Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
J Virol. 2022 Feb 9;96(3):e0145521. doi: 10.1128/JVI.01455-21. Epub 2021 Nov 24.
Susceptibility to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the outcome of coronavirus disease 2019 (COVID-19) have been linked to underlying health conditions and the age of affected individuals. Here, we assessed the effect of age on SARS-CoV-2 infection using a ferret model. For this, young (6-month-old) and aged (18- to 39-month-old) ferrets were inoculated intranasally with various doses of SARS-CoV-2. By using infectious virus shedding in respiratory secretions and seroconversion, we estimated that the infectious dose of SARS-CoV-2 in aged animals is ∼32 PFU per animal, while in young animals it was estimated to be ∼100 PFU. We showed that viral replication in the upper respiratory tract and shedding in respiratory secretions is enhanced in aged ferrets compared to young animals. Similar to observations in humans, this was associated with higher transcription levels of two key viral entry factors, ACE2 and TMPRSS2, in the upper respiratory tract of aged ferrets. In humans, ACE2 and TMPRSS2 are expressed in various cells and tissues, and differential expression has been described in young and old people, with a higher level of expressing cells being detected in the nasal brushing of older people than young individuals. We described the same pattern occurring in ferrets, and we demonstrated that age affects susceptibility of ferrets to SARS-CoV-2. Aged animals were more likely to get infected when exposed to lower infectious dose of the virus than young animals, and the viral replication in the upper respiratory tract and shedding are enhanced in aged ferrets. Together, these results suggest that the higher infectivity and enhanced ability of SARS-CoV-2 to replicate in aged individuals is associated, at least in part, with transcription levels of ACE2 and TMPRSS2 at the sites of virus entry. The young and aged ferret model developed here may represent a great platform to assess age-related differences in SARS-CoV-2 infection dynamics and replication.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的易感性和 2019 年冠状病毒病(COVID-19)的结局与潜在的健康状况和受影响个体的年龄有关。在这里,我们使用雪貂模型评估了年龄对 SARS-CoV-2 感染的影响。为此,将年轻(6 月龄)和老年(18-39 月龄)雪貂通过鼻腔接种不同剂量的 SARS-CoV-2。通过呼吸道分泌物中传染性病毒的脱落和血清转化,我们估计老年动物中 SARS-CoV-2 的感染剂量约为每只动物 32 个 PFU,而在年轻动物中估计为 100 PFU。我们表明,与年轻动物相比,老年雪貂上呼吸道中的病毒复制和呼吸道分泌物中的脱落增强。与人类的观察结果类似,这与老年雪貂上呼吸道中两个关键病毒进入因子 ACE2 和 TMPRSS2 的转录水平升高有关。在人类中,ACE2 和 TMPRSS2 在各种细胞和组织中表达,并且在年轻人和老年人中已经描述了差异表达,在老年人的鼻拭子中检测到更高水平的表达细胞。我们描述了在雪貂中也发生了相同的模式,并且我们证明了年龄会影响雪貂对 SARS-CoV-2 的易感性。与年轻动物相比,暴露于较低感染剂量的病毒时,老年动物更容易感染,并且在上呼吸道中的病毒复制和脱落在老年雪貂中增强。总之,这些结果表明,SARS-CoV-2 在老年人中的更高感染性和增强的复制能力至少部分与病毒进入部位 ACE2 和 TMPRSS2 的转录水平有关。这里开发的年轻和老年雪貂模型可能代表了一个很好的平台,可以评估 SARS-CoV-2 感染动力学和复制中与年龄相关的差异。