Immunoassay targeting nonstructural protein 5 to differentiate West Nile virus infection from Dengue and St. Louis encephalitis virus infections and from flavivirus vaccination

被引:89
作者
Wong, SJ [1 ]
Boyle, RH
Demarest, VL
Woodmansee, AN
Kramer, LD
Li, HM
Drebot, M
Koski, RA
Fikrig, E
Martin, DA
Shi, PY
机构
[1] New York State Dept Hlth, Wadsworth Ctr, Albany, NY 12201 USA
[2] SUNY Albany, Dept Biomed Sci, Albany, NY 12201 USA
[3] Hlth Canada, Natl Mocrobiol Lab, Winnipeg, MB R3E 3R2, Canada
[4] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
[5] US Dept Hlth & Human Serv, Ctr Dis Control & Prevent, Publ Hlth Serv, Div Vector Borne Infect Dis, Ft Collins, CO 80522 USA
关键词
D O I
10.1128/JCM.41.9.4217-4223.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
West Nile virus (WNV) is an emerging flavivirus that has caused frequent epidemics since 1996. Besides natural transmission by mosquitoes, WNV can also be transmitted through blood transfusion and organ transplantation, thus heightening the urgency of development of a specific and rapid serologic assay of WNV infection. The current immunoassays lack specificity because they are based on detection of antibodies against WNV structural proteins and immune responses to structural proteins among flaviviruses cross-react to each other. Here, we describe microsphere immunoassays that detect antibodies to nonstructural proteins 3 and 5 (NS3 and NS5). In contrast to immunoassays based on viral envelope and NS3 proteins, the NS5-based assay (i) reliably discriminates between WNV infections and dengue virus or St. Louis encephalitis virus infections, (ii) differentiates between flavivirus vaccination and natural WNV infection, and (iii) indicates recent infections. These unique features of the NS5-based immunoassay will be very useful for both clinical and veterinary diagnosis of WNV infection.
引用
收藏
页码:4217 / 4223
页数:7
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