在患有细菌性阴道病的妇女的阴道样本中,内溶素选择性地杀死加德纳菌。

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Lenka Podpera Tisakova, Timo Schwebs, Rocío Berdaguer, Marina von Freyberg, Philipp Foessleitner, Ann-Katrin Kieninger, Albina Poljak, Lorenzo Corsini, Alex Farr
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引用次数: 0

摘要

目前对细菌性阴道病(BV)的治疗经常导致疾病复发。加德纳菌在阴道上皮细胞上形成生物膜,是细菌性阴道炎发病机制中的关键角色。重组内溶素已显示出特异性杀死加德纳菌,但不是共生乳酸菌,在体外。本研究评估了bnt331 - endoolysin (BNT331-EL)对49例BV (Nugent评分≥7,Amsel标准,线索细胞)女性阴道样本的药理学。全基因组测序证实了bv相关的群落状态类型IV-B和III,加德纳菌在53%的样本中占主导地位,在86%的样本中存在。BNT331-EL体外处理20-50µg/mL, 19小时内使加德纳菌存活率降低≥94%。L. iners在样品中平均减少了92%,而L. crispatus在大量存在的地方增殖。内溶素处理有效地破坏了加德纳菌生物膜,并以时间和浓度依赖的方式降低了活菌负荷。这些结果为BNT331-EL首次人体试验的治疗剂量定义提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endolysin selectively kills Gardnerella ex vivo in vaginal samples from women with bacterial vaginosis.

Current treatments for bacterial vaginosis (BV) often result in recurrent disease. Gardnerella, a key player in BV pathogenesis, forms biofilms on vaginal epithelial cells. Recombinant endolysins have shown to specifically kill Gardnerella, but not commensal lactobacilli, in vitro. This study evaluated the pharmacodynamics of BNT331-endolysin (BNT331-EL) on vaginal samples from 49 women with BV (Nugent score ≥7, Amsel criteria, and clue cells). Whole genome sequencing confirmed BV-associated community state types IV-B and III, with Gardnerella dominating in 53% of samples and present in 86%. Ex vivo treatment with BNT331-EL reduced viable Gardnerella by ≥94% at 20-50 µg/mL over 19 h. L. iners was reduced by an average of 92% across samples, while L. crispatus proliferated where present in substantial amounts. Endolysin treatment effectively disrupted Gardnerella biofilms and reduced viable bacterial load in a time- and concentration-dependent manner. These results informed the definition of the treatment dose for a first-in-human trial with BNT331-EL.

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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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