Venecia Krista, Young Glenn M
Microbiology Graduate Group, University of California, Davis, California 95616, USA.
Infect Immun. 2005 Sep;73(9):5961-77. doi: 10.1128/IAI.73.9.5961-5977.2005.
Pathogenic biovars of Yersinia enterocolitica maintain the well-studied plasmid-encoded Ysc type III secretion (TTS) system, which has a definitive role in virulence. Y. enterocolitica biovar 1B additionally has a distinct chromosomal locus, the Yersinia secretion apparatus pathogenicity island (YSA PI) that encodes the Ysa TTS system. The signals to which the Ysa TTS system responds and its role in virulence remain obscure. This exploratory study was conducted to define environmental cues that promote the expression of Ysa TTS genes and to define how the Ysa TTS system influences bacterium-host interactions. Using a genetic approach, a collection of Y. enterocolitica Ysa TTS mutants was generated by mutagenesis with a transposon carrying promoterless lacZYA. This approach identified genes both within and outside of the YSA PI that contribute to Ysa TTS. Expression of these genes was regulated in response to growth phase, temperature, NaCl, and pH. Additional genetic analysis demonstrated that two regulatory genes encoding components of the YsrR-YsrS (ysrS) and RcsC-YojN-RcsB (rcsB) phosphorelay systems affect the expression of YSA PI genes and each other. The collection of Ysa TTS-defective transposon mutants, along with other strains carrying defined mutations that block Ysa and Ysc TTS, was examined for changes in virulence properties by using the BALB/c mouse model of infection. This analysis revealed that the Ysa TTS system impacts the ability of Y. enterocolitica to colonize gastrointestinal tissues. These results reveal facets of how Y. enterocolitica controls the function of the Ysa TTS system and uncovers a role for the Ysa TTS during the gastrointestinal phase of infection.
小肠结肠炎耶尔森菌的致病生物变种保留了经过充分研究的质粒编码的Ysc III型分泌(TTS)系统,该系统在毒力方面具有决定性作用。小肠结肠炎耶尔森菌生物变种1B还具有一个独特的染色体位点,即耶尔森菌分泌装置致病岛(YSA PI),它编码Ysa TTS系统。Ysa TTS系统所响应的信号及其在毒力中的作用仍不清楚。进行这项探索性研究是为了确定促进Ysa TTS基因表达的环境线索,并确定Ysa TTS系统如何影响细菌与宿主的相互作用。采用遗传学方法,通过用携带无启动子lacZYA的转座子进行诱变,构建了一组小肠结肠炎耶尔森菌Ysa TTS突变体。这种方法确定了YSA PI内外有助于Ysa TTS的基因。这些基因的表达受生长阶段、温度、NaCl和pH的调节。进一步的遗传分析表明,编码YsrR - YsrS(ysrS)和RcsC - YojN - RcsB(rcsB)磷酸转移系统组分的两个调控基因影响YSA PI基因的表达以及彼此的表达。通过使用BALB/c小鼠感染模型,检查了Ysa TTS缺陷转座子突变体的集合以及其他携带特定突变以阻断Ysa和Ysc TTS的菌株的毒力特性变化。该分析表明,Ysa TTS系统影响小肠结肠炎耶尔森菌在胃肠道组织中定殖的能力。这些结果揭示了小肠结肠炎耶尔森菌如何控制Ysa TTS系统功能的多个方面,并揭示了Ysa TTS在感染胃肠道阶段的作用。