Department of Biotechnology, Chemistry and Environmental Engineering, Aalborg University, Aalborg, Denmark.
ISME J. 2012 Jun;6(6):1094-106. doi: 10.1038/ismej.2011.176. Epub 2011 Dec 15.
Enhanced biological phosphorus removal (EBPR) is widely used for removal of phosphorus from wastewater. In this study, a metagenome (18.2 Gb) was generated using Illumina sequencing from a full-scale EBPR plant to study the community structure and genetic potential. Quantitative fluorescence in situ hybridization (qFISH) was applied as an independent method to evaluate the community structure. The results were in qualitative agreement, but a DNA extraction bias against gram positive bacteria using standard extraction protocols was identified, which would not have been identified without the use of qFISH. The genetic potential for community function showed enrichment of genes involved in phosphate metabolism and biofilm formation, reflecting the selective pressure of the EBPR process. Most contigs in the assembled metagenome had low similarity to genes from currently sequenced genomes, underlining the need for more reference genomes of key EBPR species. Only the genome of 'Candidatus Accumulibacter', a genus of phosphorus-removing organisms, was closely enough related to the species present in the metagenome to allow for detailed investigations. Accumulibacter accounted for only 4.8% of all bacteria by qFISH, but the depth of sequencing enabled detailed insight into their microdiversity in the full-scale plant. Only 15% of the reads matching Accumulibacter had a high similarity (>95%) to the sequenced Accumulibacter clade IIA strain UW-1 genome, indicating the presence of some microdiversity. The differences in gene complement between the Accumulibacter clades were limited to genes for extracellular polymeric substances and phage-related genes, suggesting a selective pressure from phages on the Accumulibacter diversity.
强化生物除磷 (EBPR) 被广泛用于从废水中去除磷。在这项研究中,使用 Illumina 测序从一个全规模的 EBPR 工厂生成了一个宏基因组(18.2 Gb),以研究群落结构和遗传潜力。定量荧光原位杂交 (qFISH) 被用作评估群落结构的独立方法。结果在定性上是一致的,但使用标准提取方案对革兰氏阳性菌的 DNA 提取存在偏差,如果不使用 qFISH,这种偏差将不会被识别。群落功能的遗传潜力显示出参与磷酸盐代谢和生物膜形成的基因富集,反映了 EBPR 过程的选择压力。组装的宏基因组中的大多数 contigs 与当前测序的基因组中的基因相似度较低,这突显了需要更多关键 EBPR 物种的参考基因组。只有“Candidatus Accumulibacter”的基因组,即除磷生物的一个属,与宏基因组中存在的物种足够接近,允许对其进行详细研究。Accumulibacter 通过 qFISH 仅占所有细菌的 4.8%,但测序的深度使我们能够深入了解它们在全规模工厂中的微观多样性。只有 15%与 Accumulibacter 匹配的读数与测序的 Accumulibacter 聚类 IIA 菌株 UW-1 基因组具有高度相似性(>95%),表明存在一些微观多样性。Accumulibacter 聚类之间的基因补充差异仅限于细胞外聚合物和噬菌体相关基因,表明噬菌体对 Accumulibacter 多样性存在选择压力。