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首页> 外文期刊>BMC Genomics >Dormant non-culturable Mycobacterium tuberculosis retains stable low-abundant mRNA
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Dormant non-culturable Mycobacterium tuberculosis retains stable low-abundant mRNA

机译:休眠不可培养的结核分枝杆菌保留稳定的低丰度mRNA

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Dormant Mycobacterium tuberculosis bacilli are believed to play an important role in latent tuberculosis infection. Previously, we have demonstrated that cultivation of M. tuberculosis in K+-deficient medium resulted in generation of dormant cells. These bacilli were non-culturable on solid media (a key feature of dormant M. tuberculosis in vivo) and characterized by low metabolism and tolerance to anti-tuberculosis drugs. The dormant bacteria demonstrated a high potential to reactivation after K+ reintroduction even after prolonged persistence under rifampicin. In this work, we studied the transcriptome and stability of transcripts in persisting dormant bacilli under arrest of mRNA de novo synthesis. RNA-seq-based analysis of the dormant non-culturable population obtained under rifampicin exposure revealed a 30–50-fold decrease of the total mRNA level, indicating global transcriptional repression. However, the analysis of persisting transcripts displayed a cohort of mRNA molecules coding for biosynthetic enzymes, proteins involved in adaptation and repair processes, detoxification, and control of transcription initiation. This ‘dormant transcriptome’ demonstrated considerable stability during M. tuberculosis persistence and mRNA de novo synthesis arrest. On the contrary, several small non-coding RNAs showed increased abundance on dormancy. Interestingly, M. tuberculosis entry into dormancy was accompanied by the cleavage of 23S ribosomal RNA at a specific point located outside the ribosome catalytic center. Dormant non-culturable M. tuberculosis bacilli are characterized by a global transcriptional repression. At the same time, the dormant bacilli retain low-abundant mRNAs, which are considerably stable during in vitro persistence, reflecting their readiness for translation upon early resuscitation steps. Increased abundance of non-coding RNAs on dormancy may indicate their role in the entry into and maintenance of M. tuberculosis dormant non-culturable state.
机译:人们认为休眠结核分枝杆菌在潜伏性结核感染中起重要作用。以前,我们已经证明在K +缺乏培养基中培养结核分枝杆菌会导致休眠细胞的产生。这些杆菌不可在固体培养基上培养(体内休眠的结核分枝杆菌的一个关键特征),其特点是新陈代谢低和对抗结核药物的耐受性。即使在利福平下长时间持续存在,休眠细菌也显示出在重新导入K +后具有很高的再活化潜能。在这项工作中,我们研究了转录的组学和转录本在持久休眠细菌在mRNA从头合成停止作用下的稳定性。在利福平暴露下获得的休眠的不可培养种群的基于RNA-seq的分析显示,总mRNA水平降低了30–50倍,表明总体转录抑制。但是,对持久性转录本的分析显示出一群编码生物合成酶,参与适应和修复过程,排毒和控制转录起始的蛋白质的mRNA分子。该“休眠转录组”在结核分枝杆菌持续存在和从头合成mRNA停止期间表现出相当大的稳定性。相反,一些小的非编码RNA显示出更多的休眠状态。有趣的是,结核分枝杆菌进入休眠状态,伴随着23S核糖体RNA的切割,位于核糖体催化中心之外的特定位置。休眠的不可培养的结核分枝杆菌的特征在于整体转录抑制。同时,休眠的细菌保留了低丰度的mRNA,这些mRNA在体外持久性过程中相当稳定,反映出它们准备在早期复苏步骤中进行翻译。非编码RNA的休眠数量增加可能表明它们在结核分枝杆菌休眠不可培养状态的进入和维持中的作用。

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