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J Clin Microbiol ; 34(8): 1949-51, 1996 Aug.
Article in English | MEDLINE | ID: mdl-8818888

ABSTRACT

PCR has been used successfully for the direct detection of Mycobacterium tuberculosis in uncultured patient samples. Its potential is hindered by the risk of false-positive results as a result of either amplicon carryover of cross-contamination between patient samples. In the present study, we investigated whether residual amplifiable human or M. tuberculosis DNA could remain in sterile bronchoscopes and potentially be a cause of false-positive PCR results in subsequent patient samples. Sterilized bronchoscopes were flushed with sterile saline, and the collected eluate was submitted for PCR amplification of IS6110 sequences and exon 8 of the human p53 gene. Of a total of 55 washes of sterile bronchoscopes from two institutions, 2 (3.6%) contained amplifiable M. tuberculosis DNA and 11 (20%) contained residual human DNA. These findings indicate that residual DNA can remain in sterilized bronchoscopes and can be a source of false-positive PCR results.


Subject(s)
Bronchoscopes , DNA, Bacterial/isolation & purification , Equipment Contamination , Polymerase Chain Reaction/methods , Tuberculosis, Pulmonary/diagnosis , False Positive Reactions , Humans , Sterilization
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