首页> 美国卫生研究院文献>PLoS Neglected Tropical Diseases >Application of a targeted-enrichment methodology for full-genome sequencing of Dengue 1-4 Chikungunya and Zika viruses directly from patient samples
【2h】

Application of a targeted-enrichment methodology for full-genome sequencing of Dengue 1-4 Chikungunya and Zika viruses directly from patient samples

机译:靶向富集方法在直接从患者样品中登革热1-4基孔肯雅热和寨卡病毒全基因组测序中的应用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The frequency of epidemics caused by Dengue viruses 1–4, Zika virus and Chikungunya viruses have been on an upward trend in recent years driven primarily by uncontrolled urbanization, mobility of human populations and geographical spread of their shared vectors, Aedes aegypti and Aedes albopictus. Infections by these viruses present with similar clinical manifestations making them challenging to diagnose; this is especially difficult in regions of the world hyperendemic for these viruses. In this study, we present a targeted-enrichment methodology to simultaneously sequence the complete viral genomes for each of these viruses directly from clinical samples. Additionally, we have also developed a customized computational tool (BaitMaker) to design these enrichment baits. This methodology is robust in its ability to capture diverse sequences and is amenable to large-scale epidemiological studies. We have applied this methodology to two large cohorts: a febrile study based in Colombo, Sri Lanka taken during the 2009–2015 dengue epidemic (n = 170) and another taken during the 2016 outbreak of Zika virus in Singapore (n = 162). Results from these studies indicate that we were able to cover an average of 97.04% ± 0.67% of the full viral genome from samples in these cohorts. We also show detection of one DENV3/ZIKV co-infected patient where we recovered full genomes for both viruses.
机译:近年来,由登革热病毒1-4,寨卡病毒和基孔肯雅病毒引起的流行频率呈上升趋势,这主要是由于不受控制的城市化,人口流动以及其共有媒介伊蚊和白纹伊蚊的地理分布所致。这些病毒的感染具有相似的临床表现,使其难以诊断。在世界上这些病毒高流行的地区,这尤其困难。在这项研究中,我们提出了一种靶向富集方法,可直接从临床样品中同时对每种病毒的完整病毒基因组进行测序。此外,我们还开发了定制的计算工具(BaitMaker)来设计这些浓缩诱饵。这种方法具有捕获各种序列的能力,并且适合大规模流行病学研究。我们已将此方法应用于两个大型队列:一项在斯里兰卡科伦坡的发热研究,在2009-2015年登革热流行期间(n = 170)进行,另一项在2016年新加坡寨卡病毒爆发期间进行(n = 162)。这些研究的结果表明,我们能够从这些人群的样本中平均覆盖整个病毒基因组的97.04%±0.67%。我们还显示了对一名DENV3 / ZIKV共感染患者的检测,在该患者中我们恢复了两种病毒的完整基因组。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号