Candida glabrata and Candida albicans co-infection of an in vitro oral epithelium
Candida albicans is regarded as the leading of candidosis. However, Candida glabrata has emerged as an important pathogen of oral mucosa, occurring both singly or in mixed species infections, often with C. albicans. Compared with C. albicans, little is known about the role of C. glabrata in oral inf...
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Veröffentlicht in: | Journal of oral pathology & medicine 2011-05, Vol.40 (5), p.421-427 |
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Zusammenfassung: | Candida albicans is regarded as the leading of candidosis. However, Candida glabrata has emerged as an important pathogen of oral mucosa, occurring both singly or in mixed species infections, often with C. albicans. Compared with C. albicans, little is known about the role of C. glabrata in oral infection. The aim of this study was to examine single and mixed species infection of oral epithelium involving C. glabrata and establish its ability to invade and damage tissue. Methods: A reconstituted human oral epithelium (RHOE) was infected only with C. glabrata, or simultaneously with C. glabrata and C. albicans. The ability of both species to invade the tissue was examined using species specific peptide nucleic acid (PNA) probe hybridization and confocal laser scanning microscopy. Epithelial damage was assessed by measuring lactate dehydrogenase (LDH) activity. Results: Candida glabrata strains were able to colonize the RHOE, in a strain dependent manner. Candida glabrata single infection after 12h, generally revealed no invasion of the RHOE, which contrasted with extensive tissue invasion demonstrated by C. albicans. Mixed infection showed that C. albicans enhanced the invasiveness of C. glabrata, and led to increased LDH release by the RHOE, which paralleled the observed histological damage. Conclusions: The results obtained demonstrating enhanced invasion and increased tissue damage caused by mixed C. glabrata and C. albicans infections have important clinical significance and highlight the need to identify Candida species involved in oral candidosis.
We would like to thank Mrs Kath Allsopp for processing and sectioning tissue samples. The authors also would like to thank Mr Mark Fiandaca of AdvanDX for provision of Yeast Traffic Light PNA FISH (TM) Kit. This work was supported by the research grant SFRH/BD/28341/2006 from the Fundacao para a Ciencia e Tecnologia (FCT), Portugal. |
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ISSN: | 0904-2512 1600-0714 |
DOI: | 10.1111/j.1600-0714.2010.00981.x |