Literature DB >> 8573483

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.

M Taghavi1, C Hayward, L I Sly, M Fegan.   

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.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8573483     DOI: 10.1099/00207713-46-1-10

Source DB:  PubMed          Journal:  Int J Syst Bacteriol        ISSN: 0020-7713


  20 in total

1.  Genetic diversity of african and worldwide strains of ralstonia solanacearum as determined by PCR-restriction fragment length polymorphism analysis of the hrp gene region

Authors: 
Journal:  Appl Environ Microbiol       Date:  1999-05       Impact factor: 4.792

2.  Phylogeny and population structure of brown rot- and Moko disease-causing strains of Ralstonia solanacearum phylotype II.

Authors:  G Cellier; B Remenant; F Chiroleu; P Lefeuvre; P Prior
Journal:  Appl Environ Microbiol       Date:  2012-01-27       Impact factor: 4.792

3.  Detection of Ralstonia solanacearum strains with a quantitative, multiplex, real-time, fluorogenic PCR (TaqMan) assay.

Authors:  S A Weller; J G Elphinstone; N C Smith; N Boonham; D E Stead
Journal:  Appl Environ Microbiol       Date:  2000-07       Impact factor: 4.792

4.  Evolutionary dynamics of Ralstonia solanacearum.

Authors:  José A Castillo; Jean T Greenberg
Journal:  Appl Environ Microbiol       Date:  2006-12-22       Impact factor: 4.792

5.  Phylogenetic analysis of Ara+ and Ara- Burkholderia pseudomallei isolates and development of a multiplex PCR procedure for rapid discrimination between the two biotypes.

Authors:  T Dharakul; B Tassaneetrithep; S Trakulsomboon; S Songsivilai
Journal:  J Clin Microbiol       Date:  1999-06       Impact factor: 5.948

6.  Detection of Ralstonia solanacearum, which causes brown rot of potato, by fluorescent in situ hybridization with 23S rRNA-targeted probes.

Authors:  B A Wullings; A R Van Beuningen; J D Janse; A D Akkermans
Journal:  Appl Environ Microbiol       Date:  1998-11       Impact factor: 4.792

7.  Specific and sensitive detection of Ralstonia solanacearum in soil on the basis of PCR amplification of fliC fragments.

Authors:  J Schönfeld; H Heuer; J D Van Elsas; K Smalla
Journal:  Appl Environ Microbiol       Date:  2003-12       Impact factor: 4.792

8.  Changes in microbial community composition and function during a polyaromatic hydrocarbon phytoremediation field trial.

Authors:  Steven D Siciliano; James J Germida; Kathy Banks; Charles W Greer
Journal:  Appl Environ Microbiol       Date:  2003-01       Impact factor: 4.792

9.  Application of variable-number tandem-repeat typing to discriminate Ralstonia solanacearum strains associated with English watercourses and disease outbreaks.

Authors:  Neil Parkinson; Ruth Bryant; Janice Bew; Christine Conyers; Robert Stones; Michael Alcock; John Elphinstone
Journal:  Appl Environ Microbiol       Date:  2013-07-26       Impact factor: 4.792

10.  A unique DNA repair and recombination gene (recN) sequence for identification and intraspecific molecular typing of bacterial wilt pathogen Ralstonia solanacearum and its comparative analysis with ribosomal DNA sequences.

Authors:  Aundy Kumar; Thekkan Puthiyaveedu Prameela; Rajamma Suseelabhai
Journal:  J Biosci       Date:  2013-06       Impact factor: 1.826

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.