First report of Turnip yellow virus (TuYV) in Brassica juncea (Indian mustard) in India

Abstract

Figure 2 A survey for Turnip yellow virus (TuYV) was carried out during October-December 2012 covering the major field crops in Rajasthan, India. Fifty leaf samples with yellowing and red stripes were collected from Brassica juncea (Indian mustard) fields. The observed symptoms and the presence of a large number of aphids (Myzus persicea) indicated the presence of a virus, possibly TuYV. To confirm the presence of TuYV, total RNA was extracted from infected leaves using the TRIZOL plant mini kit (Invitrogen), according to the manufacturer’s protocol. RT-PCR was performed in a single PCR tube with the reaction mixture (20 μl) containing 10 ng RNA, 1 μl of 20 pmol oligo d(T), 1 μl of 20 pmol of Luteovirus group primers Lu1 and Lu4 (Robertson et al., 1991), 2 μl of 10x reaction buffer, 0.5 μl of 10 mM dNTPs, 0.5 μl of 50 mM MgCl2, 0.5 μl of AMV reverse transcriptase and 0.5 μl of Taq polymerase (3U/μl). The RT-PCR was performed in a thermal cycler with the following programme: reverse transcription at 42°C for 1 hour, initial denaturation at 94°C for 2 min, followed by 35 cycles of 94°C for 30 sec, annealing at 50°C for 1 min, extension at 72°C for 1 min and a final extension of 72°C for 10 min. An amplicon of expected size (~600 nt) (Fig. 1) was sequenced and submitted to GenBank (Accession No. KC570457, isolate RP1). BLAST analysis of the nucleotide sequence showed 91-97% identity with the corresponding region of TuYV (X13063), Beet western yellows virus (BWYV; L40015, Y11531) and TuYV isolate WA-1 (JQ862472.1).