In vitro synergistic effect of farnesol and human gingival cells against Candida albicans

被引:18
作者
Saidi, Said [1 ]
Luitaud, Cyril [1 ]
Rouabhia, Mahmoud [1 ]
机构
[1] Univ Laval, Fac Med Dent, Grp Rech & Ecol Buccale, Quebec City, PQ G1K 7P4, Canada
关键词
epithelial cells; Candida albicans; candidiasis; oral mucosa; farnesol; antifungal;
D O I
10.1002/yea.1389
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Farnesol prevents the germination of yeast cells into mycelia, a fact that may be useful in eliminating C albicans pathogenicity. Given the clinical potential of farnesol, its impact on C albicans and host cells merited further investigation. We thus studied the effect of farnesol on C. albicans growth and filamentation and on gingival epithelial cells and fibroblasts and the synergistic effect of both gingival cells and farnesol on C. albicans filamentation. Repeated additions of farnesol reduced the growth of C. albicans. Farnesol was also effective at reducing C albicans germ tube formation. While farnesol inhibited germ tube formation under the conditions tested, it was most effective at inhibiting C. albicans filamentation when added to the culture medium at the same time as the serum. Farnesol also had an effect on gingival cells. In a serum-free medium, farnesol reduced fibroblast adhesion and proliferation, promoted epithelial cell differentiation and reduced proliferation up to 48 h post-treatment. These effects were not seen in the presence of serum. When C. albicans, farnesol and gingival cells were present in the same culture, significantly greater inhibition of the yeast-to-hyphal transition was observed than germ tube inhibition in cultures containing only C albicans and farnesol, suggesting a synergistic effect between the gingival cells and farnesol in inhibiting the transition. Overall, the data suggest that farnesol is effective against C albicans and may have an effect on host cells at certain concentrations. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:673 / 687
页数:15
相关论文
共 55 条
[21]   BRANCH-POINT REACTIONS IN THE BIOSYNTHESIS OF CHOLESTEROL, DOLICHOL, UBIQUINONE AND PRENYLATED PROTEINS [J].
GRUNLER, J ;
ERICSSON, J ;
DALLNER, G .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1994, 1212 (03) :259-277
[22]  
HEMMERLIN A, 2005, IN PRESS ARCH BIOCH
[23]   Modulation of hepatic and renal drug metabolizing enzyme activities in rats by subchronic administration of farnesol [J].
Horn, TL ;
Long, L ;
Cwik, MJ ;
Morrissey, RL ;
Kapetanovic, IM ;
McCormick, DL .
CHEMICO-BIOLOGICAL INTERACTIONS, 2005, 152 (2-3) :79-99
[24]   Farnesol biosynthesis in Candida albicans:: Cellular response to sterol inhibition by zaragozic acid B [J].
Hornby, JM ;
Kebaara, BW ;
Nickerson, KW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (07) :2366-2369
[25]   Quorum sensing in the dimorphic fungus Candida albicans is mediated by farnesol [J].
Hornby, JM ;
Jensen, EC ;
Lisec, AD ;
Tasto, JJ ;
Jahnke, B ;
Shoemaker, R ;
Dussault, P ;
Nickerson, KW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (07) :2982-2992
[26]  
Hudes GR, 2000, CLIN CANCER RES, V6, P3071
[27]   The two-component signal transduction protein Chk1p regulates quorum sensing in Candida albicans [J].
Kruppa, M ;
Krom, BP ;
Chauhan, N ;
Bambach, AV ;
Cihlar, RL ;
Calderone, RA .
EUKARYOTIC CELL, 2004, 3 (04) :1062-1065
[28]   In vitro susceptibility of oral Candida to seven antifungal agents [J].
Kuriyama, T ;
Williams, DW ;
Bagg, J ;
Coulter, WA ;
Ready, D ;
Lewis, MAO .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2005, 20 (06) :349-353
[29]   Candida-specific systemic cell-mediated immune reactivities in human immunodeficiency virus-positive persons with mucosal candidiasis [J].
Leigh, JE ;
Barousse, M ;
Swoboda, RK ;
Myers, T ;
Hager, S ;
Wolf, NA ;
Cutright, JL ;
Thompson, J ;
Sobel, JD ;
Fidel, PL .
JOURNAL OF INFECTIOUS DISEASES, 2001, 183 (02) :277-285
[30]   Farnesyl-O-acetylhydroquinone and geranyl-O-acetylhydroquinone suppress the proliferation of murine B16 melanoma cells, human prostate and colon adenocarcinoma cells, human lung carcinoma cells, and human leukemia cells [J].
McAnally, JA ;
Jung, M ;
Mo, HB .
CANCER LETTERS, 2003, 202 (02) :181-192