M. pneumoniae is a common causative agent of community-acquired pneumonia i
n children. The diagnosis of such infections is usually based on serology u
sing complement fixation or, more recently, enzyme-immune assays. PCR has b
een shown to be a promising alternative. We have evaluated a real-time PCR
assay targeting the pi adhesion protein gene and compared it to a conventio
nal semi-nested PCR assay with the 16S rDNA as target. Comparison of 147 sp
ecimens from 48 patients showed an overall agreement of 97.4%. Real-time PC
R proved to be of equal value on clinical specimens as conventional PCR reg
arding sensitivity and specificity, but is clearly advantageous regarding s
peed, handling and number of samples that can be analyzed per run. (C) 2000
Elsevier Science BN. All rights reserved.