Antigenic variants of influenza B viruses isolated in Japan during the 2017-2018 and 2018-2019 influenza seasons

被引:6
|
作者
Kato-Miyashita, Sari [1 ]
Sakai-Tagawa, Yuko [1 ]
Yamashita, Makoto [1 ]
Iwatsuki-Horimoto, Kiyoko [1 ]
Ito, Mutsumi [1 ]
Tokita, Akifumi [2 ,3 ]
Hagiwara, Haruhisa [3 ,4 ]
Izumida, Naomi [3 ,5 ]
Nishino, Tamon [3 ,6 ]
Wada, Noriyuki [3 ,7 ]
Koga, Michiko [8 ]
Adachi, Eisuke [9 ]
Jubishi, Daisuke [1 ,10 ]
Yotsuyanagi, Hiroshi [9 ]
Kawaoka, Yoshihiro [1 ,11 ,12 ]
Imai, Masaki [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Dept Microbiol & Immunol, Div Virol, Tokyo 1088639, Japan
[2] Clin Bambini, Tokyo, Japan
[3] Tokyo Pediat Assoc Publ Hlth Comm, Tokyo, Japan
[4] Hagiwara Clin, Tokyo, Japan
[5] Akebonocho Clin, Tokyo, Japan
[6] Alpaca Kids Ent Clin, Tokyo, Japan
[7] Wada Pediat Clin, Tokyo, Japan
[8] Univ Tokyo, Adv Clin Res Ctr, Inst Med Sci, Div Infect Dis, Tokyo, Japan
[9] Univ Tokyo, Inst Med Sci, IMSUT Hosp, Dept Infect Dis & Appl Immunol, Tokyo, Japan
[10] Nezu Clin, Tokyo, Japan
[11] Univ Wisconsin, Dept Pathobiol Sci, Sch Vet Med, Influenza Res Inst, Madison, WI 53706 USA
[12] Univ Tokyo, Int Res Ctr Infect Dis, Inst Med Sci, Dept Special Pathogens, Tokyo, Japan
关键词
antigenicity; hemagglutinin; influenza B virus; Japan; neuraminidase inhibitors; NEURAMINIDASE INHIBITORS; EXPRESSION; UPDATE;
D O I
10.1111/irv.12713
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Here, we genetically and antigenically analyzed influenza B viruses (IBVs) isolated in Japan during the 2017-2018 and 2018-2019 influenza seasons. Methods A total of 68 IBVs (61 B/Yamagata/16/88-like [B/Yamagata]-lineage and 7 B/Victoria/2/87-like [B/Victoria]-lineage) were antigenically and genetically characterized by using hemagglutination inhibition (HI) assays and phylogenetic analysis, respectively. The susceptibility of IBVs to neuraminidase (NA) inhibitors was assessed by using a fluorescence-based NA inhibition assay. Results All 61 B/Yamagata-lineage isolates were genetically closely related to B/Phuket/3073/2013, the vaccine strain for these two seasons. Eleven B/Yamagata-lineage isolates tested were antigenically similar to B/Phuket/3073/2013 by the HI test. Seven B/Victoria-lineage isolates were genetically closely related to B/Texas/02/2013, the WHO-recommended vaccine strain for the 2017-2018 season; however, they were antigenically distinct from B/Texas/02/2013 with an eightfold or 16-fold difference in HI titer. Of these 7 isolates, 4 possessed a two-amino-acid deletion at positions 162 and 163 in hemagglutinin (HA) and the other 3 had a three-amino-acid deletion at positions 162-164 in HA. Importantly, the variants with the three-amino-acid deletion appeared to be antigenically different from the B/Colorado/06/2017 virus with the two-amino-acid deletion, the vaccine strain for the 2018-2019 season with a fourfold or eightfold difference in HI titer. One B/Yamagata-lineage isolate carrying a G407S mutation in its NA showed a marked reduction in susceptibility to zanamivir, peramivir, and laninamivir. Conclusions These results highlight the need for continued monitoring for the prevalence of the antigenic variant with the three-amino-acid deletion and the variant with reduced NA inhibitor susceptibility.
引用
收藏
页码:311 / 319
页数:9
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