Concentration of fecal indicators in sources of fecal contamination

5.1 Human sources

Other than coliphages, in order to provide a better idea of the fecal load on the samples the following tables also display values for fecal indicator bacteria (fecal coliforms or thermotolerant coliforms), E. coli, enterococci (or fecal streptococci) and spores of sulfite-reducing clostridia (SSRC).

The values presented in the tables represent the most common values reported worldwide when tested by standardized methods (ISO, USEPA and standard methods)

5.1.1 Human feces

Common procedures regarding amounts of sample to analyze, extraction method, and amount of sample for quantitative or qualitative (presence/absence) determination have not been applied in different studies. Therefore values reported in different studies hinder comparisons. Even if the results are too variable, and likely to be reconsidered in the future, concentrations of bacterial indicators appear more constant than concentrations of bacteriophages. Among bacteriophages somatic coliphages appear to be more abundant than the F-specific ones (Jebri et al., 2017, link capitol 1; Simon and Gorbach, 1984)

Table 1. Most frequent values of fecal indicators in faeces
Fecal coliforms / E. coli Enterococci SSRC Somatic coliphages F-specific coliphages
Percent positive samples 100 100 100 39,7 to 100 0 to 73
Concentration range (CFU or PFU/g) 107– 108 107– 108 - <1 to 1·108 <1 to 1.2·106

5.1.2 Raw sewage (untreated municipal wastewater)

Values in raw sewage depend on the concentration of fecal remains in it, which depends mainly on the characteristics of the sewer system, rainfall of the area in the hours previous to sampling, per capita water consumption in the area and the time of day of sample collection. Values of microbial indicators are steadier than those of feces, and what is more important when tested in the same sample, most of the comparative values show the same trend. Fecal coliforms and E. coli are the most abundant with numbers 5–10 times higher than those for somatic coliphages, 5–20 times higher than enterococci, 25-100 times higher than values for SSRC and 20-80 times higher than F-specific RNA bacteriophages (Mandilara et al, 2006; Yahya et al., 2015; Blanch et al., 2006; Lucena et al., 2003; Lucena et al., 2004; Contreras-Coll et al., 2002; Lodder and de Roda Husaman, 2005).

Table 2. Most frequent values of fecal indicators in raw sewage
Fecal coliforms / E. coli Enterococci SSRC Somatic coliphages F-specific coliphages
Percent positive samples 100 100 100 100 100
Concentration range (CFU or PFU/100mL) 5x105 - 5x107 5·104 to 5·106 104 to 5·106 105 to 5.106 5·103 to 1·106

Important observations regarding the concentrations in raw sewage of the fecal indicators displayed in the tables are that they are neither seasonal nor show appreciable differences in different areas of the planet, regardless of the level of development of the area.

The raw sewage with the microbial indicator load shown in table 2 is released into the environment either untreated or treated by conventional wastewater treatment plants, mostly those based on activated sludge.

 

5.1.3 Conventional wastewater treatment plant effluents

Table 3. Most frequent values of fecal indicators in conventional wastewater water treatment plant effluents
Fecal coliforms / E. coli Enterococci SSRC Somatic coliphages F-specific coliphages
Percent positive samples 100 100 100 100 100
Concentration range (CFU or PFU/100mL) 2.0·104 to 7·106 2.5·104 to 7·105 1·104 to 3·105 1·104 to 2.0·106 <1.104 to 2.1·105

Effluent water from conventional (activated sludge digestion) wastewater treatment plants all around the world that is released into water bodies still contains important amounts of microbial indicators. The precise concentrations will depend on the performance of the treatment plant, but the relative proportions of the different indicators remain similar to those of raw sewage (Mandilara et al., 2006; Yahya et al., 2015; Lucena et al., 2004; Costan-Longares et al., 2008; Gomila et al., 2008)

Other treatments that remove similar amounts of all indicators, regardless of the extent of removal, are: primary sedimentation, flocculation-aided sedimentation, activated sludge digestion plus precipitation and trickling filters, depth filtration and precipitation/flocculation plus filtration (Harwood et al., 2005; Rose et al., 2005; Nieuwstad et al., 1988; Otosson et al., 2006).

In contrast, advanced (tertiary) treatments remove the various indicators with different efficiencies.

