The molecular basis of the pathogenicity of the Dutch highly pathogenic human influenza A H7N7 viruses
The Journal of Infectious Diseases , Volume 196 - Issue 2 p. 258- 265
During the highly pathogenic avian influenza (HPAI) H7N7 virus outbreak in The Netherlands in 2003, 88 infected persons suffered from mild illnesses, and 1 died of pneumonia. Here, we studied which of the 14 amino acid substitutions observed between the fatal case (FC) virus and a conjunctivitis case (CC) virus determined the differences in virus pathogenicity. In virus-attachment experiments, the CC and FC viruses revealed marked differences in binding to the lower respiratory tract of humans. In a mouse model, the hemagglutinin (HA) gene of the FC virus was a determinant of virus tissue distribution. The lysine at position 627 of basic polymerase 2 (PB2) of the FC virus was the major determinant of pathogenicity and tissue distribution. Thus, remarkable similarities were revealed between recent HPAI H5N1 and H7N7 viruses. We conclude that the influenza virus HA and PB2 genes should be the prime targets for molecular surveillance during outbreaks of zoonotic HPAI viruses.
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|The Journal of Infectious Diseases|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
Munster, V.J, de Wit, E, van Riel, D.A.J, Beyer, W.E.Ph, Rimmelzwaan, G.F, Osterhaus, A.D.M.E, … Fouchier, R.A.M. (2007). The molecular basis of the pathogenicity of the Dutch highly pathogenic human influenza A H7N7 viruses. The Journal of Infectious Diseases, 196(2), 258–265. doi:10.1086/518792
|publisher's version Final Version|