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海洋抗菌肽:对抗多重耐药和形成生物膜细菌的新策略

Marine Antimicrobial Peptides: Emerging Strategies Against Multidrug-Resistant and Biofilm-Forming Bacteria.

作者信息

Magalhães Rita, Mil-Homens Dalila, Cruz Sónia, Oliveira Manuela

机构信息

ECOMARE-Laboratory for Innovation and Sustainability of Marine Biological Resources, CESAM-Centre for Environmental and Marine Studies, Department of Biology, University of Aveiro, 3810-193 Aveiro, Portugal.

ITQB NOVA-Instituto de Tecnologia Química e Biológica António Xavier, NOVA University of Lisbon, Av. da República, 2780-157 Oeiras, Portugal.

出版信息

Antibiotics (Basel). 2025 Aug 7;14(8):808. doi: 10.3390/antibiotics14080808.

Abstract

The global rise in antimicrobial resistance poses a major threat to public health, with multidrug-resistant bacterial infections expected to surpass cancer in mortality by 2050. As traditional antibiotic pipelines stagnate, novel therapeutic alternatives are critically needed. Antimicrobial peptides (AMPs), particularly those derived from marine organisms, have emerged as promising antimicrobial candidates due to their broad-spectrum activity, structural diversity, and distinctive mechanisms of action. Unlike conventional antibiotics, AMPs can disrupt microbial membranes, inhibit biofilm formation, and even modulate immune responses, making them highly effective against resistant bacteria. This review highlights the potential of marine AMPs as next-generation therapeutics, emphasizing their efficacy against multidrug-resistant pathogens and biofilm-associated infections. Furthermore, marine AMPs show promise in combating persister cells and disrupting quorum sensing pathways, offering new strategies for tackling chronic infections. Despite their potential, challenges such as production scalability and limited clinical validation remain; nevertheless, the use of new technologies and bioinformatic tools is accelerating the discovery and optimization of these peptides, paving the way for bypassing these challenges. This review consolidates current findings on marine AMPs, advocating for their continued exploration as viable tools in the fight against antimicrobial resistance.

摘要

全球抗菌药物耐药性的上升对公共卫生构成了重大威胁,预计到2050年,耐多药细菌感染导致的死亡率将超过癌症。随着传统抗生素研发停滞不前,迫切需要新的治疗替代方案。抗菌肽(AMPs),尤其是那些源自海洋生物的抗菌肽,因其广谱活性、结构多样性和独特的作用机制,已成为有前景的抗菌候选物。与传统抗生素不同,抗菌肽可以破坏微生物膜、抑制生物膜形成,甚至调节免疫反应,使其对耐药细菌非常有效。这篇综述强调了海洋抗菌肽作为下一代治疗药物的潜力,重点介绍了它们对耐多药病原体和生物膜相关感染的疗效。此外,海洋抗菌肽在对抗持留菌和破坏群体感应途径方面显示出前景,为应对慢性感染提供了新策略。尽管它们具有潜力,但仍存在生产可扩展性和临床验证有限等挑战;然而,新技术和生物信息学工具的使用正在加速这些肽的发现和优化,为克服这些挑战铺平道路。这篇综述整合了关于海洋抗菌肽的当前研究结果,主张继续探索它们,使其成为对抗抗菌药物耐药性的可行工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b01/12383081/cd45a1986ef3/antibiotics-14-00808-g001.jpg

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