Secreted metalloprotease gene family of Microsporum canis

被引:81
作者
Brouta, F
Descamps, F
Monod, M
Vermout, S
Losson, B
Mignon, B
机构
[1] Univ Liege, Fac Vet Med, Dept Parasitol & Parasit Dis, B-4000 Cointe Ougree, Belgium
[2] CHU Vaudois, Serv Dermatol, CH-1011 Lausanne, Switzerland
关键词
D O I
10.1128/IAI.70.10.5676-5683.2002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Keratinolytic proteases secreted by dermatophytes are likely to be virulence-related factors. Microsporum canis, the main agent of dermatophytosis in dogs and cats, causes a zoonosis that is frequently reported. Using Aspergillus fumigatus metalloprotease genomic sequence (MEP) as a probe, three genes (MEP1, MEP2, and MEP3) were isolated from an M. canis genomic library. They presented a quite-high percentage of identity with both A. fumigatus MEP and Aspergillus oryzae neutral protease I genes. At the amino acid level, they all contained an HEXXH consensus sequence, confirming that these M. canis genes (MEP genes) encode a zinc-containing metalloprotease gene family. Furthermore, MEP3 was found to be the gene encoding a previously isolated M. canis 43.5-kDa keratinolytic metalloprotease, and was successfully expressed as an active recombinant enzyme in Pichia pastoris. Reverse transcriptase nested PCR performed on total RNA extracted from the hair of M. cants-infected guinea pigs showed that at least MEP2 and MEP3 are produced during the infection process. This is the first report describing the isolation of a gene family encoding potential virulence-related factors in dermatophytes.
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收藏
页码:5676 / 5683
页数:8
相关论文
共 53 条
[1]   REGULATION OF TRICHOPHYTON-RUBRUM PROTEOLYTIC ACTIVITY [J].
APODACA, G ;
MCKERROW, JH .
INFECTION AND IMMUNITY, 1989, 57 (10) :3081-3090
[2]   PURIFICATION AND CHARACTERIZATION OF A 27,000-MR EXTRACELLULAR PROTEINASE FROM TRICHOPHYTON-RUBRUM [J].
APODACA, G ;
MCKERROW, JH .
INFECTION AND IMMUNITY, 1989, 57 (10) :3072-3080
[3]   PURIFICATION AND CHARACTERIZATION OF MAJOR EXTRACELLULAR PROTEINASES FROM TRICHOPHYTON-RUBRUM [J].
ASAHI, M ;
LINDQUIST, R ;
FUKUYAMA, K ;
APODACA, G ;
EPSTEIN, WL ;
MCKERROW, JH .
BIOCHEMICAL JOURNAL, 1985, 232 (01) :139-144
[4]   The expression of the secreted aspartyl proteinases Sap4 to Sap6 from Candida albicans in murine macrophages [J].
Borg-von Zepelin, M ;
Beggah, S ;
Boggian, K ;
Sanglard, D ;
Monod, M .
MOLECULAR MICROBIOLOGY, 1998, 28 (03) :543-554
[5]  
Brouta F, 2001, MED MYCOL, V39, P269, DOI 10.1080/mmy.39.3.269.275
[6]   THE PMTL NIC-CLONING VECTORS .1. IMPROVED PUC POLYLINKER REGIONS TO FACILITATE THE USE OF SONICATED DNA FOR NUCLEOTIDE SEQUENCING [J].
CHAMBERS, SP ;
PRIOR, SE ;
BARSTOW, DA ;
MINTON, NP .
GENE, 1988, 68 (01) :139-149
[7]   Characteristics of the biologically active 35-kDa metalloprotease virulence factor from Listeria monocytogenes [J].
Coffey, A ;
van den Burg, B ;
Veltman, R ;
Abee, T .
JOURNAL OF APPLIED MICROBIOLOGY, 2000, 88 (01) :132-141
[8]   ROLE OF KERATINASES IN DERMATOPHYTOSIS .2. FLUORESCENT-ANTIBODY STUDIES WITH KERATINASE II-OF TRICHOPHYTON-MENTAGROPHYTES [J].
COLLINS, JP ;
GRAPPEL, SF ;
BLANK, F .
DERMATOLOGICA, 1973, 146 (02) :95-100
[9]   Evidence that members of the secretory aspartyl proteinase gene family, in particular SAP2, are virulence factors for Candida vaginitis [J].
De Bernardis, F ;
Arancia, S ;
Morelli, L ;
Hube, B ;
Sanglard, D ;
Schäfer, W ;
Cassone, A .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (01) :201-208
[10]  
DOUMAS A, 1999, J FOOD MYCOL, V2, P271