首页> 外文期刊>Letters in Applied Microbiology >Comparison of two filtration-elution procedures to improve the standard methods ISO 10705-1 & 2 for bacteriophage detection in groundwater, surface water and finished water samples.
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Comparison of two filtration-elution procedures to improve the standard methods ISO 10705-1 & 2 for bacteriophage detection in groundwater, surface water and finished water samples.

机译:比较两种过滤-洗脱程序,以改进用于检测地下水,地表水和最终水样品中噬菌体的标准方法ISO 10705-1和2。

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Aim: To select a reliable method for bacteriophage concentration prior detection by culture from surface water, groundwater and drinking water to enhance the sensitivity of the standard methods ISO 10705-1 & 2. Methods and Results: Artificially contaminated (groundwater and drinking water) and naturally contaminated (surface water) 1-litre samples were processed for bacteriophages detection. The spiked samples were inoculated with about 150 PFU of F-specific RNA bacteriophages and somatic coliphages using wastewater. Bacteriophage detection in the water samples was achieved using the standard method without and with a concentration step (electropositive Anodisc membrane or a pretreated electronegative Micro Filtration membrane, MF). For artificially contaminated matrices (drinking and ground waters), recovery rates using the concentration step were superior to 70% whilst analyses without concentration step mainly led to false negative results. Besides, the MF membrane presented higher performances compared with the Anodisc membrane. Conclusion: The concentration of a large volume of water (up to one litre) on a filter membrane avoids false negative results obtained by direct analysis as it allows detecting low number of bacteriophages in water samples. Significance and Impact of the Study: The addition of concentration step before applying the standard method could be useful to enhance the reliability of bacteriophages monitoring in water samples as bio-indicators to highlight faecal pollution
机译:目的:从地表水,地下水和饮用水中选择一种可靠的细菌培养物浓度检测方法,以便通过培养进行检测,以提高标准方法ISO 10705-1和2的灵敏度。方法和结果:人为污染(地下水和饮用水)和对自然污染的(地表水)1升样品进行处理以检测噬菌体。加标样品使用废水接种约150 PFU的F特异性RNA噬菌体和体细胞巨噬细胞。水样品中的噬菌体检测使用标准方法进行,无需进行浓缩步骤(正电阳极膜或预处理的负电微滤膜,MF)。对于人工污染的基质(饮用水和地下水),使用浓缩步骤的回收率优于70%,而没有浓缩步骤的分析主要导致假阴性结果。此外,MF膜比Anodisc膜具有更高的性能。结论:滤膜上大量水(最多一升)的浓度避免了直接分析获得的假阴性结果,因为它可以检测到水样本中的噬菌体数量少。研究的意义和影响:在应用标准方法之前添加浓缩步骤可能会有助于提高水样本中作为噬菌体污染生物指标的噬菌体监测的可靠性。

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