July 2, 2019
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Linke, R.B., Stadler, P., Reischer, G.H., Savio, D., Kollanur, D., Mayer, R., Mach, R.L., Kirschner, A.K.T., Sommer, R., Derx, J., Stadler, H. and Farnleitner, A.H. 2019. Using genetic microbial source tracking (MST) markers to identify fecal pollution sources in spring water of a large alpine karst catchment. In: J.B. Rose and B. Jiménez-Cisneros, (eds) Global Water Pathogen Project. http://www.waterpathogens.org (S. Petterson and G. Medema (eds) Part 5 Case Studies) http://www.waterpathogens.org/book/using-genetic-microbial-source-tracking-markers-to-identify-fecal-pollution-sources-in-spring-water-of-a-large-alpine-karst-catchment. Michigan State University, E. Lansing, MI, UNESCO.
|Last published: July 2, 2019|
Fecal pollution analysis still relies on cultivation-based E. coli and intestinal Enterococci (FIB) standard methods. However, these approaches do not give information on the kind of pollution sources. This study demonstrates how to identify pollution sources based on the application of genetic microbial source tracking (MST) markers at alpine spring water to guide target-oriented catchment protection and management.
The study site is located in the Northern Calcareous Alps (Austria) and drains a large Triassic limestone aquifer between 820 and 1828 m (catchment approx. 70 km2). Vegetation comprises summer pastures, natural calcareous alpine swards with open krummholz and forests. Potential fecal pollution sources include humans, livestock (cattle) and wild life. During base-flow conditions the observed spring has excellent water quality. In contrast, heavy rain events can result in high FIB concentrations.
The integrated multi-tiered approach covers, i) pollution source profiling using information from catchment survey activities, ii) hypothesis formulation on the potentially important fecal pollution sources and MST assay selection, and finally iii) hypothesis testing at the spring using hydrology-driven sampling and data stratification with concurrent analysis of FIB and genetic MST markers.
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Alpine and mountainous karstic springs are of high importance for drinking water supply worldwide (Ford and Williams, 2007). It is estimated that nearly a quarter of the world’s population is dependent on groundwater from karstic aquifers, including alpine, mountainous and low land karstic systems. In most cases, alpine karstic systems offer good raw-water quality under base flow conditions (Farnleitner et al., 2005; Wilhartitz et al., 2009). However, they are frequently very susceptible to precipitation events and a rapid decrease in water quality can often be observed during such situations. Microbial fecal pollution and input of fecal associated pathogens via rapid surface runoff, through temporarily activated karst conduits, is the most abundant quality hazard (Ford and Williams 2007; Savio et al.,2018). Thus, water resources from (alpine) karst aquifers require sustainable protection from fecal pollution within the catchment and proper microbial quality management at and after the spring (e.g. optimized spring water abstraction, adjusted treatment and disinfection measures) if used for drinking water supply (Farnleitner et al., 2018; Savio et al., 2018).
In practice, microbiological spring water quality is monitored by the application of standardized methods to enumerate fecal indictor bacteria (SFIB), most frequently using E. coli and/or intestinal enterococci as target organisms. Cultivation-based enumeration of SFIB is still regarded the “gold standard” for many water resources in order to sensitively evaluate the extent of fecal contamination (Farnleitner et al., 2010). However, detection of SFIB in water resources does not give any information on the origin of the contamination source, because SFIB do occur in wildlife, livestock and human sources (Farnleitner et al., 2010; Frick et al., 2018).
The aim of this case study is to demonstrate how SFIB spring monitoring can be complemented by applying host-associated microbial source tracking (MST) markers to identify responsible fecal sources in case of contamination. Genetic MST markers are determined by state-of-the-art quantitative PCR (qPCR) methodology. A robust and straightforward methodology (“hypothesis-driven approach”) is presented for the investigated dynamic alpine karstic water resource, integrating best available information from the catchment with monitoring efforts from the spring environment.
During base-flow conditions the investigated spring (limestone karst aquifer spring number 6; LKAS6) shows good raw water quality (Farnleitner et al., 2005; Wilhartitz et al., 2009) and - based on SFIB enumeration - microbial water quality problems do apparently not exist (SFIB are not detectable in the applied monitoring volume). Detection of fecal pollution is limited to the warm season and increased discharge situations (e.g. snow-melt, heavy rain events during summertime). For such periods, moderate to strong fecal pollution events are reported (Stadler et al., 2008; Farnleitner et al., 2011). For example, the herein presented investigation period showed pollution events in the range of log10 1.1-4.0 and of log10 0.3-3.8 CFU per 100ml for E. coli and enterococci, respectively. However, no information on the responsible fecal contamination sources was available before the application of the herein presented approach. Nevertheless, this information is considered of highest relevance for hazard- and health risk assessment and to guide target-oriented catchment management and best environmental practices.
