scholarly journals The Viral Distribution and Pathological Characteristics of BALB/c Mice Infected With Highly Pathogenic Influenza H7N9 Virus

Author(s):  
Xiao-Xin Wu ◽  
Song-Jia Tang ◽  
Shu-Hao Yao ◽  
Yu-Qin Zhou ◽  
Lan-Lan Xiao ◽  
...  

Abstract Background: 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.Methods: The mice were infected with A/Guangdong/GZ8H002/2017(H7N9) virus via nasal inoculation. Some mice were killed at 2, 3, and 7 days after infection. The other mice were used to observe their illness status and weight changes. The characteristics of viral invasion were analysed using reverse transcription polymerase chain reaction and viral isolation. The pathological changes of the main organs were observed using haematoxylin and eosin staining and immunohistochemistry.Results: The weight of mice infected with A/Guangdong/GZ8H002/2017(H7N9) virus 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 after infection and showed multiple organ injury. The emergence of viremia in mice was synchronous with lung infection. On the third day after infection, except in the brain, the virus could be isolated from all organs (lung, heart, kidney, liver, and spleen). On the seventh day after 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.Conclusion: 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.

2021 ◽  
Author(s):  
Xiao-Xin Wu ◽  
Song-Jia Tang ◽  
Shu-Hao Yao ◽  
Yu-Qin Zhou ◽  
Lan-Lan Xiao ◽  
...  

Abstract Background 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. Methods 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. Results 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. Conclusion 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.


2021 ◽  
Vol 18 (1) ◽  
Author(s):  
Xiao-Xin Wu ◽  
Song-Jia Tang ◽  
Shu-Hao Yao ◽  
Yu-Qin Zhou ◽  
Lan-Lan Xiao ◽  
...  

Abstract Background 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. Methods 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. Results 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. Conclusion 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.


Viruses ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1066 ◽  
Author(s):  
Maki Kiso ◽  
Seiya Yamayoshi ◽  
Yuri Furusawa ◽  
Masaki Imai ◽  
Yoshihiro Kawaoka

Viral neuraminidase inhibitors show limited efficacy in mice infected with H7N9 influenza A viruses isolated from humans. Although baloxavir marboxil protected mice from lethal challenge infection with a low pathogenic avian influenza H7N9 virus isolated from a human, its efficacy in mice infected with a recent highly pathogenic version of H7N9 human isolates is unknown. Here, we examined the efficacy of baloxavir marboxil in mice infected with a highly pathogenic human H7N9 virus, A/Guangdong/17SF003/2016. Treatment of infected mice with a single 1.5 mg/kg dose of baloxavir marboxil protected mice from the highly pathogenic human H7N9 virus infection as effectively as oseltamivir treatment at 50 mg/kg twice a day for five days. Daily treatment for five days at 15 or 50 mg/kg of baloxavir marboxil showed superior therapeutic efficacy, largely preventing virus replication in respiratory organs. These results indicate that baloxavir marboxil is a valuable candidate treatment for human patients suffering from highly pathogenic H7N9 virus infection.


2018 ◽  
Vol 7 (1) ◽  
pp. 1-10 ◽  
Author(s):  
Ming Tan ◽  
Lunbiao Cui ◽  
Xiang Huo ◽  
Ming Xia ◽  
Fengjuan Shi ◽  
...  

Oncotarget ◽  
2017 ◽  
Vol 8 (17) ◽  
pp. 27715-27724 ◽  
Author(s):  
Yu-Lin Xu ◽  
Hai-Lin Tang ◽  
Hao-Ran Peng ◽  
Ping Zhao ◽  
Zhong-Tian Qi ◽  
...  

2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Lei Guo ◽  
Nan Li ◽  
Wenlong Li ◽  
Jienan Zhou ◽  
Ruotong Ning ◽  
...  

Abstract Since 2013, influenza H7N9 virus has caused five epidemic waves of human infection. The virus evolved from low pathogenic to highly pathogenic in wave 5, 2017, while the prevalence of host receptor-binding tropism in human-infecting viruses maintained dual-receptor-binding property with preference for avian receptor. A human-infecting H7N9 virus was isolated after the fifth epidemic wave and possessed an avian and human dual-receptor specificity, with a moderately higher affinity for human receptor binding. A V186I (H3 numbering) substitution in the receptor-binding site of the hemagglutinin (HA) molecule is responsible for the alteration of the dual-receptor-binding tropism. Viral strains which contain I186 amino acid of avian- and human-infecting H7N9 viruses were all isolated during or after wave 5, and their HA genes clustered in a same phylogenetic clade together with 2018–9 H7N9 isolates, highlights a new evolutionary path for human adaption of natural H7N9 viruses.


2015 ◽  
Vol 21 (1) ◽  
pp. 142-145 ◽  
Author(s):  
Timothy William ◽  
Bharathan Thevarajah ◽  
Shiu Fee Lee ◽  
Maria Suleiman ◽  
Mohamad Saffree Jeffree ◽  
...  

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