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Virulence assessment of six major pathogenic Candida species in the mouse model of invasive candidiasis caused by fungal translocation
Gastrointestinal colonization has been considered as the primary source of candidaemia; however, few established mouse models are available that mimic this infection route. We therefore developed a reproducible mouse model of invasive candidiasis initiated by fungal translocation and compared the vi...
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Published in: | Scientific reports 2020-03, Vol.10 (1), p.3814-3814, Article 3814 |
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Main Authors: | , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Gastrointestinal colonization has been considered as the primary source of candidaemia; however, few established mouse models are available that mimic this infection route. We therefore developed a reproducible mouse model of invasive candidiasis initiated by fungal translocation and compared the virulence of six major pathogenic
Candida
species. The mice were fed a low-protein diet and then inoculated intragastrically with
Candida
cells. Oral antibiotics and cyclophosphamide were then administered to facilitate colonization and subsequent dissemination of
Candida
cells. Mice infected with
Candida albicans
and
Candida tropicalis
exhibited higher mortality than mice infected with the other four species. Among the less virulent species, stool titres of
Candida glabrata
and
Candida parapsilosis
were higher than those of
Candida krusei
and
Candida guilliermondii
. The fungal burdens of
C. parapsilosis
and
C. krusei
in the livers and kidneys were significantly greater than those of
C. guilliermondii
. Histopathologically,
C. albicans
demonstrated the highest pathogenicity to invade into gut mucosa and liver tissues causing marked necrosis. Overall, this model allowed analysis of the virulence traits of
Candida
strains in individual mice including colonization in the gut, penetration into intestinal mucosa, invasion into blood vessels, and the subsequent dissemination leading to lethal infections. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-020-60792-y |