Department of Entomology, Cornell Institute of Host-Microbe Interactions and Disease, Cornell University, Ithaca, NY, USA.
MedStar Georgetown Transplant Institute, Georgetown University School of Medicine, Washington, DC, USA.
Science. 2020 May 1;368(6490). doi: 10.1126/science.aau5480.
Antimicrobial peptides (AMPs) are essential components of immune defenses of multicellular organisms and are currently in development as anti-infective drugs. AMPs have been classically assumed to have broad-spectrum activity and simple kinetics, but recent evidence suggests an unexpected degree of specificity and a high capacity for synergies. Deeper evaluation of the molecular evolution and population genetics of AMP genes reveals more evidence for adaptive maintenance of polymorphism in AMP genes than has previously been appreciated, as well as adaptive loss of AMP activity. AMPs exhibit pharmacodynamic properties that reduce the evolution of resistance in target microbes, and AMPs may synergize with one another and with conventional antibiotics. Both of these properties make AMPs attractive for translational applications. However, if AMPs are to be used clinically, it is crucial to understand their natural biology in order to lessen the risk of collateral harm and avoid the crisis of resistance now facing conventional antibiotics.
抗菌肽(AMPs)是多细胞生物免疫防御的重要组成部分,目前正在开发为抗感染药物。AMPs 通常被认为具有广谱活性和简单的动力学特性,但最近的证据表明,它们具有出人意料的特异性和高度协同作用的能力。对 AMP 基因的分子进化和群体遗传学的更深入评估表明,与以前的认识相比,AMP 基因的多态性具有更多适应性维持的证据,以及 AMP 活性的适应性丧失。AMPs 表现出降低靶微生物耐药性进化的药效学特性,并且 AMPs 可以相互协同作用,并与传统抗生素协同作用。这两个特性使得 AMPs 成为具有吸引力的转化应用。然而,如果要将 AMPs 用于临床,了解它们的自然生物学是至关重要的,以降低对附带损害的风险,并避免传统抗生素目前面临的耐药危机。