SINGLE-STEP NESTED POLYMERASE CHAIN-REACTION FOR DETECTION OF DIFFERENT GENOTYPES OF HEPATITIS-C VIRUS

被引:18
|
作者
LI, JS
TONG, SP
VITVITSKI, L
TREPO, C
机构
[1] Unité de Recherche sur les Hépatites, INSERM U271, Lyon
[2] Molecular Hepatology Laboratory, Massachusetts General Hospital, Massachusetts General Hospital Cancer Center, Harvard Medical School, Charlestown, Massachusetts
关键词
NON-A; NON-B HEPATITIS; ENZYMATIC AMPLIFICATION; CLINICAL DIAGNOSIS; CONTAMINATION; METHODOLOGY;
D O I
10.1002/jmv.1890450207
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepatitis C virus (HCV) exhibits considerable sequence variability and circulates in the blood at extremely tow revels. Current methods for detecting HCV RNA are based mostly on nested polymerase chain reaction (PCR), in which part of the first amplification product is reamplified in the second tube by an internal primer pair. A novel nested PCR method was developed in which the two successive amplification processes are carried out in the same tube with a single step of physical manipulation. Careful selection of highly conserved sequences of the 5' noncoding region as primers enabled successful detection of all three major genotypes circulating in France, including the one with variation in this region. Retaining high sensitivity of the conventional nested PCR, the novel method reduced greatly the risk of carry-over contaminations. It was also cost- and time-saving. The one-step nested PCR method is especially suitable for routine diagnosis of HCV infection in clinical laboratories. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:151 / 155
页数:5
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