Flow-cytometric total bacterial cell counts as a descriptive microbiological parameter for drinking water treatment processes

被引:476
作者
Hammes, Frederik [1 ]
Berney, Michael [1 ]
Wang, Yingying [1 ,3 ]
Vital, Marius [1 ,3 ]
Koester, Oliver [2 ]
Egli, Thomas [1 ,3 ]
机构
[1] Eawag, Swiss Fed Inst Aquat Sci & Technol, CH-8600 Dubendorf, Switzerland
[2] Wasserversorgung Zurich, CH-8023 Zurich, Switzerland
[3] ETH, Inst Biogeochem & Pollutant Dynam, CH-8092 Zurich, Switzerland
关键词
adenosine tri-phosphate (ATP); drinking water; flow cytometry; heterotrophic plate counts (HPCS); total cell concentration;
D O I
10.1016/j.watres.2007.07.009
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
There are significantly more microbial cells in drinking water than what can be cultured on synthetic growth media. Nonetheless, cultivation-based heterotrophic plate counts (HPCs) are used worldwide as a general microbial quality parameter in drinking water treatment and distribution. Total bacterial cell concentrations are normally not considered during drinking water treatment as a design, operative or legislative parameters. This is mainly because easy and rapid methods for quantification of total bacterial cell concentrations have, up to now, not been available. As a consequence, the existing lack of data does not allow demonstrating the practical value of this parameter. In this study, we have used fluorescence staining of microbial cells with the nucleic acid stain SYBR(R) Green I together with quantitative flow cytometry (FCM) to analyse total cell concentrations in water samples from a drinking water pilot plant. The plant treats surface water (Lake Zilrich) through sequential ozonation, granular active carbon (GAC) filtration and membrane ultrafiltration (UF). The data were compared with adenosine tri-phosphate (ATP) measurements and conventional HPCs performed on the same water samples. We demonstrated that the impact of all three major treatment steps on the microbiology in the system could accurately be described with total cell counting: (1) ozonation caused chemical destruction of the bacterial cells; (2) GAC filtration facilitated significant regrowth of the microbial community; and (3) membrane UF physically removed the bacterial cells from the water. FCM typically detected 1-2 log units more than HPC, while ATP measurements were prone to interference from extracellular ATP released during the ozonation step in the treatment train. We have shown that total cell concentration measured with FCM is a rapid, easy, sensitive and importantly, a descriptive parameter of several widely applied drinking water treatment processes. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:269 / 277
页数:9
相关论文
共 33 条
[1]   Heterotrophic plate count bacteria - what is their significance in drinking water? [J].
Allen, MJ ;
Edberg, SC ;
Reasoner, DJ .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2004, 92 (03) :265-274
[2]  
Bartram J., 2003, Heterotrophic Plate Counts and Drinking-Water Safety: the Significance of HPCs for Water Quality and Human Health
[3]   Assessment and interpretation of bacterial viability by using the LIVE/DEAD BacLight kit in combination with flow cytometry [J].
Berney, Michael ;
Hammes, Frederik ;
Bosshard, Franziska ;
Weilenmann, Hans-Ulrich ;
Egli, Thomas .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (10) :3283-3290
[4]   Flow-cytometric study of vital cellular functions in Escherichia coli during solar disinfection (SODIS) [J].
Berney, Michael ;
Weilenmann, Hans-Ulrich ;
Egli, Thomas .
MICROBIOLOGY-SGM, 2006, 152 :1719-1729
[5]   Microbial ecology of drinking water distribution systems [J].
Berry, David ;
Xi, Chuanwu ;
Raskin, Lutgarde .
CURRENT OPINION IN BIOTECHNOLOGY, 2006, 17 (03) :297-302
[6]   LIVE/DEAD® BacLight™:: application of a new rapid staining method for direct enumeration of viable and total bacteria in drinking water [J].
Boulos, L ;
Prévost, M ;
Barbeau, B ;
Coallier, J ;
Desjardins, R .
JOURNAL OF MICROBIOLOGICAL METHODS, 1999, 37 (01) :77-86
[7]   Improved detection of bacteria by flow cytometry using a combination of antibody and viability markers [J].
Clarke, RG ;
Pinder, AC .
JOURNAL OF APPLIED MICROBIOLOGY, 1998, 84 (04) :577-584
[8]  
Deininger RA, 2005, NATO SCI S SS IV EAR, P71
[9]   An ATP-based method for monitoring the microbiological drinking water quality in a distribution network [J].
Delahaye, E ;
Welté, B ;
Levi, Y ;
Leblon, G ;
Montiel, A .
WATER RESEARCH, 2003, 37 (15) :3689-3696
[10]  
Gasol JM, 1999, APPL ENVIRON MICROB, V65, P4475