Department of Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Department of Pathology, National Cheng Kung University Hospital, Tainan, Taiwan.
PLoS Negl Trop Dis. 2024 Jun 13;18(6):e0012268. doi: 10.1371/journal.pntd.0012268. eCollection 2024 Jun.
Dengue virus (DENV) causes approximately 390 million dengue infections worldwide every year. There were 22,777 reported DENV infections in Tainan, Taiwan in 2015. In this study, we sequenced the C-prM-E genes from 45 DENV 2015 strains, and phylogenetic analysis based on C-prM-E genes revealed that all strains were classified as DENV serotype 2 Cosmopolitan genotype. Sequence analysis comparing different DENV-2 genotypes and Cosmopolitan DENV-2 sequences prior to 2015 showed a clade replacement event in the DENV-2 Cosmopolitan genotype. Additionally, a major substitution C-A314G (K73R) was found in the capsid region which may have contributed to the clade replacement event. Reverse genetics virus rgC-A314G (K73R) showed slower replication in BHK-21 and C6/36 cells compared to wildtype virus, as well as a decrease in NS1 production in BHK-21-infected cells. After a series of passaging, the C-A314G (K73R) mutation reverted to wildtype and was thus considered to be unstable. Next generation sequencing (NGS) of three sera collected from a single DENV2-infected patient at 1-, 2-, and 5-days post-admission was employed to examine the genetic diversity over-time and mutations that may work in conjunction with C-A314G (K73R). Results showed that the number of haplotypes decreased with time in the DENV-infected patient. On the fifth day after admission, two new haplotypes emerged, and a single non-synonymous NS4A-L115I mutation was identified. Therefore, we have identified a persistent mutation C-A314G (K73R) in all of the DENV-2 isolates, and during the course of an infection, a single new non-synonymous mutation in the NS4A region appears in the virus population within a single host. The C-A314G (K73R) thus may have played a role in the DENV-2 2015 outbreak while the NS4A-L115I may be advantageous during DENV infection within the host.
登革热病毒(DENV)每年在全球导致约 3.9 亿例登革热感染。2015 年,中国台湾台南报告了 22777 例登革热感染。在这项研究中,我们对 45 株 2015 年的 DENV2 分离株的 C-prM-E 基因进行了测序,基于 C-prM-E 基因的系统进化分析显示,所有分离株均被归类为 DENV 血清型 2 型世界性基因型。对 2015 年前不同 DENV-2 基因型和世界性 DENV-2 序列的序列分析显示,DENV-2 世界性基因型发生了枝替换事件。此外,在衣壳区发现了一个主要的取代 C-A314G(K73R),这可能促成了枝替换事件。逆转录病毒 rgC-A314G(K73R)在 BHK-21 和 C6/36 细胞中的复制速度比野生型病毒慢,并且在 BHK-21 感染细胞中 NS1 的产生减少。经过一系列传代,C-A314G(K73R)突变回复为野生型,因此被认为是不稳定的。对一名 2015 年登革热 2 型感染患者在入院后第 1、2 和 5 天采集的 3 份血清进行下一代测序(NGS),以检测随时间推移的遗传多样性和可能与 C-A314G(K73R)协同作用的突变。结果表明,登革热感染患者体内的单倍型数量随时间减少。入院后第 5 天,出现了两种新的单倍型,并鉴定出单个非同义 NS4A-L115I 突变。因此,我们在所有 DENV-2 分离株中发现了一个持续存在的突变 C-A314G(K73R),并且在感染过程中,单个宿主内病毒群体中出现了单个新的非同义 NS4A 区突变。因此,C-A314G(K73R)可能在 2015 年登革热疫情中发挥了作用,而 NS4A-L115I 可能在宿主内登革热感染中具有优势。