Dietary patterns drive loss of fiber-foraging species in the celiac disease patients gut microbiota compared to first-degree relatives.

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Gut Pathogens Pub Date : 2024-10-08 DOI:10.1186/s13099-024-00643-7
Ana Roque, Joyce Zanker, Sara Brígido, Maria Beatriz Tomaz, André Gonçalves, Sandra Barbeiro, Alfonso Benítez-Páez, Sónia Gonçalves Pereira
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Abstract

Background: Celiac disease is an autoimmune disorder triggered by dietary gluten in genetically predisposed individuals that primarily affects the small intestine. Studies have reported differentially abundant bacterial taxa in the gut microbiota of celiac patients compared with non-celiac controls. However, findings across studies have inconsistencies and no microbial signature of celiac disease has been defined so far.

Results: Here, we showed, by comparing celiac patients with their non-celiac 1st-degree relatives, that bacterial communities of related individuals have similar species occurrence and abundance compared with non-relatives, regardless the disease status. We also found in celiac patients a loss of bacterial species associated with fiber degradation, and host metabolic and immune modulation, as ruminiclostridia, ruminococci, Prevotella, and Akkermansia muciniphila species. We demonstrated that the differential abundance of bacterial species correlates to different dietary patterns observed between the two groups. For instance, Ruminiclostridium siraeum, Ruminococcus bicirculans, and Bacteroides plebeious, recognized as fiber-degraders, appear more abundant in non-celiac 1st-degree relatives, which have a vegetable consumption pattern higher than celiac patients. Pattern of servings per day also suggests a possible link between these species' abundance and daily calorie intake.

Conclusions: Overall, we evidenced that a kinship approach could be valuable in unveiling potential celiac disease microbial traits, as well as the significance of dietary factors in shaping microbial profiles and their influence on disease development and progression. Our results pave the way for designing and adopting novel dietary strategies based on gluten-free fiber-enriched ingredients to improve disease management and patients' quality of life.

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与一级亲属相比,饮食模式导致乳糜泻患者肠道微生物群中纤维觅食物种的减少。
背景:乳糜泻是一种自身免疫性疾病,由遗传易感人群饮食中的麸质引发,主要影响小肠。有研究报告称,与非乳糜泻对照组相比,乳糜泻患者肠道微生物群中的细菌类群丰富程度不同。然而,各项研究的结果并不一致,迄今为止还没有确定乳糜泻的微生物特征:结果:在这里,我们通过比较乳糜泻患者和他们的非乳糜泻一级亲属发现,与非亲属相比,亲缘个体的细菌群落具有相似的物种发生率和丰度,与疾病状态无关。我们还发现,在乳糜泻患者体内,与纤维降解、宿主代谢和免疫调节相关的细菌物种有所减少,如反刍动物、反刍球菌、普雷沃特氏菌和粘膜阿克曼菌等。我们的研究表明,细菌种类的丰度差异与两组观察到的不同饮食模式有关。例如,在非乳糜泻患者的一级亲属中,被认为是纤维降解菌的siraeum反刍梭菌、Ruminococcus bicirculans反刍球菌和Bacteroides plebeious的数量更多,而这些亲属的蔬菜消费模式高于乳糜泻患者。每日食用量的模式也表明,这些物种的丰富程度与每日卡路里摄入量之间可能存在联系:总之,我们证明了亲缘关系方法在揭示潜在乳糜泻微生物特征方面的价值,以及饮食因素在塑造微生物特征方面的重要性及其对疾病发生和发展的影响。我们的研究结果为设计和采用基于无麸质富含纤维成分的新型饮食策略,改善疾病管理和患者的生活质量铺平了道路。
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来源期刊
Gut Pathogens
Gut Pathogens GASTROENTEROLOGY & HEPATOLOGY-MICROBIOLOGY
CiteScore
7.70
自引率
2.40%
发文量
43
期刊介绍: Gut Pathogens is a fast publishing, inclusive and prominent international journal which recognizes the need for a publishing platform uniquely tailored to reflect the full breadth of research in the biology and medicine of pathogens, commensals and functional microbiota of the gut. The journal publishes basic, clinical and cutting-edge research on all aspects of the above mentioned organisms including probiotic bacteria and yeasts and their products. The scope also covers the related ecology, molecular genetics, physiology and epidemiology of these microbes. The journal actively invites timely reports on the novel aspects of genomics, metagenomics, microbiota profiling and systems biology. Gut Pathogens will also consider, at the discretion of the editors, descriptive studies identifying a new genome sequence of a gut microbe or a series of related microbes (such as those obtained from new hosts, niches, settings, outbreaks and epidemics) and those obtained from single or multiple hosts at one or different time points (chronological evolution).
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