This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Graf, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Graf, J.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, October 1999, p. 3194-3197, Vol. 37, No. 10
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Diverse Restriction Fragment Length Polymorphism Patterns of the PCR-Amplified 16S rRNA Genes in Aeromonas veronii Strains and Possible Misidentification of Aeromonas Species

Joerg Graf*

Institute for Medical Microbiology, University of Berne, CH-3010 Berne, Switzerland

Received 20 April 1999/Returned for modification 4 June 1999/Accepted 9 July 1999

Restriction fragment length polymorphism analysis after PCR amplification (RFLP-PCR) of the 16S rRNA gene has been previously proposed as a rapid method to identify Aeromonas species. In the present study, the precision of RFLP-PCR was evaluated with 62 Aeromonas reference strains. The analysis revealed that Aeromonas veronii biovar sobria strains produce various patterns, possibly leading to its misidentification as an environmental species. For most other Aeromonas species little variation was noted. This study supports the usefulness of RFLP-PCR analysis to separate three clinically important species but also reveals possible misidentifications that necessitate further biochemical tests to validate the preliminary identification.


* Mailing address: Institute for Medical Microbiology, University of Berne, Friedbühlstr. 51, CH-3010 Berne, Switzerland. Phone: 41-31-632-3568. Fax: 41-31-632-3550. E-mail: jgraf{at}imm.unibe.ch.


Journal of Clinical Microbiology, October 1999, p. 3194-3197, Vol. 37, No. 10
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Bossi-Kupfer, M., Genini, A., Peduzzi, R., Demarta, A. (2007). Tracheobronchitis caused by Aeromonas veronii biovar sobria after near-drowning. J Med Microbiol 56: 1563-1564 [Abstract] [Full Text]  
  • Morandi, A., Zhaxybayeva, O., Gogarten, J. P., Graf, J. (2005). Evolutionary and Diagnostic Implications of Intragenomic Heterogeneity in the 16S rRNA Gene in Aeromonas Strains. J. Bacteriol. 187: 6561-6564 [Abstract] [Full Text]  
  • Moore, J E, Millar, B C, Xu, J, Crowe, M, Redmond, A O B, Elborn, J S (2002). Misidentification of a genomovar of Burkholderia cepacia by recA restriction fragment length polymorphism. J. Clin. Pathol. 55: 309-311 [Abstract] [Full Text]  
  • Goni-Urriza, M., Arpin, C., Capdepuy, M., Dubois, V., Caumette, P., Quentin, C. (2002). Type II Topoisomerase Quinolone Resistance-Determining Regions of Aeromonas caviae, A. hydrophila, and A. sobria Complexes and Mutations Associated with Quinolone Resistance. Antimicrob. Agents Chemother. 46: 350-359 [Abstract] [Full Text]  
  • Figueras, M. J., Guarro, J., Martínez-Murcia;, A., Graf, J. (2000). Use of Restriction Fragment Length Polymorphism of the PCR-Amplified 16S rRNA Gene for the Identification of Aeromonas spp.. J. Clin. Microbiol. 38: 2023-2025 [Full Text]