Characterization of substitutions in the neuraminidase of A(H7N9) influenza viruses selected following serial passage in the presence of different neuraminidase inhibitors

• Published in: Antiviral research Vol. 168; pp. 68 - 75
• Main Authors: Farrukee, R., Butler, J., Reading, P.C., Hurt, A.C.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.08.2019
• Subjects: Antivirals; Influenza A(H7N9); Neuraminidase inhibitors; Reduced sensitivity; Resistance; Resistance; Influenza A(H7N9); Reduced sensitivity; Neuraminidase inhibitors; Antivirals
• ISSN: 0166-3542; 1872-9096
• DOI: 10.1016/j.antiviral.2019.05.009

Avian A(H7N9) infections in humans have been reported in China since 2013 and are of public health concern due to their severity and pandemic potential. Oseltamivir and peramivir are neuraminidase inhibitors (NAIs) routinely used for the treatment of A(H7N9) infections, but variants with reduced sensitivity to these drugs can emerge in patients during treatment. Zanamivir and laninamivir are NAIs that are used less frequently. Herein, we performed in vitro serial passaging experiments with recombinant viruses, containing the neuraminidase (NA) from influenza A/Anhui/1/13 (H7N9) virus, in the presence of each NAI, to determine whether variants with reduced sensitivity would emerge. NA substitutions were characterized for their effect on the NA enzymatic activity and surface expression of the A/Anhui/1/13 (Anhui/1) NA, as well as NAs originating from contemporary A(H7N9) viruses of the Yangtze River Delta and Pearl River Delta lineages. In vitro passage in the presence of oseltamivir, peramivir and laninamivir selected for substitutions associated with reduced sensitivity (E119D, R292K and R152K), whereas passage in the presence of zanamivir did not select for any viruses with reduced sensitivity. All the NA substitutions significantly reduced activity, but not the expression of the Anhui/1 NA. In contemporary N9 NAs, all substitutions tested significantly reduced NA enzyme function in the Yangtze River lineage background, but not in the Pearl River Delta lineage background. Overall, these findings suggest that zanamivir may be less likely than the other NAIs to select for resistance in A(H7N9) viruses and that the impact of substitutions that reduce NAI susceptibility or enzyme function may be less in A(H7N9) viruses from the Pearl River lineage. •Substitutions R292K was selected in vitro following passage in oseltamivir or peramivir.•Zanamivir did not select for substitutions that reduced NAI susceptibility in vitro.•R292K significantly reduced NA activity but not expression in the A/Anhui/1/13 NA background.•All NA substitutions reduced enzyme function to a greater extent in the Yangtze-NA background than Pearl-NA background.