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

被引:100
作者
Aguilar, JC
Pérez-Breña, MP
García, ML
Cruz, N
Erdman, DD
Echevarria, JE
机构
[1] Inst Salud Carlos III, Ctr Nacl Microbiol, Serv Virol, Madrid 28220, Spain
[2] Inst Salud Carlos III, Ctr Nacl Microbiol, Serv Microbiol Diagnost, Madrid 28220, Spain
[3] Hosp Severo Ochoa, Serv Pediat, Madrid, Spain
[4] Ctr Dis Control & Prevent, Resp & Enter Viruses Branch, Div Viral & Rickettsial Dis, Natl Ctr Infect Dis, Atlanta, GA 30333 USA
关键词
D O I
10.1128/JCM.38.3.1191-1195.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We describe a multiplex reverse transcription-PCR (m-RT-PCR) assay that is able to detect and differentiate all known human parainfluenza viruses (HPIVs). 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 TCID(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 HPIV-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 monoclonal antibodies for the detection of HPIV infections. Also, HPIV-4 was more frequently detected than HPIV-2 in this study, suggesting that it may have been underestimated as a lower respiratory tract pathogen because of the insensitivity of cell culture.
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页码:1191 / 1195
页数:5
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