Abstract
Resistance to neuraminidase inhibitors (NAIs) is problematic as these drugs constitute the major treatment option for severe influenza. Extensive use of the NAI oseltamivir (Tamiflu®) results in up to 865 ng/L of its active metabolite oseltamivir carboxylate (OC) in river water. There one of the natural reservoirs of influenza A, dabbling ducks, can be exposed. We previously demonstrated that an influenza A(H1N1) virus in mallards (Anas platyrhynchos) exposed to 1 µg/L of OC developed oseltamivir resistance through the mutation H274Y (N2-numbering). In this study, we assessed the resistance development in an A(H6N2) virus, which belongs to the phylogenetic N2 group of neuraminidases with distinct functional and resistance characteristics. Mallards were infected with A(H6N2) while exposed to 120 ng/L, 1.2 µg/L or 12 µg/L of OC in their sole water source. After 4 days with 12 µg/L of OC exposure, the resistance mutation R292K emerged and then persisted. Drug sensitivity was decreased ≈13,000-fold for OC and ≈7.8-fold for zanamivir. Viral shedding was similar when comparing R292K and wild-type virus indicating sustained replication and transmission. Reduced neuraminidase activity and decrease in recovered virus after propagation in embryonated hen eggs was observed in R292K viruses. The initial, but not the later R292K isolates reverted to wild-type during egg-propagation, suggesting a stabilization of the mutation, possibly through additional mutations in the neuraminidase (D113N or D141N) or hemagglutinin (E216K). Our results indicate a risk for OC resistance development also in a N2 group influenza virus and that exposure to one NAI can result in a decreased sensitivity to other NAIs as well. If established in influenza viruses circulating among wild birds, the resistance could spread to humans via re-assortment or direct transmission. This could potentially cause an oseltamivir-resistant pandemic; a serious health concern as preparedness plans rely heavily on oseltamivir before vaccines can be mass-produced.
Highlights
Resistance to the antiviral drugs neuraminidase inhibitors (NAIs) is a problem as they are the best available option for treatment and prophylaxis of influenza A virus infection
We previously found that a low-pathogenic avian influenza A(H1N1) virus developed resistance to oseltamivir when infected mallards were exposed to low, environmental-like levels of oseltamivir carboxylate (OC) (1 mg/L) [28]
We demonstrate resistance development in an influenza A(H6N2) virus in mallards exposed to 12 mg/L of OC in their sole water source
Summary
Resistance to the antiviral drugs neuraminidase inhibitors (NAIs) is a problem as they are the best available option for treatment and prophylaxis of influenza A virus infection. The NAI oseltamivir (TamifluH) has been stockpiled in large quantities in many nations as part of preparedness plans for a new influenza pandemic [1,2]. A new pandemic strain resistant to oseltamivir would be of substantial individual and public health concern. The emergence and spread of the resistant seasonal (pre-pandemic) A(H1N1) strain 2007–2009 tilted the previous concept of decreased fitness of resistant viruses [3]. If a resistance mutation occurs in a permissive genetic background the decreased fitness can be compensated for [4,5]. All studied pandemics (from the last century) have contained gene segments from avian influenza A virus lineages [7,8,9,10] and there is good reason to believe that this will be the case in future pandemics
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