The polymerase chain reaction (PCR) has been used previously for the detection and typing of adenoviruses directly in clinical samples. Since under clinical conditions subgenus-specific identification is often sufficient, we extended the genus-and type-specific PCR by a subgenusspecific PCR. By sequ
Detection and typing of respiratory adenoviruses in a single-tube multiplex polymerase chain reaction
β Scribed by Byoung-Kuk Na; Jee-Hee Kim; Gu-Choul Shin; Joo-Yeon Lee; Jin-Soo Lee; Chun Kang; Woo-Joo Kim
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 134 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0146-6615
- DOI
- 10.1002/jmv.2174
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β¦ Synopsis
Abstract
A multiplex polymerase chain reaction (PCR) assay that is capable of detecting and typing six serotypes of respiratory adenovirus (Ad) was developed, using multiple sets of typeβspecific primers. The detection of each different serotype depended on distinguishing different numbers and sizes of amplification products on agarose gels following PCR. The multiplex PCR was tested with 26 clinical Ad isolates and other respiratory viruses including influenza viruses, parainfluenza viruses, and respiratory syncytial viruses as well as respiratory bacterial pathogens such as Chlamydia pneumoniae, Streptococcus pneumoniae, Haemophilus influenzae, and Mycoplasma pneumoniae. The multiplex PCR for the detection and typing of Ads gave an excellent correlation with the results by conventional typing with typeβspecific antisera. This assay may serve as a rapid means of confirming Ad with simultaneous serotype identification of the isolates. It will also have relevance as an adjunctive tool to conventional serotyping for diagnostic and epidemiological purposes. J. Med. Virol. 66:512β517, 2002. Β© 2002 WileyβLiss, Inc.
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