Heilongjiang Key Laboratory for Animal Disease Control and Pharmaceutical Development, Northeast Agricultural University, Harbin 150036, China.
Department of Basic Veterinary Science, College of Veterinary Medicine, Northeast Agricultural University, Harbin 150036, China.
Int J Mol Sci. 2021 Dec 24;23(1):197. doi: 10.3390/ijms23010197.
Multidrug bacterial resistance endangers clinically effective antimicrobial therapy and continues to cause major public health problems, which have been upgraded to unprecedented levels in recent years, worldwide. β-Lactam antibiotics have become an important weapon to fight against pathogen infections due to their broad spectrum. Unfortunately, the emergence of antibiotic resistance genes (ARGs) has severely astricted the application of β-lactam antibiotics. Of these, New Delhi metallo-β-lactamase-1 (NDM-1) represents the most disturbing development due to its substrate promiscuity, the appearance of variants, and transferability. Given the clinical correlation of β-lactam antibiotics and NDM-1-mediated resistance, the discovery, and development of combination drugs, including NDM-1 inhibitors, for NDM-1 bacterial infections, seems particularly attractive and urgent. This review summarizes the research related to the development and optimization of effective NDM-1 inhibitors. The detailed generalization of crystal structure, enzyme activity center and catalytic mechanism, variants and global distribution, mechanism of action of existing inhibitors, and the development of scaffolds provides a reference for finding potential clinically effective NDM-1 inhibitors against drug-resistant bacteria.
多药耐药细菌耐药性危及临床有效抗菌治疗,并继续在全球范围内造成重大公共卫生问题,近年来这些问题已升级到前所未有的水平。由于广谱性,β-内酰胺类抗生素已成为对抗病原体感染的重要武器。不幸的是,抗生素耐药基因 (ARGs) 的出现严重限制了β-内酰胺类抗生素的应用。其中,新德里金属β-内酰胺酶-1 (NDM-1) 由于其底物的混杂性、变体的出现和可转移性,代表了最令人担忧的发展。鉴于β-内酰胺类抗生素与 NDM-1 介导的耐药性的临床相关性,开发包括 NDM-1 抑制剂在内的联合药物治疗 NDM-1 细菌感染似乎特别有吸引力和迫切需要。本综述总结了与开发和优化有效 NDM-1 抑制剂相关的研究。对现有抑制剂的晶体结构、酶活性中心和催化机制、变体和全球分布、作用机制的详细概括,以及支架的发展为寻找针对耐药菌的潜在临床有效 NDM-1 抑制剂提供了参考。