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Int J Syst Bacteriol 41 (1991), 535-542; DOI 10.1099/00207713-41-4-535
© 1991 Society for General Microbiology
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Differentiation of Xanthomonas campestris pv. Citri Strains by Sodium Dodecyl Sulfate-Polyacrylamide Gel Electrophoresis of Proteins, Fatty Acid Analysis, and DNA-DNA Hybridization

L. Vauterin1,*, P. Yang1, B. Hoste1, M. Vancanneyt1, E. L. Civerolo2, J. Swings1 and K. Kersters1

1Laboratorium voor Microbiologie en Microbiële Genetica, Rijksuniversiteit, K. L. Ledeganckstraat 35, B-9000 Ghent, Belgium
2Agricultural Research Service, United States Department of Agriculture, Beltsville, Maryland 20705

* Corresponding author.

ABSTRACT

A total of 61 strains, including members of all five currently described pathogenicity groups of Xanthomonas campestris pv. citri (groups A, B, C, D, and E) and representing a broad geographical diversity, were compared by using sodium dodecyl sulfate-polyacrylamide gel electrophoresis of whole-cell proteins, gas chromatographic analysis of fatty acid methyl esters, and DNA-DNA hybridization. We found that all of the pathogenicity groups were related to each other at levels of DNA binding of more than 60%, indicating that they all belong to one species. Our results do not confirm a previous reclassification of X. campestris pathogens isolated from citrus in two separate species (Gabriel et al., Int. J. Syst. Bacteriol. 39:14-22, 1989). Pathogenicity groups A and E could be clearly delineated by the three methods used, and group A was the most homogeneous group. The delineation of pathogenicity groups B, C, and D was not clear on the basis of the results of sodium dodecyl sulfate-polyacrylamide gel electrophoresis of proteins and gas chromatography of fatty acid methyl esters, although these groups constituted a third subgroup on the basis of the DNA homology results.




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