Differentiation of amphistome species of cattle in Kerala by polymerase chain reaction - restriction fragment length polymorphism

K. Thulasi, K. Devada, H. Shameem, Naicy Thomas, K. K. Jayavardhanan
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引用次数: 0

Abstract

The present study evaluated the PCR-RFLP of ITS-2+genes for species differentiation of three major amphistomes namely Gastrothylax crumenifer, Fischoederius cobboldi and Paramphistomum spp. Molecular analysis using PCR yielded amplicons of 515 bp for each species. The nucleotide differences among the sequences of the three species of amphistomes at different positions were further used for designing suitable RFLP. The amphistome parasites were distinguished taking into account the differences in the recognition sequences of TspRI on the ITS-2+ region by PCR-RFLP. The enzyme cleaved F.cobboldi at two recognition sites, CAGTG and CACTG and yielded 331, 93 and 91 bp products. Gastrothylax crumenifer had one recognition site CAGTG and resulted in 331 bp and 184 bp fragments. Since no recognition sequence was found in Paramphistomum spp., there was no cleavage. It is concluded that PCRRFLP was a promising molecular tool for species identification of amphistomes.
聚合酶链反应-限制性片段长度多态性对喀拉拉邦牛类的鉴别
本研究利用ITS-2+基因的PCR- rflp对三种主要两栖动物(Gastrothylax crumenifer, Fischoederius cobboldi和Paramphistomum spp)的物种分化进行了分析,结果显示每种物种的ITS-2+基因扩增量均为515 bp。利用三种两栖动物不同位置序列的核苷酸差异进一步设计合适的RFLP。利用TspRI在ITS-2+区识别序列的差异,采用PCR-RFLP方法对两类两栖寄生虫进行区分。该酶在两个识别位点CAGTG和CACTG上裂解f.c oboldi,得到331、93和91 bp的产物。胃蕨有一个识别位点CAGTG,分别产生331 bp和184 bp的片段。由于在副胃中未发现识别序列,因此不存在卵裂。PCRRFLP是一种很有前途的两栖动物物种鉴定分子工具。
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