Monoclonal antibody capture enzyme immunoassay for detection of Paracoccidioides brasiliensis antibodies in paracoccidioidomycosis

Four murine monoclonal antibodies (MAbs 17C, 21A, 21F, and 32B) raised against the 43-kDa glycoprotein of Paracoccidioides brasiliensis were tested in a capture enzyme immunoassay (EIA) for the detection of specific human anti-gp43 immunoglobulin G in patients with paracoccidioidomycosis (PCM). All MAbs reacted similarly in the assay. These MAbs, which detected anti-gp43 at levels of as low as 500 pg/ml, were demonstrated to specifically recognize at least two different epitopes in gp43 binding assays. Specific antibodies in the sera of patients with active PCM were detected at dilutions of as high as 1:819,200, and the reactivities of patient sera, as measured by optical densities, were found to be significantly higher than those of control sera. The comparison between classical ELISA and our capture enzyme immunoassay showed that both sensitivity and specificity were greatly improved by the latter. These MAbs represent the first specific reagents to P. brasiliensis described for use in serological tests for PCM.

[1]  M. Franco,et al.  Host-parasite relationship in paracoccidioidomycosis. , 1995, Current topics in medical mycology.

[2]  C. Taborda,et al.  Diagnosis of paracoccidioidomycosis by passive haemagglutination assay of antibody using a purified and specific antigen-gp43. , 1993, Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology.

[3]  M. Blotta,et al.  Immunological response to cell-free antigens of Paracoccidioides brasiliensis: relationship with clinical forms of paracoccidioidomycosis , 1993, Journal of clinical microbiology.

[4]  L. Travassos,et al.  The 43-kDa glycoprotein from the human pathogen Paracoccidioides brasiliensis and its deglycosylated form: excretion and susceptibility to proteolysis. , 1991, Archives of biochemistry and biophysics.

[5]  L. Travassos,et al.  43-kilodalton glycoprotein from Paracoccidioides brasiliensis: immunochemical reactions with sera from patients with paracoccidioidomycosis, histoplasmosis, or Jorge Lobo's disease , 1991, Journal of clinical microbiology.

[6]  L. Travassos,et al.  Identification of antigenic polypeptides of Paracoccidioides brasiliensis by immunoblotting. , 1989, Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology.

[7]  L. Travassos,et al.  Production of Paracoccidioides brasiliensis exoantigens for immunodiffusion tests , 1988, Journal of clinical microbiology.

[8]  E. Brummer,et al.  An evaluation of the enzyme-linked immunoabsorbent assay (ELISA) for quantitation of antibodies to Paracoccidioides brasiliensis. , 1986, Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology.

[9]  L. Travassos,et al.  Exocellular components of Paracoccidioides brasiliensis: identification of a specific antigen , 1986, Infection and immunity.

[10]  C. Lacaz,et al.  Immunoenzymatic absorption test for serodiagnosis of paracoccidioidomycosis , 1984, Journal of clinical microbiology.

[11]  J. Guesdon,et al.  Magnetic enzyme-linked immunosorbent assay (MELISA) for determination of specific IgG in paracoccidioidomycosis. , 1984, Sabouraudia.

[12]  W. Ansorge FAST VISUALISATION OF PROTEIN BANDS BY IMPREGNATION IN POTASSIUM PERMANGANATE AND SILVER NITRATE , 1983 .

[13]  J. Guesdon,et al.  Coupling of Enzymes to Antibodies and Antigens , 1978 .

[14]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.