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口服表达非洲猪瘟病毒抗原的重组体可诱导免疫反应。

Orally administered recombinant expressing African swine fever virus antigens that induced immunity responses.

作者信息

Zhang Hongliang, Zhao Saisai, Zhang Haojie, Shen Yu, Zhang Peijun, Shan Hu, Cai Xiulei

机构信息

College of Veterinary Medicine, Qingdao Agricultural University, Qingdao, Shandong, China.

College of Animal Science and Technology, Shandong Agricultural University, Tai'an, Shandong, China.

出版信息

Front Microbiol. 2023 Jan 9;13:1103327. doi: 10.3389/fmicb.2022.1103327. eCollection 2022.

Abstract

African swine fever (ASF) is a highly contagious, acute, febrile disease caused by the African swine fever virus (ASFV), with morbidity and mortality rates approaching 100% in domestic and wild swine, resulting in massive economic losses to the pig industry worldwide. This study aimed to express the p30, p54, and p72 proteins encoded by ASFV using the () expression system. Here, six new functional recombinant were constructed, and the expression of the p30 protein, p54 protein, p72 protein, p30-LTB (heat-labile enterotoxin B, LTB) fusion protein, p54-LTB fusion protein, and the p72-LTB fusion protein was successfully detected by Western blot analysis. Following oral immunization of rabbits with recombinant , serum IgG, intestinal mucosal sIgA, cytokines (IL-4 and INF-γ), and splenocyte viability were higher than in the control group ELISA. Notably, without the LTB adjuvant group, humoral and Th1 cellular immunity were promoted, whereas, with the LTB adjuvant group, local mucosal immunity, humoral immunity, and Th2 cellular immunity were promoted, providing new insights into the design and development of an ASFV subunit vaccine.

摘要

非洲猪瘟(ASF)是一种由非洲猪瘟病毒(ASFV)引起的高度传染性、急性、发热性疾病,家猪和野猪的发病率和死亡率接近100%,给全球养猪业造成巨大经济损失。本研究旨在使用()表达系统表达ASFV编码的p30、p54和p72蛋白。在此,构建了六种新的功能性重组体,并通过蛋白质印迹分析成功检测到p30蛋白、p54蛋白、p72蛋白、p30-LTB(不耐热肠毒素B,LTB)融合蛋白、p54-LTB融合蛋白和p72-LTB融合蛋白的表达。用重组体对兔进行口服免疫后,通过酶联免疫吸附测定法(ELISA)检测发现,血清IgG、肠黏膜sIgA、细胞因子(IL-4和INF-γ)以及脾细胞活力均高于对照组。值得注意的是,在没有LTB佐剂组的情况下,体液免疫和Th1细胞免疫得到促进,而在有LTB佐剂组的情况下,局部黏膜免疫、体液免疫和Th2细胞免疫得到促进,这为ASFV亚单位疫苗的设计和开发提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a71/9869048/1e485cb3f5af/fmicb-13-1103327-g001.jpg

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