Schnitzler B E, Thebo P L, Tomley F M, Uggla A, Shirley M W
Department of Parasitology, Swedish University of Agricultural Sciences & National Veterinary Institute, Uppsala, Sweden.
Avian Pathol. 1999 Feb;28(1):89-93. doi: 10.1080/03079459995091.
A polymerase chain reaction (PCR) assay, based on the amplification of internal transcribed spacer 1 (ITS1) regions of ribosomal DNA, was developed for the chicken coccidian species Eimeria maxima, E. mitis and E. praecox. Thus, taking into account our previous work, a complete set of ITS1-based, species-specific primers for the detection and discrimination of all seven Eimeria species that infect the domestic fowl is now available. ITS1 primers for each of these seven species of Eimeria were also used as capture probes in a paper chromatography assay (PACHA). The addition of PACHA to the PCR assay provided a faster, more simplified read-out compared to staining of amplified bands in an agarose gel with ethidium bromide.
基于核糖体DNA内部转录间隔区1(ITS1)区域的扩增,开发了一种聚合酶链反应(PCR)检测方法,用于检测鸡球虫种类巨型艾美耳球虫、微小艾美耳球虫和早熟艾美耳球虫。因此,考虑到我们之前的工作,现在已有一套完整的基于ITS1的物种特异性引物,用于检测和区分感染家鸡的所有七种艾美耳球虫。这七种艾美耳球虫各自的ITS1引物也被用作纸色谱分析(PACHA)中的捕获探针。与用溴化乙锭对琼脂糖凝胶中的扩增条带进行染色相比,在PCR检测中加入PACHA可提供更快、更简化的读数。