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首页> 外文期刊>International Journal of Hygiene and Environmental Health >Integration of Pseudomonas aeruginosa and Legionella pneumophila in drinking water biofilms grown on domestic plumbing materials
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Integration of Pseudomonas aeruginosa and Legionella pneumophila in drinking water biofilms grown on domestic plumbing materials

机译:铜绿假单胞菌和肺炎军团菌在家用管道材料上生长的饮用水生物膜中的整合

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Drinking water biofilms were grown on coupons of plumbing materials, including ethylene-propylene-diene-monomer (EPDM) rubber, silane cross-linked polyethylene (PE-X b), electron-ray cross-linked PE (PE-X c) and copper under constant flow-through of cold tap water. After 14 days, the biofilms were spiked with Pseudomonas aeruginosa, Legionella pneumophila and Enterobacter nimipressuralis (10~6 cells/mL each). The test bacteria were environmental isolates from contamination events in drinking water systems. After static incubation for 24 h, water flow was resumed and continued for 4 weeks. Total cell count and heterotrophic plate count (HPC) of biofilms were monitored, and P. aeruginosa, L. pneumophila and £. nimipressuralis were quantified, using standard culture-based methods or culture-independent fluorescence in situ hybridization (FISH). After 14 days total cell counts and HPC values were highest on EPDM followed by the plastic materials and copper. P. aeruginosa and L. pneumophila became incorporated into drinking water biofilms and were capable to persist in biofilms on EPDM and PE-X materials for several weeks, while copper biofilms were colonized only by L. pneumophila in low culturable numbers. E. nimipressuralis was not detected in any of the biofilms. Application of the FISH method often yielded orders of magnitude higher levels of P. aeruginosa and L pneumophila than culture methods. These observations indicate that drinking water biofilms grown under cold water conditions on domestic plumbing materials, especially EPDM and PE-X in the present study, can be a reservoir for P. aeruginosa and L pneumophila that persist in these habitats mostly in a viable but non-culturable state.
机译:饮用水生物膜生长在包括乙烯-丙烯-二烯单体(EPDM)橡胶,硅烷交联聚乙烯(PE-X b),电子射线交联PE(PE-X c)和铜在冷自来水不断流通下。 14天后,在生物膜上掺入铜绿假单胞菌,嗜肺军团菌和加压肠杆菌(每个10〜6个细胞/ mL)。测试细菌是饮用水系统中污染事件的环境分离物。静态孵育24小时后,水流恢复并持续4周。监测生物膜的总细胞数和异养平板数(HPC),以及铜绿假单胞菌,嗜肺乳杆菌和and。使用基于标准培养物的方法或与培养物无关的荧光原位杂交(FISH)来定量对nimipressuralis进行定量。 14天后,EPDM上的总细胞数和HPC值最高,其次是塑料和铜。铜绿假单胞菌和肺炎链球菌被并入饮用水生物膜中,并能够在EPDM和PE-X材料上的生物膜中保留数周,而铜生物膜仅被肺炎链球菌以低培养量定殖。在任何生物膜中均未检测到大肠杆菌。与培养方法相比,FISH方法的应用通常产生较高数量级的铜绿假单胞菌和肺炎链球菌。这些观察结果表明,在本研究中,在冷水条件下在家用水暖材料(尤其是EPDM和PE-X)上生长的饮用水生物被膜可能是铜绿假单胞菌和肺炎链球菌的储集层,这些生物膜主要在这些栖息地中存活,但没有生存能力。 -可培养状态。

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