小的非编码RNA B11调节脓肿分枝杆菌毒力的多个方面。

IF 6.7 1区 医学 Q1 Immunology and Microbiology PLoS Pathogens Pub Date : 2023-08-21 eCollection Date: 2023-08-01 DOI:10.1371/journal.ppat.1011575
Michal Bar-Oz, Maria Carla Martini, Maria Natalia Alonso, Michal Meir, Nicola Ivan Lore, Paolo Miotto, Camilla Riva, Shiva K Angala, Junpei Xiao, Catherine S Masiello, Maria-Anna Misiakou, Huaming Sun, Justin K Moy, Mary Jackson, Helle Krogh Johansen, Daniela Maria Cirillo, Scarlet S Shell, Daniel Barkan
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引用次数: 0

摘要

脓肿分枝杆菌引起囊性纤维化患者的严重疾病。脓肿分枝杆菌对小调节RNA(sRNA)在基因调控中的作用知之甚少。我们发现sRNAB11控制该病原体的基因表达和毒力相关表型。光滑菌株ATCC_19977的B11缺失产生了一个粗糙菌株,在多种感染模型中增加了促炎信号和毒力,并增加了对抗生素的耐药性。对临床分离株队列的检查确定了具有B11突变或表达减少的分离株。我们使用RNAseq和蛋白质组学来研究B11对基因表达的影响,并测试临床分离株中发现的突变的影响。超过200个基因在缺失突变体中差异表达。具有临床B11突变的菌株显示出与缺失突变相似的表达趋势,表明功能部分丧失。在B11突变体中上调的基因中,在其预测的核糖体结合位点(RBS)中具有B11互补序列的基因有很强的富集,这与B11作为负调控因子的作用一致,该负调控因子通过碱基配对抑制翻译为RBS。比较蛋白质组类似地显示上调的蛋白质强烈富集B11互补序列。有趣的是,在没有B11的情况下上调的基因包括ESX-4分泌系统的成分,这对脓肿分枝杆菌的毒力至关重要。这些基因中的许多在其RBS处具有B11互补序列,我们表明这足以通过直接结合介导B11的抑制。总之,我们的数据表明,B11作为一种直接的负调控因子,介导(可能是间接的)正调控,对脓肿分枝杆菌的基因表达和临床重要表型具有多效性影响。临床菌株中亚形态B11突变的存在与在某些临床情况下较低的B11活性可能对脓肿分枝杆菌有利的观点一致。这是首次报道sRNA在脓肿分枝杆菌中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The small non-coding RNA B11 regulates multiple facets of Mycobacterium abscessus virulence.

Mycobacterium abscessus causes severe disease in patients with cystic fibrosis. Little is known in M. abscessus about the roles of small regulatory RNAs (sRNA) in gene regulation. We show that the sRNA B11 controls gene expression and virulence-associated phenotypes in this pathogen. B11 deletion from the smooth strain ATCC_19977 produced a rough strain, increased pro-inflammatory signaling and virulence in multiple infection models, and increased resistance to antibiotics. Examination of clinical isolate cohorts identified isolates with B11 mutations or reduced expression. We used RNAseq and proteomics to investigate the effects of B11 on gene expression and test the impact of mutations found in clinical isolates. Over 200 genes were differentially expressed in the deletion mutant. Strains with the clinical B11 mutations showed expression trends similar to the deletion mutant, suggesting partial loss of function. Among genes upregulated in the B11 mutant, there was a strong enrichment for genes with B11-complementary sequences in their predicted ribosome binding sites (RBS), consistent with B11 functioning as a negative regulator that represses translation via base-pairing to RBSs. Comparing the proteomes similarly revealed that upregulated proteins were strongly enriched for B11-complementary sequences. Intriguingly, genes upregulated in the absence of B11 included components of the ESX-4 secretion system, critical for M. abscessus virulence. Many of these genes had B11-complementary sequences at their RBSs, which we show is sufficient to mediate repression by B11 through direct binding. Altogether, our data show that B11 acts as a direct negative regulator and mediates (likely indirect) positive regulation with pleiotropic effects on gene expression and clinically important phenotypes in M. abscessus. The presence of hypomorphic B11 mutations in clinical strains is consistent with the idea that lower B11 activity may be advantageous for M. abscessus in some clinical contexts. This is the first report on an sRNA role in M. abscessus.

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来源期刊
PLoS Pathogens
PLoS Pathogens 生物-病毒学
CiteScore
11.40
自引率
3.00%
发文量
598
审稿时长
2 months
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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