Probiotic cell-free supernatant as effective antimicrobials against Klebsiella pneumoniae and reduce antibiotic resistance development.

IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Anh Duy Do, Hoa Pham Quang, Quang Khai Phan
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Abstract

This study evaluated the antimicrobial activity, resistance development, and synergistic potential of cell-free supernatant (CFSs) derived from Levilactobacillus brevis (Lb-CFS) and Lactiplantibacillus plantarum (Lp-CFS) against Klebsiella pneumoniae. Both CFSs exhibited potent growth inhibition, with minimum inhibitory concentrations (MICs) of 128 μg/mL and 64 μg/mL for Lb-CFS and Lp-CFS, respectively, and demonstrated dose-dependent bactericidal activity, achieving complete bacterial eradication at minimum bactericidal concentrations (MBC) within 6 h. The CFSs suppressed the expression of virulence genes (galF, wzi, and manC) and biofilm formation in a dose-dependent manner. Synergistic interactions were observed when combining CFSs with antibiotics, resulting in 2- to fourfold reductions in antibiotic MICs and MBCs. Notably, adaptive evolution experiments revealed significantly slower resistance development in K. pneumoniae against CFSs (twofold MIC/MBC increase) compared to antibiotics (16- to 128-fold increase) after 21 days. Furthermore, CFS-adapted strains exhibited increased antibiotic susceptibility, while antibiotic-adapted strains displayed cross-resistance to multiple antibiotics. No cross-resistance occurred between Lb-CFS and Lp-CFS, suggesting distinct adaptive mechanisms. These findings highlight the potential of probiotic-derived CFSs as effective antimicrobials with a lower propensity for inducing rapid resistance compared to conventional antibiotics, suggesting their promise in combating multidrug-resistant infections.

Abstract Image

无细胞益生菌上清液可有效抗击肺炎克雷伯氏菌,并减少抗生素耐药性的产生。
本研究评估了无细胞上清液(CFSs)对肺炎克雷伯氏菌的抗菌活性、耐药性发展和协同增效潜力,这些无细胞上清液分别来自于Levilactobacillus brevis(Lb-CFS)和Lactiplantibacillus plantarum(Lp-CFS)。两种 CFS 都具有强效的生长抑制作用,Lb-CFS 和 Lp-CFS 的最低抑菌浓度(MICs)分别为 128 μg/mL 和 64 μg/mL,并表现出剂量依赖性杀菌活性,在最低杀菌浓度(MBC)下可在 6 小时内完全消灭细菌。当 CFS 与抗生素结合使用时,会产生协同作用,使抗生素的 MIC 和 MBC 降低 2 到 4 倍。值得注意的是,适应性进化实验显示,21 天后,肺炎克雷伯菌对 CFS 的耐药性发展(MIC/MBC 增加两倍)明显慢于抗生素(MIC/MBC 增加 16 到 128 倍)。此外,适应 CFS 的菌株对抗生素的敏感性增加,而适应抗生素的菌株则对多种抗生素产生交叉耐药性。Lb-CFS和Lp-CFS之间没有发生交叉耐药性,这表明两者有不同的适应机制。这些发现凸显了益生菌衍生的CFS作为有效抗菌剂的潜力,与传统抗生素相比,CFS诱导快速耐药性的倾向较低,这表明它们有望对抗耐多药感染。
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来源期刊
International Microbiology
International Microbiology 生物-生物工程与应用微生物
CiteScore
5.50
自引率
3.20%
发文量
67
审稿时长
3 months
期刊介绍: International Microbiology publishes information on basic and applied microbiology for a worldwide readership. The journal publishes articles and short reviews based on original research, articles about microbiologists and their work and questions related to the history and sociology of this science. Also offered are perspectives, opinion, book reviews and editorials. A distinguishing feature of International Microbiology is its broadening of the term microbiology to include eukaryotic microorganisms.
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