Cellular and molecular biology of Candida albicans estrogen response

被引:75
作者
Cheng, G [1 ]
Yeater, KM [1 ]
Hoyer, LL [1 ]
机构
[1] Univ Illinois, Dept Pathobiol, Urbana, IL 61802 USA
关键词
D O I
10.1128/EC.5.1.180-191.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Candida albicans is the most common etiological agent of vaginal candidiasis. Elevated host estrogen levels and the incidence of vaginal candidiasis are positively associated. Elevated estrogen levels may affect host and/or fungal cells. This study investigates the effect of 17-beta-estradiol, 17-alpha-estradiol, ethynyl estradiol, and estriol on several C albicans strains at concentrations ranging from 10(-5) to 10(-10) M. The addition of 17-beta-estradiol or ethynyl estradiol to C. albicans cells caused an increase in the number of cells forming germ tubes and an increase in germ tube length in a dose- and strain-dependent manner. The addition of 17-alpha-estradiol or estriol did not have a significant effect on germ tube formation by the cultured cells. Exposure to exogenous estrogens did not significantly change the biomass of any C albicans culture tested. The transcriptional profile of estrogen-treated C albicans cells showed increased expression of CDRI and CDR2 across several strain-estrogen concentration-time point combinations, suggesting that these genes are the most responsive to estrogen exposure. Analysis of strain DSY654, which lacks the CDR1 and CDR2 coding sequences, showed a significantly decreased number of germ tube-forming cells in the presence of 17-beta-estradiol. PDR16 was the most highly up-regulated gene in strain DSY654 under these growth conditions. The cell biology and gene expression data from this study led to a model that proposes how components of the phospholipid and sterol metabolic pathways may interact to affect C albicans germ tube formation and length.
引用
收藏
页码:180 / 191
页数:12
相关论文
共 54 条
[1]   The Candida albicans HYR1 gene, which is activated in response to hyphal development: Belongs to a gene family encoding yeast cell wall proteins [J].
Bailey, DA ;
Feldmann, PJF ;
Bovey, M ;
Gow, NAR ;
Brown, AJP .
JOURNAL OF BACTERIOLOGY, 1996, 178 (18) :5353-5360
[2]   Propranolol inhibits hyphal development in Candida albicans [J].
Baker, CA ;
Desrosiers, K ;
Dolan, JW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (11) :3617-3620
[3]   Prevalence of vulvovaginal candidiasis and susceptibility to fluconazole in women [J].
Bauters, TGM ;
Dhont, MA ;
Temmerman, MIL ;
Nelis, HJ .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2002, 187 (03) :569-574
[4]   LIPOPHILIC IMPURITIES, NOT PHENOLSULFONPHTHALEIN, ACCOUNT FOR THE ESTROGENIC ACTIVITY IN COMMERCIAL PREPARATIONS OF PHENOL RED [J].
BINDAL, RD ;
CARLSON, KE ;
KATZENELLENBOGEN, BS ;
KATZENELLENBOGEN, JA .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1988, 31 (03) :287-293
[5]   CLONING AND CHARACTERIZATION OF ECE1, A GENE EXPRESSED IN ASSOCIATION WITH CELL ELONGATION OF THE DIMORPHIC PATHOGEN CANDIDA-ALBICANS [J].
BIRSE, CE ;
IRWIN, MY ;
FONZI, WA ;
SYPHERD, PS .
INFECTION AND IMMUNITY, 1993, 61 (09) :3648-3655
[6]   Higher-risk behavioral practices associated with bacterial vaginosis compared with vaginal candidiasis [J].
Bradshaw, CS ;
Morton, AN ;
Garland, SM ;
Morris, MB ;
Moss, LM ;
Fairley, CK .
OBSTETRICS AND GYNECOLOGY, 2005, 106 (01) :105-114
[7]   Binding and reactivity of Candida albicans estrogen binding protein with steroid and other substrates [J].
Buckman, J ;
Miller, SM .
BIOCHEMISTRY, 1998, 37 (40) :14326-14336
[8]   cDNA microarray analysis of differential gene expression in Candida albicans biofilm exposed to farnesol [J].
Cao, YY ;
Cao, YB ;
Xu, Z ;
Ying, K ;
Li, Y ;
Xie, Y ;
Zhu, ZY ;
Chen, WS ;
Jiang, YY .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (02) :584-589
[9]   Pregnenolone esterification in Saccharomyces cerevisiae -: A potential detoxification mechanism [J].
Cauet, G ;
Degryse, E ;
Ledoux, C ;
Spagnoli, R ;
Achstetter, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 261 (01) :317-324
[10]   Comparison between Candida albicans agglutinin-like sequence gene expression patterns in human clinical specimens and models of vaginal candidiasis [J].
Cheng, G ;
Wozniak, K ;
Wallig, MA ;
Fidel, PL ;
Trupin, SR ;
Hoyer, LL .
INFECTION AND IMMUNITY, 2005, 73 (03) :1656-1663