The selected study site is located in the Northern Calcareous Alps (Austria) and drains a large Triassic limestone aquifer between 820 and 1828 m (catchment approx. 4 km2). The spring, LKAS6, shows a pronounced variation in flow conditions, with a mean discharge of 244 L.s-1 (range: 118 to 1150 L.s-1). Vegetation in the investigated area comprises summer pastures, natural calcareous alpine swards with open krummholz and forests (Grabherr et al., 1999). Several mountain lodges, supporting touristic activities, also exist (Reischer et al., 2011).
Hydrological characterization of the spring was achieved by collecting data on discharge, temperature, electrical conductivity, spectral absorption coefficient at 254 nm (SAC254), and turbidity measured by infield online sensors directly installed at the outlet of the spring (Farnleitner et al., 2005; Stadler et al., 2008,;Stadler et al., 2010).
Considering hydrological discharge dynamics, a nested sampling approach was followed resulting in a total of three sampling tiers. A basic monitoring sampling (BMS) was performed on a 3- to 4-weeks interval from June 2007 to November 2008 and a high-frequency sampling (HFS) during summer time (i.e., period of increased hydrological- and fecal pollution dynamics) was performed twice a week. Furthermore, one flood event (EVENT08) was analyzed in detail during late summer 2008 (cf. Figure 1).
SFIB (E. coli, enterococci), presumptive Clostridium perfringens, aerobic spore-forming bacteria and heterotrophic plate count bacteria at 22°C (HPC22) were performed for BMS, HFS and EVENT08 according to ISO standard methods (ISO 2000a; ISO 2000b; ISO 2002).
Figure 1: Hydrological situation of the spring and the applied “nested” sampling scheme. Discharge levels in the main graph show the discharge throughout the years 2007 and 2008 as daily mean values. Vertical lines mark the sampling dates during the monitoring program, green lines mark basic monitoring sampling dates, blue lines mark high frequency monitoring sampling dates during summer months, red box represents the flood event time frame, which is zoomed-in (upper right corner, linked with red dotted lines to the red flood event box), red lines within the high-resolution time scale mark event based high frequency monitoring sampling dates; discharge levels in the zoomed-in box are quarter-hourly measured values; gaps in the discharge data were due to malfunctions of the instruments necessary for the calculation of the discharge. Source: Farnleitner et al., 2011.
The presented concept is based on a three-step approach (Farnleitner et al., 2011; Reischer et al., 2013). STEP 1) A catchment survey to identify and characterize potential pollution sources – referred to as pollution source profiling (PSP; compare graphical abstract) - is undertaken. Visual inspection tours are organized to identify fecal pollution sources in the catchment. Further information for quantitative characterization of identified fecal sources is obtained from local authorities, official records, and scientific literature. Furthermore, information on the occurrence of SFIB from a broad range of animal and human sources in the catchment area was available and thus the amount of produced E. coli per source group could be estimated by the amount of environmentally available fecal material per source group x source group specific average E. coli concentrations in excreta or sewage (Farnleitner et al., 2011). STEP 2) Based on SFIB pollution load estimates, a hypothesis can be generated on the most likely pollution source(s) for the considered spring water habitat. The generated hypothesis then leads to the required sampling design and the choice of MST-markers to be applied. In the present study, a nested sampling design resulting in a total of three sampling tiers was chosen considering the hydrological discharge dynamics of the system (compare section: description of the system and applied methods; Fig. 1). STEP 3) The approach is completed by rigorous testing of the formulated hypothesis at the spring water environment by the retrieved information. For this, the generated MST-data is analyzed and discussed at 3 levels. (3.1) Comparison of the host-associated MST-maker levels in the spring water (i.e. human vs. animal marker) in context of the applied sampling regimes (here: BMS, HFS, EVENT08). (3.2) Statistical evaluation on existing associations between the MST-marker with the prevailing spring water quality situation by integrating all available hydrological, chemical, physical and microbiological parameters (i.e. multiparametric correlation analysis). (3.3) Finally (if applicable), testing the statistical predictability of SFIB pollution by the determined MST-marker concentrations.
