Infection of trigeminal ganglion by herpes simplex virus (HSV)
thymidine kinase-negative (TK-) mutants was investigated in
mixed infection studies in mice. Mice were corneally inoculated with TK- HSV alone or with mixtures of TK- HSV-TK+ HSV. When inoculated alone, an
arabinosylthymine-selected HSV type 1 TK- mutant and a HSV type 2 TK- deletion mutant infected mouse ocular tissues but rarely infected
ganglion tissues. However, both TK- mutants readily infected
ganglion tissues when they were inoculated in mixtures with TK+ HSV. By means of
mixed infection studies, it was demonstrated that TK- HSV could readily establish acute and latent
ganglion infections. It was thought that the frequent
infection of trigeminal ganglion tissue by both TK- mutants after mixed TK(-)-TK+ HSV
infection was the result of in vivo complementation. After mixed TK(-)-TK+ HSV
infection and subsequent cultivation of
ganglion explants in
arabinosylthymine, results supported the conclusion that when TK- was present in ganglia it was in the same neurons that contained TK+ HSV.