Zheng Ruiping, Feng Xuemei, Wei Xueying, Pan Xiaolei, Liu Chang, Song Ruopu, Jin Yongxin, Bai Fang, Jin Shouguang, Wu Weihui, Cheng Zhihui
Department of Microbiology, College of Life Sciences, Nankai University, Tianjin, China.
Department of Molecular Genetics and Microbiology, College of Medicine, University of Florida, Gainesville, FL, United States.
Front Microbiol. 2018 Mar 26;9:548. doi: 10.3389/fmicb.2018.00548. eCollection 2018.
, a Gram-negative opportunistic pathogenic bacterium, causes acute and chronic infections. Upon entering the host, alters global gene expression to adapt to host environment and avoid clearance by the host immune system. Proline utilization A (PutA) is a bifunctional enzyme, which converts proline to glutamate. Here we report that PutA was required for the virulence of in a murine acute pneumonia model. A mutant was more susceptible to oxidative stress compared to the wild type strain. An AraC/XylS family protein, PruR, directly bound to the upstream of -35 box in the promoter and activated expression. High concentration of proline in bacteria up-regulated expression, which led to the activation of expression. As a feedback regulation, glutamate produced by PutA released PruR from the promoter and turned off the expression. PruR affected bacterial virulence through the regulation of the expression. Altogether, these data are the first to reveal that PutA plays an important role in the pathogenesis of , as well as to describe the genetic regulation of PutA in .
[细菌名称]是一种革兰氏阴性机会致病菌,可引起急性和慢性感染。进入宿主后,[细菌名称]会改变整体基因表达以适应宿主环境并避免被宿主免疫系统清除。脯氨酸利用A(PutA)是一种双功能酶,可将脯氨酸转化为谷氨酸。在此我们报告,在小鼠急性肺炎模型中,PutA是[细菌名称]毒力所必需的。与野生型菌株相比,[细菌名称]突变体对氧化应激更敏感。一种AraC/XylS家族蛋白PruR直接结合到[细菌名称]启动子中-35框的上游并激活[细菌名称]表达。细菌中高浓度的脯氨酸上调了[细菌名称]表达,这导致了[细菌名称]表达的激活。作为一种反馈调节,PutA产生的谷氨酸将PruR从[细菌名称]启动子上释放下来并关闭[细菌名称]表达。PruR通过调节[细菌名称]表达影响细菌毒力。总之,这些数据首次揭示PutA在[细菌名称]发病机制中起重要作用,同时也描述了[细菌名称]中PutA的遗传调控。