Ali Haidar, Saleem Iffat, Ahmed Muhammad Saad, Amraiz Deeba, Shahid Imran, Al-Shahari Eman A, Yang Jing, Ali Liaqat
Department of Biological Sciences, National University of Medical Sciences (NUMS), Rawalpindi, Pakistan.
Department of Pharmacology & Toxicology, Faculty of Medicine, Umm Al-Qura University, Al-Abidiyah, P.O. Box 13578, Makkah, 21955, Saudi Arabia.
Virus Res. 2024 Dec;350:199497. doi: 10.1016/j.virusres.2024.199497. Epub 2024 Nov 23.
Dengue virus infection, caused by a single positive-stranded RNA virus from the Flaviviridae family, represents a significant public health challenge in tropical and subtropical regions. This virus has four serotypes (DENV-1, 2, 3, and 4), primarily transmitted by Aedes mosquitoes. Despite extensive research, effective antiviral treatments and vaccines remain elusive due to the viral diversity and the complex mechanisms such as antibody-dependent enhancement (ADE). In the current study, NS1-positive serum samples from dengue cases in Pakistan (2023-2024), were analyzed to determine the predominant serotype and characterize the envelope (E) gene for further exploration of antiviral targets. Out of 100 samples, 63 (63%) tested positive for DENV-2, indicating its predominance during this period, while two samples showed mixed infections with DENV-2 and DENV-3. The envelope gene was successfully amplified using nested PCR, validated through gel electrophoresis and sanger sequencing. Phylogenetic analysis revealed high similarity of the DENV-2 isolates to strains from China and India. Computational modeling of the envelope protein structure identified potential antiviral binding sites and further molecular docking studies suggested that specific antiviral compounds like Arbidol and Quercetin can inhibit early steps in viral infection. Additionally, BepiPred-3.0 predicted several B-cell epitopes, which could be useful for vaccine development. These findings enhance our understanding of dengue epidemiology in Pakistan and contribute to the development of targeted antiviral therapies, potentially informing future vaccination strategies and outbreak management.
登革病毒感染由黄病毒科的一种单链正核糖核酸病毒引起,是热带和亚热带地区重大的公共卫生挑战。该病毒有四种血清型(DENV-1、2、3和4),主要通过伊蚊传播。尽管进行了广泛研究,但由于病毒的多样性以及抗体依赖性增强(ADE)等复杂机制,有效的抗病毒治疗方法和疫苗仍然难以实现。在本研究中,对巴基斯坦(2023 - 2024年)登革热病例的NS1阳性血清样本进行分析,以确定主要血清型并对包膜(E)基因进行特征分析,以便进一步探索抗病毒靶点。在100个样本中,63个(63%)检测出DENV-2呈阳性,表明其在此期间占主导地位,而两个样本显示为DENV-2和DENV-3的混合感染。通过巢式PCR成功扩增包膜基因,并经凝胶电泳和桑格测序验证。系统发育分析显示,DENV-2分离株与来自中国和印度的毒株高度相似。包膜蛋白结构的计算模型确定了潜在的抗病毒结合位点,进一步的分子对接研究表明,像阿比多尔和槲皮素这样的特定抗病毒化合物可以抑制病毒感染的早期步骤。此外,BepiPred-3.0预测了几个B细胞表位,这可能对疫苗开发有用。这些发现加深了我们对巴基斯坦登革热流行病学的理解,并有助于开发有针对性的抗病毒疗法,可能为未来的疫苗接种策略和疫情管理提供参考。