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首页> 外文期刊>Journal of Microbiological Methods >Group-specific PCR primers for the phylum Acidobacteria designed based on the comparative analysis of 16S rRNA gene sequences
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Group-specific PCR primers for the phylum Acidobacteria designed based on the comparative analysis of 16S rRNA gene sequences

机译:基于16S rRNA基因序列比较分析设计门酸菌群特异性PCR引物

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We performed a comprehensive phylogenetic analysis of the phylum Acidobacteria and developed novel, group-specific PCR primers for Acidobacteria and its class-level subgroups. Acidobacterial 16S rRNA gene sequences deposited in the RDP database were used to construct a local database then subsequently analyzed. A total of 556 phylotypes were observed and the majority of the phylotypes belonged to five major subgroups (subgroups 1, 2, 3, 4, and 6), which comprised >80% of the acidobacterial sequences in the RDP database. Phylum-specific and subgroup-specific primers were designed from the consensus sequences of the phylotype sequences, and the specificities of the designed primers were evaluated both in silico and empirically for coverage and tolerance. The phylum-specific primer ACIDO, which was designed in this study, showed increased coverage for Acidobacteria, as compared to the previous phylum-specific primer 31F. However, the tolerance of the primer ACIDO for non-target sequences was slightly higher than that of the primer 31F. We also developed subgroup-specific PCR primers for the major subgroups of Acidobacteria, except for subgroup 4. Subgroup-specific primers 51, 52, and S3, which targeted subgroups 1, 2, and 3, respectively, showed high coverage for their target subgroups and low tolerance for non-target sequences. However, the primer S6 targeting subgroup 6 showed a lower specificity in its empirical evaluation than expected from the in silica results. The subgroup-specific primers, as well as the phylum-specific primer designed in this study, will be valuable tools in understanding the phylogenetic diversity and ecological niche of the phylum Acidobacteria and its subgroups
机译:我们对门酸杆菌进行了全面的系统发育分析,并开发了针对酸杆菌及其类水平亚组的新型,组特异性PCR引物。 RDP数据库中存放的酸性细菌16S rRNA基因序列用于构建本地数据库,然后进行分析。总共观察到556个系统型,大多数系统型属于五个主要亚组(1、2、3、4和6个亚组),它们在RDP数据库中占酸性细菌序列的80%以上。从系统型序列的共有序列中设计了植物特异性引物和亚组特异性引物,并通过计算机和经验方法对设计引物的特异性进行了覆盖和耐受性评估。与先前的门类特异性引物31F相比,本研究中设计的门类特异性引物ACIDO显示出增加了对酸性细菌的覆盖率。然而,引物ACIDO对非靶序列的耐受性略高于引物31F。除亚组4外,我们还为嗜酸细菌的主要亚组开发了亚组特异性PCR引物。分别针对亚组1、2和3的亚组特异性引物51、52和S3对它们的目标亚组具有较高的覆盖率对非目标序列的耐受性较低。然而,靶向亚组6的引物S6在其经验评估中显示的特异性低于二氧化硅结果中预期的特异性。亚组特异性引物以及本研究设计的门特异性引物,将成为了解门酸杆菌及其亚组的系统发育多样性和生态位的有价值的工具。

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