Potential of Venom-Derived Compounds for the Development of New Antimicrobial Agents.

IF 3.9 3区 医学 Q2 FOOD SCIENCE & TECHNOLOGY
Toxins Pub Date : 2025-05-11 DOI:10.3390/toxins17050238
Esraa Yasser Rabea, Esraa Dakrory Mahmoud, Nada Khaled Mohamed, Erada Rabea Ansary, Mahmoud Roushdy Alrouby, Rabab Reda Shehata, Youssef Yasser Mokhtar, Prakash Arullampalam, Ahmed M Hegazy, Ahmed Al-Sabi, Tarek Mohamed Abd El-Aziz
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引用次数: 0

Abstract

The emergence of antimicrobial resistance is a significant challenge in global healthcare, necessitating innovative techniques to address multidrug-resistant pathogens. Multidrug-resistant pathogens like Klebsiella pneumoniae, Acinetobacter baumannii, and Pseudomonas aeruginosa pose significant public health threats, as they are increasingly resistant to common antibiotics, leading to more severe and difficult-to-treat infections. These pathogens are part of the ESKAPE group, which includes Enterococcus faecium, Staphylococcus aureus, and Enterobacter species. Animal venoms, derived from a wide range of species such as snakes, scorpions, spiders, bees, wasps, and ants, represent a rich source of bioactive peptides. Venoms have been a valuable source for drug discovery, providing unique compounds with therapeutic potential. Venom-derived drugs are known for their increased bioactivity, specificity, and stability compared to synthetic alternatives. These compounds are being investigated for various conditions, including treatments for diabetes, pain relief, cancer, and infections, showcasing their remarkable antimicrobial efficacy. In this review, we provide a comprehensive investigation into the potential of venom-derived compounds for developing new antimicrobial agents, including antibacterial, antifungal, antiviral, and antiparasitic therapeutics. Key venom components, including melittin from bee venom, phospholipase A2 from snake venom, and chlorotoxin from scorpion venom, exhibit potent antimicrobial effects through mechanisms such as membrane disruption, enzymatic inhibition, and immune modulation. We also explore the challenges related to the development and clinical use of venom-derived antimicrobials, including toxicity, stability, and delivery mechanisms. These compounds hold immense promise as transformative tools against resistant pathogens, offering a unique avenue for groundbreaking advancements in antimicrobial research and therapeutic development.

毒液衍生化合物开发新型抗菌药物的潜力。
抗菌素耐药性的出现是全球卫生保健面临的重大挑战,需要创新技术来应对耐多药病原体。肺炎克雷伯菌、鲍曼不动杆菌和铜绿假单胞菌等多重耐药病原体对公共卫生构成重大威胁,因为它们对常见抗生素的耐药性日益增强,导致更严重和更难治疗的感染。这些病原体是ESKAPE组的一部分,其中包括屎肠球菌、金黄色葡萄球菌和肠杆菌。动物毒液是生物活性肽的丰富来源,其来源广泛,如蛇、蝎子、蜘蛛、蜜蜂、黄蜂和蚂蚁。毒液一直是药物发现的宝贵来源,提供具有治疗潜力的独特化合物。与合成替代品相比,毒液衍生药物以其更高的生物活性、特异性和稳定性而闻名。这些化合物正在被研究用于各种疾病,包括治疗糖尿病、缓解疼痛、癌症和感染,显示出它们卓越的抗菌功效。在这篇综述中,我们提供了全面的研究潜力,毒液衍生化合物开发新的抗微生物药物,包括抗菌,抗真菌,抗病毒和抗寄生虫治疗。关键的毒液成分,包括蜂毒中的蜂毒素、蛇毒中的磷脂酶A2和蝎子毒液中的氯毒素,通过膜破坏、酶抑制和免疫调节等机制表现出强大的抗菌作用。我们还探讨了与开发和临床使用毒液源抗微生物药物相关的挑战,包括毒性、稳定性和给药机制。这些化合物作为抗耐药病原体的变革性工具具有巨大的前景,为抗菌研究和治疗开发提供了突破性进展的独特途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Toxins
Toxins TOXICOLOGY-
CiteScore
7.50
自引率
16.70%
发文量
765
审稿时长
16.24 days
期刊介绍: Toxins (ISSN 2072-6651) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to toxins and toxinology. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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