Experimental induction of fluconazole resistance in Candida tropicalis ATCC 750

Détails

ID Serval
serval:BIB_5B89097B5A6F
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Experimental induction of fluconazole resistance in Candida tropicalis ATCC 750
Périodique
Antimicrobial Agents and Chemotherapy
Auteur⸱e⸱s
Barchiesi  F., Calabrese  D., Sanglard  D., Falconi Di Francesco  L., Caselli  F., Giannini  D., Giacometti  A., Gavaudan  S., Scalise  G.
ISSN
0066-4804 (Print)
Statut éditorial
Publié
Date de publication
06/2000
Volume
44
Numéro
6
Pages
1578-84
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Jun
Résumé
Candida tropicalis is less commonly isolated from clinical specimens than Candida albicans. Unlike C. albicans, which can be occasionally found as a commensal, C. tropicalis is almost always associated with the development of fungal infections. In addition, C. tropicalis has been reported to be resistant to fluconazole (FLC). To analyze the development of FLC resistance in C. tropicalis, an FLC-susceptible strain (ATCC 750) (MIC = 1.0 microg/ml) was cultured in liquid medium containing increasing FLC concentrations from 8.0 to 128 microg/ml. The strain developed variable degrees of FLC resistance which paralleled the concentrations of FLC used in the medium. The highest MICs of FLC were 16, 256, and 512 microg/ml for strains grown in medium with 8.0, 32, and 128 microg of FLC per ml, respectively. Development of resistance was rapid and could be observed already after a single subculture in azole-containing medium. The resistant strains were cross-resistant to itraconazole (MIC > 1.0 microg/ml) and terbinafine (MIC > 512 microg/ml) but not to amphotericin B. Isolates grown in FLC at concentrations of 8.0 and 32 microg/ml reverted to low MICs (1.0 microg/ml) after 12 and 11 passages in FLC-free medium, respectively. The MIC for one isolate grown in FLC (128 microg/ml) (128 R) reverted to 16 microg/ml but remained stable over 60 passages in FLC-free medium. Azole-resistant isolates revealed upregulation of two different multidrug efflux transporter genes: the major facilitators gene MDR1 and the ATP-binding cassette transporter CDR1. The development of FLC resistance in vitro correlated well with the results obtained in an experimental model of disseminated candidiasis. While FLC given at 10 mg/kg of body weight/day was effective in reducing the fungal burden of mice infected with the parent strain, the same dosing regimen was ineffective in mice infected with strain 128 R. Finally, the acquisition of in vitro FLC resistance in strain 128 R was related to a loss of virulence. The results of our study elucidate important characteristics and potential mechanisms of FLC resistance in C. tropicalis.
Mots-clé
Animals Candida/*drug effects/*genetics *Drug Resistance, Microbial Fluconazole/*pharmacology Gene Expression Regulation, Fungal Mice Virulence
Pubmed
Web of science
Création de la notice
25/01/2008 14:40
Dernière modification de la notice
20/08/2019 14:14
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