Wong Christopher W, Albert Thomas J, Vega Vinsensius B, Norton Jason E, Cutler David J, Richmond Todd A, Stanton Lawrence W, Liu Edison T, Miller Lance D
Genome Institute of Singapore, Singapore 138672, Republic of Singapore.
Genome Res. 2004 Mar;14(3):398-405. doi: 10.1101/gr.2141004.
Mutations in the SARS-Coronavirus (SARS-CoV) can alter its clinical presentation, and the study of its mutation patterns in human populations can facilitate contact tracing. Here, we describe the development and validation of an oligonucleotide resequencing array for interrogating the entire 30-kb SARS-CoV genome in a rapid, cost-effective fashion. Using this platform, we sequenced SARS-CoV genomes from Vero cell culture isolates of 12 patients and directly from four patient tissues. The sequence obtained from the array is highly reproducible, accurate (>99.99% accuracy) and capable of identifying known and novel variants of SARS-CoV. Notably, we applied this technology to a field specimen of probable SARS and rapidly deduced its infectious source. We demonstrate that array-based resequencing-by-hybridization is a fast, reliable, and economical alternative to capillary sequencing for obtaining SARS-CoV genomic sequence on a population scale, making this an ideal platform for the global monitoring of SARS-CoV and other small-genome pathogens.
严重急性呼吸综合征冠状病毒(SARS-CoV)的突变可改变其临床表现,而对其在人群中的突变模式进行研究有助于接触者追踪。在此,我们描述了一种寡核苷酸重测序阵列的开发与验证,该阵列能够以快速且经济高效的方式对整个30 kb的SARS-CoV基因组进行检测。利用这个平台,我们对12例患者的Vero细胞培养分离株以及直接从4例患者组织中提取的SARS-CoV基因组进行了测序。从阵列获得的序列具有高度可重复性、准确性高(准确率>99.99%),并且能够识别SARS-CoV的已知和新型变体。值得注意的是,我们将这项技术应用于一份可能感染SARS的现场样本,并迅速推断出其传染源。我们证明,基于阵列的杂交重测序是一种在群体规模上获取SARS-CoV基因组序列的快速、可靠且经济的替代毛细管测序的方法,使其成为全球监测SARS-CoV和其他小基因组病原体的理想平台。