Department of Agricultural and Environmental Sciences, College of Agriculture, Tennessee State University, 3500 John A. Merritt Boulevard, Nashville, TN, USA.
Department of Anatomy and Physiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA.
Int J Obes (Lond). 2019 Nov;43(11):2134-2142. doi: 10.1038/s41366-019-0323-2. Epub 2019 Jan 22.
Obesity has become a worldwide epidemic affecting millions of people. Obesity and associated health consequences tend to be complicated by diverse causes and multi-systemic involvement. Previous studies have investigated obesity induced by a single factor, such as a high-fat diet (HF) of typical energy-dense food and infection by an adipogenic virus, such as a widely studied human adenovirus serotype 36 (Ad-36). In this study, we hypothesized and investigated the synergistic effect of two causal factors, HF and Ad-36, in obesity induction.
The 7-week-old Wistar rats (n = 1214/group) were randomly divided into weight-matched groups and induced for obesity with mock-control, HF, Ad-36, or HF + Ad-36 for 8-30 weeks, and compared for obesity phenotype. A global transcriptomic RNA-Seq analysis was used to profile signature gene response pathways in ileal tissues from 8-week control and obese animals during this early phase of obesity induction.
HF only and particularly co-administration of Ad-36 and HF (HF + Ad-36) induced significant obesity in rats (p < 0.05 or p < 0.005). Compared with either Ad-36 or HF alone, HF + Ad-36 treatment significantly aggravates obesity in rats regarding body weight (n = 12-14/group) and adiposity index (n = 6-7). Genome-wide transcriptomic analyses of intestinal tissues revealed signature genes on an inter-systemic scale, including many genes in the pathways of circadian rhythm and antiviral immunity focusing on IFN signaling.
Ad-36 exacerbated the induction of obesity in rats compared with those treated with HF alone. Gene-responsive pathways involved in circadian rhythm and antiviral immunity in ileal tissues were significantly (p < 0.05, and FDR < 0.01) regulated during the early phase of obesity induction. This study provided a co-factorial model for obesity induction and profiled molecular targets for further validation and molecular manipulation.
肥胖已成为影响数百万人的全球性流行病。肥胖症及其相关健康后果往往因多种原因和多系统参与而变得复杂。以前的研究已经调查了由单一因素引起的肥胖,例如高脂肪饮食(HF)和致肥胖病毒(如广泛研究的人腺病毒 36 型(Ad-36))的感染。在这项研究中,我们假设并研究了两个因果因素,HF 和 Ad-36,在肥胖诱导中的协同作用。
7 周龄 Wistar 大鼠(每组 n=1214)随机分为体重匹配组,并分别用模拟对照、HF、Ad-36 或 HF+Ad-36 诱导肥胖 8-30 周,并比较肥胖表型。使用全局转录组 RNA-Seq 分析在肥胖诱导的早期阶段分析 8 周龄对照和肥胖动物回肠组织中的特征基因反应途径。
HF 仅和特别是 Ad-36 和 HF(HF+Ad-36)联合给药可显著诱导大鼠肥胖(p<0.05 或 p<0.005)。与 Ad-36 或 HF 单独治疗相比,HF+Ad-36 治疗显著加重了大鼠的肥胖程度,表现在体重(每组 n=12-14)和肥胖指数(每组 n=6-7)。肠道组织的全基因组转录组分析揭示了系统性特征基因,包括昼夜节律和抗病毒免疫途径中的许多基因,重点是 IFN 信号。
与单独用 HF 治疗相比,Ad-36 可加剧大鼠肥胖的诱导。在肥胖诱导的早期阶段,回肠组织中涉及昼夜节律和抗病毒免疫的基因反应途径明显(p<0.05,FDR<0.01)受到调节。这项研究提供了肥胖诱导的协同因素模型,并对分子靶标进行了分析,以进一步验证和分子操作。