MINERVA: A Facile Strategy for SARS-CoV-2 Whole-Genome Deep Sequencing of Clinical Samples

Mol Cell. 2020 Dec 17;80(6):1123-1134.e4. doi: 10.1016/j.molcel.2020.11.030. Epub 2020 Nov 20.

Abstract

Analyzing the genome of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) from clinical samples is crucial for understanding viral spread and evolution as well as for vaccine development. Existing RNA sequencing methods are demanding on user technique and time and, thus, not ideal for time-sensitive clinical samples; these methods are also not optimized for high performance on viral genomes. We developed a facile, practical, and robust approach for metagenomic and deep viral sequencing from clinical samples. We demonstrate the utility of our approach on pharyngeal, sputum, and stool samples collected from coronavirus disease 2019 (COVID-19) patients, successfully obtaining whole metatranscriptomes and complete high-depth, high-coverage SARS-CoV-2 genomes with high yield and robustness. With a shortened hands-on time from sample to virus-enriched sequencing-ready library, this rapid, versatile, and clinic-friendly approach will facilitate molecular epidemiology studies during current and future outbreaks.

Keywords: COVID-19, SARS-CoV-2, whole-genome sequencing, metagenomics.

MeSH terms

  • Animals
  • COVID-19 / genetics*
  • Genome, Viral*
  • High-Throughput Nucleotide Sequencing*
  • Humans
  • Mice
  • NIH 3T3 Cells
  • RNA, Viral / genetics*
  • RNA, Viral / metabolism
  • SARS-CoV-2 / genetics*
  • SARS-CoV-2 / metabolism
  • Whole Genome Sequencing*

Substances

  • RNA, Viral