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dc.contributor.authorRadzijevskaja, Jana
dc.contributor.authorPaulauskas, Algimantas
dc.contributor.authorRosef, Olav
dc.date.accessioned2009-07-09T12:02:26Z
dc.date.accessioned2017-04-19T12:25:04Z
dc.date.available2009-07-09T12:02:26Z
dc.date.available2017-04-19T12:25:04Z
dc.date.issued2008
dc.identifier.citationInternational journal of medical microbiology 298(2008), Suppl.1, p. 218-221
dc.identifier.issn1618-0607
dc.identifier.issn1438-4221
dc.identifier.urihttp://hdl.handle.net/11250/2438029
dc.description.abstractWe detected Anaplasma phagocytophilum and Babesia divergens in Ixodes ricinus ticks collected from different locations in Lithuania and Norway by using the Taq Man based real-time PCR method. The msp2 gene of A. phagocytophilum and the 18S rRNA gene of B. divergens have been chosen as amplification targets. The overall infection rate of A. phagocytophilum in Norwegian ticks was 4.5% (10/224) and in Lithuanian ticks 3% (4/140). The prevalence varied in locations between 0% and 9% in Lithuania and in Norway. Three out of 140 (2%) ticks were infected with B. divergens in Lithuania and two out of 224 (0.9%) in Norway. The prevalence of B. divergens infection varied from 0% to 3% and from 0% to 4% in different sites in Lithuania and Norway, respectively.
dc.language.isoeng
dc.publisherElsevier
dc.subjectTicks
dc.subjectReal-time PCR
dc.subjectAnaplasma phagocytophilum
dc.subjectBabesia divergens
dc.titlePrevalence of Anaplasma phagocytophilum and Babesia divergens in Ixodes ricinus ticks from Lithuania and Norway
dc.typeJournal article
dc.typePeer reviewed
dc.subject.nsi715
dc.subject.nsi474
dc.source.journalInternational journal of medical microbiology
dc.identifier.doihttp://dx.doi.org/10.1016/j.ijmm.2008.01.008


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