The 2022 RSV surge was driven by multiple viral lineages
Adams, G.; Moreno, G. K.; Petros, B. A.; Uddin, R.; Levine, Z.; Kotzen, B.; Messer, K.; Dobbins, S.; Deruff, K. C.; Loreth, C.; Brock-Fisher, T.; Schaffner, S. F.; Chaluvadi, S.; Kanjilal, S.; Luban, J.; Ozonoff, A.; Park, D.; Turbett, S.; Siddle, K. J.; MacInnis, B.; Sabeti, P.; Lemieux, J.
Show abstract
The US experienced an early and severe respiratory syncytial virus (RSV) surge in autumn 2022. Despite the pressure this has put on hospitals and care centers, the factors promoting the surge in cases are unknown. To investigate whether viral characteristics contributed to the extent or severity of the surge, we sequenced 105 RSV-positive specimens from symptomatic patients diagnosed with RSV who presented to the Massachusetts General Hospital (MGH) and its outpatient practices in the Greater Boston Area. Genomic analysis of the resulting 77 genomes (54 with >80% coverage, and 23 with >5% coverage) demonstrated that the surge was driven by multiple lineages of RSV-A (91%; 70/77) and RSV-B (9%; 7/77). Phylogenetic analysis of all US RSV-A revealed 12 clades, 4 of which contained Massachusetts and Washington genomes. These clades individually had times to most recent common ancestor (tMRCA) between 2014 and 2017, and together had a tMRCA of 2009, suggesting that they emerged well before the COVID-19 pandemic. Similarly, the RSV-B genomes had a tMRCA between 2016 and 2019. We found that the RSV-A and RSV-B genomes in our sample did not differ statistically from the estimated clock rate of the larger phylogenetic tree (10.6 and 12.4 substitutions per year, respectively). In summary, the polyphyletic nature of viral genomes sequenced in the US during the autumn 2022 surge is inconsistent with the emergence of a single, highly transmissible causal RSV lineage.
Matching journals
The top 8 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- SARS-CoV-2 within-host population expansion, diversification and adaptation in zoo tigers, lions and hyenas 94%
- Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions 94%
- Polymerase mutations underlie early adaptation of H5N1 influenza virus to dairy cattle and other mammals. 93%
Similar papers in this journal
- Antibody evasion and receptor binding of SARS-CoV-2 LP.8.1.1, NB.1.8.1, XFG, and related subvariants 94%
- Systems immunology of transcriptional responses to viral infection identifies conserved antiviral pathways across macaques and humans 94%
- Antibody evasiveness of SARS-CoV-2 subvariants KP.3.1.1 and XEC 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.