Clotrimazole-induced shifts in vaginal bacteriome and lipid metabolism: insights into recovery mechanisms in vulvovaginal candidiasis.

IF 3.2 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of Applied Microbiology Pub Date : 2024-11-04 DOI:10.1093/jambio/lxae269
Jingjing Wang, Xiaowen Pu, Zhengrong Gu
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Abstract

Aims: Vulvovaginal candidiasis (VVC) is a prevalent condition affecting a significant proportion of women worldwide, with recurrent episodes leading to detrimental effects on quality of life. While treatment with clotrimazole is common, the specific alterations it evokes in the vaginal bacteriome and metabolome were previously underexplored.

Methods and results: In this prospective study, we enrolled reproductive-age women diagnosed with single VVC and conducted comprehensive analyses of vaginal fungi, bacteriome, and metabolome before and after local clotrimazole treatment. We observed a significant reduction in Candida albicans and notable improvements in vaginal cleanliness. Advanced sequencing revealed substantial shifts in the vaginal bacteriome, with an increase in Lactobacillus-dominant communities post-treatment. Our findings identified 17 differentially abundant bacterial species, including notable decreases in pathogenic anaerobes such as Gardnerella vaginalis, Dialister micraerophilus, and Aerococcus christensenii, suggesting a restoration of a healthier microbial balance. Furthermore, metabolomic analysis revealed significant changes in 230 metabolites, particularly within lipid metabolism pathways, with marked downregulation of lipid-related compounds linked to inflammation. Correlation studies indicated a strong interplay between lipid metabolites and specific bacterial species, emphasizing the influence of clotrimazole treatment on microbial and metabolic interactions. Importantly, predictive models using microbiota and metabolite signatures demonstrated high accuracy in distinguishing pre- and post-treatment states.

Conclusions: This research highlights clotrimazole's dual role in effectively clearing Candida infection and promoting a healthier vaginal microenvironment, paving the way for novel microbial and metabolomic-based diagnostic approaches to enhance VVC management and understand its underlying mechanisms.

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克霉唑诱导的阴道菌群和脂质代谢变化:外阴阴道念珠菌病恢复机制的启示。
目的:外阴阴道念珠菌病(VVC)是一种流行病,影响着全球相当一部分妇女,反复发作会对生活质量造成不利影响。虽然克霉唑治疗很常见,但它在阴道细菌组和代谢组中引起的具体改变以前却未得到充分探讨:在这项前瞻性研究中,我们招募了被诊断为单发 VVC 的育龄妇女,并对局部克霉唑治疗前后的阴道真菌、细菌组和代谢组进行了全面分析。我们观察到白色念珠菌明显减少,阴道清洁度显著提高。高级测序显示阴道细菌组发生了重大变化,治疗后以乳酸杆菌为主的群落有所增加。我们的研究结果发现了 17 种数量不同的细菌,其中包括致病性厌氧菌,如阴道加德纳菌、嗜酸性小肠球菌和克里斯滕森气球菌的明显减少,这表明微生物恢复了更健康的平衡。此外,代谢组学分析显示,230 种代谢物发生了显著变化,尤其是脂质代谢途径中的代谢物,与炎症有关的脂质相关化合物明显下调。相关性研究表明,脂质代谢物与特定细菌种类之间存在强烈的相互作用,强调了克霉唑治疗对微生物和代谢相互作用的影响。重要的是,使用微生物群和代谢物特征的预测模型在区分治疗前和治疗后状态方面表现出很高的准确性:这项研究强调了克霉唑在有效清除念珠菌感染和促进更健康的阴道微环境方面的双重作用,为基于微生物和代谢组学的新型诊断方法铺平了道路,以加强 VVC 管理并了解其潜在机制。
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来源期刊
Journal of Applied Microbiology
Journal of Applied Microbiology 生物-生物工程与应用微生物
CiteScore
7.30
自引率
2.50%
发文量
427
审稿时长
2.7 months
期刊介绍: Journal of & Letters in Applied Microbiology are two of the flagship research journals of the Society for Applied Microbiology (SfAM). For more than 75 years they have been publishing top quality research and reviews in the broad field of applied microbiology. The journals are provided to all SfAM members as well as having a global online readership totalling more than 500,000 downloads per year in more than 200 countries. Submitting authors can expect fast decision and publication times, averaging 33 days to first decision and 34 days from acceptance to online publication. There are no page charges.
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