Abstract
This study was conducted to assess potential human health risks presented by pathogenic bacteria in a protected multi-use lake-reservoir (Lake Ma Vallée) located in west of Kinshasa, Democratic Republic of Congo (DRC). Water and surface sediments from several points of the Lake were collected during summer. Microbial analysis was performed for Escherichia coli, Enterococcus (ENT), Pseudomonas species and heterotrophic plate counts. PCR amplification was performed for the confirmation of E. coli, ENT, Pseudomonas spp. and Pseudomonas aeruginosa isolated from samples. The results reveal low concentration of bacteria in water column of the lake, the bacterial quantification results observed in this study for the water column were below the recommended limits, according to WHO and the European Directive 2006/7/CE, for bathing water. However, high concentration of bacteria was observed in the sediment samples; the values of 2.65 × 103, 6.35 × 103, 3.27 × 103 and 3.60 × 108 CFU g−1 of dry sediment for E. coli, ENT, Pseudomonas spp. and heterotrophic plate counts, respectively. The results of this study indicate that sediments of the Lake Ma Vallée can constitute a reservoir of pathogenic microorganisms which can persist in the lake. Possible resuspension of faecal indicator bacteria and pathogens would affect water quality and may increase health risks to the population during recreational activities. Our results indicate that the microbial sediment analysis provides complementary and important information for assessing sanitary quality of surface water under tropical conditions.
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Introduction
The contamination of drinking and recreational water resources by pathogenic organisms and micropollutants is a major problem in many parts of the world. In developing countries, the diarrheal diseases, mainly due to the consumption of microbiologically contaminated drinking water, cause about one billion illnesses and 2.2 million deaths per year (Montgomery and Elimelech 2007). Although most infections occur in developing countries, waterborne diseases are a worldwide problem that also concern industrialized societies where highly populated centres draw their supply of drinking water (Thevenon et al. 2013; Poté et al. 2009a). Faecal pollution can originate from a variety of human and non-human sources, but faecal indicator bacteria (FIB) contamination from human faecal material is generally considered to be a greater risk to human health as it is more likely to contain human enteric pathogens (Scott et al. 2003; Haller et al. 2009a).
FIB reside in the gastrointestinal tracts of humans and animals, and are commonly used to assess the microbiological safety of drinking and recreational waters. Although indicator bacteria do not necessarily cause illness, their presence indicates that the water has been contaminated by faecal material and indicates therefore the potential presence of pathogens (An et al. 2002; Noble et al. 2003). The surface recreation water generally contains indigenous microorganisms, pathogenic and non-pathogenic microbes. The choice of bacterial indicators is thus very important for the management of aquatic environmental quality. The US Environmental Protection Agency and the European Union recommend the use of Escherichia coli, a subset of the faecal coliform group, and members of the genus Enterococcus (ENT), to assess the hygienic safety of recreational waters (USEPA 2000; WHO 2004; EU 2006). Both, heterotrophic plate count (HPC) and Pseudomonas aeruginosa, an opportunistic pathogen responsible for numerous infections especially for the persons with weakened immune systems, are often used as additional water quality indicators (Poté et al. 2009a; Varga 2001).
Exposure to bathing waters with high concentrations of E. coli, ENT and P. aeruginosa are documented in epidemiological studies as being associated with an increased risk of contracting gastrointestinal and respiratory illnesses. It has been demonstrated that during recreational activities, exposure to high concentrations of the faecal bacteria in recreational waters may increase the risk of illness and disease, including gastrointestinal, respiratory illnesses and skin, ear and eye infections (Crabelli 1983; Kay et al. 1994; Prüss 1998; Haile et al. 1999).
Sediments may contain (100 to 1,000×) more FIB as the overlying water (Davies et al. 1995; Poté et al. 2010). Recent studies demonstrated that the evaluation of FIB in sediments may be a more stable index of overall or long-term water quality than in the overlying water (Laliberte and Grimes 1982; Ferguson et al. 2005; Haller et al. 2009b). Thus, the monitoring of FIB levels in the water column, accumulation and resuspension of FIB from sediments should also be taken into account. Depending on sediment characteristics, coastal sediments can act as a reservoir of FIB. Analysis of water quality alone may underestimate the risk of exposure to potentially pathogenic microbes in recreational waters (Craig et al. 2002; Poté et al. 2009b). Some studies demonstrated that sediments can constitute as an important reservoir for FIB in freshwater environments (LaLiberte and Grimes 1982; Burton et al. 1987; An et al. 2002; Haller et al. 2009a).
