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dc.contributor.authorNúñez-Egido, Sandra
dc.contributor.authorLowther, Andrew
dc.contributor.authorNymo, Ingebørg H.
dc.contributor.authorKlein, Jörn
dc.contributor.authorBreines, Eva Marie
dc.contributor.authorTryland, Morten
dc.date.accessioned2021-11-09T09:02:09Z
dc.date.available2021-11-09T09:02:09Z
dc.date.created2021-01-05T15:24:08Z
dc.date.issued2020
dc.identifier.citationPolar Research. 2020, 39 1-11.
dc.identifier.issn0800-0395
dc.identifier.urihttps://hdl.handle.net/11250/2828563
dc.description.abstractKnowledge of the health status and potential effect of disease outbreaks among Southern Ocean fauna may be decisive for its conservation. We assessed the exposure and infection of Antarctic fur seals (Arctocephalus gazella, AFS) and Southern elephant seals (Mirounga leonine, SES) to parapoxvirus, Phocid alphaherpesvirus-1 (PhHV-1), smooth Brucella spp. and Toxoplasma gon-dii. AFS (n = 65) serum and swab samples, and SES (n = 13) serum samples from the sub- Antarctic island of Bouvetøya (54°25’S, 03°22’E) were collected during two austral summers (2014/15, 2017/18). Three polymerase chain reaction (PCR) tests amplifying the DNA polymerase, B2L and GIF parapoxvi-rus genomic regions were performed, investigating DNA from mucosal swab samples. The glycoprotein B gene was targeted to detect PhHV-1 viral DNA. Sera were assayed for T. gondii and smooth Brucella spp. antibodies with indi-rect enzyme-linked immunosorbent assays. Parapoxvirus PCR amplicons of the expected size were generated in two of the 29 AFS pups (nasal swabs, 2014/15), targeting the B2L (n = 2) and DNA polymerase (n = 1) genes, whereas the GIF PCR did not amplify target sequences. The PCR amplicons were sequenced and blasted in GenBank, revealing highest similarity with a seal parapoxvirus, confirming the presence of the virus in AFS for the first time. No PhHV-1 amplicons were generated, and antibodies against T. gondii or smooth Brucella spp. were not detected. Our data indicate that these seals are host for parapoxvirus but are neither exposed to smooth Brucella spp. nor T. gondii. Evidence of PhHV-1 shedding was not detected .
dc.language.isoeng
dc.subjectSel
dc.subjectPinnipeds
dc.subjectDyrehelse
dc.subjectAnimal health
dc.titlePathogen surveillance in Southern Ocean pinnipeds
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.33265/polar.v39.3841
dc.identifier.cristin1865797
dc.source.journalPolar Research
dc.source.volume39
dc.source.pagenumber1-11


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