Enaud Raphaël, Hooks Katarzyna B, Barre Aurélien, Barnetche Thomas, Hubert Christophe, Massot Marie, Bazin Thomas, Clouzeau Haude, Bui Stéphanie, Fayon Michael, Berger Patrick, Lehours Philippe, Bébéar Cécile, Nikolski Macha, Lamireau Thierry, Delhaes Laurence, Schaeverbeke Thierry
Centre de Recherche Cardio-Thoracique de Bordeaux, INSERM, University Bordeaux, U1045, F-33000 Bordeaux, France.
CRCM Pédiatrique, CHU Bordeaux, CIC 1401, F-33000 Bordeaux, France.
J Clin Med. 2019 May 10;8(5):645. doi: 10.3390/jcm8050645.
Cystic fibrosis (CF) is a systemic genetic disease that leads to pulmonary and digestive disorders. In the majority of CF patients, the intestine is the site of chronic inflammation and microbiota disturbances. The link between gut inflammation and microbiota dysbiosis is still poorly understood. The main objective of this study was to assess gut microbiota composition in CF children depending on their intestinal inflammation. We collected fecal samples from 20 children with CF. Fecal calprotectin levels were measured and fecal microbiota was analyzed by 16S rRNA sequencing. We observed intestinal inflammation was associated with microbiota disturbances characterized mainly by increased abundances of , and , along with decreased abundances of , , and . Those changes exhibited similarities with that of Crohn's disease (CD), as evidenced by the elevated CD Microbial-Dysbiosis index that we applied for the first time in CF. Furthermore, the significant over-representation of in children with intestinal inflammation appears to be specific to CF and raises the issue of gut-lung axis involvement. Taken together, our results provide new arguments to link gut microbiota and intestinal inflammation in CF and suggest the key role of the gut-lung axis in the CF evolution.
囊性纤维化(CF)是一种导致肺部和消化系统疾病的全身性遗传疾病。在大多数CF患者中,肠道是慢性炎症和微生物群紊乱的部位。肠道炎症与微生物群失调之间的联系仍知之甚少。本研究的主要目的是根据CF儿童的肠道炎症情况评估其肠道微生物群组成。我们收集了20名CF儿童的粪便样本。测量了粪便钙卫蛋白水平,并通过16S rRNA测序分析了粪便微生物群。我们观察到肠道炎症与微生物群紊乱有关,其主要特征是[具体微生物名称1]、[具体微生物名称2]和[具体微生物名称3]丰度增加,同时[具体微生物名称4]、[具体微生物名称5]和[具体微生物名称6]丰度降低。这些变化与克罗恩病(CD)的变化相似,我们首次在CF中应用的CD微生物失调指数升高就证明了这一点。此外,肠道炎症儿童中[具体微生物名称7]的显著过度表现似乎是CF特有的,并引发了肠肺轴参与的问题。综上所述,我们的结果为CF中肠道微生物群与肠道炎症之间的联系提供了新的证据,并表明肠肺轴在CF进展中的关键作用。