Genomics and Bioinformatics Department, Biological Defense Research Directorate, Naval Medical Research Center - Frederick, Fort Detrick, Frederick, MD, 21702, USA.
Uniformed Services University of the Health Sciences, Bethesda, MD, 20814, USA.
BMC Genomics. 2019 Feb 26;20(1):155. doi: 10.1186/s12864-019-5543-2.
Sequencing-based detection and characterization of viruses in complex samples can suffer from lack of sensitivity due to a variety of factors including, but not limited to, low titer, small genome size, and contribution of host or environmental nucleic acids. Hybridization-based target enrichment is one potential method for increasing the sensitivity of viral detection via high-throughput sequencing.
This study expands upon two previously developed panels of virus enrichment probes (for filoviruses and for respiratory viruses) to include other viruses of biodefense and/or biosurveillance concern to the U.S. Department of Defense and various international public health agencies. The newly expanded and combined panel is tested using carefully constructed synthetic metagenomic samples that contain clinically relevant amounts of viral genetic material. Target enrichment results in a dramatic increase in sensitivity for virus detection as compared to shotgun sequencing, yielding full, deeply covered viral genomes from materials with Ct values suggesting that amplicon sequencing would be likely to fail. Increased pooling to improve cost- and time-effectiveness does not negatively affect the ability to obtain full-length viral genomes, even in the case of co-infections, although as expected, it does decrease depth of coverage.
Hybridization-based target enrichment is an effective solution to obtain full-length viral genomes for samples from which virus detection would fail via unbiased, shotgun sequencing or even via amplicon sequencing. As the development and testing of probe sets for viral target enrichment expands and continues, the application of this technique, in conjunction with deeper pooling strategies, could make high-throughput sequencing more economical for routine use in biosurveillance, biodefense and outbreak investigations.
基于测序的病毒检测和鉴定在复杂样本中可能会由于多种因素(包括但不限于低滴度、小基因组大小以及宿主或环境核酸的贡献)而缺乏敏感性。基于杂交的靶向富集是一种通过高通量测序提高病毒检测灵敏度的潜在方法。
本研究扩展了之前开发的两种病毒富集探针(用于丝状病毒和呼吸道病毒),以包括美国国防部和各种国际公共卫生机构关注的其他生物防御和/或生物监测病毒。新扩展和组合的探针组使用精心构建的含有临床相关病毒遗传物质的合成宏基因组样本进行测试。与 shotgun 测序相比,靶向富集显著提高了病毒检测的灵敏度,从 Ct 值表明扩增子测序可能失败的材料中获得了完整、深度覆盖的病毒基因组。为了提高成本效益和时间效率而增加池化不会影响获得全长病毒基因组的能力,即使在合并感染的情况下也是如此,尽管正如预期的那样,它确实会降低覆盖深度。
基于杂交的靶向富集是一种有效的解决方案,可以从通过无偏 shotgun 测序甚至扩增子测序检测病毒失败的样本中获得全长病毒基因组。随着用于病毒靶向富集的探针组的开发和测试的扩展和继续,这种技术与更深层次的池化策略相结合,可以使高通量测序在生物监测、生物防御和疫情调查中的常规应用更加经济。