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Genome Scanning for Conditionally Essential Genes in Salmonella enterica Serotype Typhimurium

机译:肠道沙门氏菌血清型鼠伤寒中有条件必需基因的基因组扫描。

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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:Tn 5 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:Tn 5 mutagenesis has been established.
机译:随着越来越多的全基因组序列变得可用,对将基因链接到表型,促进新基因功能发现的高通量方法的需求不断增长。在这项研究中,我们描述了Tn-seq方法的新版本,其中涉及经过修饰的EZ:Tn 5转座子,可利用全基因组平行Illumina测序对整个突变体文库中的所有插入片段进行全基因组范围内的定量和定量作图。将此Tn-seq方法应用于在3种不同的体外生长条件下(从稀释的Luria-Bertani [LB]培养基,LB培养基和胆汁酸和LB培养基在42° C),模仿宿主压力源的某些方面。我们确定了S中105个蛋白质编码基因的重叠集。在至少一种上述选择性条件下有条件必需的鼠伤寒。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,从而验证了该方法在发现新基因功能中的实用性。随着下一代测序技术的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种已经进行EZ:Tn 5诱变的细菌物种中尚未探索的遗传决定因素以及各种生物过程的潜在机制。成立。

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