An Economical Tandem Multiplex Real-Time PCR Technique for the Detection of a Comprehensive Range of Respiratory Pathogens

被引:48
|
作者
Chidlow, Glenys R. [1 ,2 ]
Harnett, Gerry B. [1 ]
Shellam, Geoffrey R. [2 ]
Smith, David W. [1 ,2 ]
机构
[1] Univ Western Australia, Queen Elizabeth II Med Ctr, Dept Microbiol, Pathwest Lab Med WA, Nedlands, WA 6009, Australia
[2] Univ Western Australia, Sch Biomed Biomol & Chem Sci M502, Nedlands, WA 6009, Australia
来源
VIRUSES-BASEL | 2009年 / 1卷 / 01期
关键词
respiratory pathogens; tandem multiplex real-time PCR; mixed infections; POLYMERASE-CHAIN-REACTION; REVERSE TRANSCRIPTION-PCR; COMMUNITY-ACQUIRED PNEUMONIA; TRACT INFECTIONS; SYNCYTIAL-VIRUS; NESTED-PCR; NASOPHARYNGEAL SAMPLES; ACUTE BRONCHIOLITIS; HUMAN RHINOVIRUSES; CLINICAL-SAMPLES;
D O I
10.3390/v1010042
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This study used real-time PCR assays to screen small sample volumes for a comprehensive range of 35 respiratory pathogens. Initial thermocycling was limited to 20 cycles to avoid competition for reagents, followed by a secondary real-time multiplex PCR. Supplementary semi-nested human metapneumovirus and picornavirus PCR assays were required to complete the acute respiratory pathogen profile. Potential pathogens were detected in 85 (70%) of pernasal aspirates collected from 121 children with acute respiratory symptoms. Multiple pathogens were detected in 29 (24%) of those samples. The tandem multiplex real-time PCR was an efficient method for the rapid detection of multiple pathogens.
引用
收藏
页码:42 / 56
页数:15
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