Detection and identification of human parainfluenza viruses 1, 2, 3, and 4in clinical samples of pediatric patients by multiplex reverse transcription-PCR

We describe a multiplex reverse transcription-PCR (m-RT-PCR) assay that is able to detect and differentiate all known human parainfluenza viruses (HPI Vs). Serial dilution experiments with reference strains that compared cell culture isolation and m-RT-PCR showed sensitivities ranging from 0.0004 50% tissue culture infective dose (TCID50) for HPIV type 4B (HPN-4B) to 32 TCI D(50)s for HPIV-3. As few as 10 plasmids containing HPIV PCR products could be detected in all cases. When 201 nasopharyngeal aspirate specimens from pediatric patients hospitalized for lower respiratory illness were tested, m-RT-PCR assay detected 64 HPIVs (24 HPIV-3, 23 HPIV-1, 10 HPIV-4, and 7 HP IV-2), while only 42 of them (21 HPIV-1, 14 HPIV-3, 6 HPIV-2, and 1 HPIV-4 isolates) grew in cell culture. Our m-RT-PCR assay was more sensitive than either cell culture isolation or indirect immunofluorescence with monoclona l antibodies for the detection of HPIV infections. Also, HPIV-4 was more fr equently detected than HPIV-2 in this study, suggesting that it may have be en underestimated as a lower respiratory tract pathogen because of the inse nsitivity of cell culture.