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人类腺病毒 36 的基因组特征,一种可能的肥胖因子。

Genomic characterization of human adenovirus 36, a putative obesity agent.

机构信息

Department of Pediatrics, Division of Infectious Diseases, Naval Medical Center San Diego, San Diego, CA, USA.

出版信息

Virus Res. 2010 May;149(2):152-61. doi: 10.1016/j.virusres.2010.01.011. Epub 2010 Jan 28.

Abstract

Increased levels of serum antibody titers against human adenovirus 36 (HAdV-D36) are associated with human obesity and experimental obesity in laboratory animals. While HAdV-D36 has been studied as an infectious agent implicated in obesity for over a decade, the complete genome sequence and its analysis have yet to be reported. A detailed analysis of the genome sequence of HAdV-D36 may be important to understand its role in obesity. Genomic and bioinformatic comparisons with other HAdVs identified differences that suggested unique functions. Global pairwise genome alignment with all sequenced human adenovirus D (HAdV-D) genomes revealed areas of nonconserved sequences in the hexon, E3 CR1 beta, E3 CR1 gamma, and fiber genes. Phylogenetic analysis of all HAdV-D36 proteins confirmed that this virus belongs to species Human adenovirus D. This genomic analysis of HAdV-D36 provides an important tool for comprehending the role that this unique adenovirus may play in human obesity. Low amino acid sequence identity in the E3 CR1 beta and CR1 gamma genes may suggest distinctive roles for these proteins. Furthermore, the predicted molecular models of the HAdV-D36 fiber protein seem to implicate a unique tissue tropism for HAdV-D36.

摘要

血清中针对人腺病毒 36(HAdV-D36)的抗体滴度升高与人类肥胖和实验动物肥胖有关。虽然 HAdV-D36 作为一种与肥胖相关的传染性病原体已经研究了十多年,但它的完整基因组序列及其分析尚未报道。对 HAdV-D36 基因组序列的详细分析对于理解其在肥胖中的作用可能很重要。与其他 HAdV 的基因组和生物信息学比较显示出一些差异,这些差异表明其具有独特的功能。与所有已测序的人腺病毒 D(HAdV-D)基因组的全球成对基因组比对显示,在六邻体、E3 CR1 beta、E3 CR1 gamma 和纤维基因中存在非保守序列区域。对所有 HAdV-D36 蛋白的系统发育分析证实,该病毒属于人类腺病毒 D 种。对 HAdV-D36 的基因组分析为理解这种独特的腺病毒在人类肥胖中的作用提供了一个重要的工具。E3 CR1 beta 和 CR1 gamma 基因中低的氨基酸序列同一性可能表明这些蛋白具有独特的作用。此外,HAdV-D36 纤维蛋白的预测分子模型似乎暗示了 HAdV-D36 具有独特的组织嗜性。

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