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微小隐孢子虫、肠内 septata 菌和米氏艾美球虫的核糖体 RNA 序列:系统发育构建与结构对应关系

Ribosomal RNA sequences of Enterocytozoon bieneusi, Septata intestinalis and Ameson michaelis: phylogenetic construction and structural correspondence.

作者信息

Zhu X, Wittner M, Tanowitz H B, Cali A, Weiss L M

机构信息

Department of Pathology, Albert Einstein College of Medicine, Bronx, New York 10461.

出版信息

J Eukaryot Microbiol. 1994 May-Jun;41(3):204-9. doi: 10.1111/j.1550-7408.1994.tb01498.x.

DOI:10.1111/j.1550-7408.1994.tb01498.x
PMID:8049683
Abstract

The microsporidian species Enterocytozoon bieneusi, Septata intestinalis and Ameson michaelis were compared by using sequence data of their rRNA gene segments, which were amplified by polymerized chain reaction and directly sequenced. The forward primer 530f (5'-GTGCCATCCAGCCGCGG-3') was in the small subunit rRNA (SSU-rRNA) and the reverse primer 580r (5'-GGTCCGTGTTTCAAGACGG-3') was in the large subunit rRNA (LSU-rRNA). We have utilized these sequence data, the published data on Encephalitozoon cuniculi and Encephalitozoon hellem and our cloned SSU-rRNA genes from E. bieneusi and S. intestinalis to develop a phylogenetic tree for the microsporidia involved in human infection. The higher sequence similarities demonstrated between S. intestinalis and E. cuniculi support the placement of S. intestinalis in the family Encephalitozoonidae. This method of polymerized chain reaction rRNA phylogeny allows the establishment of phylogenetic relationships on limiting material where culture and electron microscopy are difficult or impossible and can be applied to archival material to expand the molecular phylogenetic analysis of the phylum Microspora. In addition, the highly variable region (E. coli numbering 590-650) and intergenic spacer regions in the microsporidia were noted to have structural correspondence, suggesting the possibility that they are coevolving.

摘要

通过聚合酶链反应扩增并直接测序,利用其核糖体RNA(rRNA)基因片段的序列数据,对微孢子虫物种肠脑炎微孢子虫、肠 septata 和米氏阿梅森微孢子虫进行了比较。正向引物530f(5'-GTGCCATCCAGCCGCGG-3')位于小亚基rRNA(SSU-rRNA)中,反向引物580r(5'-GGTCCGTGTTTCAAGACGG-3')位于大亚基rRNA(LSU-rRNA)中。我们利用这些序列数据、已发表的关于兔脑炎微孢子虫和海伦脑炎微孢子虫的数据以及我们从肠脑炎微孢子虫和肠 septata 克隆的SSU-rRNA基因,构建了涉及人类感染的微孢子虫的系统发育树。肠 septata 和兔脑炎微孢子虫之间较高的序列相似性支持将肠 septata 归入脑炎微孢子虫科。这种聚合酶链反应rRNA系统发育方法能够在难以或无法进行培养和电子显微镜观察的有限材料上建立系统发育关系,并且可以应用于存档材料,以扩展对微孢子虫门的分子系统发育分析。此外,注意到微孢子虫中的高变区(大肠杆菌编号590-650)和基因间隔区具有结构对应性,这表明它们可能在共同进化。

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