GeneScan reverse transcription-PCR assay for detection of six common respiratory viruses in young children hospitalized with acute respiratory illness

被引:92
作者
Erdman, DD
Weinberg, GA
Edwards, KM
Walker, FJ
Anderson, BC
Winter, J
González, M
Anderson, LJ
机构
[1] Ctr Dis Control & Prevent, Resp & Enter Viruses Branch, Atlanta, GA 30333 USA
[2] Univ Rochester, Dept Pediat, Rochester, NY 14642 USA
[3] Vanderbilt Univ, Dept Pediat, Nashville, TN 37235 USA
[4] Hosp Cent Fuerzas Armadas, Montevideo, Uruguay
关键词
D O I
10.1128/JCM.41.9.4298-4303.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A reverse transcription-PCR (RT-PCR) assay based on automated fluorescent capillary electrophoresis and GeneScan software analysis was developed to detect six common respiratory viruses in clinical specimens from young children. Assays for human respiratory syncytial virus (HRSV); human parainfluenza viruses 1, 2, and 3 (HPIV1, -2, and -3, respectively); and influenza A and B viruses were incorporated into a single standard assay format. The optimized assay panel was used to test 470 respiratory specimens obtained from 462 children hospitalized with acute respiratory illness that had been previously tested by viral culture (405 specimens) or direct immunofluorescence staining (DIF) (65 specimens). Of 93 specimens positive for respiratory viruses by culture or DIF, 86 (92%) were positive by RT-PCR, including 66 HRSV, 2 HPIV2, 5 HPIV3, 3 influenza A virus, and 10 influenza B virus specimens. An additional 119 respiratory viruses were identified by RT-PCR in 116 patients for whom results were negative by viral isolation or DIF. We conclude that the GeneScan RT-PCR panel can markedly improve detection of acute respiratory virus infections in young children.
引用
收藏
页码:4298 / 4303
页数:6
相关论文
共 41 条
[1]   Detection and identification of human parainfluenza viruses 1, 2, 3, and 4 in clinical samples of pediatric patients by multiplex reverse transcription-PCR [J].
Aguilar, JC ;
Pérez-Breña, MP ;
García, ML ;
Cruz, N ;
Erdman, DD ;
Echevarria, JE .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (03) :1191-1195
[2]   COMPARISON OF NASOPHARYNGEAL ASPIRATE AND NASOPHARYNGEAL SWAB SPECIMENS FOR RESPIRATORY SYNCYTIAL VIRUS DIAGNOSIS BY CELL-CULTURE, INDIRECT IMMUNOFLUORESCENCE ASSAY, AND ENZYME-LINKED-IMMUNOSORBENT-ASSAY [J].
AHLUWALIA, G ;
EMBREE, J ;
MCNICOL, P ;
LAW, B ;
HAMMOND, GW .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (05) :763-767
[3]   TYPE-SPECIFIC IDENTIFICATION OF INFLUENZA VIRUS-A, VIRUS-B AND VIRUS-C BY THE POLYMERASE CHAIN-REACTION [J].
CLAAS, ECJ ;
SPRENGER, MJW ;
KLETER, GEM ;
VANBEEK, R ;
QUINT, WGV ;
MASUREL, N .
JOURNAL OF VIROLOGICAL METHODS, 1992, 39 (1-2) :1-13
[4]   A multiplex RT-PCR for the detection of parainfluenza viruses 1-3 in clinical samples [J].
Corne, JM ;
Green, S ;
Sanderson, G ;
Caul, EO ;
Johnston, SL .
JOURNAL OF VIROLOGICAL METHODS, 1999, 82 (01) :9-18
[5]  
Echevarría JE, 1998, J CLIN MICROBIOL, V36, P1388
[6]   Multiplex reverse transcription PCR for surveillance of influenza A and B viruses in England and Wales in 1995 and 1996 [J].
Ellis, JS ;
Fleming, DM ;
Zambon, MC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (08) :2076-2082
[7]   Detection of respiratory syncytial virus A and B and parainfluenzavirus 3 sequences in respiratory tracts of infants by a single PCR with primers targeted to the L-polymerase gene and differential hybridization [J].
Eugene-Ruellan, G ;
Freymuth, F ;
Bahloul, C ;
Badrane, H ;
Vabret, A ;
Tordo, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (03) :796-801
[8]   Rapid simultaneous diagnosis of infections with respiratory syncytial viruses A and B, influenza viruses A and B, and human parainfluenza virus types 1, 2, and 3 by multiplex quantitative reverse transcription-polymerase chain reaction enzyme hybridization assay (Hexaplex) [J].
Fan, J ;
Henrickson, KJ ;
Savatski, LL .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (06) :1397-1402
[9]  
Fredricks DN, 1999, CLIN INFECT DIS, V29, P475, DOI 10.1086/598618
[10]   Detection of respiratory syncytial virus, parainfluenzavirus 3, adenovirus and rhinovirus sequences in respiratory tract of infants by polymerase chain reaction and hybridization [J].
Freymuth, F ;
Vabret, A ;
GalateauSalle, F ;
Ferey, J ;
Eugene, G ;
Petitjean, J ;
Gennetay, E ;
Brouard, J ;
Jokik, M ;
Duhamel, JF ;
Guillois, B .
CLINICAL AND DIAGNOSTIC VIROLOGY, 1997, 8 (01) :31-40