Wang Yufei, Ke Yuehua, Xu Jie, Wang Ligui, Wang Tongkun, Liang Hui, Zhang Wei, Gong Chunli, Yuan Jiuyun, Zhuang Yubin, An Chang, Lei Shuangshuang, Du Xinying, Wang Zhoujia, Li Wenna, Yuan Xitong, Huang Liuyu, Yang Xiaoli, Chen Zeliang
Department of Laboratory Medicine, The General Hospital of Chinese People's Armed Police Forces , Beijing , China.
Department of Infectious Disease Control, Institute of Disease Control and Prevention, Academy of Military Medical Sciences , Beijing , China.
Front Microbiol. 2015 Mar 19;6:164. doi: 10.3389/fmicb.2015.00164. eCollection 2015.
Bacterial small non-coding RNAs (sRNAs) are gene expression modulators respond to environmental changes, stressful conditions, and pathogenesis. In this study, by using a combined bioinformatic and experimental approach, eight novel sRNA genes were identified in intracellular pathogen Brucella melitensis. BSR0602, one sRNA that was highly induced in stationary phase, was further examined and found to modulate the intracellular survival of B. melitensis. BSR0602 was present at very high levels in vitro under stresses similar to those encountered during infection in host macrophages. Furthermore, BSR0602 was found to be highly expressed in the spleens of infected mice, suggesting its potential role in the control of pathogenesis. BSR0602 targets the mRNAs coding for gntR, a global transcriptional regulator, which is required for B. melitensis virulence. Overexpression of BSR0602 results in distinct reduction in the gntR mRNA level. B. melitensis with high level of BSR0602 is defective in bacteria intracellular survival in macrophages and defective in growth in the spleens of infected mice. Therefore, BSR0602 may directly inhibit the expression of gntR, which then impairs Brucellae intracellular survival and contributes to Brucella infection. Our findings suggest that BSR0602 is responsible for bacterial adaptation to stress conditions and thus modulate B. melitensis intracellular survival.
细菌小非编码RNA(sRNA)是响应环境变化、应激条件和发病机制的基因表达调节剂。在本研究中,通过结合生物信息学和实验方法,在细胞内病原体布鲁氏菌中鉴定出8个新的sRNA基因。对其中一个在稳定期高度诱导的sRNA BSR0602进行了进一步研究,发现它可调节布鲁氏菌的细胞内存活。在类似于宿主巨噬细胞感染期间遇到的应激条件下,BSR0602在体外的水平非常高。此外,发现BSR0602在感染小鼠的脾脏中高度表达,表明其在发病机制控制中的潜在作用。BSR0602靶向编码全局转录调节因子gntR的mRNA,gntR是布鲁氏菌毒力所必需的。BSR0602的过表达导致gntR mRNA水平明显降低。具有高水平BSR0602的布鲁氏菌在巨噬细胞中的细胞内存活存在缺陷,并且在感染小鼠的脾脏中生长存在缺陷。因此,BSR0602可能直接抑制gntR的表达,进而损害布鲁氏菌的细胞内存活并导致布鲁氏菌感染。我们的研究结果表明,BSR0602负责细菌对应激条件的适应,从而调节布鲁氏菌的细胞内存活。