College of Animal Science and Technology, Jilin Provincial Engineering Research Center of Animal Probiotics, Key Laboratory of Animal Production and Product Quality Safety of Ministry of Education, Jilin Agricultural University, 2888 Xincheng Street, Changchun, 130118, China.
Appl Microbiol Biotechnol. 2018 Jun;102(12):5077-5088. doi: 10.1007/s00253-018-8924-6. Epub 2018 Apr 19.
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.
禽流感病毒(AIV)可以感染家禽、哺乳动物和其他宿主,给全球家禽业造成巨大的经济损失。在这项研究中,为了开发一种基于植物乳杆菌(L. plantarum)的新型、有效的口服疫苗来控制 AIV 在家禽业中的传播,我们构建了一株表达流感病毒 3M2e-HA2 蛋白的重组植物乳杆菌菌株,并确定了 N/pgsA'-3M2e-HA2 对雏鸡的抗 AIV 作用。我们首先通过流式细胞术和免疫荧光实验证实了 3M2e-HA2 融合蛋白在植物乳杆菌表面的表达。我们的实验结果表明,用 N/pgsA'-3M2e-HA2 免疫的雏鸡可以诱导特异性体液、黏膜和 T 细胞介导的免疫反应,使宿主自身能够抵御 AIV。此外,与口服相比,滴鼻免疫 N/pgsA'-3M2e-HA2 能够引起更强的免疫反应,产生有效的保护作用,阻止体重减轻,降低肺部病毒滴度,并减少肺部和喉咙的病理损伤。因此,我们的结果表明,我们的新方法是促进黏膜免疫的有效疫苗设计方法。