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Genetic characterization of influenza A virus and assessment of vaccine efficacy in Yantai from 2014 to 2017

tetano

Editor, Senior Moderator
Zhonghua Yu Fang Yi Xue Za Zhi. 2019 Aug 6;53(8):840-842. doi: 10.3760/cma.j.issn.0253-9624.2019.08.008.
[h=1][Genetic characterization of influenza A virus and assessment of vaccine efficacy in Yantai from 2014 to 2017].[/h] [Article in Chinese; Abstract available in Chinese from the publisher]
Liu J[SUP]1[/SUP], Xu YC, Sun ZL, Gao Q, Dong ZJ, Xu XW, Gong LF.
[h=3]Author information[/h]

[h=3]Abstract[/h] in English, Chinese
In this study, the swabs were collected among patients with an influenza-like illness (ILI) admitted to 2 sentinel surveillance hospitals of Yantai from April 2014 to August 2017. All specimen were cultured and identified by hemagglutination inhibition assay. Complete sequences of Hemagglutinin (HA) of influenza A were amplified, sequenced and analyzed using molecular and phylogenetic methods. The potential vaccine efficacy were calculated using Pepitope model. The results showed that the antigenicity of A (H3N2) had changed greatly. 8 strains of influenza A (H1N1) pdm09 belonged to subclade 6B.1 and 14 strains clustered in 6B.2. 12 strains of influenza A (H3N2) fell into subgroup 3C.3a and 33 strains clustered in 3C.2a. Several residues at antigen sites and potential glycosylation sites had changed in influenza A strains. Vaccine efficacy of influenza A (H1N1) pdm09 in 2015/2016 and 2016/2017 seasons were 77.29% and 79.11% of that of a perfect match with vaccine strain, meanwhile vaccine efficacy of influenza A (H3N2) in 2014/2015, 2015/2016 and 2016/2017 were-5.18%, 16.97% and 42.05% separately. In conclusion, the influenza A virus circulated in Yantai from 2014 to 2017 presented continual genetic variation. The recommended vaccine strains still afforded protection against influenza A (H1N1) pdm09 strains and provided suboptimal protection against influenza A (H3N2) strains.


[h=4]KEYWORDS:[/h] Antigenic variation; Hemagglutinins, viral; Influenza A virus; Survalleince; Vaccine efficacy

PMID: 31378046 DOI: 10.3760/cma.j.issn.0253-9624.2019.08.008
 
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