Lavignon M, Walker J L, Perryman S M, Malik F G, Khan A S, Theodore T S, Evans L H
Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, Hamilton, Montana 59840.
J Virol. 1994 Aug;68(8):5194-203. doi: 10.1128/JVI.68.8.5194-5203.1994.
Polytropic murine leukemia viruses (MuLVs) arise in mice by recombination of ecotropic MuLVs with endogenous retroviral envelope genes and have been implicated in the induction of hematopoietic proliferative diseases. Inbred mouse strains contain many endogenous sequences which are homologous to the polytropic env genes; however, the extent to which particular sequences participate in the generation of the recombinants is unknown. Previous studies have established antigenic heterogeneity among the env genes of polytropic MuLVs, which may reflect recombination with distinct endogenous genes. In the present study, we have examined many polytropic MuLVs and found that nearly all isolates fall into two mutually exclusive antigenic subclasses on the basis of the ability of their SU proteins to react with one of two monoclonal antibodies, termed Hy 7 and MAb 516. Epitope-mapping studies revealed that reactivity to the two antibodies is dependent on the identity of a single amino acid residue encoded in a variable region of the receptor-binding domain of the env gene. This indicated that the two antigenic subclasses of MuLVs arose by recombination with distinct sets of endogenous genes. Evaluation of polytropic MuLVs in mice revealed distinctly different ratios of the two subclasses after inoculation of different ecotropic MuLVs, suggesting that individual ecotropic MuLVs preferentially recombine with distinct sets of endogenous polytropic env genes.
多嗜性鼠白血病病毒(MuLVs)在小鼠体内通过嗜亲性MuLVs与内源性逆转录病毒包膜基因重组产生,并与造血增殖性疾病的诱导有关。近交系小鼠品系含有许多与多嗜性env基因同源的内源性序列;然而,特定序列参与重组体产生的程度尚不清楚。先前的研究已经证实多嗜性MuLVs的env基因之间存在抗原异质性,这可能反映了与不同内源性基因的重组。在本研究中,我们检测了许多多嗜性MuLVs,发现几乎所有分离株根据其SU蛋白与两种单克隆抗体(称为Hy 7和MAb 516)之一反应的能力,分为两个相互排斥的抗原亚类。表位作图研究表明,对这两种抗体的反应性取决于env基因受体结合域可变区编码的单个氨基酸残基的同一性。这表明MuLVs的两个抗原亚类是通过与不同的内源性基因集重组产生的。在小鼠中对多嗜性MuLVs的评估显示,接种不同的嗜亲性MuLVs后,这两个亚类的比例明显不同,这表明单个嗜亲性MuLVs优先与不同的内源性多嗜性env基因集重组。