Antimicrobial Research Unit, School of Health Sciences, University of KwaZulu-Natal, Durban, South Africa
Biomedical Resource Unit, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa.
Appl Environ Microbiol. 2018 Aug 31;84(18). doi: 10.1128/AEM.00698-18. Print 2018 Sep 15.
The worldwide proliferation of life-threatening metallo-β-lactamase (MBL)-producing Gram-negative bacteria is a serious concern to public health. MBLs are compromising the therapeutic efficacies of β-lactams, particularly carbapenems, which are last-resort antibiotics indicated for various multidrug-resistant bacterial infections. Inhibition of enzymes mediating antibiotic resistance in bacteria is one of the major promising means for overcoming bacterial resistance. Compounds having potential MBL-inhibitory activity have been reported, but none are currently under clinical trials. The need for developing safe and efficient MBL inhibitors (MBLIs) is obvious, particularly with the continuous spread of MBLs worldwide. In this review, the emergence and escalation of MBLs in Gram-negative bacteria are discussed. The relationships between different class B β-lactamases identified up to 2017 are represented by a phylogenetic tree and summarized. In addition, approved and/or clinical-phase serine β-lactamase inhibitors are recapitulated to reflect the successful advances made in developing class A β-lactamase inhibitors. Reported MBLIs, their inhibitory properties, and their purported modes of inhibition are delineated. Insights into structural variations of MBLs and the challenges involved in developing potent MBLIs are also elucidated and discussed. Currently, natural products and MBL-resistant β-lactam analogues are the most promising agents that can become clinically efficient MBLIs. A deeper comprehension of the mechanisms of action and activity spectra of the various MBLs and their inhibitors will serve as a bedrock for further investigations that can result in clinically useful MBLIs to curb this global menace.
全球范围内危及生命的金属β-内酰胺酶(MBL)-产生革兰氏阴性菌的扩散是对公共卫生的严重关注。MBLs 削弱了β-内酰胺类药物(尤其是碳青霉烯类药物)的治疗效果,碳青霉烯类药物是用于多种耐多药细菌感染的最后手段抗生素。抑制介导细菌抗生素耐药性的酶是克服细菌耐药性的主要有前途的手段之一。已经报道了具有潜在 MBL 抑制活性的化合物,但目前没有在临床试验中。开发安全有效的 MBL 抑制剂(MBLIs)的需求显而易见,特别是随着 MBL 在全球范围内的不断传播。在这篇综述中,讨论了革兰氏阴性菌中 MBL 的出现和升级。通过系统发育树和总结,展示了截至 2017 年鉴定的不同 B 类β-内酰胺酶之间的关系。此外,综述了已批准和/或临床阶段的丝氨酸β-内酰胺酶抑制剂,以反映在开发 A 类β-内酰胺酶抑制剂方面取得的成功进展。描述了报道的 MBLIs、它们的抑制特性以及它们假定的抑制模式。还阐明和讨论了 MBL 结构变化和开发有效 MBLIs 所涉及的挑战。目前,天然产物和 MBL 耐药的β-内酰胺类似物是最有前途的能够成为临床有效的 MBLIs 的药物。深入了解各种 MBL 及其抑制剂的作用机制和活性谱将为进一步的研究提供基础,这些研究可能会产生临床有用的 MBLIs 来遏制这一全球性威胁。