Multiplex real-time RT-PCR for the simultaneous detection and quantification of GI, GII and GIV noroviruses

J Virol Methods. 2015 Oct:223:109-14. doi: 10.1016/j.jviromet.2015.07.020. Epub 2015 Aug 3.

Abstract

Noroviruses are important causes of acute gastroenteritis and are classified into six genogroups with GI, GII and GIV containing human pathogens. This high genetic diversity represents a significant challenge for diagnostic assay development. Genogroup specific monoplex and multiplex real time RT-PCR assays are widely used for the detection of GI and GII noroviruses. On the other hand, GIV norovirus detection is not part of routine laboratory diagnosis. This study describes the development and evaluation of a one tube, real time RT-PCR assay for the simultaneous detection and quantification of GI, GII and GIV noroviruses, including both GIV.1 (human) and GIV.2 (animal) strains. Assay performance was evaluated on a panel of norovirus positive clinical samples by comparison of monoplex and multiplex standard curves and Ct values. The multiplex assay demonstrated equal sensitivity and specificity to the monoplex assays and was able to detect all GI, GII and GIV noroviruses with Ct values equal to that of the monoplex assays. The multiplex assay described in this study will be instrumental for the better understanding of GIV norovirus epidemiology, including their possible zoonotic nature.

Keywords: Calicivirus; Diagnosis; Norovirus; Real time RT-PCR.

Publication types

  • Evaluation Study

MeSH terms

  • Animals
  • Caliciviridae Infections / diagnosis*
  • Caliciviridae Infections / veterinary
  • Caliciviridae Infections / virology*
  • Genotype
  • Humans
  • Molecular Diagnostic Techniques / methods*
  • Multiplex Polymerase Chain Reaction / methods*
  • Norovirus / classification*
  • Norovirus / genetics
  • Norovirus / isolation & purification*
  • Real-Time Polymerase Chain Reaction / methods*
  • Sensitivity and Specificity
  • Viral Load / methods