Supplementary Figure

PVY CP-F PLRV CP-F PVA CI-F PVA CI-R PLRV CP-R PVY CP -R PLRV CP PVA CI PVY CP Fig. S1 PLRV CP PVA CIPVY CP attB1 attB2 LB Intron P35S RB 600bp T35S Kan T35SF Intron FIntron RP35SR pK7GWIWG2(I) (a) (c) (b)

Fig. S1 Strategy used for amplifying viral segments of 200 bp and joining the segments to generate 600-bp tandem fusions. (a) Six primers were used for the PCR to generate the three 200-bp segments, as well as the 600 bp tandem fusions. The internal primers contained 5 proximal sequences of the flanking virus sequence complementary to the 3 proximal sequences of another primer for synthesis on the opposite strand. This was used to produce the overlapping sequences necessary to facilitate joining of the 200-bp PCR products to form various fusions. (b) The 600-bp tandem fusion was amplified using primers for the various attachment regions required for cloning by using the Gateway system. Different primers were required to attach the attB1 and attB2 for constructing inserts with the IN orientation versus the OUT orientation. (c) After cloning into the Gateway entry vector pDONR207, the cassette of tandem, fused viral segments was introduced into the plant transformation vector pKGWIWG2(I) twice, in opposite orientations, via the gateway recombination system. The sequences of the various primers required are given in Table S1

PLRV-inoculated IN34 Mock-inoculated Non-transformed VS Fig. S2

Fig. S2 Potato plants of cv. Vales Sovereign (VS) inoculated with PLRV using aphids. Transgenic potato plants (line pK7GWIWG2(I)/ IN34 and non-transformed potato plants were inoculated with PLRV using 10 aphids per plant or mock-inoculated, respectively. Plants were assessed for infection 30 days after inoculation

PVA-inoculated IN34 Mock-inoculated Non-transformed VS Fig. S3

Fig. S3 Potato plants of cv. Vales Sovereign (VS) inoculated with PVA using aphids. Transgenic potato plants (line pK7GWIWG2(I)/ IN34 and non-transformed potato plants were inoculated with PVA using 10 aphids per plant or mock-inoculated, respectively. Plants were assessed for infection 30 days after inoculation