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.

Nature
|July 12, 2013
PubMed

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.