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首页> 外文期刊>Journal of digestive diseases >Detection of clarithromycin resistance in Helicobacter pylori following noncryogenic storage of rapid urease tests for 30 days
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Detection of clarithromycin resistance in Helicobacter pylori following noncryogenic storage of rapid urease tests for 30 days

机译:非尿素快速尿素酶检测30天后,检测幽门螺杆菌对克拉霉素的耐药性

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Objective: Traditional Helicobacter pylori (H. pylori) eradication therapy has been undermined by increasing antimicrobial, especially clarithromycin, resistance. Susceptibility testing in some areas is difficult to achieve or unavailable. We aimed to determine whether gastric biopsy specimens stored at room temperature for rapid urease test (RUT) were suitable for clarithromycin susceptibility testing of H. pylori. Methods: After 30 days of storage at room temperature, DNA was extracted from gastric biopsies present in RUTs (Hpfast). H.pylori status and clarithromycin susceptibility were evaluated using H.pylori-specific polymerase chain reaction (PCR) for ureA, vacA, and allele-specific primer-PCR of the 23S rRNA genes. The PCR results were compared with histology, RUT, and culture results. H.pylori positive was defined as RUT and either culture or histology positive; H.pylori negative as RUT, culture and histology negative. Results: Samples from 31 patients were evaluated; 11 were H.pylori positive including 9 by culture; seven of which had allele-specific primer-PCR results from the RUT specimen for the detection of mutations of the 23S rRNA gene. When both tests were available, culture and PCR results were concordant in 7 cases. In 15 of the 20 histology, RUT and culture negative patients, three PCR were negative. In one patient, all of the three tests were positive; and in three only the 23S rRNA was positive and in one only ureA was positive. Conclusion: Gastric biopsy specimens stored in the gel of RUT for 30 days can be used for molecular testing to confirm the diagnosis of H.pylori infection and test for clarithromycin susceptibility. Published 2011. This article is a US Government work and is in the public domain in the USA. Journal of Digestive Diseases
机译:目的:传统的幽门螺杆菌(H. pylori)根除疗法已通过增加抗菌素特别是克拉霉素的耐药性而遭到破坏。在某些地区很难进行敏感性测试或无法进行。我们旨在确定在室温下储存的用于快速尿素酶测试(RUT)的胃活检标本是否适合幽门螺杆菌的克拉霉素敏感性测试。方法:在室温下保存30天后,从RUT(Hpfast)中存在的胃活检组织中提取DNA。使用幽门螺杆菌特异性聚合酶链反应(PCR)对23S rRNA基因的ureA,vacA和等位基因特异性引物PCR,评估幽门螺杆菌状态和克拉霉素敏感性。将PCR结果与组织学,RUT和培养结果进行比较。幽门螺杆菌阳性定义为RUT,文化或组织学阳性;幽门螺杆菌阴性为RUT,文化和组织学阴性。结果:对31例患者的样本进行了评估;幽门螺杆菌阳性11例,其中9例阳性。其中有7份来自RUT标本的等位基因特异性引物-PCR结果用于检测23S rRNA基因的突变。当两种测试均可用时,在7例中培养和PCR结果一致。在20例组织学,RUT和培养阴性患者中,有15例PCR阴性。一名患者的三项检查均呈阳性。仅有3例中23S rRNA呈阳性,而仅有ureA呈阳性。结论:在RUT凝胶中保存30天的胃活检标本可用于分子检测,以确认幽门螺杆菌感染的诊断和克拉霉素敏感性的检测。 2011年发布。本文是美国政府的工作,在美国属于公共领域。消化系统疾病杂志

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