首页> 外文期刊>The Korean Journal of Parasitology >Sensitive and Rapid Detection of Giardia lamblia Infection in Pet Dogs using Loop-Mediated Isothermal Amplification
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Sensitive and Rapid Detection of Giardia lamblia Infection in Pet Dogs using Loop-Mediated Isothermal Amplification

机译:使用回路介导的等温扩增灵敏和快速检测宠物狗中的贾第鞭毛虫感染

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Giardia lamblia is recognized as one of the most prevalent parasites in dogs. The present study aimed to establish a loop-mediated isothermal amplification (LAMP) assay for rapid and specific detection of G. lamblia from dogs. The fecal samples were collected and prepared for microscopic analysis, and then the genomic DNA was extracted directly from purified cysts. The concentration of DNA samples of G. lamblia were diluted by 10-fold serially ranging from 10-1 to 10-5 ng/μl for LAMP and PCR assays. The LAMP assay allows the amplification to be finished within 60 min under isothermal conditions of 63℃ by employing 6 oligonucleotide primers designed based on G. lamblia elongation factor 1 alpha (EF1α) gene sequence. Our tests showed that the specific amplification products were obtained only with G. lamblia, while no amplification products were detected with DNA of other related protozoans. Sensitivity evaluation indicated that the LAMP assay was sensitive 10 times more than PCR. It is concluded that LAMP is a rapid, highly sensitive and specific DNA amplification technique for detection of G. lamblia, which has implications for effective control and prevention of giardiasis.
机译:贾第鞭毛虫被认为是犬中最普遍的寄生虫之一。本研究旨在建立一种循环介导的等温扩增(LAMP)测定法,用于从狗中快速,特异性地检测出兰氏菌。收集粪便样品并准备进行显微镜分析,然后直接从纯化的囊肿中提取基因组DNA。以10 sup -1 到10 s -5 ng s /μl的浓度连续10倍稀释兰氏革兰氏菌DNA样品,以进行LAMP和PCR分析。通过使用基于兰伯氏菌延伸因子1α(EF1α)基因序列设计的6个寡核苷酸引物,LAMP分析可在63℃等温条件下在60分钟内完成扩增。我们的测试表明,特异性扩增产物仅通过兰氏菌获得,而其他相关原生动物的DNA未检测到扩增产物。敏感性评估表明,LAMP测定的灵敏度是PCR的10倍。结论是,LAMP是一种快速,高度灵敏和特异的DNA扩增技术,用于检测兰氏假单胞菌,对有效控制和预防贾第鞭毛虫病具有重要意义。

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