scholarly journals Avian Influenza (H7N9) Virus Infection in Chinese Tourist in Malaysia, 2014

2015 ◽  
Vol 21 (1) ◽  
pp. 142-145 ◽  
Author(s):  
Timothy William ◽  
Bharathan Thevarajah ◽  
Shiu Fee Lee ◽  
Maria Suleiman ◽  
Mohamad Saffree Jeffree ◽  
...  
2018 ◽  
Vol 7 (1) ◽  
pp. 1-10 ◽  
Author(s):  
Ming Tan ◽  
Lunbiao Cui ◽  
Xiang Huo ◽  
Ming Xia ◽  
Fengjuan Shi ◽  
...  

2014 ◽  
Vol 23 (6) ◽  
pp. 237-240 ◽  
Author(s):  
Rui-Yuan Cao ◽  
Jun-Hai Xiao ◽  
Bin Cao ◽  
Song Li ◽  
Yohichi Kumaki ◽  
...  

Background: A novel reassortant avian-origin influenza A (H7N9) virus was isolated from respiratory specimens obtained from three patients and was identified as H7N9 in China. Antiviral agents are required to treat patients with avian influenza H7N9 virus infection. Methods: In this study, we assessed the antiviral potential of oseltamivir, peramivir, favipiravir (T-705), amantadine and rimantadine against novel reassortant avian-origin influenza H7N9 virus in vitro. Results: All three avian influenza H7N9 virus strains were sensitive to oseltamivir, peramivir and favipiravir (T-705), but resistant to amantadine and rimantadine. Conclusions: Our data show a pattern of antiviral sensitivity for this novel H7N9 strain of influenza that suggests the compounds oseltamivir, peramivir and favipiravir should be useful for therapy.


Viruses ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 871
Author(s):  
Swan Tan ◽  
Muhammad Farhan Sjaugi ◽  
Siew Chinn Fong ◽  
Li Chuin Chong ◽  
Hadia Syahirah Abd Raman ◽  
...  

Avian influenza virus A (H7N9), after circulating in avian hosts for decades, was identified as a human pathogen in 2013. Herein, amino acid substitutions possibly essential for human adaptation were identified by comparing the 4706 aligned overlapping nonamer position sequences (1–9, 2–10, etc.) of the reported 2014 and 2017 avian and human H7N9 datasets. The initial set of virus sequences (as of year 2014) exhibited a total of 109 avian-to-human (A2H) signature amino acid substitutions. Each represented the most prevalent substitution at a given avian virus nonamer position that was selectively adapted as the corresponding index (most prevalent sequence) of the human viruses. The majority of these avian substitutions were long-standing in the evolution of H7N9, and only 17 were first detected in 2013 as possibly essential for the initial human adaptation. Strikingly, continued evolution of the avian H7N9 virus has resulted in avian and human protein sequences that are almost identical. This rapid and continued adaptation of the avian H7N9 virus to the human host, with near identity of the avian and human viruses, is associated with increased human infection and a predicted greater risk of human-to-human transmission.


Vaccine ◽  
2015 ◽  
Vol 33 (18) ◽  
pp. 2152-2158 ◽  
Author(s):  
Ye V. Liu ◽  
Michael J. Massare ◽  
Melissa B. Pearce ◽  
Xiangjie Sun ◽  
Jessica A. Belser ◽  
...  

2014 ◽  
Vol 20 (2) ◽  
Author(s):  
Xian Qi ◽  
Lunbiao Cui ◽  
Ke Xu ◽  
Bin Wu ◽  
Fenyang Tang ◽  
...  

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.


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