Chamorro Nayaret, Montero David A, Gallardo Pablo, Farfán Mauricio, Contreras Mauricio, De la Fuente Marjorie, Dubois Karen, Hermoso Marcela A, Quera Rodrigo, Pizarro-Guajardo Marjorie, Paredes-Sabja Daniel, Ginard Daniel, Rosselló-Móra Ramon, Vidal Roberto
Programa de Microbiología y Micología, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile, Chile.
Programa de Inmunología, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile, Chile.
Microb Cell. 2021 Jun 18;8(9):223-238. doi: 10.15698/mic2021.09.760. eCollection 2021 Sep 6.
Inflammatory bowel diseases (IBDs), which include ulcerative colitis (UC) and Crohn's disease (CD), cause chronic inflammation of the gut, affecting millions of people worldwide. IBDs have been frequently associated with an alteration of the gut microbiota, termed dysbiosis, which is generally characterized by an increase in abundance of Proteobacteria such as , and a decrease in abundance of Firmicutes such as (an indicator of a healthy colonic microbiota). The mechanisms behind the development of IBDs and dysbiosis are incompletely understood. Using samples from colonic biopsies, we studied the mucosa-associated intestinal microbiota in Chilean and Spanish patients with IBD. In agreement with previous studies, microbiome comparison between IBD patients and non-IBD controls indicated that dysbiosis in these patients is characterized by an increase of pro-inflammatory bacteria (mostly Proteobacteria) and a decrease of commensal beneficial bacteria (mostly Firmicutes). Notably, bacteria typically residing on the mucosa of healthy individuals were mostly obligate anaerobes, whereas in the inflamed mucosa an increase of facultative anaerobe and aerobic bacteria was observed. We also identify potential co-occurring and mutually exclusive interactions between bacteria associated with the healthy and inflamed mucosa, which appear to be determined by the oxygen availability and the type of respiration. Finally, we identified a panel of bacterial biomarkers that allow the discrimination between eubiosis from dysbiosis with a high diagnostic performance (96% accurately), which could be used for the development of non-invasive diagnostic methods. Thus, this study is a step forward towards understanding the landscapes and alterations of mucosa-associated intestinal microbiota in patients with IBDs.
炎症性肠病(IBDs)包括溃疡性结肠炎(UC)和克罗恩病(CD),会引发肠道慢性炎症,影响着全球数百万人。IBDs常与肠道微生物群的改变相关,即生态失调,其一般特征是变形菌门等菌的丰度增加,而厚壁菌门等菌的丰度降低(这是健康结肠微生物群的一个指标)。IBDs和生态失调发展背后的机制尚未完全明了。我们使用结肠活检样本,研究了智利和西班牙IBD患者的黏膜相关肠道微生物群。与之前的研究一致,IBD患者与非IBD对照之间的微生物组比较表明,这些患者的生态失调特征为促炎细菌(主要是变形菌门)增加,共生有益细菌(主要是厚壁菌门)减少。值得注意的是,通常存在于健康个体黏膜上的细菌大多是专性厌氧菌,而在发炎的黏膜中则观察到兼性厌氧菌和好氧细菌有所增加。我们还确定了与健康和发炎黏膜相关细菌之间潜在的共存和互斥相互作用,这些相互作用似乎由氧气可用性和呼吸类型决定。最后,我们确定了一组细菌生物标志物,可用于以高诊断性能(96%准确率)区分正常微生物群与失调微生物群,这可用于开发非侵入性诊断方法。因此,这项研究朝着理解IBD患者黏膜相关肠道微生物群的情况和改变迈出了一步。