Mouse mammary tumor virus (MMTV) has been shown to preferentially infect B
lymphocytes in vivo. We have used recombinant envelope-coated fluospheres a
nd highly purified MMTV particles to study the distribution of the viral re
ceptors on fresh mouse lymphocytes. A preferential dose-dependent binding t
o B lymphocytes was observed which could be competed with neutralizing anti
bodies. In contrast, T-lymphocyte binding remained at background levels. Th
ese results strongly suggest a higher density of viral receptor molecules o
n B lymphocytes than on T lymphocytes and correlate with the preferential i
nitial infection of B lymphocytes observed in vivo.