Herman Allison, Serfecz Jacquelyn, Kinnally Alexandra, Crosby Kathleen, Youngman Matthew, Wykoff Dennis, Wilson James W
Villanova University, Department of Biology, Villanova, Pennsylvania, USA.
Villanova University, Department of Biology, Villanova, Pennsylvania, USA
J Bacteriol. 2016 Jul 28;198(16):2166-79. doi: 10.1128/JB.00144-16. Print 2016 Aug 15.
The iprA gene (formerly known as yaiV or STM0374) is located in a two-gene operon in the Salmonella enterica serovar Typhimurium genome and is associated with altered expression during spaceflight and rotating-wall-vessel culture conditions that increase virulence. However, iprA is uncharacterized in the literature. In this report, we present the first targeted characterization of this gene, which revealed that iprA is highly conserved across Enterobacteriaceae We found that S Typhimurium, Escherichia coli, and Enterobacter cloacae ΔiprA mutant strains display a multi-log-fold increase in oxidative stress resistance that is complemented using a plasmid-borne wild-type (WT) copy of the S Typhimurium iprA gene. This observation was also associated with increased catalase activity, increased S Typhimurium survival in macrophages, and partial dependence on the katE gene and full dependence on the rpoS gene. Our results indicate that IprA protein activity is sensitive to deletion of the N- and C-terminal 10 amino acids, while a region that includes amino acids 56 to 80 is dispensable for activity. RNA sequencing (RNA-Seq) analysis revealed several genes altered in expression in the S Typhimurium ΔiprA mutant strain compared to the WT, including those involved in fimbria formation, spvABCD-mediated virulence, ethanolamine utilization, the phosphotransferase system (PTS) transport, and flagellin phase switching from FlgB to FliC (likely a stochastic event) and several genes of hypothetical or putative function.
Overall, this work reveals that the conserved iprA gene measurably influences bacterial biology and highlights the pool of currently uncharacterized genes that are conserved across bacterial genomes. These genes represent potentially useful targets for bacterial engineering, vaccine design, and other possible applications.
iprA基因(以前称为yaiV或STM0374)位于鼠伤寒沙门氏菌基因组中的一个双基因操纵子中,并且与在增加毒力的太空飞行和旋转壁式容器培养条件下的表达改变有关。然而,iprA在文献中尚未得到充分表征。在本报告中,我们首次对该基因进行了靶向表征,结果表明iprA在肠杆菌科中高度保守。我们发现,鼠伤寒沙门氏菌、大肠杆菌和阴沟肠杆菌ΔiprA突变株对氧化应激的抗性呈多对数级增加,使用携带鼠伤寒沙门氏菌iprA基因野生型(WT)拷贝的质粒可使其恢复。这一观察结果还与过氧化氢酶活性增加、鼠伤寒沙门氏菌在巨噬细胞中的存活率提高以及对katE基因的部分依赖性和对rpoS基因的完全依赖性有关。我们的结果表明,IprA蛋白活性对N端和C端10个氨基酸的缺失敏感,而包含第56至80位氨基酸的区域对活性而言是可有可无的。RNA测序(RNA-Seq)分析显示,与野生型相比,鼠伤寒沙门氏菌ΔiprA突变株中有几个基因的表达发生了改变,包括那些参与菌毛形成、spvABCD介导的毒力、乙醇胺利用、磷酸转移酶系统(PTS)转运以及鞭毛蛋白从FlgB向FliC的相位转换(可能是一个随机事件)的基因,以及几个具有假设或推定功能的基因。
总体而言,这项工作表明保守的iprA基因可显著影响细菌生物学,并突出了目前在细菌基因组中保守但尚未充分表征的基因库。这些基因代表了细菌工程、疫苗设计和其他可能应用的潜在有用靶点。