Abstract
Infection with Borrelia burgdorferi, the etiologic agent of Lyme disease, is associated with an early and dominant humoral response to the spirochete's 23-kDa outer surface protein C (OspC). We have cloned and expressed OspC as a fusion protein in Escherichia coli and have shown that patient serum samples react with it in an enzyme-linked immunosorbent assay (ELISA) (S. J. Padula, A. Sampieri, F. Dias, A. Szczepanski, and R. W. Ryan, Infect. Immun. 61:5097-5105, 1993). Now we have compared the detection of B. burgdorferi-specific immunoglobulin M antibodies in 74 individuals with culture-positive erythema migrans by a whole-cell ELISA, immunoblot, and the recombinant OspC (rOspC) ELISA. Seventy-six negative controls were also studied. With all of the tests, there was a statistically significant association between the duration of disease and the frequency of a positive result. With the rOspC ELISA, the predictive value of a positive test was 100% and the predictive value of a negative test was 74%. Similar results were obtained with the whole-cell ELISA and with the immunoblot using as the source of test antigen a strain of B. burgdorferi which expresses abundant levels of OspC. We conclude that the use of rOspC in an ELISA is a convenient, readily automated, and easily standardized test for the serodiagnosis of early Lyme disease.
MeSH Terms
Antibodies, Bacterial/blood
Antigens, Bacterial
Bacterial Outer Membrane Proteins/blood
Borrelia burgdorferi Group/immunology
Enzyme-Linked Immunosorbent Assay/methods
Humans
Immunoglobulin M/blood
Lyme Disease/blood,diagnosis
Predictive Value of Tests
Serologic Tests
Chemicals
Antibodies, Bacterial
Antigens, Bacterial
Bacterial Outer Membrane Proteins
Immunoglobulin M
OspC protein
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Padula S J
Department of Medicine, University of Connecticut Health Center, Farmington 06030.
Dias F
Sampieri A
Craven R B
Ryan R W
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