Evaluation of Immunomagnetic Separation Method for the Recovery of Hepatitis A Virus and GI.1 and GII.4 Norovirus Strains Seeded on Oyster and Mussel

Food Environ Virol. 2014 Dec;6(4):290-6. doi: 10.1007/s12560-014-9156-2. Epub 2014 Jun 22.

Abstract

Outbreaks of viral diseases are frequently associated with the consumption of minimally processed shellfish. Among the viruses in these outbreaks, hepatitis A virus (HAV) and human norovirus (NoV) have been increasingly reported as the most common food-borne pathogens. These viruses must be concentrated in tested samples in order to be detected. In this study, a method for the detection of NoV and HAV in shellfish using an immuno-magnetic separation (IMS) procedure combined with reverse transcriptase (RT)-PCR was developed. The IMS/RT-PCR method was applied to investigate the recovery rates of HAV, NoV GI.1, and GII.4 from oyster and mussel. Based on IMS/RT-PCR results, recovery rates for HAV from oyster and mussel test samples were 2.4 and 1.1%, respectively. The NoV GI.1 recovery rates from oyster and mussel samples were 4.9-9.2% (mean 6.9%) and 4.3-8.6% (mean 6.2%), respectively, and the NoV GII.4 recovery rates were 8.8 and 8.5%, respectively. These results verified that HAV, NoV GI.1, and GII.4 can be detected in all the test samples using the IMS/RT-PCR method, although the three inoculated viruses were recovered with low efficiency. In conclusion, the IMS/RT-PCR method can be used to efficiently and rapidly detect viruses such as HAV and NoV in shellfish such as oyster and mussel.

Keywords: Hepatitis A virus; Immunomagnetic separation; Mussel; Norovirus; Oyster.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caliciviridae Infections / epidemiology
  • Caliciviridae Infections / prevention & control
  • Caliciviridae Infections / virology
  • Crassostrea / virology*
  • Disease Outbreaks / prevention & control
  • Feces / virology
  • Food Contamination* / prevention & control
  • Food Inspection / methods*
  • Foodborne Diseases / epidemiology
  • Foodborne Diseases / prevention & control
  • Foodborne Diseases / virology
  • Gastroenteritis / epidemiology
  • Gastroenteritis / prevention & control
  • Gastroenteritis / virology
  • Hepatitis A / epidemiology
  • Hepatitis A / prevention & control
  • Hepatitis A / virology
  • Hepatitis A Virus, Human / classification
  • Hepatitis A Virus, Human / isolation & purification*
  • Hepatitis A Virus, Human / metabolism
  • Humans
  • Immunomagnetic Separation
  • Molecular Typing
  • Mytilus / virology*
  • Norovirus / classification
  • Norovirus / isolation & purification*
  • Norovirus / metabolism
  • RNA, Viral / isolation & purification
  • RNA, Viral / metabolism
  • Real-Time Polymerase Chain Reaction
  • Reproducibility of Results
  • Republic of Korea / epidemiology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Shellfish / virology*

Substances

  • RNA, Viral