We have analyzed if different populations of retroviral particles carrying
the viral and cellular receptors of membrane viruses, respectively, are abl
e to specifically fuse with each other. Using the glycoprotein of human imm
unodeficiency virus type 1 and its cellular receptor complex, we demonstrat
e that interviral membrane fusion can, indeed, occur and that the resultant
fused viral structures are able to infect cells and transduce a marker gen
e. On the one hand, these results have relevance for the development of vac
cine strategies based on fusion-induced conformational epitopes on the vira
l glycoprotein. However, in addition to this potential practical applicatio
n, the results obtained (which were extended to include analyses with the v
esicular stomatitis virus G protein and its cellular receptor) have far-rea
ching implications for in vivo situations in which simultaneous infections
with different membrane viruses can occur. (C) 2000 Academic Press.