|
|
||||||||
1 Cooperative Research Centre for Tropical Plant Pathology, The University of Queensland, Queensland 4072, Brisbane, Australia
2 Department of Microbiology, Centre for Bacterial Diversity and Identification, The University of Queensland, Queensland 4072, Brisbane, Australia
* Corresponding author.
ABSTRACT
We determined nearly complete 16S rRNA gene sequences for 19 isolates of Burkholderia solanacearum, three isolates of the blood disease bacterium of bananas, and two isolates of Pseudomonas syzygii, the cause of Sumatra disease of cloves. The dendrogram produced by comparing all of these sequences revealed that there were two divisions, which corresponded to the results obtained previously in a restriction fragment length polymorphism analysis (D. Cook, E. Barlow, and L. Sequeira. Mol. Plant Microbe Interact. 2:113–121, 1989) and a total 16S ribosomal DNA (rDNA) sequence analysis of four isolates representing four biovars of B. solanacearum (X. Li, M. Dorsch. T. Del Dot, L. I. Sly, E. Stackebrandt, and A. C. Hayward, J. Appl. Bacteriol. 74:324–329, 1993). Division 1 comprised biovars 3, 4, and 5 and an aberrant biovar 2 isolate (strain ACH0732), and division 2 included biovars 1, 2, and N2, the blood disease bacterium, and P. syzygii. Specific nucleotides at positions 458 to 460 (UUC) and 474 (A) characterized division 2, whereas in division 1 the nucleotides at these positions were ACU and U, respectively. However, strain ACH0732 had a U at position 458, as did division 2 isolates, and G instead of U at position 474. Division 2 consisted of two subdivisions; one subdivision contained two B. solanacearum isolates that originated from Indonesia, P. syzygii strains, and blood disease bacterium strains, and the other subdivision contained all of the other division 2 isolates. Within division 1, the level of 16S rDNA sequence similarity ranged from 99.8 to 100%, and within division 2, the levels of 16S rDNA sequence similarity ranged from 99.1 to 100%. The division 1 isolates exhibited an average level of 16S rDNA sequence similarity to division 2 isolates of 99.3% (range, 99.1 to 99.5%). The occurrence of consistent polymorphisms in the 16S rDNA sequences of B. solanacearum strains, in particular unique 16S rDNA sequence differences in aberrant biovar 2 isolate ACH0732, and the occurrence of the Indonesian subdivision of division 2 suggest that this group is a rapidly evolving (tachytelic) group.
This article has been cited by other articles:
![]() |
J. A. Castillo and J. T. Greenberg Evolutionary Dynamics of Ralstonia solanacearum Appl. Envir. Microbiol., February 15, 2007; 73(4): 1225 - 1238. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Guidot, P. Prior, J. Schoenfeld, S. Carrere, S. Genin, and C. Boucher Genomic Structure and Phylogeny of the Plant Pathogen Ralstonia solanacearum Inferred from Gene Distribution Analysis J. Bacteriol., January 15, 2007; 189(2): 377 - 387. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Vaneechoutte, P. Kampfer, T. De Baere, E. Falsen, and G. Verschraegen Wautersia gen. nov., a novel genus accommodating the phylogenetic lineage including Ralstonia eutropha and related species, and proposal of Ralstonia [Pseudomonas] syzygii (Roberts et al. 1990) comb. nov. Int J Syst Evol Microbiol, March 1, 2004; 54(2): 317 - 327. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Schonfeld, H. Heuer, J. D. van Elsas, and K. Smalla Specific and Sensitive Detection of Ralstonia solanacearum in Soil on the Basis of PCR Amplification of fliC Fragments Appl. Envir. Microbiol., December 1, 2003; 69(12): 7248 - 7256. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Coenye, J. Goris, P. De Vos, P. Vandamme, and J. J. LiPuma Classification of Ralstonia pickettii-like isolates from the environment and clinical samples as Ralstonia insidiosa sp. nov. Int J Syst Evol Microbiol, July 1, 2003; 53(4): 1075 - 1080. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. D. Siciliano, J. J. Germida, K. Banks, and C. W. Greer Changes in Microbial Community Composition and Function during a Polyaromatic Hydrocarbon Phytoremediation Field Trial Appl. Envir. Microbiol., January 1, 2002; 69(1): 483 - 489. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. A. Weller, J. G. Elphinstone, N. C. Smith, N. Boonham, and D. E. Stead Detection of Ralstonia solanacearum Strains with a Quantitative, Multiplex, Real-Time, Fluorogenic PCR (TaqMan) Assay Appl. Envir. Microbiol., July 1, 2000; 66(7): 2853 - 2858. [Abstract] [Full Text] |
||||
![]() |
S. Poussier, D. Trigalet-Demery, P. Vandewalle, B. Goffinet, J. Luisetti, and A. Trigalet Genetic diversity of Ralstonia solanacearum as assessed by PCR-RFLP of the hrp gene region, AFLP and 16S rRNA sequence analysis, and identification of an African subdivision Microbiology, July 1, 2000; 146(7): 1679 - 1692. [Abstract] [Full Text] |
||||
![]() |
T. Dharakul, B. Tassaneetrithep, S. Trakulsomboon, and S. Songsivilai Phylogenetic Analysis of Ara+ and Ara- Burkholderia pseudomallei Isolates and Development of a Multiplex PCR Procedure for Rapid Discrimination between the Two Biotypes J. Clin. Microbiol., June 1, 1999; 37(6): 1906 - 1912. [Abstract] [Full Text] |
||||
![]() |
S. Poussier, P. Vandewalle, and J. Luisetti Genetic Diversity of African and Worldwide Strains of Ralstonia solanacearum as Determined by PCR-Restriction Fragment Length Polymorphism Analysis of the hrp Gene Region Appl. Envir. Microbiol., May 1, 1999; 65(5): 2184 - 2194. [Abstract] [Full Text] |
||||
![]() |
B. A. Wullings, A. R. Van Beuningen, J. D. Janse, and A. D. L. Akkermans Detection of Ralstonia solanacearum, Which Causes Brown Rot of Potato, by Fluorescent In Situ Hybridization with 23S rRNA-Targeted Probes Appl. Envir. Microbiol., November 1, 1998; 64(11): 4546 - 4554. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |