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Utility of the Focus Technologies West Nile Virus Immunoglobulin M Capture Enzyme-linked Immunosorbent Assay for Testing Cerebrospinal Fluid

Overview
Specialty Microbiology
Date 2004 Jan 13
PMID 14715725
Citations 6
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Abstract

Focus Technologies has developed an immunoglobulin M (IgM) capture enzyme-linked immunosorbent assay (ELISA) kit that utilizes recombinant West Nile virus (WNV) antigens to detect WNV IgM in serum. We evaluate here the utility of the kit for detecting WNV IgM in cerebrospinal fluid (CSF). The sensitivity was evaluated by using 52 CSF specimens from the 2002 WNV season that were positive in both the Public Health Service Laboratories WNV IgM ELISA and an in-house WNV IgM ELISA with native WNV antigen. The specificity was evaluated with two groups of specimens: (i). 73 CSF specimens submitted for in-house WNV IgM ELISA testing from February through April 2003 and yielding a negative WNV IgM result and (ii). 60 CSF specimens determined to be positive for another virus by PCR testing. Using these 185 CSF specimens at a screening dilution of 1:2, the kit was determined to be 100% sensitive and 100% specific. Endpoint titers were determined for 20 IgM-positive CSF specimens by testing serial twofold dilutions and ranged from 1:8 to 1:512. Index values (specimen absorbance value/calibrator absorbance value) for the screening dilution (1:2) showed no correlation with IgM titers, whereas index values for higher dilutions showed significant correlation with IgM titers. CSF screening dilutions of greater than 1:2 are not recommended, however, due to the risk of obtaining false-negative results. These findings show that the Focus Technologies WNV IgM capture ELISA, when utilized as recommended, offers accurate qualitative detection of WNV IgM in CSF specimens.

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References
1.
Malan A, Stipanovich P, Martins T, Hill H, Litwin C . Detection of IgG and IgM to West Nile virus. Development of an immunofluorescence assay. Am J Clin Pathol. 2003; 119(4):508-15. DOI: 10.1309/WJJ7-UE42-DFHT-TF1X. View

2.
Prince H, Hogrefe W . Detection of West Nile virus (WNV)-specific immunoglobulin M in a reference laboratory setting during the 2002 WNV season in the United States. Clin Diagn Lab Immunol. 2003; 10(5):764-8. PMC: 193906. DOI: 10.1128/cdli.10.5.764-768.2003. View

3.
Besselaar T, Blackburn N, Aldridge N . Comparison of an antibody-capture IgM enzyme-linked immunosorbent assay with IgM-indirect immunofluorescence for the diagnosis of acute Sindbis and West Nile infections. J Virol Methods. 1989; 25(3):337-45. DOI: 10.1016/0166-0934(89)90060-8. View

4.
Briese T, Jia X, Huang C, Grady L, Lipkin W . Identification of a Kunjin/West Nile-like flavivirus in brains of patients with New York encephalitis. Lancet. 1999; 354(9186):1261-2. DOI: 10.1016/s0140-6736(99)04576-6. View

5.
Davis B, Chang G, Cropp B, Roehrig J, Martin D, Mitchell C . West Nile virus recombinant DNA vaccine protects mouse and horse from virus challenge and expresses in vitro a noninfectious recombinant antigen that can be used in enzyme-linked immunosorbent assays. J Virol. 2001; 75(9):4040-7. PMC: 114149. DOI: 10.1128/JVI.75.9.4040-4047.2001. View