Ramie (Boehmeria nivea) is a perennial herbaceous plant which produces strong and lustrous bast fibre. It is native to East Asia and is mainly grown in china, India, Taiwan, Philippines, Thailand, Brazil, and South Korea (Sarkar et al. 2012). In May 2013, ramie plants exhibiting yellow mosaic symptoms were noted in experimental fields of the CRIJAF research farm, Barrackpore, India. In young green leaves vein-clearing was prominent, whereas the older leaves showed complete yellowing. Plants were stunted and bushy. The incidence of the disease varied from 2% to 10 %. Five symptomatic and five asymptomatic samples were collected from the field and DNA was extracted by using CTAB method (Biswas et al. 2013). DNA samples were tested for begomovirus infection by PCR using universal primer pair PAL1v1978B/PAR1c715H (Rojas et al. 1993). Only the symptomatic samples showed amplification of a 1.5 kb product suggesting that plants were infected by a begomovirus. Furthermore, circular DNA was amplified by rolling circle amplification (RCA) with Illustra TempliPhi Kit (GE Healthcare, UK) according to the manufacturer’s instructions. RCA product was digested with EcoRI, BamHI, EcoRI, KpnI, Hind III and PstI (New England Biolabs) respectively. The fragments of 2.1 kbp (with BamHI digestion) and 1.5 kbp (with KpnI digestion) were cloned and sequenced. The sequence of the 2.1 kbp fragment showed similarity with published sequences of begomovirus DNA-A component. From 2.1 kbp sequence a pair of primers was designed to obtain full length DNA -A component viz. JAF1 (5′-CTTCATCGTTTCTCAGCATCAT-3′) and JAR1 (5′-CACTTGCACACGATCTCTAAGA-3′). The full-length DNA-A was 2686 bp nucleotides and encoded six putative ORFs (GenBank Accession No. KF962542). The sequence of the 1.5 kbp fragment shared similarity with DNA-B. The begomoviral circular DNA-B was amplified using the pair of primers JBF1 (5′-GTAACACCCGAAGTGCACG-3′) and JBR1 (5′-AAAGGAGAGACACCAGTCTGCC-3′) designed from the 1.5-kbp sequence. PCR yielded full-length DNA-B sequence of 2666 bp nucleotides and encoded two putative ORFs (GenBank Accession No. KF962543). BLASTn analysis revealed that DNA-A from the ramie begomovirus isolate has 100% nucleotide sequence identity with complete sequence of DNA-A component of Corchorus golden mosaic virus (Accession no: FJ463902). Similarly, DNA-B also has 100% identity with complete sequence of CoGMV DNA-B component (Accession no: FJ455448). Based on BLASTn analysis and sequence analysis using MEGALIGN (DNASTAR), the virus causing symptoms in ramie appears to be CoGMV which is a New World begomovirus from the Old World infecting jute (Corchorus capsularis) (Ha et al. 2006). To the best of our knowledge this is the first report that CoGMV infects ramie plants. The incidence of CoGMV in ramie is relatively low but in future it may negatively affect the yield. References: Biswas, C. et al., 2013. Lett. Appl. Microbiol. 56:105. Ha, C. et al., 2006. J.Gen. Virol. 87:997. Rojas, M R. et al., 1993. Plant Dis. 77:340. Sarkar, D. et al., 2012. Curr. Sci. 98:1570.