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Clinical and vaccine immunology : CVI2009; 16(5); 667-671; doi: 10.1128/CVI.00043-09

Enzyme-linked immunosorbent assay using glycoprotein and monoclonal antibody for detecting antibodies to vesicular stomatitis virus serotype New Jersey.

Abstract: In this study, an enzyme-linked immunosorbent assay (ELISA) using glycoprotein and a monoclonal antibody (MAb) was developed for the detection of antibodies to vesicular stomatitis virus (VSV) serotype New Jersey (NJ). The glycoprotein to be used as a diagnostic antigen was extracted from partially purified VSV-NJ, and a neutralizing MAb specific to VSV-NJ was incorporated to compete with antibodies in a blocking ELISA using glycoprotein (GP ELISA). The cutoff of the GP ELISA was set at 40% inhibition, which corresponded to a virus neutralization test (VNT) titer of 32. With this threshold, the GP ELISA exhibited 99.6% specificity for naïve sera (n = 3,005) from cattle (n = 1,040), pigs (n = 1,120), and horses (n = 845) from domestic farms. The GP ELISA did not cross-react with sera positive for foot-and-mouth disease virus, swine vesicular disease virus, or VSV serotype Indiana. The GP ELISA was more compatible with the VNT than was the nucleocapsid-based ELISA for VSV-NJ-positive sera (n = 19). Taken together, this GP ELISA could be a useful tool as an alternative to the VNT for detecting antibodies specific to VSV-NJ.
Publication Date: 2009-03-11 PubMed ID: 19279165PubMed Central: PMC2681588DOI: 10.1128/CVI.00043-09Google Scholar: Lookup
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  • Evaluation Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research carefully developed and examined an enzyme-linked immunosorbent assay, making use of a glycoprotein and a monoclonal antibody, which can efficiently detect antibodies to vesicular stomatitis virus serotype New Jersey.

Research Methodology

  • The study focused on creating an enzyme-linked immunosorbent assay (ELISA) which employed a glycoprotein and a monoclonal antibody (MAb) to detect antibodies to vesicular stomatitis virus (VSV) serotype New Jersey (NJ).
  • The researchers extracted the required glycoprotein from partially purified VSV-NJ, which served as a diagnostic antigen.
  • A neutralizing MAb, specific to VSV-NJ, was used to compete with the antibodies in a blocking ELISA using the glycoprotein, known as the GP ELISA.

Observations and Findings

  • The cutoff for the GP ELISA was set at 40% inhibition, equivalent to a virus neutralization test (VNT) titer of 32.
  • At this cutoff, the GP ELISA demonstrated 99.6% specificity when tested on naïve sera (protein portion of blood) collected from a number of domesticated animals (n = 3,005) from different cattle, horses and pig farms.
  • The GP ELISA did not exhibit cross-reactivity with sera positive for other viruses like foot-and-mouth disease virus, swine vesicular disease virus, or VSV serotype Indiana.
  • The researchers observed that GP ELISA was more compatible with VNT than the nucleocapsid-based ELISA for VSV-NJ-positive sera (n = 19).

Conclusion

  • The study concludes that the developed GP ELISA is a useful tool and a reliable alternative to the VNT for detecting antibodies specific to VSV-NJ.

Cite This Article

APA
Lee HS, Heo EJ, Jeoung HY, Ko HR, Kweon CH, Youn HJ, Ko YJ. (2009). Enzyme-linked immunosorbent assay using glycoprotein and monoclonal antibody for detecting antibodies to vesicular stomatitis virus serotype New Jersey. Clin Vaccine Immunol, 16(5), 667-671. https://doi.org/10.1128/CVI.00043-09

Publication

ISSN: 1556-679X
NlmUniqueID: 101252125
Country: United States
Language: English
Volume: 16
Issue: 5
Pages: 667-671

Researcher Affiliations

Lee, Hyang-Sim
  • National Veterinary Research and Quarantine Service, Anyang, Gyeonggi-do, Republic of Korea.
Heo, Eun-Jeong
    Jeoung, Hye-Young
      Ko, Hyo-Rim
        Kweon, Chang-Hee
          Youn, Hee-Jeong
            Ko, Young-Joon

              MeSH Terms

              • Animals
              • Antibodies
              • Antibodies, Monoclonal
              • Antibodies, Viral / blood
              • Cattle
              • Cattle Diseases / diagnosis
              • Cattle Diseases / virology
              • Enzyme-Linked Immunosorbent Assay / methods
              • Glycoproteins
              • Horse Diseases / diagnosis
              • Horse Diseases / virology
              • Horses
              • Rhabdoviridae Infections / diagnosis
              • Rhabdoviridae Infections / veterinary
              • Rhabdoviridae Infections / virology
              • Sensitivity and Specificity
              • Swine
              • Swine Diseases / diagnosis
              • Swine Diseases / virology
              • Vesicular stomatitis New Jersey virus / isolation & purification

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              Citations

              This article has been cited 1 times.
              1. Lin T, Shao J, Chang H, Gao S, Cong G, Du J. Generation of monoclonal antibodies against non-structural protein 3AB of foot-and-mouth disease virus. Virol Sin 2012 Oct;27(5):316-9.
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