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Impact of Chloramination on the Development of Laboratory-Grown Biofilms Fed with Filter-Pretreated Groundwater

机译:氯化处理对用过滤器预处理的地下水喂养的实验室生长生物膜发育的影响

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摘要

This study evaluated the continuous impact of monochloramine disinfection on laboratory-grown biofilms through the characterization of biofilm architecture and microbial community structure. Biofilm development and disinfection were achieved using CDC (Centers for Disease Control and Prevention) biofilm reactor systems with polyvinyl chloride (PVC) coupons as the substratum and sand filter-pretreated groundwater as the source of microbial seeding and growth nutrient. After 2 weeks of growth, the biofilms were subjected to chloramination for 8 more weeks at concentrations of 7.5±1.4 to 9.1±0.4 mg Cl2 L−1. Control reactors received no disinfection during the development of biofilms. Confocal laser scanning microscopy and image analysis indicated that chloramination could lead to 81.4–83.5% and 86.3–95.6% reduction in biofilm biomass and thickness, respectively, but could not eliminate biofilm growth. 16S rRNA gene terminal restriction fragment length polymorphism analysis indicated that microbial community structures between chloraminated and non-chloraminated biofilms exhibited different successional trends. 16S rRNA gene pyrosequencing analysis further revealed that chloramination could select members of Actinobacteria and Acidobacteria as the dominant populations, whereas natural development leads to the selection of members of Nitrospira and Bacteroidetes as dominant biofilm populations. Overall, chloramination treatment could alter the growth of multi-species biofilms on the PVC surface, shape the biofilm architecture, and select a certain microbial community that can survive or proliferate under chloramination.
机译:这项研究通过表征生物膜结构和微生物群落结构,评估了一氯胺消毒对实验室生长的生物膜的持续影响。使用CDC(疾病控制和预防中心)生物膜反应器系统可实现生物膜的发育和消毒,其中聚氯乙烯(PVC)试样作为基质,砂滤预处理的地下水作为微生物播种和生长养分的来源。生长2周后,将生物膜以7.5±1.4至9.1±0.4 mg Cl2 L -1 的浓度再氯化8周。对照反应器在生物膜形成过程中未进行消毒。共聚焦激光扫描显微镜和图像分析表明,氯化作用可分别使生物膜生物量和厚度减少81.4–83.5%和86.3–95.6%,但不能消除生物膜的生长。 16S rRNA基因末端限制性片段长度多态性分析表明,在氯化和非氯化生物膜之间的微生物群落结构表现出不同的演替趋势。 16S rRNA基因焦磷酸测序分析进一步表明,氯化作用可以选择放线菌和酸性细菌的成员作为主要种群,而自然发育导致选择硝化螺菌和拟杆菌的成员作为主要生物膜种群。总体而言,氯化处理可以改变PVC表面上多种生物膜的生长,改变生物膜的结构,并选择可以在氯化作用下生存或增殖的微生物群落。

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