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dc.rights.licenseopenen_US
dc.contributor.authorHUITS, R.
dc.contributor.authorDE SMET, B.
dc.contributor.authorGRARD, G.
dc.contributor.authorEGGERMONT, K.
dc.contributor.authorMINTO-BAIN, C.
dc.contributor.authorJESS, N.
dc.contributor.authorLEPARC-GOFFART, I.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorMALVY, Denis
dc.contributor.authorCNOPS, L.
dc.date.accessioned2021-01-26T14:59:19Z
dc.date.available2021-01-26T14:59:19Z
dc.date.issued2020
dc.identifier.issn1537-6613 (Electronic) 0022-1899 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/26033
dc.description.abstractEnBackground Persistence of Zika virus (ZIKV) ribonucleic acid (RNA) in semen is common after infection. Methods We designed a reverse-transcription polymerase chain reaction assay that targets antisense ZIKV RNA (asRNA) to assess ZIKV replication competence in ZIKV RNA-positive semen samples. Results We detected ZIKV asRNA in semen of 9 of 19 men (47.4%) diagnosed with ZIKV infection. All asRNA-positive samples had high ZIKV loads (cycle threshold values <26) and were obtained within 21 days of symptom onset. Conclusions The sensitivity of the asRNA assay for detection of ZIKV replication was higher than that of conventional virus isolation methods (47.4% vs 21.1%, P = .032).
dc.language.isoENen_US
dc.subjectIDLIC
dc.title.enDetection of Zika Virus Replication in Human Semen by Reverse-Transcription Polymerase Chain Reaction Targeting of Antisense Ribonucleic Acid
dc.title.alternativeJ Infect Disen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/infdis/jiaa070en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
bordeaux.journalJournal of Infectious Diseasesen_US
bordeaux.page319-323en_US
bordeaux.volume222en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - U1219en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.teamIDLICen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03121809
hal.version1
hal.date.transferred2021-01-26T14:59:22Z
hal.exporttrue
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