加塞乳杆菌和阴道加德纳菌产生的细胞外囊泡有助于发挥阴道微生物群的功能,并调节宿主与阴道毛滴虫之间的相互作用。

IF 2.6 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Molecular Microbiology Pub Date : 2024-09-01 Epub Date: 2023-07-24 DOI:10.1111/mmi.15130
Anastasiia Artuyants, Jiwon Hong, Priscila Dauros-Singorenko, Anthony Phillips, Augusto Simoes-Barbosa
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引用次数: 0

摘要

阴道毛滴虫是人类泌尿生殖道的一种细胞外原生动物寄生虫,是一种流行的性传播感染。滴虫性阴道炎伴有微生物群落失调,其特点是宿主保护性共生菌(如加塞利乳杆菌)枯竭,而与细菌性阴道病相似的细菌群落(包括创始菌阴道加德纳菌)却蓬勃发展。已知这两种阴道细菌对阴道加德纳菌的致病性有相反的影响。对细胞外囊泡(EVs)的研究主要集中在微生物生产者(共生菌或病原体)对宿主接受者的定向上,而且主要是在肠道微生物组的背景下进行的。在这里,我们利用人类宫颈阴道微生物组的简单性,确定了由 L. gasseri 和 G. vaginalis 产生的 EVs 的分子货物,并研究了这些囊泡如何调节 T. vaginalis 与宿主细胞的相互作用。我们发现,这些EVs携带有特定的蛋白质,其功能可归因于这些细菌在阴道生物群中扮演的相反角色。此外,这些细菌的EVs被输送到宿主细胞和原生动物细胞,以模拟这些细菌对阴道球菌致病性的相反作用的方式调节宿主与病原体之间的相互作用。这是首次研究并列描述两种属于微生物组相反谱系的细菌产生的EVs的蛋白质组成,并证明这些囊泡能调节原生动物寄生虫的致病性。在滴虫病等疾病中,感染和菌群失调经常同时发生,导致严重的并发症。因此,此类研究为开发抗菌疗法提供了知识,这些疗法旨在清除感染,同时恢复健康的微生物群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lactobacillus gasseri and Gardnerella vaginalis produce extracellular vesicles that contribute to the function of the vaginal microbiome and modulate host-Trichomonas vaginalis interactions.

Trichomonas vaginalis is an extracellular protozoan parasite of the human urogenital tract, responsible for a prevalent sexually transmitted infection. Trichomoniasis is accompanied by a dysbiotic microbiome that is characterised by the depletion of host-protective commensals such as Lactobacillus gasseri, and the flourishing of a bacterial consortium that is comparable to the one seen for bacterial vaginosis, including the founder species Gardnerella vaginalis. These two vaginal bacteria are known to have opposite effects on T. vaginalis pathogenicity. Studies on extracellular vesicles (EVs) have been focused on the direction of a microbial producer (commensal or pathogen) to a host recipient, and largely in the context of the gut microbiome. Here, taking advantage of the simplicity of the human cervicovaginal microbiome, we determined the molecular cargo of EVs produced by L. gasseri and G. vaginalis and examined how these vesicles modulate the interaction of T. vaginalis and host cells. We show that these EVs carry a specific cargo of proteins, which functions can be attributed to the opposite roles that these bacteria play in the vaginal biome. Furthermore, these bacterial EVs are delivered to host and protozoan cells, modulating host-pathogen interactions in a way that mimics the opposite effects that these bacteria have on T. vaginalis pathogenicity. This is the first study to describe side-by-side the protein composition of EVs produced by two bacteria belonging to the opposite spectrum of a microbiome and to demonstrate that these vesicles modulate the pathogenicity of a protozoan parasite. Such as in trichomoniasis, infections and dysbiosis co-occur frequently resulting in significant co-morbidities. Therefore, studies like this provide the knowledge for the development of antimicrobial therapies that aim to clear the infection while restoring a healthy microbiome.

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来源期刊
Molecular Microbiology
Molecular Microbiology 生物-生化与分子生物学
CiteScore
7.20
自引率
5.60%
发文量
132
审稿时长
1.7 months
期刊介绍: Molecular Microbiology, the leading primary journal in the microbial sciences, publishes molecular studies of Bacteria, Archaea, eukaryotic microorganisms, and their viruses. Research papers should lead to a deeper understanding of the molecular principles underlying basic physiological processes or mechanisms. Appropriate topics include gene expression and regulation, pathogenicity and virulence, physiology and metabolism, synthesis of macromolecules (proteins, nucleic acids, lipids, polysaccharides, etc), cell biology and subcellular organization, membrane biogenesis and function, traffic and transport, cell-cell communication and signalling pathways, evolution and gene transfer. Articles focused on host responses (cellular or immunological) to pathogens or on microbial ecology should be directed to our sister journals Cellular Microbiology and Environmental Microbiology, respectively.
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