Rajput Akanksha, Seif Yara, Choudhary Kumari Sonal, Dalldorf Christopher, Poudel Saugat, Monk Jonathan M, Palsson Bernhard O
Systems Biology Research Group, Department of Bioengineering, University of California, San Diego, San Diego, California, USA.
Systems Biology Research Group, Department of Bioengineering, University of California, San Diego, San Diego, California, USA
mSystems. 2021 Jan 26;6(1):e00981-20. doi: 10.1128/mSystems.00981-20.
The two-component system (TCS) helps bacteria sense and respond to environmental stimuli through histidine kinases and response regulators. TCSs are the largest family of multistep signal transduction processes, and they are involved in many important cellular processes such as antibiotic resistance, pathogenicity, quorum sensing, osmotic stress, and biofilms. Here, we perform the first comprehensive study to highlight the role of TCSs as potential drug targets against ESKAPEE (, , , , , spp., and ) pathogens through annotation, mapping, pangenomic status, gene orientation, and sequence variation analysis. The distribution of the TCSs is group specific with regard to Gram-positive and Gram-negative bacteria, except for KdpDE. The TCSs among ESKAPEE pathogens form closed pangenomes, except for Furthermore, their conserved nature due to closed pangenomes might make them good drug targets. Fitness score analysis suggests that any mutation in some TCSs such as BaeSR, ArcBA, EvgSA, and AtoSC, etc., might be lethal to the cell. Taken together, the results of this pangenomic assessment of TCSs reveal a range of strategies deployed by the ESKAPEE pathogens to manifest pathogenicity and antibiotic resistance. This study further suggests that the conserved features of TCSs might make them an attractive group of potential targets with which to address antibiotic resistance. The ESKAPEE pathogens are the leading cause of health care-associated infections worldwide. Two-component systems (TCSs) can be used as effective targets against pathogenic bacteria since they are ubiquitous and manage various vital functions such as antibiotic resistance, virulence, biofilms, quorum sensing, and pH balance, among others. This study provides a comprehensive overview of the pangenomic status of the TCSs among ESKAPEE pathogens. The annotation and pangenomic analysis of TCSs show that they are significantly distributed and conserved among the pathogens, as most of them form closed pangenomes. Furthermore, our analysis also reveals that the removal of the TCSs significantly affects the fitness of the cell. Hence, they may be used as promising drug targets against bacteria.
双组分系统(TCS)通过组氨酸激酶和反应调节因子帮助细菌感知并响应环境刺激。TCS是多步信号转导过程中最大的家族,它们参与许多重要的细胞过程,如抗生素抗性、致病性、群体感应、渗透胁迫和生物膜形成。在此,我们进行了首次全面研究,通过注释、图谱绘制、泛基因组状态、基因方向和序列变异分析,突出TCS作为针对ESKAPEE(粪肠球菌、屎肠球菌、金黄色葡萄球菌、肺炎克雷伯菌、鲍曼不动杆菌、铜绿假单胞菌和肠杆菌属)病原体的潜在药物靶点的作用。除了KdpDE外,TCS在革兰氏阳性菌和革兰氏阴性菌中的分布具有菌群特异性。除了[此处原文缺失相关内容]外,ESKAPEE病原体中的TCS形成封闭的泛基因组。此外,由于封闭的泛基因组,它们的保守性质可能使它们成为良好的药物靶点。适应性评分分析表明,某些TCS(如BaeSR、ArcBA、EvgSA和AtoSC等)中的任何突变可能对细胞是致命的。综上所述,TCS的泛基因组评估结果揭示了ESKAPEE病原体为表现出致病性和抗生素抗性而采用的一系列策略。这项研究进一步表明,TCS的保守特征可能使它们成为解决抗生素抗性问题的有吸引力的潜在靶点群体。ESKAPEE病原体是全球医疗保健相关感染的主要原因。双组分系统(TCS)可作为针对病原菌的有效靶点,因为它们普遍存在并管理各种重要功能,如抗生素抗性、毒力、生物膜、群体感应和pH平衡等。本研究全面概述了ESKAPEE病原体中TCS的泛基因组状态。TCS的注释和泛基因组分析表明,它们在病原体中显著分布且保守,因为它们中的大多数形成封闭的泛基因组。此外,我们的分析还表明,去除TCS会显著影响细胞的适应性。因此,它们可作为针对细菌的有前景的药物靶点。