Human norovirus detection and production, quantification, and storage of virus-like particles

Curr Protoc Microbiol. 2013 Nov 5:31:15K.1.1-15K.1.45. doi: 10.1002/9780471729259.mc15k01s31.

Abstract

Human noroviruses constitute a significant worldwide disease burden. Each year, noroviruses cause over 267 million infections, deaths in over 200,000 children under the age of five, and over 50% of U.S. food-borne illness. Due to the absence of a tissue culture model or small animal model to study human norovirus, virus-like particles (VLPs) and ELISA-based biological assays have been used to answer questions about norovirus evolution and immunity as well to provide a potential vaccine platform. This chapter outlines the protocols for norovirus detection in stool, as well as norovirus VLP design, production, purification, and storage using a Venezuelan equine encephalitis virus (VEE)-based virus replicon particle (VRP) expression system.

Keywords: Venezuelan equine encephalitis virus; norovirus; virus replicon particle; virus-like particle; virus-like particle purification.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Encephalitis Virus, Venezuelan Equine / genetics
  • Feces / virology
  • Genetic Vectors
  • Humans
  • Norovirus / genetics
  • Norovirus / growth & development*
  • Norovirus / isolation & purification*
  • Preservation, Biological / methods*
  • Virology / methods*