Protective effects of farnesol against oral candidiasis in mice

被引:53
作者
Hisajima, Tatsuya [1 ,2 ]
Maruyama, Naho [1 ]
Tanabe, Yuko
Ishibashi, Hiroko [1 ]
Yamada, Tsuyoshi [1 ]
Makimura, Koichi [1 ]
Nishiyama, Yayoi [1 ]
Funakoshi, Kengo [2 ]
Oshima, Haruyuki
Abe, Shigeru [1 ]
机构
[1] Teikyo Univ, Inst Med Mycol, Tokyo 1920395, Japan
[2] Yokohama City Univ, Sch Med, Dept Neuroanat, Yokohama, Kanagawa 232, Japan
关键词
Candida mycelial growth; dimorphic switch; mucosal infection; tongue lesion;
D O I
10.1111/j.1348-0421.2008.00044.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Farnesol is known as a quorum-sensing molecule for Candida albicans and is recognized to play pathogenic roles in Candida infection. To assess the possible role of farnesol in mucosal C. albicans infection, the effects of farnesol treatment against experimental oral candidiasis in mice were examined. Prednisolone-pretreated ICR mice were orally infected with C. albicans and 3, 24 and 30 hr later the animals were orally given farnesol. Forty-eight hr later they were killed for observation. Farnesol treatment in a dose ranging between 1.125 and 9 mu mol/mouse showed a protective effect against oral candidiasis in a dose-dependent manner, at least as estimated by symptom scores of tongues. At 9 mu mol/mouse it decreased bodyweight loss. Histological studies of 2.25 mu mol/mouse farnesol-treated animals indicated that farnesol suppressed mycelial growth of C. albicans on the surface of tongues, but microbiological study did not prevent the change of CFU of C. albicans cells not only on tongues but also in feces, kidneys and livers. These results suggest that farnesol has very characteristic roles in protection against mucosal candidiasis.
引用
收藏
页码:327 / 333
页数:7
相关论文
共 14 条
[1]
A RAPID COLORIMETRIC ASSAY FOR DETERMINATION OF LEUKOCYTE-MEDIATED INHIBITION OF MYCELIAL GROWTH OF CANDIDA-ALBICANS [J].
ABE, S ;
SATOH, T ;
TOKUDA, Y ;
TANSHO, S ;
YAMAGUCHI, H .
MICROBIOLOGY AND IMMUNOLOGY, 1994, 38 (05) :385-388
[2]
[Anonymous], 1988, CANDIDA CANDIDIASIS
[3]
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
[4]
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
[5]
A novel murine model of pharyngeal candidiasis with local symptoms characteristic of pharyngeal thrush produced by using an inhaled corticosteroid [J].
Hu, Weimin ;
Ninomiya, Kentaro ;
Ishibashi, Hiroko ;
Maruyama, Naho ;
Oshima, Haruyuki ;
Yamaguchi, Hideyo ;
Abe, Shigeru .
MEDICAL MYCOLOGY, 2007, 45 (02) :143-148
[6]
Nonfilamentous C-albicans mutants are avirulent [J].
Lo, HJ ;
Kohler, JR ;
DiDomenico, B ;
Loebenberg, D ;
Cacciapuoti, A ;
Fink, GR .
CELL, 1997, 90 (05) :939-949
[7]
Exogenous farnesol interferes with the normal progression of cytokine expression during candidiasis in a mouse model [J].
Navarathna, Dhammika H. M. L. P. ;
Nickerson, Kenneth W. ;
Duhamel, Gerald E. ;
Jerrels, Thomas R. ;
Petro, Thomas M. .
INFECTION AND IMMUNITY, 2007, 75 (08) :4006-4011
[8]
Effect of farnesol on a mouse model of systemic candidiasis, determined by use of a DPP3 knockout mutant of Candida albicans [J].
Navarathna, Dhammika H. M. L. P. ;
Hornby, Jacob M. ;
Krishnan, Navasona ;
Parkhurst, Anne ;
Duhamel, Gerald E. ;
Nickerson, Kenneth W. .
INFECTION AND IMMUNITY, 2007, 75 (04) :1609-1618
[9]
Quorum sensing in dimorphic fungi: Farnesol and beyond [J].
Nickerson, KW ;
Atkin, AL ;
Hornby, JM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (06) :3805-3813
[10]
Inhibition of Candida albicans biofilm formation by farnesol, a quorum-sensing molecule [J].
Ramage, G ;
Saville, SP ;
Wickes, BL ;
López-Ribot, JL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (11) :5459-5463