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Impact of Bioreactor Environment and Recovery Method on the Profile of Bacterial Populations from Water Distribution Systems

机译:生物反应器环境和回收方法对配水系统细菌种群分布的影响

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摘要

Multiple rotating annular reactors were seeded with biofilms flushed from water distribution systems to assess (1) whether biofilms grown in bioreactors are representative of biofilms flushed from the water distribution system in terms of bacterial composition and diversity, and (2) whether the biofilm sampling method affects the population profile of the attached bacterial community. Biofilms were grown in bioreactors until thickness stabilized (9 to 11 weeks) and harvested from reactor coupons by sonication, stomaching, bead-beating, and manual scraping. High-throughput sequencing of 16S rRNA amplicons was used to profile bacterial populations from flushed biofilms seeded into bioreactors as well as biofilms recovered from bioreactor coupons by different methods. β diversity between flushed and reactor biofilms was compared to β diversity between (i) biofilms harvested from different reactors and (ii) biofilms harvested by different methods from the same reactor. These analyses showed that average diversity between flushed and bioreactor biofilms was double the diversity between biofilms from different reactors operated in parallel. The diversity between bioreactors was larger than the diversity associated with different biofilm recovery methods. Compared to other experimental variables, the method used to recover biofilms had a negligible impact on the outcome of water biofilm analyses based on 16S amplicon sequencing. Results from this study show that biofilms grown in reactors over 9 to 11 weeks are not representative models of the microbial populations flushed from a distribution system. Furthermore, the bacterial population profile of biofilms grown in replicate reactors from the same flushed water are likely to diverge. However, four common sampling protocols, which differ with respect to disruption of bacterial cells, provide similar information with respect to the 16S rRNA population profile of the biofilm community.
机译:在多个旋转环形反应器中接种从水分配系统冲洗的生物膜,以评估(1)就细菌组成和多样性而言,在生物反应器中生长的生物膜是否代表从水分配系统冲洗的生物膜,以及(2)是否使用生物膜采样方法影响附属细菌群落的种群概况。生物膜在生物反应器中生长,直到厚度稳定(9至11周),然后通过超声处理,鼓胃,打珠和手动刮擦从反应器试片中收获生物膜。 16S rRNA扩增子的高通量测序用于从接种到生物反应器中的冲洗过的生物膜以及通过不同方法从生物反应器试样中回收的生物膜中分析细菌种群。将冲洗和反应器生物膜之间的β多样性与(i)从不同反应器收获的生物膜和(ii)通过不同方法从同一反应器收获的生物膜之间的β多样性进行比较。这些分析表明,冲洗和生物反应器生物膜之间的平均多样性是并行运行的不同反应器中生物膜之间的多样性的两倍。生物反应器之间的多样性大于与不同生物膜回收方法相关的多样性。与其他实验变量相比,用于回收生物膜的方法对基于16S扩增子测序的水生物膜分析结果的影响可忽略不计。这项研究的结果表明,在反应器中生长超过9到11周的生物膜不是从分配系统冲洗掉的微生物种群的代表性模型。此外,在相同的冲洗水中,在复制反应器中生长的生物膜的细菌种群分布可能会发散。但是,关于细菌细胞破坏的不同,有四种常见的采样方案,它们针对生物膜群落的16S rRNA种群概况提供了相似的信息。

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