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A computational strategy for the search of regulatory small RNAs in Actinobacillus pleuropneumoniae

机译:在胸膜肺炎放线杆菌中搜索调节性小RNA的计算策略

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Bacterial regulatory small RNAs (sRNAs) play important roles in gene regulation and are frequently connected to the expression of virulence factors in diverse bacteria. Only a few sRNAs have been described for Pasteurellaceae pathogens and no in-depth analysis of sRNAs has been described for Actinobacillus pleuropneumoniae, the causative agent of porcine pleuropneumonia, responsible for considerable losses in the swine industry. To search for sRNAs in A. pleuropneumoniae, we developed a strategy for the computational analysis of the bacterial genome by using four algorithms with different approaches, followed by experimental validation. The coding strand and expression of 17 out of 23 RNA candidates were confirmed by Northern blotting, RT-PCR, and RNA sequencing. Among them, two are likely riboswitches, three are housekeeping regulatory RNAs, two are the widely studied GcvB and 6S sRNAs, and 10 are putative novel trans-acting sRNAs, never before described for any bacteria. The latter group has several potential mRNA targets, many of which are involved with virulence, stress resistance, or metabolism, and connect the sRNAs in a complex gene regulatory network. The sRNAs identified are well conserved among the Pasteurellaceae that are evolutionarily closer to A. pleuropneumoniae and/or share the same host. Our results show that the combination of newly developed computational programs can be successfully utilized for the discovery of novel sRNAs and indicate an intricate system of gene regulation through sRNAs in A. pleuropneumoniae and in other Pasteurellaceae, thus providing clues for novel aspects of virulence that will be explored in further studies.
机译:细菌调控小RNA(sRNA)在基因调控中发挥重要作用,并经常与各种细菌中毒力因子的表达有关。对于巴斯德杆菌病原体,仅描述了几种sRNA,而对于猪胸膜肺炎的致病因子胸膜肺炎放线杆菌却没有对sRNA的深入分析,这在猪业造成了巨大损失。为了在胸膜肺炎链球菌中搜索sRNA,我们开发了一种策略,通过使用四种具有不同方法的算法对细菌基因组进行计算分析,然后进行实验验证。通过RNA印迹,RT-PCR和RNA测序证实了23种RNA候选物中的17种的编码链和表达。其中,两个可能是核糖开关,三个是管家调节RNA,两个是广泛研究的GcvB和6S sRNA,还有十个是推定的新型反式sRNA,以前从未对任何细菌进行过描述。后一组具有几个潜在的mRNA靶标,其中许多与毒力,抗逆性或代谢有关,并将sRNA连接在复杂的基因调控网络中。所鉴定的sRNA在巴斯德杆菌科中是保守的,它们进化上更靠近胸膜肺炎放线杆菌和/或共享同一宿主。我们的结果表明,新开发的计算程序的组合可以成功地用于发现新的sRNA,并表明通过胸膜肺炎放线杆菌和其他巴斯德杆菌科中的sRNA进行复杂的基因调控,从而为新的毒力方面提供了线索有待进一步研究。

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