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使用改良引物通过实时聚合酶链反应检测溃疡分枝杆菌

Detection of Mycobacterium ulcerans by real-time PCR with improved primers.

作者信息

Shinoda Noriko, Nakamura Hajime, Watanabe Mineo

机构信息

Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641 Japan.

Research Institute of Tuberculosis, Japan Anti-Tuberculosis Association, 3-1-24 Matsuyama, Kiyose, Tokyo 204-8533 Japan.

出版信息

Trop Med Health. 2016 Aug 19;44(1):28. doi: 10.1186/s41182-016-0028-3. eCollection 2016.

Abstract

BACKGROUND

Buruli ulcer is a severe skin disease caused by Mycobacterium ulcerans. Real-time PCR targeting the IS2404 sequence has been used as a reliable and rapid method for the diagnosis of Buruli ulcer and detection of M. ulcerans in the environment. The genome of M. ulcerans contains hundreds of IS2404 copies, which have variability in certain sequences. Therefore, the design of new primers specific to conserved IS2404 regions may potentially improve the sensitivity of M. ulcerans detection and, consequently, the diagnosis of Buruli ulcer, thus ensuring timely treatment of the disease.

RESULTS

In silico analysis indicates that DNA sequences of the IS2404 elements are highly variable within a single strain. As the binding sites of conventional IS2404-specific primers used for M. ulcerans detection contain polymorphic sequences, we designed new primers, which enabled the detection of M. ulcerans by real-time PCR with higher sensitivity and similar specificity with respect to that of conventional primers. However, the increase in sensitivity with the new primers depended on the M. ulcerans strain.

CONCLUSIONS

The results suggest that real-time PCR based on the new primers could improve Buruli ulcer diagnosis and M. ulcerans detection in environmental samples.

摘要

背景

布鲁里溃疡是由溃疡分枝杆菌引起的一种严重皮肤病。针对IS2404序列的实时PCR已被用作诊断布鲁里溃疡和检测环境中溃疡分枝杆菌的可靠且快速的方法。溃疡分枝杆菌的基因组包含数百个IS2404拷贝,这些拷贝在某些序列上存在变异性。因此,设计针对保守IS2404区域的新引物可能会提高溃疡分枝杆菌检测的灵敏度,进而改善布鲁里溃疡的诊断,从而确保对该疾病的及时治疗。

结果

电子分析表明,IS2404元件的DNA序列在单个菌株内高度可变。由于用于检测溃疡分枝杆菌的传统IS2404特异性引物的结合位点包含多态性序列,我们设计了新引物,通过实时PCR检测溃疡分枝杆菌时,其灵敏度更高,特异性与传统引物相似。然而,新引物灵敏度的提高取决于溃疡分枝杆菌菌株。

结论

结果表明,基于新引物的实时PCR可改善布鲁里溃疡的诊断以及环境样本中溃疡分枝杆菌的检测。

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