婴儿肠道中的噬菌体被广泛诱导,并可能调节其宿主的功能。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Tamsin A Redgwell, Jonathan Thorsen, Marie-Agnès Petit, Ling Deng, Gisle Vestergaard, Jakob Russel, Bo Chawes, Klaus Bønnelykke, Hans Bisgaard, Dennis S Nielsen, Søren Sørensen, Jakob Stokholm, Shiraz A Shah
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引用次数: 0

摘要

肠道微生物组(GM)的组成和功能对人类健康和疾病至关重要,其中病毒的重要性日益得到认识。然而,对婴儿肠道中噬菌体及其诱导模式的研究仍不充分。在这里,我们从COPSAC2010母婴队列的1岁儿童的662个宏基因组中鉴定了10645个推定的噬菌体,并研究了它们的潜在功能。未发现核心原病毒体,因为仅在约70%的样品中鉴定出最普遍的vOTU。队列中最显性的vOTUs簇与拟杆菌噬菌体Hanky p00'有关,它携带了多样性生成逆转录因子和荚膜多糖合成相关基因。对来自相同样本的病毒组和宏基因组的配对分析显示,婴儿肠道内的大多数噬菌体是诱导的,并且诱导不受一系列环境干扰因素的影响。综上所述,噬菌体是婴儿肠道的主要组成部分,可能对微生物群及其宿主产生深远的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prophages in the infant gut are pervasively induced and may modulate the functionality of their hosts.

Gut microbiome (GM) composition and function is pivotal for human health and disease, of which the virome's importance is increasingly recognised. However, prophages and their induction patterns in the infant gut remain understudied. Here, we identified 10645 putative prophages in 662 metagenomes from 1-year-old children in the COPSAC2010 mother-child cohort and investigated their potential functions. No core provirome was found as the most prevalent vOTU was identified in only ~70% of the samples. The most dominant cluster of vOTUs in the cohort was related to Bacteroides phage Hanky p00', and it carried both diversity generating retroelements and genes involved in capsular polysaccharide synthesis. Paired analysis of viromes and metagenomes from the same samples revealed that most prophages within the infant gut were induced and that induction was unaffected by a range of environmental perturbers. In summary, prophages are major components of the infant gut that may have far reaching influences on the microbiome and its host.

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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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