tetano
Editor, Senior Moderator
Nat Commun
. 2024 Jan 20;15(1):648.
doi: 10.1038/s41467-024-44803-4. Using big sequencing data to identify chronic SARS-Coronavirus-2 infections
Sheri Harari[SUP] #[/SUP][SUP] 1 2 [/SUP], Danielle Miller[SUP] #[/SUP][SUP] 1 2 [/SUP], Shay Fleishon[SUP] 3 [/SUP], David Burstein[SUP] 1 2 [/SUP], Adi Stern[SUP] 4 5 [/SUP]
Affiliations
The evolution of SARS-Coronavirus-2 (SARS-CoV-2) has been characterized by the periodic emergence of highly divergent variants. One leading hypothesis suggests these variants may have emerged during chronic infections of immunocompromised individuals, but limited data from these cases hinders comprehensive analyses. Here, we harnessed millions of SARS-CoV-2 genomes to identify potential chronic infections and used language models (LM) to infer chronic-associated mutations. First, we mined the SARS-CoV-2 phylogeny and identified chronic-like clades with identical metadata (location, age, and sex) spanning over 21 days, suggesting a prolonged infection. We inferred 271 chronic-like clades, which exhibited characteristics similar to confirmed chronic infections. Chronic-associated mutations were often high-fitness immune-evasive mutations located in the spike receptor-binding domain (RBD), yet a minority were unique to chronic infections and absent in global settings. The probability of observing high-fitness RBD mutations was 10-20 times higher in chronic infections than in global transmission chains. The majority of RBD mutations in BA.1/BA.2 chronic-like clades bore predictive value, i.e., went on to display global success. Finally, we used our LM to infer hundreds of additional chronic-like clades in the absence of metadata. Our approach allows mining extensive sequencing data and providing insights into future evolutionary patterns of SARS-CoV-2.
. 2024 Jan 20;15(1):648.
doi: 10.1038/s41467-024-44803-4. Using big sequencing data to identify chronic SARS-Coronavirus-2 infections
Sheri Harari[SUP] #[/SUP][SUP] 1 2 [/SUP], Danielle Miller[SUP] #[/SUP][SUP] 1 2 [/SUP], Shay Fleishon[SUP] 3 [/SUP], David Burstein[SUP] 1 2 [/SUP], Adi Stern[SUP] 4 5 [/SUP]
Affiliations
- PMID: 38245511
- PMCID: PMC10799923
- DOI: 10.1038/s41467-024-44803-4
The evolution of SARS-Coronavirus-2 (SARS-CoV-2) has been characterized by the periodic emergence of highly divergent variants. One leading hypothesis suggests these variants may have emerged during chronic infections of immunocompromised individuals, but limited data from these cases hinders comprehensive analyses. Here, we harnessed millions of SARS-CoV-2 genomes to identify potential chronic infections and used language models (LM) to infer chronic-associated mutations. First, we mined the SARS-CoV-2 phylogeny and identified chronic-like clades with identical metadata (location, age, and sex) spanning over 21 days, suggesting a prolonged infection. We inferred 271 chronic-like clades, which exhibited characteristics similar to confirmed chronic infections. Chronic-associated mutations were often high-fitness immune-evasive mutations located in the spike receptor-binding domain (RBD), yet a minority were unique to chronic infections and absent in global settings. The probability of observing high-fitness RBD mutations was 10-20 times higher in chronic infections than in global transmission chains. The majority of RBD mutations in BA.1/BA.2 chronic-like clades bore predictive value, i.e., went on to display global success. Finally, we used our LM to infer hundreds of additional chronic-like clades in the absence of metadata. Our approach allows mining extensive sequencing data and providing insights into future evolutionary patterns of SARS-CoV-2.