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PdtaS 缺乏影响分枝杆菌对核糖体靶向抗生素的抗性。

PdtaS Deficiency Affects Resistance of Mycobacteria to Ribosome Targeting Antibiotics.

作者信息

Dadura Karolina, Płocińska Renata, Rumijowska-Galewicz Anna, Płociński Przemysław, Żaczek Anna, Dziadek Bożena, Zaborowski Andrzej, Dziadek Jarosław

机构信息

Institute for Medical Biology, Polish Academy of Sciences, Łódź, Poland.

Department of Biochemistry and Cell Biology, University of Rzeszów, Rzeszów, Poland.

出版信息

Front Microbiol. 2017 Nov 3;8:2145. doi: 10.3389/fmicb.2017.02145. eCollection 2017.

Abstract

Two-component regulatory systems (TCSSs) are key regulatory elements responsible for the adaptation of bacteria to environmental stresses. A classical TCSS is typically comprised of a sensory histidine kinase and a corresponding response regulator. Here, we used homologous recombination to construct a mutant defective in the synthesis of cytosolic histidine kinase PdtaS (Msmeg_1918). The resulting Δ mutant strain was tested in the Phenotype Microarray screening system, which allowed us to identify aminoglycoside antibiotic sensitivity, tetracyclines antibiotic resistance as well as membrane transport and respiration, as the main processes affected by removal of . The antibiotic sensitivity profiles were confirmed by survival assessment and complementation studies. To gain insight into the molecular mechanisms responsible for the observed phenotype, we compared ribosomal RNA and protein profiles of the mutant and wild-type strains. We carried out Northern blotting and qRT-PCR to compare rRNA levels and analyzed ribosome sedimentation patterns of the wild-type and mutant strains on sucrose gradients. Isolated ribosomes were further used to estimate relative abundance of individual proteins in the ribosomal subunits using label free mass spectrometry analysis. Additionally, the Δ mutant revealed lower activity of the respiratory chain as measured by the rate of TTC (triphenyltetrazolium chloride) reduction, while at the same time showing only insignificant changes in the uptake of aminoglycosides. We postulate that deficiency of PdtaS affects the oxidative respiration rates and ribosomal composition causing relevant changes to intrinsic resistance or susceptibility to antibiotics targeting ribosomes, which are commonly used to treat mycobacterial infections.

摘要

双组分调节系统(TCSSs)是负责细菌适应环境压力的关键调节元件。经典的双组分调节系统通常由一个传感组氨酸激酶和一个相应的反应调节因子组成。在此,我们利用同源重组构建了一个胞质组氨酸激酶PdtaS(Msmeg_1918)合成缺陷的突变体。在表型微阵列筛选系统中对所得的Δ突变株进行了测试,这使我们能够确定氨基糖苷类抗生素敏感性、四环素类抗生素抗性以及膜转运和呼吸作用,这些是去除该激酶后受影响的主要过程。通过生存评估和互补研究证实了抗生素敏感性谱。为了深入了解导致观察到的表型的分子机制,我们比较了突变株和野生型菌株的核糖体RNA和蛋白质谱。我们进行了Northern印迹和qRT-PCR以比较rRNA水平,并分析了野生型和突变株在蔗糖梯度上的核糖体沉降模式。使用无标记质谱分析进一步利用分离的核糖体来估计核糖体亚基中各个蛋白质的相对丰度。此外,通过TTC(氯化三苯基四氮唑)还原速率测量,Δ突变株显示出较低的呼吸链活性,而与此同时,其氨基糖苷类药物摄取仅显示出微不足道的变化。我们推测,PdtaS的缺陷会影响氧化呼吸速率和核糖体组成,从而导致对常用于治疗分枝杆菌感染的靶向核糖体的抗生素的内在抗性或敏感性发生相关变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27ad/5676007/0d6f931a82a1/fmicb-08-02145-g001.jpg

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