tetano
Editor, Senior Moderator
Nat Commun
. 2025 Jan 11;16(1):594.
doi: 10.1038/s41467-025-55938-3. Evolution of Omicron lineage towards increased fitness in the upper respiratory tract in the absence of severe lung pathology
Arthur Wickenhagen[SUP] #[/SUP][SUP] 1 [/SUP], Meaghan Flagg[SUP] #[/SUP][SUP] 1 [/SUP], Julia R Port[SUP] 1 2 [/SUP], Claude Kwe Yinda[SUP] 1 [/SUP], Kerry Goldin[SUP] 1 [/SUP], Shane Gallogly[SUP] 1 [/SUP], Jonathan E Schulz[SUP] 1 [/SUP], Tessa Lutterman[SUP] 1 [/SUP], Brandi N Williamson[SUP] 1 [/SUP], Franziska Kaiser[SUP] 1 [/SUP], Reshma K Mukesh[SUP] 1 [/SUP], Sarah van Tol[SUP] 1 [/SUP], Brian Smith[SUP] 3 [/SUP], Neeltje van Doremalen[SUP] 1 [/SUP], Colin A Russell[SUP] 4 [/SUP], Emmie de Wit[SUP] 5 [/SUP], Vincent J Munster[SUP] 6 [/SUP]
Affiliations
The emergence of the Omicron lineage represented a major genetic drift in SARS-CoV-2 evolution. This was associated with phenotypic changes including evasion of pre-existing immunity and decreased disease severity. Continuous evolution within the Omicron lineage raised concerns of potential increased transmissibility and/or disease severity. To address this, we evaluate the fitness and pathogenesis of contemporary Omicron variants XBB.1.5, XBB.1.16, EG.5.1, and JN.1 in the upper (URT) and lower respiratory tract (LRT). We compare in vivo infection in Syrian hamsters with infection in primary human nasal and lung epithelium cells and assess differences in transmissibility, antigenicity, and innate immune activation. Omicron variants replicate efficiently in the URT but display limited pathology in the lungs compared to previous variants and fail to replicate in human lung organoids. JN.1 is attenuated in both URT and LRT compared to other Omicron variants and fails to transmit in the male hamster model. Our data demonstrate that Omicron lineage evolution has favored increased fitness in the URT.
. 2025 Jan 11;16(1):594.
doi: 10.1038/s41467-025-55938-3. Evolution of Omicron lineage towards increased fitness in the upper respiratory tract in the absence of severe lung pathology
Arthur Wickenhagen[SUP] #[/SUP][SUP] 1 [/SUP], Meaghan Flagg[SUP] #[/SUP][SUP] 1 [/SUP], Julia R Port[SUP] 1 2 [/SUP], Claude Kwe Yinda[SUP] 1 [/SUP], Kerry Goldin[SUP] 1 [/SUP], Shane Gallogly[SUP] 1 [/SUP], Jonathan E Schulz[SUP] 1 [/SUP], Tessa Lutterman[SUP] 1 [/SUP], Brandi N Williamson[SUP] 1 [/SUP], Franziska Kaiser[SUP] 1 [/SUP], Reshma K Mukesh[SUP] 1 [/SUP], Sarah van Tol[SUP] 1 [/SUP], Brian Smith[SUP] 3 [/SUP], Neeltje van Doremalen[SUP] 1 [/SUP], Colin A Russell[SUP] 4 [/SUP], Emmie de Wit[SUP] 5 [/SUP], Vincent J Munster[SUP] 6 [/SUP]
Affiliations
- PMID: 39799119
- PMCID: PMC11724920
- DOI: 10.1038/s41467-025-55938-3
The emergence of the Omicron lineage represented a major genetic drift in SARS-CoV-2 evolution. This was associated with phenotypic changes including evasion of pre-existing immunity and decreased disease severity. Continuous evolution within the Omicron lineage raised concerns of potential increased transmissibility and/or disease severity. To address this, we evaluate the fitness and pathogenesis of contemporary Omicron variants XBB.1.5, XBB.1.16, EG.5.1, and JN.1 in the upper (URT) and lower respiratory tract (LRT). We compare in vivo infection in Syrian hamsters with infection in primary human nasal and lung epithelium cells and assess differences in transmissibility, antigenicity, and innate immune activation. Omicron variants replicate efficiently in the URT but display limited pathology in the lungs compared to previous variants and fail to replicate in human lung organoids. JN.1 is attenuated in both URT and LRT compared to other Omicron variants and fails to transmit in the male hamster model. Our data demonstrate that Omicron lineage evolution has favored increased fitness in the URT.