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Vulvovaginal candidosis (VVC) is a common condition with severe symptoms and high recurrence rates. Probiotic lactobacilli are explored as alternatives to azole treatments. Although the vaginal microbiota is generally not depleted in lactobacilli during VVC, studies indicate that the functionality and antimicrobial activity of the lactobacilli is impaired. We selected three strains from the Lactobacillus genus complex (L. rhamnosus GG, L. pentosus KCA1 and L. plantarum WCFS1) based on in vitro evaluation and formulated them in a gel for vaginal application. This gel was evaluated in 20 patients suffering from acute VVC, who were followed for four weeks including a 10-day treatment period. The microbiome was assessed through 16S rRNA (bacteria) and internal transcribed spacer (ITS; fungi) amplicon sequencing, supplemented with quantitative PCR, culture and microscopy for Candida evaluation. 45% of women did not require rescue medication (3×200 mg fluconazole), implying an improvement of their symptoms. These women showed similar end concentrations of fungi as women treated with fluconazole. Moreover, fluconazole appeared to reduce numbers of endogenous lactobacilli. Our study points towards important aspects for future selection of lactobacilli for probiotic use in VVC and the need to investigate possible negative influences of azoles on the vaginal bacterial community.
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http://dx.doi.org/10.1038/s41598-020-64705-x | DOI Listing |
Vulvovaginal candidiasis (VVC), caused by the commensal pathobiont affects >75% of women, marring quality of life and incurring significant health costs. Estrogen (E2) activity is tightly linked to VVC susceptibility, and preclinical models employ E2 to establish vaginal colonization. Unlike most forms of candidiasis, VVC is not considered to be a condition of immune compromise.
View Article and Find Full Text PDFmSystems
September 2025
Department of Microbiology, Faculty of Science, University of Manitoba, Winnipeg, Manitoba, Canada.
Unlabelled: Vulvovaginal candidiasis is a very common human fungal infection. Most are successfully treated with antifungal drugs, yet ~8% lead to recurrent vulvovaginal candidiasis (RVVC). Vaginal and rectal populations have been previously found to be closely related in RVVC.
View Article and Find Full Text PDFInt J Microbiol
August 2025
Department of Mycology and Molecular Diagnostic Laboratory, School of Biochemistry and Biological Sciences, Universidad Nacional del Litoral, Santa Fe de la Vera Cruz, Santa Fe, Argentina.
complex species are the main cause of candidiasis. The purpose of this study was to report the prevalence and genetic diversity of complex using hyphal wall protein 1 (HWP1) gene size polymorphism, as well as the susceptibility patterns to fluconazole and voriconazole. A total of 170 yeast isolates were obtained from vulvovaginal samples, and phenotypic and proteomic identification was performed.
View Article and Find Full Text PDFCurr Opin Obstet Gynecol
August 2025
Department of Urogynecology, Hartford Hospital, Hartford, Connecticut, USA.
Purpose Of Review: The vaginal microbiome plays an important role in protecting the vagina and bladder from infection. There is significant interest in understanding whether probiotics can normalize the vaginal microbiome and lead to decreased incidence of vulvovaginal-associated infections. Probiotics are an appealing treatment option as they are well tolerated, have a low risk profile, and potentially can reduce antibiotic usage.
View Article and Find Full Text PDFPharmacol Res
August 2025
Toxicology and Drug Metabolism Group, Department of Pharmacy, University of Copenhagen, Copenhagen, Denmark.
During pregnancy there is an increased risk of vulvovaginal candidiasis that if left untreated is associated with pregnancy complications. First choice of treatment are over-the-counter azole antifungal drugs (AADs): miconazole, and clotrimazole, or prescription drug: fluconazole, which are suspected endocrine disruptive compounds. To investigate foetal exposure and endocrine disrupting effects of AADs on the human placenta, we added R-miconazole, S-miconazole, clotrimazole and fluconazole to the maternal reservoir of a dually recirculating ex vivo human term placental perfusion model.
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