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Structural resilience of the gut microbiota in adult mice under high-fat dietary perturbations

机译:高脂饮食对成年小鼠肠道菌群结构弹性的影响

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摘要

Disruption of the gut microbiota by high-fat diet (HFD) has been implicated in the development of obesity. It remains to be elucidated whether the HFD-induced shifts occur at the phylum level or whether they can be attributed to specific phylotypes; additionally, it is unclear to what extent the changes are reversible under normal chow (NC) feeding. One group (diet-induced obesity, DIO) of adult C57BL/6J mice was fed a HFD for 12 weeks until significant obesity and insulin resistance were observed, and then these mice were switched to NC feeding for 10 weeks. Upon switching to NC feeding, the metabolic deteriorations observed during HFD consumption were significantly alleviated. The second group (control, CHO) remained healthy under continuous NC feeding. UniFrac analysis of bar-coded pyrosequencing data showed continued structural segregation of DIO from CHO on HFD. At 4 weeks after switching back to NC, the gut microbiota in the DIO group had already moved back to the CHO space, and continued to progress along the same age trajectory and completely converged with CHO after 10 weeks. Redundancy analysis identified 77 key phylotypes responding to the dietary perturbations. HFD-induced shifts of these phylotypes all reverted to CHO levels over time. Some of these phylotypes exhibited robust age-related changes despite the dramatic abundance variations in response to dietary alternations. These findings suggest that HFD-induced structural changes of the gut microbiota can be attributed to reversible elevation or diminution of specific phylotypes, indicating the significant structural resilience of the gut microbiota of adult mice to dietary perturbations.
机译:高脂饮食(HFD)破坏肠道菌群与肥胖的发展有关。尚需阐明,HFD诱导的转变是否发生在门的水平上,或者是否可以归因于特定的门型。另外,尚不清楚在正常的食物(NC)下,这种变化在多大程度上是可逆的。给一组(饮食诱发的肥胖症,DIO)成年C57BL / 6J小鼠喂食HFD 12周,直到观察到明显的肥胖症和胰岛素抵抗,然后将这些小鼠转为NC喂养10周。改用NC喂养后,HFD消耗期间观察到的代谢恶化得到了明显缓解。第二组(对照组,CHO)在连续NC喂养下保持健康。 UniFrac对条形码焦磷酸测序数据的分析表明,在HFD上DIO与CHO的结构持续分离。改回NC后第4周,DIO组的肠道菌群已经移回CHO空间,并继续沿着相同的年龄轨迹发展,并在10周后完全与CHO融合。冗余分析确定了77种对饮食扰动有反应的主要系统型。随着时间的流逝,HFD诱导的这些系统型的转变全部恢复为CHO水平。尽管响应饮食交替的丰度变化很大,但其中一些系统型仍表现出与年龄相关的强烈变化。这些发现表明,HFD诱导的肠道菌群的结构变化可归因于特定系统型的可逆升高或减少,这表明成年小鼠的肠道菌群对饮食扰动具有显着的结构弹性。

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