Precocious Eimeria magna transgenically expressing RHDV P2 subdomain induces immune responses in rabbits.

IF 6.5 1区 医学 Q1 IMMUNOLOGY
Wenxuan Chen, Jingxia Suo, Jiahua Kong, Chunxia Lu, Xiaomin Ge, Fang Yu, Xinming Tang, Xun Suo, Xianyong Liu
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Abstract

Rabbit coccidiosis and rabbit haemorrhagic disease (RHD) pose major threats to the rabbit industry, causing significant economic losses. Developing a multivalent vaccine to concurrently protect rabbits against Eimeria and RHDV infections would provide dual protection through a single immunization protocol. Here, we utilized a precocious line of E. magna (EmagPWT) as a vaccine vector to express P2 subdomain of RHDV capsid protein VP60. We constructed three transgenic parasites expressing (i) RHDV1-P2 subdomain, (ii) RHDV2-P2 subdomain, and (iii) 2 copies of P2 subdomains from both RHDV1 and RHDV2. We found that all transgenic parasites elicited detectable neutralizing antibodies and robust mucosal immune response following secondary immunization. In conclusion, our results indicate genetically manipulated precocious Eimeria parasite expressing heterologous antigens, such as P2 subdomain, holds promise as a vector for developing a multivalent vaccine against RHD and Eimeria infections in rabbits.

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转基因表达RHDV P2亚结构域的早熟大艾美球虫诱导兔免疫应答。
兔球虫病和兔出血性疾病(RHD)对家兔产业构成重大威胁,造成重大经济损失。开发一种多价疫苗,同时保护家兔免受艾美耳球虫和狂犬病病毒感染,将通过单一免疫方案提供双重保护。在这里,我们利用E. magna早熟系(EmagPWT)作为疫苗载体表达RHDV衣壳蛋白VP60的P2亚域。我们构建了三种转基因寄生虫,分别表达(i) RHDV1-P2子域,(ii) RHDV2-P2子域,以及(iii)来自RHDV1和RHDV2的P2子域的2个拷贝。我们发现所有转基因寄生虫在二次免疫后都能引起可检测的中和抗体和强大的粘膜免疫反应。总之,我们的研究结果表明,基因操纵的表达异源抗原(如P2亚结构域)的早熟艾美球虫寄生虫有望作为开发抗RHD和家兔艾美球虫感染的多价疫苗的载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
NPJ Vaccines
NPJ Vaccines Immunology and Microbiology-Immunology
CiteScore
11.90
自引率
4.30%
发文量
146
审稿时长
11 weeks
期刊介绍: Online-only and open access, npj Vaccines is dedicated to highlighting the most important scientific advances in vaccine research and development.
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