Targeting H3N2 Influenza Virus RNA-dependent RNA Polymerase by Using Bioactives from Essential Oils from Eucalyptus polybrachtea, Cymbopogon citratus and Cymbopogon khasianus

Arun Dev Sharma, Inderjeet Kaur
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Abstract

A dramatic surge of H3N2 influenza virus is of grave concern worldwide and particularly in India. H3N2 cause acute respiratory infection, however, a few drugs are available for its mitigation. Subsequently, researchers have been involved in efforts to discover novel antiviral mechanisms that can lay the basis for new anti-influenza drugs. Influenza virus RNA-dependent RNA polymerase (RdRP) is a multi-functional hetero-trimer, implicated in the production of viral mRNA, hence plays a major role in viral infectivity thus directly associated with survival of the virus. RdRP have been cited as anappropriate target for therapeutic drug design. In the present study molecular docking was designed to estimate the effect of potent bioactive moleculesfrom essential oils from Eucalyptus polybrachtea (eucalyptus oil, EO), Cymbopogon citratus (lemon grass essential oil, LEO) and Cymbopogon khasianus (palmarosa essential oil, PEO) against RdRP protein. GC-FID (gas chromatography with flame-ionization detection) based composition profile, and in-silico docking study was conducted by using CB-dock 2 analysis followed by 2D interactions. GC-FID revealed eucalyptol, geranial and geraniolas major phytocompounds in EO, LEO and PEO respectively. The docking score indicated effective binding of ligands to RdRP. Interactions results indicated that, RdRP/ligand complexes form hydrogen, van der waals forces, pi-alkyl, alkyl, and pi-Sigma interactions. Based on above findings of aroma profile and docking, therefore, it was recommended that essential oils from above mentioned aromatic cropsmay represent potential herbal treatment to mitigate H3N2 infections.
利用聚茶桉、香蒲和香蒲精油的生物活性靶向H3N2流感病毒RNA依赖性RNA聚合酶
H3N2流感病毒的急剧增加在全世界引起严重关切,特别是在印度。H3N2引起急性呼吸道感染,然而,有几种药物可用于减轻其感染。随后,研究人员一直致力于发现新的抗病毒机制,为新的抗流感药物奠定基础。流感病毒RNA依赖性RNA聚合酶(RdRP)是一种多功能的异源三聚体,与病毒mRNA的产生有关,因此在病毒感染性中起主要作用,从而与病毒的存活直接相关。RdRP被认为是治疗性药物设计的合适靶点。本研究采用分子对接的方法,研究了桉树精油(Eucalyptus oil, EO)、香茅精油(Cymbopogon citratus, LEO)和棕榈草精油(Cymbopogon khasianus, PEO)对RdRP蛋白的活性作用。基于GC-FID(气相色谱-火焰电离检测)的成分分析,并通过CB-dock 2分析和2D相互作用进行了硅对接研究。GC-FID分析表明,EO、LEO和PEO中的主要植物成分分别为桉油、香叶和香叶。对接评分表明配体与RdRP有效结合。相互作用结果表明,RdRP/配体配合物形成氢、范德华力、pi-烷基、烷基和pi-Sigma相互作用。因此,基于上述香气特征和对接的发现,建议上述芳香作物的精油可能是缓解H3N2感染的潜在草药治疗方法。
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