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Published on: August 2, 2011
Pathogenesis and transmission of avian influenza A (H7N9) virus in ferrets and mice
Jessica A Belser1, Kortney M Gustin, Melissa B Pearce
1Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
Abstract:
On 29 March 2013, the Chinese Center for Disease Control and Prevention confirmed the first reported case of human infection with an avian influenza A(H7N9) virus. The recent human infections with H7N9 virus, totalling over 130 cases with 39 fatalities to date, have been characterized by severe pulmonary disease and acute respiratory distress syndrome (ARDS). This is concerning because H7 viruses have typically been associated with ocular disease in humans, rather than severe respiratory disease. This recent outbreak underscores the need to better understand the pathogenesis and transmission of these viruses in mammals. Here we assess the ability of A/Anhui/1/2013 and A/Shanghai/1/2013 (H7N9) viruses, isolated from fatal human cases, to cause disease in mice and ferrets and to transmit to naive animals. Both H7N9 viruses replicated to higher titre in human airway epithelial cells and in the respiratory tract of ferrets compared to a seasonal H3N2 virus. Moreover, the H7N9 viruses showed greater infectivity and lethality in mice compared to genetically related H7N9 and H9N2 viruses. The H7N9 viruses were readily transmitted to naive ferrets through direct contact but, unlike the seasonal H3N2 virus, did not transmit readily by respiratory droplets. The lack of efficient respiratory droplet transmission was corroborated by low receptor-binding specificity for human-like α2,6-linked sialosides. Our results indicate that H7N9 viruses have the capacity for efficient replication in mammals and human airway cells and highlight the need for continued public health surveillance of this emerging virus.
Insights
Avian influenza A(H7N9) viruses caused severe respiratory disease in humans. These H7N9 viruses efficiently replicated in mammals and human airway cells, but transmission was mainly via direct contact, not respiratory droplets.
Area of Science:
- Virology
- Infectious Diseases
- Public Health
Background:
- The 2013 avian influenza A(H7N9) outbreak in China marked a shift from typical H7 virus ocular disease to severe respiratory illness.
- Over 130 human cases and 39 deaths were reported, necessitating research into H7N9 pathogenesis and mammalian transmission.
Purpose of the Study:
- To evaluate the pathogenicity and transmissibility of H7N9 viruses in mammalian models.
- To compare H7N9 virus replication and disease severity against a seasonal influenza virus.
Main Methods:
- Infection of mice and ferrets with H7N9 viruses (A/Anhui/1/2013, A/Shanghai/1/2013).
- Assessment of viral replication in human airway epithelial cells and ferret respiratory tracts.
- Evaluation of direct contact and respiratory droplet transmission in ferrets.
- Analysis of viral receptor-binding specificity.
Main Results:
- H7N9 viruses replicated to higher titers in human airway cells and ferret respiratory tracts compared to a seasonal H3N2 virus.
- H7N9 viruses exhibited increased infectivity and lethality in mice versus related H7N9 and H9N2 viruses.
- Efficient direct contact transmission occurred in ferrets, but respiratory droplet transmission was limited, correlating with low binding to human-like receptors.
Conclusions:
- Avian influenza A(H7N9) viruses possess the capacity for efficient mammalian replication and infection of human airway cells.
- Limited respiratory droplet transmission suggests a lower pandemic potential via this route, but highlights the need for ongoing surveillance.
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