Department of Physiology, Genetics, and Microbiology, University of Alicante, Alicante, Spain.
Bigelow Laboratory for Ocean Sciences, East Boothbay, ME, USA.
Environ Microbiol. 2021 Mar;23(3):1584-1593. doi: 10.1111/1462-2920.15375. Epub 2021 Jan 17.
Metagenomics and single-cell genomics have enabled the discovery of relevant uncultured microbes. Recently, single-virus genomics (SVG), although still in an incipient stage, has opened new avenues in viral ecology by allowing the sequencing of one single virus at a time. The investigation of methodological alternatives and optimization of existing procedures for SVG is paramount to deliver high-quality genomic data. We report a sequencing dataset of viral single-amplified genomes (vSAGs) from cultured and uncultured viruses obtained by applying different conditions in each SVG step, from viral preservation and novel whole-genome amplification (WGA) to sequencing platforms and genome assembly. Sequencing data showed that cryopreservation and mild fixation were compatible with WGA, although fresh samples delivered better genome quality data. The novel TruPrime WGA, based on primase-polymerase features, and WGA-X employing a thermostable phi29 polymerase, were proven to be with sufficient sensitivity in SVG. The Oxford Nanopore (ON) sequencing platform did not provide a significant improvement of vSAG assembly compared to Illumina alone. Finally, the SPAdes assembler performed the best. Overall, our results represent a valuable genomic dataset that will help to standardized and advance new tools in viral ecology.
宏基因组学和单细胞基因组学已经能够发现相关的未培养微生物。最近,虽然单病毒基因组学(SVG)仍处于起步阶段,但通过一次对单个病毒进行测序,为病毒生态学开辟了新途径。调查替代方法和优化 SVG 的现有程序对于提供高质量的基因组数据至关重要。我们报告了一个通过在每个 SVG 步骤中应用不同条件(从病毒保存到新型全基因组扩增(WGA)再到测序平台和基因组组装)从培养和未培养病毒中获得的病毒单扩增基因组(vSAG)的测序数据集。测序数据表明,低温保存和温和固定与 WGA 兼容,尽管新鲜样本提供了更好的基因组质量数据。基于引物酶-聚合酶特性的新型 TruPrime WGA 和采用热稳定 phi29 聚合酶的 WGA-X 已被证明在 SVG 中具有足够的灵敏度。与单独使用 Illumina 相比,Oxford Nanopore(ON)测序平台并未为 vSAG 组装提供显著改进。最后,SPAdes 组装器的表现最好。总体而言,我们的结果代表了一个有价值的基因组数据集,将有助于病毒生态学的标准化和新工具的推进。