Evidence map›Paper›PMID 35037399›Full record

ArticleInfluenza and other respiratory viruses2022

Homologous PB1 gene promotes the replication efficiency of avian influenza H7N4 candidate vaccine virus.

Liqi Liu, Zi Li, Jianfang Zhou, Jia Liu, Xiyan Li, Weijuan Huang, Ning Xiao, Dayan Wang

Abstract read
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Article in Influenza and other respiratory viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Liqi LiuChinese National Influenza Center, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
Zi LiChinese National Influenza Center, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
Jianfang ZhouChinese National Influenza Center, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
Jia LiuChinese National Influenza Center, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
Xiyan LiChinese National Influenza Center, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
Weijuan HuangChinese National Influenza Center, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
Ning XiaoChinese National Influenza Center, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
Dayan WangChinese National Influenza Center, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.ORCID 0000-0002-4990-1016

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe first and only case of human infection with the avian influenza A (H7N4) virus in China emerged in 2018. The H7N4 virus was distinct from previous H7N9 viruses and raised public concerns. Therefore, developing a suitable H7N4 candidate vaccine virus (CVV) remains crucial for potential pandemic preparedness.

methodsWe constructed a reassortant virus with a (6 + 2) genome composition, then introduced the polymerase basic protein 1 (PB1) from a wild-type virus to develop a (5 + 3) reassortant virus through reverse genetics. We performed whole-genome sequencing to confirm the genome stability, assessed the growth ability in MDCK cells, and analyzed virus antigenicity using hemagglutination inhibition assays. Subsequently, the effect of homologous PB1 on polymerase activity, viral protein yield, and pathogenicity was assessed.

resultsThe (5 + 3) virus harbouring the homologous PB1 gene exhibited significantly improved growth characteristics, higher viral protein yield, and polymerase activity than the (6 + 2) virus. After successive passage in embryonated eggs, glutamic acid (E) substituted glycine(G) at position 218 (H3 numbering) in the hemagglutinin (HA) gene of both (5 + 3) and (6 + 2) viruses. The substitution improved the growth of the (6 + 2) virus but exhibited no significant effect or alteration on the antigenicity of the (5 + 3) virus. Moreover, the (5 + 3) virus exhibited low pathogenicity in chickens and ferrets.

conclusionHomologous PB1 of the H7N4 virus improves the growth ability while sustaining low pathogenicity. Collectively, the gene composition of the (5 + 3) reassortant virus is a suitable H7N4 CVV for potential pandemic preparedness.

Indexed as

Influenza A Virus, H7N9 SubtypeInfluenza in BirdsInfluenza VaccinesVaccinesAnimalsChickensFerretsHumansReassortant VirusesVirus ReplicationInfluenza VaccinesVaccinesavian influenza H7N4 viruscandidate vaccine viruspolymerase basic protein 1reverse genetics

Identifiers

PMID35037399
PMCPMC8983892

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