Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, United States; Department of Environmental Health Sciences, University of South Carolina, Columbia, SC, 29208, United States.
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, United States.
Biomaterials. 2024 Dec;311:122690. doi: 10.1016/j.biomaterials.2024.122690. Epub 2024 Jun 28.
The escalating rise in antimicrobial resistance (AMR) coupled with a declining arsenal of new antibiotics is imposing serious threats to global public health. A pervasive aspect of many acquired AMR infections is that the pathogenic microorganisms exist as biofilms, which are equipped with superior survival strategies. In addition, persistent and recalcitrant infections are seeded with bacterial persister cells at infection sites. Together, conventional antibiotic therapeutics often fail in the complete treatment of infections associated with bacterial persisters and biofilms. Novel therapeutics have been attempted to tackle AMR, biofilms, and persister-associated complex infections. This review focuses on the progress in designing molecular biomaterials and therapeutics to address acquired and intrinsic AMR, and the fundamental microbiology behind biofilms and persisters. Starting with a brief introduction of AMR basics and approaches to tackling acquired AMR, the emphasis is placed on various biomaterial approaches to combating intrinsic AMR, including (1) semi-synthetic antibiotics; (2) macromolecular or polymeric biomaterials mimicking antimicrobial peptides; (3) adjuvant effects in synergy; (4) nano-therapeutics; (5) nitric oxide-releasing antimicrobials; (6) antimicrobial hydrogels; (7) antimicrobial coatings. Particularly, the structure-activity relationship is elucidated in each category of these biomaterials. Finally, illuminating perspectives are provided for the future design of molecular biomaterials to bypass AMR and cure chronic multi-drug resistant (MDR) infections.
抗生素耐药性(AMR)的不断上升,加上新抗生素储备的不断减少,对全球公共卫生构成了严重威胁。许多获得性 AMR 感染的一个普遍方面是,病原微生物以生物膜的形式存在,而生物膜则具备更优越的生存策略。此外,在感染部位,持续性和难治性感染会以细菌持久细胞为种子。总之,传统的抗生素疗法常常无法完全治疗与细菌持久细胞和生物膜相关的感染。人们已经尝试了新的疗法来应对 AMR、生物膜和与持久细胞相关的复杂感染。本综述重点介绍了设计分子生物材料和疗法以应对获得性和固有 AMR 以及生物膜和持久细胞背后的基本微生物学的进展。本文首先简要介绍了 AMR 的基础知识和应对获得性 AMR 的方法,重点介绍了各种生物材料方法来对抗固有 AMR,包括(1)半合成抗生素;(2)模拟抗菌肽的大分子或聚合物生物材料;(3)协同增效的佐剂作用;(4)纳米疗法;(5)释放一氧化氮的抗菌剂;(6)抗菌水凝胶;(7)抗菌涂层。特别是,在这些生物材料的每一类中都阐明了结构-活性关系。最后,为未来设计分子生物材料以绕过 AMR 和治疗慢性多药耐药(MDR)感染提供了有启发性的观点。