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PCR detection of clarithromycin-susceptible and -resistant Helicobacter pylori from formalin-fixed, paraffin-embedded gastric biopsies

机译:从福尔马林固定,石蜡包埋的胃活组织检查中对克拉霉素敏感性和耐药性幽门螺杆菌的PCR检测

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Antimicrobial resistance to clarithromycin is a growing concern in the treatment of Helicobacter pylori and is associated with three major point mutations of the 23S rRNA, A2142C, A2142G, and A2143G. The use of traditional culture-based methods for determination of clarithromycin resistance in H. pylori are time consuming and lack sensitivity. We implemented a real-time PCR with melt curve analysis to detect and characterize H. pylori in formalin-fixed, paraffin-embedded gastric biopsy specimens to assess the frequency of clarithromycin resistance mutations in our study population. One hundred and fifty-three formalin-fixed, paraffin-embedded gastric biopsies were chosen on the basis of positive immunohistochemical staining for H. pylori and an accompanying histopathological diagnosis of Helicobacter-associated gastritis. New adjacent sections were taken for immunohistochemical staining and DNA extraction with subsequent testing by PCR assay and melt curve analysis using a primer and probe combination first described by Oleastro et al.12 One hundred and forty-six samples demonstrated adequate amplification of a human DNA control target. Of these, there were 122 H. pylori immunohistochemistry-positive samples. In all, 103 out of 122 (84%) immunohistochemistry-positive samples demonstrated amplifiable H. pylori 23S rRNA gene target and 19 (16%) demonstrated no amplification of H. pylori. Twenty-two samples were negative for H. pylori by immunohistochemistry and PCR. Two were negative for H. pylori by immunohistochemistry, but were positive for H. pylori by PCR. In all, 52 out of 105 (50%) PCR-positive samples demonstrated resistance mutations, and it was determined that a heterogeneous population of mutated and unmutated organisms was present in 11 out of 52 samples. The use of PCR assays allows for a timely assessment of clarithromycin resistance status without the disadvantages of culture-based methods, and may lead to a decrease in treatment failure rates.
机译:对幽门螺杆菌的抗药性在幽门螺杆菌的治疗中日益引起关注,并且与23S rRNA,A2142C,A2142G和A2143G的三个主要点突变有关。使用传统的基于文化的方法确定幽门螺杆菌对克拉霉素的耐药性既费时又缺乏敏感性。我们实施了带有融解曲线分析的实时PCR,以检测和表征福尔马林固定,石蜡包埋的胃活检标本中的幽门螺杆菌,以评估研究人群中克拉霉素抗性突变的频率。基于对幽门螺杆菌的阳性免疫组织化学染色和伴随的幽门螺杆菌相关性胃炎的组织病理学诊断,选择了一百三十三份福尔马林固定,石蜡包埋的胃活检组织。取新的相邻切片用于免疫组织化学染色和DNA提取,随后通过PCR分析进行测试,并使用由Oleastro等人首先描述的引物和探针组合进行熔解曲线分析[12] 146个样品显示了对人类DNA对照的充分扩增目标。其中,有122例幽门螺杆菌免疫组织化学阳性样品。在122个免疫组织化学阳性样本中,总共有103个(84%)表现出可扩增的幽门螺杆菌23S rRNA基因靶标,而19个样本(16%)没有显示幽门螺杆菌的扩增。通过免疫组织化学和PCR,22个样品的幽门螺杆菌阴性。通过免疫组织化学,有两个幽门螺杆菌阴性,而通过PCR阳性的幽门螺杆菌阳性。总共105份(50%)PCR阳性样本中有52份表现出抗性突变,并且确定52份样本中有11份存在异种突变和未突变生物种群。 PCR测定法的使用允许及时评估克拉霉素的耐药性状态,而没有基于培养的方法的缺点,并且可能导致治疗失败率降低。

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