Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/115623
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorShrestha, A.C.-
dc.contributor.authorFlower, R.L.-
dc.contributor.authorSeed, C.R.-
dc.contributor.authorKeller, A.J.-
dc.contributor.authorHarley, R.-
dc.contributor.authorChan, H.-T.-
dc.contributor.authorHoad, V.-
dc.contributor.authorWarrilow, D.-
dc.contributor.authorNorthill, J.-
dc.contributor.authorHolmberg, J.A.-
dc.contributor.authorFaddy, H.M.-
dc.date.issued2016-
dc.identifier.citationTransfusion, 2016; 56(12):3086-3093-
dc.identifier.issn0041-1132-
dc.identifier.issn1537-2995-
dc.identifier.urihttp://hdl.handle.net/2440/115623-
dc.description.abstractBackground: Hepatitis E virus (HEV) poses a risk to transfusion safety. In Australia, locally acquired HEV is rare and cases are mainly reported in travelers returning from countries endemic for HEV. The risk posed by HEV to transfusion safety in Australia is unknown; therefore, we aimed to measure the rate of current HEV infection in Australian blood donations. Study Design and Methods: A total of 14,799 blood donations were tested for HEV RNA by transcription-mediated amplification, with confirmatory testing by reverse transcription–polymerase chain reaction. Viral load quantification and phylogenetic analysis was performed on HEV RNA–positive samples. Results: One (0.0068%; 95% confidence interval [CI], 0.0002%-0.0376%) sample was confirmed positive for HEV RNA, resulting in a risk of collecting a HEV-viremic donation of 1 in 14,799 (95% CI, 1 in 584,530 to 1 in 2,657). The viral load in this sample was approximately 15,000 IU/mL, and it was determined to be Genotype 3. Discussion: Our finding of 1 in 14,799 Australian donations positive for HEV RNA is lower than that from many other developed countries; this is consistent with the relatively low seroprevalence in Australia. As this HEV RNA–positive sample was Genotype 3, it seems likely that this infection was acquired through zoonotic transmission, either within Australia or overseas in a developed nation. HEV has the potential to pose a risk to transfusion safety in Australia; however, additional, larger studies are required to quantify the magnitude of this risk.-
dc.description.statementofresponsibilityAshish C. Shrestha, Robert L.P. Flower, Clive R. Seed, Anthony J. Keller, Robert Harley, Hiu-Tat Chan, Veronica Hoad, David Warrilow, Judith Northill, Jerry A. Holmberg, and Helen M. Faddy-
dc.language.isoen-
dc.publisherWiley-
dc.rights© 2016 AABB-
dc.source.urihttp://dx.doi.org/10.1111/trf.13799-
dc.subjectHumans-
dc.subjectHepatitis E virus-
dc.subjectHepatitis E-
dc.subjectRNA, Viral-
dc.subjectViral Load-
dc.subjectSeroepidemiologic Studies-
dc.subjectPolymerase Chain Reaction-
dc.subjectPhylogeny-
dc.subjectBlood Donors-
dc.subjectAustralia-
dc.subjectBlood Safety-
dc.subjectTransfusion Reaction-
dc.titleHepatitis E virus RNA in Australian blood donations-
dc.typeJournal article-
dc.identifier.doi10.1111/trf.13799-
pubs.publication-statusPublished-
dc.identifier.orcidShrestha, A.C. [0000-0001-5049-8351]-
Appears in Collections:Aurora harvest 3
Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.