Oral colonization by Candida albicans

被引:213
作者
Cannon, RD
Chaffin, WL
机构
[1] Univ Otago, Fac Dent, Dept Oral Sci & Orthodont, Dunedin, New Zealand
[2] Texas Tech Univ, Hlth Sci Ctr, Dept Microbiol & Immunol, Lubbock, TX 79430 USA
关键词
Candida albicans; colonization; adherence; candidiasis;
D O I
10.1177/10454411990100030701
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Candida albicans is a commensal yeast normally present in small numbers in the oral flora of a large proportion of humans. Colonization of the oral cavity by C. albicans involves the acquisition and maintenance of a stable yeast population. Micro-organisms are continually being removed from the oral cavity by host clearance mechanisms, and so, in order to survive and inhabit this eco-system, C. albicans cells have to adhere and replicate. The oral cavity presents many niches for C. albicans colonization, and the yeast is able to adhere to a plethora of ligands. These include epithelial and bacterial cell-surface molecules, extracellular matrix proteins, and dental acrylic. In addition, saliva molecules, including basic proline-rich proteins, adsorbed to many oral surfaces promote C. albicans adherence. Several adhesins present in the C. albicans cell wall have now been partially characterized. Adherence involves lectin, protein-protein, and hydrophobic interactions. As C. albicans cells evade host defenses and colonize new environments by penetrating tissues, they are exposed to new adherence receptors and respond by expressing alternative adhesins. The relatively small number of commensal Candida cells in the oral flora raises the possibility that strategies can be devised to prevent oral colonization and infection. However, the variety of oral niches and the complex adherence mechanisms of the yeast mean that such a goal will remain elusive until more is known about the contribution of each mechanism to colonization.
引用
收藏
页码:359 / 383
页数:25
相关论文
共 265 条
[1]   ISOLATION AND BIOCHEMICAL-CHARACTERIZATION OF THE IC3B RECEPTOR OF CANDIDA-ALBICANS [J].
ALAEI, S ;
LARCHER, C ;
EBENBICHLER, C ;
PRODINGER, WM ;
JANATOVA, J ;
DIERICH, MP .
INFECTION AND IMMUNITY, 1993, 61 (04) :1395-1399
[2]   Multiple efflux mechanisms are involved in Candida albicans fluconazole resistance [J].
Albertson, GD ;
Niimi, M ;
Cannon, RD ;
Jenkinson, HF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (12) :2835-2841
[3]   Antifungal resistance trends towards the year 2000 - Implications for therapy and new approaches [J].
Alexander, BD ;
Perfect, JR .
DRUGS, 1997, 54 (05) :657-678
[4]   CHARACTERIZATION OF INVIVO SALIVARY-DERIVED ENAMEL PELLICLE [J].
ALHASHIMI, I ;
LEVINE, MJ .
ARCHIVES OF ORAL BIOLOGY, 1989, 34 (04) :289-295
[5]  
Alloush HM, 1996, J MED VET MYCOL, V34, P91
[6]  
Annaix V, 1990, FEMS Microbiol Immunol, V2, P147
[7]   ORAL CANDIDAL POPULATIONS IN HEALTH AND DISEASE [J].
ARENDORF, TM ;
WALKER, DM .
BRITISH DENTAL JOURNAL, 1979, 147 (10) :267-272
[8]   THE PREVALENCE AND INTRA-ORAL DISTRIBUTION OF CANDIDA-ALBICANS IN MAN [J].
ARENDORF, TM ;
WALKER, DM .
ARCHIVES OF ORAL BIOLOGY, 1980, 25 (01) :1-10
[9]   ADHERENCE OF CANDIDA-ALBICANS TO HUMAN BUCCAL EPITHELIAL-CELLS - HOST-INDUCED PROTEIN-SYNTHESIS AND SIGNALING EVENTS [J].
BAILEY, A ;
WADSWORTH, E ;
CALDERONE, R .
INFECTION AND IMMUNITY, 1995, 63 (02) :569-572
[10]  
BECKSAGUE CM, 1993, J INFECT DIS, V167, P1247, DOI 10.1093/infdis/167.5.1247