Department of Molecular Sciences, Macquarie University, Sydney, Australia.
ARC Centre of Excellence in Synthetic Biology, Macquarie University, Sydney, Australia.
J Bacteriol. 2021 Mar 8;203(7). doi: 10.1128/JB.00432-20.
Gene essentiality studies have been performed on numerous bacterial pathogens, but essential gene sets have been determined for only a few plant-associated bacteria. Pf-5 is a plant-commensal, biocontrol bacterium that can control disease-causing pathogens on a wide range of crops. Work on Pf-5 has mostly focused on secondary metabolism and biocontrol genes, but genome-wide approaches such as high-throughput transposon mutagenesis have not yet been used for this species. In this study, we generated a dense Pf-5 transposon mutant library and used transposon-directed insertion site sequencing (TraDIS) to identify 446 genes essential for growth on rich media. Genes required for fundamental cellular machinery were enriched in the essential gene set, while genes related to nutrient biosynthesis, stress responses, and transport were underrepresented. The majority of Pf-5 essential genes were part of the core genome. Comparison of the essential gene set of Pf-5 with those of two plant-associated pseudomonads, and , and the well-studied opportunistic human pathogen PA14 showed that the four species share a large number of essential genes, but each species also had uniquely essential genes. Comparison of the Pf-5 -predicted and -determined essential gene sets highlighted the essential cellular functions that are over- and underestimated by each method. Expanding essentiality studies into bacteria with a range of lifestyles may improve our understanding of the biological processes important for bacterial survival and growth. Essential genes are those crucial for survival or normal growth rates in an organism. Essential gene sets have been identified in numerous bacterial pathogens but only a few plant-associated bacteria. Employing genome-wide approaches, such as transposon insertion sequencing, allows for the concurrent analyses of all genes of a bacterial species and rapid determination of essential gene sets. We have used transposon insertion sequencing to systematically analyze thousands of Pf-5 genes and gain insights into gene functions and interactions that are not readily available using traditional methods. Comparing Pf-5 essential genes with those of three other pseudomonads highlights how gene essentiality varies between closely related species.
基因必需性研究已经在许多细菌病原体上进行,但只有少数植物相关细菌的必需基因集被确定。Pf-5 是一种植物共生、生物防治细菌,可以控制广泛作物上的致病病原体。Pf-5 的工作主要集中在次生代谢和生物防治基因上,但基因组范围的方法,如高通量转座子诱变,尚未用于该物种。在这项研究中,我们生成了一个密集的 Pf-5 转座子突变体文库,并使用转座子定向插入位点测序 (TraDIS) 来鉴定 446 个在丰富培养基上生长所必需的基因。必需基因集中富含基本细胞机制所需的基因,而与营养生物合成、应激反应和运输相关的基因则代表性不足。Pf-5 必需基因的大多数是核心基因组的一部分。将 Pf-5 的必需基因集与两种植物相关的假单胞菌 和 以及研究充分的机会性病原体 PA14 进行比较,发现这四个物种共享大量必需基因,但每个物种也有独特的必需基因。Pf-5 预测和确定的必需基因集的比较突出了每种方法高估和低估的必需细胞功能。将必需性研究扩展到具有不同生活方式的细菌中,可能会提高我们对细菌生存和生长重要的生物学过程的理解。必需基因是指对生物体的生存或正常生长速率至关重要的基因。必需基因集已在许多细菌病原体中被确定,但只有少数植物相关细菌的必需基因集被确定。采用基因组范围的方法,如转座子插入测序,可以同时分析一个细菌物种的所有基因,并快速确定必需基因集。我们已经使用转座子插入测序来系统地分析数千个 Pf-5 基因,并深入了解使用传统方法不易获得的基因功能和相互作用。将 Pf-5 的必需基因与其他三种假单胞菌的必需基因进行比较,突出了密切相关的物种之间基因必需性的差异。