Identification of <i>Lily mottle virus</i> and <i>Lily symptomless virus</i> Co-infecting Asiatic Lily in Ohio

Fig. 2. PCR detection of LMoV from cDNAs synthesized from immunocaptured virions with TBV/LMoVfwd540+rev1370 (Lane 1) and TBV/LMoVfwd900+rev2005 (Lane 2) primers. Water controls with TBV/LMoVfwd540+rev1370 (Lane 3), TBV/LMoVfwd900+rev2005 (Lane 4), LSV-RdRp (Lane 5), and LSV-CP (Lane 6) primers. LSV clones with LSV-RdRp (Lane 7) and CP (Lane 8) primers used as positive PCR controls because of compatible reaction and cycling conditions. M = 1 Kb DNA ladder (250, 500, 750, 1000, and 1500 bp markers indicated). Electrophoresis was performed in 0.8% agarose at 100 volts for 60 min in 1X TAE buffer. Gel was stained with ethidium bromide. LMoV amplicons are 829 bp and 1102 bp, respectively.



Image from Plant Health Progress article:
Identification of Lily mottle virus and Lily symptomless virus Co-infecting Asiatic Lily in Ohio