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H9亚型禽流感病毒mRNA疫苗的构建与效力评价

黄程 刘月焕 杨志远 林健 程慧敏 王米 毛惠琳 王国良 刘贵明 赵际成

畜牧兽医学报2025,Vol.56Issue(4):1843-1853,11.
畜牧兽医学报2025,Vol.56Issue(4):1843-1853,11.DOI:10.11843/j.issn.0366-6964.2025.04.032

H9亚型禽流感病毒mRNA疫苗的构建与效力评价

Construction and Efficacy Evaluation of mRNA Vaccines against H9 Subtype Avian Influenza Virus

黄程 1刘月焕 1杨志远 1林健 1程慧敏 1王米 2毛惠琳 2王国良 3刘贵明 3赵际成1

作者信息

  • 1. 北京市农林科学院畜牧兽医研究所,北京 100097
  • 2. 苏州近岸蛋白质科技股份有限公司,苏州 215200
  • 3. 北京市农林科学院生物技术研究所,北京 100097
  • 折叠

摘要

Abstract

H9 subtype of avian influenza(AI)poses a significant threat to the poultry industry,particular the broiler industry.As current inactivated vaccine cannot effectively prevent virus in-fection and replication in the upper respiratory tract of chickens,it is necessary to generate an mRNA vaccine targeting the hemagglutinin(HA)gene of H9 subtype avian influenza virus(AIV).Based on the HA gene sequences available on GenBank in 2022,full-length of the HA sequences(HA)and its extracellular domain(HAe)were optimized,and cloned into the pUC57 vector to construct transcription templates in vitro.After transcription in vitro,capping,and purification,the mRNAs were encapsulated in lipid nanoparticles(LNPs)and transfected into human embryonic kidney cells(293T),baby hamster kidney cells(BHK-21),and chicken em-bryo fibroblast cells(DF-1).HA protein expression was confirmed via Western blot.Twenty 3-week-old SPF chickens were randomly divided into four groups(n=5).Each chicken was im-munized with 0.3 mL PBS,25 μg HA mRNA LNP,25 μg HAe mRNA LNP and 0.3 mL H9 subtype AI inactivated vaccine,respectively.Serum samples was collected 4 weeks post-immuni-zation to assess hemagglutination inhibition(HI)antibody titers.All animals were intranasally and ocularly challenged with 0.2 mL of H9N2 subtype AIV(containing 106.0EID50).Oral swabs were collected 5 days post-challenge to detect virus isolation,and peripheral blood mononuclear cells(PBMCs)were collected for the measurement of expression levels of IFN-γ and IL-4,along-side observing pathological changes of tracheal tissue.Western blot analysis showed that both 2 mRNA HA proteins were successfully expressed and could be effectively translated into cells fol-lowing LNP encapsulation.The mean HI antibody titers(log2)post immunization with HA mR-NA LNP and HAe mRNA LNP in SPF chickens were 5.6 and 3,respectively.The H9 subtype AI inactivated vaccine induced significantly higher antibody titer(9.8),compared to both two mRNA LNP groups(P<0.01).Virus isolation rates of the challenge control,HA mRNA LNP,HAe mRNA LNP,and H9 subtype AI inactivated vaccine groups were 5/5,1/5,4/5,and 2/5,respectively.The HA mRNA LNP group exhibited significantly higher IFN-γ expression levels compared to other groups(P<0.05),while the HAe mRNA LNP group showed signifi-cantly lower IL-4 expression levels(P<0.05).The pathological changes of tracheal tissue indi-cated that immunization with HA mRNA LNP and H9 subtype AI inactivated vaccine effectively mitigated damage of H9 subtype AIV to tracheal epithelial cells in SPF chickens.The constructed mRNA vaccine with HA full-length of H9N2 subtype AIV could provide an effective protection to chickens on H9 subtype AIV attack,while mRNA vaccine with HA extracellular domain could not provide an effective immune protection.

关键词

H9亚型/禽流感病毒/mRNA疫苗/LNP/免疫保护

Key words

H9 subtype/avian influenza virus/mRNA vaccine/LNP/immune protection

分类

畜牧业

引用本文复制引用

黄程,刘月焕,杨志远,林健,程慧敏,王米,毛惠琳,王国良,刘贵明,赵际成..H9亚型禽流感病毒mRNA疫苗的构建与效力评价[J].畜牧兽医学报,2025,56(4):1843-1853,11.

基金项目

北京市农林科学院院长基金(YZJJ202102) (YZJJ202102)

北京市农林科学院青年科研基金(QNJJ202234) (QNJJ202234)

现代农业产业技术体系北京市家禽创新团队(BAIC06-2024) (BAIC06-2024)

畜牧兽医学报

OA北大核心

0366-6964

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