空间宿主-微生物组分析显示儿童回肠克罗恩病中细菌相关的宿主转录改变。

IF 12.7 1区 生物学 Q1 MICROBIOLOGY
Sooyoung Jang, Eun Joo Lee, Sowon Park, Hyeji Lim, Byungsoo Ahn, Yoon Huh, Hong Koh, Yu Rang Park
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引用次数: 0

摘要

背景:克罗恩病(CD)是一种慢性炎症性肠病,涉及肠道微生物群和宿主免疫系统之间的复杂关系。然而,组织驻留细菌和宿主细胞在CD发病机制中的空间关系仍然知之甚少。我们开发了一种空间宿主-微生物组分析方法,以高分类学分辨率同时检测儿童回肠CD组织中的宿主转录组学和细菌种类。结果:在这项前瞻性病例对照研究中,我们分析了来自6名儿童回肠CD患者和2名对照组的14例晚期回肠组织样本。空间宿主-微生物组测序,结合空间转录组学和原位聚腺苷酸化,以及散装散弹枪宏基因组测序。我们开发了一个全面的生物信息学管道来鉴定细菌种类,并在细胞分辨率上分析宿主-微生物组的相互作用,结果分析了13,876个细胞。我们的方法显示,与对照组相比,乳糜泻组织中的细菌丰度增加。诊断时细菌浸润的程度与疾病预后和内镜检查的严重程度相关。我们在回肠CD中鉴定了16个潜在的有益微生物群和9个致病微生物群成员,包括一些新发现的风险调节细菌物种。细胞类型特异性宿主基因表达分析揭示了在多种细菌存在下与细菌防御机制相关的转录组改变。结论:我们的空间宿主-微生物组分析方法可以同时识别细菌和宿主转录组学。它揭示了宿主细胞和细菌之间复杂的相互作用,为CD的发病机制提供了细胞水平的见解。我们的方法为研究各种微生物组相关疾病中的宿主-微生物组相互作用提供了一个强大的工具,以指导基于微生物组的治疗和预后标志物的新策略。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spatial host-microbiome profiling demonstrates bacterial-associated host transcriptional alterations in pediatric ileal Crohn's disease.

Background: Crohn's disease (CD) is a chronic inflammatory bowel disease involving complex relationships between the gut microbiome and host immune system. However, the spatial relationships between tissue-resident bacteria and host cells in CD pathogenesis remain poorly understood. We developed a spatial host-microbiome profiling approach to simultaneously detect host transcriptomics and bacterial species at high taxonomic resolution in pediatric ileal CD tissues.

Results: In this prospective case-control study, we analyzed 14 terminal ileal tissue samples from six pediatric patients with ileal CD and two controls. Spatial host-microbiome sequencing, combined spatial transcriptomics and in-situ polyadenylation, and bulk shotgun metagenome sequencing were performed. We developed a comprehensive bioinformatics pipeline to identify bacterial species and analyze host-microbiome interactions at cellular resolution, resulting in 13,876 analyzed cells. Our approach revealed increased bacterial abundance in CD tissues compared with controls. The extent of bacterial infiltration at diagnosis correlated with disease prognosis and severity of endoscopic findings. We identified 16 potentially beneficial and nine pathogenic microbiome members in ileal CD, including several newly discovered risk-modulating bacterial species. Cell-type-specific host gene expression analysis revealed transcriptome alterations related to bacterial defense mechanisms in the presence of various bacterial species.

Conclusions: Our spatial host-microbiome profiling approach enables simultaneous species-level identification of bacteria and host transcriptomics. It reveals the intricate interactions between host cells and bacteria, providing cellular-level insights into CD pathogenesis. Our approach offers a powerful tool for investigating host-microbiome interactions in various microbiome-associated diseases to direct new strategies for microbiome-based therapeutics and prognostic markers. Video Abstract.

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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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