tetano
Editor, Senior Moderator
PLoS Pathog
. 2023 Apr 5;19(4):e1011265.
doi: 10.1371/journal.ppat.1011265. eCollection 2023 Apr.
Developing an appropriate evolutionary baseline model for the study of SARS-CoV-2 patient samples
John W Terbot 2nd[SUP] 1 2 [/SUP], Parul Johri[SUP] 2 [/SUP], Schuyler W Liphardt[SUP] 1 [/SUP], Vivak Soni[SUP] 2 [/SUP], Susanne P Pfeifer[SUP] 2 [/SUP], Brandon S Cooper[SUP] 1 [/SUP], Jeffrey M Good[SUP] 1 [/SUP], Jeffrey D Jensen[SUP] 2 [/SUP]
Affiliations
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.
. 2023 Apr 5;19(4):e1011265.
doi: 10.1371/journal.ppat.1011265. eCollection 2023 Apr.
Developing an appropriate evolutionary baseline model for the study of SARS-CoV-2 patient samples
John W Terbot 2nd[SUP] 1 2 [/SUP], Parul Johri[SUP] 2 [/SUP], Schuyler W Liphardt[SUP] 1 [/SUP], Vivak Soni[SUP] 2 [/SUP], Susanne P Pfeifer[SUP] 2 [/SUP], Brandon S Cooper[SUP] 1 [/SUP], Jeffrey M Good[SUP] 1 [/SUP], Jeffrey D Jensen[SUP] 2 [/SUP]
Affiliations
- PMID: 37018331
- DOI: 10.1371/journal.ppat.1011265
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.