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

Commun Biol. 2022 Sep 28;5(1):1026. doi: 10.1038/s42003-022-04005-4.

Abstract

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.

Trial registration: ClinicalTrials.gov NCT03684044.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use
  • Drug Resistance, Viral / genetics
  • Ferrets
  • Humans
  • Influenza A Virus, H1N1 Subtype* / genetics
  • Influenza, Human* / drug therapy
  • Neuraminidase / genetics
  • Virus Replication / genetics

Substances

  • Antiviral Agents
  • Neuraminidase

Associated data

  • figshare/10.6084/m9.figshare.21008614
  • ClinicalTrials.gov/NCT03684044