Identification of Erwinia amylovora, the fireblight pathogen, by colony hybridization with DNA from plasmid pEA29

• Published in: Applied and Environmental Microbiology 1988-11, Vol.54 (11), p.2798-2802
• Main Authors: Falkenstein, H, Bellemann, P, Walter, S, Zeller, W, Geider, K
• Format: Article
• Language: English
• Subjects: Bacterial plant pathogens; Biological and medical sciences; Biotechnology; ERWINIA AMYLOVORA; Fundamental and applied biological sciences. Psychology; GENE; GENES; Genetic engineering; Genetic technics; Methods. Procedures. Technologies; Microorganism-Plant Interactions; Molecular cloning; Phytopathology. Animal pests. Plant and forest protection; PLASMIDE; PLASMIDIOS; ROSACEAE; Systematics. Structure, properties and multiplication. Genetics
• ISSN: 0099-2240; 1098-5336
• DOI: 10.1128/AEM.54.11.2798-2802.1988

All strains of Erwinia amylovora characterized carry a medium-size plasmid of 29 kilobases (pEA29). We mapped this plasmid with various restriction enzymes, cloned the whole DNA into an Escherichia coli plasmid, and subcloned restriction fragments. These DNA species were used for identification of E. amylovora after handling of strains in the laboratory and also in field isolates. About 70 strains of E. amylovora and 24 strains from nine other species, mainly found in plant habitats, were checked in a colony hybridization test. Virulent and avirulent E. amylovora strains reacted positively, whereas the other species were negative. Apart from the hybridization assay, the positive strains were additionally tested for ooze production on rich agar with 5% sucrose and on immature-pear slices. Unspecific background hybridization of non-E. amylovora strains found for hybridization with the whole E. amylovora plasmid was almost eliminated when a 5-kilobase SalI fragment from pEA29 was used as a probe and when the washes after the hybridization procedure were done with high stringency. Under these conditions, E. amylovora could be readily identified from field isolates