Affiliation:
1. Department of Microbiology and Immunology1 and
2. Department of Medicine,2 Albert Einstein College of Medicine, Bronx, New York 10461
Abstract
ABSTRACT
Cryptococcus neoformans
var.
neoformans
strains have historically been divided into serotypes A and D on the basis of reactivity with rabbit sera. Previously, we noted that two murine immunoglobulin M monoclonal antibodies (MAbs) to the capsular glucuronoxylomannan produced different indirect immunofluorescence (IF) patterns, described as annular and punctate, when bound to
C. neoformans
cells from different strains. In this study, we examined the reactivity of these two MAbs, known as 12A1 and 13F1, with 20
C. neoformans
var.
neoformans
strains, of which 13 were serotype A and 7 were serotype D. For all strains, MAb binding was studied by IF and agglutination assays. In addition, we blindly tested the IF patterns of 22
C. neoformans
var.
neoformans
strains. For selected strains, MAb binding was studied by flow cytometry (FACScan) and phagocytosis assays. The epitopes recognized by MAbs 12A1 and 13F1 were found in all of the strains. MAb 12A1 binding produced an annular IF pattern with all of the strains, irrespective of the serotype classification. MAb 13F1 binding produced annular binding with all of the serotype A strains and punctate binding with 19 of 20 serotype D strains. In general, the punctate IF pattern was associated with lower fluorescence intensity, a requirement for higher antibody concentrations to produce yeast cell agglutination, and lower opsonic efficacy. Our results provide strong support for the existing classification of two serological types for strains assigned to variety
neoformans
and indicate qualitative and quantitative antigenic differences among serotype A and D strains.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
Cited by
51 articles.
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