Pétursson G, Andrésdóttir V, Andrésson O, Torsteinsdóttir S, Georgsson G, Pálsson P A
Institute for Experimental Pathology, University of Iceland, Reykjavík.
Comp Immunol Microbiol Infect Dis. 1991;14(4):277-87. doi: 10.1016/0147-9571(91)90133-x.
Maedi-visna virus (MVV) of sheep was the first lentivirus to be isolated. The genomic organization of MVV is very similar to that of human immunodeficiency virus (HIV) with several genes regulating the expression of the viral genome. Viral replication is severely restricted in the host and some cells apparently contain the genetic information in a DNA provirus form with little or no expression of viral antigens. This seems to be a major factor in causing the "slowness" of lentiviral infections and the persistence of the virus in the host since the immune system may not recognize the provirus-containing cells. The target cells for HIV and MVV are similar although T4 lymphocytes are not specifically destroyed in maedi-visna. There are also certain similarities in the pathological changes in both diseases, both in the central nervous system, the lungs and the lymphatic system. Although the severe final immunodeficiency state characteristic of AIDS has not been observed in maedi-visna, the basic biological features of the MVV and its interaction with host cells are so similar to HIV infection, that we consider ovine maedi-visna useful animal model for the human lentivirus infections.
绵羊梅迪-维斯纳病毒(MVV)是最早分离出的慢病毒。MVV的基因组结构与人类免疫缺陷病毒(HIV)非常相似,有几个基因调控病毒基因组的表达。病毒复制在宿主体内受到严重限制,一些细胞显然以DNA原病毒形式包含遗传信息,很少或根本没有病毒抗原的表达。这似乎是导致慢病毒感染“缓慢”以及病毒在宿主体内持续存在的一个主要因素,因为免疫系统可能无法识别含有原病毒的细胞。HIV和MVV的靶细胞相似,尽管在梅迪-维斯纳病中T4淋巴细胞不会被特异性破坏。两种疾病在中枢神经系统、肺部和淋巴系统的病理变化也有一定相似性。虽然在梅迪-维斯纳病中未观察到艾滋病特有的严重终末期免疫缺陷状态,但MVV的基本生物学特征及其与宿主细胞的相互作用与HIV感染非常相似,因此我们认为绵羊梅迪-维斯纳病是人类慢病毒感染的有用动物模型。