Literature DB >> 12789481

False-positive Mycobacterium tuberculosis culture revealed by restriction fragment length polymorphism analysis.

O D Schoch1, G E Pfyffer, D Buhl, A Paky.   

Abstract

BACKGROUND: The microbiological analysis of respiratory specimens is the most reliable approach to diagnose active pulmonary tuberculosis. PATIENT AND METHODS: We report a 60-year-old female patient (index patient) who underwent diagnostic bronchoscopy for chronic cough. No acid-fast bacilli were detected in bronchial washings. Although cough subsided with symptomatic treatment, Mycobacterium tuberculosis grew on egg-based media after 12 weeks. A false-positive culture result was suspected. Chart review and DNA fingerprinting were carried out.
RESULTS: The bronchoscope used to examine the index patient was previously used for a 30-year-old patient (source patient) with smear- and culture-positive pulmonary tuberculosis. Restriction fragment length polymorphism (RFLP) analysis based on the IS 6110 element confirmed that the two strains were identical.
CONCLUSION: Cross-contamination is a reason for false-positive cultures with M. tuberculosis and should be suspected in patients with a low clinical probability for active tuberculosis.

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Year:  2003        PMID: 12789481     DOI: 10.1007/s15010-002-3060-7

Source DB:  PubMed          Journal:  Infection        ISSN: 0300-8126            Impact factor:   3.553


  2 in total

1.  Evaluation of low-colony-number counts of Mycobacterium tuberculosis on solid media as a microbiological marker of cross-contamination.

Authors:  F K C Ribeiro; E M Lemos; D J Hadad; S C Leão; C Viana-Niero; R Dietze; J L Johnson; K D Eisenach; M Palaci
Journal:  J Clin Microbiol       Date:  2009-04-08       Impact factor: 5.948

2.  Rapid detection of laboratory cross-contamination with Mycobacterium tuberculosis using multispacer sequence typing.

Authors:  Zoheira Djelouadji; Jean Orehek; Michel Drancourt
Journal:  BMC Microbiol       Date:  2009-03-03       Impact factor: 3.605

  2 in total

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