TY - JOUR
T1 - Developing an appropriate evolutionary baseline model for the study of SARS-CoV-2 patient samples
AU - Terbot, John W.
AU - Johri, Parul
AU - Liphardt, Schuyler W.
AU - Soni, Vivak
AU - Pfeifer, Susanne P.
AU - Cooper, Brandon S.
AU - Good, Jeffrey M.
AU - Jensen, Jeffrey D.
N1 - Funding Information: Research reported in this publication was supported by the National Institute of General Medical Sciences of the National Institutes of Health (NIH) under Award Numbers P20GM102546 and P30GM140963. NIH awards R35GM124701 (BSC) and R35GM139383 (JDJ) also supported this work. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We would like to thank Jeremy Kamil and Timothy Kowalik for helpful comments on the manuscript, and Will Conner, David Xing, and the University of Montana Genomics Core for data contributions. Publisher Copyright: © 2023 Terbot et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2023/4
Y1 - 2023/4
N2 - AU Over: Pleaseconfirmthatallheadinglevelsarerepresentedcorrectly the past 3 years, Severe Acute Respiratory Syndrome:Coronavirus 2 (SARS-CoV-2) has spread through human populations in several waves, resulting in a global health crisis. In response, genomic surveillance efforts have proliferated in the hopes of tracking and anticipating the evolution of this virus, resulting in millions of patient isolates now being available in public databases. Yet, while there is a tremendous focus on identifying newly emerging adaptive viral variants, this quantification is far from trivial. Specifically, multiple co-occurring and interacting evolutionary processes are constantly in operation and must be jointly considered and modeled in order to perform accurate inference. We here outline critical individual components of such an evolutionary baseline model—mutation rates, recombination rates, the distribution of fitness effects, infection dynamics, and compartmentalization—and describe the current state of knowledge pertaining to the related parameters of each in SARS-CoV-2. We close with a series of recommendations for future clinical sampling, model construction, and statistical analysis.
AB - AU Over: Pleaseconfirmthatallheadinglevelsarerepresentedcorrectly the past 3 years, Severe Acute Respiratory Syndrome:Coronavirus 2 (SARS-CoV-2) has spread through human populations in several waves, resulting in a global health crisis. In response, genomic surveillance efforts have proliferated in the hopes of tracking and anticipating the evolution of this virus, resulting in millions of patient isolates now being available in public databases. Yet, while there is a tremendous focus on identifying newly emerging adaptive viral variants, this quantification is far from trivial. Specifically, multiple co-occurring and interacting evolutionary processes are constantly in operation and must be jointly considered and modeled in order to perform accurate inference. We here outline critical individual components of such an evolutionary baseline model—mutation rates, recombination rates, the distribution of fitness effects, infection dynamics, and compartmentalization—and describe the current state of knowledge pertaining to the related parameters of each in SARS-CoV-2. We close with a series of recommendations for future clinical sampling, model construction, and statistical analysis.
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U2 - 10.1371/journal.ppat.1011265
DO - 10.1371/journal.ppat.1011265
M3 - Review article
C2 - 37018331
SN - 1553-7366
VL - 19
JO - PLoS pathogens
JF - PLoS pathogens
IS - 4
M1 - e1011265
ER -