Volume 25, Number 11—November 2019
Dispatch
Human-to-Human Transmission of Influenza A(H3N2) Virus with Reduced Susceptibility to Baloxavir, Japan, February 2019
Table 2
Susceptibility of influenza A(H3N2) virus carrying polymerase acidic I38T substitution detected in children within family cluster, February 2019, compared with 2018–19 seasonal virus, Japan*
Influenza virus | Median IC50 + SD, nmol/L |
||||
---|---|---|---|---|---|
Baloxavir | NA inhibitors (WHO criteria) |
||||
Oseltamivir | Peramivir | Zanamivir | Laninamivir | ||
A/Kanagawa/IC18141/2019 | 236.08 | 0.37 (NI) | 0.18 (NI) | 1.01 (NI) | 1.27 (NI) |
A(H3N2) of 2018–19 | 1.27 + 1.08† | 0.37 + 0.17‡ | 0.13 + 0.03‡ | 0.79 + 0.33‡ | 1.00 + 0.21‡ |
*We determined antiviral susceptibilities using a focus reduction assay and a fluorescent NA inhibition assay (NA-Fluor Influenza Neuraminidase Assay Kit; Applied Biosystems, https://www.thermofisher.com) (4) and calculated IC50 values using MikroWin 2010 (Labsis, https://labsis.de). We expressed NA inhibitor susceptibilities using WHO criteria for influenza A virus inhibition, which define susceptibility on the basis of the -fold change in IC50 compared with the IC50 of reference isolates (6). WHO inhibition was defined as normal (<10-fold increase), reduced (10–100-fold increase), or highly reduced (>100-fold increase) in comparison with the median value of isolates from the same influenza season. IC50, 50% inhibitory concentration; NA, neuraminidase; NI, normal inhibition; WHO, World Health Organization.
†n = 83.
‡n = 170.
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