A recombinant envelope protein-based enzyme-linked immunosorbent assay for West Nile virus serodiagnosis.
Abstract: Recombinant West Nile virus envelope (E) protein was examined in enzyme-linked immunosorbent assay (ELISA) to detect antibodies elicited during West Nile virus infection. Horses (nine of 10) and humans (six of six) with confirmed West Nile virus infection had IgG and/or IgM antibodies to the E protein. Antibodies to the recombinant West Nile virus membrane and nonstructural 1 proteins were not detected in any of these sera. An E protein-based ELISA may aid in the serological diagnosis of West Nile virus infection.
Publication Date: 2003-03-26 PubMed ID: 12653304DOI: 10.1089/153036602321131904Google Scholar: Lookup
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- Journal Article
- Research Support
- U.S. Gov't
- Non-P.H.S.
Summary
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The research article features a study conducted to investigate whether the recombinant West Nile virus envelope protein could be utilized in enzyme-linked immunosorbent assay (ELISA) to identify antibodies generated during a West Nile virus infection.
Objective and Methodology of the Study
- The main goal of the researchers was to examine whether a recombinant envelope protein from the West Nile virus could be used in an Enzyme-Linked Immunosorbent Assay (ELISA) to detect antibodies produced during an infection with the West Nile virus.
- To achieve this, researcher used samples from human and horses with confirmed cases of West Nile virus infections. This was done to investigate if immunoglobulins IgG and/or IgM (types of antibodies) would be detected against the said protein.
Findings of the Study
- Out of the ten horses they tested, antibodies to the E protein were detected in nine cases, showing a strong indication that the Envelope (E) protein from the West Nile virus does elicit an immune response.
- Similarly, all six human samples tested positive for antibodies to the E protein, further affirming the result.
- However, antibodies to other recombinant West Nile virus proteins like the membrane and nonstructural 1 proteins were not detected in any of the samples. This suggests that the immune response may be specifically targeted towards the E protein.
Conclusion of the Study
- The ending note of the study suggests that an ELISA based on the E protein of the West Nile virus could potentially aid in the serological diagnosis of West Nile virus infections. Such a diagnostic tool would be useful in accurately identifying cases of West Nile virus, thereby enabling prompt and effective treatment.
Cite This Article
APA
Wang T, Magnarelli LA, Anderson JF, Gould LH, Bushmich SL, Wong SJ, Fikrig E.
(2003).
A recombinant envelope protein-based enzyme-linked immunosorbent assay for West Nile virus serodiagnosis.
Vector Borne Zoonotic Dis, 2(2), 105-109.
https://doi.org/10.1089/153036602321131904 Publication
Researcher Affiliations
- Section of Rheumatology, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06520-8031, USA.
MeSH Terms
- Animals
- Antibodies, Viral / blood
- Enzyme-Linked Immunosorbent Assay / methods
- Horses / immunology
- Horses / virology
- Humans
- Immunoglobulin G / blood
- Immunoglobulin M / blood
- Recombinant Proteins / immunology
- Viral Envelope Proteins / immunology
- West Nile Fever / diagnosis
- West Nile Fever / virology
- West Nile virus / immunology
- West Nile virus / isolation & purification
Citations
This article has been cited 3 times.- Martín-Acebes MA, Saiz JC. West Nile virus: A re-emerging pathogen revisited.. World J Virol 2012 Apr 12;1(2):51-70.
- Yeh JY, Chung KM, Song J. Differentiation of West Nile virus-infected animals from vaccinated animals by competitive ELISA using monoclonal antibodies against non-structural protein 1.. Vector Borne Zoonotic Dis 2012 May;12(5):380-7.
- Choi KS, Ko YJ, Nah JJ, Kim YJ, Kang SY, Yoon KJ, Joo YS. Monoclonal antibody-based competitive enzyme-linked immunosorbent assay for detecting and quantifying West Nile virus-neutralizing antibodies in horse sera.. Clin Vaccine Immunol 2007 Feb;14(2):134-8.
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