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Applied and Environmental Microbiology, January 1999, p. 322-326, Vol. 65, No. 1
Laboratoire de Virologie,
Received 3 August 1998/Accepted 28 October 1998
To quantify hepatitis A virus (HAV) in experimentally contaminated
mussels, we developed an internal standard RNA with a 7-nucleotide deletion for competitive reverse transcription (RT)-PCR. Deposited directly into the sample, this standard was used both as extraction control and as quantification tool. After coextraction and competitive RT-PCR, standard and wild-type products were detected by differential hybridization with specific probes and a DNA enzyme immunoassay. The
quantifiable range with this reproducible method was 104 to
107 copies of HAV/gram or 400 to 106 50%
tissue culture infective doses/ml.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Quantification of Hepatitis A Virus in Shellfish by Competitive
Reverse Transcription-PCR with Coextraction of Standard
RNA
*
Corresponding author. Mailing address: Laboratoire de
Virologie, Institut de Biologie, Centre Hospitalier Universitaire, 9 Quai Moncousu, 44093 Nantes Cedex, France. Phone: (33) 2 40 08 41 05. Fax: (33) 2 44 20 41 14. E-mail:
sbi{at}sante.univ-nantes.fr.
Applied and Environmental Microbiology, January 1999, p. 322-326, Vol. 65, No. 1
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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