Previous Article | Next Article 
Journal of Clinical Microbiology, February 1999, p. 464-466, Vol. 37, No. 2
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Gram Type-Specific Broad-Range PCR Amplification
for Rapid Detection of 62 Pathogenic Bacteria
Alfred
Klausegger,1
Markus
Hell,2
Alexandra
Berger,1
Kerstin
Zinober,1
Sabine
Baier,1
Neil
Jones,1
Wolfgang
Sperl,1 and
Barbara
Kofler1,*
Children's Hospital1
and
Institute of Bacteriology,2 General
Hospital Salzburg, Salzburg, Austria
Received 11 June 1998/Returned for modification 22 July
1998/Accepted 2 November 1998
Broad-range PCR has proven to be useful for the detection of
bacteria. A set of broad-range PCR primers directed against conserved regions in the 16S rRNA gene was designed to specifically amplify either gram-positive or gram-negative bacteria. The gram type-specific broad-range PCR correctly classified all 62 pathogenic species tested.
*
Corresponding author. Mailing address: Children's
Hospital, General Hospital Salzburg, Müllner Hauptstr. 48, A-5020
Salzburg, Austria. Phone: 43 662 4482 2650. Fax: 43 662 4482 2604. E-mail: b.kofler{at}lkasbg.gv.at.
Journal of Clinical Microbiology, February 1999, p. 464-466, Vol. 37, No. 2
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
-
Goldschmidt, P, Degorge, S, Benallaoua, D, Basli, E, Batellier, L, Boutboul, S, Allouch, C, Borderie, V, Laroche, L, Chaumeil, C
(2009). New test for the diagnosis of bacterial endophthalmitis. Br J Ophthalmol
93: 1089-1095
[Abstract]
[Full Text]
-
Wu, Y.-D., Chen, L.-H., Wu, X.-J., Shang, S.-Q., Lou, J.-T., Du, L.-Z., Zhao, Z.-Y.
(2008). Gram Stain-Specific-Probe-Based Real-Time PCR for Diagnosis and Discrimination of Bacterial Neonatal Sepsis. J. Clin. Microbiol.
46: 2613-2619
[Abstract]
[Full Text]
-
Pingle, M. R., Granger, K., Feinberg, P., Shatsky, R., Sterling, B., Rundell, M., Spitzer, E., Larone, D., Golightly, L., Barany, F.
(2007). Multiplexed Identification of Blood-Borne Bacterial Pathogens by Use of a Novel 16S rRNA Gene PCR-Ligase Detection Reaction-Capillary Electrophoresis Assay. J. Clin. Microbiol.
45: 1927-1935
[Abstract]
[Full Text]
-
Newsome, T., Li, B.-J., Zou, N., Lo, S.-C.
(2004). Presence of Bacterial Phage-Like DNA Sequences in Commercial Taq DNA Polymerase Reagents. J. Clin. Microbiol.
42: 2264-2267
[Abstract]
[Full Text]
-
Hill, K.E., Davies, C.E., Wilson, M.J., Stephens, P., Harding, K.G., Thomas, D.W.
(2003). Molecular analysis of the microflora in chronic venous leg ulceration. J Med Microbiol
52: 365-369
[Abstract]
[Full Text]
-
Klaschik, S., Lehmann, L. E., Raadts, A., Book, M., Hoeft, A., Stuber, F.
(2002). Real-Time PCR for Detection and Differentiation of Gram-Positive and Gram-Negative Bacteria. J. Clin. Microbiol.
40: 4304-4307
[Abstract]
[Full Text]
-
Nadkarni, M. A., Martin, F. E., Jacques, N. A., Hunter, N.
(2002). Determination of bacterial load by real-time PCR using a broad-range (universal) probe and primers set. Microbiology
148: 257-266
[Abstract]
[Full Text]
-
Louie, M., Louie, L., Simor, A. E.
(2000). The role of DNA amplification technology in the diagnosis of infectious diseases. CMAJ
163: 301-309
[Abstract]
[Full Text]
-
Corless, C. E., Guiver, M., Borrow, R., Edwards-Jones, V., Kaczmarski, E. B., Fox, A. J.
(2000). Contamination and Sensitivity Issues with a Real-Time Universal 16S rRNA PCR. J. Clin. Microbiol.
38: 1747-1752
[Abstract]
[Full Text]