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Inhibitory Effects of Vaginal Lactobacilli on Candida albicans Growth, Hyphal Formation, Biofilm Development, and Epithelial Cell Adhesion

Authors :
Tomonori Takano
Hayami Kudo
Shuhei Eguchi
Asami Matsumoto
Kentaro Oka
Yukitaka Yamasaki
Motomichi Takahashi
Takuro Koshikawa
Hiromu Takemura
Yuka Yamagishi
Hiroshige Mikamo
Hiroyuki Kunishima
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

Antifungal agents are not always efficient in resolving vulvovaginal candidiasis (VVC), a common genital infection caused by overgrowth of Candida spp., including Candida albicans, or preventing recurrent infections. Although lactobacilli (which are dominant microorganisms constituting healthy human vaginal microbiota) are important barriers against VVC, the Lactobacillus metabolite concentration needed to suppress VVC is unknown. Therefore, we quantitatively evaluated Lactobacillus metabolite concentrations to determine their effect on Candida spp., including 27 vaginal strains of Lactobacillus crispatus, Lactobacillus jensenii, Lactobacillus gasseri, Lacticaseibacillus rhamnosus, and Limosilactobacillus vaginalis, with inhibitory abilities against biofilms of Candida clinical isolates. Lactobacillus culture supernatants suppressed viable bacteria by approximately 24%-92% relative to preformed Candida biofilms, but their suppression differed between strains, not species. Lactate production was necessary to suppress preformed biofilms and hyphal elongation of C. albicans, whereas hydrogen peroxide was not always essential. Both lactic acid and hydrogen peroxide were required to suppress Candida planktonic cell growth. Lactobacillus strains that significantly inhibited biofilm formation in culture supernatant also inhibited Candida adhesion to epithelial cells in an actual live bacterial adhesion competition test. Healthy human microflora and their metabolites may play important roles in the development of new antifungal agent against VVC caused by C. albicans.

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........484d4407614cc1f208cef9c60a49c5f2
Full Text :
https://doi.org/10.20944/preprints202209.0424.v1