Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, USA.
Yale Institute for Global Health, Yale University, New Haven, Connecticut, USA.
BMC Genomics. 2024 May 1;25(1):433. doi: 10.1186/s12864-024-10350-x.
The increasing burden of dengue virus on public health due to more explosive and frequent outbreaks highlights the need for improved surveillance and control. Genomic surveillance of dengue virus not only provides important insights into the emergence and spread of genetically diverse serotypes and genotypes, but it is also critical to monitor the effectiveness of newly implemented control strategies. Here, we present DengueSeq, an amplicon sequencing protocol, which enables whole-genome sequencing of all four dengue virus serotypes.
We developed primer schemes for the four dengue virus serotypes, which can be combined into a pan-serotype approach. We validated both approaches using genetically diverse virus stocks and clinical specimens that contained a range of virus copies. High genome coverage (>95%) was achieved for all genotypes, except DENV2 (genotype VI) and DENV 4 (genotype IV) sylvatics, with similar performance of the serotype-specific and pan-serotype approaches. The limit of detection to reach 70% coverage was 10-100 RNA copies/μL for all four serotypes, which is similar to other commonly used primer schemes. DengueSeq facilitates the sequencing of samples without known serotypes, allows the detection of multiple serotypes in the same sample, and can be used with a variety of library prep kits and sequencing instruments.
DengueSeq was systematically evaluated with virus stocks and clinical specimens spanning the genetic diversity within each of the four dengue virus serotypes. The primer schemes can be plugged into existing amplicon sequencing workflows to facilitate the global need for expanded dengue virus genomic surveillance.
登革热病毒给公共卫生带来的负担日益加重,因为其爆发更加猛烈且更为频繁,这凸显了加强监测和控制的必要性。对登革热病毒进行基因组监测不仅可以深入了解遗传上多样化的血清型和基因型的出现和传播,而且对于监测新实施的控制策略的效果也至关重要。在这里,我们提出了 DengueSeq,这是一种扩增子测序方案,可实现所有四种登革热病毒血清型的全基因组测序。
我们为这四种登革热病毒血清型开发了引物方案,这些方案可以组合成一种泛血清型方法。我们使用遗传上多样化的病毒株和包含一系列病毒拷贝的临床标本对这两种方法进行了验证。除了 DENV2(VI 型)和 DENV4(IV 型)野毒株之外,所有基因型的基因组覆盖率均达到了>95%(DENV2 和 DENV4 野毒株除外),两种方法的性能相似。达到 70%覆盖率的检测限为所有四种血清型的 10-100 RNA 拷贝/μL,与其他常用的引物方案相似。DengueSeq 便于对未知血清型的样本进行测序,允许在同一样本中检测多种血清型,并且可以与各种文库制备试剂盒和测序仪器一起使用。
我们用涵盖了四种登革热病毒血清型内每种血清型遗传多样性的病毒株和临床标本对 DengueSeq 进行了系统评估。这些引物方案可以被整合到现有的扩增子测序工作流程中,以满足全球对扩大登革热病毒基因组监测的需求。