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肠道微生物组中颗粒大小与微生物生态学的相互作用。

Interplay between particle size and microbial ecology in the gut microbiome.

机构信息

Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC 27710, United States.

Duke Office of Clinical Research, Duke University School of Medicine, Durham, NC 27710, United States.

出版信息

ISME J. 2024 Jan 8;18(1). doi: 10.1093/ismejo/wrae168.

Abstract

Physical particles can serve as critical abiotic factors that structure the ecology of microbial communities. For non-human vertebrate gut microbiomes, fecal particle size (FPS) has been known to be shaped by chewing efficiency and diet. However, little is known about what drives FPS in the human gut. Here, we analyzed FPS by laser diffraction across a total of 76 individuals and found FPS to be strongly individualized. Contrary to our initial hypothesis, a behavioral intervention with 41 volunteers designed to increase chewing efficiency did not impact FPS. Dietary patterns could also not be associated with FPS. Instead, we found evidence that human and mouse gut microbiomes shaped FPS. Fecal samples from germ-free and antibiotic-treated mice exhibited increased FPS relative to colonized mice. In humans, markers of longer transit time were correlated with smaller FPS. Gut microbiota diversity and composition were also associated with FPS. Finally, ex vivo culture experiments using human fecal microbiota from distinct donors showed that differences in microbiota community composition can drive variation in particle size. Together, our results support an ecological model in which the human gut microbiome plays a key role in reducing the size of food particles during digestion. This finding has important implications for our understanding of energy extraction and subsequent uptake in gastrointestinal tract. FPS may therefore be viewed as an informative functional readout, providing new insights into the metabolic state of the gut microbiome.

摘要

物理颗粒可以作为关键的非生物因素,影响微生物群落的生态结构。对于非人类脊椎动物肠道微生物组,粪便颗粒大小(FPS)已知受咀嚼效率和饮食影响。然而,对于人类肠道中什么因素驱动 FPS 知之甚少。在这里,我们通过激光衍射分析了总共 76 个人的 FPS,发现 FPS 具有很强的个体差异性。与我们最初的假设相反,一项旨在提高咀嚼效率的 41 名志愿者的行为干预并没有影响 FPS。饮食模式也与 FPS 无关。相反,我们有证据表明人类和小鼠肠道微生物组塑造了 FPS。无菌和抗生素处理的小鼠的粪便样本与定植小鼠相比,FPS 增加。在人类中,较长的转运时间标志物与较小的 FPS 相关。肠道微生物多样性和组成也与 FPS 相关。最后,使用来自不同供体的人类粪便微生物组进行的离体培养实验表明,微生物群落组成的差异可以驱动颗粒大小的变化。总之,我们的结果支持一种生态模型,即人类肠道微生物组在消化过程中减小食物颗粒大小方面发挥着关键作用。这一发现对我们理解胃肠道中的能量提取和随后的吸收具有重要意义。因此,FPS 可以被视为一种信息丰富的功能指标,为我们了解肠道微生物组的代谢状态提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7393/11406467/41be5f6f2c21/wrae168ga1.jpg

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