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构建并评价重组干酪乳杆菌表达维氏气单胞菌外膜蛋白 OmpAI 作为分子佐剂的免疫效果。

Construction and immune efficacy of recombinant Lactobacillus casei expressing OmpAI of Aeromonas veronii C5-I as molecular adjuvant.

机构信息

College of Animal Science and Technology, Jilin Agricultural University, Changchun, 130118, China.

College of Animal Science and Technology, Jilin Agricultural University, Changchun, 130118, China; College of Life Science, Changchun Sci-Tech University Shuangyang District, Changchun, Jilin, 130118, China.

出版信息

Microb Pathog. 2021 Jul;156:104827. doi: 10.1016/j.micpath.2021.104827. Epub 2021 Apr 21.

Abstract

Despite advancements in diagnosis and control, Aeromonas infections are considered the leading cause of economic aquaculture loss. In this study, to enhance DNA vaccine efficacy against Aeromonas infections, a fused DNA fragment (1504 bp) of the OmpAI gene from Aeromonas veronii (A. veronii) combined with the C5-I gene from the common carp was generated with splicing by overlapping PCR (SOE-PCR) and expressed in Lactobacillus casei strain CC16. Protein C5-I served as a molecular adjuvant for the antigen OmpAI. Two types of fusion antigens were developed (anchored and secretory). Generally, anchored-type antigens are more effective in inducing immune responses in fish than secretory antigens. Western blot analysis showed that the bands of both antigens were present at 58 kDa. After oral immunization, both DNA vaccines enhanced the serum levels of AKP, ACP, SOD and LZM in immunized carp; the genes IL-10, IL-1β, TNF-α, and IFN-γ in the heart, liver, spleen, head kidney, and intestinal tract were upregulated; and a stronger phagocytic response was triggered in immunized fish. In addition, common carp administered the fused antigens were more protected from Aeromonas challenge (60-73.3% protection). Recombinant Lactobacillus bacteria expressing the fused protein showed a greater propensity for colonization in the intestinal tract in immunized fish than in controls. Here, we provide a promising approach to improve DNA vaccine immunogenicity for protecting common carp from A. veronii infections.

摘要

尽管在诊断和控制方面取得了进展,但气单胞菌感染仍是水产养殖经济损失的主要原因。在本研究中,为了提高针对气单胞菌感染的 DNA 疫苗效力,采用重叠 PCR(SOE-PCR)融合了维氏气单胞菌(A. veronii)的 OmpAI 基因和鲤鱼的 C5-I 基因的融合 DNA 片段(1504bp),并在干酪乳杆菌 CC16 中表达。C5-I 蛋白作为抗原 OmpAI 的分子佐剂。开发了两种融合抗原(锚定型和分泌型)。一般来说,锚定型抗原比分泌型抗原更能有效诱导鱼类的免疫反应。Western blot 分析表明,两种抗原的条带均在 58kDa 处出现。经口服免疫后,两种 DNA 疫苗均能提高免疫鲤鱼血清中 AKP、ACP、SOD 和 LZM 的水平;心脏、肝脏、脾脏、头肾和肠道中的 IL-10、IL-1β、TNF-α 和 IFN-γ 基因上调;并引发免疫鱼更强的吞噬反应。此外,接受融合抗原免疫的鲤鱼对气单胞菌攻毒的保护率更高(60-73.3%)。表达融合蛋白的重组干酪乳杆菌在免疫鱼的肠道中更倾向于定植,而对照组则不然。本研究为提高 DNA 疫苗免疫原性,保护鲤鱼免受维氏气单胞菌感染提供了一种有前途的方法。

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