J Med Microbiol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


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 Email this article to a friend
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 arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Alfaresi, M.
Right arrow Articles by Elkosh, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Alfaresi, M.
Right arrow Articles by Elkosh, A.
Agricola
Right arrow Articles by Alfaresi, M.
Right arrow Articles by Elkosh, A.
J Med Microbiol 55 (2006), 1711-1715; DOI: 10.1099/jmm.0.46593-0
© 2006 Society for General Microbiology
ISSN 1473-5644

Rapid identification of clinically relevant Nocardia species using real-time PCR with SYBR Green and melting-curve analysis

Mubarak Alfaresi and Abida Elkosh

Department of Pathology and Laboratory Medicine – Microbiology Division, Zayed Military Hospital, Abu Dhabi, United Arab Emirates

Correspondence
Mubarak Alfaresi
uaenow{at}emirates.net.ae

Received 26 February 2006
Accepted 21 August 2006


The objective of this study was to develop and evaluate a rapid new method of identifying clinically relevant Nocardia species. DNA extracted from different Nocardia strains was used in a real-time PCR assay with SYBR Green and melting-curve analysis to identify Nocardia species. Ten control strains and four bacterial strains of closely related genera were employed, and samples from 28 patients were used. All Nocardia strains were identified correctly, and there was no cross-reaction with strains from genera closely related to Nocardia. The sensitivity and specificity of the method were 90 and 100 %, respectively. This method can be used to rapidly detect Nocardia species in culture, without cross-reaction with other closely related genera.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL J MED MICROBIOL MICROBIOLOGY J GEN VIROL ALL SGM JOURNALS
Copyright © 2006 Society for General Microbiology.