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Protection of Litopenaeus vannamei against White Spot Syndrome Virus using bacterially expressed recombinant envelope proteins VP39 and VP28

机译:使用细菌表达的重组包膜蛋白VP39和VP28保护凡纳滨对虾对白斑综合症病毒的保护

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摘要

White spot syndrome virus (WSSV) is a highly virulent shrimp pathogen, causing huge economic loss to the aquaculture industry. We investigated the efficacy of recombinant VP39 protein against WSSV infection in Litopenaeus vannamei by intramuscular and oral administration, and also compared the efficacy with recombinant VP28 (rVP28). The VP39 is a 283 amino acid protein encoded by the structural gene vp39 which acts as an important mediator for virus entry to the host. Shrimp orally vaccinated with rVP39 and rVP28 showed a cumulative mortality of 50% and 60% respectively following challenge, and this indicates that rVP39 had a better protective effect against WSSV infection compared with rVP28. Vaccination by intramuscular injection with rVP39 and rVP28 resulted in survival rate of 60% and 50%, respectively. The transcriptional profiling of viral genes of vaccinated shrimp with recombinant viral proteins of VP28 showed higher transcriptional levels than VP39. The transcriptional level of rVP39 vaccinated animals was delayed by 6 days after WSSV infection, while the delay was only 4 days in the case of rVP28. These results indicate that vaccination delays the transcription of envelope genes of WSSV in shrimp. The present study could demonstrate the importance of VP39 as a prominent candidate for vaccination against WSSV.
机译:白斑综合症病毒(WSSV)是一种高毒性虾病原体,给水产养殖业造成了巨大的经济损失。我们通过肌肉内和口服给药研究了重组VP39蛋白针对南美白对虾WSSV感染的功效,并与重组VP28(rVP28)进行了比较。 VP39是由结构基因vp39编码的283个氨基酸的蛋白质,它是病毒进入宿主的重要介体。挑战后口服rVP39和rVP28接种的虾的累积死亡率分别为50%和60%,这表明与rVP28相比,rVP39对WSSV感染具有更好的保护作用。肌内注射rVP39和rVP28疫苗接种的存活率分别为60%和50%。 VP28重组病毒蛋白对虾的病毒基因转录谱显示出比VP39高的转录水平。 WSSV感染后,接种rVP39的动物的转录水平延迟了6天,而使用rVP28的动物仅延迟了4天。这些结果表明疫苗接种延迟了虾中WSSV的包膜基因的转录。本研究可以证明VP39作为针对WSSV疫苗的杰出候选者的重要性。

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