Blackwood Christopher B, Oaks Adam, Buyer Jeffrey S
School of Natural Resources and the Environment, University of Michigan, 440 Church St., Ann Arbor, MI 48109-1041, USA.
Appl Environ Microbiol. 2005 Oct;71(10):6193-8. doi: 10.1128/AEM.71.10.6193-6198.2005.
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.
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。