AJTMH Transactions of the Royal Society of Tropical Medicine and Hygiene
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Am. J. Trop. Med. Hyg., 34(2), 1985, pp. 346-354
Copyright © 1985 by The American Society of Tropical Medicine and Hygiene

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Rapid Serodiagnosis of Leptospirosis Using the IgM-Specific Dot-ELISA: Comparison with the Microscopic Agglutination Test*

Michael G. Pappas{dagger}, W. Ripley Ballou{dagger}, Michael R. Gray{ddagger}, Ernest T. Takafuji, Richard N. Miller AND Wayne T. Hockmeyer{dagger}
{dagger} Department of Immunology
the Division of Preventive Medicine, Walter Reed Army Institute of Research, Washington, D.C. 20307
{ddagger} Veterinary Laboratory Service, Brooke Army Medical Center, Fort Sam Houston, Texas 78324

The dot enzyme-linked immunosorbent assay (Dot-ELISA) was compared to the microscopic agglutination test (MA test) for the diagnosis of human leptospirosis. Of 177 sera from 68 soldiers who trained in the Republic of Panama, 102 sera were positive in the MA test and 93 of these sera were positive in the IgM-specific Dot-ELISA. Incidence of infection was 50 of 68 patients with the MA test and 48 of 68 in the IgM Dot-ELISA. Five MA test-positive sera were reactive only in the IgG-specific Dot-ELISA, suggesting previous exposure. All 21 infecting serovars of Leptospira interrogans, as determined by positive reactions in the MA test or culture of blood and urine specimens, were reactive in the Dot-ELISA. Of 75 sera negative in the MA test, 61 were nonreactive in the Dot-ELISA. However, 9 of these 14 Dot-ELISA-positive/MA test-negative sera were acute samples from patients whose later sera were MA test-positive. Positive reactions in the IgM Dot-ELISA occurred in 2 of 30 control, 4 of 10 Lyme disease, 1 of 11 relapsing fever, and 1 of 8 yaws sera; 10 syphilis patient sera were nonreactive. The IgM-specific Dot-ELISA appears to be sensitive and specific for the serodiagnosis of acute leptospirosis. In addition, this rapid test is inexpensive, simple to perform, utilizes minute volumes of killed leptospiral antigen and is easily adaptable to field use.

Accepted for publication October 17, 1984.


* A preliminary report of this work was presented at the American Leptospirosis Conference in Chicago, Illinois, September 1983.

The views of the authors do not purport to reflect the position of the Department of the Army or the Department of Defense (Para. 4-3, AR 360-5).

Address reprint requests to: Michael G. Pappas, Ph.D., Covalent Technology Corp., P.O. Box 1868, Ann Arbor, Michigan 48106.







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Copyright © 1985 by the American Society of Tropical Medicine and Hygiene.