Abstract
An enzyme-linked immunosorbent assay (ELISA) and indirect fluorescent-antibody test were used to detect antibodies to Borrelia burgdorferi, the causative agent of Lyme disease, in Peromyscus leucopus (white-footed mouse). Of the 661 mice captured in Connecticut, Rhode Island, and New York during 1980 and 1983 to 1987, 166 (25.1%) had antibodies to B. burgdorferi by ELISA. Comparative analyses of 210 serum specimens, collected in areas where Lyme disease is endemic, revealed a threefold difference in sensitivity between the ELISA (38.1% positive) and the indirect fluorescent-antibody method (12.4%). Although prevalence of seropositive P. leucopus was highest during June, elevated amounts of antibody (1:1,280 to 1:2,560) were detected in mice that harbored spirochetes during all seasons. Being reservoirs for B. burgdorferi, these rodents are suitable for monitoring spirochete infections at foci and should be included in field evaluations of control programs aimed at suppressing Lyme disease.
MeSH Terms
Animals
Antigens, Bacterial/analysis
Borrelia/immunology
Disease Vectors/microbiology
Enzyme-Linked Immunosorbent Assay
Peromyscus/microbiology
Seasons
United States
Chemicals
Antigens, Bacterial
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Magnarelli L A
Department of Entomology, Connecticut Agricultural Experiment Station, New Haven 06504.
Anderson J F
Hyland K E
Fish D
Mcaninch J B
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