Home LiteratureArticle Details
PMID: 7538282 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Identification of aquatic Burkholderia (Pseudomonas) cepacia by hybridization with species-specific rRNA gene probes.

Applied and environmental microbiology ·Vol. 61 ·No. 4 ·1995-04-00 ·Pages 1634-6

Leff LG, Kernan RM, McArthur JV, Shimkets LJ

Abstract

Burkholderia (Pseudomonas) cepacia is a common environmental bacterium which can be pathogenic for plants and humans. In this study, four strategies were used to identify aquatic isolates: API test strips, hybridization with species-specific DNA probes for the 16S and 23S rRNA genes, fatty acid methyl ester (FAME) profiles, and growth on selective medium (TB-T agar [C. Hagedorn, W. D. Gould, T. R. Bardinelli, and D. R. Gustarson, Appl. Environ. Microbiol. 53:2265-2268, 1987]). Only 59% of the isolates identified as B. cepacia with the API test strips were confirmed as B. cepacia by using fatty acid profiles. The 23S rRNA probe generated a few false-positive results but dramatically underestimated the number of B. cepacia isolates (i.e., 40% of the colonies that did not hybridize to the probe were B. cepacia, as determined by FAME). The 16S rRNA probe generated more false-positive results than the 23S rRNA probe but was effective in identifying the majority of the B. cepacia isolates. The selective medium was only partially successful in recovering B. cepacia. Use of the B. cepacia-specific 16S rRNA probe was the most efficient and accurate way of identifying B. cepacia.

MeSH Terms
Base Sequence Burkholderia cepacia/genetics,isolation & purification,pathogenicity DNA Probes/genetics Humans Molecular Sequence Data Nucleic Acid Hybridization RNA, Bacterial/genetics RNA, Ribosomal, 16S/genetics RNA, Ribosomal, 23S/genetics Species Specificity Water Microbiology
Chemicals
DNA Probes RNA, Bacterial RNA, Ribosomal, 16S RNA, Ribosomal, 23S
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Leff L G
Department of Microbiology and Savannah River Ecology Laboratory, University of Georgia, Athens 30602, USA.
Kernan R M
McArthur J V
Shimkets L J
References (6)
6 references, click to expand
  1. Use of recombination techniques to examine the structure of the csg locus of Myxococcus xanthus.
    Mol Gen Genet. 1988 Jan;211(1):63-71 PMID: 2830469
  2. Evidence that associated soil bacteria may influence root hair infection of actinorhizal plants by Frankia.
    Can J Microbiol. 1980 Aug;26(8):971-7 PMID: 7459718
  3. Use of a simplified cell blot technique and 16S rRNA-directed probes for identification of common environmental isolates.
    Appl Environ Microbiol. 1993 Oct;59(10):3219-24 PMID: 7504429
  4. Subgrouping of Pseudomonas cepacia by cellular fatty acid composition.
    J Clin Microbiol. 1989 Dec;27(12):2640-6 PMID: 2687315
  5. A selective medium for enumeration and recovery of Pseudomonas cepacia biotypes from soil.
    Appl Environ Microbiol. 1987 Sep;53(9):2265-8 PMID: 3674874
  6. Genetic diversity in natural populations of a soil bacterium across a landscape gradient.
    Proc Natl Acad Sci U S A. 1988 Dec;85(24):9621-4 PMID: 16594009
Article Info
Journal
Applied and environmental microbiology
Abbr.
Appl Environ Microbiol
ISSN
0099-2240
Published
1995-04-00
Pages
1634-6
Language
English
Region
United States
NLM ID
7605801
PMCID
PMC167421
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com