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dc.contributor.authorTešović, Bojana
dc.contributor.authorNišavić, Jakov
dc.contributor.authorBanović Đeri, Bojana
dc.contributor.authorPetrović, Tamaš
dc.contributor.authorRadalj, Andrea
dc.contributor.authorŠekler, Milanko
dc.contributor.authorMatović, Kazimir
dc.contributor.authorDebeljak, Zoran
dc.contributor.authorVasković, Nikola
dc.contributor.authorDmitrić, Marko
dc.contributor.authorVidanović, Dejan
dc.date.accessioned2022-11-27T09:40:33Z
dc.date.available2022-11-27T09:40:33Z
dc.date.issued2023
dc.identifier.issn0732-8893
dc.identifier.urihttps://repo.niv.ns.ac.rs/xmlui/handle/123456789/586
dc.description.abstractWest Nile virus (WNV) can affect humans, birds, horses and another mammals, causing asymptomatic infection, mild febrile disease, neurological and systematic disease and death. In order to gain insight into the prevalence of WNV, a monitoring program has been established in the Republic of Serbia. Whole genome sequencing is essential for the molecular epizootiological analysis of virus entry and transmission routes, especially in high-risk regions. This paper describes the development of a multiplex PCR based NGS protocol for whole genome sequencing of WNV lineage 2 directly from biological samples using Oxford Nanopore (ONT) platform. The results obtained using this platform, confirmed by Sanger sequencing, indicate that this protocol can be applied to obtain whole sequences of the WNV genome, even when the virus concentration in the sample is medium, Ct value is approximately 30. The use of this protocol does not require prior virus isolation on cell culture nor the depletion of host nucleic acids.en_US
dc.language.isoenen_US
dc.sourceDiagnostic Microbiology and Infectious Diseaseen
dc.subjectWest Nile virusen_US
dc.subjectlineage 2en_US
dc.subjectmultiplex PCRen_US
dc.subjectnext generation sequencingen_US
dc.subjectMinIONen_US
dc.subjectOxford Nanopore platformen_US
dc.titleDevelopment of multiplex PCR based NGS protocol for whole genome sequencing of West Nile virus lineage 2 directly from biological samples using Oxford Nanopore platformen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.diagmicrobio.2022.115852


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