Sex differences in lung imaging and SARS-CoV-2 antibody responses in a COVID-19 golden Syrian hamster model.
Santosh DhakalCamilo A Ruiz-BedoyaRuifeng ZhouPatrick CreisherJason VillanoKirsten LittlefieldJennie CastilloPaula MarinhoAnne JedlickaAlvaro OrdonezNatalia MajewskaMichael BetenbaughKelly FlavahanAlice MuellerMonika LooneyDarla QuijadaFilipa MotaSarah E BeckJacqueline K BrockhurstAlicia BraxtonNatalie CastellFranco D'AlessioKelly A Metcalf PatePetros C KarakousisJoseph L MankowskiAndrew S PekoszSanjay K JainSabra L KleinPublished in: bioRxiv : the preprint server for biology (2021)
In the ongoing 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 compared with 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 (8-10 weeks of age) were inoculated intranasally with 10 5 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, developing more extensive pneumonia as noted on chest computed tomography, and recovering 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 IFNb and TNFa, were comparable between the sexes. However, during the recovery phase of infection, females mounted two-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.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- computed tomography
- gene expression
- pulmonary hypertension
- magnetic resonance imaging
- endothelial cells
- adipose tissue
- type diabetes
- coronary artery disease
- early onset
- cardiovascular disease
- risk factors
- extracorporeal membrane oxygenation
- magnetic resonance
- zika virus
- cardiovascular events
- disease virus
- insulin resistance
- young adults
- respiratory tract
- dna binding
- pet ct