Lake Ma Vallée is a scenic African Lake surrounded by the equatorial forest. The lake is well protected and known as a place of leisure, sports and relaxation by different classes of population. A small dam, a creek mouth and water form an intimate lake and the surrounding forest is still primitive. The lake is considered as a reservoir for various activities including swimming, canoe, fishing and rowing boats. To our knowledge, no regular water quality monitoring and research programmes have been conducted to assess the microbial and physico-chemical qualities of the lake. Thus, the present research was carried out to assess the microbial quality of the lake. The assessment is based on the quantification and characterization of Pseudomonas spp., FIB including E. coli, ENT and HPC in both, water column and sediments from the lake. The spatial microbial distribution was performed by sampling sediments from eight sites distributed on either sides of the lake. The influence of sediment characteristics including sediment grain size and organic matter content on FIB accumulation and persistence was also examined.
Materials and methods
Study site and sampling procedure
Lake Ma Vallée is located about 30 km west of the city of Kinshasa with a surface area of 2.44 km2 (6 km long). Each month, approximately 640 peoples visit the lake for different recreational activities. Sampling was done during low flow of water with stratified lake conditions on June 2013. Canoes were used to collect core sediment samples and water samples from the lake. Water samples (250 mL) were duplicated from three sites (EM, stream inlet; MM, middle of lake; and SM, stream outlet) and pooled in 1 L sterile bottles. Surface sediment (n = 8) was sampled from both the banks of the lake: on the right bank side noticed 1D–4D and the left side noticed 1G–4G (Fig. 1). The samples were placed in sterile containers and stored in an icebox at 4 °C and transported to laboratory. At the point of sampling, physico-chemical characteristics of water, such pH, electrical conductivity and temperature were measured using a Multi 350i (WTW, Germany).
Sediment characterization
The grain size distribution was measured using a particle size analyzer Coulter ® LS-100 (Beckman Coulter, Fullerton, CA, USA), following ultrasonic dispersal in deionized water (Loizeau et al. 1994). The proportions of three major size classes (clays <2 μm; silts 2–63 μm; and sand >63 μm) were determined from size distributions, as well as the median grain size. Sediment total water content was measured by drying the samples at 60 °C for overnight and the weight loss was taken for the percentage of water content. Sediment total organic matter content and CaCO3 was estimated by loss on ignition for 1 h in Salvis oven (Salvis AG, Emmenbrücke, Luzern, Switzerland).
Bacteria analysis by selective culture method
The FIB (E. coli and ENT) were quantified in the water and sediment samples using the method previously described by Balkwill and Ghiorse (1985) and modified by Haller et al. (2009a). Bacterial analysis in the water and sediment supernatant was estimated according to the international standard methods for water quality determination using the membrane filtration method (APHA 2005; Haller et al. 2009a, b). Briefly, the sediments were resuspended by adding 100 g of fresh sediment to 500 mL of 0.2 % Na6(PO3)6 in 1 L sterile plastic bottles and mixed for 30 min using the agitator rotary printing-press Watson-Marlow 601 controller (Skan, Switzerland). The mixture was then centrifuged at 4,000 rpm for 15 min at 15 °C. For each sample, triplicates of serially diluted sediment supernatant (100 mL) was passed through a 0.45-μm filter (47 mm diameter, Millipore, Bedford, USA) and placed on different selective culture media (Biolife Italiana) supplemented with the anti-fungal compound Nystatin (100 μg mL−1 final concentration), using the following incubation conditions: E. coli—Tryptone Soy Agar (TSA) medium, incubated at 37 °C for 4 h and transferred to Tryptone Bile X-Gluc Agar (TBX) medium at 44 °C for 24 h; ENT—Slanetz Bartley Agar (SBA) medium, incubated at 44 °C for 48 h and transferred into Bile Aesculin Agar (BAA) medium at 44 °C for 4 h; Pseudomonas spp.—Pseudomonas selective Agar incubated for 24 h at 37 °C. The HPC were determined using spread plate method on TSA after 48–72 h incubation at 28 °C (Poté et al. 2009b). The results are expressed as colony forming units per 100 mL of water (CFU 100 mL−1) or 100 g of dry sediments (CFU 100 g−1). The reproducibility of the whole experimental procedure was tested by means of triplicates on selected sediment samples.
