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An improved quantitative real-time polymerase chain reaction technology for Helicobacter pylori detection in stomach tissue and its application value in clinical precision testing

机译:一种改进的胃组织幽门螺杆菌检测的定量实时聚合酶链反应技术及其在临床精密测试中的应用价值

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Helicobacter pylori (H. pylori) infection is a serious human health threat. The empiric H. pylori treatment paradigm guided by traditional testing technologies has led to antibiotic resistance. Here, we improved the qPCR method to provide technical support for precision H. pylori diagnosis and treatment. Two pairs of primers and probes targeting the glmM gene were designed to detect H. pylori, and a multiplex qPCR method was established for virulence factor detection. Then, a rapid urease test (RUT), culturing and qPCR were performed on 141 specimens collected from Xinqiao Hospital of China in 2017 to evaluate the qPCR detection capability. Finally, the H. pylori infectious amount and virulence genes were detected by qPCR. 1. The improved qPCR method which used two pairs of primers had a higher detection rate (100%) and better accuracy (p?=?0.000), compared with the qPCR using a pair of primers. It also had better consistency with the bacterial culture than with RUT (Kappa =0.440, p??0.001). 2. The H. pylori infectious amount was significantly positively associated with gastritis in corpus (p?=?0.003) and gastric erosion (p?=?0.043). The H. pylori infectious amount in gastric precancerous patients was significantly lower than that in H. pylori-positive patients (p??0.05), and the infectious H. pylori-vacA s1 amount was significantly greater than that of H. pylori-vacA s1- (p??0.05). 3. The vacA s1 frequency was significantly higher than that of vacA m1/cagA /babA2 in chronic superficial gastritis (p?=?0.000), peptic ulcer (p?=?0.037) and gastric erosion (p?=?0.009). The H. pylori-vacA /cagA /babA2 frequency showed a significant positive correlation (p??0.05). The H. pylori infectious amount and presence of H. pylori virulence factors showed complex correlations with gastric disease occurrence and development. The improved qPCR with good detection performance can be used for quantitative H. pylori detection and testing for the virulence genes vacA s1, vacA m1, cagA and babA2 simultaneously. These findings will provide valuable information for disease diagnosis and treatment.
机译:幽门螺杆菌(H. pylori)感染是严重的人类健康威胁。传统测试技术指导的透视H.幽门治疗范式导致抗生素抗性。在这里,我们改进了QPCR方法,为精密H.幽门诊断和治疗提供了技术支持。设计了两对靶向GLMM基因的引物和探针以检测H. Pylori,并建立多重QPCR方法进行毒力因子检测。然后,在2017年从中国新桥医院收集的141标本中进行了快速的脲酶测试(RUT),培养和QPCR,以评估QPCR探测能力。最后,通过QPCR检测到幽门螺杆菌传染量和毒力基因。 1.与使用一对引物的QPCR相比,使用两对引物的改进QPCR方法具有较高的检测率(100%)和更好的精度(P?= 0.000)。它也与细菌培养相比的份额比与车辙(Kappa = 0.440,p≤0.001)。 2.幽门螺杆菌传染量与语料库中的胃炎显着呈正相关(p?= 0.003)和胃腐蚀(p?= 0.043)。胃预态患者的H.幽门螺杆菌传染量显着低于H.幽门阳性患者(P?<β05),传染性H. Pylori-Vaca S1量明显大于H. Pylori- vaca s1-(p?<?0.05)。 3. VACA S1频率显着高于慢性浅表胃炎(P?= 0.000),消化性溃疡(P?= 0.037)和胃腐蚀(P?= 0.009)。 H. Pylori-Vaca / Caga / Baba2频率显示出显着的正相关(P?<?0.05)。 H.幽门螺杆菌传染量和H.幽门螺杆菌毒力因子的存在表现出与胃病的复杂相关性和发育。具有良好检测性能的改进QPCR可用于同时定量H.幽门螺杆检测和检测毒力基因Vaca S1,Vaca M1,Caga和Baba2。这些调查结果将为疾病诊断和治疗提供有价值的信息。

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