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“Candidatus Accumulibacter” Population Structure in Enhanced Biological Phosphorus Removal Sludges as Revealed by Polyphosphate Kinase Genes▿

机译:多磷酸盐激酶基因揭示的增强型生物除磷污泥中的“ Candidatus Accumulibacter”种群结构Structure

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摘要

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.
机译:我们使用聚磷酸盐激酶1基因(ppk1)作为遗传标记,研究了增强型生物除磷(EBPR)系统中“细小球菌”谱系的小规模种群结构。我们从一个实验室规模的和几个完整规模的EBPR系统中检索了“ Candidatus Accumulibacter” 16S rRNA和ppk1基因的片段。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可以提供更高的系统发育分辨率和更清晰的树形拓扑结构,因此,与16S rRNA相比,它是更好的遗传标记,可揭示“ Candidatus Accumulibacter”谱系中的种群结构。通过ppk1靶向PCR回收了至少5个进化枝“ Candidatus Accumulibacter”进化枝的序列,随后设计了特异性引物对每个进化枝的ppk1基因进行靶向。开发了使用“ Candidatus Accumulibacter”特异的16S rRNA和“ Candidatus Accumulibacter” clade特异的ppk1引物的定量实时PCR(qPCR)分析,并在三个实验室规模和九个全规模EBPR样品以及两个全规模非EBPR样品上进行-EBPR样本,用于确定“累计阴茎细菌”谱系的丰度以及五个“累计阴茎细菌”进化枝的相对分布和丰度。基于qPCR的使用16S rRNA基因测量的“累计念珠菌”级分占细菌群落比例的估算值与使用ppk1测量的估算值没有显着差异,证明了ppk1作为检测所有细菌的遗传标记的能力目前定义的“ Candidatus Accumulibacter”进化枝。在不同的EBPR系统之间,以及在系统内的时间上,“累积杆菌”进化枝的相对分布都不同。我们的结果表明,“ Candidatus Accumulibacter”谱系比以前意识到的要多样化,并且谱系中的不同进化枝在生态学上是不同的。

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