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VapC Toxins from Mycobacterium tuberculosis Are Ribonucleases that Differentially Inhibit Growth and Are Neutralized by Cognate VapB Antitoxins

机译:来自结核分枝杆菌的VapC毒素是核糖核酸酶,可差异地抑制生长,并被同源VapB抗毒素中和。

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摘要

The chromosome of Mycobacterium tuberculosis (Mtb) encodes forty seven toxin-antitoxin modules belonging to the VapBC family. The role of these modules in the physiology of Mtb and the function(s) served by their expansion are unknown. We investigated ten vapBC modules from Mtb and the single vapBC from M. smegmatis. Of the Mtb vapCs assessed, only Rv0549c, Rv0595c, Rv2549c and Rv2829c were toxic when expressed from a tetracycline-regulated promoter in M. smegmatis. The same genes displayed toxicity when conditionally expressed in Mtb. Toxicity of Rv2549c in M. smegmatis correlated with the level of protein expressed, suggesting that the VapC level must exceed a threshold for toxicity to be observed. In addition, the level of Rv2456 protein induced in M. smegmatis was markedly lower than Rv2549c, which may account for the lack of toxicity of this and other VapCs scored as ‘non-toxic’. The growth inhibitory effects of toxic VapCs were neutralized by expression of the cognate VapB as part of a vapBC operon or from a different chromosomal locus, while that of non-cognate antitoxins did not. These results demonstrated a specificity of interaction between VapCs and their cognate VapBs, a finding corroborated by yeast two-hybrid analyses. Deletion of selected vapC or vapBC genes did not affect mycobacterial growth in vitro, but rendered the organisms more susceptible to growth inhibition following toxic VapC expression. However, toxicity of ‘non-toxic’ VapCs was not unveiled in deletion mutant strains, even when the mutation eliminated the corresponding cognate VapB, presumably due to insufficient levels of VapC protein. Together with the ribonuclease (RNase) activity demonstrated for Rv0065 and Rv0617 – VapC proteins with similarity to Rv0549c and Rv3320c, respectively – these results suggest that the VapBC family potentially provides an abundant source of RNase activity in Mtb, which may profoundly impact the physiology of the organism.
机译:结核分枝杆菌(Mtb)的染色体编码属于VapBC家族的47个毒素-抗毒素模块。这些模块在Mtb生理学中的作用及其扩展所发挥的作用尚不清楚。我们研究了来自Mtb的十个vapBC模块和来自耻垢分枝杆菌的单个vapBC。在经耻垢分枝杆菌中由四环素调节的启动子表达时,在评估的Mtb vapC中,只有Rv0549c,Rv0595c,Rv2549c和Rv2829c有毒。当在Mtb中有条件表达时,相同的基因显示出毒性。 Rv2549c在耻垢分枝杆菌中的毒性与表达的蛋白质水平相关,这表明VapC水平必须超过观察到的毒性阈值。此外,在耻垢分枝杆菌中诱导的Rv2456蛋白水平明显低于Rv2549c,这可能解释了这种和其他被评定为“无毒”的VapC的毒性。有毒VapCs的生长抑制作用通过作为VapBC操纵子一部分或来自不同染色体基因座的同源VapB的表达而被中和,而非同源抗毒素则没有。这些结果证明了VapCs及其同源VapBs之间相互作用的特异性,这一发现被酵母两杂交分析所证实。选定的vapC或vapBC基因的删除不会影响分枝杆菌的体外生长,但是使该生物体在毒性VapC表达后更容易受到生长抑制的影响。但是,即使突变消除了相应的同源VapB,也可能是由于缺乏足够的VapC蛋白水平,因此在缺失突变株中未显示出“无毒” VapCs的毒性。结合Rv0065和Rv0617 – VapC蛋白所证实的核糖核酸酶(RNase)活性,分别与Rv0549c和Rv3320c相似,这些结果表明VapBC家族潜在地提供了Mtb中RNase活性的丰富来源,这可能会深刻影响Mtb的生理学。有机体。

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