Immune responses induced by recombinant Lactobacillus plantarum expressing the spike protein derived from transmissible gastroenteritis virus in piglets

被引:27
|
作者
Jin, Yu-Bei [1 ]
Yang, Wen-Tao [1 ]
Shi, Chun-Wei [1 ]
Feng, Bo [1 ]
Huang, Ke-Yan [1 ]
Zhao, Guang-Xun [1 ]
Li, Qiong-Yan [1 ]
Xie, Jing [1 ]
Huang, Hai-Bin [1 ]
Jiang, Yan-Long [1 ]
Wang, Jian-Zhong [1 ]
Wang, Guan [1 ]
Kang, Yuan-Huan [1 ]
Yang, Gui-Lian [1 ]
Wang, Chun-Feng [1 ]
机构
[1] Jilin Agr Univ, Lab Anim Prod & Qual Secur, Jilin Prov Engn Res Ctr Anim Probiot, Minist Educ,Coll Anim Sci & Technol, 2888 Xincheng St, Changchun 130118, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
TGEV S protein; Lactobacillus plantarum; Oral immunization; DCpep; Bcells; Immune response; PORCINE EPIDEMIC DIARRHEA; AVIAN INFLUENZA-VIRUS; DENDRITIC CELLS; IMMUNOLOGICAL EVALUATION; PROTECTIVE IMMUNITY; LACTOCOCCUS-LACTIS; B-CELLS; SURFACE; VACCINE; CONSTRUCTION;
D O I
10.1007/s00253-018-9205-0
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
Transmissible gastroenteritis coronavirus (TGEV) is one of the most severe threats to the swine industry. In this study, we constructed a suite of recombinant Lactobacillus plantarum with surface displaying the spike (S) protein coming from TGEV and fused with DC cells targeting peptides (DCpep) to develop an effective, safe, and convenient vaccine against transmissible gastroenteritis. Our research results found that the recombinant Lactobacillus plantarum (NC8-pSIP409-pgsA-S-DCpep) group expressing S fused with DCpep could not only significantly increase the percentages of MHC-II(+)CD80(+) B cells and CD3(+)CD4(+) T cells but also the number of IgA(+) B cells and CD3(+)CD4(+) T cells of ileum lamina propria, which elevated the specific secretory immunoglobulin A (SIgA) titers in feces and IgG titers in serum. Taken together, these results suggest that NC8-pSIP409-pgsA-S-DCpep expressing the S of TGEV fused with DCpep could effectively induce immune responses and provide a feasible original strategy and approach for the design of TGEV vaccines.
引用
收藏
页码:8403 / 8417
页数:15
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