In summer 2004, five Dahlia cultorum plants of unknown cultivar, grown in garden plots in Skierniewice, Poland, exhibited bushy growth accompanied by shoot proliferation, narrowed leaf and flower bud deficiency. Research in Italy (Marzachi et al ., 1999) had indicated that stunted growth and shoot proliferation symptoms in some dahlia plants was associated with aster yellows phytoplasma infection. To detect the possible presence of phytoplasmas in dahlias in Poland, three plants showing symptoms and two symptomless plants were assayed for the presence of phytoplasma 16S rDNA by PCR. Nucleic acids were extracted from leaves and roots using DNeasy Plant Mini Kit (Qiagen). A nested PCR was done using the universal phytoplasma primer pair P1/P7, followed by primers fA/rA or R16F2n/R16R2. To detect potential mixed infection in dahlias, the phytoplasma 16SrI or 16SrX group-specific primer pairs (R16(I)F1/R16(I)R1, fAT/rAS, fAT/rPRUS or fPD/rAT) were used for nested PCR. Phytoplasma identification was accompanied by restriction fragment length polymorphism (RFLP) analysis of R16F2n/R16R2-primed PCR product digested with Alu I, Mse I, Hha I, Hpa II, Ssp I or Rsa I endonucleases.Products were generated by nested PCRs with universal and groupspecific 16(I)F1/R16(I)R1 and fAT/rAS primer pairs exclusively from two diseased D. cultorum plants. No bands were amplified from one dahlia with disease symptoms or from healthy dahlia and Catharanthus roseus plants.