Linoleic acid acts as a potential anti-virulence agent in Klebsiella pneumoniae.

IF 1.7 Q3 INFECTIOUS DISEASES
GERMS Pub Date : 2024-06-30 eCollection Date: 2024-06-01 DOI:10.18683/germs.2024.1426
Jayalaxmi Wangkheimayum, Tuhina Banerjee, Somorita Baishya, Swati Sharma, Manabendra Dutta Choudhury, Monjur Ahmed Laskar, Amitabha Bhattacharjee
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Abstract

Introduction: The rise in antimicrobial resistance among bacterial pathogens is a global concern, and anti-virulence therapy may be an alternative strategy to address the issue. Multidrug resistant (MDR) hypervirulent Klebsiella pneumoniae (HvKp) is known to be associated with healthcare associated infections. These are often challenging to treat and here anti-virulence therapy may be a treatment option. The study of anti-virulence compounds against HvKp by in-silico prediction, in-vitro experiments and in-vivo assay enables to determine which anti-virulence compounds are suitable for an alternative approach MDR HvKp.

Methods: Modeling of the proteins, ligand binding and molecular docking were performed targeting different hypervirulence genes viz., rmpA, rmpA2 and, iroC by in-silico analysis using different bioinformatics tool and software. Minimum inhibitory concentration (MIC) was determined for six anti-virulence compounds; curcumin, eugenol, reserpine, linoleic acid, ε-anethole, and α-thujone by standard protocol. Quantitative real-time PCR was performed selecting two isolates harboring rmpA, rmpA2 and iroC genes. Galleria mellonella larva killing assay was used for in-vivo experiment.

Results: In-silico analysis observed that linoleic acid could be the best fit in comparison with the other compounds. None of the anti-virulence compounds showed any inhibitory activity and upon transcriptional expression analysis of the hypervirulence genes; rmpA was marginally increased for both the isolates when linoleic acid exposure was given.

Conclusions: In-vivo study revealed that linoleic acid and reserpine showed anti-virulence activity.

亚油酸是肺炎克雷伯氏菌的一种潜在抗病毒剂。
导言:细菌病原体的抗菌药耐药性上升是一个全球关注的问题,而抗病毒疗法可能是解决这一问题的另一种策略。众所周知,耐多药(MDR)高病毒性肺炎克雷伯菌(HvKp)与医疗相关感染有关。这些细菌的治疗通常具有挑战性,而抗病毒治疗可能是一种治疗选择。通过室内预测、体外实验和体内检测对 HvKp 的抗病毒化合物进行研究,可以确定哪些抗病毒化合物适合作为 MDR HvKp 的替代方法:方法:使用不同的生物信息学工具和软件,针对不同的高侵染性基因(即 rmpA、rmpA2 和 iroC)进行了蛋白质建模、配体结合和分子对接。通过标准方案测定了六种抗病毒化合物的最低抑菌浓度(MIC):姜黄素、丁香酚、雷公藤碱、亚油酸、ε-茴香醚和α-麝香酮。对携带 rmpA、rmpA2 和 iroC 基因的两个分离物进行了定量实时 PCR 检测。在体内实验中使用了杀幼虫剂:结果:体内分析表明,与其他化合物相比,亚油酸最合适。没有一种抗病毒化合物显示出任何抑制活性,在对高病毒性基因进行转录表达分析时,当亚油酸暴露于两种分离物时,rmpA 都略有增加:体内研究表明,亚油酸和利血平具有抗病毒活性。
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
GERMS
GERMS INFECTIOUS DISEASES-
CiteScore
2.80
自引率
5.00%
发文量
36
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