Improved sero-monitoring assay for classical swine fever (CSF) using the recombinant E2 protein of a recent Korean isolate.

Res Vet Sci

Department of Infectious Diseases, College of Veterinary Medicine, KRF Priority Zoonotic Disease Research Institute and Brain Korea 21 Program for Veterinary Science, Seoul National University, Seoul 151-742, South Korea.

Published: April 2011

AI Article Synopsis

  • Classical swine fever (CSF) is a serious, contagious disease affecting pigs and can lead to severe symptoms and death.
  • The study focuses on the E2 protein of the virus, which plays a key role in virus entry and immune response, and involves cloning the E2 gene from a recent Korean isolate for further analysis.
  • An ELISA test was developed using this E2 protein, showing high sensitivity and specificity in detecting CSFV, but some samples gave conflicting results with existing tests, indicating varied immune responses in pig infections.

Article Abstract

Classical swine fever (CSF) is a highly contagious disease of pigs that causes fever, diarrhea and paralysis, often resulting in death. E2 is the major structural protein of the CSF virus (CSFV) and mediates the entrance of the virus, subsequently inducing a neutralizing immune response. In this study, the E2 gene of a recent Korean isolate of CSF, SW03, was cloned and the DNA sequence was compared to other strains via phylogenetic analysis. With the purified E2 protein, an enzyme-linked immunosorbent assay (ELISA) was developed for the serodiagnosis of CSFV infection. The sensitivity and specificity of the E2-ELISA were 96.1% and 94.8%, respectively. A total of 17 out of 485 field-collected pig sera tested demonstrated conflicting results between two ELISA methods, a commercial kit and the E2-ELISA. Of these sera, 60% were determined to be CSFV positive by a virus neutralization test (VNT), suggesting involvement of different immune responses in the cases of CSFV infection. As the E2-ELISA was developed using a recent Korean isolate, SW03, this assay is capable of rapidly identifying newly emerging CSFV strains.

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http://dx.doi.org/10.1016/j.rvsc.2010.06.003DOI Listing

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