Heterogeneity of metallo and serine extracellular proteinases in oral clinical isolates of Candida albicans in HIV-positive and healthy children from Rio de Janeiro, Brazil

被引:31
作者
Costa, EMMD
dos Santos, ALS
Cardoso, AS
Portela, MB
Abreu, CM
Alviano, CS
Hagler, AN
Soares, RMD
机构
[1] Univ Fed Rio de Janeiro, IMPPG, Dept Microbiol Geral, CCS, BR-21941590 Rio de Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Dept Ortodontia & Odontopediat, Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Fac Odontol, Dept Diagnost & Patol Oral, Rio de Janeiro, Brazil
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2003年 / 38卷 / 02期
关键词
CD4+ T cell; extracellular proteolytic activity; HIV-infected child; oral clinical isolate; serine and metalloproteinase; Candida albicans;
D O I
10.1016/S0928-8244(03)00145-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Candida yeasts frequently cause life-threatening systemic infections in immunocompromised hosts. In the present study, gelatin-SDS-PAGE analysis was used to characterize extracellular proteinases in 44 oral clinical isolates of Candida albicans from HIV-positive (29/50) and healthy children (15150). Our survey indicates that these oral clinical isolates of C albicans have complex extracellular proteolytic activity profiles, which illustrates the heterogeneity of this species. We showed four distinct proteolytic patterns composed of distinct serine (30-58 kDa) and metalloproteinase (64-95 kDa) activities, based on the inhibition profile with phenylmethylsulfonyl fluoride and 1,10-phenanthroline, respectively. This is the first report on secreted serine and metalloproteinases present in the culture supernatant fluids of C albicans; however, we did not observe a significant correlation between proteolytic profile expressed by the C albicans isolates from HIV-positive children and CD4(+) T cell count and plasma viral load. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:173 / 180
页数:8
相关论文
共 47 条
[1]   Trichophyton tonsurans exocellular protease expression:: correlation with clinical presentation in tinea capitis [J].
Abdel-Rahman, SM .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2002, 27 (04) :268-271
[2]  
ATKINSON JC, 1990, J ACQ IMMUN DEF SYND, V3, P41
[3]  
ATKINSON R, 1989, J PHYS CHEM REF DATA, V1, P18
[4]   IN-VITRO ACTIVITY OF A NEW ANTIFUNGAL TRIAZOLE, D0870, AGAINST CANDIDA-ALBICANS ISOLATES FROM ORAL CAVITIES OF PATIENTS INFECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS [J].
BARCHIESI, F ;
COLOMBO, AL ;
MCGOUGH, DA ;
FOTHERGILL, AW ;
RINALDI, MG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (11) :2553-2556
[5]  
BEDOYAESCOBAR VI, 1993, J MED VET MYCOL, V31, P299
[6]   CLUSTER OF ORAL ATYPICAL CANDIDA-ALBICANS ISOLATES IN A GROUP OF HUMAN IMMUNODEFICIENCY VIRUS-POSITIVE DRUG-USERS [J].
BOERLIN, P ;
BOERLINPETZOLD, F ;
DURUSSEL, C ;
ADDO, M ;
PAGANI, JL ;
CHAVE, JP ;
BILLE, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (05) :1129-1135
[7]   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
[8]  
Calderone R, 1994, Trends Microbiol, V2, P461, DOI 10.1016/0966-842X(94)90647-5
[9]  
CALDERONE RA, 1989, MYCOSES, V32, P12
[10]   Oral colonization by Candida albicans [J].
Cannon, RD ;
Chaffin, WL .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1999, 10 (03) :359-383