首页> 外文期刊>Journal of food protection >Researhc Note: An Oligonucleotide-Ligation Assay for the Differentiation Between Cyclospora and Eimeria spp. Polymerase Chain Reaction Amplification Products.
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Researhc Note: An Oligonucleotide-Ligation Assay for the Differentiation Between Cyclospora and Eimeria spp. Polymerase Chain Reaction Amplification Products.

机译:研究注:区分环孢菌和艾美球虫属的寡核苷酸连接法。聚合酶链反应扩增产物。

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摘要

An oligonucleotide-ligation assay (OLA) was developed and compared to a restriction fragment length polymrphism (RFLP) test for distinguishing between 294-bp polymerase chain reaction (PCR) amplification products of the 18S rRNA gene from Cyclospora and Eimeria spp. The PCR/OLA correctly distinguished between there Cyclospora, three E. Tenella, and one E. mitis strains and the ratio of positive to negative spectrophotometric absorbance (A_490) values for each strain ranged form 4.086 to 15.280 (median 9.5). PCR/OLA provides a rapid, reliable, spectrophotometric alternative to PCR/RFLP.
机译:开发了寡核苷酸连接测定法(OLA),并将其与限制性片段长度多态性(RFLP)测试进行了比较,以区分Cyclospora和Eimeria spp的18S rRNA基因的294-bp聚合酶链反应(PCR)扩增产物。 PCR / OLA正确地区分了这三个环孢菌,三个大肠杆菌和一个大肠杆菌,每个菌株的正负分光光度吸收比(A_490)值范围为4.086至15.280(中位数9.5)。 PCR / OLA提供了一种快速,可靠的分光光度法替代PCR / RFLP。

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