4.6 Article

Dengue Virus Serotype 2 Intrahost Diversity in Patients with Different Clinical Outcomes

期刊

VIRUSES-BASEL
卷 13, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/v13020349

关键词

dengue virus; serotype 2; intrahost diversity; severe disease

类别

资金

  1. International Development Research Centre (IDRC) Canada [108411-001]
  2. French Government's Investissement d'Avenir program, Laboratoire d'Excellence Integrative Biology of Emerging Infectious Diseases [ANR-10LABX-62-IBEID]
  3. Faperj [E-26/2002.930/2016]

向作者/读者索取更多资源

The study found significant differences in viral population structure among different clinical classifications of Dengue virus serotype 2 circulating in Brazil, driven mainly by different infection times and selection pressures rather than clinical outcomes. However, diversity in the NS2B gene was found to be constrained, regardless of clinical outcome and infection time. High frequency of non-synonymous intrahost single-nucleotide variants were identified among cases with warning signs and severe cases, but no single variant appeared to characterize cases of greater severity independently.
Intrahost genetic diversity is thought to facilitate arbovirus adaptation to changing environments and hosts, and it might also be linked to viral pathogenesis. Dengue virus serotype 2 (DENV-2) has circulated in Brazil since 1990 and is associated with severe disease and explosive outbreaks. Intending to shed light on the viral determinants for severe dengue pathogenesis, we sought to analyze the DENV-2 intrahost genetic diversity in 68 patient cases clinically classified as dengue fever (n = 31), dengue with warning signs (n = 19), and severe dengue (n = 18). Unlike previous DENV intrahost diversity studies whose approaches employed PCR, here we performed viral whole-genome deep sequencing from clinical samples with an amplicon-free approach, representing the real intrahost diversity scenario. Striking differences were detected in the viral population structure between the three clinical categories, which appear to be driven mainly by different infection times and selection pressures, rather than being linked with the clinical outcome itself. Diversity in the NS2B gene, however, showed to be constrained, irrespective of clinical outcome and infection time. Finally, 385 non-synonymous intrahost single-nucleotide variants located along the viral polyprotein, plus variants located in the untranslated regions, were consistently identified among the samples. Of them, 124 were exclusively or highly detected among cases with warning signs and among severe cases. However, there was no variant that by itself appeared to characterize the cases of greater severity, either due to its low intrahost frequency or the conservative effect on amino acid substitution. Although further studies are necessary to determine their real effect on viral proteins, this heightens the possibility of epistatic interactions. The present analysis represents an initial effort to correlate DENV-2 genetic diversity to its pathogenic potential and thus contribute to understanding the virus's dynamics within its human host.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据