STEP 1 (pollution source profiling at the catchment). Before the systematic investigation, humans were suspected the major source of fecal pollution due to the presence of significant touristic activities in the area (waste water, cesspits and/or illegal turnout thereof). Cattle grazing on pastures were assumed to play a minor role.
Results from the PSP, however, identified ruminants (cattle and wildlife) as the most important potential source of fecal pollution. Their daily production of environmentally available fecal matter was estimated to amount to 3.6 tons (equivalent to an E. coli load of 5.2 x 1013 CFU/d) in the catchment area (Farnleitner et al., 2011). Environmentally available fecal matter from human sources, in contrast, was negligible despite the presence of significant touristic activities in the area (0.04 kg wet weight/day; equivalent to an E. coli load of 3.6 x 109 CFU/d; Farnleitner et al., 2011). This was attributed to the fact that sufficient sanitary facilities at restaurants and lodges exist which reduce direct fecal pollution from hikers and climbers to a minimum (i.e. low environmental availability of the produced fecal material). Moreover, state-of-the-art sewage disposal facilities at restaurants and lodges further minimize the input of fecal pollution of human origin to the environment.
STEP 2 (hypothesis generation and study design formulation). From PSP results, it was hypothesized that ruminants instead of originally suspected human fecal excreta and sewage were responsible for the occasionally observed high levels of fecal indicator bacteria in the spring water of LKAS6. Based on these findings MST-tools to detect human and ruminant associated fecal pollution were chosen to test this hypothesis. To target fecal pollution of human origin the BacH assay (Reischer et al., 2007) was chosen and for the detection of fecal pollution originating from ruminants (wildlife and cattle) the BacR assay (Reischer et al., 2006) was chosen. Both assays target Bacteroidetes populations associated with their hosts. Concerning performance criteria of MST-tools, it has been suggested that no fixed performance thresholds categorize an assay as suitable/applicable (Harwood et al., 2011; Belanche et al., 2011). Instead, to ensure applicability of a MST assay its performance must match the requirements for each MST problem and the conditions within the study area specifically (Reischer et al., 2013). For the investigated LKAS6 catchment, Reischer et al., (2011) used an approach based on Bayes' theorem to estimate the probability for the correct detection of a specific source of pollution under different pollution scenarios (Reischer et al. 2011; Kildare et al., 2007). In addition, both, the BacH and BacR assay, were tested for their level of specificity and sensitivity for the respective fecal source group(s) on samples from the LKAS6 catchment.
STEP 3 (multi-parametric hypothesis testing at the spring environment) All microbiological and most of the physicochemical parameter values showed strong variations throughout the year and the nested sampling design nicely covered the system dynamics (Fig. 1).
Level 1 – analysis: Regarding the results of the genetic Bacteroidetes markers associated with either human (BacH) or ruminant (BacR) fecal pollution, BacR marker levels were found to be several orders of magnitude higher than those of BacH, irrespective of the sampling tier investigated (Fig. 2). BacH levels were frequently close to or below the detection threshold. Since BacH marker concentration in human fecal material was shown to be around 1 order of magnitude higher than BacR marker concentrations in ruminant feces the BacH marker concentrations have additionally been corrected for the higher abundance to allow a quantitative direct comparison of fecal input from human versus ruminants in spring water (BacH corr., Fig. 2). The finding of higher levels of BacR clearly supports the hypothesis that ruminants (cattle and wildlife) instead of humans were the most abundant source of fecal pollution in the catchment area.
Figure 2. Abundances of the BacR and BacH marker in LKAS6 during basic monitoring sampling (BMS), high frequency sampling (HFS) and flood event monitoring (EVENT08). Box plots show the distribution of BacR and BacH marker values (whiskers, 10th and 90th percentile; boxes, 25th and 75th percentile; bold lines within the box, median). BacR, ruminant-associated marker (red boxes and dot symbols); BacH, human-associated marker (green boxes and triangle symbols); BacH corr., human-associated marker after correction for the higher abundance in feces as compared to ruminant marker. Data is directly derived from BacH results after consideration of the correction factor (0.10); ME, marker equivalent; n, number of samples; data is given after log+1- transformation. Source: modified from Farnleitner et al., 2011.
