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含Montanide佐剂的细胞培养来源的罗非鱼湖病毒灭活疫苗对罗非鱼病毒攻击提供高度保护。

Cell Culture-Derived Tilapia Lake Virus-Inactivated Vaccine Containing Montanide Adjuvant Provides High Protection against Viral Challenge for Tilapia.

作者信息

Zeng Weiwei, Wang Yingying, Hu Huzi, Wang Qing, Bergmann Sven M, Wang Yahui, Li Bo, Lv Yuefeng, Li Hua, Yin Jiyuan, Li Yingying

机构信息

Guangdong Provincial Key Laboratory of Animal Molecular Design and Precise Breeding, School of Life Science and Engineering, Foshan University, Foshan 528000, China.

Key Laboratory of Aquatic Animal Immune Technology, Key Laboratory of Fishery Drug Development, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Ministry of Agriculture, Guangzhou 510380, China.

出版信息

Vaccines (Basel). 2021 Jan 25;9(2):86. doi: 10.3390/vaccines9020086.

DOI:10.3390/vaccines9020086
PMID:33503930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7911875/
Abstract

Tilapia lake virus (TiLV) is a newly emerging pathogen responsible for high mortality and economic losses in the global tilapia industry. Currently, no antiviral therapy or vaccines are available for the control of this disease. The goal of the present study was to evaluate the immunological effects and protective efficacy of formaldehyde- and β-propiolactone-inactivated vaccines against TiLV in the presence and absence of the Montanide IMS 1312 VG adjuvant in tilapia. We found that β-propiolactone inactivation of viral particles generated a vaccine with a higher protection efficacy against virus challenge than did formaldehyde. The relative percent survivals of vaccinated fish at doses of 10, 10, and 10 50% tissue culture infectious dose (TCID)/mL were 42.9%, 28.5%, and 14.3% in the absence of the adjuvant and 85.7%, 64.3%, and 32.1% in its presence, respectively. The vaccine generated specific IgM and neutralizing antibodies against TiLV at 3 weeks following immunization that were significantly increased after a second booster immunization. The steady state mRNA levels of the genes tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), interferon γ (IFN-γ), cluster of differentiation 4 (CD4), major histocompatibility complex (MHC)-Ia, and MHC-II were all increased and indicated successful immune stimulation against TiLV. The vaccine also significantly lowered the viral loads and resulted in significant increases in survival, indicating that the vaccine may also inhibit viral proliferation as well as stimulate a protective antibody response. The β-propiolactone-inactivated TiLV vaccine coupled with the adjuvant Montanide IMS 1312 VG and booster immunizations can provide a high level of protection from virus challenge in tilapia.

摘要

罗非鱼湖病毒(TiLV)是一种新出现的病原体,在全球罗非鱼养殖业中导致高死亡率和经济损失。目前,尚无抗病毒疗法或疫苗可用于控制这种疾病。本研究的目的是评估在有和没有Montanide IMS 1312 VG佐剂的情况下,甲醛和β-丙内酯灭活疫苗对罗非鱼体内TiLV的免疫效果和保护效力。我们发现,病毒颗粒经β-丙内酯灭活后产生的疫苗对病毒攻击的保护效力高于甲醛灭活疫苗。在无佐剂的情况下,接种剂量为10、10²和10³ 50%组织培养感染剂量(TCID)/mL的鱼的相对存活率分别为42.9%、28.5%和14.3%;在有佐剂的情况下,相对存活率分别为85.7%、64.3%和32.1%。该疫苗在免疫后3周产生了针对TiLV的特异性IgM和中和抗体,在第二次加强免疫后显著增加。肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)、干扰素γ(IFN-γ)、分化簇4(CD4)、主要组织相容性复合体(MHC)-Ia和MHC-II基因的稳态mRNA水平均升高,表明对TiLV的免疫刺激成功。该疫苗还显著降低了病毒载量,并导致存活率显著提高,表明该疫苗可能还能抑制病毒增殖以及刺激保护性抗体反应。β-丙内酯灭活的TiLV疫苗与佐剂Montanide IMS 1312 VG结合并进行加强免疫,可以为罗非鱼提供高水平的病毒攻击保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/53bc208d933b/vaccines-09-00086-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/5bbcc6bf5feb/vaccines-09-00086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/fcdd811d2ea4/vaccines-09-00086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/984a8cbdd628/vaccines-09-00086-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/83d2b47cf2da/vaccines-09-00086-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/53bc208d933b/vaccines-09-00086-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/5bbcc6bf5feb/vaccines-09-00086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/fcdd811d2ea4/vaccines-09-00086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/984a8cbdd628/vaccines-09-00086-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/83d2b47cf2da/vaccines-09-00086-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9e/7911875/53bc208d933b/vaccines-09-00086-g005.jpg

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