缺失 L60L 和 CD2v 基因的新型减毒 ASFV 对同源挑战的保护评估

Viruses Pub Date : 2024-09-14 DOI:10.3390/v16091464
Jinjin Yang, Rongnian Zhu, Nan Li, Yanyan Zhang, Xintao Zhou, Huixian Yue, Qixuan Li, Yu Wang, Faming Miao, Teng Chen, Fei Zhang, Shoufeng Zhang, Aidong Qian, Rongliang Hu
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摘要

非洲猪瘟(ASF)是一种急性传染病,家猪和野猪的死亡率都很高。由于非洲猪瘟病原体非洲猪瘟病毒(ASFV)的结构和基因组复杂多样,目前还没有针对非洲猪瘟的商业疫苗或抗病毒药物。近年来,关于非洲猪瘟减毒疫苗候选株的报道层出不穷。在本研究中,我们通过同时删除高毒力毒株 SY18 的 L60L 基因和 CD2v 基因,获得了名为 SY18ΔL60LΔCD2v 的重组病毒。在体外,与亲本 SY18 相比,SY18ΔL60LΔCD2v 的生长动力学有所下降。在体内,高剂量(105 TCID50)的 SY18ΔL60LΔCD2v 能保护猪(5/5)免受亲本 SY18 株(102 TCID50)的攻击。低剂量(102 TCID50)的 SY18ΔL60LΔCD2v 只能保护 20% 的猪(1/5)免受亲本 SY18 株(102 TCID50)的攻击。结果表明,SY18 中这两个基因的缺失可诱导对同源亲本毒株的保护,并且没有明显的临床症状或病毒血症。这些结果表明,SY18ΔL60LΔCD2v 株可作为一种新的减毒活疫苗候选株,用于预防和控制 ASFV 感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protection Evaluation of a New Attenuated ASFV by Deletion of the L60L and CD2v Genes against Homologous Challenge
African swine fever (ASF) is an acute infectious disease with a high mortality rate in both domestic and wild boars. Commercial vaccines or antiviral drugs for ASF were not available due to the complex diversity of the structure and genome of its pathogen African swine fever virus (ASFV). In recent years, there have been many reports on candidate strains of attenuated vaccines for ASFV. In this study, we obtained a recombinant virus named SY18ΔL60LΔCD2v by simultaneously deleting the L60L gene and CD2v gene from highly virulent strain SY18. In vitro, SY18ΔL60LΔCD2v displayed a decreased growth kinetic compared to that of parental SY18. In vivo, high doses (105 TCID50) of SY18ΔL60LΔCD2v can protect pigs (5/5) from attacks by the parental SY18 strain (102 TCID50). Low doses (102 TCID50) of SY18ΔL60LΔCD2v only protected 20% of pigs (1/5) from attacks by the parental SY18 strain (102 TCID50). The results indicated that the absence of these two genes in SY18 could induce protection against the homologous parental strain, and there were no obvious clinical symptoms or viremia. These results indicate that the SY18ΔL60LΔCD2v strain can serve as a new live attenuated vaccine candidate for the prevention and control of ASFV infection.
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