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口服微囊化疫苗负载海藻酸钠可有效增强草鱼对 GCRV 感染的保护作用。

An Oral Microencapsulated Vaccine Loaded by Sodium Alginate Effectively Enhances Protection Against GCRV Infection in Grass Carp ().

机构信息

Department of Aquatic Animal Medicine, College of Fisheries, Huazhong Agricultural University, Wuhan, China.

Laboratory for Marine Biology and Biotechnology, Pilot National Laboratory for Marine Science and Technology, Qingdao, China.

出版信息

Front Immunol. 2022 Mar 24;13:848958. doi: 10.3389/fimmu.2022.848958. eCollection 2022.

Abstract

Grass carp reovirus (GCRV) is highly infectious and lethal to grass carp, causing huge economic losses to the aquaculture industry annually. Currently, vaccination is the most effective method against viral infections. Among the various vaccination methods, the oral vaccination is an ideal way in aquaculture. However, low protective efficiency is the major problem for oral vaccination owing to some reasons, such as antigen degradation and low immunogenicity. In our study, we screened the antigenic epitopes of GCRV-II and prepared an oral microencapsulated vaccine using sodium alginate (SA) as a carrier and flagellin B (FlaB) as an adjuvant, and evaluated its protective effects against GCRV-II infection in grass carp. The full length and three potential antigenic epitope regions of GCRV-II VP56 gene were expressed in and purified by glutathione affinity column respectively. The optimal antigen (VP56-3) was screened by enzyme-linked immunosorbent assay (ELISA). Adjuvant FlaB was also expressed in and purified by Ni affinity column. Subsequently, we prepared the oral vaccines using sodium alginate as a carrier. The vaccine (SA-VP56-3/FlaB) forms microsphere (1.24 ± 0.22 μm), examined by transmission electron microscopy, scanning electron microscopy, and dynamic light scattering assay. SA-VP56-3/FlaB vaccine has excellent stability, slow-release, and low toxicity by dynamic light scattering assay, release dynamic assay, fluorescence imaging system, hemolytic activity and cytotoxicity. Then we vaccinated grass carp orally with SA-VP56-3/FlaB and measured immune-related parameters (serum neutralizing antibody titer, serum enzyme activity (TSOD, LZM, C3), immune-related genes ((IgM, IFN1, MHC-II, CD8 in head kidney and spleen), IgZ in hindgut)). The results showed that SA-VP56-3/FlaB significantly induced strong immune responses, compared to other groups. The highest survival rate achieved in SA-VP56-3/FlaB microencapsulated vaccine (56%) in 2 weeks post GCRV challenge, while 10% for the control group. Meanwhile, the tissue virus load in survival grass carp is lowest in SA-VP56-3/FlaB group. These results indicated that SA-VP56-3/FlaB could be a candidate oral vaccine against GCRV-II infection in aquaculture.

摘要

草鱼呼肠孤病毒(GCRV)对草鱼具有高度传染性和致死性,每年给水产养殖业造成巨大的经济损失。目前,疫苗接种是对抗病毒感染最有效的方法。在各种疫苗接种方法中,口服疫苗接种是水产养殖中的一种理想方式。然而,由于抗原降解和免疫原性低等原因,口服疫苗接种的保护效率较低是主要问题。在我们的研究中,我们筛选了 GCRV-II 的抗原表位,并使用海藻酸钠(SA)作为载体和鞭毛蛋白 B(FlaB)作为佐剂制备了口服微囊化疫苗,并评估了其对草鱼 GCRV-II 感染的保护效果。全长和三个潜在的 GCRV-II VP56 基因的抗原表位区域分别在 中表达,并通过谷胱甘肽亲和柱进行纯化。通过酶联免疫吸附试验(ELISA)筛选出最佳抗原(VP56-3)。佐剂 FlaB 也在 中表达,并通过 Ni 亲和柱进行纯化。随后,我们使用海藻酸钠作为载体制备口服疫苗。通过透射电子显微镜、扫描电子显微镜和动态光散射分析观察到,疫苗(SA-VP56-3/FlaB)形成微球(1.24±0.22μm)。通过动态光散射分析、释放动态分析、荧光成像系统、溶血活性和细胞毒性检测,SA-VP56-3/FlaB 疫苗具有良好的稳定性、缓慢释放和低毒性。然后,我们通过口服方式给草鱼接种 SA-VP56-3/FlaB,并测量免疫相关参数(血清中和抗体滴度、血清酶活性(TSOD、LZM、C3)、免疫相关基因((头肾和脾脏中的 IgM、IFN1、MHC-II、CD8)、后肠中的 IgZ)。结果表明,与其他组相比,SA-VP56-3/FlaB 显著诱导了强烈的免疫反应。在 GCRV 攻毒后 2 周,SA-VP56-3/FlaB 微囊化疫苗组的存活率最高(56%),而对照组为 10%。同时,SA-VP56-3/FlaB 组存活草鱼组织中的病毒载量最低。这些结果表明,SA-VP56-3/FlaB 可以作为一种候选口服疫苗,用于防治水产养殖中的 GCRV-II 感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ba1/8987307/70a3da4b5939/fimmu-13-848958-g001.jpg

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