Gupta Rinki, Singh Mangal, Pathania Ranjana
Department of Biosciences and Bioengineering, Indian Institute of Technology Roorkee Roorkee - 247 667 Uttarakhand India
RSC Med Chem. 2023 Aug 30;14(11):2125-2154. doi: 10.1039/d3md00143a. eCollection 2023 Nov 15.
Antimicrobial resistance (AMR) in bacterial pathogens is a worldwide health issue. The innovation gap in discovering new antibiotics has remained a significant hurdle in combating the AMR problem. Currently, antibiotics target various vital components of the bacterial cell envelope, nucleic acid and protein biosynthesis machinery and metabolic pathways essential for bacterial survival. The critical role of the bacterial cell envelope in cell morphogenesis and integrity makes it an attractive drug target. While a significant number of in-clinic antibiotics target peptidoglycan biosynthesis, several components of the bacterial cell envelope have been overlooked. This review focuses on various antibacterial targets in the bacterial cell wall and the strategies employed to find their novel inhibitors. This review will further elaborate on combining forward and reverse chemical genetic approaches to discover antibacterials that target the bacterial cell envelope.
细菌病原体中的抗菌药物耐药性(AMR)是一个全球性的健康问题。在发现新抗生素方面的创新差距一直是对抗AMR问题的重大障碍。目前,抗生素作用于细菌细胞壁包膜的各种重要成分、核酸和蛋白质生物合成机制以及细菌生存所必需的代谢途径。细菌细胞壁包膜在细胞形态发生和完整性方面的关键作用使其成为一个有吸引力的药物靶点。虽然大量临床使用的抗生素作用于肽聚糖生物合成,但细菌细胞壁包膜的几个成分一直被忽视。本综述重点关注细菌细胞壁中的各种抗菌靶点以及寻找其新型抑制剂所采用的策略。本综述还将进一步阐述如何结合正向和反向化学遗传学方法来发现作用于细菌细胞壁包膜的抗菌药物。