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Impact of PepT1 deletion on microbiota composition and colitis requires multiple generations

机译:Pept1缺失对微生物异症酵母组成和结肠炎的影响需要多个世代

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摘要

Colon tissues and feces were collected from 6-month-old PepT1−/− and WT mice. a Representative images of confocal microscopy analyses of microbiota localization in Carnoy-fixed colonic tissues of WT and PepT1−/− mice, showing mucus thickness (upper right) and distance of the closest bacteria to the intestinal epithelium (lower right) per genotype across five high-powered fields. Green, Muc2; purple, actin; red, bacteria; blue, DNA. Scale bar: 10 μm. b PCR-based quantification of bacterial load in feces (upper) and adhered to the mucosa (lower). c–e Total RNA was extracted from colons, and the expression levels of Zg16 (c), Lyz1 (d) and Defb1 (e) were quantified by qPCR and normalized to those of 36B4. f Enzymatic activity of lysozyme against peptidoglycan in feces supernatants. Data are presented as the mean ± SEM. Significance was determined by unpaired two-tailed student’s t-test (n = 5–6 mice/group; *P < 0.05, n.s. non-significant).
机译:从6个月历史的Pept1 - / - 和WT小鼠收集结肠组织和粪便。 WT和PEPT1 - / - 小鼠Carnoya固定结肠组织中微生物群定位的共聚焦显微镜分析的代表性图像,显示粘液厚度(右上)和最近的细菌在五个基因型中最近的肠上皮(右下)的距离高功率字段。绿色,muc2;紫色,肌动蛋白;红色,细菌;蓝色,DNA。秤栏:10μm。 B PCR基于粪便(上)的细菌载荷量化并粘附到粘膜(下)。从结肠中提取C-E总RNA,通过QPCR定量Zg16(c),Lyz1(d)和Defb1(e)的表达水平,并将其标准化为36b4。钙酰胺对粪便上清液肽聚糖的酶活性。数据显示为平均值±SEM。由未配对的双尾学生的T检验(n = 5-6只小鼠/组; * P <0.05,N.S.非重大)确定意义。

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