The viral distribution and pathological characteristics of BALB/c mice infected with highly pathogenic Influenza H7N9 virus

• Published in: Virology journal Vol. 18; no. 1; p. 237
• Main Authors: Wu, Xiao-Xin, Tang, Song-Jia, Yao, Shu-Hao, Zhou, Yu-Qin, Xiao, Lan-Lan, Cheng, Lin-Fang, Liu, Fu-Ming, Wu, Nan-Ping, Yao, Hang-Ping, Li, Lan-Juan
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 29-11-2021; BioMed Central; BMC
• Subjects: Animals; Avian flu; Avian influenza; Bronchopulmonary infection; Complications and side effects; Development and progression; Experimental infection; Experiments; Highly pathogenic H7N9; Humans; Immunohistochemistry; Infections; Influenza; Influenza A Virus, H7N9 Subtype; Influenza, Human; Inoculation; Kidneys; Laboratory animals; Lung - pathology; Lungs; Medical research; Mice; Mice, Inbred BALB C; Mortality; Multiple organ dysfunction syndrome; Multiple organ injury; Mutation; Orthomyxoviridae Infections; Pandemics; Pathological changes; Polymerase chain reaction; Poultry; Reverse transcription; Spleen; Swine flu; Vaccines; Viral distribution; Viral infections; Viremia; Viruses; China; United States > US; Zhejiang China; Pathological changes; Viral distribution; Highly pathogenic H7N9; Multiple organ injury
• ISSN: 1743-422X; 1743-422X
• 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.