Nkouawa Agathe, Sako Yasuhito, Okamoto Munehiro, Ito Akira
Department of Parasitology, Asahikawa Medical University, Asahikawa, Japan; Medical Research Centre, Institute of Medical Research and Medicinal Plants Studies (IMPM), Ministry of Scientific Research and Innovation, Yaoundé, Cameroon; Center for Human Evolution Modeling Research, Primate Research Institute, Kyoto University, Inuyama, Japan
Department of Parasitology, Asahikawa Medical University, Asahikawa, Japan; Medical Research Centre, Institute of Medical Research and Medicinal Plants Studies (IMPM), Ministry of Scientific Research and Innovation, Yaoundé, Cameroon; Center for Human Evolution Modeling Research, Primate Research Institute, Kyoto University, Inuyama, Japan.
Am J Trop Med Hyg. 2016 Jun 1;94(6):1318-23. doi: 10.4269/ajtmh.15-0829. Epub 2016 Apr 4.
For differential detection of Taenia solium, Taenia saginata, and Taenia asiatica, loop-mediated isothermal amplification (LAMP) assay targeting the cytochrome c oxidase subunit 1 gene has been recently developed and shown to be sensitive, specific, and effective. However, to achieve differential identification, one specimen requires three reaction mixtures containing a primer set of each Taenia species separately, which is complex and time consuming and increases the risk of cross-contamination. In this study, we developed a simple differential identification of human Taenia species using multiplex LAMP (mLAMP) in combination with dot enzyme-linked immunosorbent assay (dot-ELISA). Forward inner primers of T. solium, T. saginata, and T. asiatica labeled with fluorescein isothiocyanate (FITC), digoxigenin (DIG), and tetramethylrhodamine (TAMRA), respectively, and biotin-labeled backward inner primers were used in mLAMP. The mLAMP assay succeeded in specific amplification of each respective target gene in a single tube. Furthermore, the mLAMP product from each species was easily distinguished by dot-ELISA with an antibody specific for FITC, DIG, or TAMRA. The mLAMP assay in combination with dot-ELISA will make identification of human Taenia species simpler, easier, and more practical.
为了对猪带绦虫、牛带绦虫和亚洲带绦虫进行鉴别检测,最近开发了一种针对细胞色素c氧化酶亚基1基因的环介导等温扩增(LAMP)检测方法,该方法已被证明具有灵敏性、特异性和有效性。然而,为了实现鉴别鉴定,一个样本需要三个反应混合物,分别包含每种带绦虫物种的一组引物,这既复杂又耗时,还增加了交叉污染的风险。在本研究中,我们开发了一种简单的方法,通过多重LAMP(mLAMP)结合斑点酶联免疫吸附测定(dot-ELISA)来鉴别人类带绦虫物种。猪带绦虫、牛带绦虫和亚洲带绦虫的正向内引物分别用异硫氰酸荧光素(FITC)、地高辛(DIG)和四甲基罗丹明(TAMRA)标记,生物素标记的反向内引物用于mLAMP。mLAMP检测成功地在单个管中特异性扩增了各自的目标基因。此外,通过使用针对FITC、DIG或TAMRA的特异性抗体的dot-ELISA,可以轻松区分每种物种的mLAMP产物。mLAMP检测与dot-ELISA相结合将使人类带绦虫物种的鉴定更简单、更容易且更实用。