Rapid diagnosis of LaCrosse encephalitis: detection of specific immunoglobulin M in cerebrospinal fluid

Author:

Dykers T I,Brown K L,Gundersen C B,Beaty B J

Abstract

An immunoglobulin M (IgM) antibody capture enzyme immunoassay (MAC-EIA) was developed for the rapid and early diagnosis of LaCrosse (LAC) virus infections. The MAC-EIA was a sensitive and specific technique for the detection of IgM antibodies to LAC virus in cerebrospinal fluid specimens and in acute-phase serum specimens. In a retrospective study, cerebrospinal fluid and acute-phase serum paired samples from 108 patients were tested by the MAC-EIA and by an IgM immunofluorescence assay. The results were compared with the original diagnosis, which was made by using a variety of classical serological tests including serum neutralization, hemagglutination inhibition, and complement fixation. Thirty patients were confirmed as having LAC virus infections; of these, 30 (100%) were diagnosed as positive by serum MAC-EIA, and 27 (90%) were positive by cerebrospinal fluid MAC-EIA. The MAC-EIA was more sensitive than the IgM immunofluorescence assay. Two patients who were not previously confirmed as positive cases were diagnosed as having LAC virus infections by the MAC-EIA. One patient who was subsequently diagnosed as having a Jamestown Canyon virus infection and two patients who were previously infected with Jamestown Canyon virus were not falsely identified as having LAC virus infections by the MAC-EIA.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference19 articles.

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3. Beaty B. J. T. L. Jamnback and S. W. Hildreth. 1983. Rapid diagnosis of LaCrosse virus infections: evaluation of serologic and antigen detection techniques for the clinically relevant diagnosis of LaCrosse encephalitis p. 293-302. In C. H. Calisher and W. H. Thompson (ed.) California serogroup viruses. A. R. Liss Inc. New York.

4. Antibody capture immunoassay detection of Japanese encephalitis virus immunoglobulin M and G antibodies in cerebrospinal fluid;Burke D. S.;J. Clin. Microbiol.,1982

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