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Journal of Clinical Microbiology, Dec 1996, 2894-2896, Vol 34, No. 12
A Ibrahim, P Gerner-Smidt and A Sjostedt
By use of primers specific to conserved regions of the rRNA gene cluster, a
discrete amplicon of approximately 5 kb was amplified by PCR from all 21
bacterial genera investigated. Subsequent endonuclease digestion of the PCR
product with HaeIII distinguished between the three species of the human
pathogen Francisella spp. on the one hand and four clinically relevant
genomic groups of Acinetobacter spp. on the other hand. The described
technique has the potential as a rapid method for discriminating between
closely related species that are of clinical importance.
Copyright © 1996 by the American Society for Microbiology. All rights reserved.
Amplification and restriction endonuclease digestion of a large fragment of genes coding for rRNA as a rapid method for discrimination of closely related pathogenic bacteria
Department of Clinical Microbiology, Statens Seruminstitut, Copenhagen, Denmark. ashegy@ume.foa.se
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