Abstract

COVID-19 global cases have climbed to more than 33 million, with over a million total deaths, as of September, 2020. Real-time massive SARS-CoV-2 whole genome sequencing is key to tracking chains of transmission and estimating the origin of disease outbreaks. Yet no methods have simultaneously achieved high precision, simple workflow, and low cost. We developed a high-precision, cost-efficient SARS-CoV-2 whole genome sequencing platform for COVID-19 genomic surveillance, CorvGenSurv (Coronavirus Genomic Surveillance). CorvGenSurv directly amplified viral RNA from COVID-19 patients’ Nasopharyngeal/Oropharyngeal (NP/OP) swab specimens and sequenced the SARS-CoV-2 whole genome in three segments by long-read, high-throughput sequencing. Sequencing of the whole genome in three segments significantly reduced sequencing data waste, thereby preventing dropouts in genome coverage. We validated the precision of our pipeline by both control genomic RNA sequencing and Sanger sequencing. We produced near full-length whole genome sequences from individuals who were COVID-19 test positive during April to June 2020 in Los Angeles County, California, USA. These sequences were highly diverse in the G clade with nine novel amino acid mutations including NSP12-M755I and ORF8-V117F. With its readily adaptable design, CorvGenSurv grants wide access to genomic surveillance, permitting immediate public health response to sudden threats.

Highlights

  • COVID-19 global cases have climbed to more than 33 million, with over a million total deaths, as of September, 2020

  • After de-multiplexing, we built the consensus sequence of each of the three segments, correcting sequencing errors. These overlapping consensus sequences were assembled into a near fulllength SARS-CoV-2 whole genome sequence for each COVID-19 case

  • We developed CorvGenSurv (Coronavirus Genomic Surveillance), a streamlined, high-resolution, and costeffective SARS-CoV-2 whole genome sequencing method in which viral RNA is directly amplified, indexed, and sequenced

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Summary

Introduction

COVID-19 global cases have climbed to more than 33 million, with over a million total deaths, as of September, 2020. We produced near full-length whole genome sequences from individuals who were COVID-19 test positive during April to June 2020 in Los Angeles County, California, USA These sequences were highly diverse in the G clade with nine novel amino acid mutations including NSP12-M755I and ORF8-V117F. SARS-CoV-2 whole genome sequencing has important utility in the surveillance of amino acid mutations that may result in changes to viral protein physical ­structures[12,13] Such changes in structure can potentially alter virus ­transmissibility[14], disease ­severity[15], or reduce vaccine ­efficacy[16,17]. CorvGenSurv is a streamlined, high-resolution, and cost-effective pipeline that facilitates the deployment of real-time SARS-CoV-2 whole genome sequencing for public health

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