State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou, China.
Dongguan Institute of Paediatrics, Dongguan Children's Hospital, The Eighth People's Hospital of Dongguan City, Guangdong Medical University, Dongguan, China.
Front Immunol. 2021 May 13;12:665197. doi: 10.3389/fimmu.2021.665197. eCollection 2021.
Coxsackievirus A6 (CVA6) is recognized as a major enterovirus type that can cause severe hand, foot, and mouth disease and spread widely among children. Vaccines and antiviral drugs may be developed more effectively based on a stable and easy-to-operate CVA6 mouse infection model. In this study, a wild CVA6-W strain was sub-cultured in newborn mice of different ages (in days), for adaptation. Therefore, a CVA6-A mouse-adapted strain capable of stably infecting the mice was generated, and a fatal model was built. As the result indicated, CVA6-A could infect the 10-day-old mice to generate higher levels of IFN-γ, IL-6, and IL-10. The mice infected with CVA6-A were treated with IFN-α1b at a higher dose, with complete protection. Based on this strain, an animal model with active immunization was built to evaluate antiviral protection by active immunization. The three-day-old mice were pre-immunized with inactivated CVA6 thereby generating IgM and IgG antibodies within 7 days that enabled complete protection of the pre-immunized mice following the CVA6 virus challenge. There were eight mutations in the genome of CVA6-A than in that of CVA6-W, possibly attributed to the virulence of CVA6 in mice. Briefly, the CVA6 infection model of the 10-day-old mice built herein, may serve as an applicable preclinical evaluation model for CVA6 antiviral drugs and vaccine study.
柯萨奇病毒 A6(Coxsackievirus A6,CVA6)是一种主要的肠道病毒,可引起严重的手足口病,在儿童中广泛传播。基于稳定且易于操作的 CVA6 小鼠感染模型,可更有效地开发疫苗和抗病毒药物。本研究通过对不同日龄(天)新生小鼠进行 CVA6-W 野毒株的连续传代适应,获得了一株可稳定感染小鼠的 CVA6-A 适应株,并构建了致死性感染模型。结果表明,CVA6-A 可感染 10 日龄小鼠,诱导高水平的 IFN-γ、IL-6 和 IL-10。高剂量 IFN-α1b 处理可完全保护 CVA6-A 感染的小鼠。基于该适应株,建立了主动免疫的动物模型,评价主动免疫的抗病毒保护作用。3 日龄小鼠经 CVA6 灭活疫苗预先免疫,7 天内产生 IgM 和 IgG 抗体,可完全保护预先免疫的小鼠免受 CVA6 病毒攻击。CVA6-A 的基因组与 CVA6-W 相比有 8 个突变,可能与 CVA6 在小鼠中的毒力有关。总之,本研究建立的 10 日龄小鼠 CVA6 感染模型,可为 CVA6 抗病毒药物和疫苗的研究提供一种可行的临床前评价模型。