蝎毒衍生肽 IsCT 的截短类似物对铜绿假单胞菌的抗生物膜和抗炎特性

IF 4.3 2区 医学 Q1 INFECTIOUS DISEASES
Pornpimon Jantaruk, Kittitat Teerapo, Supattra Charoenwutthikun, Sittiruk Roytrakul, Duangkamol Kunthalert
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引用次数: 0

摘要

铜绿假单胞菌(Pseudomonas aeruginosa)是人类的一种机会性病原体,也是造成严重院内感染和免疫力低下人群致命感染的常见原因。铜绿假单胞菌具有形成生物膜的能力,这是它对几乎所有传统抗生素产生抗药性的主要原因,从而限制了治疗效果。为了发现新型治疗药物来对抗与铜绿假单胞菌相关的生物膜感染,我们合成了蝎毒衍生肽 IsCT 的截短类似物,并研究了它们的抗生物膜特性。在所研究的肽中,IsCT-Δ6-8肽明显表现出最潜在的抗铜绿假单胞菌生物膜活性,而且这种作用不是由于抑制细菌生长而产生的。IsCT-Δ6-8 肽还对铜绿假单胞菌的重要毒力因子--脓青素的产生具有抑制作用。此外,IsCT-Δ6-8 肽还能显著抑制一氧化氮和白细胞介素-6 在绿脓杆菌 LPS 诱导的巨噬细胞中的产生。由于其对哺乳动物细胞的细胞毒性较低,IsCT-Δ6-8 肽有望成为一种具有显著抗生物膜和抗炎特性的候选物质。这些发现突显了它在治疗与铜绿假单胞菌相关的生物膜感染方面的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-Biofilm and Anti-Inflammatory Properties of the Truncated Analogs of the Scorpion Venom-Derived Peptide IsCT against Pseudomonas aeruginosa.

Pseudomonas aeruginosa is an opportunistic pathogen in humans and a frequent cause of severe nosocomial infections and fatal infections in immunocompromised individuals. Its ability to form biofilms has been the main driving force behind its resistance to almost all conventional antibiotics, thereby limiting treatment efficacy. In an effort to discover novel therapeutic agents to fight P. aeruginosa-associated biofilm infections, the truncated analogs of scorpion venom-derived peptide IsCT were synthesized and their anti-biofilm properties were examined. Among the investigated peptides, the IsCT-Δ6-8 peptide evidently showed the most potential anti-P. aeruginosa biofilm activity and the effect was not due to bacterial growth inhibition. The IsCT-Δ6-8 peptide also exhibited inhibitory activity against the production of pyocyanin, an important virulence factor of P. aeruginosa. Furthermore, the IsCT-Δ6-8 peptide significantly suppressed the production of inflammatory mediators nitric oxide and interleukin-6 in P. aeruginosa LPS-induced macrophages. Due to its low cytotoxicity to mammalian cells, the IsCT-Δ6-8 peptide emerges as a promising candidate with significant anti-biofilm and anti-inflammatory properties. These findings highlight its potential application in treating P. aeruginosa-related biofilm infections.

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来源期刊
Antibiotics-Basel
Antibiotics-Basel Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
7.30
自引率
14.60%
发文量
1547
审稿时长
11 weeks
期刊介绍: Antibiotics (ISSN 2079-6382) is an open access, peer reviewed journal on all aspects of antibiotics. Antibiotics is a multi-disciplinary journal encompassing the general fields of biochemistry, chemistry, genetics, microbiology and pharmacology. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers.
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