Few foamy (spuma) retroviruses have been investigated in molecular det
ail, despite their previous isolation from several mamalian species, i
ncluding ten neutralization serotypes from various primates. Here, we
have studied a new gorilla foamy virus (SFV-Gg) and investigated its f
unctional and phylogenetic relationship to the human (HFV) and other p
rimate foamy viruses, including that recently described in orangutans
(SFV-11). Nucleotide sequencing of PCR products obtained from the R/U5
region of the LTR, gag, and pol genes revealed a close relationship b
etween HFV and three chimpanzee isolates (SFV-6, SFV-7, and SN-cpz). T
he SFV-Gg, SFV-11, rhesus macaque (SFV-1), and African green monkey (S
FV-3) isolates were more divergent. To explore functional relationship
s, primate foamy Virus transactivation of HFV LTR driven beta-galactos
idase expression in a newly constructed cell line, BHLL, was investiga
ted. HFV, SFV-6, and SFV-7 potently transactivated HFV LTR driven lacZ
gene expression, SFV-Gg induced expression approximately 10-fold less
efficiently, and SFV types 1, 2, 3, and 11 did not significantly tran
sactivate the HFV LTR. It was, thus, possible to assay serum neutraliz
ing activity in SFV-infected primates against HFV, SFV-6, and SFV-7 by
reduction of beta-galactosidase activity following infection of the i
ndicator cell line. Sera from infected chimpanzees and gorillas neutra
lized, to varying degrees, each of these three viruses, whereas orangu
tan sera did not. Our results, based on DNA sequences and functional a
ssays, support the conclusion that HN is closely related to foamy viru
ses of chimpanzee origin. (C) 1995 Academic Press, Inc.