Secapin: a promising antimicrobial peptide against multidrug-resistant Acinetobacter baumannii.

IF 1.7 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
GMS Hygiene and Infection Control Pub Date : 2024-07-09 eCollection Date: 2024-01-01 DOI:10.3205/dgkh000491
Zohreh Sadeghi Rad, Mahnaz Farahmand, Mahsa Kavousi
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引用次数: 0

Abstract

Introduction: Acinetobacter baumannii, renowned for its exceptional multidrug resistance and its role as a prevalent nosocomial pathogen, poses a formidable challenge to conventional antibiotic therapies. The primary objective of this investigation was to evaluate the efficacy of Secapin, an antimicrobial peptide, against multidrug-resistant (MDR) baumannii. Furthermore, the mechanisms underlying Secapin's antibacterial and antibiofilm activities were elucidated.

Methods: The antimicrobial and antibiofilm effectiveness of Secapin against MDR A. baumannii was assessed through a series of experiments. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of Secapin were determined using established protocols. Time-kill kinetic analysis was performed to assess the concentration-dependent bactericidal effect of Secapin. Additionally, the capacity of Secapin to impede biofilm formation and eradicate A. b aumannii biofilms was investigated. Hemolytic potential was evaluated using human red blood cells, while mammalian cell viability was examined at varying Secapin concentrations.

Results: Secapin exhibited robust bactericidal activity at minimal concentrations, with an MIC of 5 µg/mL and an MBC of 10 µg/mL against MDR A. baumannii. The time-kill kinetic analysis confirmed the concentration-dependent efficacy of Secapin in diminishing bacterial viability. Moreover, Secapin demonstrated the ability to prevent biofilm formation and eliminate established A. baumannii biofilms. Notably, Secapin exhibited no hemolytic activity and preserved mammalian cell viability up to a concentration of 100 µg/mL.

Conclusion: These findings underscore the substantial potential of Secapin as a potent agent against multidrug-resistant A. baumannii, showcasing its efficacy in both antibacterial and antibiofilm capacities. The favorable attributes of Secapin, characterized by its minimal hemolytic effects and high mammalian cell viability, position it as a promising contender in the fight against antibiotic resistance.

塞卡平:一种针对耐多药鲍曼不动杆菌的前景看好的抗菌肽。
导言:鲍曼不动杆菌(Acinetobacter baumannii)以其特殊的多重耐药性和作为流行的院内病原体而闻名,对传统的抗生素疗法提出了严峻的挑战。这项研究的主要目的是评估抗菌肽塞卡平对耐多药(MDR)鲍曼不动杆菌的疗效。此外,还阐明了塞卡平抗菌和抗生物膜活性的机制:方法:通过一系列实验评估了塞卡平对 MDR 鲍曼尼氏菌的抗菌和抗生物膜效果。采用既定方案测定了塞卡平的最低抑菌浓度(MIC)和最低杀菌浓度(MBC)。进行了时间杀灭动力学分析,以评估塞卡平的杀菌效果与浓度有关。此外,还研究了塞卡平阻碍生物膜形成和根除鲍曼不动杆菌生物膜的能力。利用人体红细胞评估了溶血潜能,并在不同浓度的塞卡平作用下检测了哺乳动物细胞的存活率:结果:塞卡平在最低浓度下表现出强大的杀菌活性,对 MDR 鲍曼尼氏菌的 MIC 为 5 µg/mL,MBC 为 10 µg/mL。时间杀伤动力学分析证实,塞卡平在降低细菌活力方面的功效与浓度有关。此外,塞卡平还能防止生物膜的形成并消除已形成的鲍曼不动杆菌生物膜。值得注意的是,塞卡平没有溶血活性,并且在浓度达到 100 µg/mL 时仍能保持哺乳动物细胞的活力:这些发现强调了塞卡平作为抗耐多药鲍曼不动杆菌的强效制剂的巨大潜力,展示了其在抗菌和抗生物膜方面的功效。塞卡平溶血作用小、哺乳动物细胞存活率高,这些有利特性使其成为抗击抗生素耐药性的有力竞争者。
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
GMS Hygiene and Infection Control
GMS Hygiene and Infection Control PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
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10 weeks
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