomicsen
dc.rights© 2008 Hjerde et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly citeden
dc.subjectWidespread colonization islanden
dc.subjectBacterium vibrio-furnissiien
dc.subjectChitin-binding proteinsen
dc.subject2 tonb systemsen
dc.subjectSalmo-salar len
dc.subjectAtlantic-salmonen
dc.subjectMolecular-cloningen
dc.subjectEscherichia-colien
dc.subjectCausative agenten
dc.subjectCholeraeen
dc.subjectQH426 Geneticsen
dc.subjectQL Zoologyen
dc.subject.lccQH426en
dc.subject.lccQLen
dc.titleThe genome sequence of the fish pathogen Aliivibrio salmonicida strain LFI1238 shows extensive evidence of gene decayen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Infection Groupen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doihttps://doi.org/10.1186/1471-2164-9-616
dc.description.statusPeer revieweden


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