5.1.2 Untreated sludge

Conventional wastewater treatment plants produce huge amounts of sludge that constitutes an important source of microbial indicators. Theoretically, the sludges generated in conventional plants cannot be released untreated into the environment, but in many areas of the world it still is.

The results available in the scientific literature for untreated sludge are not easy to interpret because of the differences when reporting the concentration (wet versus dry matter, different amounts of sample reported, etc.), and a degree of uncertainty regarding the tested sludge characteristics (primary, activates, mixed, dewatered, etc.).

Table 4. Fecal contamination indicators in untreated sludge from municipal wastewater
Fecal coliforms / E. coli Enterococci SSRC Somatic coliphages F-specific coliphages
Percent positive samples 100 100 100 100 100
Concentration range (CFU or PFU per g of dry matter) 5x106-1x108 1.105-5x106 5.105-1.107 5·106 to 5·107 5·105 to 1·107

However, instead of the variability of results reported in the scientific literature, untreated sewage sludge contains great amounts of fecal indicators. In fact, they are concentrated regarding their numbers in raw sewage. As for the proportions between different indicators, they remain similar to those of raw sewage (Mandilara et al., 2006; Guzman et al., 2007).

The effect of the most frequent treatment of sludges, anaerobic mesophilic digestion, has a very modest impact on the reduction in the numbers of indicators without significant differences between them (Mandilara et al., 2006; Guzman et al., 2007). In contrast, further treatments such as pasteurization, composting, etc., bring about important and differential reductions (Guzman et al., 2007; Astals et al., 2012).

5.2 Animal sources

In the previous section we looked at the numbers of the indicators for wastewater originated by human populations.

Regarding animal sources we take into account wastewater from slaughterhouses and slurries generated in farms.

If we take a look at the numbers, we can observe that in the case of animal sources the amount of bacterial and viral indicators appear to be more variable than those from a human population (animal sources often present higher maximums and lower minimums for every indicator). This higher variability may be due to the higher variability of the sources studied.

Table 5. Presence of indicators from slaughterhouses and slurry from farms of different locations. Concentrations in CFU or PFU 100 mL (Data extracted from Blanch et al, 2006)
Indicator Number of samples % positive Minimum value Maximum value
Fecal coliforms 111 100 1.0x104 1.7x1010
Enterococci 111 100 1.5x104 8x108
SSRC 111 100 2.0x103 2.0x108
Somatic coliphages 110 100 5.0x10 4.5x109
F-specific RNA phages 110 80 < 5.0x10 4.0x108
Phages infecting GA17 strain* 73 7 < 5.0x10 1.103
Phages infecting GA17 strain 73** 98.6   < 5.0x10 7.3x105
*Ga17 is a strain infecting Bacteroides (Payan et al., 2005 )
 **Municipal raw sewage

As shown in table 5, the relative abundances of indicators of fecal contamination are very similar for both animal and human contamination sources (Table 2).

In light of the results, the only conclusion we can come to is that there are no significant differences between animal fecal pollution and human fecal pollution in terms of the concentrations of fecal bacteria indicators and coliphages, with the exception of phages infecting strain GA17 of Bacteroides that is a marker of fecal contamination of human origin.

References

Astals, S, C Venegas, M Peces, J Jofre, F Lucena and J Mata-Alvarez. 2012. Balancing hygienization and anaerobic digestion of raw sewage sludge. Water Research 46: 6218-6227.

Blanch, A., L. Belanche-Muñoz, X. Bonjoch, J. Ebdon, C. Gantzer, F. Lucena, J. Ottoson, C. Kourtis, A. Iversen, I. Kühn, L. Mocé, M. Muniesa, ……… and J. Jofre. 2006. Integrated analysis of established and novel microbial and chemical methods for microbial source tracking. Applied and Environmental Microbiology 72: 5915-5926.

Contreras-Coll, N.; Lucena, F.; Mooijman, K.; Havelaar, A.; Pierz, V.; Boque, M.; Gawler, A.; Holler, C.; Lambiri, M.; Mirolo, G.; Moreno, B.; Niemi, M.; Sommer, R.; Valentin, B.; Wiedenmann, A.; Young, V.; Jofre, J. 2002. Occurrence and levels of indicator bacteriophages in bathing waters throughout Europe. WaterResearch 36: 4963-4974.

