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减毒Orf病毒株D1701的基因组重排及随后的基因缺失分析。

Analysis of genomic rearrangement and subsequent gene deletion of the attenuated Orf virus strain D1701.

作者信息

Cottone R, Büttner M, Bauer B, Henkel M, Hettich E, Rziha H J

机构信息

Federal Research Centre for Virus Diseases of Animals, Institute For Vaccines, Tübingen, Federal Republic of Germany.

出版信息

Virus Res. 1998 Jul;56(1):53-67. doi: 10.1016/s0168-1702(98)00056-2.

DOI:10.1016/s0168-1702(98)00056-2
PMID:9784065
Abstract

The orf virus (OV) strain D1701 belongs to the genetically heterogenous parapoxvirus (PPV) genus of the family Poxviridae. The attenuated OV D1701 has been licensed as a live vaccine against contagious ecthyma in sheep. Detailed knowledge on the genetic structure and organization of this PPV vaccine strain is an important prerequisite to reveal possible genetic mechanisms of PPV attenuation. The present study demonstrates a genomic map of the approximately 158 kbp DNA of OV D1701 established by hybridization studies of cloned restriction fragments covering the complete viral genome. The results show an enlargement of the inverted terminal repeats (ITR) to up to 18 kbp due to recombination between nonhomologous sequences during cell culture adaptation. DNA sequencing of the region adjacent to the ITR junction revealed the absence of one open reading frame designated E2L. In contrast to a transposition-deletion variant of the New Zealand OV strain NZ2 (Fleming et al., 1995) the two genes E3L (a homologue of dUTPase) and G1L neighbouring E2L are retained in OV D1701. DNA and RNA analyses proved the presence of E2L gene in wild-type OV isolated directly from scab material. The data presented indicate that the E2L gene is nonessential for virus replication in vitro and in vivo, and may represent one important viral gene in determining virulence and pathogenesis of OV.

摘要

羊口疮病毒(OV)D1701株属于痘病毒科中基因异质性的副痘病毒(PPV)属。减毒的OV D1701已被批准作为预防绵羊传染性脓疱性皮炎的活疫苗。详细了解该PPV疫苗株的遗传结构和组织是揭示PPV减毒可能遗传机制的重要前提。本研究展示了通过对覆盖完整病毒基因组的克隆限制性片段进行杂交研究建立的OV D1701约158 kbp DNA的基因组图谱。结果显示,由于细胞培养适应过程中非同源序列之间的重组,反向末端重复序列(ITR)扩大至18 kbp。对ITR连接处相邻区域的DNA测序显示,一个名为E2L的开放阅读框缺失。与新西兰OV株NZ2的转座缺失变体(Fleming等人,1995年)不同,与E2L相邻的两个基因E3L(dUTPase的同源物)和G1L在OV D1701中保留。DNA和RNA分析证明,直接从痂皮材料中分离的野生型OV中存在E2L基因。所呈现的数据表明,E2L基因在体外和体内病毒复制中并非必需,可能是决定OV毒力和发病机制的一个重要病毒基因。

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