Shen Yifei, Qu Wenxin, Song Mengdi, Zhang Tianyu, Liu Chang, Shi Xiaofeng, Xu Xinxin, Jiang Jingjing, Ding Liguo, Mo Fangyu, Mao Zheying, Huang Mingzhu, Xu Ziye, Chen Jiaye, Shen Enhui, Ruan Jian, Liu Jiong, Timko Michael P, Chen Yu, Fan Longjiang, Zheng Shufa, Wang Yongcheng
Department of Laboratory Medicine of The First Affiliated Hospital & Liangzhu Laboratory Zhejiang University School of Medicine Hangzhou China.
Key Laboratory of Clinical In Vitro Diagnostic Techniques of Zhejiang Province Hangzhou China.
Imeta. 2025 Apr 17;4(3):e70035. doi: 10.1002/imt2.70035. eCollection 2025 Jun.
The human body is inhabited by trillions of microorganisms that play a crucial role in health and diseases. Our understanding of the species and functional composition of the human gut microbiome is rapidly expanding, but it is still mainly based on taxonomic profiles or gene abundance measurements. As such, little is known about the species-function heterogeneity and dynamic activities in human microecosystem niches. By applying a novel gut-specific single-microbe ribonucleic acid (RNA) sequencing and analytical framework on three healthy donors with distinct enterotypes, we created a comprehensive transcriptional landscape of the human gut microbiome and dissected functional specialization in 38,922 single microbes across 198 species. We investigated the functional redundancy and complementarity involved in short-chain fatty acids related central carbon metabolism and studied the heterogeneity and covariation of single-microbe metabolic capacity. Comparing the human gut microbiome at different times throughout the day, we were able to map diurnal dynamic activities of the gut microbiome and discovered its association with sub-population functional heterogeneous. Remarkably, using single-microbe RNA sequencing, we systematically dissected the metabolic function heterogeneity of , a keystone species in Asian populations. Together with in vitro and in vivo experimental validations, we proved can effectively improve mineral absorption through exogenous phytic acid degradation, which could potentially serve as a probiotic that reduces malnutrition caused by deficiency of mineral elements. Our results indicated that species-function heterogeneity widely exists and plays important roles in the human gut microbiome, and through single-microbe RNA sequencing, we have been able to capture the transcriptional activity variances and identify keystone species with specialized metabolic functions of possible biological and clinical importance.
人体中栖息着数万亿微生物,它们在健康和疾病中发挥着关键作用。我们对人类肠道微生物组的物种和功能组成的理解正在迅速扩展,但仍主要基于分类学图谱或基因丰度测量。因此,对于人类微生态系统生态位中的物种功能异质性和动态活动知之甚少。通过对三名具有不同肠型的健康供体应用一种新颖的肠道特异性单微生物核糖核酸(RNA)测序和分析框架,我们创建了人类肠道微生物组的全面转录图谱,并剖析了198个物种中38,922个单微生物的功能特化。我们研究了与短链脂肪酸相关的中心碳代谢中涉及的功能冗余和互补性,并研究了单微生物代谢能力的异质性和协变。通过比较一天中不同时间的人类肠道微生物组,我们能够绘制肠道微生物组的昼夜动态活动图谱,并发现其与亚群功能异质性的关联。值得注意的是,使用单微生物RNA测序,我们系统地剖析了亚洲人群中的关键物种——[具体物种名称未给出]的代谢功能异质性。结合体外和体内实验验证,我们证明[具体物种名称未给出]可以通过外源性植酸降解有效改善矿物质吸收,这可能潜在地作为一种益生菌来减少由矿物质元素缺乏引起的营养不良。我们的结果表明,物种功能异质性广泛存在并在人类肠道微生物组中发挥重要作用,并且通过单微生物RNA测序,我们能够捕捉转录活性差异并识别具有可能具有生物学和临床重要性的专门代谢功能的关键物种。