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我国不同疫区杜氏利什曼原虫ITS-1片段序列的多态性分析 被引量:8

Sequence polymorphism analysis of the ITS-1 gene of Leishmania donovani isolates from different epidemic foci in China
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摘要 目的确定rDNA的内转录间隔区Ⅰ(ITS-1)是否可作为我国杜氏利什曼原虫(Leishmania donovani)分类的分子遗传标记。方法对我国不同疫区杜氏利什曼原虫分离株(L.d.SD1、L.d.SC7、L.d.XJ3、L.d.JS12)的ITS-1进行PCR扩增、克隆、测序,并分析它们的ITS-1序列多态性。结果 4个不同疫区的利什曼原虫分离株(L.d.SD1、L.d.SC7、L.d.XJ3、L.d.JS12)经PCR均扩增出一条约320bp的ITS-1片段,其序列大小分别为:317bp、323bp、317bp、316bp。序列分析表明:序列之间在多处位点发生了不同类型的突变,存在明显的序列多态性,其中伽师县突变的频率最为频繁,序列多态性最为显著。结论 ITS-1可以作为Leishmania donovani种内分类的分子遗传标记,有利于我国内脏利什慢原虫病的防治、诊断和治疗。 Objective To determine whether the first internal transcribed spacer ( ITS-1) of ribosomal DNA ( rDNA) could be used as a genetic marker of Leishmania donovani with different geographic origins in China.Methods The ITS-1 rDNA from L.d.SD1 isolate,L.d.SC7 isolate,L.d.XJ3 isolate,and L.d.JS12 isolate was amplified by PCR,cloned,sequenced,and then analyzed for sequence polymorphism.Results ITS-1 from L.d.SD1 isolate,L.d.SC7 isolate,L.d.XJ3 isolate,and L.d.JS12 isolate had a sequence size of 317 bp,323 bp,317 bp,and 316 bp,respectively.Different types of mutations occurred in the four sequences of ITS-1.Mutation of the ITS-1 from L.d.JS12 isolate in particular was the most frequent and its sequence polymorphism was the most significant.Conclusion ITS-1 can serve as a molecular genetic marker of Leishmania donovani with different geographic origins in China.
出处 《中国病原生物学杂志》 CSCD 2010年第7期520-523,共4页 Journal of Pathogen Biology
基金 中国医学科学院病原生物所资助项目
关键词 杜氏利什慢原虫 PCR 内转录间隔区Ⅰ 序列多态性分析 Leishmania donovani PCR first internal transcribed spacer ( ITS-1) sequence polymorphism analysis
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  • 1Chu, Li CP, Ho HY. The first internal transcribed spacer(ITS-I) of ribosomalDNA as amolecular marker for phylogenetic analyses in Crustacea[J]. Marine Biotechnology, 2001,3 : 355-61.
  • 2李一明,管立人.陇南、川北山区黑热病的调查报告[J].中国寄生虫病防治杂志,1990,3(1):13-16. 被引量:15
  • 3Smyth AJ,Ghosh A, Hassan MQ,et al. Rapid and sensitive detection of Leishmania kinetoplast DNA from spleen and blood sampies of kala-azar patients[J]. Parasitology, 1992,105 : 183.
  • 4Fairlamb AH, Weisogel PD, Hoejmakers JHJ, et al. Isolation and characterization of kinetoplast DNA from blood stream of Trypanosoma bruucei [J]. J Cell Biol, 1978,76 : 293-309.
  • 5Nasereddin A, Hermano EB, Charles LJ. Molecular diagnosis of old world cutaneous leishmaniasis and species identification by use of a reverse line blothybridization assay[J]. J Clin Microbiol, 2008,9: 2848-55.
  • 6Berzunza-Cruz M, Cabrera N, Crippa-Rossi M, et al. Polymorphism analysis of the internaltranscribed spacer and small subunit of ribosomal RNA genes of Leishmania mexicana [J]. Parasitol, 2002,88: 918-25.
  • 7周荣琼,李国清,肖淑敏,郭远忠,夏艳勋,林瑞庆,朱兴全.安氏隐孢子虫ITS-1序列的PCR扩增、克隆及分析[J].中国预防兽医学报,2005,27(5):369-372. 被引量:7
  • 8翁亚彪,谢德华,林瑞庆,李华文,张德林,吴绍强,朱兴全.弓形虫ITS及5.8S序列的PCR扩增、克隆及分析[J].畜牧兽医学报,2005,36(1):70-73. 被引量:16
  • 9温少芳,卢思奇,王凤云.蓝氏贾第鞭毛虫C2株rRNA基因ITS1-5.8SrDNA-ITS2序列测定与分析[J].首都医科大学学报,2005,26(6):769-770. 被引量:2

二级参考文献31

  • 1萨姆布鲁克J 拉塞尔DW 黄培堂 译.分子克隆实验指南[M](第3版)[M].北京:科学出版社,2002.463-465.
  • 2Zangerle A, Allerberger F, Pohl P, et al. High risk of developing toxoplasmic encephalitis in AIDS patients seropositive to Toxoplasma gondii [J]. Medical Microbiological Immunology, 1991, 180:59-66.
  • 3Gasser R B, Rossi L, Zhu X Q. Identification of Nematodirus species ( Nematoda: Molineidae) from wild ruminants in Italy using gentic markers in ribosomal DNA[J]. International Journal for Parasitology. 1999, 29: 1809-1817.
  • 4Zhu X Q, D'Amelio S, Paggi L, et al. Assessing sequence variation in the internal transcribed spacers of ribosomal DNA within and among members of the Contracaecum osculatum complex (Nematoda: Ascaridoidea: Anisakidae) [J]. Parasitology Research,2000, 86: 677-683.
  • 5Gasser R B, Zhu X Q, Beveridge I, et al. Mutation scanning analysis of sequence heterogenity in the second internal transcribed spacer (rDNA) within some members of the Hypodontus rnacropi (Nematoda: Strongyloidea) complex[J]. Electrophoresis, 2001,22 :1076-1085.
  • 6Zhu X Q, Gasser R B, Chilton N B, et al. Molecular approaches for studying ascaridoid nematodes with zoonotic potential, with an emphasis on Toxocara Species (an invited review) [J]. Journal of Helminthology, 2001, 75: 101-108.
  • 7Zhu X Q, D'Amelio S, Palm H W, et al. SSCP-based identification of members within the Pseudoterranova decipiens complex (Nematoda : Ascaridoidea : Anisakidae) using gentic markers in the internal transcribed spacers of ribosomal DNA[J]. Parasitology. 2002, 124: 615-623.
  • 8Suzanne P, John E. Detection of Neospora caninum DNA by the polymerase chain reaction[J]. International Journal for Parasitology, 1996, 26 (4): 347-351.
  • 9Homan W L, Limper L, Verlaan M, et al. Comparison of the internal transcribed spacer, ITS 1, from Toxoplasma gondii isolates and Neospora caninum [J]. Parasitology Research, 1997, 83(3): 285-289.
  • 10Jauregui L H, Higgins J, Zarlenga D, et al. Development of a Real-Time PCR assay for detection of Toxoplasma gondii in pig and mouse tissues[J]. Journal of Clinical Microbiology,2001,39(6) :2065-2071.

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