Usai Carla, Pailler-García Lola, Lorca-Oró Cristina, Fernández-Bastit Leira, Roca Núria, Brustolin Marco, Rodon Jordi, Pérez Mónica, Cantero Guillermo, Carrillo Jorge, Izquierdo-Useros Nuria, Blanco Julià, Clotet Bonaventura, Napp Sebastián, Segalés Joaquim, Vergara-Alert Júlia
Unitat Mixta d'Investigació IRTA-UAB en Sanitat Animal, Centre de Recerca en Sanitat Animal (CReSA), Campus de la Universitat Autònoma de Barcelona (UAB), Bellaterra, Catalonia, Spain.
IRTA Programa de Sanitat Animal, Centre de Recerca en Sanitat Animal (CReSA), Campus de la UAB, Bellaterra, Catalonia, Spain.
Front Microbiol. 2022 Nov 15;13:1016201. doi: 10.3389/fmicb.2022.1016201. eCollection 2022.
Rodents are widely used for the development of COVID-19-like animal models, the virological outcome being determined through several laboratory methods reported in the literature. Our objective was to assess the agreement between methods performed on different sample types from 342 rodents experimentally infected with SARS-CoV-2 (289 golden Syrian hamsters and 53 K18-hACE2 mice). Our results showed moderate agreement between methods detecting active viral replication, and that increasing viral loads determined by either RT-qPCR or infectious viral titration corresponded to increasing immunohistochemical scores. The percentage of agreement between methods decreased over experimental time points, and we observed poor agreement between RT-qPCR results and viral titration from oropharyngeal swabs. In conclusion, RT-qPCR and viral titration on tissue homogenates are the most reliable techniques to determine the presence and replication of SARS-CoV-2 in the early and peak phases of infection, and immunohistochemistry is valuable to evaluate viral distribution patterns in the infected tissues.
啮齿动物被广泛用于开发类似 COVID-19 的动物模型,病毒学结果通过文献中报道的几种实验室方法来确定。我们的目标是评估对 342 只经实验感染 SARS-CoV-2 的啮齿动物(289 只金黄叙利亚仓鼠和 53 只 K18-hACE2 小鼠)的不同样本类型进行检测的方法之间的一致性。我们的结果表明,检测病毒活跃复制的方法之间存在中等程度的一致性,并且通过 RT-qPCR 或感染性病毒滴定法测定的病毒载量增加与免疫组织化学评分增加相对应。方法之间的一致性百分比在实验时间点上有所下降,并且我们观察到 RT-qPCR 结果与口咽拭子的病毒滴定之间的一致性较差。总之,对组织匀浆进行 RT-qPCR 和病毒滴定是确定 SARS-CoV-2 在感染早期和高峰期的存在和复制的最可靠技术,免疫组织化学对于评估感染组织中的病毒分布模式很有价值。