Strain-level variation among vaginal Lactobacillus crispatus and Lactobacillus iners as identified by comparative metagenomics.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Sai Ravi Chandra Nori, Calum J Walsh, Fionnuala M McAuliffe, Rebecca L Moore, Douwe Van Sinderen, Conor Feehily, Paul D Cotter
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Abstract

The vaginal microbiome, a relatively simple, low diversity ecosystem crucial for female health, is often dominated by Lactobacillus spp. Detailed strain-level data, facilitated by shotgun sequencing, can provide a greater understanding of the mechanisms of colonization and host-microbe interactions. We analysed 354 vaginal metagenomes from pregnant women in Ireland to investigate metagenomic community state types and strain-level variation, focusing on cell surface interfaces. Our analysis revealed multiple subspecies, with Lactobacillus crispatus and Lactobacillus iners being the most dominant. We found genes, including putative mucin-binding genes, distinct to L. crispatus subspecies. Using 337 metagenome-assembled genomes, we observed a higher number of strain-specific genes in L. crispatus related to cell wall biogenesis, carbohydrate and amino acid metabolism, many under positive selection. A cell surface glycan gene cluster was predominantly found in L. crispatus but absent in L. iners and Gardnerella vaginalis. These findings highlight strain-specific factors associated with colonisation and host-microbe interactions.

比较宏基因组学鉴定阴道crispatus乳杆菌和乳杆菌iners菌株水平差异。
阴道微生物群是一个相对简单、低多样性的生态系统,对女性健康至关重要,通常由乳杆菌(Lactobacillus spp)主导。通过鸟枪法测序,详细的菌株水平数据可以更好地了解定植和宿主-微生物相互作用的机制。我们分析了来自爱尔兰孕妇的354个阴道宏基因组,以调查宏基因组群落状态类型和菌株水平变化,重点关注细胞表面界面。我们的分析显示了多个亚种,以crispatus和Lactobacillus iners为最优势。我们发现了一些基因,包括假定的黏液结合基因,与crispatus亚种不同。利用337个元基因组组装的基因组,我们观察到与细胞壁生物发生、碳水化合物和氨基酸代谢相关的菌株特异性基因数量较多,其中许多基因处于正选择状态。一个细胞表面聚糖基因簇主要存在于葡萄球菌中,而在葡萄球菌和阴道加德纳菌中不存在。这些发现强调了与定植和宿主-微生物相互作用相关的菌株特异性因素。
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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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