PCR for confirmation of E. coli, ENT, Pseudomonas spp. and P. aeruginosa
General confirmation of E. coli, ENT, Pseudomonas spp. and P. aeruginosa were performed by PCR assay using specific primers and operational conditions as summarized in Table 5. PCR assay were performed on genomic DNA extracted from the isolated colonies grown on selective media. Genomic DNA was extracted using 5 % Chelex® 100 and proteinase K as described by Walsh et al. (1991) and Yang et al. (2008). Briefly, 5 g of Chelex resin (Bio-Rad) and 0.02 g of Proteinase K were dissolved in 100 mL of molecular grade water, mixed thoroughly and refrigerated. Two hundred microlitres of this solution was dispensed to sterile 1.5 mL tubes and a loopful (10 μL) of bacterial colonies grown on selective media were added to the aliquot and incubated at 56 °C for 4–6 h or overnight, and vortexed briefly. The tubes were then boiled at 95 °C for 8–10 min and cooled in a freezer for 15–20 min, centrifuged at 13,000 rpm and the supernatant was transferred to fresh tubes. The extracted DNA was quantified spectrophotometrically (OD260) and the quality was assessed on selected samples by electrophoresis on 1 % agarose gel stained with 1× SYBR safe DNA gel stain (Invitrogen) in 1× TAE buffer. DNA was stored at −20 °C until used.
PCR was performed on Biometra thermocycler (BIOLABO) in a 20-μL reaction mixture containing 1 μL of processed DNA template, 0.4 μmol of each primer (Invitrogen), 200 μmol of dNTP mix (Sigma Aldrich), 1 unit of RED Taq DNA polymerase (Sigma Aldrich) and 1× PCR buffer (containing 1.1 mM of MgCl2). Samples were subjected to the following thermal cycling conditions: initial denaturation 94 °C for 5 min, following 35 cycles at 94 °C for 30 s, appropriate annealing temperature (Table 5) for 1 min, 72 °C for 1 min and final 10-min extension at 72 °C. PCR products were visualized on 1.3 % agarose gel stained with 1× SYBR safe DNA gel stain in 1× TAE buffer.
The experiment was conducted in triplicate with each set of conditions. Negative (without DNA) and positive (genomic DNA extracted from BD Microtrol™ E. coli ATCC25922, Enterococcus faecalis ATCC 29212 and P. aeruginosa ATCC 27853) were used for each set of PCR assay.
Data analysis
For all analyses, the triplicate measurements have been performed on selected sediment samples. Statistical treatment of data (Spearman rank order correlation) has been realized using SigmaStat11.0 (Systat Software, Inc., USA).
Results and discussion
Physico-chemical analysis of water and sediment
The physico-chemical parameters of water and sediments are given in Tables 1 and 2. The pH value 5.9 of lake water was observed in all parts of the lake. The lake temperature ranged between 23.7 and 25.3 °C. The water electrical conductivity and dissolved oxygen in water are very low, with maximum value of 12.8 μS cm−1 and 1 %, respectively. The samples were collected during summer period and the flow of the lake was almost stabilized. There are many aspects which can explain the low values of pH, conductivities and dissolved oxygen in the water, including the presence of equatorial forest surrounding the lake (organic matter input, low mineralization under tropical condition), and the presence of silicate and aluminium compounds in the area. Additionally, the probable low contribution of ground water into the lake and the probable high primary production can explain the low value of dissolved oxygen.
