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肠道微生物群菌株丰富度具有物种特异性,并影响植入。

Gut microbiota strain richness is species specific and affects engraftment.

作者信息

Chen-Liaw Alice, Aggarwala Varun, Mogno Ilaria, Haifer Craig, Li Zhihua, Eggers Joseph, Helmus Drew, Hart Amy, Wehkamp Jan, Lamousé-Smith Esi S N, Kerby Robert L, Rey Federico E, Colombel Jean Frédéric, Kamm Michael A, Olle Bernat, Norman Jason M, Menon Rajita, Watson Andrea R, Crossette Emily, Terveer Elisabeth M, Keller Josbert J, Borody Thomas J, Grinspan Ari, Paramsothy Sudarshan, Kaakoush Nadeem O, Dubinsky Marla C, Faith Jeremiah J

机构信息

Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Nature. 2025 Jan;637(8045):422-429. doi: 10.1038/s41586-024-08242-x. Epub 2024 Nov 27.

DOI:10.1038/s41586-024-08242-x
PMID:39604726
Abstract

Despite the fundamental role of bacterial strain variation in gut microbiota function, the number of unique strains of a species that can stably colonize the human intestine is still unknown for almost all species. Here we determine the strain richness (SR) of common gut species using thousands of sequenced bacterial isolates with paired metagenomes. We show that SR varies across species, is transferable by faecal microbiota transplantation, and is uniquely low in the gut compared with soil and lake environments. Active therapeutic administration of supraphysiologic numbers of strains per species increases recipient SR, which then converges back to the population average after dosing is ceased. Stratifying engraftment outcomes by high or low SR shows that SR predicts microbial addition or replacement in faecal transplants. Together, these results indicate that properties of the gut ecosystem govern the number of strains of each species colonizing the gut and thereby influence strain addition and replacement in faecal microbiota transplantation and defined live biotherapeutic products.

摘要

尽管细菌菌株变异在肠道微生物群功能中具有重要作用,但几乎所有物种中能够稳定定殖于人类肠道的独特菌株数量仍不明确。在此,我们利用数千株测序的细菌分离株及配对宏基因组来确定常见肠道物种的菌株丰富度(SR)。我们发现,SR因物种而异,可通过粪便微生物群移植进行转移,并且与土壤和湖泊环境相比,肠道中的SR特别低。对每个物种进行超生理数量菌株的主动治疗性给药可增加受体的SR,给药停止后,SR又会收敛至群体平均值。根据SR的高低对移植结果进行分层显示,SR可预测粪便移植中微生物的添加或替代情况。这些结果共同表明,肠道生态系统的特性决定了定殖于肠道的每个物种的菌株数量,从而影响粪便微生物群移植和特定活生物治疗产品中菌株的添加和替代。

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