A random-primed cDNA expression library constructed from the mRNA of neurob
lastoma cells (NG108) was used to clone a specific rabies virus (RV) recept
or. A soluble form of the RV glycoprotein (G(s)) was utilized as a ligand t
o detect positive cells. We identified the murine low-affinity nerve-growth
factor receptor, p75NTR, BSR cells stably expressing p75NTR were able to b
ind G(s) and G-expressing lepidopteran cells. The ability of the RV glycopr
otein to bind p75NTR was dependent on the presence of a lysine and arginine
in positions 330 and 333 respectively of antigenic site III, which is know
n to control virus penetration into motor and sensory neurons of adult mice
. P75NTR-expressing BSR cells were permissive for a non-adapted fox RV isol
ate (street virus) and nerve growth factor (NGF) decreased this infection.
In infected cells, p75NTR associates with the RV glycoprotein and could be
precipitated with anti-G monoclonal antibodies. Therefore, p75NTR is a rece
ptor for street RV.