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Understanding the multifaceted roles of the phosphoenolpyruvate: Phosphotransferase system in regulation of Salmonella virulence using a mutant defective in ptsl and err expression

机译:了解磷酸丙酮酸的多方型作用:P6SL和ERR表达中突变缺陷调节沙门氏菌毒力的调节

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The phosphoenolpyruvate (PEP):carbohydrate phosphotransferase system (PTS) catalyzes the translocation of sugar substrates with their concomitant phosphorylation in bacteria. In addition to its intrinsic role in sugar transport and metabolism, numerous recent studies report the versatility of the PTS to interconnect energy and signal transduction in response to sugar availability. In this study, the role of PTS in Salmonella virulence regulation was explored. To decipher the regulatory network coordinated by the PTS during Salmonella infection, a transcriptomic approach was applied to a transposon insertion mutant with defective expression of ptsl and crr, which encode enzyme I and enzyme IIA~(Glc) of the PTS, respectively. There were 114 differentially expressed genes (DEGs) exhibiting two-fold or higher expression changes in the transposon mutant strain, with 13 up-regulated genes versus 101 down-regulated genes. One-third of the DEGs were associated with energy production and carbohydrate/aminoacid metabolism pathways, implicating the prominent role of the PTS in carbohydrate transport. With regard to regulation of virulence, the tested mutant decreased the expression of genes associated with quorum sensing, Salmonella pathogenicity islands, flagella, and the PhoPQ regulon. We investigated the possibility of PTS-mediated regulation of virulence determinants identified in the transcriptomic analysis and proposed a regulatory circuit orchestrated by the PTS in Salmonella infection of host cells. These results suggest that Salmonella divergently controls virulence attributes in accordance with the availability of carbohydrates in the environment.
机译:磷酸丙酯(PEP):碳水化合物磷酸转移酶系统(PTS)催化糖底物的易位与细菌中的伴随磷酸化。除了在糖转运和新陈代谢中的内在作用外,近期研究报告了PTS以响应于糖可用性而互连能量和信号转导的通用性。在这项研究中,探讨了PTS在沙门氏菌毒力调节中的作用。为了破译Salmonella感染期间PTS协调的调节网络,将转录组方法应用于转座子插入突变体,其PTS1和CRR的缺陷表达分别编码PTS的酶I和酶IIA〜(GLC)。存在114个差异表达的基因(DEGS),其在转座子突变体菌株中表现出两倍或更高的表达变化,13个上调基因与101个下调基因。三分之一的DEG与能量产生和碳水化合物/氨基酸代谢途径有关,暗示PTS在碳水化合物运输中的突出作用。关于毒力的调节,测试突变体降低了与法定感测,沙门氏菌致病性岛,鞭毛和PhoPQ调节件相关的基因的表达。我们研究了在转录组分析中鉴定的毒力决定因素的PTS介导的调节的可能性,并提出了由宿主细胞的沙门氏菌感染的PTS策划的调节赛道。这些结果表明,沙门氏菌根据环境中的碳水化合物的可用性来致病地控制毒力属性。

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