Suppr超能文献

对多重耐药病原体具有强效活性的两亲性肽类抗生素。

Amphipathic Peptide Antibiotics with Potent Activity against Multidrug-Resistant Pathogens.

作者信息

Shi Jingru, Chen Chen, Wang Dejuan, Tong Ziwen, Wang Zhiqiang, Liu Yuan

机构信息

College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China.

Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, China.

出版信息

Pharmaceutics. 2021 Mar 24;13(4):438. doi: 10.3390/pharmaceutics13040438.

Abstract

The emergence and prevalence of multidrug-resistant (MDR) bacteria have posed a serious threat to public health. Of particular concern are methicillin-resistant (MRSA) and , and (X)-positive Gram-negative pathogens. The fact that few new antibiotics have been approved in recent years exacerbates this global crisis, thus, new alternatives are urgently needed. Antimicrobial peptides (AMPs) originated from host defense peptides with a wide range of sources and multiple functions, are less prone to achieve resistance. All these characteristics laid the foundation for AMPs to become potential antibiotic candidates. In this study, we revealed that peptide WW307 displayed potent antibacterial and bactericidal activity against MDR bacteria, including MRSA and Gram-negative bacteria carrying , or (X4). In addition, WW307 exhibited great biofilm inhibition and eradication activity. Safety and stability experiments showed that WW307 had a strong resistance against various physiological conditions and displayed relatively low toxicity. Mechanistic experiments showed that WW307 resulted in membrane damage by selectively targeting bacterial membrane-specific components, including lipopolysaccharide (LPS), phosphatidylglycerol (PG), and cardiolipin (CL). Moreover, WW307 dissipated membrane potential and triggered the production of reactive oxygen species (ROS). Collectively, these results demonstrated that WW307 represents a promising candidate for combating MDR pathogens.

摘要

多重耐药(MDR)细菌的出现和流行对公众健康构成了严重威胁。特别令人担忧的是耐甲氧西林金黄色葡萄球菌(MRSA)以及产超广谱β-内酰胺酶(ESBL)和碳青霉烯酶(KPC)的革兰氏阴性病原体。近年来获批的新抗生素寥寥无几,这加剧了这场全球危机,因此迫切需要新的替代药物。抗菌肽(AMPs)源自宿主防御肽,来源广泛且功能多样,较不易产生耐药性。所有这些特性为抗菌肽成为潜在的抗生素候选物奠定了基础。在本研究中,我们发现肽WW307对包括MRSA以及携带ESBL、KPC或新德里金属β-内酰胺酶-4(NDM-4)的革兰氏阴性菌在内的多重耐药菌表现出强大的抗菌和杀菌活性。此外,WW307表现出很强的生物膜抑制和清除活性。安全性和稳定性实验表明,WW307对各种生理条件具有很强的耐受性,且毒性相对较低。机制实验表明,WW307通过选择性靶向细菌膜特异性成分,包括脂多糖(LPS)、磷脂酰甘油(PG)和心磷脂(CL),导致膜损伤。此外,WW307使膜电位消散并引发活性氧(ROS)的产生。总的来说,这些结果表明WW307是对抗多重耐药病原体的一个有前景的候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76a6/8063935/33d32cf499e0/pharmaceutics-13-00438-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验