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PMID: 10066176 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Adhesive and mammalian transglutaminase substrate properties of Candida albicans Hwp1.

Science (New York, N.Y.) ·Vol. 283 ·No. 5407 ·1999-03-05 ·Pages 1535-8

Staab JF, Bradway SD, Fidel PL, Sundstrom P

Abstract

The pathogenesis of candidiasis involves invasion of host tissues by filamentous forms of the opportunistic yeast Candida albicans. Morphology-specific gene products may confer proinvasive properties. A hypha-specific surface protein, Hwp1, with similarities to mammalian small proline-rich proteins was shown to serve as a substrate for mammalian transglutaminases. Candida albicans strains lacking Hwp1 were unable to form stable attachments to human buccal epithelial cells and had a reduced capacity to cause systemic candidiasis in mice. This represents a paradigm for microbial adhesion that implicates essential host enzymes.

MeSH Terms
Animals Candida albicans/pathogenicity,physiology Candidiasis/microbiology Candidiasis, Oral/microbiology Cell Adhesion Epithelial Cells/enzymology,microbiology Fungal Proteins GTP Phosphohydrolases/metabolism GTP-Binding Proteins Genes, Fungal Humans Membrane Glycoproteins/genetics,physiology Mice Mice, Inbred CBA Mouth Mucosa/enzymology,microbiology Protein Glutamine gamma Glutamyltransferase 2 Recombinant Proteins/metabolism Transglutaminases/metabolism
Chemicals
Fungal Proteins HWP1 protein, Candida albicans Membrane Glycoproteins Recombinant Proteins Protein Glutamine gamma Glutamyltransferase 2 Transglutaminases GTP Phosphohydrolases GTP-Binding Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Staab J F
Department of Medical Microbiology and Immunology, College of Medicine and Public Health, Ohio State University, 333 West Tenth Avenue, Columbus, OH 43210, USA.
Bradway S D
Fidel P L
Sundstrom P
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1999-03-05
Pages
1535-8
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIDCR NIH HHS · 1 R01 DE11375-05A2 · United States
NIAID NIH HHS · AI32556 · United States
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