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FEMS immunology and medical microbiology2005; 44(1); 91-97; doi: 10.1016/j.femsim.2004.12.002

Ribotyping of Burkholderia mallei isolates.

Abstract: In this study, the subspecies differentiation of 25 isolates of Burkholderia mallei was attempted based on their ribotype polymorphisms. The isolates were from human and equine infections that occurred at various times around the world. DNA samples from each isolate were digested separately with PstI and EcoRI enzymes and probed with an Escherichia coli-derived 18-mer rDNA sequence to identify diagnostic fragments. Seventeen distinct ribotypes were identified from the combined data obtained with the two restriction enzymes. The results demonstrate the general utility of ribotyping for the subspecies identification of B. mallei isolates.
Publication Date: 2005-03-23 PubMed ID: 15780581DOI: 10.1016/j.femsim.2004.12.002Google Scholar: Lookup
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  • Journal Article

Summary

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This research article discusses the use of ribotype polymorphisms to differentiate subspecies of Burkholderia mallei, a bacteria associated with human and equine infections.

Overview of the Research

  • The researchers conducted a study to differentiate various isolates of Burkholderia mallei, a bacterial species associated with diseases in humans and horses.
  • The focus is on using ribotype polymorphisms for identification and classification. Ribotyping is a technique that analyzes patterns in ribosomal DNA to categorize microorganisms.

Methodology

  • The study used 25 different isolates of Burkholderia mallei, taken from instances of infections in both humans and horses across various locations and timelines.
  • These DNA samples from each isolate were subjected to enzymatic digestion with two enzymes – PstI and EcoRI. Enzymatic digestion is a process involving use of enzymes to break down the DNA into smaller fragments.
  • The digested fragments of DNA were then probed with an 18-mer rDNA sequence derived from a different strain of bacteria, Escherichia coli, aiming to identify diagnostic fragments – distinctive pieces of DNA that can differentiate between subspecies.

Results

  • The combination of data from both PstI and EcoRI digestions resulted in the identification of 17 distinct ribotypes.
  • This reflects a significant level of diversity among the isolates, supporting the value of ribotyping as a method for subspecies identification of Burkholderia mallei.

Conclusions

  • The study has demonstrated that ribotyping can effectively differentiate between various subspecies of B. mallei.
  • This technique has the potential to improve our understanding and categorization of diverse bacterial strains participating in human and equine diseases.
  • The research advances the field of pathogen typing and may contribute to more precise diagnostic and treatment strategies.

Cite This Article

APA
Harvey SP, Minter JM. (2005). Ribotyping of Burkholderia mallei isolates. FEMS Immunol Med Microbiol, 44(1), 91-97. https://doi.org/10.1016/j.femsim.2004.12.002

Publication

ISSN: 0928-8244
NlmUniqueID: 9315554
Country: England
Language: English
Volume: 44
Issue: 1
Pages: 91-97

Researcher Affiliations

Harvey, Steven P
  • US Army Edgewood Chemical Biological Center, 5138 Blackhawk Road, Aberdeen Proving Ground, MD 21010-5424, USA. steve.harvey@us.army.mil
Minter, Jennifer M

    MeSH Terms

    • Animals
    • Burkholderia mallei / classification
    • Burkholderia mallei / genetics
    • Burkholderia mallei / isolation & purification
    • DNA Fingerprinting
    • DNA, Bacterial / genetics
    • DNA, Bacterial / isolation & purification
    • DNA, Ribosomal / genetics
    • DNA, Ribosomal / isolation & purification
    • Glanders / microbiology
    • Horses
    • Humans
    • Polymorphism, Genetic
    • Polymorphism, Restriction Fragment Length
    • Ribotyping / methods
    • Species Specificity

    Citations

    This article has been cited 4 times.
    1. Brangsch H, Singha H, Laroucau K, Elschner M. Sequence-based detection and typing procedures for Burkholderia mallei: Assessment and prospects.. Front Vet Sci 2022;9:1056996.
      doi: 10.3389/fvets.2022.1056996pubmed: 36452150google scholar: lookup
    2. Shanmugasundaram K, Singha H, Saini S, Tripathi BN. 16S rDNA and ITS Sequence Diversity of Burkholderia mallei Isolated from Glanders-Affected Horses and Mules in India (2013-2019).. Curr Microbiol 2021 Dec 18;79(1):31.
      doi: 10.1007/s00284-021-02701-8pubmed: 34921617google scholar: lookup
    3. Ferrari RG, Panzenhagen PHN, Conte-Junior CA. Phenotypic and Genotypic Eligible Methods for Salmonella Typhimurium Source Tracking.. Front Microbiol 2017;8:2587.
      doi: 10.3389/fmicb.2017.02587pubmed: 29312260google scholar: lookup
    4. U'Ren JM, Schupp JM, Pearson T, Hornstra H, Friedman CL, Smith KL, Daugherty RR, Rhoton SD, Leadem B, Georgia S, Cardon M, Huynh LY, DeShazer D, Harvey SP, Robison R, Gal D, Mayo MJ, Wagner D, Currie BJ, Keim P. Tandem repeat regions within the Burkholderia pseudomallei genome and their application for high resolution genotyping.. BMC Microbiol 2007 Mar 30;7:23.
      doi: 10.1186/1471-2180-7-23pubmed: 17397553google scholar: lookup