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dc.contributor.authorFlannery, John
dc.contributor.authorVan Rijn, Piet A.
dc.contributor.authorRajko-Nenow, Paulina
dc.contributor.authorArnold, Hannah
dc.contributor.authorVan Weezep, Erik
dc.date.accessioned2019-10-01T07:22:51Z
dc.date.available2019-10-01T07:22:51Z
dc.date.issued2019
dc.identifier.citationFlannery, J. et al. 2019. Improved PCR diagnostics using up-to-date in silico validation: an F-gene RT-qPCR assay for the detection of all four lineages of peste des petits ruminants virus. Journal of virological methods, 274: Article no 113735. [https://doi.org/10.1016/j.jviromet.2019.113735]en_US
dc.identifier.issn0166-0934
dc.identifier.issn1879-0984 (Online)
dc.identifier.urihttp://hdl.handle.net/10394/33377
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0166093419302848/pdfft?md5=ed907fa2d4db8eda44e8b77d6f08ac40&pid=1-s2.0-S0166093419302848-main.pdf
dc.identifier.urihttps://doi.org/10.1016/j.jviromet.2019.113735
dc.description.abstractPeste des petits ruminants (PPR) is a globally significant disease of small ruminants caused by the peste des petits ruminants virus (PPRV) that is considered for eradication by 2030 by the United Nations Food and Agriculture Organisation (FAO). Critical to the eradication of PPR are accurate diagnostic assays. RT-qPCR assays targeting the nucleocapsid gene of PPRV have been successfully used for the diagnosis of PPR. We describe the development of an RT-qPCR assay targeting an alternative region (the fusion (F) gene) based on the most up-to-date PPRV sequence data. In silico analysis of the F-gene RT-qPCR assay performed using PCRv software indicated 98% sensitivity and 100% specificity against all PPRV sequences published in Genbank. The assay indicated the greatest in silico sensitivity in comparison to other previously published and recommended PPRV RT-qPCR assays. We evaluated the assay using strains representative of all 4 lineages in addition to samples obtained from naturally and experimentally-infected animals. The F-gene RT-qPCR assay showed 100% diagnostic specificity and demonstrated a limit of detection of 10 PPRV genome copies per μl. This RT-qPCR assay can be used in isolation or in conjunction with other assays for confirmation of PPR and should support the global efforts for eradicationen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectRapid detectionen_US
dc.subjectIn silicoen_US
dc.subjectPPRVen_US
dc.subjectRT-qPCRen_US
dc.titleImproved PCR diagnostics using up-to-date in silico validation: an F-gene RT-qPCR assay for the detection of all four lineages of peste des petits ruminants virusen_US
dc.typeArticleen_US
dc.contributor.researchID24551287 - Van Rijn, Petrus Antonius


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