Degregori Samuel, Manus Melissa B, Qu Evan B, Mendall Calen P, Baker Jacob S, Hopper Lydia M, Amato Katherine R, Lieberman Tami D
Department of Anthropology, Northwestern University, Evanston, Illinois, USA.
Department of Anthropology, University of Texas at San Antonio, San Antonio, Texas, USA.
mSystems. 2025 Jun 17;10(6):e0008125. doi: 10.1128/msystems.00081-25. Epub 2025 May 28.
The human facial skin microbiome is remarkably similar across all people sampled to date, dominated by facultative anaerobe . The origin of this genus is unknown, with no close relatives currently described from samples of primate skin. This apparent human-specific bacterial taxon could reflect the unique nature of human skin, which is significantly more oily than that of our closest primate relatives. However, previous studies have not sampled the facial skin microbiome of our closest primates. Here, we profiled the skin microbiome of zoo-housed chimpanzees () and gorillas (), alongside their human care staff, using both 16S and shotgun sequencing. We showed that facial skin microbiomes differ significantly across host species, with humans having the lowest diversity and the most unique community among the three species. We were unable to find a close relative of on either chimpanzee or gorilla facial skin, consistent with human specificity. Hominid skin microbiome functional profiles were more functionally similar compared to their taxonomic profiles. However, we still found notable functional differences, including lower proportions of fatty acid biosynthesis in humans, consistent with microbes' reliance on host-derived lipids. Our study highlights the uniqueness of the human facial skin microbiome and supports a horizontal acquisition of its dominant resident from a yet unknown source.IMPORTANCEUnderstanding how and why human skin bacteria differ from our closest animal relatives provides crucial insights into human evolution and health. While we have known that human facial skin hosts distinct bacteria-particularly -we did not know if these bacteria and their associated genes were also present on the faces of our closest relatives, chimpanzees and gorillas. Our study shows that human facial skin hosts markedly different bacteria than other primates, with being uniquely abundant on human faces. This finding suggests that this key bacterial species may have adapted specifically to human skin, which produces more oils than other primates.
迄今为止,在所有采样的人群中,人类面部皮肤微生物群非常相似,以兼性厌氧菌为主。该属的起源尚不清楚,目前在灵长类动物皮肤样本中未发现其近亲。这种明显的人类特异性细菌分类群可能反映了人类皮肤的独特性质,人类皮肤比我们最亲近的灵长类亲属的皮肤油腻得多。然而,以前的研究没有对我们最亲近的灵长类动物的面部皮肤微生物群进行采样。在这里,我们使用16S和鸟枪法测序,对圈养在动物园的黑猩猩()和大猩猩()以及它们的人类饲养员的皮肤微生物群进行了分析。我们发现,不同宿主物种的面部皮肤微生物群存在显著差异,在这三个物种中,人类的多样性最低,群落最为独特。我们在黑猩猩或大猩猩的面部皮肤上均未找到与 密切相关的物种,这与人类特异性相符。与分类学特征相比,人科动物皮肤微生物群的功能特征在功能上更为相似。然而,我们仍然发现了显著的功能差异,包括人类脂肪酸生物合成比例较低,这与微生物对宿主衍生脂质的依赖一致。我们的研究突出了人类面部皮肤微生物群的独特性,并支持其优势常驻菌是从一个未知来源水平获得的。重要性了解人类皮肤细菌与我们最亲近的动物亲属不同的方式和原因,对于深入了解人类进化和健康至关重要。虽然我们已经知道人类面部皮肤存在独特的细菌,特别是 ,但我们不知道这些细菌及其相关基因是否也存在于我们最亲近的亲属黑猩猩和大猩猩的脸上。我们的研究表明,人类面部皮肤携带的细菌与其他灵长类动物明显不同, 在人类面部特别丰富。这一发现表明,这种关键的细菌物种可能已经特别适应了人类皮肤,因为人类皮肤比其他灵长类动物产生更多的油脂。