| Literature DB >> 31727377 |
Alejandra Rojas1, Victoria Stittleburg2, Fátima Cardozo3, Nathen Bopp4, César Cantero1, Sanny López1, Cynthia Bernal1, Laura Mendoza3, Patricia Aguilar4, Benjamin A Pinsky5, Yvalena Guillén1, Malvina Páez3, Jesse J Waggoner6.
Abstract
Oropouche virus (OROV) causes an acute, systemic febrile illness, and in certain regions of South America, this represents the second most common human arboviral infection after dengue virus. A new real-time RT-PCR was developed for OROV and reassortant species. The new OROV rRT-PCR proved linear across 6-7 orders of magnitude with a lower limit of 95% detection of 5.6-10.8 copies/μL. Upon testing dilutions of OROV and Iquitos virus reference genomic RNA, all dilutions with >10 copies/μL were detected in both the OROV rRT-PCR and a comparator molecular assay, but the OROV rRT-PCR detected more samples with ≤10 copies/μL (8/14 vs 0/13, respectively, P = 0.002). In a set of 100 acute-phase clinical samples from Paraguay patients with a suspected arboviral illness, no patients tested positive for OROV RNA using either assay. The OROV rRT-PCR provides a sensitive molecular assay for the study of this important yet neglected tropical arboviral infection.Entities:
Keywords: Oropouche virus; Orthobunyavirus; Quantitative real-time PCR; Reverse transcriptase PCR
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Year: 2019 PMID: 31727377 PMCID: PMC6906250 DOI: 10.1016/j.diagmicrobio.2019.114894
Source DB: PubMed Journal: Diagn Microbiol Infect Dis ISSN: 0732-8893 Impact factor: 2.803