1. Molecular mechanism of azoles resistant Candida albicans in a patient with chronic mucocutaneous candidiasis
- Author
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Fei Zhao, Mou Yan, Sha Lv, Fuqiu Li, Ying Zhou, Mingrui Zhang, Shuang Wang, and Yao Chunli
- Subjects
Azoles ,Male ,0301 basic medicine ,Antifungal Agents ,Adolescent ,030106 microbiology ,Case Report ,Microbial Sensitivity Tests ,Drug resistance ,Microbiology ,lcsh:Infectious and parasitic diseases ,Fungal Proteins ,03 medical and health sciences ,Minimum inhibitory concentration ,symbols.namesake ,Chronic mucocutaneous candidiasis ,STAT1 ,Drug Resistance, Fungal ,Gene Expression Regulation, Fungal ,Candida albicans ,medicine ,Humans ,lcsh:RC109-216 ,Immunodeficiency ,Sanger sequencing ,Mouth ,biology ,business.industry ,Candidiasis, Chronic Mucocutaneous ,Membrane Transport Proteins ,medicine.disease ,biology.organism_classification ,Corpus albicans ,030104 developmental biology ,Infectious Diseases ,Over-expression ,Mutation ,symbols ,Azoles resistance ,Drug efflux ,Efflux ,business - Abstract
Background More and more azole-resistant strains emerged through the development of acquired resistance and an epidemiological shift towards inherently less susceptible species. The mechanisms of azoles resistance of Candida albicans is very complicated. In this study, we aim to investigate the mechanism of azole-resistant C. albicans isolated from the oral cavity of a patient with chronic mucocutaneous candidiasis (CMC). Case presentation CMC diagnosis was given based on clinical manifestations, laboratory test findings and gene sequencing technique. Minimum inhibitory concentration (MIC) of the fungal isolate, obtained from oral cavity termed as CA-R, was obtained by in vitro anti-fungal drugs susceptibility test. To further investigate the resistant mechanisms, we verified the mutations of drug target genes (i.e. ERG11 and ERG3) by Sanger sequencing, and verified the over-expression of ERG11 and drug efflux genes (i.e. CDR1 and CDR2) by RT-PCR. A heterozygous mutation of c.1162A > G resulting in p.K388E was detected in STAT1 of the patient. The expression of CDR1 and CDR2 in CA-R was 4.28-fold and 5.25-fold higher than that of type strain SC5314, respectively. Conclusions Up-regulation of CDR1 and CDR2 was mainly responsible for the resistance of CA-R. For CMC or other immunodeficiency patients, drug resistance monitoring is necessary.
- Published
- 2020