Cameron C, Hota-Mitchell S, Chen L, Barrett J, Cao J X, Macaulay C, Willer D, Evans D, McFadden G
Department of Microbiology, The University of Western Ontario, London, Ontario, Canada.
Virology. 1999 Nov 25;264(2):298-318. doi: 10.1006/viro.1999.0001.
Myxomatosis in European rabbits is a severely debilitating disease characterized by profound systemic cellular immunosuppression and a high rate of mortality. The causative agent, myxoma virus, is a member of the poxvirus family and prototype of the Leporipoxvirus genus. As a major step toward defining the genetic strategies by which the virus circumvents host antiviral responses, the genomic DNA sequence of myxoma virus, strain Lausanne, was determined. A total of 171 open reading frames were assigned to cover the 161.8-kb genome, including two copies each of the 12 genes that map within the 11.5-kb terminal inverted repeats. Database searches revealed a central core of approximately 120 kb that encodes more than 100 genes that exhibit close relationships to the conserved genes of members of other poxvirus genera. Open reading frames with predicted signal sequences, localization motifs, or homology to known proteins with immunomodulatory or host-range functions were examined more extensively for predicted features such as hydrophobic regions, nucleic acid binding domains, ankyrin repeats, serpin signatures, lectin domains. and structural cysteine spacings. As a result, several novel, potentially immunomodulatory proteins have been identified, including a family with multiple ankyrin-repeat domains, an OX-2 like member of the neural cell adhesion molecule family, a third myxoma serpin, a putative chemokine receptor fragment, two natural killer receptor-like species, and a variety of species with domains closely related to diverse host immune regulatory proteins. Coupled with the genomic sequencing of the related leporipoxvirus Shope fibroma virus, this work affirms the existence of a conserved complement of poxvirus-specific core genes and expands the growing repertoire of virus genes that confer the unique capacity of each poxvirus family member to counter the immune responses of the infected host.
欧洲兔的黏液瘤病是一种严重的消耗性疾病,其特征是全身性细胞免疫抑制严重且死亡率高。致病因子黏液瘤病毒是痘病毒科的成员,也是兔痘病毒属的原型。作为确定该病毒规避宿主抗病毒反应的遗传策略的重要一步,已确定了洛桑株黏液瘤病毒的基因组DNA序列。总共分配了171个开放阅读框来覆盖161.8 kb的基因组,包括位于11.5 kb末端反向重复序列内的12个基因的两个拷贝。数据库搜索显示,大约120 kb的核心区域编码了100多个与其他痘病毒属成员的保守基因密切相关的基因。对具有预测信号序列、定位基序或与具有免疫调节或宿主范围功能的已知蛋白质具有同源性的开放阅读框,更广泛地检查了预测特征,如疏水区域、核酸结合结构域、锚蛋白重复序列、丝氨酸蛋白酶抑制剂特征、凝集素结构域和结构半胱氨酸间距。结果,鉴定出了几种新的、潜在的免疫调节蛋白,包括一个具有多个锚蛋白重复结构域的家族、神经细胞粘附分子家族的一个类OX-2成员、第三个黏液瘤丝氨酸蛋白酶抑制剂、一个假定的趋化因子受体片段、两个自然杀伤受体样物种,以及多种与不同宿主免疫调节蛋白密切相关的结构域的物种。结合相关兔痘病毒肖普纤维瘤病毒的基因组测序,这项工作证实了痘病毒特异性核心基因保守互补的存在,并扩展了不断增加的病毒基因库,这些基因赋予每个痘病毒家族成员对抗感染宿主免疫反应的独特能力。