Costán-Longares, A., M. Montemayor, A. Payán, J. Mendez, J. Jofre, R. Mujeriego and F. Lucena. 2008. Microbial indicators and pathogens: removal, relationships and predictive capabilities in water reclamation facilities. Water Research 42 : 4439-4448.

Gomila, M.; Solis, J.J.; David, Z.; Ramon, C.; Lalucat, J. Comparative reductions of bacterial indicators, bacteriophage-infecting enteric bacteria and enteroviruses in wastewater tertiary treatments by lagooning and UV-radiation. Water Sci. Technol. 2008, 58, 2223–2233.

Guzman, C., J. Jofre. M. Montemayor and F. Lucena. 2007. Occurrence and levels of indicators and selected pathogens in different sludges and biosolids. Journal of Applied Microbiology 103: 2420- 2429.

Harwood, V.J.; Levine, A.D.; Scott, T.M.; Chivukula, V.; Lukasik, J.; Farrah, S.R.; Rose, J.B. Validity of the indicator organism paradigm for pathogen reduction in reclaimed water and public health protection. Appl. Environ. Microbiol. 2005, 71, 3163–3170.

Lodder, W.J.; de RodaHusman, A.M. Presence of noroviruses and other enteric viruses in sewage and surface waters in The Netherlands. Appl. Environ. Microbiol. 2005, 71, 1453–1461.

Lucena, F. X. Mendez, A. Morón, E. Calderón, C. Campos, A. Guerrero, M. Cárdenas, C. Gantzer, L. Schwartzbrood, S. Skraber and J. Jofre. 2003. Occurrence and densities of bacteriophages proposed as indicators and bacterial indicators in river waters from Europe and South America. Journal of Applied Microbiology 94: 808- 815.

Lucena, F., A.E. Duran, A. Moron, E. Calderon, C. Campos, C. Gantzer, S. Skraber and J. Jofre. 2004. Reduction of bacterial indicators and bacteriophages infecting faecal bacteria in primary and secondary wasterwater treatments. Journal of Applied Microbiology 97: 1069-1076.    

Mandilara, GD, Smeti, EM, Mavridou, ATh, Lambiri, MP, Vatopoulos, AC and Rigas, FP (2006a). Correlation between bacterial indicators and bacteriophages in sewage and sludge. FEMS microbiology letters. 263, pp. 119–26.

Mandilara, G.; Mavridou, A.; Lambiri, M.; Vatopoulos, A.; Rigas, F. The use of bacteriophages for monitoring the microbiological quality of sewage sludge. Environ. Technol. 2006b, 27, 367–375

Nieuwstad, T.J.; Mulder, E.P.; Havelaar, A.H.; Van Olphen, M. Elimination of micro-organisms from wastewater by tertiary precipitation and simultaneous precipitation followed by filtration. Water Res. 1988, 22, 1389–1397.

Ottoson, J.; Hansen, A.; Westrell, T.; Johansen, K.; Norder, H.; Stenström, T.A. Removal of noro- and enteroviruses, Giardia cysts, Cryptosporidium oocysts, and fecal indicators at four secondary wastewater treatment plants in Sweden. Water Environ. Res. 2006, 78, 828–834.

Payan, A., J. Ebdon, H. Taylor, C. Gantzer, J. Ottoson, G. T. Papageorgiou, A. R. Blanch, F. Lucena, J. Jofre and M. Muniesa. 2005. Method for isolation of Bacteroides bacteriophage host strains suitable for tracking sources of fecal pollution in water. Applied and Environmental Microbiology 71: 5659-5662.

Rose, J.B.; Farrah, S.R.; Harwood, V. Reduction of Pathogens, Indicator Bacteria, and Alternative Indicators by Wastewater Treatment and Reclamation Processes; IWA Publishing: Lodon, UK;Water Environment Research Foundation: Alexandria, VA, USA, 2005

Simon, G.L. and Gorbach, S.L. (1984) Intestinal Flora in Health and Disease. Gastroenterology 86, 174-193.

Yahya, M., F. Hmaied, S. Jebri, J. Jofre and M. Hamdi. 2015. Bacteriophages as indicators of human and animal faecal contamination in raw and treated wastewaters from Tunissia.J. Applied Microbiol 118: 1271-1225.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we’ll assume that you are happy to receive cookies on the COLIPHAGES website. Please, take a look at our Cookies policy

ACEPTAR
Aviso de cookies
Share This