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Gut Microbiota in Health and Disease: Cecal versus fecal microbiota in Ossabaw swine and implications for obesity

机译:肠道菌群在健康与疾病中的应用:s鼠猪的盲肠菌群与粪便菌群及其对肥胖的影响

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摘要

The gut microbiome plays a critical role in the onset and progression of obesity and the metabolic syndrome. However, it is not well documented whether the cecal vs. the fecal microbiome is more relevant when assessing their contributions to these diseases. Here, we amplified the V4 region of the 16S rRNA gene from cecal and fecal samples of female Ossabaw swine fed a low-fat control diet (10.5% fat, n = 4) or Western diet (43.0% fat, 17.8% high fructose corn syrup, 2% cholesterol; n = 3) for 36 wk. Obesity significantly lowered alpha-diversity (P < 0.05), and there was clear separation in beta-diversity between lean and obese pigs, as well as between cecal and fecal samples (P < 0.05). Obesity dramatically increased (P < 0.05) the Firmicutes:Bacteroidetes ratio in fecal samples, and Actinobacteria was higher (P < 0.05) in fecal vs. cecal samples in obese pigs. Cyanobacteria, Proteobacteria, and Fusobacteria were increased (P < 0.05), while Spirochaetes, Tenericutes, and Verrucomicrobia were decreased (P < 0.05) in obese vs. lean pigs. Prevotellaceae was reduced (P < 0.05) in obese fecal vs. cecal samples. Moreover, cecal samples in obese had greater (P < 0.05) predicted metabolic capacity for glycan biosynthesis and metabolism and LPS biosynthesis compared with fecal. Obese pigs also had greater (P < 0.05) capacity for carbohydrate metabolism, which was driven by obese fecal rather than cecal samples and was opposite in lean pigs (P < 0.05). The observed differences in pro-inflammatory microbiota and their metabolic capacity in cecal vs. fecal samples of obese pigs provide new insight into evaluating the microbiome in the pathogenesis of obesity and metabolic disease.
机译:肠道微生物组在肥胖症和代谢综合征的发作和发展中起着至关重要的作用。然而,当评估盲肠微生物与粪便微生物组对这些疾病的贡献时,盲肠与粪便微生物组是否更相关尚无充分文献记载。在这里,我们从饲喂低脂对照饮食(10.5%脂肪,n = 4)或西方饮食(43.0%脂肪,17.8%高果糖玉米)的雌性奥萨巴猪的盲肠和粪便样本中扩增了16S rRNA基因的V4区域。糖浆,含2%胆固醇; n = 3),连续36周。肥胖显着降低了α-多样性(P <0.05),瘦猪和肥胖猪之间以及盲肠和粪便样品之间的β-多样性之间存在明显的分离(P <0.05)。粪便样本中肥胖者的盲肠菌比拟杆菌比率显着提高(P <0.05),而粪便样本中肥胖者的盲肠放线菌比盲肠菌更高(P <0.05)。与肥胖猪相比,肥胖猪的蓝细菌,变形杆菌和融合细菌增加(P <0.05),而螺旋体,tenericutes和疣状微生物减少(P <0.05)。与盲肠相比,肥胖的粪便中的前牡蛎科减少(P <0.05)。此外,与粪便相比,肥胖者的盲肠样品具有更高的(P <0.05)预测的糖代谢和LPS生物合成代谢能力。肥胖猪的碳水化合物代谢能力也更高(P <0.05),这是由肥胖的粪便而非盲肠样品驱动的,而瘦肉猪则相反(P <0.05)。在肥胖猪的盲肠和粪便样品中观察到的促炎微生物群及其代谢能力的差异,为评估微生物组在肥胖症和代谢性疾病发病机理中的应用提供了新的见识。

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