SummaryFlavescence dorée (FD), a yellows disease of grapevine is caused by a non cultivable mycoplasma‐like organism (MLO) transmitted in vineyards by the leafhopper vectorScaphoideus titanus.In the laboratory, FD is transmitted from broadbean to broadbean by the leafhopperEuscelidius variegatus.Total DNA from FD‐diseased broadbean was centrifuged in a bisbenzimide‐CsCl density gradient. Low density DNA was collected from the gradient, digested withHindIII, ligated into plasmid pUC18 and cloned inEscherichia coli.Trans‐formants were differentially screened by colony hybridisation with32P‐iabelled healthy and FD‐infected leafhopper DNA as probes. The selected clones were shown to carry inserts which all hybridised with FD‐diseased host DNA and not with DNA from healthy host. These32P‐labelled inserts, used as probes in dot blot hybridisation, enabled detection of FD‐MLO in field‐collected samples of grapevine. However, because of the low MLO titre in this plant, an MLO enrichment procedure using tissue from main leaf veins was necessary to ensure effi