Pesquisa Veterinária Brasileira (Jan 2015)

Development of a Real-time PCR test for porcine group A rotavirus diagnosis

  • Elizabeth C.M. Marconi,
  • Nara T.C.G. Bernardes,
  • Laila A.R. Beserra,
  • Fernanda D.F. Silva,
  • Fabio Gregori

DOI
https://doi.org/10.1590/S0100-736X2015000100009
Journal volume & issue
Vol. 35, no. 1
pp. 39 – 43

Abstract

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Group A Rotavirus (RVA) is one of the most common causes of diarrhea in humans and several animal species. A SYBR-Green Real-Time polymerase chain reaction (PCR) was developed to diagnose RVA from porcine fecal samples, targeting amplification of a 137-bp fragment of nonstructural protein 5 (NSP5) gene using mRNA of bovine NADH-desidrogenase-5 as exogenous internal control. Sixty-five samples were tested (25 tested positive for conventional PCR and genetic sequencing). The overall agreement (kappa) was 0.843, indicating 'very good' concordance between tests, presenting 100% of relative sensitivity (25+ Real Time PCR/25+ Conventional PCR) and 87.5% of relative sensitivity (35- Real Time PCR/40- Conventional PCR). The results also demonstrated high intra- and inter-assay reproducibility (coefficient of variation ≤1.42%); thus, this method proved to be a fast and sensitive approach for the diagnosis of RVA in pigs.

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