Dhakal Santosh, Ruiz-Bedoya Camilo A, Zhou Ruifeng, Creisher Patrick, Villano Jason, Littlefield Kirsten, Castillo Jennie, Marinho Paula, Jedlicka Anne, Ordonez Alvaro, Majewska Natalia, Betenbaugh Michael, Flavahan Kelly, Mueller Alice, Looney Monika, Quijada Darla, Mota Filipa, Beck Sarah E, Brockhurst Jacqueline K, Braxton Alicia, Castell Natalie, D'Alessio Franco, Metcalf Pate Kelly A, Karakousis Petros C, Mankowski Joseph L, Pekosz Andrew, Jain Sanjay K, Klein Sabra L
bioRxiv. 2021 Apr 4:2021.04.02.438292. doi: 10.1101/2021.04.02.438292.
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 TCID 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.
在由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019年冠状病毒病(COVID-19)大流行中,据报道男性的病情比女性更严重,包括住院和死亡情况。动物模型可为从机制上探究SARS-CoV-2发病机制中性别差异的原因提供机会。将成年雄性和雌性金黄叙利亚仓鼠(8至10周龄)经鼻接种10 TCID的SARS-CoV-2/USA-WA1/2020,并在感染的急性期(即病毒活跃复制期)和恢复期(即感染性病毒已清除后)的多个时间点实施安乐死。没有出现死亡情况,但感染的雄性仓鼠发病率更高,体重减轻的百分比更大,胸部计算机断层扫描显示肺炎范围更广,且恢复得比雌性仓鼠慢。用雌二醇治疗雄性仓鼠并未改变肺部损伤情况。包括鼻甲、气管和肺在内的呼吸道组织中的病毒滴度以及包括IFNb和TNFa在内的肺部细胞因子浓度在两性之间相当。然而,在感染的恢复期,雌性仓鼠在血浆和呼吸道组织中针对刺突蛋白受体结合域(S-RBD)产生的IgM、IgG和IgA反应是雄性的两倍。雌性仓鼠针对全灭活SARS-CoV-2和突变S-RBD的IgG抗体以及血浆中的病毒中和抗体也明显更多。开发用于研究COVID-19性别差异的动物模型将有助于从机制上更深入地了解在人类群体中观察到的与SARS-CoV-2相关的性别差异。