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作 者:高世同[1] 李晓恒[1] 耿艺介[1] 谢旭[1] 梅树江[1] 黄达娜[1]
机构地区:[1]深圳市疾病预防控制中心传染病监控重点实验室,深圳518055
出 处:《中华地方病学杂志》2016年第9期636-639,共4页Chinese Journal of Endemiology
摘 要:目的基于线粒体16SrDNA序列对深圳水库区双脐螺进行分子鉴定。方法以双脐螺基因组DNA为模板,聚合酶链反应扩增16SrDNA目的基因片段,并以pMDl8.T载体克隆后进行序列测定,采用BLAST和MEGA4软件分析序列特征。结果双脐螺线粒体16SrDNA扩增片段大小约为466bp:测定序列与GenBank中1株巴西藁杆双脐螺(Biomphalaria straminea,B.straminea)同源性为99%;与3株库恩双脐螺(B.kuhniana)同源性均为98%;与1株中介双脐螺(B.intermedia)和1株双脐螺(B.edisoni)的同源性分别为95%和94%。深圳水库区2株双脐螺与巴西藁杆双脐螺(序列号AY030213.1)的遗传距离为O:基于16SrDNA序列,采用MEGA4软件作系统发生分析,以邻位连接法(NJ)和非加权组平均法(UPGMA)构建的系统发生树,水库区双脐螺与该藁杆双脐螺属于同一个分支。结论根据16SrDNA序列特征,深圳水库区双脐螺可归类为藁杆双脐螺。Objective To identify the species of Biomphalaria snails collected in Shenzhen reservoir, based on the mitochondrial 16S rDNA sequences. Methods The 16S rDNA fragments were amplified by PCR from the genome DNA of Biomphalaria snails, and inserted in plasmid pMD-18T for sequencing. The sequence of 16S rDNA fragment and its phylogenetic relationships with those of other species of Biomphalaria snails were analyzed with BLAST and MEGA4 software. Results The amplified 16S rDNA fragment of the Biomphalaria snails was about 466 bp in length. As aligned with the corresponding sequences of the related Biomphalaria species, the identity of nucleotides was 99% with 1 isolate of Biomphalaria straminea (B. straminea), 98% with 3 isolates of B. kuhniana, 95% with 1 isolate of B. intermedia, and 94% with 1 isolate of B. edisoni. Based on the 16S rDNA sequence, the results of phylogenetic analysis with neighbor-joining (N J) and unweighted pair-group method with arithmetic means (UPGMA) indicated that the snails had close genetic relationships with the B. straminea isolate (Genbank accession NO.AY030213.1) Conclusion The Biomphalaria snails collected in Shenzhen reservoir could be classified as B. straminea based on the characteristics of 16S rDNA sequence.
分 类 号:R383.2[医药卫生—医学寄生虫学]
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