Comparative analysis of the complete genome sequence of the California MSW strain of myxoma virus reveals potential host adaptations

dc.contributor.authorKerr, Peter J.
dc.contributor.authorRogers, Matthew B.
dc.contributor.authorFitch, Adam
dc.contributor.authorDepasse, Jay V.
dc.contributor.authorCattadori, Isabella M
dc.contributor.authorHudson, Peter J.
dc.contributor.authorTscharke, David C.
dc.contributor.authorHolmes, Edward C.
dc.contributor.authorGhedin, Elodie
dc.date.accessioned2015-03-13T00:30:32Z
dc.date.available2015-03-13T00:30:32Z
dc.date.issued2013-11
dc.date.updated2015-12-11T09:00:51Z
dc.description.abstractMyxomatosis is a rapidly lethal disease of European rabbits that is caused by myxoma virus (MYXV). The introduction of a South American strain of MYXV into the European rabbit population of Australia is the classic case of host-pathogen coevolution following cross-species transmission. The most virulent strains of MYXV for European rabbits are the Californian viruses, found in the Pacific states of the United States and the Baja Peninsula, Mexico. The natural host of Californian MYXV is the brush rabbit, Sylvilagus bachmani. We determined the complete sequence of the MSW strain of Californian MYXV and performed a comparative analysis with other MYXV genomes. The MSW genome is larger than that of the South American Lausanne (type) strain of MYXV due to an expansion of the terminal inverted repeats (TIRs) of the genome, with duplication of the M156R, M154L, M153R, M152R, and M151R genes and part of the M150R gene from the right-hand (RH) end of the genome at the left-hand (LH) TIR. Despite the extreme virulence of MSW, no novel genes were identified; five genes were disrupted by multiple indels or mutations to the ATG start codon, including two genes, M008.1L/R and M152R, with major virulence functions in European rabbits, and a sixth gene, M000.5L/R, was absent. The loss of these gene functions suggests that S. bachmani is a relatively recent host for MYXV and that duplication of virulence genes in the TIRs, gene loss, or sequence variation in other genes can compensate for the loss of M008.1L/R and M152R in infections of European rabbits.
dc.description.sponsorshipThis work was funded in part by grant R01 AI093804 from the National Institute of Allergy and Infectious Diseases, National Institutes of Health. E.C.H. was supported by an NHMRC Australia Fellowship, and D.C.T. was supported by an ARC Future Fellowship.en_AU
dc.identifier.issn0022-538X
dc.identifier.urihttp://hdl.handle.net/1885/12901
dc.publisherAmerican Society for Microbiology
dc.rightshttp://www.sherpa.ac.uk/romeo/issn/0022-538X/..."Author's post-print on funder's repositories, institutional repository or subject-based repositories. Publisher's version/PDF may be used on author's personal website or employers website" from SHERPA/RoMEO site (as at 13/03/15)
dc.sourceJournal of virology
dc.subjectAdaptation, Physiological
dc.subjectAnimals
dc.subjectBase Sequence
dc.subjectBiological Evolution
dc.subjectCalifornia
dc.subjectEurope
dc.subjectMexico
dc.subjectMolecular Sequence Data
dc.subjectMyxoma virus
dc.subjectMyxomatosis, Infectious
dc.subjectPhylogeny
dc.subjectRabbits
dc.subjectSequence Homology, Nucleic Acid
dc.subjectTerminal Repeat Sequences
dc.subjectTumor Virus Infections
dc.subjectViral Proteins
dc.subjectVirulence
dc.subjectVirus Replication
dc.subjectGenome, Viral
dc.titleComparative analysis of the complete genome sequence of the California MSW strain of myxoma virus reveals potential host adaptations
dc.typeJournal article
dcterms.dateAccepted2013-08-22
local.bibliographicCitation.issue22en_AU
local.bibliographicCitation.lastpage12089en_AU
local.bibliographicCitation.startpage12080en_AU
local.contributor.affiliationTscharke, D. C. Research School of Biology, The Australian National Universityen_AU
local.contributor.authoremaildavid.tscharke@anu.edu.auen_AU
local.contributor.authoruidu4334102en_AU
local.identifier.absfor110700 - IMMUNOLOGY
local.identifier.absfor060500 - MICROBIOLOGY
local.identifier.ariespublicationf5625xPUB4542
local.identifier.citationvolume87en_AU
local.identifier.doi10.1128/JVI.01923-13en_AU
local.identifier.essn1098-5514en_AU
local.identifier.scopusID2-s2.0-84886243948
local.identifier.thomsonID000325865400010
local.identifier.uidSubmittedByu4334102en_AU
local.publisher.urlhttp://www.asm.org/en_AU
local.type.statusPublished Versionen_AU

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