6-Aminoflavone Inhibits Planktonic Growth, Disrupts Biofilm Architecture, and Regulates Quorum Sensing in Klebsiella pneumoniae.

IF 2.9 Q2 BIOCHEMICAL RESEARCH METHODS
Biochemistry Research International Pub Date : 2026-08-21 eCollection Date: 2026-01-01 DOI:10.1155/bri/8058282
Pooja Pandey, T Tushar, Lakshmi Sirisha Vavilala
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引用次数: 0

Abstract

Antibiotic resistance has emerged as a major global health challenge, particularly in biofilm-forming pathogens that exhibit enhanced tolerance to antimicrobial therapies. K. pneumoniae, a multidrug-resistant pathogen, is a leading cause of hospital-acquired infections, including pneumonia, septicemia, and device-associated infections. Its robust biofilm-forming capacity facilitates immune evasion, restricts antibiotic penetration, and contributes to recurrent infections. Therefore, the identification of agents capable of targeting both planktonic bacterial growth and biofilm architecture is of considerable therapeutic importance. In the present study, the antibacterial, antibiofilm, and antivirulence potential of 6-Aminoflavone was investigated against K. pneumoniae. Antibacterial activity was evaluated using growth inhibition assays, time-kill kinetics, and clonogenic survival analysis. Mechanistic investigations revealed significant intracellular ROS accumulation, increased oxidative stress susceptibility, and induction of apoptosis-like cell death, suggesting ROS-mediated antibacterial activity. In addition to suppressing bacterial proliferation, 6-Aminoflavone exhibited promising antibiofilm efficacy, inhibiting biofilm formation by 86.23% and eradicating 84.77% of established biofilms. These effects were associated with a substantial reduction in cell surface hydrophobicity (∼45.39%), and EPS levels were reduced to ∼2.33% as compared to untreated controls, indicating severe destabilization of the biofilm matrix. Furthermore, eDNA, a key structural component of the biofilm scaffold, exhibited a maximum ∼2.13-fold reduction following treatment. Confocal microscopy confirmed marked disruption and collapse of biofilm architecture. Additionally, quorum sensing (QS)-regulated virulence factors, including urease (∼51.92%), protease (∼55.18%), and lipase (∼44.90%), were significantly attenuated. These findings demonstrate that 6-Aminoflavone exerts antimicrobial activity by inducing oxidative stress-mediated apoptosis-like bacterial death, disrupting biofilm structural components, and suppressing QS-regulated virulence in K. pneumoniae.

6-氨基黄酮抑制肺炎克雷伯菌浮游生物生长,破坏生物膜结构并调节群体感应。
抗生素耐药性已成为一项重大的全球健康挑战,特别是在对抗菌素疗法表现出增强耐受性的生物膜形成病原体中。肺炎克雷伯菌是一种多重耐药病原体,是医院获得性感染的主要原因,包括肺炎、败血症和器械相关感染。其强大的生物膜形成能力促进免疫逃避,限制抗生素渗透,并有助于复发性感染。因此,确定能够同时针对浮游细菌生长和生物膜结构的药物具有相当大的治疗意义。在本研究中,研究了6-氨基黄酮对肺炎克雷伯菌的抗菌、抗生物膜和抗毒潜力。抗菌活性通过生长抑制试验、时间杀伤动力学和克隆生存分析进行评估。机制研究显示细胞内ROS积累显著,增加氧化应激敏感性,诱导细胞凋亡样死亡,提示ROS介导的抗菌活性。除了抑制细菌增殖外,6-氨基黄酮还表现出良好的抗生物膜效果,抑制生物膜形成86.23%,根除已建立的生物膜84.77%。这些影响与细胞表面疏水性大幅降低(~ 45.39%)有关,与未经处理的对照组相比,EPS水平降低至~ 2.33%,表明生物膜基质严重不稳定。此外,eDNA(生物膜支架的关键结构成分)在处理后表现出最大约2.13倍的减少。共聚焦显微镜证实了明显的生物膜结构破坏和崩溃。此外,群体感应(QS)调节的毒力因子,包括脲酶(~ 51.92%)、蛋白酶(~ 55.18%)和脂肪酶(~ 44.90%),显著减弱。这些发现表明,6-氨基黄酮通过诱导氧化应激介导的细胞凋亡样细菌死亡、破坏生物膜结构成分和抑制qs调节的肺炎克雷伯菌毒力来发挥抗菌活性。
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
Biochemistry Research International
Biochemistry Research International BIOCHEMICAL RESEARCH METHODS-
CiteScore
6.30
自引率
0.00%
发文量
27
审稿时长
14 weeks
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