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系统注释和分析“virmugens”-毒力因子,其突变体可用作活减毒疫苗。

Systematic annotation and analysis of "virmugens"-virulence factors whose mutants can be used as live attenuated vaccines.

机构信息

College of Literature, Science, and the Arts, University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

Vaccine. 2013 Jan 21;31(5):797-805. doi: 10.1016/j.vaccine.2012.11.066. Epub 2012 Dec 6.

Abstract

Live attenuated vaccines are usually generated by mutation of genes encoding virulence factors. "Virmugen" is coined here to represent a gene that encodes for a virulent factor of a pathogen and has been proven feasible in animal models to make a live attenuated vaccine by knocking out this gene. Not all virulence factors are virmugens. VirmugenDB is a web-based virmugen database (http://www.violinet.org/virmugendb). Currently, VirmugenDB includes 225 virmugens that have been verified to be valuable for vaccine development against 57 bacterial, viral, and protozoan pathogens. Bioinformatics analysis has revealed significant patterns in virmugens. For example, 10 Gram-negative and 1 Gram-positive bacterial aroA genes are virmugens. A sequence analysis has revealed at least 50% of identities in the protein sequences of the 10 Gram-negative bacterial aroA virmugens. As a pathogen case study, Brucella virmugens were analyzed. Out of 15 verified Brucella virmugens, 6 are related to carbohydrate or nucleotide transport and metabolism, and 2 involving cell membrane biogenesis. In addition, 54 virmugens from 24 viruses and 12 virmugens from 4 parasites are also stored in VirmugenDB. Virmugens tend to involve metabolism of nutrients (e.g., amino acids, carbohydrates, and nucleotides) and cell membrane formation. Host genes whose expressions were regulated by virmugen mutation vaccines or wild type virulent pathogens have also been annotated and systematically compared. The bioinformatics annotation and analysis of virmugens helps to elucidate enriched virmugen profiles and the mechanisms of protective immunity, and further supports rational vaccine design.

摘要

活疫苗通常通过突变编码毒力因子的基因产生。这里创造了“Virmugen”一词来代表编码病原体毒力因子的基因,并且已经在动物模型中证明通过敲除该基因可以制造活减毒疫苗。并非所有毒力因子都是 Virmugen。VirmugenDB 是一个基于网络的 Virmugen 数据库(http://www.violinet.org/virmugendb)。目前,VirmugenDB 包括 225 种已被证实可用于针对 57 种细菌、病毒和原生动物病原体开发疫苗的 Virmugen。生物信息学分析揭示了 Virmugen 中的显著模式。例如,10 种革兰氏阴性和 1 种革兰氏阳性细菌的 aroA 基因是 Virmugen。序列分析显示,这 10 种革兰氏阴性细菌 aroA Virmugen 的蛋白质序列中有至少 50%的同一性。作为病原体案例研究,分析了布鲁氏菌 Virmugen。在 15 种已验证的布鲁氏菌 Virmugen 中,有 6 种与碳水化合物或核苷酸的运输和代谢有关,有 2 种涉及细胞膜生物发生。此外,VirmugenDB 还存储了来自 24 种病毒的 54 种 Virmugen 和来自 4 种寄生虫的 12 种 Virmugen。Virmugen 倾向于参与营养物质(例如氨基酸、碳水化合物和核苷酸)的代谢和细胞膜的形成。还对表达受 Virmugen 突变疫苗或野生型毒力病原体调节的宿主基因进行了注释,并进行了系统比较。Virmugen 的生物信息学注释和分析有助于阐明丰富的 Virmugen 特征和保护性免疫机制,并进一步支持合理的疫苗设计。

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