Fast Evaluation of Viral Emerging Risks (FEVER): A computational tool for biosurveillance, diagnostics, and mutation typing of emerging viral pathogens

Zachary R. Stromberg, James Theiler, Brian T. Foley, Adán Myers y. Gutiérrez, Attelia Hollander, Samantha J. Courtney, Jason Gans, Alina Deshpande, Ebany J. Martinez-Finley, Jason Mitchell, Harshini Mukundan, Karina Yusim, Jessica Z. Kubicek-Sutherland

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Viral pathogens can rapidly evolve, adapt to novel hosts, and evade human immunity. The early detection of emerging viral pathogens through biosurveillance coupled with rapid and accurate diagnostics are required to mitigate global pandemics. However, RNA viruses can mutate rapidly, hampering biosurveillance and diagnostic efforts. Here, we present a novel computational approach called FEVER (Fast Evaluation of Viral Emerging Risks) to design assays that simultaneously accomplish: 1) broad-coverage biosurveillance of an entire group of viruses, 2) accurate diagnosis of an outbreak strain, and 3) mutation typing to detect variants of public health importance. We demonstrate the application of FEVER to generate assays to simultaneously 1) detect sarbecoviruses for biosurveillance; 2) diagnose infections specifically caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2); and 3) perform rapid mutation typing of the D614G SARS-CoV-2 spike variant associated with increased pathogen transmissibility. These FEVER assays had a high in silico recall (predicted positive) up to 99.7% of 525,708 SARS-CoV-2 sequences analyzed and displayed sensitivities and specificities as high as 92.4% and 100% respectively when validated in 100 clinical samples. The D614G SARS-CoV-2 spike mutation PCR test was able to identify the single nucleotide identity at position 23,403 in the viral genome of 96.6% SARS-CoV-2 positive samples without the need for sequencing. This study demonstrates the utility of FEVER to design assays for biosurveillance, diagnostics, and mutation typing to rapidly detect, track, and mitigate future outbreaks and pandemics caused by emerging viruses.

Original languageEnglish
Article numbere0000207
JournalPLOS Global Public Health
Volume2
Issue number2 February
DOIs
StatePublished - Feb 2022

Funding

This research was funded by Los Alamos National Laboratory Exploratory Research and Development grant number 20190392ER (to J.K.S and K.Y.) and Los Alamos National Laboratory Technology Evaluation and Demonstration Funds. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors would like to thank the Presbyterian Clinical Research team (Brigitte Holder, Susan Salazar, and Maria Vahtel) for their contributions to this study. We are also grateful to the patients who volunteered to take part in this study. Dr. Karina Yusim passed away before the submission of the final version of this manuscript. Dr. Jessica Kubicek-Sutherland accepts responsibility for the integrity and validity of the data collected and analyzed.

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