Proviruses were cloned directly from a cat that developed neurological
disorders approximately 28 months after inoculation with a molecularl
y 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 a-like variant in brain, bon
e marrow, and lymph node that apparently had acquired the major portio
n of its extracellular envelope gene (gp70) from endogenous FeLV-relat
ed 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 f
rom brain tissue encoded a replication-defective virus. A chimera enco
ding 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 e
xtended host range properties of FeLV-B. (C) 1994 Academic Press, Inc.