Asaji Naoki, Inoue Jun, Hayashi Hiroki, Tokunaga Eri, Shimamoto Yusaku, Kinoshita Masato, Tanaka Takeshi, Sakai Arata, Yano Yoshihiko, Ueda Yoshihide, Kodama Yuzo
Department of Internal Medicine, Division of Gastroenterology Kobe University Graduate School of Medicine Kobe Japan.
Division of Gastroenterology Kita-Harima Medical Center Ono Japan.
JGH Open. 2022 Aug 29;6(10):677-684. doi: 10.1002/jgh3.12803. eCollection 2022 Oct.
Regarding the gut-liver axis, fecal dysbiosis is implicated in the pathogenesis of non-alcoholic fatty liver disease (NAFLD). The significance of mucosa-associated microbiota (MAM, which is present in the mucin layer covering the intestinal mucosa) has not been well explored. We aimed to clarify the characteristics of MAM in patients with NAFLD.
MAM were obtained from seven patients with early-stage NAFLD and seven controls by colonoscopy in five locations (terminal ileum, cecum, ascending and sigmoid colon, and rectum) using mucosal brushes. The microbial 16S rDNA profiles of the MAM and fecal microbiota of patients in the NAFLD and control groups were analyzed.
α-diversities of fecal microbiota were decreased in patients with NAFLD (observed species, Shannon index, and Chao1: 174.57 134.86, 5.51 4.65, and 206.34 167.91; = 0.048, 0.067, and 0.087, respectively), and microbial composition analyses by principal coordinate analysis differed between the fecal microbiota of patients with NAFLD and those of controls (permutational analysis of variance [PERMANOVA] of weighted and unweighted: Pseud-: 1.4179/-value: 0.05 and Pseud-: 2.1497/-value: 0.049, respectively). However, α-diversities or microbial composition of MAM in most parts of the intestine did not differ significantly between the NAFLD and control groups. Unclassified , Oscillospira, Odoribacter, unclassified , and were decreased in the feces of patients with NAFLD (determined by linear discriminant analysis effect size), but five (except ) of the six genera were not decreased in the MAM of these patients.
In early-stage NAFLD, MAM was uniform and relatively stable throughout the intestine, even when fecal dysbiosis appeared.
关于肠-肝轴,粪便微生物群失调与非酒精性脂肪性肝病(NAFLD)的发病机制有关。黏膜相关微生物群(MAM,存在于覆盖肠黏膜的黏液层中)的意义尚未得到充分研究。我们旨在阐明NAFLD患者中MAM的特征。
通过结肠镜检查,使用黏膜刷在五个部位(回肠末端、盲肠、升结肠和乙状结肠以及直肠)从7例早期NAFLD患者和7例对照中获取MAM。分析NAFLD组和对照组患者MAM和粪便微生物群的微生物16S rDNA谱。
NAFLD患者粪便微生物群的α多样性降低(观察到的物种数、香农指数和Chao1指数分别为:174.57±134.86、5.51±4.65和206.34±167.91;P值分别为0.048、0.067和0.087),通过主坐标分析的微生物组成分析显示,NAFLD患者的粪便微生物群与对照组不同(加权和未加权的置换方差分析[PERMANOVA]:伪F值:1.4179/P值:0.05和伪F值:2.1497/P值:0.049)。然而,NAFLD组和对照组在肠道大部分部位的MAM的α多样性或微生物组成没有显著差异。NAFLD患者粪便中未分类的[菌属名称未给出]、颤螺菌属、气味杆菌属、未分类的[菌属名称未给出]和[菌属名称未给出]减少(通过线性判别分析效应大小确定),但这六个属中的五个属(除[菌属名称未给出]外)在这些患者的MAM中没有减少。
在早期NAFLD中,即使出现粪便微生物群失调,MAM在整个肠道中也是均匀且相对稳定的。