Use of cRNA digoxigenin-labelled probes for detection of enteroviruses in humans and in the environment

J Virol Methods. 1993 May;42(2-3):217-26. doi: 10.1016/0166-0934(93)90034-o.

Abstract

A dot blot hybridization test for enteroviruses is described using non-radioactive digoxigenin-labelled probes and a chemiluminescent detection. The use of a 5' non-coding riboprobe which detects all enteroviruses and a VP1 probe that detects the three serotypes of polioviruses allows the rapid detection of polioviruses and non-polio enteroviruses in human specimens or environmental water samples. The assay is strictly enterovirus specific and sensitive (800 fg RNA) and offers several advantages over conventional diagnosis or radioactive probes.

MeSH terms

  • Capsid / genetics*
  • Capsid Proteins
  • Digoxigenin
  • Enterovirus / genetics
  • Enterovirus / isolation & purification*
  • Enterovirus Infections / diagnosis*
  • Enterovirus Infections / epidemiology
  • Enterovirus Infections / genetics
  • France / epidemiology
  • Humans
  • Luminescent Measurements
  • Nucleic Acid Hybridization / methods
  • Poliovirus / genetics
  • Poliovirus / isolation & purification
  • RNA Probes
  • RNA, Viral / isolation & purification*
  • Water Microbiology*

Substances

  • Capsid Proteins
  • RNA Probes
  • RNA, Viral
  • VP1 protein, Poliovirus
  • Digoxigenin