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高通量系统用于革兰氏阳性菌分泌蛋白和表面暴露蛋白在功能宏基因组学研究中的展示。

High-throughput system for the presentation of secreted and surface-exposed proteins from Gram-positive bacteria in functional metagenomics studies.

机构信息

INRA, UMR1319 Micalis, Jouy-en-Josas, France.

出版信息

PLoS One. 2013 Jun 14;8(6):e65956. doi: 10.1371/journal.pone.0065956. Print 2013.

Abstract

Complex microbial ecosystems are increasingly studied through the use of metagenomics approaches. Overwhelming amounts of DNA sequence data are generated to describe the ecosystems, and allow to search for correlations between gene occurrence and clinical (e.g. in studies of the gut microbiota), physico-chemical (e.g. in studies of soil or water environments), or other parameters. Observed correlations can then be used to formulate hypotheses concerning microbial gene functions in relation to the ecosystem studied. In this context, functional metagenomics studies aim to validate these hypotheses and to explore the mechanisms involved. One possible approach is to PCR amplify or chemically synthesize genes of interest and to express them in a suitable host in order to study their function. For bacterial genes, Escherichia coli is often used as the expression host but, depending on the origin and nature of the genes of interest and the test system used to evaluate their putative function, other expression systems may be preferable. In this study, we developed a system to evaluate the role of secreted and surface-exposed proteins from Gram-positive bacteria in the human gut microbiota in immune modulation. We chose to use a Gram-positive host bacterium, Bacillus subtilis, and modified it to provide an expression background that behaves neutral in a cell-based immune modulation assay, in vitro. We also adapted an E. coli-B. subtilis shuttle expression vector for use with the Gateway high-throughput cloning system. Finally, we demonstrate the functionality of this host-vector system through the cloning and expression of a flagellin-coding sequence, and show that the expression-clone elicits an inflammatory response in a human intestinal epithelial cell line. The expression host can easily be adapted to assure neutrality in other assay systems, allowing the use of the presented presentation system in functional metagenomics of the gut and other ecosystems.

摘要

复杂的微生物生态系统越来越多地通过使用宏基因组学方法进行研究。为了描述这些生态系统,生成了大量的 DNA 序列数据,以寻找基因出现与临床(例如在肠道微生物组研究中)、物理化学(例如在土壤或水生态系统研究中)或其他参数之间的相关性。然后,可以使用观察到的相关性来提出有关微生物基因功能与所研究生态系统之间关系的假设。在这种情况下,功能宏基因组学研究旨在验证这些假设并探索所涉及的机制。一种可能的方法是通过 PCR 扩增或化学合成感兴趣的基因,并在合适的宿主中表达它们,以研究它们的功能。对于细菌基因,大肠杆菌通常被用作表达宿主,但根据感兴趣的基因的来源和性质以及用于评估其潜在功能的测试系统,可能需要使用其他表达系统。在这项研究中,我们开发了一种系统来评估来自革兰氏阳性菌的分泌和表面暴露蛋白在人类肠道微生物群中对免疫调节的作用。我们选择使用革兰氏阳性宿主细菌枯草芽孢杆菌,并对其进行修饰,以提供在体外基于细胞的免疫调节测定中表现中性的表达背景。我们还对大肠杆菌-枯草芽孢杆菌穿梭表达载体进行了改造,使其可用于 Gateway 高通量克隆系统。最后,我们通过克隆和表达鞭毛编码序列证明了这个宿主-载体系统的功能,并表明表达克隆在人肠上皮细胞系中引发了炎症反应。表达宿主可以很容易地适应其他测定系统以确保其中性,从而允许在肠道和其他生态系统的功能宏基因组学中使用所提出的表达系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e26/3682982/ee37f601d30d/pone.0065956.g001.jpg

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