Cardona Silvia T, Choy Matthew, Hogan Andrew M
Department of Microbiology, University of Manitoba, Buller Building, Room 213, Winnipeg, MB, R3T 2N2, Canada.
Department of Medical Microbiology & Infectious Disease, University of Manitoba, Winnipeg, MB, Canada.
J Membr Biol. 2018 Feb;251(1):75-89. doi: 10.1007/s00232-017-9995-5. Epub 2017 Nov 2.
Novel therapies are urgently needed to alleviate the current crisis of multiple drug-resistant infections. The bacterial signal transduction mechanisms, known as two-component systems (TCSs), are ideal targets of novel inhibitory molecules. Highly restricted to the bacterial world, TCSs control a diverse set of cellular functions, namely virulence, response to cell envelope stress, and drug efflux. Impaired regulation of any of these aspects could affect the susceptibility of bacterial pathogens to antibiotics, which highlights the potential of TCS as targets of antibiotic adjuvant therapies. Moreover, new high-density transposon mutagenesis methods have revealed the existence of TCSs required for growth and viability. Experimental validation of gene essentiality and phenotypic characterization of knockdown mutants indicate that essential TCSs regulate aspects of the cell envelope homeostasis in coordination with cell division. In this review, we describe essential TCSs, and their potentials as targets for antibacterial molecules. We also discuss methods for the identification of small molecules that inhibit TCSs and possible reasons why antibacterial molecules targeting essential TCSs have not yet reached clinical trials.
迫切需要新的治疗方法来缓解当前多重耐药感染的危机。被称为双组分系统(TCSs)的细菌信号转导机制是新型抑制分子的理想靶点。TCSs高度局限于细菌界,控制着一系列不同的细胞功能,即毒力、对细胞壁应激的反应和药物外排。这些方面中任何一个的调节受损都可能影响细菌病原体对抗生素的敏感性,这突出了TCS作为抗生素辅助治疗靶点的潜力。此外,新的高密度转座子诱变方法揭示了生长和生存所需的TCSs的存在。基因必需性的实验验证和敲除突变体的表型特征表明,必需的TCSs与细胞分裂协同调节细胞壁稳态的各个方面。在这篇综述中,我们描述了必需的TCSs及其作为抗菌分子靶点的潜力。我们还讨论了鉴定抑制TCSs的小分子的方法,以及针对必需TCSs的抗菌分子尚未进入临床试验的可能原因。