State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Centre for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, 79 Qing Chun Road, Hangzhou, 310003, Zhejiang, China.
Plastic and Aesthetic Surgery Department, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, Zhejiang, China.
Virol J. 2021 Nov 29;18(1):237. doi: 10.1186/s12985-021-01709-7.
The highly pathogenic Influenza H7N9 virus is believed to cause multiple organ infections. However, there have been few systematic animal experiments demonstrating the virus distribution after H7N9 virus infection. The present study was carried out to investigate the viral distribution and pathological changes in the main organs of mice after experimental infection with highly pathogenic H7N9 virus.
Infection of mice with A/Guangdong/GZ8H002/2017(H7N9) virus was achieved via nasal inoculation. Mice were killed at 2, 3, and 7 days post infection. The other mice were used to observe their illness status and weight changes. Reverse transcription polymerase chain reaction and viral isolation were used to analyse the characteristics of viral invasion. The pathological changes of the main organs were observed using haematoxylin and eosin staining and immunohistochemistry.
The weight of H7N9 virus-infected mice increased slightly in the first two days. However, the weight of the mice decreased sharply in the following days, by up to 20%. All the mice had died by the 8th day post infection and showed multiple organ injury. The emergence of viremia in mice was synchronous with lung infection. On the third day post infection, except in the brain, the virus could be isolated from all organs (lung, heart, kidney, liver, and spleen). On the seventh day post infection, the virus could be detected in all six organs. Brain infection was detected in all mice, and the viral titre in the heart, kidney, and spleen infection was high.
Acute diffuse lung injury was the initial pathogenesis in highly pathogenic H7N9 virus infection. In addition to lung infection and viremia, the highly pathogenic H7N9 virus could cause multiple organ infection and injury.
高致病性 H7N9 流感病毒被认为会导致多器官感染。然而,很少有系统的动物实验证明 H7N9 病毒感染后的病毒分布。本研究旨在探讨实验感染高致病性 H7N9 病毒后小鼠主要器官的病毒分布和病理变化。
通过鼻腔接种感染小鼠 A/Guangdong/GZ8H002/2017(H7N9)病毒。感染后 2、3 和 7 天处死小鼠。其余小鼠用于观察其疾病状态和体重变化。采用逆转录聚合酶链反应和病毒分离分析病毒侵袭的特征。采用苏木精和伊红染色和免疫组织化学观察主要器官的病理变化。
H7N9 病毒感染小鼠的体重在头两天略有增加。然而,在接下来的几天里,体重急剧下降,最多下降 20%。所有小鼠在感染后第 8 天死亡,并表现出多器官损伤。病毒血症的出现与肺部感染同步。感染后第 3 天,除大脑外,所有器官(肺、心、肾、肝和脾)均可分离出病毒。感染后第 7 天,可在所有 6 个器官中检测到病毒。所有小鼠均出现脑部感染,心、肾和脾感染的病毒滴度较高。
急性弥漫性肺损伤是高致病性 H7N9 病毒感染的初始发病机制。除肺部感染和病毒血症外,高致病性 H7N9 病毒还可引起多器官感染和损伤。