Isenbarger Thomas A, Finney Michael, Ríos-Velázquez Carlos, Handelsman Jo, Ruvkun Gary
Department of Bacteriology, University of Wisconsin-Madison, 1550 Linden Drive, Madison, WI 53706-1521, USA.
Appl Environ Microbiol. 2008 Feb;74(3):840-9. doi: 10.1128/AEM.01933-07. Epub 2007 Dec 14.
Molecular methods based on the 16S rRNA gene sequence are used widely in microbial ecology to reveal the diversity of microbial populations in environmental samples. Here we show that a new PCR method using an engineered polymerase and 10-nucleotide "miniprimers" expands the scope of detectable sequences beyond those detected by standard methods using longer primers and Taq polymerase. After testing the method in silico to identify divergent ribosomal genes in previously cloned environmental sequences, we applied the method to soil and microbial mat samples, which revealed novel 16S rRNA gene sequences that would not have been detected with standard primers. Deeply divergent sequences were discovered with high frequency and included representatives that define two new division-level taxa, designated CR1 and CR2, suggesting that miniprimer PCR may reveal new dimensions of microbial diversity.
基于16S rRNA基因序列的分子方法在微生物生态学中被广泛应用,以揭示环境样本中微生物种群的多样性。我们在此表明,一种使用工程化聚合酶和10核苷酸“微型引物”的新型PCR方法,将可检测序列的范围扩展到了使用更长引物和Taq聚合酶的标准方法所能检测的序列之外。在计算机模拟中测试该方法以鉴定先前克隆的环境序列中的 divergent核糖体基因后,我们将该方法应用于土壤和微生物垫样本,发现了一些用标准引物无法检测到的新型16S rRNA基因序列。高频发现了深度 divergent序列,其中包括定义了两个新的门级分类群(命名为CR1和CR2)的代表序列,这表明微型引物PCR可能揭示微生物多样性的新维度。