Developing an appropriate evolutionary baseline model for the study of SARS-CoV-2 patient samples
Over 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...
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Published in | PLoS pathogens Vol. 19; no. 4; p. e1011265 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
01.04.2023
Public Library of Science (PLoS) |
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Abstract | Over 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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AbstractList | Over 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. |
Audience | Academic |
Author | Cooper, Brandon S Jensen, Jeffrey D Good, Jeffrey M Terbot, 2nd, John W Soni, Vivak Johri, Parul Liphardt, Schuyler W Pfeifer, Susanne P |
AuthorAffiliation | University of Alberta, CANADA 1 University of Montana, Division of Biological Sciences, Missoula, Montana, United States of America 2 Arizona State University, School of Life Sciences, Center for Evolution & Medicine, Tempe, Arizona, United States of America |
AuthorAffiliation_xml | – name: University of Alberta, CANADA – name: 2 Arizona State University, School of Life Sciences, Center for Evolution & Medicine, Tempe, Arizona, United States of America – name: 1 University of Montana, Division of Biological Sciences, Missoula, Montana, United States of America |
Author_xml | – sequence: 1 givenname: John W surname: Terbot, 2nd fullname: Terbot, 2nd, John W organization: Arizona State University, School of Life Sciences, Center for Evolution & Medicine, Tempe, Arizona, United States of America – sequence: 2 givenname: Parul surname: Johri fullname: Johri, Parul organization: Arizona State University, School of Life Sciences, Center for Evolution & Medicine, Tempe, Arizona, United States of America – sequence: 3 givenname: Schuyler W surname: Liphardt fullname: Liphardt, Schuyler W organization: University of Montana, Division of Biological Sciences, Missoula, Montana, United States of America – sequence: 4 givenname: Vivak surname: Soni fullname: Soni, Vivak organization: Arizona State University, School of Life Sciences, Center for Evolution & Medicine, Tempe, Arizona, United States of America – sequence: 5 givenname: Susanne P surname: Pfeifer fullname: Pfeifer, Susanne P organization: Arizona State University, School of Life Sciences, Center for Evolution & Medicine, Tempe, Arizona, United States of America – sequence: 6 givenname: Brandon S orcidid: 0000-0002-8269-7731 surname: Cooper fullname: Cooper, Brandon S organization: University of Montana, Division of Biological Sciences, Missoula, Montana, United States of America – sequence: 7 givenname: Jeffrey M orcidid: 0000-0003-0707-5374 surname: Good fullname: Good, Jeffrey M organization: University of Montana, Division of Biological Sciences, Missoula, Montana, United States of America – sequence: 8 givenname: Jeffrey D orcidid: 0000-0002-4786-8064 surname: Jensen fullname: Jensen, Jeffrey D organization: Arizona State University, School of Life Sciences, Center for Evolution & Medicine, Tempe, Arizona, United States of America |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37018331$$D View this record in MEDLINE/PubMed |
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Copyright | 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. COPYRIGHT 2023 Public Library of Science 2023 Terbot et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2023 Terbot et al 2023 Terbot et al |
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SubjectTerms | Analysis Biology and life sciences Coronaviruses COVID-19 Estimates Evolution Evolutionary biology Genetic diversity Genetic variation Genomes Genomics Global health Health aspects Human populations Humans Infections Mathematical models Medicine and health sciences Methods Mutation Mutation rates Public health Recombination Review SARS-CoV-2 Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Statistical analysis Viral diseases Viruses |
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Title | Developing an appropriate evolutionary baseline model for the study of SARS-CoV-2 patient samples |
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