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Lorf9 缺失显著消除了由 meq 缺失的超强毒马立克氏病病毒引起的淋巴器官萎缩。

Lorf9 deletion significantly eliminated lymphoid organ atrophy induced by meq-deleted very virulent Marek's disease virus.

机构信息

College of Animal Sciences and Veterinary Medicine, Henan Agricultural University, Zhengzhou, 450002, Henan, PR China.

Key laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, 450002, Henan, PR China.

出版信息

Vet Microbiol. 2019 Aug;235:164-169. doi: 10.1016/j.vetmic.2019.06.020. Epub 2019 Jul 2.

Abstract

Marek's disease virus (MDV) is a highly contagious alphaherpesvirus that causes rapid onset of T cell lymphomas in chickens. MDV continues to break through vaccinal immunity due to the emergence of highly virulent field strains. Earlier studies revealed that deletion of the meq gene from MDV results in attenuated vaccines that protect against disease when chickens are infected with highly virulent strains. However, meq-deleted viruses still retain the ability to induce lymphoid organ atrophy, which raises safety concerns. In an earlier study, we found that deletion of lorf9 counteracts this lymphoid organ atrophy. Here, we describe the generation of a double deletion mutant virus lacking virus-encoded meq and lorf9. In vitro studies revealed that during replication, the mutant virus had kinetic characteristics similar to the parental virus; however, in vivo the replication capability was significantly reduced. Results of animal studies revealed no obvious MDV-specific symptoms and lesions. Importantly, the double deletion mutant virus lost the capacity to induce lymphoid organ atrophy, which has been the main obstacle during development of a good vaccine candidate.

摘要

马立克氏病病毒(MDV)是一种高度传染性的α疱疹病毒,可导致鸡的 T 细胞淋巴瘤迅速发作。由于高毒力田间毒株的出现,MDV 继续突破疫苗免疫。早期研究表明,从 MDV 中删除 meq 基因可导致减毒疫苗,当鸡感染高毒力毒株时,可预防疾病。然而,缺失 meq 的病毒仍然保留诱导淋巴器官萎缩的能力,这引发了安全性问题。在早期的一项研究中,我们发现删除 lorf9 可拮抗这种淋巴器官萎缩。在这里,我们描述了一种缺失病毒编码的 meq 和 lorf9 的双重缺失突变病毒的产生。体外研究表明,在复制过程中,突变病毒具有与亲本病毒相似的动力学特征;然而,在体内,其复制能力显著降低。动物研究结果显示没有明显的 MDV 特异性症状和病变。重要的是,双重缺失突变病毒丧失了诱导淋巴器官萎缩的能力,这是开发良好疫苗候选物的主要障碍。

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