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本文引用的文献

1
Terminal restriction pattern analysis of 16S rRNA genes for the characterization of bacterial communities of activated sludge.用于活性污泥细菌群落特征分析的16S rRNA基因末端限制性片段长度多态性分析
J Biosci Bioeng. 2000;90(2):148-56. doi: 10.1016/s1389-1723(00)80102-4.
2
ARB: a software environment for sequence data.ARB:一种用于序列数据的软件环境。
Nucleic Acids Res. 2004 Feb 25;32(4):1363-71. doi: 10.1093/nar/gkh293. Print 2004.
3
Review and re-analysis of domain-specific 16S primers.特定领域16S引物的综述与重新分析。
J Microbiol Methods. 2003 Dec;55(3):541-55. doi: 10.1016/j.mimet.2003.08.009.
4
Fidelity of select restriction endonucleases in determining microbial diversity by terminal-restriction fragment length polymorphism.通过末端限制性片段长度多态性分析确定微生物多样性时所选限制性内切酶的保真度
Appl Environ Microbiol. 2003 Aug;69(8):4823-9. doi: 10.1128/AEM.69.8.4823-4829.2003.
5
A census of rRNA genes and linked genomic sequences within a soil metagenomic library.土壤宏基因组文库中rRNA基因及相关基因组序列的普查。
Appl Environ Microbiol. 2003 May;69(5):2684-91. doi: 10.1128/AEM.69.5.2684-2691.2003.
6
Potential bias of fungal 18S rDNA and internal transcribed spacer polymerase chain reaction primers for estimating fungal biodiversity in soil.用于评估土壤中真菌生物多样性的真菌18S核糖体DNA和内转录间隔区聚合酶链反应引物的潜在偏差
Environ Microbiol. 2003 Jan;5(1):36-47. doi: 10.1046/j.1462-2920.2003.00383.x.
7
The Ribosomal Database Project (RDP-II): previewing a new autoaligner that allows regular updates and the new prokaryotic taxonomy.核糖体数据库项目(RDP-II):预览一种允许定期更新的新型自动比对工具和新的原核生物分类法。
Nucleic Acids Res. 2003 Jan 1;31(1):442-3. doi: 10.1093/nar/gkg039.
8
Molecular community analysis of microbial diversity.微生物多样性的分子群落分析
Curr Opin Biotechnol. 2002 Jun;13(3):213-7. doi: 10.1016/s0958-1669(02)00314-2.
9
Analysis of bacterial community composition by oligonucleotide fingerprinting of rRNA genes.通过rRNA基因的寡核苷酸指纹分析细菌群落组成。
Appl Environ Microbiol. 2002 Jul;68(7):3243-50. doi: 10.1128/AEM.68.7.3243-3250.2002.
10
Empirical and theoretical bacterial diversity in four Arizona soils.亚利桑那州四种土壤中的经验性和理论性细菌多样性。
Appl Environ Microbiol. 2002 Jun;68(6):3035-45. doi: 10.1128/AEM.68.6.3035-3045.2002.

用于一般微生物群落分析的门和类特异性PCR引物。

Phylum- and class-specific PCR primers for general microbial community analysis.

作者信息

Blackwood Christopher B, Oaks Adam, Buyer Jeffrey S

机构信息

School of Natural Resources and the Environment, University of Michigan, 440 Church St., Ann Arbor, MI 48109-1041, USA.

出版信息

Appl Environ Microbiol. 2005 Oct;71(10):6193-8. doi: 10.1128/AEM.71.10.6193-6198.2005.

DOI:10.1128/AEM.71.10.6193-6198.2005
PMID:16204538
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1265930/
Abstract

Amplification of a particular DNA fragment from a mixture of organisms by PCR is a common first step in methods of examining microbial community structure. The use of group-specific primers in community DNA profiling applications can provide enhanced sensitivity and phylogenetic detail compared to domain-specific primers. Other uses for group-specific primers include quantitative PCR and library screening. The purpose of the present study was to develop several primer sets targeting commonly occurring and important groups. Primers specific for the 16S ribosomal sequences of Alphaproteobacteria, Betaproteobacteria, Bacilli, Actinobacteria, and Planctomycetes and for parts of both the 18S ribosomal sequence and the internal transcribed spacer region of Basidiomycota were examined. Primers were tested by comparison to sequences in the ARB 2003 database, and chosen primers were further tested by cloning and sequencing from soil community DNA. Eighty-five to 100% of the sequences obtained from clone libraries were found to be placed with the groups intended as targets, demonstrating the specificity of the primers under field conditions. It will be important to reevaluate primers over time because of the continual growth of sequence databases and revision of microbial taxonomy.

摘要

通过聚合酶链式反应(PCR)从生物体混合物中扩增特定DNA片段是检测微生物群落结构方法中常见的第一步。与结构域特异性引物相比,在群落DNA分析应用中使用组特异性引物可提高灵敏度并提供系统发育细节。组特异性引物的其他用途包括定量PCR和文库筛选。本研究的目的是开发几套针对常见且重要类群的引物组。对靶向α-变形菌纲、β-变形菌纲、芽孢杆菌纲、放线菌纲和浮霉菌纲16S核糖体序列以及担子菌门18S核糖体序列和内部转录间隔区部分的特异性引物进行了检测。通过与ARB 2003数据库中的序列进行比较来测试引物,并通过从土壤群落DNA中克隆和测序对所选引物进行进一步测试。从克隆文库获得的序列中有85%至100%被发现与预期作为目标的类群归为一类,这证明了这些引物在田间条件下的特异性。由于序列数据库的不断增长和微生物分类学的修订,随着时间的推移重新评估引物将很重要。