In:
Yeast, Wiley, Vol. 25, No. 2 ( 2008-02), p. 141-154
Abstract:
The dimorphic fungus Paracoccidioides brasiliensis is the causative agent of the most frequent systemic mycosis in Latin America. In humans, infection starts by inhalation of fungal propagules, which reach the pulmonary epithelium and differentiate into the yeast parasitic phase. Here we describe the characterization of a Dfg5p ( d efective for f ilamentous g rowth) homologue of P. brasiliensis , a predictable cell wall protein, first identified in Saccharomyces cerevisiae . The protein, the cDNA and genomic sequences were analysed. The cloned cDNA was expressed in Escherichia coli and the purified r Pb Dfg5p was used to obtain polyclonal antibodies. Immunoelectron microscopy and biochemical studies demonstrated the presence of Pb Dfg5p in the fungal cell wall. Enzymatic treatments identified Pb Dfg5p as a β‐glucan linked protein that undergoes N ‐glycosylation. The r Pb Dfg5p bound to extracellular matrix components, indicating that those interactions could be important for initial steps leading to P. brasiliensis attachment and colonization of host tissues. The P. brasiliensis dfg5 nucleotide and deduced protein, Pb Dfg5p, sequences reported in this paper had been submitted to the GenBank database under Accession Nos AY307855 (cDNA) and DQ534495 (genomic). Copyright © 2007 John Wiley & Sons, Ltd.
Type of Medium:
Online Resource
ISSN:
0749-503X
,
1097-0061
Language:
English
Publisher:
Wiley
Publication Date:
2008
detail.hit.zdb_id:
1479172-9
SSG:
12
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