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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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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:沙门氏菌血清型伤寒菌 tsx 基因编码的孔蛋白有助于核苷的导入。当血清型伤寒菌在厌氧条件下生长时,Tsx就是外膜蛋白之一,其表达急剧增加。表达的这种增加至少部分是由于转录增加,并且取决于Fnr,而不取决于ArcA。带有 tsx 基因缺失的血清型鼠伤寒菌株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,内膜核苷通透酶缺陷的原本同基因的 nupG nupC 双突变体是原营养型。由于厌氧生长增强了鼠伤寒血清的毒力,因此我们评估了 tsx 基因在致病性中的作用,发现鼠伤寒血清型Typh STH2370Δ tsx 突变体在在人类巨噬细胞样U937细胞内存活。为了了解为什么Δ tsx 突变体是营养缺陷型,我们选择了在恢复原营养的Δ tsx 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Δ tsx 突变的T-POP插入位于 pyrD 基因的上游。逆转录PCR分析结果表明,诱导剂的加入降低了 pyrD 的转录速率。这些结果表明,Tsx孔蛋白和 tsx 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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