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阴道毛滴虫dsRNA病毒部分基因的克隆与序列分析 被引量:3

Cloning and Sequence Analysis of a Partial Gene of Trichomonas vaginalis dsRNA Virus
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摘要 提取阴道毛滴虫总核酸为模板,根据GenBank中发表的阴道毛滴虫病毒序列(U08999,NC003873,NC003824,NC003834)设计1对简并引物,经RT-PCR得到与预计大小一致的PCR特异性产物,将其进行克隆、测序,得到目的基因片段长度为1454bp,与阴道毛滴虫病毒T1株(U08999)的序列同源性最高为82.9%。 A pair of degenerate primers were designed following the published nucleotide sequence of Trichomonas vaginalis virus(U08999, NC003873, NC003824, NC003834). Using the total nucleic acids extracted from the Trichomonas vaginalis as template, RT-PCR was performed with the primers to obtain a fragment of the TVV. The product was cloned, sequenced and compared with the sequences available in the GenBank. The size of the amplified gene was 1 454bp, which shares 82.9% sequence identity with the Trichoraonas vaginalis virus T1.
出处 《中国寄生虫学与寄生虫病杂志》 CAS CSCD 北大核心 2006年第5期389-390,共2页 Chinese Journal of Parasitology and Parasitic Diseases
基金 总后卫生部留学回国人员基金(No.98H025)~~
关键词 阴道毛滴虫 dsRNA病毒 克隆 序列分析 Trichomonas vaginalis dsRNA virus Cloning Sequencing
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同被引文献42

  • 1郭步平,李宇飞.不同pH肝浸汤培养基培养阴道毛滴虫的观察[J].中国病原生物学杂志,2006,1(1):20-21. 被引量:6
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