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Mapping and Regulation of Genes within Salmonella Pathogenicity Island 12 That Contribute to In Vivo Fitness of Salmonella enterica Serovar Typhimurium

机译:沙门氏菌致病岛12中的基因的映射和调节,有助于肠道沙门氏菌血清鼠伤寒的适应性。

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Salmonella pathogenicity island 12 (SPI-12) of Salmonella enterica serovar Typhimurium is a 15-kb region that encompasses genes STM2230 to STM2245 and encodes a remnant phage known to contribute to bacterial virulence. In mouse infection experiments and replication assays in macrophages, we demonstrated a role for four genes in SPI-12 for bacterial survival in the host. STM2239, a potential Q antiterminator, showed a prominent contribution to bacterial fitness. Transcriptional reporter experiments, quantitative reverse transcription-PCR (RT-PCR), and immunoblotting demonstrated that the virulence regulator SsrB and STM2239 contribute to transcriptional activation of genes in SPI-12. SsrB was found to indirectly regulate this locus by transcriptional read-through from the sspH2 (STM2241) promoter. Chromatin immunoprecipitation showed that STM2239 copurified with the promoter regulating STM2237, suggesting that STM2239 may function as an antiterminator to activate adjacent genes. These results demonstrate that bacteriophage genes may be adapted by pathogenic bacteria to improve fitness in the host.
机译:鼠伤寒沙门氏菌鼠伤寒沙门氏菌的致病岛12(SPI-12)是一个15 kb的区域,涵盖STM2230至STM2245基因,并编码已知有助于细菌毒性的残留噬菌体。在巨噬细胞中的小鼠感染实验和复制试验中,我们证明了SPI-12中四个基因对于宿主中细菌存活的作用。 STM2239是一种潜在的Q抗终止剂,对细菌的适应性具有显着贡献。转录报告实验,定量逆转录PCR(RT-PCR)和免疫印迹证明,毒力调节剂SsrB和STM2239有助于SPI-12中基因的转录激活。发现ssrB通过从sspH2(STM2241)启动子的转录读取间接调控该基因座。染色质免疫沉淀表明STM2239与调节STM2237的启动子共纯化,提示STM2239可能起激活终止基因的抗终止剂的作用。这些结果证明,噬菌体基因可以被病原细菌适应以改善宿主的适应性。

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