Using protein blot assays, a 94-kDa thrips protein was identified that
exhibited specific binding to tomato spotted wilt virus (TSWV) partic
les. Renaturation of the 94-kDa protein, which is conserved among the
two major vector species of TSWV, Frankliniella occidentalis and Thrip
s tabaci, was crucial for its virus-binding properties, whereas under
the same conditions no specific binding was observed with aphid (Myzus
persicae) proteins. The 94-kDa protein species was present in all dev
elopmental stages of both vectoring thrips, whereas it was present mai
nly in the adult stage of a nonvectoring thrips species, Parthenothrip
s dracenae. Using antibodies against the different TSWV structural pro
teins, the G2 envelope glycoprotein was identified as the viral determ
inant involved. Because the virus-binding protein is present throughou
t the thrips body, but not in the gut, it may represent a receptor pro
tein involved during circulation of the virus through its vector but p
robably not during viral uptake in the midgut.