Metaproteomics reveals diet-induced changes in gut microbiome function according to Crohn's disease location.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-10-23 DOI:10.1186/s40168-024-01927-5
Stefano Levi Mortera, Valeria Marzano, Federica Rapisarda, Chiara Marangelo, Ilaria Pirona, Pamela Vernocchi, Marta Di Michele, Federica Del Chierico, Maria A Quintero, Irina Fernandez, Hajar Hazime, Rose M Killian, Norma Solis, Mailenys Ortega, Oriana M Damas, Siobhan Proksell, David H Kerman, Amar R Deshpande, Luis Garces, Franco Scaldaferri, Antonio Gasbarrini, Maria T Abreu, Lorenza Putignani
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Abstract

Background: Crohn's disease (CD) is characterized by chronic intestinal inflammation. Diet is a key modifiable factor influencing the gut microbiome (GM) and a risk factor for CD. However, the impact of diet modulation on GM function in CD patients is understudied. Herein, we evaluated the effect of a high-fiber, low-fat diet (the Mi-IBD diet) on GM function in CD patients. All participants were instructed to follow the Mi-IBD diet for 8 weeks. One group of CD patients received one-time diet counseling only (Gr1); catered food was supplied for the other three groups, including CD patients (Gr2) and dyads of CD patients and healthy household controls (HHCs) residing within the same household (Gr3-HHC dyads). Stool samples were collected at baseline, week 8, and week 36, and analyzed by liquid chromatography-tandem mass spectrometry.

Results: At baseline, the metaproteomic profiles of CD patients and HHCs differed. The Mi-IBD diet significantly increased carbohydrate and iron transport and metabolism. The predicted microbial composition underlying the metaproteomic changes differed between patients with ileal only disease (ICD) or colonic involvement: ICD was characterized by decreased Faecalibacterium abundance. Even on the Mi-IBD diet, the CD patient metaproteome displayed significant underrepresentation of carbohydrate and purine/pyrimidine synthesis pathways compared to that of HHCs. Human immune-related proteins were upregulated in CD patients compared to HHCs.

Conclusions: The Mi-IBD diet changed the microbial function of CD patients and enhanced carbohydrate metabolism. Our metaproteomic results highlight functional differences in the microbiome according to disease location. Notably, our dietary intervention yielded the most benefit for CD patients with colonic involvement compared to ileal-only disease. Video Abstract.

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元蛋白质组学揭示了根据克罗恩病发病部位饮食诱导的肠道微生物组功能变化。
背景:克罗恩病(CD)以慢性肠道炎症为特征。饮食是影响肠道微生物组(GM)的一个关键可调节因素,也是克罗恩病的一个危险因素。然而,饮食调节对 CD 患者肠道微生物组功能的影响尚未得到充分研究。在此,我们评估了高纤维、低脂肪饮食(Mi-IBD 饮食)对 CD 患者肠道微生物组功能的影响。所有参与者都被要求遵循 Mi-IBD 饮食 8 周。其中一组 CD 患者只接受一次性饮食指导(Gr1);其他三组包括 CD 患者(Gr2)和居住在同一家庭中的 CD 患者和健康家庭对照组(HHCs)(Gr3-HHC dyads)。在基线、第8周和第36周收集粪便样本,并采用液相色谱-串联质谱法进行分析:结果:基线时,CD 患者和 HHC 的元蛋白组图谱不同。Mi-IBD饮食明显增加了碳水化合物和铁的转运和代谢。回肠疾病(ICD)或结肠受累患者的元蛋白组变化所依据的微生物组成预测不同:回肠疾病患者的粪便杆菌丰度降低。即使使用 Mi-IBD 饮食,CD 患者元蛋白质组中碳水化合物和嘌呤/嘧啶合成途径的代表性也明显低于 HHCs。与HHCs相比,CD患者的人类免疫相关蛋白上调:结论:Mi-IBD饮食改变了CD患者的微生物功能,促进了碳水化合物代谢。我们的元蛋白组学结果凸显了不同疾病部位微生物组的功能差异。值得注意的是,与单纯回肠疾病相比,我们的饮食干预对结肠受累的 CD 患者最有益。视频摘要。
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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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