Abstract

The cost and complexity of traditional methods for the detection of faecal indicator bacteria, including E. coli, hinder widespread monitoring of drinking water quality, especially in low-income countries and outside controlled laboratory settings. In these settings the problem is exacerbated by the lack of inexpensive media for the detection of E. coli in drinking water. We developed a new low-cost growth medium, aquatest (AT), and validated its use for the direct detection of E. coli in temperate and sub-tropical drinking waters using IDEXX Quanti-Tray®. AT was compared with IDEXX Colilert-18® and either EC-MUG or MLSB for detecting low levels of E. coli from water samples from temperate (n = 140; Bristol, UK) and subtropical regions (n = 50, Pretoria/Tshwane, South Africa). Confirmatory testing (n = 418 and 588, respectively) and the comparison of quantitative results were used to assess performance. Sensitivity of AT was higher than Colilert-18® for water samples in the UK [98.0% vs. 86.9%; p<0.0001] and South Africa [99.5% vs. 93.2%; p = 0.0030]. There was no significant difference in specificity, which was high for both media (>95% in both settings). Quantitative results were comparable and within expected limits. AT is reliable and accurate for the detection of E. coli in temperate and subtropical drinking water. The composition of the new medium is reported herein and can be used freely.

Highlights

  • The WHO/UNICEF Joint Monitoring Programme for Water Supply and Sanitation estimates that 663 million people do not have access to an improved source of drinking water [1]

  • The performance of AT was compared to three established procedures for the determination of E. coli in drinking water: C-18 (IDEXX), LTB/ EC-MUG (Oxoid), MLSB (Oxoid) and MacConkey Agar (Oxoid) [10,11]

  • EC-MUG was used in a five tube ten-fold dilution format (5 x 10 mL, 5 x 1 mL and 5 x 0.1 mL) and MLSB using membrane filtration according to standard methods [11]

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Summary

Objectives

The objective of this study was to evaluate the performance of AT in a variety of settings and using various strains of E. coli

Methods
Results
Discussion
Conclusion

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