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Journal of Clinical Microbiology, April 2000, p. 1672-1675, Vol. 38, No. 4
School of Medical
Technology,1 Laser Medicine Research
Center,3 and Department of Surgery
(Neurosurgery),4 National Taiwan University
College of Medicine, and Department of Laboratory Medicine,
National Taiwan University Hospital,2 Taipei,
Taiwan
Received 11 November 1999/Returned for modification 21 December
1999/Accepted 1 February 2000
Bacteroides thetaiotaomicron is the second most
frequently encountered species of the anaerobes isolated from clinical
specimens. We developed a PCR-based assay for the rapid identification
of B. thetaiotaomicron. Specific primers were based on
shared amplicons of about 1.2 kb generated from B. thetaiotaomicron by randomly amplified polymorphic DNA. This
1.2-kb fragment was sequenced and then used to design a set of PCR
amplification primers. This PCR generated an amplification product of
721 bp, which was unique to all 65 isolates of B. thetaiotaomicron tested. There was no amplification with isolates
of other bacterial species. Restriction enzyme digestion of the
amplification product and dot blot hybridization further verified the
specificity of the assay. These results suggest that this PCR assay
targets a nucleotide sequence that is strongly conserved in B. thetaiotaomicron. This simple and rapid PCR assay provides a
rapid and accurate method for identification of B. thetaiotaomicron and shows promise for the detection of B. thetaiotaomicron in clinical samples.
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
PCR Assay for Species-Specific Identification of
Bacteroides thetaiotaomicron
*
Corresponding author. Mailing address: School of
Medical Technology, National Taiwan University College of Medicine, No.
1, Chang-Te St., Taipei 100, Taiwan. Phone: 886-2-23970800 ext. 6918. Fax: 886-2-23959794. E-mail:
ljteng{at}ha.mc.ntu.edu.tw.
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