IJSEM Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Int J Syst Bacteriol 46 (1996), 10-15; DOI 10.1099/00207713-46-1-10
© 1996 Society for General Microbiology
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by TAGHAVI, M.
Right arrow Articles by FEGAN, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by TAGHAVI, M.
Right arrow Articles by FEGAN, M.
Agricola
Right arrow Articles by TAGHAVI, M.
Right arrow Articles by FEGAN, M.

Analysis of the Phylogenetic Relationships of Strains of Burkholderia solanacearum, Pseudomonas syzygii, and the Blood Disease Bacterium of Banana Based on 16S rRNA Gene Sequences

MOHSEN TAGHAVI1,2, CHRIS HAYWARD1,2, LINDSAY I. SLY1,2 and MARK FEGAN1,*

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:


Home page
Appl. Environ. Microbiol.Home page
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]


Home page
J. Bacteriol.Home page
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]


Home page
Int. J. Syst. Evol. Microbiol.Home page
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]


Home page
Appl. Environ. Microbiol.Home page
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]


Home page
Int. J. Syst. Evol. Microbiol.Home page
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]


Home page
Appl. Environ. Microbiol.Home page
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]


Home page
Appl. Environ. Microbiol.Home page
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]


Home page
MicrobiologyHome page
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]


Home page
J. Clin. Microbiol.Home page
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]


Home page
Appl. Environ. Microbiol.Home page
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]


Home page
Appl. Environ. Microbiol.Home page
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
Copyright © 1996 by the International Union of Microbiological Societies.