A blind study of the polymerase chain reaction for the detection of Mycobacterium tuberculosis DNA

Abstract Setting: Nine French laboratories routinely involved in mycobacterial work. Objective: To assess the detection of Mycobacterium tuberculosis in experimental samples by polymerase chain reaction (PCR) using the insertion sequence IS 6110 as a target for deoxyribonucleic acid (DNA) amplification. Design: Nine laboratories participated in a blind study of the detection of M. tuberculosis by PCR in 20 coded samples containing either a definite number of M. tuberculosis complex (positive samples) or environmental mycobacteria (four samples) or no mycobacteria (five samples). Results: Five laboratories reported false-positive PCR results, with an average rate of 7%. All laboratories except one reported positive PCR results for samples containing 10 5 cfu/ml or more. M. tuberculosis DNA was detected in two thirds of samples containing 10 4 and 10 3 cfu/ml, and in one third of the samples containing 10 2 cfu/ml. Conclusion: The results of the study suggest that PCR using IS 6110 as a target for DNA amplication is neither very sensitive nor really specific for the detection of M. tuberculosis .