Murine mammary tumor viruses are retroviruses which encode superantige
ns capable of stimulating T cells via superantigen-reactive T-cell rec
eptor V beta chains. Murine mammary tumor viruses are transmitted to t
he suckling offspring through the milk. We have established that B cel
l-deficient pups which were foster-nursed by virus-secreting mice do n
ot transfer infectious murine mammary tumor viruses to their offspring
. No murine mammary tumor virus proviruses could be detected in the sp
leen and mammary tissue of these mice. We conclude that B cells are es
sential for the completion of the viral life cycle in vile. This indic
ates that B cells are infected first and that viral amplification take
s place only if infected B cells present the murine mammary tumor viru
s superantigen on their surface, which, in turn, results in activation
of T cells expressing the appropriate T-cell receptor V beta chains.
These activated T cells secrete factors which stimulate B cells, enabl
ing viral replication.