Assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model

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Harry L. Stannard
Edin J. Mifsud
Steffen Wildum
Sook Kwan Brown
Paulina Koszalka
Takao Shishido
Satoshi Kojima
Shinya Omoto
Keiko Baba
Klaus Kuhlbusch
Aeron C. Hurt
Ian G. Barr
机构
[1] WHO Collaborating Centre for Reference and Research on Influenza,Department of Microbiology and Immunology, at the Peter Doherty Institute for Infection and Immunity
[2] at the Peter Doherty Institute for Infection and Immunity,undefined
[3] F. Hoffmann-La Roche Ltd,undefined
[4] Shionogi & Co.,undefined
[5] Ltd,undefined
[6] the University of Melbourne,undefined
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Influenza antivirals are important tools in our fight against annual influenza epidemics and future influenza pandemics. Combinations of antivirals may reduce the likelihood of drug resistance and improve clinical outcomes. Previously, two hospitalised immunocompromised influenza patients, who received a combination of a neuraminidase inhibitor and baloxavir marboxil, shed influenza viruses resistant to both drugs. Here-in, the replicative fitness of one of these A(H1N1)pdm09 virus isolates with dual resistance mutations (NA-H275Y and PA-I38T) was similar to wild type virus (WT) in vitro, but reduced in the upper respiratory tracts of challenged ferrets. The dual-mutant virus transmitted well between ferrets in an airborne transmission model, but was outcompeted by the WT when the two viruses were co-administered. These results indicate the dual-mutant virus had a moderate loss of viral fitness compared to the WT virus, suggesting that while person-to-person transmission of the dual-resistant virus may be possible, widespread community transmission is unlikely.
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