Li C, Ha T, Chi D S, Ferguson D A, Jiang C, Laffan J J, Thomas E
Department of Internal Medicine, Quillen College of Medicine, East Tennessee State University, and VA Medical Center, Johnson City 37684, USA.
J Clin Microbiol. 1997 Dec;35(12):3021-5. doi: 10.1128/jcm.35.12.3021-3025.1997.
Recent studies have shown the usefulness of PCR-based restriction fragment length polymorphism (RFLP) analysis for differentiating Helicobacter pylori strains isolated by culture. For this study, a PCR-based RFLP assay was developed for directly typing H. pylori strains from gastric biopsy specimens. Nineteen gastric biopsy specimens obtained from patients undergoing endoscopy for gastrointestinal complaints were cultured for isolation of H. pylori. Genomic DNA preparations from these gastric biopsy specimens and the corresponding H. pylori isolates were tested by our PCR-based RFLP assay. The 1,179-bp H. pylori DNA fragments amplified by the PCR assay were digested with the restriction enzymes HhaI, MboI, and AluI and analyzed by agarose gel electrophoresis. HhaI, MboI, and AluI digestion produced 11, 10, and 6 distinguishable digestion patterns, respectively, from the 19 H. pylori isolates tested and generated 13, 11, and 6 different patterns, respectively, from the 19 gastric biopsy specimens. The patterns from 13 of the 19 gastric biopsy specimens matched those of the H. pylori isolates from the corresponding patients. The patterns from the remaining six biopsy specimens appeared to represent infection by two strains of H. pylori; the pattern of one strain was identical to that of the isolate from the corresponding patient. By combining all the restriction enzyme digestion patterns obtained by using HhaI, MboI, and AluI, we observed 19 distinct RFLP patterns from the 19 specimens. The results suggest that the PCR-based RFLP analysis method may be useful as a primary technique to identify and distinguish H. pylori strains directly from gastric biopsy specimens without culture of the organisms.
最近的研究表明,基于聚合酶链反应(PCR)的限制性片段长度多态性(RFLP)分析对于区分培养分离出的幽门螺杆菌菌株很有用。在本研究中,开发了一种基于PCR的RFLP检测方法,用于直接对胃活检标本中的幽门螺杆菌菌株进行分型。从因胃肠道不适接受内镜检查的患者中获取19份胃活检标本,培养以分离幽门螺杆菌。用我们基于PCR的RFLP检测方法对这些胃活检标本以及相应的幽门螺杆菌分离株的基因组DNA制剂进行检测。通过PCR检测扩增出的1179 bp幽门螺杆菌DNA片段用限制性内切酶HhaI、MboI和AluI进行消化,并用琼脂糖凝胶电泳进行分析。HhaI、MboI和AluI消化分别从19株受试幽门螺杆菌分离株中产生了11、10和6种可区分的消化模式,从19份胃活检标本中分别产生了13、11和6种不同模式。19份胃活检标本中的13份的模式与相应患者的幽门螺杆菌分离株的模式相匹配。其余6份活检标本的模式似乎代表了两种幽门螺杆菌菌株的感染;其中一种菌株的模式与相应患者分离株的模式相同。通过合并使用HhaI、MboI和AluI获得的所有限制性内切酶消化模式,我们从19份标本中观察到了19种不同的RFLP模式。结果表明,基于PCR的RFLP分析方法可能作为一种主要技术有用,可直接从胃活检标本中鉴定和区分幽门螺杆菌菌株,而无需对该生物体进行培养。