Nested-polymerase chain reaction for the detection of Helicobacter pylori infection with novel primers designed by sequence analysis of urease A gene in clinically isolated bacterial strains

被引:39
作者
Kawamata, O
Yoshida, H
Hirota, K
Yoshida, A
Kawaguchi, R
Shiratori, Y
Omata, M
机构
[1] UNIV TOKYO, FAC MED, DEPT INTERNAL MED 2, BUNKYO KU, TOKYO 113, JAPAN
[2] SRL INC, CTR MOLEC BIOL & CYTOGENET, HACHIOJI, TOKYO 192, JAPAN
[3] MITO SAISEIKAI HOSP, DEPT INTERNAL MED, MITO, IBARAKI 31141, JAPAN
关键词
D O I
10.1006/bbrc.1996.0216
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have established a highly sensitive semi-nested PCR assay for the detection of H. pylori infection using gastric juice sampler, which can be aspirated with disposable nasogastric tubes. The primers targeting H. pylori urease A gene were designed based on tile sequence conservation analysis of sixteen H. pylori strains isolated from Japanese patients. The efficacy of the PCR assay, designated as the URA-PCR, was confirmed by in vitro and in vivo assessments. Its sensitivity was 97.5% in the gastric juice samples aspirated from forty patients with proven H. pylori infection, and was significantly higher than that obtained with previously described PCR assays. (C) 1996 Academic Press, Inc.
引用
收藏
页码:266 / 272
页数:7
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