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Identification of a Novel Small Non-Coding RNA Modulating the Intracellular Survival of Brucella melitensis

机译:新型小型非编码RNA调控布鲁氏菌布鲁氏菌细胞内存活的鉴定。

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摘要

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.
机译:细菌小非编码RNA(sRNA)是基因表达调节剂,可响应环境变化,压力条件和发病机理。在这项研究中,通过结合使用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八个新的sRNA基因。 BSR0602,一种在固定相中被高度诱导的sRNA,经过进一步检查,发现它调节了B. melitensis的细胞内存活。 BSR0602在体外的压力很高,与宿主巨噬细胞在感染过程中遇到的压力相似。此外,发现BSR0602在受感染小鼠的脾脏中高度表达,表明其在控制发病机理中的潜在作用。 BSR0602靶向编码gntR的mRNA,而gntR是melitensis毒力所必需的。 BSR0602的过表达导致gntR mRNA水平明显降低。高水平BSR0602的B. melitensis在巨噬细胞的细菌细胞内存活缺陷,在被感染小鼠的脾脏中生长缺陷。因此,BSR0602可能直接抑制gntR的表达,从而损害布鲁氏菌细胞内存活,并导致布鲁氏菌感染。我们的研究结果表明BSR0602负责细菌适应压力条件,从而调节B. melitensis细胞内存活。

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