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Vaginal microbiota: different roles of lactobacilli and community instability in chronic vulvovaginal discomfort

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dc.rights.license CC BY eng
dc.contributor.author Buchta, Vladimir cze
dc.contributor.author Nekvindova, Jana cze
dc.contributor.author Lesko, Daniel cze
dc.contributor.author Vrbacky, Filip cze
dc.contributor.author Vescicik, Peter cze
dc.contributor.author Uhlirova, Zuzana cze
dc.contributor.author Andrys, Ctirad cze
dc.contributor.author Bolehovska, Radka cze
dc.contributor.author Kacerovsky, Marian cze
dc.contributor.author Spacek, Jiri cze
dc.contributor.author Mrkvicova, Alena cze
dc.contributor.author Skalská, Hana cze
dc.contributor.author Pliskova, Lenka cze
dc.date.accessioned 2025-12-05T16:12:15Z
dc.date.available 2025-12-05T16:12:15Z
dc.date.issued 2025 eng
dc.identifier.issn 2235-2988 eng
dc.identifier.uri http://hdl.handle.net/20.500.12603/2476
dc.description.abstract Background Chronic vulvovaginal discomfort (CVD) is a complex syndrome with many unresolved questions regarding its etiology, diagnosis, and management in relation to the vaginal microbiota.Methods Cervicovaginal fluid of 91 CVD patients and 35 healthy controls was obtained at the beginning and end of the follow-up period. The bacterial community state types (CST) in the vagina were assessed using next-generation sequencing (NGS). CVD patients were divided into four study groups by etiology: non-specific, yeast, bacterial, and mixed.Results The vaginal microbiota was characterized by 1) predominance of CST3 in all study groups, 2) a relatively higher proportion of CST2 (29.2%) and CST4 (20.0%) in the non-specific group and controls, respectively, 3) lack of CST4 (4.0%) in the yeast group, and 4) an effect of clinical status (CVD vs. health) on CST stability and microbiota composition. The vaginal environment was shaped by lactobacilli except for CST4. CVD patients had a higher proportion of G-positive cocci than controls; the non-specific group had significantly higher L. gasseri abundance than other CVD etiologies. There was a negative correlation between L. crispatus and L. iners, between G-positive cocci and L. iners, and a positive correlation between G-positive cocci and non-bivia Prevotella species. CST3 in CVD patients represented the most stable CST and was the community to which other CSTs were most often converted, whereas in healthy controls, CST3 was the most labile CST, with a preferential shift to CST4. The distribution of unstable CSTs was similar in both main cohorts, but within CVD group, non-specific etiology showed significantly higher proportion of unstable CSTs and L. gasseri.Conclusion Our results revealed an opposing trend in the abundance of L. iners and L. gasseri between CVD patients and healthy controls, depending on CST stability. We hypothesize that the increased prevalence of CST2 and CST3 may result either from persistent CVD-associated pressure (CST2 and partially CST3), or from enhanced community stability (CST3). The finding that the importance and behavior of Lactobacillus species depend on the patient's clinical status and microbiota context (CST) should contribute to more accurate diagnoses (correct interpretation of laboratory findings) and management of CVD. eng
dc.format p. "Article Number: 1636873" eng
dc.language.iso eng eng
dc.publisher Frontiers Media S.A. eng
dc.relation.ispartof Frontiers in cellular and infection microbiology, volume 15, issue: August eng
dc.subject chronic vulvovaginal discomfort eng
dc.subject vaginal microbiota eng
dc.subject community state type (CST) eng
dc.subject CST shift eng
dc.subject CST stability eng
dc.subject <italic>Lactobacillus iners</italic> eng
dc.subject next generation sequencing (NGS) eng
dc.title Vaginal microbiota: different roles of lactobacilli and community instability in chronic vulvovaginal discomfort eng
dc.type article eng
dc.identifier.obd 43882282 eng
dc.identifier.wos 001560856700001 eng
dc.identifier.doi 10.3389/fcimb.2025.1636873 eng
dc.publicationstatus postprint eng
dc.peerreviewed yes eng
dc.source.url https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2025.1636873/full cze
dc.relation.publisherversion https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2025.1636873/full eng
dc.rights.access Open Access eng


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