Tariq Faaria, Irfan Muhammad, Farooq Saba, Iqbal Hana'a, Khan Ishtiaq Ahmad, Iftner Thomas, Choudhary M Iqbal
National Institute of Virology, Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan.
Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan.
Sci Rep. 2025 Jul 2;15(1):22703. doi: 10.1038/s41598-025-07606-1.
Dengue virus (DENV) poses a critical health threat causing millions of cases every year. The absence of proof-reading activity of the RNA-dependent RNA polymerases (RdRp) leads to significant mutations in its genome. This may result in genetic diversity among the genotypes which contribute to severe complications during the infection. Targeting these mutations may help to understand the viral transmission and identify a potential treatment. An aggregate of 152 dengue positive serum samples were collected from different tertiary care hospitals in Karachi. RNA isolation, cDNA synthesis as well as amplification of the C-prM region was performed, followed by the Sanger sequencing. The resultant sequences of each serotype were aligned with their respective genome sequences and phylogenetic trees based on genotypes were constructed using Maximum Likelihood (ML) method with 1000 bootstraps replicates. The sequences were then converted to the amino acid sequence and genetic variations in comparison to the reference genomes were evaluated. The results showed that there was a higher number of positive cases in males (58%) than in females (42%). The most affected age group was 21-30. The study suggested that the dominant serotype in the population of Karachi was DENV-1 (78.33%), followed by DENV- 2 (15%) and DENV-3 (6.66%). Overall, the acquired data provide the information about genetic variation in the C-prM region of dengue virus in Karachi, Pakistan.
登革病毒(DENV)对健康构成严重威胁,每年导致数百万病例。RNA依赖性RNA聚合酶(RdRp)缺乏校对活性导致其基因组发生显著突变。这可能导致基因型之间的遗传多样性,从而在感染期间引发严重并发症。针对这些突变可能有助于了解病毒传播并确定潜在的治疗方法。从卡拉奇不同的三级护理医院收集了152份登革热阳性血清样本。进行了RNA分离、cDNA合成以及C-prM区域的扩增,随后进行桑格测序。将每种血清型的所得序列与其各自的基因组序列进行比对,并使用最大似然法(ML)和1000次重复自展构建基于基因型的系统发育树。然后将序列转换为氨基酸序列,并评估与参考基因组相比的遗传变异。结果显示,男性阳性病例数(58%)高于女性(42%)。受影响最大的年龄组是21至30岁。该研究表明,卡拉奇人群中占主导地位的血清型是DENV-1(78.33%),其次是DENV-2(15%)和DENV-3(6.66%)。总体而言,所获得的数据提供了关于巴基斯坦卡拉奇登革病毒C-prM区域遗传变异的信息。