Exposure route, sex, and age influence disease outcome in a golden Syrian hamster model of SARS-CoV-2 infection
Griffin, B. D.; Warner, B. M.; Chan, M.; Mendoza, E. J.; Tailor, N.; Banadyga, L.; Leung, A.; He, S.; Boese, A. S.; Audet, J.; Cao, W.; Moffat, E.; Garnett, L.; Tierney, K.; Tran, K. N.; Albietz, A.; Manguiat, K.; Soule, G.; Bello, A.; Vendramelli, R.; Lin, J.; Deschambault, Y.; Zhu, W.; Safronetz, D.; Wood, H.; Mubareka, S.; Strong, J. E.; Embury-Hyatt, C.; Kobasa, D.
Show abstract
The emergence of Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the resultant pandemic of coronavirus disease 2019 (COVID-19) has led to over one hundred million confirmed infections, greater than three million deaths, and severe economic and social disruption. Animal models of SARS-CoV-2 are critical tools for the pre-clinical evaluation of antivirals, vaccines, and candidate therapeutics currently under urgent development to curb COVID-19-associated morbidity and mortality. The golden (Syrian) hamster model of SARS-CoV-2 infection recapitulates key characteristics of severe COVID-19, including high-titer viral replication in the upper and lower respiratory tract and the development of pathogenic lesions in the lungs. In this work we examined the influence of the route of exposure, sex, and age on SARS-CoV-2 pathogenesis in golden hamsters. We report that delivery of SARS-CoV-2 primarily to the nasal passages (low-volume intranasal), the upper and lower respiratory tract (high-volume intranasal), or the digestive tract (intragastric) results in comparable viral titers in the lung tissue and similar levels of viral shedding during acute infection. However, low-volume intranasal exposure results in milder weight loss during acute infection while intragastric exposure leads to a diminished capacity to regain body weight following the period of acute illness. Further, we examined both sex and age differences in response to SARS-CoV-2 infection. Male hamsters, and to a greater extent older male hamsters, display an impaired capacity to recover from illness and a delay in viral clearance compared to females. Lastly, route of exposure, sex, and age were found to influence the nature of the host inflammatory cytokine response, but they had a minimal effect on both the quality and durability of the humoral immune response as well as the susceptibility of hamsters to SARS-CoV-2 re-infection. Together, these data indicate that the route of exposure, sex, and age have a meaningful impact SARS-CoV-2 pathogenesis in hamsters and that these variables should be considered when designing pre-clinical challenge studies.
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Evolution of Omicron lineage towards increased fitness in the upper respiratory tract in the absence of severe lung pathology 96%
- B.1.1.7 and B.1.351 variants are highly virulent in K18-ACE2 transgenic mice and show different pathogenic patterns from early SARS-CoV-2 strains 96%
- A live-attenuated SARS-CoV-2 vaccine candidate with accessory protein deletions 95%
Similar papers in this journal
- Prior aerosol infection with lineage A SARS-CoV-2 variant protects hamsters from disease, but not reinfection with B.1.351 SARS-CoV-2 variant 96%
- Defining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection 95%
- Cross-neutralization and viral fitness of SARS-CoV-2 Omicron sublineages 93%
Similar papers in this journal
Similar papers in this journal
- SARS-CoV-2 infection of African green monkeys results in mild respiratory disease discernible by PET/CT imaging and prolonged shedding of infectious virus from both respiratory and gastrointestinal tracts 95%
- Breakthrough infections by SARS-CoV-2 variants boost cross-reactive hybrid immune responses in mRNA-vaccinated Golden Syrian Hamsters 95%
- Human FcRn expression and Type I Interferon signaling control Echovirus 11 pathogenesis in mice 95%
Similar papers in this journal
- Disruption of Adaptive Immunity Enhances Disease in SARS-CoV-2 Infected Syrian Hamsters 97%
- A monoclonal antibody targeting the Nipah virus fusion glycoprotein apex imparts protection from disease 94%
- NVX-CoV2373 ancestral and NVX-CoV2540 BA.5 protein nanoparticle vaccines protect against Omicron BA.5 variant in Syrian hamsters 94%
"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.