The expression of the secreted aspartyl proteinases Sap4 to Sap6 from Candida albicans in murine macrophages

Details

Serval ID
serval:BIB_097CC08812BE
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
The expression of the secreted aspartyl proteinases Sap4 to Sap6 from Candida albicans in murine macrophages
Journal
Molecular Microbiology
Author(s)
Borg-von Zepelin  M., Beggah  S., Boggian  K., Sanglard  D., Monod  M.
ISSN
0950-382X (Print)
Publication state
Published
Issued date
05/1998
Volume
28
Number
3
Pages
543-54
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: May
Abstract
Medically important yeasts of the genus Candida secrete aspartyl proteinases (Sap), which are of particular interest as virulence factors. Six closely related gene sequences, SAP1 to SAP6, for secreted proteinases are present in Candida albicans. The methylotrophic yeast Pichia pastoris was chosen as an expression system for preparing substantial amounts of each Sap isoenzyme. Interestingly, Sap4, Sap5 and Sap6, which have not yet been detected in C. albicans cultures in vitro, were produced as active recombinant enzymes. Different Sap polyclonal antibodies were raised in rabbits and tested before further application by enzyme-linked immunosorbent assay (ELISA) against each recombinant Sap. Two antisera recognized only Sap4 to Sap6. Using these antisera, together with sap null mutants obtained by targeted mutagenesis, we could demonstrate a high production of Sap4, Sap5 and Sap6 by C. albicans cells after phagocytosis by murine peritoneal macrophages. Furthermore, a delta sap4,5,6 null mutant was killed 53% more effectively after contact with macrophages than the wild-type strain. These results support a role for Sap4 to Sap6 in pathogenicity.
Keywords
Animals Antibodies, Fungal/immunology Antigens, Fungal/analysis Aspartic Endopeptidases/genetics/immunology/isolation & purification/*metabolism Candida albicans/*enzymology/genetics/growth & development/pathogenicity Cross Reactions Enzyme-Linked Immunosorbent Assay Fluorescent Antibody Technique *Fungal Proteins Hydrogen-Ion Concentration Isoenzymes/metabolism Macrophages, Peritoneal/*microbiology Mice Phagocytosis Pichia/enzymology Plasmids/genetics Rabbits Recombinant Fusion Proteins/isolation & purification/metabolism
Pubmed
Web of science
Open Access
Yes
Create date
25/01/2008 17:47
Last modification date
20/08/2019 13:31
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