Rapid detection of laboratory cross-contamination with <it>Mycobacterium tuberculosis </it>using multispacer sequence typing

<p>Abstract</p> <p>Background</p> <p>The ability to culture <it>Mycobacterium tuberculosis </it>from clinical specimens serves as the gold standard for the diagnosis of tuberculosis. However, a number of false-positive diagnoses may be due to cross-contamina...

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Main Authors: Orehek Jean, Drancourt Michel, Djelouadji Zoheira
Format: Article
Language:English
Published: BMC 2009-03-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/9/47
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spelling doaj-ce31c7a8b64048eb9e218cb8b2a4ea5b2020-11-24T21:33:40ZengBMCBMC Microbiology1471-21802009-03-01914710.1186/1471-2180-9-47Rapid detection of laboratory cross-contamination with <it>Mycobacterium tuberculosis </it>using multispacer sequence typingOrehek JeanDrancourt MichelDjelouadji Zoheira<p>Abstract</p> <p>Background</p> <p>The ability to culture <it>Mycobacterium tuberculosis </it>from clinical specimens serves as the gold standard for the diagnosis of tuberculosis. However, a number of false-positive diagnoses may be due to cross-contamination of such specimens. We herein investigate such episode of cross-contamination by using a technique known as multispacer sequence typing (MST). This technique was applied to six <it>M. tuberculosis </it>isolates prepared within the same laboratory over a two-week period of time.</p> <p>Results</p> <p>MST analysis indicated a unique and common sequence profile between a strain isolated from a patient with proven pulmonary tuberculosis and a strain isolated from a patient diagnosed with lung carcinoma. Using this approach, we were able to provide a clear demonstration of laboratory cross-contamination within just four working days. Further epidemiological investigations revealed that the two isolates were processed for culture on the same day.</p> <p>Conclusion</p> <p>The application of MST has been demonstrated to serve as a rapid and efficient method to investigate cases of possible cross-contamination with <it>M. tuberculosis</it>.</p> http://www.biomedcentral.com/1471-2180/9/47
collection DOAJ
language English
format Article
sources DOAJ
author Orehek Jean
Drancourt Michel
Djelouadji Zoheira
spellingShingle Orehek Jean
Drancourt Michel
Djelouadji Zoheira
Rapid detection of laboratory cross-contamination with <it>Mycobacterium tuberculosis </it>using multispacer sequence typing
BMC Microbiology
author_facet Orehek Jean
Drancourt Michel
Djelouadji Zoheira
author_sort Orehek Jean
title Rapid detection of laboratory cross-contamination with <it>Mycobacterium tuberculosis </it>using multispacer sequence typing
title_short Rapid detection of laboratory cross-contamination with <it>Mycobacterium tuberculosis </it>using multispacer sequence typing
title_full Rapid detection of laboratory cross-contamination with <it>Mycobacterium tuberculosis </it>using multispacer sequence typing
title_fullStr Rapid detection of laboratory cross-contamination with <it>Mycobacterium tuberculosis </it>using multispacer sequence typing
title_full_unstemmed Rapid detection of laboratory cross-contamination with <it>Mycobacterium tuberculosis </it>using multispacer sequence typing
title_sort rapid detection of laboratory cross-contamination with <it>mycobacterium tuberculosis </it>using multispacer sequence typing
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2009-03-01
description <p>Abstract</p> <p>Background</p> <p>The ability to culture <it>Mycobacterium tuberculosis </it>from clinical specimens serves as the gold standard for the diagnosis of tuberculosis. However, a number of false-positive diagnoses may be due to cross-contamination of such specimens. We herein investigate such episode of cross-contamination by using a technique known as multispacer sequence typing (MST). This technique was applied to six <it>M. tuberculosis </it>isolates prepared within the same laboratory over a two-week period of time.</p> <p>Results</p> <p>MST analysis indicated a unique and common sequence profile between a strain isolated from a patient with proven pulmonary tuberculosis and a strain isolated from a patient diagnosed with lung carcinoma. Using this approach, we were able to provide a clear demonstration of laboratory cross-contamination within just four working days. Further epidemiological investigations revealed that the two isolates were processed for culture on the same day.</p> <p>Conclusion</p> <p>The application of MST has been demonstrated to serve as a rapid and efficient method to investigate cases of possible cross-contamination with <it>M. tuberculosis</it>.</p>
url http://www.biomedcentral.com/1471-2180/9/47
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