灭活假单胞菌PE(ΔIII)外毒素融合中和PEDV S蛋白的表位,在小鼠中产生特异性免疫反应。

动物疾病(英文) Pub Date : 2021-01-01 Epub Date: 2021-10-08 DOI:10.1186/s44149-021-00021-9
Leqiang Sun, Yajie Tang, Keji Yan, Huanchun Chen, Huawei Zhang
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引用次数: 3

摘要

猪流行性腹泻(PED)是由猪流行性腹泻病毒(PEDV)引起的一种严重的传染性和破坏性猪疾病,在世界范围内给养猪业造成了严重的经济损失。自2010年以来,许多国家报告了由变体PEDV引起的PED病例数量增加。S蛋白是主要的免疫原性蛋白,含有一些b细胞表位,可以诱导PEDV的中和抗体。本研究以铜绿假单胞菌(Pseudomonas aeruginosa)外毒素A (PE) (without domain III) (PEΔIII)为载体,构建、表达和纯化PEDV S-A或S-B。PE(ΔIII) PEDV S-A和PE(ΔIII) PEDV S-B重组蛋白通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和Western blot分析得到证实。研究了PEDV S-A和PEDV S-B亚单位疫苗在小鼠体内的免疫原性。结果表明,PEDV-S-B疫苗不仅能诱导小鼠特异性体液免疫和Th1型优势细胞免疫应答,还能刺激小鼠PEDV-S-B特异性粘膜免疫应答。PEDV- s - b亚单位疫苗是一种新的抗PEDV感染的候选粘膜疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inactivated Pseudomonas PE(ΔIII) exotoxin fused to neutralizing epitopes of PEDV S proteins produces a specific immune response in mice.

Inactivated Pseudomonas PE(ΔIII) exotoxin fused to neutralizing epitopes of PEDV S proteins produces a specific immune response in mice.

Inactivated Pseudomonas PE(ΔIII) exotoxin fused to neutralizing epitopes of PEDV S proteins produces a specific immune response in mice.

Inactivated Pseudomonas PE(ΔIII) exotoxin fused to neutralizing epitopes of PEDV S proteins produces a specific immune response in mice.

Porcine epidemic diarrhea (PED) caused by the porcine epidemic diarrhea virus (PEDV), is a severe infectious and devastating swine disease that leads to serious economic losses in the swine industry worldwide. An increased number of PED cases caused by variant PEDV have been reported in many countries since 2010. S protein is the main immunogenic protein containing some B-cell epitopes that can induce neutralizing antibodies of PEDV. In this study, the construction, expression and purification of Pseudomonas aeruginosa exotoxin A (PE) without domain III (PEΔIII) as a vector was performed for the delivery of PEDV S-A or S-B. PE(ΔIII) PEDV S-A and PE(ΔIII) PEDV S-B recombinant proteins were confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blot analysis. The immunogenicity of PEDV S-A and PEDV S-B subunit vaccines were evaluated in mice. The results showed that PEDV-S-B vaccine could not only induce specific humoral and Th1 type-dominant cellular immune responses, but also stimulate PEDV-specific mucosal immune responses in mice. PEDV-S-B subunit vaccine is a novel candidate mucosal vaccine against PEDV infection.

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