Cloning and disruption of the antigenic catalase gene of Aspergillus fumigatus

被引:103
|
作者
Calera, JA
Paris, S
Monod, M
Hamilton, AJ
Debeaupuis, JP
Diaquin, M
LopezMedrano, R
Leal, F
Latge, JP
机构
[1] INST PASTEUR, LAB ASPERGILLUS, F-75724 PARIS 15, FRANCE
[2] CHU VAUDOIS, SERV DERMATOL, CH-1011 LAUSANNE, SWITZERLAND
[3] GUYS HOSP, DERMATOL LAB, LONDON SE1 9RT, ENGLAND
[4] UNIV SALAMANCA, DEPT GENET & MICROBIOL, E-37008 SALAMANCA, SPAIN
关键词
D O I
10.1128/IAI.65.11.4718-4724.1997
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aspergillus fumigatus possesses two catalases (described as fast and slow on the basis of their electrophoretic mobility). The slow catalase has been recognized as a diagnostic antigen for aspergillosis in immunocompetent patients. The antigenic catalase has been purified. The enzyme is a tetrameric protein composed of 90-kDa subunits. The corresponding cat1 gene was cloned, and sequencing data show that the cat1 gene codes for a 728-amino-acid polypeptide. A recombinant protein expressed in Pichia pastoris is enzymatically active and has biochemical and antigenic properties that are similar to those of the wild-type catalase. Molecular experiments reveal that CAT1 contains a signal peptide and a propeptide of 15 and 12 amino acrid residues, respectively. cat1-disrupted mutants that were unable to produce the slow catalase were as sensitive to H2O2 and polymorphonuclear cells as the wild-type strain. In addition, there was no difference in pathogenicity between the cat1 mutant and its parental cat1(+) strain in a murine model of aspergillosis.
引用
收藏
页码:4718 / 4724
页数:7
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