Differential expression of Candida albicans secreted aspartyl proteinase and phospholipase B genes in humans correlates with active oral and vaginal infections

被引:155
作者
Naglik, JR
Rodgers, CA
Shirlaw, PJ
Dobbie, JL
Fernandes-Naglik, LL
Greenspan, D
Agabian, N
Challacombe, SJ
机构
[1] Univ London Kings Coll, Dept Oral Med Pathol & Immunol, GKT Dent Inst, London SE1 9RT, England
[2] St Thomas Hosp, Dept Genitourinary & HIV Med, Guys & St Thomas Hosp Trust, London, England
[3] Univ Calif San Francisco, Dept Stomatol, San Francisco, CA 94143 USA
关键词
D O I
10.1086/376536
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The in vivo expression of Candida albicans secreted aspartyl proteinase (SAP1-SAP8) and phospholipase B (PLB1 and PLB2) genes was analyzed in 137 human subjects with oral and vaginal candidiasis or carriage. Total RNA was isolated from whole unstimulated saliva or vaginal swabs, and the expression of SAP1-8 and PLB1-2 was evaluated by reverse-transcriptase polymerase chain reaction using specific primer sets. A spectrum of SAP gene expression profiles was obtained from different C. albicans strains during symptomatic disease and asymptomatic carriage. SAP2 and SAP5 were the most common genes expressed during both infection and carriage. SAP1, SAP3, SAP4, SAP7, SAP8, and PLB1 expression was correlated with oral disease, whereas SAP1, SAP3, and SAP6-SAP8 expression was correlated with vaginal disease. Furthermore, SAP1, SAP3, and SAP8 were preferentially expressed in vaginal, rather than oral, infections. This study demonstrates the differential expression of the hydrolytic enzyme genes in humans and correlates the expression of specific Candida species virulence genes with active disease and anatomical location.
引用
收藏
页码:469 / 479
页数:11
相关论文
共 50 条
[1]  
AGABIAN N, 1994, J MED VET MYCOL, V32, P229
[2]  
BANNO Y, 1985, SABOURAUDIA, V23, P47
[3]  
BARRETTBEE K, 1985, J GEN MICROBIOL, V131, P1217
[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]   HIV-protease inhibitors reduce cell adherence of Candida albicans strains by inhibition of yeast secreted aspartic proteases [J].
Borg-von Zepelin, M ;
Meyer, I ;
Thomssen, R ;
Würzner, R ;
Sanglard, D ;
Telenti, A ;
Monod, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 113 (05) :747-751
[6]   Virulence factors of Candida albicans [J].
Calderone, RA ;
Fonzi, WA .
TRENDS IN MICROBIOLOGY, 2001, 9 (07) :327-335
[7]   In vitro and in vivo anticandidal activity of human immunodeficiency virus protease inhibitors [J].
Cassone, A ;
De Bernardis, F ;
Torosantucci, A ;
Tacconelli, E ;
Tumbarello, M ;
Cauda, R .
JOURNAL OF INFECTIOUS DISEASES, 1999, 180 (02) :448-453
[8]   A SIMPLE PROCEDURE FOR OPTIMIZING THE POLYMERASE CHAIN-REACTION (PCR) USING MODIFIED TAGUCHI METHODS [J].
COBB, BD ;
CLARKSON, JM .
NUCLEIC ACIDS RESEARCH, 1994, 22 (18) :3801-3805
[9]   PUTATIVE VIRULENCE FACTORS OF CANDIDA-ALBICANS [J].
CUTLER, JE .
ANNUAL REVIEW OF MICROBIOLOGY, 1991, 45 :187-218
[10]   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