Detection and Identification of Human Parainfluenza Viruses 1, 2, 3, and 4 in Clinical Samples of Pediatric Patients by Multiplex Reverse Transcription-PCR

Author:

Aguilar Jose C.1,Pérez-Breña María P.1,García María L.2,Cruz Nieves1,Erdman Dean D.3,Echevarría Juan Emilio4

Affiliation:

1. Servicio de Virologı́a1 and

2. Servicio de Pediatrı́a, Hospital Severo Ochoa, Leganes,2 Madrid, Spain, and

3. Respiratory and Enteric Viruses Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 303333

4. Servicio de Microbiologı́a Diagnóstica,4 Centro Nacional de Microbiologı́a, Instituto de Salud Carlos III, Carretera de Majadahonda Pozuelo s/n, 28220 Majadahonda, and

Abstract

ABSTRACT 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 (TCID 50 ) for HPIV type 4B (HPIV-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.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference32 articles.

1. Antigenic variation among new isolated strains of parainfluenza type 4 virus;Canchola J.;Am. J. Hyg.,1964

2. Detection of enteroviral RNA and specific DNA of herpesviruses by multiplex genome amplification;Casas I.;J. Virol. Methods,1997

3. New method for the extraction of viral RNA and DNA from cerebrospinal fluid for use in the polymerase chain reaction assay;Casas I.;J. Virol. Methods,1995

4. NCI-H292 as an alternative cell line for the isolation and propagation of the human paramyxoviruses;Castells E.;Arch. Virol.,1990

5. Collins P. L. Chanock R. M. McIntosh K. Parainfluenza viruses Fields virology 3rd ed. Fields B. N. Knipe D. M. Howley P. M. 1996 1205 1241 Lippincott-Raven Publications Philadelphia Pa

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3