Local areas of conserved amino acids sequences in the RNA dependent RNA polymerase gene (RdRp), denoted as pre-motif A, motifs A and C, of viruses putatively belonging to the newly established genus Emaravirus, were used for designating sets of downstream and upstream degenerate oligonucleotide primers able to amplify in reverse transcription-polymerase chain reaction assay (RT-PCR) DNA fragments of 276 bp and 360 bp in size. These primers were efficient to detect Emaraviruses with known sequences available in database, i.e., Fig mosaic virus (FMV) and European mountain ash ringspot-associated virus (EMARaV), together with Pigeonpea sterility mosaic virus (PPSMV) and Maize red stripe virus (MRSV), of which only short sequences limitedly to their RNA3 segments constitute the unique molecular information available in Genbank. In particular, the degenerate primers designated on pre-motif A and motif A sequences were successful to amplify (276 bp) the four Emaraviruses used as positive controls while those of motifs A and C have failed to detect only MRSV. The amino acids sequences obtained from PPSMV and MRSV shared the highest identity with those of RRV (69%) and RYRV (60%), respectively. The phylogenetic tree constructed with RNA1 sequences of Emaravirus-like viruses clustered PPSMV and MRSV in two separate clades close to RRV and RLBV, respectively. The newly developed degenerate primers have proved their efficacy to amplify new Emaravirus-specific sequences and accordingly they could be useful to fish-out new Emaravirus-like viruses present in nature similarly to those reported in the literature and commonly used for virus identification.