Natural and Synthetic AMPs from Latin America across Diversity Engineering and Applications

IF 4.5 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2026-08-14 Epub Date: 2026-07-27 DOI:10.1021/acsinfecdis.6c00394
José Brango-Vanegas, Elizabete de Souza Cândido, Juliana Carneiro, Nanci Almeida Ribeiro, Octávio Luiz Franco
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引用次数: 0

Abstract

Latin America’s biodiversity accounts for approximately 60% of the world’s total, fueling scientific research into natural products, a highly relevant area in drug discovery to this day. This is accompanied by an increasing number of antimicrobial peptides (AMPs) derived from natural products in the region, which over the past decade have been redesigned through modifications, enhancements, and refinements of their physicochemical properties and antimicrobial potency, using approaches that range from rational design and structure–activity relationship (SAR) studies to artificial intelligence and machine learning methodologies. AMPs and their derivatives represent a vast chemical space with potential for antibacterial, antifungal, antiviral, and antiparasitic therapies, with emerging applications beyond infectious diseases. Over the years, studies have identified these peptides from a wide range of sources, including amphibians, reptiles, invertebrates, and microorganisms from South America, highlighting their diverse biological activities. This raises important questions about whether Latin America is a fertile source of inspiration for the development of AMPs. It also prompts an examination of the region’s historical and ongoing contributions to the field of natural and synthetic AMPs with anti-infective potential. Additionally, it highlights the need to assess the region’s progress in keeping pace with the recent advancements in engineering AMPs to combat resistant bacteria. This mini-review addresses these topics and related issues, exploring Latin America’s discoveries, challenges, and innovations in AMPs and their applications, particularly in anti-infective agents.

来自拉丁美洲的天然和合成amp跨越多样性工程和应用
拉丁美洲的生物多样性约占世界总量的60%,促进了对天然产品的科学研究,这是迄今为止与药物发现高度相关的领域。与此同时,来自该地区天然产物的抗菌肽(amp)数量不断增加,在过去的十年中,这些抗菌肽通过修改、增强和改进其物理化学性质和抗菌效力而重新设计,使用的方法从合理设计和结构-活性关系(SAR)研究到人工智能和机器学习方法。抗菌肽及其衍生物在抗菌、抗真菌、抗病毒和抗寄生虫治疗方面具有广阔的化学空间,在传染病之外也有新的应用。多年来,研究已经从广泛的来源确定了这些肽,包括两栖动物,爬行动物,无脊椎动物和来自南美洲的微生物,突出了它们的多样性生物活性。这就提出了一个重要的问题:拉丁美洲是否为amp的发展提供了丰富的灵感来源。它还促使人们审视该地区在具有抗感染潜力的天然和合成抗菌药物领域的历史和持续贡献。此外,报告强调有必要评估该地区在与抗药抗菌肽工程的最新进展保持同步方面取得的进展。这篇小型综述探讨了这些主题和相关问题,探讨了拉丁美洲在amp及其应用方面的发现、挑战和创新,特别是在抗感染药物方面。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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