Rapid Detection of Human Pathogenic Orthobunyaviruses

Author:

Weidmann Manfred1,Rudaz Veronique1,Nunes Marcio R. T.2,Vasconcelos Pedro F. C.2,Hufert Frank T.1

Affiliation:

1. Department of Virology, Institute of Medical Microbiology and Hygiene, University of Freiburg, 79104 Freiburg, Germany

2. Department of Arbovirus, Instituto Evandro Chagas, 66090-000 Belém, PA, Brazil

Abstract

ABSTRACT Modern detection and identification tools can help to provide answers to urgent questions about the incidence, prevalence, and epidemiology of currently emerging diseases. We developed highly sensitive one-step TaqMan reverse transcription-PCR assays with sensitivities ranging from 10 4 to 10 1 molecules for 11 human pathogens of the orthobunyaviruses. We compared the performances of these assays on three currently available cyclers (ABI-PRISM 7700, LightCycler, and SmartCycler). The assay for Oropouche virus (OROV) was tested using sera collected from days 1 to 5 after onset of OROV disease and was found to be greatly superior to an established nested PCR system. A mean copy number of 1.31 × 10 7 OROV RNA/ml of serum was detected. Diagnostic RNA detection can be used as early as day 1 after onset of OROV disease. The use of a mobile SmartCycler and a hands-on time of less than 3 h could help to intensify outbreak surveillance and control, especially in field studies.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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