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Clinical and Diagnostic Laboratory Immunology, March 2005, p. 371-374, Vol. 12, No. 3
1071-412X/05/$08.00+0 doi:10.1128/CDLI.12.3.371-374.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Public Health Virology Laboratory, Queensland Health Scientific Services, Cooper's Plains, Australia1
Received 29 June 2004/ Returned for modification 22 September 2004/ Accepted 7 December 2004
We report the development of a flavivirus immunoglobulin M (IgM) capture enzyme-linked immunosorbent assay (MAC-ELISA) which improves the determination of an infecting flavivirus serotype over that by current serological methods. A panel of 165 IgM-positive sera from flavivirus patients with specific diagnostic results was tested by the flavivirus MAC-ELISA using a panel of 10 antigens. For 134 of these sera (81.2%), the highest reactivity was demonstrated against the infecting virus, which was consistent with the original diagnostic result. Specific antibody reactions inconsistent with the original diagnosis were found for six sera (3.6%). In our experience, the flavivirus-serotyping ELISA provides a rapid and accurate alternative to other serological tests, such as hemagglutination inhibition, for the specific diagnosis of flavivirus infections.
| Antimicrob. Agents Chemother. | Clin. Microbiol. Rev. | Infect. Immun. |
|---|---|---|
| J. Clin. Microbiol. | J. Virol. | ALL ASM JOURNALS |