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全基因组筛选细菌包膜生物发生突变体鉴定涉及细胞壁前体代谢的新型因子。

A genome-wide screen for bacterial envelope biogenesis mutants identifies a novel factor involved in cell wall precursor metabolism.

机构信息

Department of Microbiology, Infectiology and Immunology, Université de Montréal, Montréal, Québec, Canada.

European Molecular Biology Laboratory, Genome Biology Unit, Heidelberg, Germany.

出版信息

PLoS Genet. 2014 Jan;10(1):e1004056. doi: 10.1371/journal.pgen.1004056. Epub 2014 Jan 2.

Abstract

The cell envelope of Gram-negative bacteria is a formidable barrier that is difficult for antimicrobial drugs to penetrate. Thus, the list of treatments effective against these organisms is small and with the rise of new resistance mechanisms is shrinking rapidly. New therapies to treat Gram-negative bacterial infections are therefore sorely needed. This goal will be greatly aided by a detailed mechanistic understanding of envelope assembly. Although excellent progress in the identification of essential envelope biogenesis systems has been made in recent years, many aspects of the process remain to be elucidated. We therefore developed a simple, quantitative, and high-throughput assay for mutants with envelope biogenesis defects and used it to screen an ordered single-gene deletion library of Escherichia coli. The screen was robust and correctly identified numerous mutants known to be involved in envelope assembly. Importantly, the screen also implicated 102 genes of unknown function as encoding factors that likely impact envelope biogenesis. As a proof of principle, one of these factors, ElyC (YcbC), was characterized further and shown to play a critical role in the metabolism of the essential lipid carrier used for the biogenesis of cell wall and other bacterial surface polysaccharides. Further analysis of the function of ElyC and other hits identified in our screen is likely to uncover a wealth of new information about the biogenesis of the Gram-negative envelope and the vulnerabilities in the system suitable for drug targeting. Moreover, the screening assay described here should be readily adaptable to other organisms to study the biogenesis of different envelope architectures.

摘要

革兰氏阴性菌的细胞包膜是一个难以穿透的强大障碍,使抗菌药物难以发挥作用。因此,能够有效治疗这些生物体的治疗方法很少,而且随着新的耐药机制的出现,这种方法迅速减少。因此,非常需要新的疗法来治疗革兰氏阴性菌感染。如果对包膜组装有详细的机制理解,这一目标将得到极大的帮助。尽管近年来在鉴定必需的包膜生物发生系统方面取得了出色的进展,但该过程的许多方面仍有待阐明。因此,我们开发了一种简单、定量和高通量的突变体包膜生物发生缺陷检测方法,并将其用于筛选大肠杆菌的有序单基因缺失文库。该筛选方法稳健且正确地鉴定了许多已知参与包膜组装的突变体。重要的是,该筛选还暗示了 102 个未知功能的基因编码可能影响包膜生物发生的因素。作为原理验证,对这些因素之一,ElyC(YcbC)进行了进一步表征,并表明其在用于细胞壁和其他细菌表面多糖生物发生的必需脂质载体的代谢中起着关键作用。进一步分析我们筛选中鉴定的 ElyC 和其他命中因素的功能可能会揭示有关革兰氏阴性菌包膜生物发生和适合药物靶向的系统弱点的大量新信息。此外,这里描述的筛选方法应该很容易适应其他生物体,以研究不同包膜结构的生物发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1e3/3879167/f18c4da1e2df/pgen.1004056.g001.jpg

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