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Identification of Attenuated Yersinia pseudotuberculosis Strains and Characterization of an Orogastric Infection in BALB/c Mice on Day 5 Postinfection by Signature-Tagged Mutagenesis

机译:减毒的耶尔森氏菌假结核菌的鉴定和BALB / c小鼠在感染后第5天通过特征标记诱变的胃胃感染的特征

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摘要

Yersinia pseudotuberculosis localizes to the distal ileum, cecum, and proximal colon of the gastrointestinal tract after oral infection. Using signature-tagged mutagenesis, we isolated 13 Y. pseudotuberculosis mutants that failed to survive in the cecum of mice after orogastric inoculation. Twelve of these mutants were also attenuated for replication in the spleen after intraperitoneal infection, whereas one strain, mutated the gene encoding invasin, replicated as well as wild-type bacteria in the spleen. Several mutations were in operons encoding components of the type III secretion system, including components involved in translocating Yop proteins into host cells. This indicates that one or more Yops may be necessary for survival in the gastrointestinal tract. Three mutants were defective in O-antigen biosynthesis; these mutants were also unable to invade epithelial cells as efficiently as wild-type Y. pseudotuberculosis. Several other mutations were in genes that had not previously been associated with growth in a host, including cls, ksgA, and sufl. In addition, using Y. pseudotuberculosis strains marked with signature tags, we counted the number of different bacterial clones that were present in the cecum, mesenteric lymph nodes, and spleen 5 days postinfection. We find barriers in the host animal that limit the number of bacteria that succeed in reaching and/or replicating in the mesenteric lymph nodes and spleen after breaching the gut mucosa.
机译:口腔感染后假性耶尔森氏菌位于回肠远端,盲肠和胃肠道近端结肠。使用标记标签的诱变,我们分离了13种假性结核杆菌突变体,这些突变体在口胃接种后无法在小鼠的盲肠中存活。这些突变体中的十二个在腹膜内感染后在脾脏中的复制也被减弱,而一种菌株突变了编码入侵蛋白的基因,并且在脾脏中复制了野生型细菌。在操纵子中编码III型分泌系统成分的一些突变,包括参与将Yop蛋白转运到宿主细胞中的成分。这表明在胃肠道中生存可能需要一个或多个Yops。三个突变体在O抗原生物合成方面存在缺陷。这些突变体也不能像野生型假结核耶尔森氏菌一样有效地侵入上皮细胞。以前与宿主生长无关的基因中还有其他几种突变,包括cls,ksgA和suf1。此外,使用带有标记标签的假结核耶尔森氏菌菌株,我们对感染后5天的盲肠,肠系膜淋巴结和脾脏中存在的不同细菌克隆进行了计数。我们在宿主动物中发现了一些障碍,这些障碍限制了突破肠道粘膜后成功进入和/或在肠系膜淋巴结和脾中复制的细菌数量。

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