A CANDIDA-ALBICANS SURFACE-ANTIGEN MEDIATING ADHESION AND AUTOAGGREGATION IN SACCHAROMYCES-CEREVISIAE

Citation
M. Barki et al., A CANDIDA-ALBICANS SURFACE-ANTIGEN MEDIATING ADHESION AND AUTOAGGREGATION IN SACCHAROMYCES-CEREVISIAE, Infection and immunity, 62(10), 1994, pp. 4107-4111
Citations number
29
Categorie Soggetti
Immunology,"Infectious Diseases
Journal title
ISSN journal
00199567
Volume
62
Issue
10
Year of publication
1994
Pages
4107 - 4111
Database
ISI
SICI code
0019-9567(1994)62:10<4107:ACSMAA>2.0.ZU;2-4
Abstract
In a previous study (M. Barki, Y. Koltin, M. Yanko, A. Tamarkin, and M . Rosenberg, J. Bacteriol. 175:5683-5689, 1993), a 3.3-kb DNA fragment from Candida albicans which confers adhesion and autoaggregation in S accharomyces cerevisiae was isolated and partially characterized. In t his report, evidence is presented that the adhesion-autoaggregation ph enotype observed in S. cerevisiae cells transformed with the candidal DNA fragment is due to expression of a C. albicans surface antigen. Ra bbit antiserum, prepared against transformant S. cerevisiae cells, was adsorbed with S. cerevisiae bearing the vector alone. Immunofluoresee nce micrography showed that the adsorbed antiserum bound to the surfac e of transformant S. cerevisiae cells as sell as to C. albicans cells, but only marginally to the S. cerevisiae control. The adsorbed antise rum specifically inhibited autoaggregation of transformant cells. Furt her adsorption of the antiserum with transformant cells eliminated bot h inhibition and immunofluorescence. Autoaggregative activity and immu nofluorescence of transformant cells were abolished following proteoly tic treatment. Western blot (immunoblot) analysis of candidal extracts revealed that the absorbed antiserum recognized a major candidal anti gen of ca. 30 kDa which was present on both yeast-phase and germ tube cells. The data suggest that the observed adhesion-autoaggregation phe notype is due to the presence of a specific candidal antigen on the ou ter surface of the transformant cells.