Azrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel.
Racah Institute of Physics, The Hebrew University, Jerusalem, Israel.
Sci Adv. 2024 Sep 13;10(37):eadp4119. doi: 10.1126/sciadv.adp4119. Epub 2024 Sep 11.
Antibiotic use is a risk factor for development of inflammatory bowel diseases (IBDs). IBDs are characterized by a damaged mucus layer, which does not separate the intestinal epithelium from the microbiota. Here, we hypothesized that antibiotics affect the integrity of the mucus barrier, which allows bacterial penetrance and predisposes to intestinal inflammation. We found that antibiotic treatment led to breakdown of the colonic mucus barrier and penetration of bacteria into the mucus layer. Using fecal microbiota transplant, RNA sequencing followed by machine learning, ex vivo mucus secretion measurements, and antibiotic treatment of germ-free mice, we determined that antibiotics induce endoplasmic reticulum stress in the colon that inhibits colonic mucus secretion in a microbiota-independent manner. This antibiotic-induced mucus secretion flaw led to penetration of bacteria into the colonic mucus layer, translocation of microbial antigens into circulation, and exacerbation of ulcerations in a mouse model of IBD. Thus, antibiotic use might predispose to intestinal inflammation by impeding mucus production.
抗生素的使用是炎症性肠病 (IBD) 发展的一个风险因素。IBD 的特征是粘液层受损,这使得肠上皮细胞不能与微生物群分离。在这里,我们假设抗生素会影响粘液屏障的完整性,使细菌穿透并导致肠道炎症。我们发现抗生素治疗导致结肠粘液屏障的破坏和细菌穿透粘液层。通过粪便微生物群移植、RNA 测序和机器学习、离体粘液分泌测量以及无菌小鼠的抗生素治疗,我们确定抗生素在结肠中诱导内质网应激,以非微生物群依赖的方式抑制结肠粘液分泌。这种抗生素诱导的粘液分泌缺陷导致细菌穿透结肠粘液层,微生物抗原易位到循环中,并在 IBD 小鼠模型中加剧溃疡。因此,抗生素的使用可能通过阻碍粘液生成而导致肠道炎症易感性。