Lactobacillus plantarum displaying conserved M2e and HA2 fusion antigens induces protection against influenza virus challenge

被引:23
作者
Yang, Wen-Tao [1 ]
Yang, Gui-Lian [1 ]
Zhao, Liang [1 ]
Jin, Yu-Bei [1 ]
Jiang, Yan-Long [1 ]
Huang, Hai-Bin [1 ]
Shi, Chun-Wei [1 ]
Wang, Jian-Zhong [1 ]
Wang, Guan [1 ]
Kang, Yuan-Huan [1 ]
Wang, Chun-Feng [1 ]
机构
[1] Jilin Agr Univ, Coll Anim Sci & Technol, Jilin Prov Engn Res Ctr Anim Probiot, Key Lab Anim Prod & Prod Qual Safety,Minist Educ, 2888 Xincheng St, Changchun 130118, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Conserved antigen; Lactobacillus plantarum; Influenza virus; Mucosal immunity; LACTIC-ACID BACTERIA; A H5N6 VIRUS; AVIAN INFLUENZA; IMMUNE-RESPONSES; BALB/C MICE; EXPRESSING HEMAGGLUTININ; NEUTRALIZING ANTIBODIES; H9N2; INFLUENZA; HIGH-LEVEL; INFECTION;
D O I
10.1007/s00253-018-8924-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Avian influenza virus (AIV) can infect poultry, mammals, and other hosts and causes enormous economic losses to the global poultry industry. In this study, to develop a novel and potent oral vaccine based on Lactobacillus plantarum (L. plantarum) for controlling the spread of AIV in the poultry industry, we constructed a recombinant L. plantarum strain displaying the 3M2e-HA2 protein of the influenza virus and determined the effect of N/pgsA'-3M2e-HA2 against AIV in chicks. We first confirmed that the 3M2e-HA2 fusion protein was expressed on the surface of L. plantarum via flow cytometry and immunofluorescence experiments. Our experimental results demonstrated that chicks immunized with N/pgsA'-3M2e-HA2 could induce specific humoral, mucosal, and T cell-mediated immune responses, eliciting the host body to protect itself against AIV. Additionally, compared to oral administration, the intranasal immunization of chicks with N/pgsA'-3M2e-HA2 provided a stronger immune response, resulting in a potent protective effect that hindered the loss of body weight, decreasing pulmonary virus titers and reducing lung and throat pathological damages. Thus, our results indicate that our novel approach is an effective method of vaccine design to promote mucosal immunity.
引用
收藏
页码:5077 / 5088
页数:12
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