Age-dependent pathogenic characteristics of SARS-CoV-2 infection in ferrets.
Young-Il KimKwang-Min YuJune-Young KohEun-Ha KimSe-Mi KimEun Ji KimMark Anthony B CaselRare RollonSeung-Gyu JangMin-Suk SongSu-Jin ParkHye Won JeongEung Gook KimOk-Jun LeeYong-Dae KimYounho ChoiShin-Ae LeeYoun Jung ChoiSu-Hyung ParkJae U JungDavid Hyunjung ChungPublished in: Nature communications (2022)
While the seroprevalence of SARS-CoV-2 in healthy people does not differ significantly among age groups, those aged 65 years or older exhibit strikingly higher COVID-19 mortality compared to younger individuals. To further understand differing COVID-19 manifestations in patients of different ages, three age groups of ferrets are infected with SARS-CoV-2. Although SARS-CoV-2 is isolated from all ferrets regardless of age, aged ferrets (≥3 years old) show higher viral loads, longer nasal virus shedding, and more severe lung inflammatory cell infiltration, and clinical symptoms compared to juvenile (≤6 months) and young adult (1-2 years) groups. Furthermore, direct contact ferrets co-housed with the virus-infected aged group shed more virus than direct-contact ferrets co-housed with virus-infected juvenile or young adult ferrets. Transcriptome analysis of aged ferret lungs reveals strong enrichment of gene sets related to type I interferon, activated T cells, and M1 macrophage responses, mimicking the gene expression profile of severe COVID-19 patients. Thus, SARS-CoV-2-infected aged ferrets highly recapitulate COVID-19 patients with severe symptoms and are useful for understanding age-associated infection, transmission, and pathogenesis of SARS-CoV-2.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- young adults
- genome wide
- end stage renal disease
- early onset
- ejection fraction
- copy number
- gene expression
- adipose tissue
- cardiovascular disease
- oxidative stress
- chronic kidney disease
- newly diagnosed
- physical activity
- drug induced
- type diabetes
- peritoneal dialysis
- prognostic factors
- depressive symptoms
- bone marrow
- sleep quality
- disease virus
- mesenchymal stem cells
- patient reported outcomes
- childhood cancer