Microbial Pathogenesis Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA.
BMC Genomics. 2014 Mar 25;15:229. doi: 10.1186/1471-2164-15-229.
Upon infection of a mammalian host, Bacillus anthracis responds to host cues, and particularly to elevated temperature (37°C) and bicarbonate/CO2 concentrations, with increased expression of virulence factors that include the anthrax toxins and extracellular capsular layer. This response requires the presence of the pXO1 virulence plasmid-encoded pleiotropic regulator AtxA. To better understand the genetic basis of this response, we utilized a controlled in vitro system and Next Generation sequencing to determine and compare RNA expression profiles of the parental strain and an isogenic AtxA-deficient strain in a 2 × 2 factorial design with growth environments containing or lacking carbon dioxide.
We found 15 pXO1-encoded genes and 3 chromosomal genes that were strongly regulated by the separate or synergistic actions of AtxA and carbon dioxide. The majority of the regulated genes responded to both AtxA and carbon dioxide rather than to just one of these factors. Interestingly, we identified two previously unrecognized small RNAs that are highly expressed under physiological carbon dioxide concentrations in an AtxA-dependent manner. Expression levels of the two small RNAs were found to be higher than that of any other gene differentially expressed in response to these conditions. Secondary structure and small RNA-mRNA binding predictions for the two small RNAs suggest that they may perform important functions in regulating B. anthracis virulence.
A majority of genes on the virulence plasmid pXO1 that are regulated by the presence of either CO2 or AtxA separately are also regulated synergistically in the presence of both. These results also elucidate novel pXO1-encoded small RNAs that are associated with virulence conditions.
当感染哺乳动物宿主时,炭疽芽孢杆菌会对宿主发出的信号做出反应,特别是对温度升高(37°C)和碳酸氢盐/二氧化碳浓度的变化做出反应,从而增加包括炭疽毒素和细胞外荚膜层在内的毒力因子的表达。这种反应需要存在 pXO1 毒力质粒编码的多效调节因子 AtxA。为了更好地理解这种反应的遗传基础,我们利用了一个受控的体外系统和下一代测序技术,以确定并比较在含有或不含有二氧化碳的 2×2 析因设计的生长环境中,亲本菌株和同源 AtxA 缺陷菌株的 RNA 表达谱。
我们发现了 15 个 pXO1 编码基因和 3 个染色体基因,这些基因受到 AtxA 和二氧化碳的单独或协同作用的强烈调节。大多数受调节的基因对 AtxA 和二氧化碳都有反应,而不仅仅是对其中一个因素有反应。有趣的是,我们鉴定了两个以前未被识别的小 RNA,它们在生理二氧化碳浓度下以 AtxA 依赖的方式高度表达。这两个小 RNA 的表达水平被发现高于对这些条件有差异表达的任何其他基因的表达水平。对这两个小 RNA 的二级结构和小 RNA-mRNA 结合预测表明,它们可能在调节炭疽杆菌毒力方面发挥重要作用。
在存在 CO2 或 AtxA 的情况下分别调节的毒力质粒 pXO1 上的大多数基因,在两者同时存在的情况下也协同调节。这些结果还阐明了与毒力条件相关的新型 pXO1 编码小 RNA。