Duke-NUS Medical School, Singapore.
National University of Singapore, Saw Swee Hock School of Public Health, Singapore.
PLoS Negl Trop Dis. 2019 Apr 25;13(4):e0007184. doi: 10.1371/journal.pntd.0007184. eCollection 2019 Apr.
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.
近年来,登革热病毒 1-4 型、寨卡病毒和基孔肯雅热病毒引起的流行频率呈上升趋势,主要原因是城市化失控、人口流动以及它们共同的传播媒介埃及伊蚊和白纹伊蚊的地理传播。这些病毒的感染表现出相似的临床症状,使得诊断具有挑战性;在这些病毒高度流行的世界区域,这尤其困难。在这项研究中,我们提出了一种靶向富集方法,可直接从临床样本中同时对这些病毒的完整病毒基因组进行测序。此外,我们还开发了一种定制的计算工具(BaitMaker)来设计这些富集探针。该方法在捕获多样化序列方面具有强大的能力,并且适用于大规模的流行病学研究。我们已经将该方法应用于两个大队列:一个是在斯里兰卡科伦坡进行的发热研究,该研究是在 2009-2015 年登革热流行期间进行的(n = 170),另一个是在 2016 年新加坡寨卡病毒爆发期间进行的(n = 162)。这些研究的结果表明,我们能够覆盖这些队列中样本的病毒全基因组的平均 97.04% ± 0.67%。我们还显示出检测到一名 DENV3/ZIKV 合并感染患者,我们从该患者中恢复了两种病毒的完整基因组。