The role of Candida albicans NOT5 in virulence depends upon diverse host factors in vivo

被引:13
作者
Cheng, SJ
Clancy, CJ
Checkley, MA
Zhang, ZD
Wozniak, KL
Seshan, KR
Jia, HY
Fidel, P
Cole, G
Nguyen, MH
机构
[1] Univ Florida, Coll Med, Dept Med, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Dept Mol Genet, Gainesville, FL 32610 USA
[3] Univ Florida, Coll Med, Dept Microbiol, Gainesville, FL 32610 USA
[4] VA Med Ctr, Dept Med, Gainesville, FL USA
[5] Louisiana State Univ, Hlth Sci Ctr, Dept Microbiol Immunol & Parasitol, New Orleans, LA 70112 USA
[6] Med Coll Ohio, Dept Microbiol & Immunol, Toledo, OH 43699 USA
关键词
D O I
10.1128/IAI.73.11.7190-7197.2005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We previously identified Candida albicans Not5p as an immunogenic protein expressed during oropharyngeal candidiasis (OPC). In this study, we demonstrate that C. albicans NOT5 reverses the growth defects of a Saccharomyces cerevisiae not5 mutant strain at 37 degrees C, suggesting that the genes share at least some functional equivalence. We implicate C. albicans NOT5 in the pathogenesis of disseminated candidiasis (DC) induced by intravenous infection among neutropenic and nonimmunosuppressed mice, as well as in that of OPC in mice immunosuppressed with corticosteroids. We find no role in virulence, however, among neutropenic and corticosteroid-suppressed mice with DC resulting from gastrointestinal translocation, nor do we implicate the gene in vulvovaginal candidiasis among mice in pseudoestrus. These findings suggest that the role of NOT5 in virulence depends on the specific in vivo environment and is influenced by diverse factors such as tissue site, portal of entry, and the status of host defenses. NOT5 is necessary for normal adherence to colonic and cervical epithelial cells in vitro, demonstrating that such assays cannot fully replicate disease processes in vivo. Lastly, antibody responses against Not5p do not differ in the sera of patients with OPC, patients with DC, and healthy controls, suggesting that the protein is associated with both commensalism and the pathogenesis of disease.
引用
收藏
页码:7190 / 7197
页数:8
相关论文
共 27 条
[11]  
Ebersole J L, 1987, Oral Microbiol Immunol, V2, P53, DOI 10.1111/j.1399-302X.1987.tb00290.x
[12]  
FONZI WA, 1993, GENETICS, V134, P717
[13]   ISOLATION OF THE CANDIDA-ALBICANS GENE FOR OROTIDINE-5'-PHOSPHATE DECARBOXYLASE BY COMPLEMENTATION OF S-CEREVISIAE URA3 AND ESCHERICHIA-COLI PYRF MUTATIONS [J].
GILLUM, AM ;
TSAY, EYH ;
KIRSCH, DR .
MOLECULAR & GENERAL GENETICS, 1984, 198 (01) :179-182
[14]   Contribution of Candida albicans ALS1 to the pathogenesis of experimental oropharyngeal candidiasis [J].
Kamai, Y ;
Kubota, M ;
Kamai, Y ;
Hosokawa, T ;
Fukuoka, T ;
Filler, SG .
INFECTION AND IMMUNITY, 2002, 70 (09) :5256-5258
[15]   Deletion of the NOT4 gene impairs hyphal development and pathogenicity in Candida albicans [J].
Krueger, KE ;
Ghosh, AK ;
Krom, BP ;
Cihlar, RL .
MICROBIOLOGY-SGM, 2004, 150 :229-240
[16]   DNA array studies demonstrate convergent regulation of virulence factors by Cph1, Cph2, and Efg1 in Candida albicans [J].
Lane, S ;
Birse, C ;
Zhou, S ;
Matson, R ;
Liu, HP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (52) :48988-48996
[17]   Saccharomyces cerevisiae Ccr4-Not complex contributes to the control of Msn2p-dependent transcription by the Ras/cAMP pathway [J].
Lenssen, E ;
Oberholzer, U ;
Labarre, J ;
De Virgilio, C ;
Collart, MA .
MOLECULAR MICROBIOLOGY, 2002, 43 (04) :1023-1037
[18]   Glucocorticoids and invasive fungal infections [J].
Lionakis, MS ;
Kontoyiannis, DP .
LANCET, 2003, 362 (9398) :1828-1838
[19]   The NOT proteins are part of the CCR4 transcriptional complex and affect gene expression both positively and negatively [J].
Liu, HY ;
Badarinarayana, V ;
Audino, DC ;
Rappsilber, J ;
Mann, M ;
Denis, CL .
EMBO JOURNAL, 1998, 17 (04) :1096-1106
[20]   SELECTION OF BACTERIAL VIRULENCE GENES THAT ARE SPECIFICALLY INDUCED IN HOST TISSUES [J].
MAHAN, MJ ;
SLAUCH, JM ;
MEKALANOS, JJ .
SCIENCE, 1993, 259 (5095) :686-688