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蛇毒化合物:对抗抗生素耐药性感染的新前沿。

Snake Venom Compounds: A New Frontier in the Battle Against Antibiotic-Resistant Infections.

作者信息

Muttiah Barathan, Hanafiah Alfizah

机构信息

Department of Medical Microbiology and Immunology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras, Kuala Lumpur 56000, Malaysia.

GUT Research Group, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.

出版信息

Toxins (Basel). 2025 May 1;17(5):221. doi: 10.3390/toxins17050221.

Abstract

The occurrence of antibiotic-resistant bacteria is a serious global health issue, and it emphasizes the need for novel antimicrobial agents. This review explores the potential of snake venom as another alternative strategy against antimicrobial resistance. Snake venoms are complex combinations of bioactive peptides and proteins, including metalloproteases (MPs), serine proteases (SPs), phospholipase A (PLA) enzymes, three-finger toxins (3FTXs), cysteine-rich secretory proteins (CRISPs), L-amino acid oxidases (LAAOs), and antimicrobial peptides (AMPs). The antibacterial products possess wide-spectrum antibacterial activity against resistant microbes via diverse mechanisms such as cell membrane disruption, enzymatic hydrolysis of microbial structures, generation of oxidative stress, inhibition of biofilms, and immunomodulation. Strong antimicrobial activity is reported by most studies, but these are mostly restricted to in vitro testing with low translational use. Although preliminary insights into molecular targets and physiological effects exist, further studies are needed to clarify long-term safety and therapeutic potential. Special attention is given to snake venom-derived extracellular vesicles (SVEVs), which enhance the therapeutic potential of venom toxins by protecting them from degradation, improving bioavailability, and facilitating targeted delivery. Furthermore, innovative delivery strategies such as PEGylation, liposomes, hydrogels, microneedle patches, biopolymer films, and nanoparticles are discussed for their role in reducing systemic toxicity and enhancing antimicrobial efficacy. The rational modification of venom-derived peptides further expands their therapeutic utility by improving pharmacokinetics and minimizing off-target effects. Together, these approaches highlight the translational potential of snake venom-based therapies as next-generation antimicrobials in the fight against resistant infections. By outlining these challenges and directions, this review positions snake venom as an overlooked but fertile resource in the battle against antibiotic resistance.

摘要

抗生素耐药菌的出现是一个严重的全球健康问题,这凸显了对新型抗菌药物的需求。本综述探讨了蛇毒作为对抗抗菌耐药性的另一种替代策略的潜力。蛇毒是生物活性肽和蛋白质的复杂组合,包括金属蛋白酶(MPs)、丝氨酸蛋白酶(SPs)、磷脂酶A(PLA)酶、三指毒素(3FTXs)、富含半胱氨酸的分泌蛋白(CRISPs)、L-氨基酸氧化酶(LAAOs)和抗菌肽(AMPs)。这些抗菌产物通过多种机制,如细胞膜破坏、微生物结构的酶促水解、氧化应激的产生、生物膜的抑制和免疫调节,对耐药微生物具有广谱抗菌活性。大多数研究都报道了很强的抗菌活性,但这些大多局限于体外测试,临床转化应用较少。尽管对分子靶点和生理效应已有初步认识,但仍需要进一步研究以阐明其长期安全性和治疗潜力。特别关注蛇毒衍生的细胞外囊泡(SVEVs),它们通过保护毒液毒素不被降解、提高生物利用度和促进靶向递送,增强了毒液毒素的治疗潜力。此外,还讨论了聚乙二醇化、脂质体、水凝胶、微针贴片、生物聚合物膜和纳米颗粒等创新递送策略在降低全身毒性和提高抗菌疗效方面的作用。对毒液衍生肽进行合理修饰,通过改善药代动力学和最小化脱靶效应,进一步扩大了它们的治疗效用。总之,这些方法凸显了基于蛇毒的疗法作为对抗耐药感染的下一代抗菌药物的临床转化潜力。通过概述这些挑战和方向,本综述将蛇毒定位为对抗抗生素耐药性斗争中一种被忽视但潜力巨大的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c74/12116190/62789cd7a784/toxins-17-00221-g001.jpg

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