Level 2 – analysis: Among all investigated parameters, BacR revealed the highest association with E. coli and enterococci (ENT). It is interesting to note that correlation coefficients between BacR and SFIB increased with the rising hydrological dynamics. For example, correlation coefficients between BacR and ENT increased from 0.59 to 0.80 and 0.96 for the BMS, the HFS and the EVENT08 sampling, respectively (Tab. 1). This effect can be explained by the different persistence of applied markers and indicators becoming less influential with decreasing average residence times of the water masses (i.e., less time available for different die-off or degradation effects). In contrast to BacR, BacH did not show any relevant correlations with E. coli or ENT.
Table 1: Correlation analysis of data collected during basic monitoring sampling (BMS; n=23), high-frequency sampling (HFS; n=75–76) and flood event 2008 based sampling (EVENT08; n = 29). Abbreviations: Aerob: aerobic spore formers, BacH: human-associated genetic Bacteroidetes marker, BacR: ruminant-associated genetic Bacteroidetes marker, Cond: conductivity, Dis: discharge, EC: E. coli, ENT: enterococci, HPC22: heterotrophic plate count at 22°C, pCP: presumptive Clostridium perfringens, SAC254: spectral absorption coefficient at 254 nm, Turb: turbidity. Source: Farnleitner et al., 2011.
Level 3 – analysis: E. coli and BacR were selected for further statistical analysis due to the high identified association between these parameters (see level 2). Using regression analysis for the parameters E. coli and BacR, it was able to predict 90% of the E. coli variation using BacR values (Fig. 3), providing strong support that E. coli was predominantly derived from ruminant fecal pollution sources (Farnleitner et al., 2011). BacH could not be used for regression analysis as indicated by the correlation analysis above, with most values being below the level of detection.
Figure 3. Regression analysis of BacR and E. coli data of flood event 2008 in LKAS6. BacR, ruminant-specific marker; ME, marker equivalents; CFU, colony forming units; solid line, regression curve; R², coefficient of determination for linear regression; data is given after log10-transformation and addition of 1 to a given value. Source: Farnleitner et al., 2011
In conclusion, all 3 levels of analysis indicated that ruminant instead of previously suspected human sources were responsible for the occasionally observed high levels of SFIB in spring water of the LKAS6 catchment.
In this case study, we introduced a robust and relatively simple approach to guide environmental authorities and water utilities for pollution source identification in case standard fecal indicators (E. coli and enterococci) are detected in spring water. Microbial source tracking by using host-associated bacterial genetic fecal makers was successfully applied as a supporting technique to complement standardized fecal indicator bacteria assays to answer the crucial question which source(s) of fecal pollution had to be considered (human vs. livestock, wildlife) in the catchment. By this approach, the “black box” of fecal pollution can be opened and responsible sources can be unraveled in the catchment area (Savio et al., 2018).
The presented concept based on Pollution Source Profiling (PSP), hypothesis formulation, definition of MST requirements and hypothesis testing, is also easily applicable for other types of “headwater” catchments and not restricted to alpine karst water resources. Complementation with standard methods is easy to perform by filtering additional water samples in addition to SFIB determination. The filters can be stored (‑80°C) and analyzed in case needed (e.g. periodic detection of fecal pollution). Numbers and types of applicable MST assays available in the literature are increasing rapidly, reducing limitations due to lacking assays for specific sources and/or habitats. Identifying the sources of fecal pollution in the water resource, as originally determined by standardized SFIB assays, can be an essential part for system assessment (i.e. water safety planning, sanitation safety planning), target-oriented catchment management, and finally, can serve also as a very important starting point for hazard- and risk assessment and MST-guided QMRA (Savio et al., 2018).
This case study was derived from a previous research project, the results of which are published in the following book chapter:
Farnleitner, A. H., Reischer, G. H., Stadler, H., Kollanur, D., Sommer, R., Zerobin, W., Blöschl, G., Barrella, K. M., Truesdayle, J. A., Casarez, E. A. & Di Giovanni, G. D. (2011). Agricultural and rural watersheds. In Microbial Source Tracking: Methods, Applications, and Case Studies (pp. 399-431). Springer, New York, NY. https://link.springer.com/book/10.1007/978-1-4419-9386-1
This paper was supported by Vienna Water (MA31) and the Science Call 2015 "Ressource und Lebensgrundlage Wasser“ Projekt SC15-016, supported by the Niederösterreichischen Forschungs- und Bildungsgesellschaft (NFB). This is a joint study effort of the ICC Water & Health (www.waterandhealth.at).