April 29, 2013
Clues in H7N9 Influenza Genetic Sequences
On March 31, 2013, the Chinese Center for Disease Control and Prevention (Chinese CDC) reported the first cases associated with the H7N9 influenza virus. As of April 21, 2013, 104 human infections had been confirmed, with 21 deaths. To date, the outbreak has been limited to eastern China, and there’s been no evidence of transmission between people.
A team of researchers set out to analyze the novel virus. They were led by Dr. Masato Tashiro of the National Institute of Infectious Diseases in Japan and Dr. Yoshihiro Kawaoka of the University of Wisconsin-Madison and the University of Tokyo. The team studied the genetic sequences of viruses isolated from 4 of the earliest fatal cases. Sequences were provided by the Chinese CDC. The analysis was funded by NIH’s National Institute of Allergy and Infectious Diseases (NIAID) and Japanese organizations. Results appeared on April 11, 2013, in Eurosurveillance.
Influenza virus strains are classified and named based on the viral surface proteins hemagglutinin (HA) and neuraminidase (NA). The combination of H7 HA and N9 NA has previously been seen only in birds. The scientists concluded that the novel strain likely got its surface protein genes from the H7N3 and H11N9 avian influenza strains. Other genes came from H9N2 influenza viruses recently circulating in poultry in China.
While H7N9 causes mild disease in birds, the analysis revealed mutations that may allow it to more efficiently cause disease in mammals. The HA sequences have mutations that have been shown to improve the virus’s ability to bind to human cells. The sequences also contain mutations associated with improved virus reproduction within human cells and with more severe disease in mammals.
The researchers found that the novel H7N9 viruses are likely to be treatable using NA inhibitors, a class of anti-influenza drugs that includes oseltamivir (Tamiflu) and zanamivir (Relenza). However, the novel strain won’t likely be treatable with ion channel inhibitors, another major class of anti-influenza drugs.
“The H7N9 influenza virus is a new concern that the public health and scientific communities will continue to track closely, including watching for any genetic mutations that might enable the virus to become transmissible from person to person or to cause more severe disease,” says NIAID Director Dr. Anthony Fauci. “Having rapid access to the viral genetic information is essential to understanding how the virus is evolving and ultimately to developing a candidate vaccine, if warranted.”
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Funding: NIH’s National Institute of Allergy and Infectious Diseases (NIAID); the Ministry of Health, Labour and Welfare, Japan; the Ministry of Education, Culture, Sports, Science, and Technology, Japan; and by ERATO, Japan.