S. agalactiae 促进 G. vaginalis 生物膜形成导致 BV 复发的机制。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Meng Li, Zhen Zeng, Xiaoqian Wang, Ying Liu, Hongbo Wei, Jun Liu, Simin Zhu, Qingyun Jiang, Ke Zhang, Yifan Wu, Shuai Liu, Juhyun Kim, Qinping Liao, Lei Zhang
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引用次数: 0

摘要

以往的研究表明,阴道加德纳菌(GV)生物膜的形成是细菌性阴道病(BV)复发的主要原因之一。本研究首次在共培养情况下探讨了无乳链球菌(B 组链球菌,GBS)对 GV 生物膜的影响。结果发现,在48小时的双菌种生物膜中,GBS能显著增加GV的生物量。在双菌种生物膜中,GBS的luxS基因含量明显升高,而敲除luxS基因会导致单菌种和双菌种生物膜的生物量明显降低。同时,体外添加AI-2(luxS基因的产物)可大幅增加生物膜的生物量。此外,我们还发现,在接收到AI-2信号后,GV中与生物膜形成相关的两个基因的表达明显升高。总之,这些研究结果表明,在体外共培养模型中,GBS通过luxS/AI-2增强了GV生物膜的形成,这反过来又可能促进BV的复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanisms of S. agalactiae promoting G. vaginalis biofilm formation leading to recurrence of BV.

Previous research has established that the formation of Gardnerella vaginalis (GV) biofilm is one of the primary reasons for bacterial vaginosis (BV) recurrence. This study was the first to explore the impact of Streptococcus agalactiae (group B Streptococcus, GBS) on GV biofilm in a co-culture scenario. The results revealed that GBS could significantly increased the GV biomass in 48-hours dual-species biofilms. The luxS gene of GBS was significantly higher in dual-species biofilm, while knockdown of the luxS gene resulted in a significant decrease in mono- and dual-species biofilms. Meanwhile, in vitro addition of AI-2 (product of luxS gene) substantially increased biofilm biomass. Furthermore, we found that the expression of two genes related to biofilm formation was notably elevated in GV after receiving AI-2 signals. Collectively, these findings suggest that GBS enhances GV biofilm formation via luxS/AI-2 in an in vitro co-culture model, which in turn may promotes recurrence of BV.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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