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肠回肠黏膜病毒组在克罗恩病患者中受到干扰,并在小鼠中加剧肠道炎症。

The gut ileal mucosal virome is disturbed in patients with Crohn's disease and exacerbates intestinal inflammation in mice.

机构信息

Key Laboratory of Human Microbiome and Chronic Diseases (Sun Yat-sen University), Ministry of Education, Guangzhou, Guangdong, China.

Guangdong Institute of Gastroenterology, The Sixth Affiliated Hospital of Sun Yat-sen University, Sun Yat-sen University, Guangzhou, Guangdong, China.

出版信息

Nat Commun. 2024 Feb 22;15(1):1638. doi: 10.1038/s41467-024-45794-y.

Abstract

Gut bacteriome dysbiosis is known to be implicated in the pathogenesis of inflammatory bowel disease (IBD). Crohn's disease (CD) is an IBD subtype with extensive mucosal inflammation, yet the mucosal virome, an empirical modulator of the bacteriome and mucosal immunity, remains largely unclear regarding its composition and role. Here, we exploited trans-cohort CD patients and healthy individuals to compositionally and functionally investigate the small bowel (terminal ileum) virome and bacteriome. The CD ileal virome was characterised by an under-representation of both lytic and temperate bacteriophages (especially those targeting bacterial pathogens), particularly in patients with flare-up. Meanwhile, the virome-bacteriome ecology in CD ileal mucosa was featured by a lack of Bifidobacterium- and Lachnospiraceae-led mutualistic interactions between bacteria and bacteriophages; surprisingly it was more pronounced in CD remission than flare-up, underlining the refractory and recurrent nature of mucosal inflammation in CD. Lastly, we substantiated that ileal virions from CD patients causally exacerbated intestinal inflammation in IBD mouse models, by reshaping a gut virome-bacteriome ecology preceding intestinal inflammation (microbial trigger) and augmenting microbial sensing/defence pathways in the intestine cells (host response). Altogether, our results highlight the significance of mucosal virome in CD pathogenesis and importance of mucosal virome restoration in CD therapeutics.

摘要

肠道细菌组失调被认为与炎症性肠病(IBD)的发病机制有关。克罗恩病(CD)是一种具有广泛黏膜炎症的 IBD 亚型,然而,黏膜病毒组作为细菌组和黏膜免疫的经验调节剂,其组成和作用在很大程度上仍不清楚。在这里,我们利用跨队列 CD 患者和健康个体,对小肠(末端回肠)病毒组和细菌组进行了组成和功能研究。CD 回肠病毒组的特点是裂解性和温和性噬菌体(尤其是针对细菌病原体的噬菌体)均存在代表性不足,尤其是在病情发作的患者中。同时,CD 回肠黏膜中的病毒组-细菌组生态系统的特点是双歧杆菌和lachnospiraceae 引导的细菌和噬菌体之间的互利相互作用缺乏;令人惊讶的是,在缓解期比发作期更为明显,这强调了 CD 中黏膜炎症的难治性和复发性。最后,我们证实 CD 患者的回肠病毒颗粒通过重塑肠道病毒组-细菌组生态系统,从而在肠道炎症之前(微生物触发)增强肠道细胞中的微生物感知/防御途径,从而在 IBD 小鼠模型中因果加剧了肠道炎症,在肠道炎症之前(微生物触发)增强肠道细胞中的微生物感知/防御途径,从而在 IBD 小鼠模型中因果加剧了肠道炎症。总之,我们的研究结果强调了黏膜病毒组在 CD 发病机制中的重要性,以及黏膜病毒组恢复在 CD 治疗中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f6/10884039/3af76a783d67/41467_2024_45794_Fig1_HTML.jpg

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