ABSTRACT In the coronavirus disease 2019 (COVID-19) pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), more severe outcomes are reported in males than in females, including hospitalizations and deaths. Animal models can provide an opportunity to mechanistically interrogate causes of sex differences in the pathogenesis of SARS-CoV-2. Adult male and female golden Syrian hamsters (8 to 10 weeks of age) were inoculated intranasally with 10 5 50% tissue culture infective dose (TCID 50 ) of SARS-CoV-2/USA-WA1/2020 and euthanized at several time points during the acute (i.e., virus actively replicating) and recovery (i.e., after the infectious virus has been cleared) phases of infection. There was no mortality, but infected male hamsters experienced greater morbidity, losing a greater percentage of body mass, developed more extensive pneumonia as noted on chest computed tomography, and recovered more slowly than females. Treatment of male hamsters with estradiol did not alter pulmonary damage. Virus titers in respiratory tissues, including nasal turbinates, trachea, and lungs, and pulmonary cytokine concentrations, including interferon-β (IFN-β) and tumor necrosis factor-α (TNF-α), were comparable between the sexes. However, during the recovery phase of infection, females mounted 2-fold greater IgM, IgG, and IgA responses against the receptor-binding domain of the spike protein (S-RBD) in both plasma and respiratory tissues. Female hamsters also had significantly greater IgG antibodies against whole-inactivated SARS-CoV-2 and mutant S-RBDs as well as virus-neutralizing antibodies in plasma. The development of an animal model to study COVID-19 sex differences will allow for a greater mechanistic understanding of the SARS-CoV-2-associated sex differences seen in the human population.
【저자키워드】 COVID-19, animal model, Receptor-binding domain, SARS-CoV-2 variants, sex differences, 【초록키워드】 coronavirus disease, SARS-CoV-2, IgG, IgM, Tumor, Coronavirus disease 2019, coronavirus, pandemic, Pathogenesis, Mortality, Hospitalization, Pneumonia, Infection, interferon, animal model, cytokine, animal models, outcome, severe acute respiratory syndrome Coronavirus, virus, Spike protein, Computed tomography, Chest computed tomography, IgG antibody, tumor necrosis factor, Receptor-binding domain, Culture, IgG antibodies, animal, S-RBD, Lungs, morbidity, hospitalizations, male, female, estradiol, plasma, age, mutant, hamster, respiratory, Sex difference, Infective dose, TNF-α, Infectious virus, dose, RBDs, deaths, Trachea, tissue culture, human population, virus titers, tumor necrosis, nasal turbinates, body mass, tumor necrosis factor-α, acute respiratory syndrome, acute respiratory syndrome coronavirus, tissue, acute respiratory syndrome coronavirus 2, IFN-β, causes, respiratory tissues, virus-neutralizing antibodies, IgA responses, pulmonary damage, TCID, infective, IgA response, pathogenesis of SARS-CoV-2, females, Alter, concentrations, virus-neutralizing antibody, greater, caused, significantly, intranasally, reported, inoculated, the spike protein, the receptor-binding domain, comparable, cause, euthanized, mounted, 【제목키워드】 SARS-CoV-2, response, imaging, Model, hamster, difference,