[核糖体DNA内转录间隔2序列作为旋毛虫线虫鉴定的系统发育标记]。

I M Odoyevskaya, S E Spiridonov
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引用次数: 0

摘要

通过对几种引物组合的测试,选择最佳引物组合扩增核糖体DNA内部转录间隔2 (ITS2)区域(直接引物:Tri58s f5 CGG TGG ATC RCT TGG CTC GTA CG和反向引物:AB28 Rr (CGA CCG CTT ATT GAT ATG C),得到900 bp的PCR产物。对来自俄罗斯联邦不同地区的8株旋毛虫分离株的ITS2序列进行比较分析,可以有效区分这些寄生线虫的不同种类和个体基因型。
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[RIBOSOMAL DNA INTERNAL TRANSCRIBED SPACER 2 SEQUENCE AS A PHYLOGENETIC MARKER FOR THE IDENTIFICATION OF TRICHINELLA NEMATODES].

The results of testing several primer combinations were used to choose an optimal pair for the amplification of the internal transcribed spacer 2 (ITS2) region of ribosomal DNA (direct: Tri58s F 5 CGG TGG ATC RCT TGG CTC GTA CG and reverse: AB28 Rr (CGA CCG CTT ATT GAT ATG C). This pair of primers yields a 900 bp PCR product. Comparative analysis of obtained ITS2 sequences, for 8 Trichinella isolates from different regions of the Russian Federation permits different species and individual genotypes of these parasitic nematodes to be validly distinguished.

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