Boomer S, Gasper P, Whalen L R, Overbaugh J
Department of Microbiology, University of Washington, Seattle 98195.
Virology. 1994 Nov 1;204(2):805-10. doi: 10.1006/viro.1994.1597.
Proviruses were cloned directly from a cat that developed neurological disorders approximately 28 months after inoculation with a molecularly cloned, minimally pathogenic subgroup A feline leukemia virus (FeLV-A). In addition to FeLV-A proviruses that were nearly identical to the inoculated virus, we detected a subgroup B-like variant in brain, bone marrow, and lymph node that apparently had acquired the major portion of its extracellular envelope gene (gp70) from endogenous FeLV-related sequences. A similar recombinant was also detected, by PCR, at low levels in bone marrow from an early time postinfection (2.5 months). A full-length proviral variant with this recombinant structure cloned from brain tissue encoded a replication-defective virus. A chimera encoding the 5' gag-pol portion of FeLV-A and the 3' env-LTR portion of the defective brain-derived clone was replication-competent and had the extended host range properties of FeLV-B.
前病毒直接从一只猫身上克隆而来,这只猫在接种分子克隆的低致病性A亚群猫白血病病毒(FeLV-A)约28个月后出现神经紊乱症状。除了与接种病毒几乎相同的FeLV-A前病毒外,我们在脑、骨髓和淋巴结中检测到一种B亚群样变体,该变体显然从内源性FeLV相关序列中获得了其细胞外包膜基因(gp70)的主要部分。通过PCR在感染后早期(2.5个月)的骨髓中也检测到低水平的类似重组体。从脑组织中克隆的具有这种重组结构的全长前病毒变体编码一种复制缺陷型病毒。一种嵌合体编码FeLV-A的5'gag-pol部分和缺陷型脑源克隆的3'env-LTR部分,具有复制能力,并具有FeLV-B的扩展宿主范围特性。