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The Salmonella enterica Serovar Typhi tsx Gene, Encoding a Nucleoside-Specific Porin, Is Essential for Prototrophic Growth in the Absence of Nucleosides

机译:沙门氏菌血清型鼠伤寒沙门氏菌tsx基因,编码一种核苷特异的孔蛋白,是缺乏核苷时原养型生长所必需的

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摘要

The Salmonella enterica serovar Typhi tsx gene encodes a porin that facilitates the import of nucleosides. When serovar Typhi is grown under anaerobic conditions, Tsx is among the outer membrane proteins whose expression increases dramatically. This increase in expression is due, at least in part, to increased transcription and is dependent on Fnr but not on ArcA. A mutant derivative of serovar Typhi strain STH2370 with a deletion of the tsx gene is an auxotroph that requires either adenosine or thymidine for growth on minimal medium. In contrast, an otherwise isogenic nupG nupC double mutant, defective in the inner membrane nucleoside permeases, is a prototroph. Because anaerobic growth enhances the virulence of serovar Typhi in vitro, we assessed the role that the tsx gene plays in pathogenicity and found that the serovar Typhi STH2370 Δtsx mutant is defective in survival within human macrophage-like U937 cells. To understand why the Δtsx mutant is an auxotroph, we selected for insertions of minitransposon T-POP in the Δtsx genetic background that restored prototrophy. One T-POP insertion that suppressed the Δtsx mutation in the presence of the inducer tetracycline was located upstream of the pyrD gene. The results of reverse transcription-PCR analysis showed that addition of the inducer decreased the rate of pyrD transcription. These results suggest that the Tsx porin and the balance of products of the tsx and pyrD genes play critical roles in membrane assembly and integrity and thus in the virulence of serovar Typhi.
机译:肠炎沙门氏菌鼠伤寒沙门氏菌tsx基因编码的孔蛋白有助于核苷的导入。当血清型伤寒在厌氧条件下生长时,Tsx是其外膜蛋白表达急剧增加的蛋白质之一。表达的这种增加至少部分地是由于转录的增加,并且取决于Fnr,而不取决于ArcA。带有tsx基因缺失的血清型Typhi菌株STH2370的突变体衍生物是营养缺陷型,需要腺苷或胸苷才能在基本培养基上生长。相比之下,在内膜核苷通透酶中有缺陷的本来是同基因的nupG nupC双突变体是原营养型。由于厌氧菌的生长会增强鼠伤寒血清的毒力,因此我们评估了tsx基因在致病性中的作用,并发现鼠伤寒Typhi STH2370Δtsx突变体在人类巨噬细胞样U937细胞中的存活存在缺陷。为了了解为什么Δtsx突变体是营养缺陷型,我们选择在恢复原营养的Δtsx遗传背景中插入小转座子T-POP。一种在诱导物四环素存在下抑制Δtsx突变的T-POP插入位于pyrD基因的上游。逆转录-PCR分析的结果表明,添加诱导剂降低了pyrD转录的速率。这些结果表明,Tsx孔蛋白以及tsx和pyrD基因产物的平衡在膜组装和完整性以及血清型伤寒菌的毒力中起关键作用。

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