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Journal of Clinical Microbiology, June 1998, p. 1544-1548, Vol. 36, No. 6
Virus Laboratory, Laboratory Centre for
Disease Control, Tunney's Pasture, Ottawa, Ontario, Canada K1A 0L2
Received 2 December 1997/Returned for modification 2 February
1998/Accepted 12 March 1998
A quick genetic approach for the screening of influenza virus
variants was developed in this laboratory (S. Zou, J. Clin. Microbiol. 35:2623-2627, 1997). It uses multiplex reverse
transcription and multiplex PCR to amplify and differentiate the
variable region of the hemagglutinin genes of different types and
subtypes of influenza viruses. Variants within the same type or subtype
are then identified by the heteroduplex mobility shift assay of the amplicons. The method was used to screen influenza virus isolates received from provincial laboratories during the 1996-1997 season and
was able to identify new influenza B virus variants. Sequencing of the
amplicons derived from the hemagglutinin gene of the identified variants and comparison with the vaccine strain B/Harbin/7/94 showed
substitution rates of 2.26 to 2.55% at the nucleotide level and 4.26 to 4.68% at the amino acid level. The result further demonstrated that
the approach provides a quick, sensitive, and reliable screening for
influenza virus variants. It also suggested the necessity of close
monitoring of influenza B virus isolates in the 1997-1998 season and
critical evaluation of the reference strain for the type B influenza
virus.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Identification of New Influenza B Virus Variants
by Multiplex Reverse Transcription-PCR and the Heteroduplex
Mobility Assay
*
Corresponding author. Mailing address: Postal Locator
3005A, Laboratory Centre for Disease Control, 11 Holland Ave., Suite 511, Ottawa, Ontario, Canada K1A 0L2. Phone: (613) 946-8819. Fax: (613)
952-6668. E-mail: shimian_zou{at}inet.hwc.ca.
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