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鼠伤寒沙门氏菌条件必需基因的基因组扫描。

Genome scanning for conditionally essential genes in Salmonella enterica Serotype Typhimurium.

机构信息

Cell and Molecular Biology Program, University of Arkansas, Fayetteville, Arkansas, USA.

出版信息

Appl Environ Microbiol. 2012 May;78(9):3098-107. doi: 10.1128/AEM.06865-11. Epub 2012 Feb 24.

Abstract

As more whole-genome sequences become available, there is an increasing demand for high-throughput methods that link genes to phenotypes, facilitating discovery of new gene functions. In this study, we describe a new version of the Tn-seq method involving a modified EZ:Tn5 transposon for genome-wide and quantitative mapping of all insertions in a complex mutant library utilizing massively parallel Illumina sequencing. This Tn-seq method was applied to a genome-saturating Salmonella enterica serotype Typhimurium mutant library recovered from selection under 3 different in vitro growth conditions (diluted Luria-Bertani [LB] medium, LB medium plus bile acid, and LB medium at 42°C), mimicking some aspects of host stressors. We identified an overlapping set of 105 protein-coding genes in S. Typhimurium that are conditionally essential under at least one of the above selective conditions. Competition assays using 4 deletion mutants (pyrD, glnL, recD, and STM14_5307) confirmed the phenotypes predicted by Tn-seq data, validating the utility of this approach in discovering new gene functions. With continuously increasing sequencing capacity of next generation sequencing technologies, this robust Tn-seq method will aid in revealing unexplored genetic determinants and the underlying mechanisms of various biological processes in Salmonella and the other approximately 70 bacterial species for which EZ:Tn5 mutagenesis has been established.

摘要

随着越来越多的全基因组序列可用,人们对能够将基因与表型联系起来的高通量方法的需求不断增加,这有助于发现新的基因功能。在这项研究中,我们描述了一种新的 Tn-seq 方法,该方法涉及一种改良的 EZ:Tn5 转座子,用于利用大规模平行的 Illumina 测序对复杂突变体文库中的所有插入进行全基因组和定量映射。该 Tn-seq 方法应用于从 3 种不同的体外生长条件(稀释 LB 培养基、LB 培养基加胆汁酸和 42°C 的 LB 培养基)下选择回收的全基因组饱和沙门氏菌肠炎 Typhimurium 突变体文库,模拟宿主应激的某些方面。我们鉴定了在至少一种上述选择条件下条件必需的 105 个重叠的编码蛋白基因。使用 4 个缺失突变体(pyrD、glnL、recD 和 STM14_5307)进行的竞争测定证实了 Tn-seq 数据预测的表型,验证了该方法在发现新基因功能方面的实用性。随着下一代测序技术测序能力的不断提高,这种强大的 Tn-seq 方法将有助于揭示沙门氏菌和其他大约 70 种已建立 EZ:Tn5 诱变的细菌物种中尚未探索的遗传决定因素和各种生物学过程的潜在机制。

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