Correlations between total cell concentration, total adenosine tri-phosphate concentration and heterotrophic plate counts during microbial monitoring of drinking water

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Abstract

The generalmicrobial quality of drinking water is normallymonitored by heterotrophic plate counts (HPC). This method has been used for more than 100 years and is recommended in drinking water guidelines. However, the HPC method is handicapped because it is time-consuming and restricted to culturable bacteria. Recently, rapid and accurate detection methods have emerged, such as adenosine tri-phosphate (ATP) measurements to assess microbial activity in drinking water, and flow cytometry (FCM) to determine the total cell concentration (TCC). It is necessary and important for drinking water quality control to understand the relationships among the conventional and new methods. In the current study, all three methods were applied to 200 drinking water samples obtained from two local buildings connected to the same distribution system. Samples were taken both on normal working days and weekends, and the correlations between the different microbiological parameters were determined. TCC in the samples ranged from 0.37-5.61×105 cells/ml, and two clusters, the so-called high (HNA) and low (LNA) nucleic acid bacterial groups, were clearly distinguished. The results showed that the rapid determination methods (i.e., FCM and ATP) correlated well (R2 =0.69), but only a weak correlation (R2 =0.31) was observed between the rapid methods and conventional HPC data. With respect to drinking water monitoring, both FCM and ATP measurements were confirmed to be useful and complimentary parameters for rapid assessing of drinking water microbial quality. © Author(s) 2008.

Figures

  • Figure 1. A 2-dimensional flow cytometry dot-plot of green fluorescence (520 nm) and sideward scattered light (SSC), distinguishing so-called high nucleic acid (HNA) and low nucleic acid (LNA) content bacteria.
  • Figure 2. Daily changes of total cell counts (TCC), colony forming units (CFU) and total adenosine tri-phosphate (ATP) concentration for one representative drinking water tap, sampled on a normal working day. Error bars indicate the standard deviation on triplicate measurements.
  • Figure 2. Daily changes of total cell counts (TCC), colony forming units (CFU) and total
  • Table 1. Linear regression analysis of different measurement parameters. R2-values were calculated from different buildings, on different days and all data summarized (n=200).
  • Figure 4. Correlation between total ATP concentrations heterotrophic plate counts (HPC) of all samples (n=200). All data points represent average values of triplicate measurements.

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APA

Siebel, E., Wang, Y., Egli, T., & Hammes, F. (2008). Correlations between total cell concentration, total adenosine tri-phosphate concentration and heterotrophic plate counts during microbial monitoring of drinking water. Drinking Water Engineering and Science, 1(1), 1–6. https://doi.org/10.5194/dwes-1-1-2008

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