Liu Qianhong, Liu Xingyu, Yan Feng, He Yuhua, Wei Jie, Zhang Yuanyuan, Liu Lu, Sun Youpeng
Jilin Agricultural Science and Technology University, Jilin 132101, China.
Guangzhou Airport Entry-Exit Inspection and Quarantine Brueau of P.R.C, Guangzhou 510470, China.
Microb Pathog. 2016 Feb;91:92-8. doi: 10.1016/j.micpath.2015.11.007. Epub 2015 Dec 12.
Brucella melitensis, encounters a very stressful environment in phagosomes, especially low pH levels. So identifying the genes that contribute to the replication and survival within an acidic environment is critical in understanding the pathogenesis of the Brucella bacteria. In our research, comparative transcriptome with RNA-seq were used to analyze the changes of genes in normal-medium culture and in pH4.4-medium culture. The results reveal that 113 genes expressed with significant differences (|log2Ratio| ≥ 3); about 44% genes expressed as up-regulated. With GO term analysis, structural constituent of the ribosome, rRNA binding, structural molecule activity, and cation-transporting ATPase activity were significantly enriched (p-value ≤ 0.05). These genes distributed in 51 pathways, in which ribosome and photosynthesis pathways were significantly enriched. Six pathways (oxidative phosphorylation, iron-transporting, bacterial secretion system, transcriptional regulation, two-component system, and ABC transporters pathways) tightly related to the intracellular survival and virulence of Brucella were analyzed. A two-component response regulator gene in the transcriptional regulation pathway, identified through gene deletion and complementary technologies, played an important role in the resistance to the acid-resistance and virulence of Brucella.
羊种布鲁氏菌在吞噬体中会遇到非常恶劣的环境,尤其是低pH值水平。因此,鉴定有助于在酸性环境中复制和存活的基因对于理解布鲁氏菌的发病机制至关重要。在我们的研究中,利用RNA测序进行比较转录组分析,以分析正常培养基培养和pH4.4培养基培养中基因的变化。结果显示,有113个基因表达存在显著差异(|log2Ratio|≥3);约44%的基因表达上调。通过基因本体(GO)术语分析,核糖体的结构成分、rRNA结合、结构分子活性和阳离子转运ATP酶活性显著富集(p值≤0.05)。这些基因分布在51条通路中,其中核糖体和光合作用通路显著富集。分析了与布鲁氏菌细胞内存活和毒力密切相关的6条通路(氧化磷酸化、铁转运、细菌分泌系统、转录调控、双组分系统和ABC转运蛋白通路)。通过基因缺失和互补技术鉴定出转录调控通路中的一个双组分反应调节基因,该基因在布鲁氏菌的耐酸性和毒力抗性中起重要作用。