Division of Infectious Diseases, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Department of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Infect Immun. 2018 Feb 20;86(3). doi: 10.1128/IAI.00626-17. Print 2018 Mar.
infection and high dietary salt intake are risk factors for the development of gastric adenocarcinoma. One possible mechanism by which a high-salt diet could influence gastric cancer risk is by modulating gene expression. In this study, we utilized transcriptome sequencing (RNA-seq) methodology to compare the transcriptional profiles of grown in media containing different concentrations of sodium chloride. We identified 118 differentially expressed genes (65 upregulated and 53 downregulated in response to high-salt conditions), including multiple members of 14 operons. Twenty-nine of the differentially expressed genes encode proteins previously shown to undergo salt-responsive changes in abundance, based on proteomic analyses. Real-time reverse transcription (RT)-PCR analyses validated differential expression of multiple genes encoding outer membrane proteins, including adhesins (SabA and HopQ) and proteins involved in iron acquisition (FecA2 and FecA3). Transcript levels of , , and are increased under high-salt conditions, whereas transcript levels of and are decreased under high-salt conditions. Transcription of , , , and is derepressed in an mutant strain, but salt-responsive transcription of these genes is not mediated by the ArsRS two-component system, and the CrdRS and FlgRS two-component systems do not have any detectable effects on transcription of these genes. In summary, these data provide a comprehensive view of transcriptional alterations that occur in response to high-salt environmental conditions.
感染和高盐饮食是胃腺癌发展的危险因素。高盐饮食可能通过调节基因表达影响胃癌风险的一个可能机制。在这项研究中,我们利用转录组测序(RNA-seq)方法比较了在含有不同浓度氯化钠的培养基中生长的的转录谱。我们鉴定出 118 个差异表达基因(65 个在高盐条件下上调,53 个下调),包括 14 个操纵子的多个成员。29 个差异表达基因编码的蛋白质以前根据蛋白质组分析显示丰度发生盐响应变化。实时逆转录(RT)-PCR 分析验证了多个编码外膜蛋白的基因的差异表达,包括粘附素(SabA 和 HopQ)和参与铁摄取的蛋白质(FecA2 和 FecA3)。在高盐条件下, 、 、 和 的转录水平增加,而在高盐条件下, 、 和 的转录水平降低。在 突变株中, 、 、 和 的转录被解除阻遏,但这些基因的盐响应转录不是由 ArsRS 双组分系统介导的,CrdRS 和 FlgRS 双组分系统对这些基因的转录没有任何可检测到的影响。总之,这些数据提供了一个全面的视角,了解了 对高盐环境条件的反应所发生的转录改变。