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通过核心基因的密码子对去优化来衰减马立克氏病病毒。

Attenuation of Marek's disease virus by codon pair deoptimization of a core gene.

机构信息

Avian Disease and Oncology Laboratory, Agricultural Research Service, U.S. Department of Agriculture, 4279 East Mount Hope Road, East Lansing, MI 48823, United States.

Avian Disease and Oncology Laboratory, Agricultural Research Service, U.S. Department of Agriculture, 4279 East Mount Hope Road, East Lansing, MI 48823, United States; Michigan State University College of Veterinary Medicine, East Lansing, MI 48824, United States.

出版信息

Virology. 2018 Mar;516:219-226. doi: 10.1016/j.virol.2018.01.020.

Abstract

Marek's disease virus (MDV) is an oncogenic alphaherpesvirus of Gallus gallus, the domesticated chicken. Control strategies rely upon vaccination with live attenuated viruses of antigenically similar avian herpesviruses or attenuated strains of MDV. Recent studies in other viruses have shown that recoding certain viral genes to employ synonymous but rarely-used codon pairs resulted in viral attenuation. We deoptimized two MDV proteins, UL54/ICP27 and UL49/VP22, and demonstrate that the more severely deoptimized variant of UL54 accumulates significantly less gene product in vitro. Using these UL54 deoptimized mutants, we further demonstrate that animals infected with the UL54-recoded recombinant virus exhibited decreased viral genome copy number in lymphocytes, reduced lymphoid atrophy and reduced tumor incidence. This study demonstrates that codon pair deoptimization of a single viral gene can produce attenuated strains of MDV. This approach may be useful as a rational way of making novel live attenuated virus vaccines for MDV.

摘要

马立克氏病病毒(MDV)是一种致瘤性的α疱疹病毒,宿主为家鸡。目前的防控策略主要依赖于接种具有相似抗原性的禽疱疹病毒的活减毒疫苗或马立克氏病病毒的减毒株。最近在其他病毒上的研究表明,对某些病毒基因进行密码子重编码,使用同义但很少使用的密码子对,可导致病毒减毒。我们对马立克氏病病毒的两个蛋白 UL54/ICP27 和 UL49/VP22 进行了去优化,并证实 UL54 的去优化变体在体外的基因产物积累明显减少。利用这些 UL54 去优化突变体,我们进一步证实,感染 UL54 重编码重组病毒的动物的淋巴细胞中的病毒基因组拷贝数减少,淋巴组织萎缩减少,肿瘤发生率降低。本研究表明,单个病毒基因的密码子对重编码可产生马立克氏病病毒的减毒株。这种方法可能作为一种合理的策略,用于开发马立克氏病病毒的新型活减毒疫苗。

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