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. 2012 Sep;223(7):4039-4046.
doi: 10.1007/s11270-012-1171-z. Epub 2012 Apr 26.

Culture-Dependent and Culture-Independent Methods in Evaluation of Emission of Enterobacteriaceae from Sewage to the Air and Surface Water

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Culture-Dependent and Culture-Independent Methods in Evaluation of Emission of Enterobacteriaceae from Sewage to the Air and Surface Water

Ewa Korzeniewska et al. Water Air Soil Pollut. 2012 Sep.

Abstract

The number of Enterobacteriaceae, with particular attention given to the presence of Escherichia coli and Klebsiella pneumoniae, was determined in hospital effluents and municipal wastewater after various stages of purification. The emission of these microorganisms to the ambient air near wastewater treatment plant (WWTP) facilities and to the river water, which is a receiver of the WWTP effluent, was also studied using fluorescence in situ hybridization (FISH) and cultivation methods. The number of Enterobacteriaceae determined by cultivation and fluorescence methods in different kinds of sewage sample ranged from 0.5 × 10(3) to 2.9 × 10(6) CFU/ml and from 2.2 × 10(5) to 1.3 × 10(8) cells/ml, respectively. Their removal rates during treatment processes were close to 99 %, but the number of these bacteria in the WWTP outflow was quite high and ranged from 5.9 × 10(3) to 3.5 × 10(4) CFU/ml and from 1.1 × 10(5) to 6.1 × 10(5) cells/ml, respectively. In the river water and the air samples, the number of Enterobacteriaceae was also high and ranged from 4.1 × 10(3) to 7.9 × 10(3) CFU/ml and from 3 to 458 CFU/m(3), respectively. The numbers of these microorganisms obtained from fluorescence and cultivation methods were statistically and significantly correlated; however, the analysis of the studied samples indicated that the FISH method gave values up to 10(3)-fold times greater than those obtained by the cultivation method. From a sanitary point of view, this means that the number of viable fecal bacteria is systematically underestimated by traditional culture-based methods. Thus, the FISH proves to be a method that could be used to estimate bacterial load, particularly in air samples and less contaminated river water.

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References

    1. Amann RI, Binder BJ, Olson RJ, Chisholm SW, Devereux R, Stahl DA. Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations. Applied and Environmental Microbiology. 1990;56:1919–1925. - PMC - PubMed
    1. Amann RI, Ludwig W, Schleifer K-H. Phylogenetic identification and in situ detection of individual microbial cells without cultivation. Microbiological Reviews. 1995;59:143–169. - PMC - PubMed
    1. Amann R, Snaidr J, Wagner M, Ludwig W, Schleifer K-H. In situ visualization of high genetic diversity in a natural microbial community. Journal of Bacteriology. 1996;178:3496–3500. - PMC - PubMed
    1. Bertaux J, Gloger U, Schmid M, Hartmann A, Scheu S. Routine fluorescence in situ hybridization in soil. Journal of Microbiological Methods. 2007;69:451–460. doi: 10.1016/j.mimet.2007.02.012. - DOI - PubMed
    1. Bitzan M, Richardson S, Huang C, Boyd B, Petric M, Karmali MA. Evidence that verotoxins (Shiga-like toxins) from Escherichia coli bind to P blood group antigens of human erythrocytes in vitro. Infection and Immunity. 1994;62(8):3337–3347. - PMC - PubMed

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