人类和非人类灵长类动物的链球菌丰度和口腔向性反映了宿主和生活方式的差异。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Irina M Velsko, Christina Warinner
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引用次数: 0

摘要

链球菌属是高度多样化的,是灵长类动物口腔微生物群的核心成员。链球菌至少分为8个进化支系,其中5个支系几乎只存在于口腔中。我们从多个口腔地点、古代和现代人类以及非人类灵长类动物的样本中探索了占优势的链球菌进化支系,发现支系优势在人类口腔中是保守的,大多数链球菌的reads被分配到属于Sanguinis或Mitis支系的物种。然而,每个分支中单个物种的存在和丰度存在微小差异,从而区分了人类的生活方式,其中中华链球菌的消失似乎与刷牙有关。在非人类灵长类动物中,只有狒狒表现出与人类相似的进化分支丰度模式,这表明与早期人类相似的栖息地和饮食可能有利于血猿和猴猿进化分支物种的生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Streptococcus abundance and oral site tropism in humans and non-human primates reflects host and lifestyle differences.

The genus Streptococcus is highly diverse and a core member of the primate oral microbiome. Streptococcus species are grouped into at least eight phylogenetically-supported clades, five of which are found almost exclusively in the oral cavity. We explored the dominant Streptococcus phylogenetic clades in samples from multiple oral sites and from ancient and modern-day humans and non-human primates and found that clade dominance is conserved across human oral sites, with most Streptococcus reads assigned to species falling in the Sanguinis or Mitis clades. However, minor differences in the presence and abundance of individual species within each clade differentiated human lifestyles, with loss of S. sinensis appearing to correlate with toothbrushing. Of the non-human primates, only baboons show clade abundance patterns similar to humans, suggesting that a habitat and diet similar to that of early humans may favor the growth of Sanguinis and Mitis clade species.

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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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