4.5 Article

Evaluation of overtime phenotypic variation of yeasts in chronic vulvovaginal candidosis cases

Journal

MEDICAL MYCOLOGY
Volume 59, Issue 12, Pages 1166-1173

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/mmy/myab048

Keywords

chronic; recurrence; vulvovaginal candidosis; molecular typing; antifungal resistance; biofilm

Funding

  1. Health Sciences Research Center (CICS-UBI) through National Funds by Fundacao para a Ciencia e Tecnologia (FCT) [UID/Multi/00709/2019]
  2. Instituto Nacional de Administracao e Gestao de Bolsas de Estudo (INAGBE), Angola
  3. FCT, Portugal [SFRH/BPD/115145/2016, SFRH/BPD/124437/2016]
  4. European Regional Development Fund (ERDF), through the Centro 2020 Regional Operational Programme [UIDB/04539/2020]
  5. Fundação para a Ciência e a Tecnologia [SFRH/BPD/115145/2016] Funding Source: FCT

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This study aimed to assess the mechanisms leading to Candida spp persistence in women with chronic vulvovaginal candidosis, focusing on strains genotypes, azole resistance, and ability to form biofilms. The results showed that related strains with increased fluconazole resistance and enhanced biofilm formation capacity were correlated with recurrent cases caused by C. glabrata, highlighting the importance of these factors in enhancing persistence in the vaginal mucosa for this particular species.
Chronic vulvovaginal candidosis results either from reinfection or from the ability of Candida spp. to persist in the vulva and/or vagina. Persistence is usually associated with increased antifungal (mainly azoles) resistance rates, which can explain treatment failure, and/or increased expression of virulence factors by Candida spp. The aim of this study was to assess the mechanisms leading to Candida spp persistence, by studying sequential isolates from women with chronic vulvovaginal candidosis, focusing on strains genotypes, azole resistance, and ability to form biofilms along the period of clinical evaluation. The strains were identified at species level by automated analysis of biochemical profiles and molecular typing evaluated by polymorphic DNA analysis. The capacity to form biofilm was assessed with a microtiter plate assay. Fluconazole susceptibility was determined by the microdilution broth assay at both pH 7 (following the recommended guideline) and pH 4.5 (as representative of vaginal pH). We studied samples from 17 clinically recurrent cases. In 53% of the chronic cases there were two or more isolates that had a phylogenetic relationship while the remaining (47%) were caused by different species. In those cases where related strains were involved in recurrence, we verified an increase in MIC at pH 7 and also an increased capacity to form biofilms over time. Significant correlation between these two parameters was observed only in cases caused by C. glabrata, evidencing the importance of these two factors to enhance persistence in the vaginal mucosa for this particular species.

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