He Shaomei, Gall Daniel L, McMahon Katherine D
Department of Civil and Environmental Engineering, University of Wisconsin-Madison, Madison, WI 53706, USA.
Appl Environ Microbiol. 2007 Sep;73(18):5865-74. doi: 10.1128/AEM.01207-07. Epub 2007 Aug 3.
We investigated the fine-scale population structure of the "Candidatus Accumulibacter" lineage in enhanced biological phosphorus removal (EBPR) systems using the polyphosphate kinase 1 gene (ppk1) as a genetic marker. We retrieved fragments of "Candidatus Accumulibacter" 16S rRNA and ppk1 genes from one laboratory-scale and several full-scale EBPR systems. Phylogenies reconstructed using 16S rRNA genes and ppk1 were largely congruent, with ppk1 granting higher phylogenetic resolution and clearer tree topology and thus serving as a better genetic marker than 16S rRNA for revealing population structure within the "Candidatus Accumulibacter" lineage. Sequences from at least five clades of "Candidatus Accumulibacter" were recovered by ppk1-targeted PCR, and subsequently, specific primer sets were designed to target the ppk1 gene for each clade. Quantitative real-time PCR (qPCR) assays using "Candidatus Accumulibacter"-specific 16S rRNA and "Candidatus Accumulibacter" clade-specific ppk1 primers were developed and conducted on three laboratory-scale and nine full-scale EBPR samples and two full-scale non-EBPR samples to determine the abundance of the total "Candidatus Accumulibacter" lineage and the relative distributions and abundances of the five "Candidatus Accumulibacter" clades. The qPCR-based estimation of the total "Candidatus Accumulibacter" fraction as a proportion of the bacterial community as measured using 16S rRNA genes was not significantly different from the estimation measured using ppk1, demonstrating the power of ppk1 as a genetic marker for detection of all currently defined "Candidatus Accumulibacter" clades. The relative distributions of "Candidatus Accumulibacter" clades varied among different EBPR systems and also temporally within a system. Our results suggest that the "Candidatus Accumulibacter" lineage is more diverse than previously realized and that different clades within the lineage are ecologically distinct.
我们以多聚磷酸盐激酶1基因(ppk1)作为遗传标记,研究了强化生物除磷(EBPR)系统中“候选聚磷菌属”谱系的精细种群结构。我们从一个实验室规模和几个全规模的EBPR系统中获取了“候选聚磷菌属”16S rRNA和ppk1基因的片段。使用16S rRNA基因和ppk1重建的系统发育在很大程度上是一致的,ppk1具有更高的系统发育分辨率和更清晰的树形拓扑结构,因此作为一种遗传标记,在揭示“候选聚磷菌属”谱系内的种群结构方面比16S rRNA更好。通过靶向ppk1的PCR回收了至少五个“候选聚磷菌属”进化枝的序列,随后,针对每个进化枝设计了靶向ppk1基因的特异性引物组。使用“候选聚磷菌属”特异性16S rRNA和“候选聚磷菌属”进化枝特异性ppk1引物开发了定量实时PCR(qPCR)检测方法,并在三个实验室规模和九个全规模的EBPR样品以及两个全规模非EBPR样品上进行检测,以确定“候选聚磷菌属”总谱系的丰度以及五个“候选聚磷菌属”进化枝的相对分布和丰度。基于qPCR对使用16S rRNA基因测量的细菌群落中“候选聚磷菌属”总比例的估计与使用ppk1测量的估计没有显著差异,这证明了ppk1作为检测所有当前定义的“候选聚磷菌属”进化枝的遗传标记的能力。“候选聚磷菌属”进化枝的相对分布在不同的EBPR系统之间以及系统内随时间而变化。我们的结果表明,“候选聚磷菌属”谱系比之前认识到的更加多样化,并且该谱系内的不同进化枝在生态上是不同的。