Frank Thieme, Ralf Koebnik, Thomas Bekel, Carolin Berger, Jens Boch, Daniela Büttner, Camila Caldana, Lars Gaigalat, Alexander Goesmann, Sabine Kay, Oliver Kirchner, Christa Lanz, Burkhard Linke, Alice C. McHardy, Folker Meyer, Gerd Mittenhuber, Dietrich H. Nies, Ulla Niesbach-Klösgen, Thomas Patschkowski, Christian Rückert, Oliver Rupp, Susanne Schneiker, Stephan C. Schuster, Frank Vorhölter, Ernst Weber, Alf Pühler, Ulla Bonas, Daniela Bartels, and Olaf Kaiser (2005)

Insights into genome plasticity and pathogenicity of the plant pathogenic bacterium Xanthomonas campestris pv. vesicatoria revealed by the complete genome sequence

Journal of Bacteriology 187 (21) 7254-7266

The gram-negative plant-pathogenic bacterium Xanthomonas campestris pv. vesicatoria is the causative agent of bacterial spot disease in pepper and tomato plants, which leads to economically important yield losses. This pathosystem has become a well-established model for studying bacterial infection strategies. Here, we present the whole-genome sequence of the pepper-pathogenic Xanthomonas campestris pv. vesicatoria strain 85-10, which comprises a 5.17-Mb circular chromosome and four plasmids. The genome has a high G+C content (64.75%) and signatures of extensive genome plasticity. Whole-genome comparisons revealed a gene order similar to both Xanthomonas axonopodis pv. citri and Xanthomonas campestris pv. campestris and a structure completely different from Xanthomonas oryzae pv. oryzae. A total of 548 coding sequences (12.2%) are unique to X. campestris pv. vesicatoria. In addition to a type III secretion system, which is essential for pathogenicity, the genome of strain 85-10 encodes all other types of protein secretion systems described so far in gram-negative bacteria. Remarkably, one of the putative type IV secretion systems encoded on the largest plasmid is similar to the Icm/Dot systems of the human pathogens Legionella pneumophila and Coxiella burnetii. Comparisons with other completely sequenced plant pathogens predicted six novel type III effector proteins and several other virulence factors, including adhesins, cell wall-degrading enzymes, and extracellular polysaccharides.

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