A novel immunochromatographic test applied to a serological survey of Japanese encephalitis virus on pig farms in Korea

PLoS One. 2015 May 20;10(5):e0127313. doi: 10.1371/journal.pone.0127313. eCollection 2015.

Abstract

Among vertebrate species, pigs are a major amplifying host of Japanese encephalitis virus (JEV) and measuring their seroconversion is a reliable indicator of virus activity. Traditionally, the hemagglutination inhibition test has been used for serological testing in pigs; however, it has several limitations and, thus, a more efficient and reliable replacement test is required. In this study, we developed a new immunochromatographic test for detecting antibodies to JEV in pig serum within 15 min. Specifically, the domain III region of the JEV envelope protein was successfully expressed in soluble form and used for developing the immunochromatographic test. The test was then applied to the surveillance of Japanese encephalitis (JE) in Korea. We found that our immunochromatographic test had good sensitivity (84.8%) and specificity (97.7%) when compared with an immunofluorescence assay used as a reference test. During the surveillance of JE in Korea in 2012, the new immunochromatographic test was used to test the sera of 1,926 slaughtered pigs from eight provinces, and 228 pigs (11.8%) were found to be JEV-positive. Based on these results, we also produced an activity map of JEV, which marked the locations of pig farms in Korea that tested positive for the virus. Thus, the immunochromatographic test reported here provides a convenient and effective tool for real-time monitoring of JEV activity in pigs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animal Husbandry*
  • Animals
  • Blotting, Western
  • Chromatography, Affinity / methods*
  • Cloning, Molecular
  • DNA, Complementary / genetics
  • Encephalitis Virus, Japanese / immunology*
  • Encephalitis Virus, Japanese / isolation & purification
  • Geography
  • Protein Structure, Tertiary
  • Protein Subunits / isolation & purification
  • Reagent Kits, Diagnostic
  • Recombinant Proteins / metabolism
  • Republic of Korea
  • Serologic Tests / methods*
  • Surveys and Questionnaires*
  • Sus scrofa / immunology*
  • Sus scrofa / virology*
  • Viral Proteins / chemistry
  • Viral Proteins / metabolism

Substances

  • DNA, Complementary
  • Protein Subunits
  • Reagent Kits, Diagnostic
  • Recombinant Proteins
  • Viral Proteins

Grants and funding

This research was undertaken with a grant from the National Institute of Health, Korea Centers for Disease Control and Prevention (Code: 4847-311-210-13).