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Journal of Clinical Microbiology, September 1999, p. 2813-2816, Vol. 37, No. 9
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Rapid Detection of Human Rhinoviruses in
Nasopharyngeal Aspirates by a Microwell Reverse
Transcription-PCR-Hybridization Assay
S.
Blomqvist,
A.
Skyttä,
M.
Roivainen, and
T.
Hovi*
Department of Virology, National Public
Health Institute (KTL), Helsinki, Finland
Received 28 January 1999/Returned for modification 16 March
1999/Accepted 7 June 1999
A rapid and sensitive microwell reverse transcription
(RT)-PCR-hybridization assay was developed to detect human
rhinoviruses in clinical specimens and cell culture suspensions. Two
hundred three nasopharyngeal aspirates collected from children with
symptoms of respiratory disease were analyzed by a classical
rolling-tube cell culture method, microwell culture of HeLa Ohio cell
monolayers, and RT-PCR with detection of the amplicons in a microwell
hybridization assay. The RT-PCR was also done with harvests of the
microwell cultures. RNA was extracted with a commercial kit, and the
RT-PCR procedure was carried out with microtiter-format equipment. A confirmatory test that exploited a blocking oligonucleotide at the
hybridization step was developed to reliably identify marginally positive specimens. Of the 203 nasopharyngeal aspirate specimens, rhinovirus or rhinoviral RNA was detected in 111 specimens (55%). Ninety-eight specimens (48%) were found to be positive by RT-PCR of
the original nasopharyngeal aspirates, while the conventional rolling-tube cell culture method yielded 52 (26%) positive specimens. This RT-PCR method with solid-phase hybridization is easy to perform, sensitive, and specific and will be especially useful for analysis of
large numbers of clinical specimens.
*
Corresponding author. Mailing address: Department of
Virology, National Public Health Institute, Mannerheimintie 166, FIN-00300 Helsinki, Finland. Phone: 358-9-47448321. Fax:
358-9-47448355. E-mail: tapani.hovi{at}ktl.fi.
Journal of Clinical Microbiology, September 1999, p. 2813-2816, Vol. 37, No. 9
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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