Bent Zachary W, Poorey Kunal, Brazel David M, LaBauve Annette E, Sinha Anupama, Curtis Deanna J, House Samantha E, Tew Karen E, Hamblin Rachelle Y, Williams Kelly P, Branda Steven S, Young Glenn M, Meagher Robert J
Department of Systems Biology, Sandia National Laboratories, Livermore, California, USA
Department of Systems Biology, Sandia National Laboratories, Livermore, California, USA.
Infect Immun. 2015 Jul;83(7):2672-85. doi: 10.1128/IAI.02922-14. Epub 2015 Apr 20.
Yersinia enterocolitica is typically considered an extracellular pathogen; however, during the course of an infection, a significant number of bacteria are stably maintained within host cell vacuoles. Little is known about this population and the role it plays during an infection. To address this question and to elucidate the spatially and temporally dynamic gene expression patterns of Y. enterocolitica biovar 1B through the course of an in vitro infection, transcriptome sequencing and differential gene expression analysis of bacteria infecting murine macrophage cells were performed under four distinct conditions. Bacteria were first grown in a nutrient-rich medium at 26 °C to establish a baseline of gene expression that is unrelated to infection. The transcriptomes of these bacteria were then compared to bacteria grown in a conditioned cell culture medium at 37 °C to identify genes that were differentially expressed in response to the increased temperature and medium but not in response to host cells. Infections were then performed, and the transcriptomes of bacteria found on the extracellular surface and intracellular compartments were analyzed individually. The upregulated genes revealed potential roles for a variety of systems in promoting intracellular virulence, including the Ysa type III secretion system, the Yts2 type II secretion system, and the Tad pilus. It was further determined that mutants of each of these systems had decreased virulence while infecting macrophages. Overall, these results reveal the complete set of genes expressed by Y. enterocolitica in response to infection and provide the groundwork for future virulence studies.
小肠结肠炎耶尔森菌通常被认为是一种胞外病原体;然而,在感染过程中,大量细菌能稳定地存在于宿主细胞液泡内。人们对这群细菌及其在感染过程中所起的作用知之甚少。为了解决这个问题,并阐明小肠结肠炎耶尔森菌生物变种1B在体外感染过程中的时空动态基因表达模式,在四种不同条件下对感染小鼠巨噬细胞的细菌进行了转录组测序和差异基因表达分析。细菌首先在富含营养的培养基中于26°C培养,以建立与感染无关的基因表达基线。然后将这些细菌的转录组与在条件细胞培养基中于37°C培养的细菌进行比较,以鉴定对温度和培养基升高有差异表达但对宿主细胞无差异表达的基因。接着进行感染,并分别分析细胞外表面和细胞内区室中细菌的转录组。上调的基因揭示了多种系统在促进细胞内毒力方面的潜在作用,包括Ysa III型分泌系统、Yts2 II型分泌系统和Tad菌毛。进一步确定,这些系统的每个突变体在感染巨噬细胞时毒力都有所下降。总体而言,这些结果揭示了小肠结肠炎耶尔森菌在感染时表达的完整基因集,并为未来的毒力研究奠定了基础。