肺炎克雷伯菌
微生物学
粘菌素
最低杀菌浓度
最小抑制浓度
抗菌剂
生物
溶解
生物膜
抗菌活性
抗菌肽
肽
细菌
大肠杆菌
分子生物学
生物化学
基因
遗传学
作者
William Gustavo Lima,Rayssa Maria Rodrigues Laia,Júlio César Moreira Brito,Daniel Augusto Guedes Reis Michel,Rodrigo M. Verly,Jarbas M. Resende,Maria Elena de Lima
出处
期刊:Toxins
[Multidisciplinary Digital Publishing Institute]
日期:2025-06-25
卷期号:17 (7): 325-325
标识
DOI:10.3390/toxins17070325
摘要
Klebsiella pneumoniae can acquire resistance mechanisms to colistin and present a pan-resistant phenotype. Therefore, new alternative agents are imperative to control this pathogen, and the peptide Jelleine-I stands out as a promising prototype. Here, the antibacterial activity of Jelleine-I against clinical isolates of colistin-resistant K. pneumoniae (CRKP) was investigated. Antimicrobial activity was assessed by determining the minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and time kill-curve assay. The release of 260 nm-absorbing materials (DNA/RNA) and the release of proteins were used in the lysis assay. Anti-biofilm activity was studied in microplates. In vivo activity was determined by the lethality assay using Tenebrio molitor larvae. The results show that the MIC of Jelleine-I ranged from 16 to 128 µM and the MBC was on average 128 µM. Jelleine-I at 200 µM killed all CRKP cells in suspension (106 colony-forming units (CFU)/mL) after 150 min of incubation. Jelleine-I acts on the CRKP cell membrane inducing lysis. Biomass and viability of CRKP-induced biofilms are reduced after treatment with Jelleine-I, and the use of this peptide in T. molitor larvae infected with CRKP reduces lethality and improves overall larval health. In conclusion, Jelleine-I is a potential prototype for the development of new antimicrobial agents.
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