The open reading frame encoding the polyprotein precursor to the tomat
o spotted wilt tospovirus (TSWV) G1 and G2 glycoproteins was cloned as
cDNA and used to produce a recombinant baculovirus. Protein expressio
n was monitored in recombinant baculovirus-infected Spodoptera frugipe
rda IPLB-SF21 (SF21) cells with monoclonal antibodies raised to TSWV G
1 and G2. Western blot analysis demonstrated expression, proteolytic p
rocessing, and glycosylation of the G1G2 polyprotein to yield proteins
with serological specificities and electrophoretic mobilities similar
to the G1 and G2 proteins found in TSWV virions. Indirect immunofluor
escence localization of G1 and G2 in infected SF21 cells revealed accu
mulation of the glycoproteins in the plasmalemma. These experiments es
tablish that the glycoproteins of TSWV, a plant-infecting virus in the
family Bunyaviridae, can be processed in the absence of other viral p
roteins.