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治疗学洞察:包含免疫药理学的人轮状病毒A治疗腹泻的阐释

Therapeutics Insight with Inclusive Immunopharmacology Explication of Human Rotavirus A for the Treatment of Diarrhea.

作者信息

Hossain Mohammad Uzzal, Hashem Abu, Keya Chaman Ara, Salimullah Md

机构信息

Department of Biotechnology and Genetic Engineering, Life Science Faculty, Mawlana Bhashani Science and Technology University Tangail, Bangladesh.

Microbial Biotechnology Division, National Institute of Biotechnology Dhaka, Bangladesh.

出版信息

Front Pharmacol. 2016 Jun 23;7:153. doi: 10.3389/fphar.2016.00153. eCollection 2016.

Abstract

Rotavirus is the most common cause of severe infant and childhood diarrhea worldwide, and the morbidity and mortality rate is going to be outnumbered in developing countries like Bangladesh. To mitigate this substantial burden of disease, new therapeutics such as vaccine and drug are swiftly required against rotavirus. The present therapeutics insight study was performed with comprehensive immunoinformatics and pharmacoinformatics approach. T and B-cell epitopes were assessed in the conserved region of outer capsid protein VP4 among the highly reviewed strains from different countries including Bangladesh. The results suggest that epitope SU1 (TLKNLNDNY) could be an ideal candidate among the predicted five epitopes for both T and B-cell epitopes for the development of universal vaccine against rotavirus. This research also suggests five novel drug compounds from medicinal plant Rhizophora mucronata Lamk. for better therapeutics strategies against rotavirus diarrhea based on 3D structure building, pharmacophore, ADMET, and QSAR properties. The exact mode of action between drug compounds and target protein VP4 were revealed by molecular docking analysis. Drug likeness and oral bioavailability further confirmed the effectiveness of the proposed drugs against rotavirus diarrhea. This study might be implemented for experimental validation to facilitate the novel vaccine and drug design.

摘要

轮状病毒是全球婴幼儿严重腹泻的最常见病因,在孟加拉国等发展中国家,其发病率和死亡率将居高不下。为减轻这一巨大的疾病负担,迫切需要针对轮状病毒的新型治疗方法,如疫苗和药物。本治疗学洞察研究采用了综合免疫信息学和药物信息学方法。在包括孟加拉国在内的不同国家的高评价菌株中,对外衣壳蛋白VP4的保守区域进行了T细胞和B细胞表位评估。结果表明,在预测的五个表位中,表位SU1(TLKNLNDNY)可能是开发抗轮状病毒通用疫苗的T细胞和B细胞表位的理想候选者。本研究还基于三维结构构建、药效团、ADMET和QSAR特性,从药用植物红树Rhizophora mucronata Lamk.中提出了五种新型药物化合物,用于更好地治疗轮状病毒腹泻。通过分子对接分析揭示了药物化合物与靶蛋白VP4之间的确切作用模式。药物相似性和口服生物利用度进一步证实了所提出药物对轮状病毒腹泻的有效性。本研究可用于实验验证,以促进新型疫苗和药物设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ada/4917548/e064c8472a2d/fphar-07-00153-g0001.jpg

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