Abstract |
We used PCR for hepatitis C virus (HCV) genotyping with type-specific primers from the core and NS5 genes. Type I was predominant in the general population (58% in blood donors) as well as in different risk groups, such as intravenous drug abusers (58%), blood transfusion recipients (64%), hemophiliacs (62%), and patients with HCV chronic liver disease (76%). Types II, III, and IV were less prevalent in Canada, being found in 10.92, 6.72, and 5.88% of the population, respectively. The type II core primer was not type specific and reacted with the majority of our type I HCV samples, suggesting a false-positive dual infection with two different genotypes (I and II). Digestion of these amplified type I and type II products with restriction endonuclease AccI proved to be very useful in the exclusion of false-positive dual type I and type II infections.
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Authors | A Andonov, R K Chaudhary |
Journal | Journal of clinical microbiology
(J Clin Microbiol)
Vol. 32
Issue 8
Pg. 2031-4
(Aug 1994)
ISSN: 0095-1137 [Print] United States |
PMID | 7989565
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- DNA Primers
- DNA, Viral
- Deoxyribonucleases, Type II Site-Specific
- GTMKAC-specific type II deoxyribonucleases
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Topics |
- Base Sequence
- Canada
(epidemiology)
- DNA Primers
- DNA, Viral
(genetics)
- Deoxyribonucleases, Type II Site-Specific
(metabolism)
- Genotype
- Hepacivirus
(classification, genetics)
- Hepatitis C
(blood, epidemiology)
- Humans
- Molecular Sequence Data
- Polymerase Chain Reaction
(methods)
- Risk Factors
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