tetano
Editor, Senior Moderator
Influenza Other Respir Viruses
. 2020 Oct 24.
doi: 10.1111/irv.12821. Online ahead of print.
Comprehensive assessment of amino acid substitutions in the trimeric RNA polymerase complex of influenza A virus detected in clinical trials of baloxavir marboxil
Takashi Hashimoto[SUP] 1 2 [/SUP], Keiko Baba[SUP] 1 [/SUP], Kae Inoue[SUP] 2 [/SUP], Miyako Okane[SUP] 2 [/SUP], Satoshi Hata[SUP] 2 [/SUP], Takao Shishido[SUP] 1 [/SUP], Akira Naito[SUP] 1 [/SUP], Steffen Wildum[SUP] 3 [/SUP], Shinya Omoto[SUP] 1 [/SUP]
Affiliations
Abstract
Background: Baloxavir marboxil (BXM) is an approved drug that selectively targets cap-dependent endonuclease on PA subunit in the RNA polymerase complex of influenza A and B viruses. Amino acid substitutions at position 38 in the PA subunit were identified as a major pathway for reduced susceptibility to baloxavir acid (BXA), the active form of BXM. Additionally, substitutions found at positions E23, A37, and E199 in the PA subunit impact BXA susceptibility by less than 10-fold.
Methods: We comprehensively evaluated the impact of novel amino acid substitutions identified in PA, PB1, and PB2 subunits in BXM clinical trials and influenza sequence databases by means of drug susceptibility and replicative capacity.
Results: PA/I38N in A(H1N1)pdm09 and PA/I38R in A(H3N2) were newly identified as treatment-emergent substitutions in the CAPSTONE-2 study. The I38N substitution conferred reduced susceptibility by 24-fold, whereas replicative capacity of the I38N-substituted virus was impaired compared with the wild-type. The I38R-substituted virus was not viable in cell culture. All other mutations assessed in this extensive study did not significantly affect BXA susceptibility (< 2.4-fold change).
Conclusion: These results provide additional information on the impact of amino acid substitutions in the trimeric viral polymerase complex to BXA susceptibility and will further support influenza surveillance.
Keywords: antiviral; baloxavir; influenza virus; replicative capacity; susceptibility.
. 2020 Oct 24.
doi: 10.1111/irv.12821. Online ahead of print.
Comprehensive assessment of amino acid substitutions in the trimeric RNA polymerase complex of influenza A virus detected in clinical trials of baloxavir marboxil
Takashi Hashimoto[SUP] 1 2 [/SUP], Keiko Baba[SUP] 1 [/SUP], Kae Inoue[SUP] 2 [/SUP], Miyako Okane[SUP] 2 [/SUP], Satoshi Hata[SUP] 2 [/SUP], Takao Shishido[SUP] 1 [/SUP], Akira Naito[SUP] 1 [/SUP], Steffen Wildum[SUP] 3 [/SUP], Shinya Omoto[SUP] 1 [/SUP]
Affiliations
- PMID: 33099886
- DOI: 10.1111/irv.12821
Abstract
Background: Baloxavir marboxil (BXM) is an approved drug that selectively targets cap-dependent endonuclease on PA subunit in the RNA polymerase complex of influenza A and B viruses. Amino acid substitutions at position 38 in the PA subunit were identified as a major pathway for reduced susceptibility to baloxavir acid (BXA), the active form of BXM. Additionally, substitutions found at positions E23, A37, and E199 in the PA subunit impact BXA susceptibility by less than 10-fold.
Methods: We comprehensively evaluated the impact of novel amino acid substitutions identified in PA, PB1, and PB2 subunits in BXM clinical trials and influenza sequence databases by means of drug susceptibility and replicative capacity.
Results: PA/I38N in A(H1N1)pdm09 and PA/I38R in A(H3N2) were newly identified as treatment-emergent substitutions in the CAPSTONE-2 study. The I38N substitution conferred reduced susceptibility by 24-fold, whereas replicative capacity of the I38N-substituted virus was impaired compared with the wild-type. The I38R-substituted virus was not viable in cell culture. All other mutations assessed in this extensive study did not significantly affect BXA susceptibility (< 2.4-fold change).
Conclusion: These results provide additional information on the impact of amino acid substitutions in the trimeric viral polymerase complex to BXA susceptibility and will further support influenza surveillance.
Keywords: antiviral; baloxavir; influenza virus; replicative capacity; susceptibility.