Sediment particle size and organic matter content in sampled sediments are shown in Table 2. The sediments present high organic matter content with the values range from 10.3 to 16.6 %. The maximum value was observed in the site 2D (16.6 %). The sediments were composed majorly with silts, the values ranged from 30.7 to 69.6 %. Except for the sites 1D (54.4 % of sand) and 4D (43.9 % of sand), all sampled sites are especially constituted with silts and clay. The lowest concentration of sand was observed in the sites 1G (0.7 %) and 3G (0.0 %). The high sediment median grain size value was observed in the site 1D (105.8 μm) and lowest (4.30 μm) for the site 3G. CaCO3 values were very less for all sediment samples and do not exceed 2 % with all the studied samples.
The particle size distribution is found to be influenced by the hydrodynamic aspects of the lake, probably by the dynamic of stream input action and wave that can create a high energy. Coarser sediments were located close to the shores, especially in the stream outlet (site 1D), with median value of 105 μm and values of 30.6, 14.8 and 54.4 % for silts, clays and sand, respectively. Around the stream inlet (site 1G), sediments contained a quite proportion of sand (0.72 %), which is a result of the river organic matter deposition. This hypothesis can be confirmed by the correlation between other physico-chemical parameters including organic matter (OM), silts and clays in this site (Haller et al. 2009a, b). Past studies have reported that distribution of sediment OM and grain size have displayed large variations on these parameters in freshwaters, lakes, rivers and reservoir (Haller et al. 2009a; Poté et al. 2008). According to their results, the organic matter in non-contaminated freshwater sediments varied from 0.2 to 6.0 %. The sediment of Lake Ma Vallée could therefore be considered as rich in organic matter content, but not polluted by organic matter. For, e.g. sediments contaminated by the municipal WWTP effluent waters, OM can reach the values of 30 % (Poté et al. 2008). The high organic matter in the sediment of the Lake Ma Vallée can also be explained by the presence of both the agricultural crops in watershed and the dense tropical forest surrounding the lake.
Bacteria levels in water column
The bacterial concentration in the water column is presented in Table 1. In general, the FIB concentration in the water column is low. The maximum values were observed in the water samples from the middle of the bay (site MM) and stream outlet of the lake (site SM). For the site SM, values of E. coli and ENT were 66 and 88 CFU 100 mL−1, respectively. The same tendency was observed for HPC and Pseudomonas values. In the SM site, the maximum obtained values were 5.1 × 104 and 12 CFU 100 mL−1 for HPC and Pseudomonas spp., respectively. This finding illustrates the homogeneous distribution of bacteria in the water column of the lake.
According to the European Directive 2006/7/CE concerning the management of bathing water quality, recreational waters are to be classified as poor, if concentrations of E. coli exceed 900 CFU 100 mL−1 and concentrations of ENT exceed 330 CFU 100 mL−1, based upon a 90-percentile evaluation. The concentrations of FIB obtained in the water column of the Lake Ma Vallée are under the values requirement for recreational/bathing waters. Thus, the Lake Ma Vallée can be considered as moderately contaminated by faecal indicator bacteria and cannot present important human risk. However, even if FIB concentrations in the water samples are low, their presence suggests that pathogenic bacteria of intestinal origin may also be present (Haller et al. 2009a). In this study, the presence of opportunist pathogens, P. aeruginosa, was detected in water and this identification reveals that there are more possible chances for the survival of pathogens in the Lake Ma Vallée.
In the vicinity of Lake Ma Vallée, there is no permanent source of pollution input, such as sewage treatment plant or a permanent urban landfill. The pollution of the lake can be explained by several aspects including domestic waste by the tourists, human visitors or wild animals; runoff of wastewater from septic tank and watershed of the lake; or as a result of contamination by human visitors or neighbouring animals. The water sampling took place in June, during dry/stratified period (no rainfall recorded). According to the sampling season, the sunlight (presence of UV radiation) can activate the decay of FIB in the water column (Hughes 2003; Sinton et al. 1999). Additionally, other factors such as the presence of protozoans and bacteriophages and competing autochthonous bacteria can cause considerable inactivation of FIB in the water column (Davies and Bavor 2000; Poté et al. 2009a; Chandran et al. 2011). Thus, increased temperatures, biological activity and potential presence of predation by bacterivores organisms, as well as intense UV radiation, further can contribute to the reduction of FIB levels in the water column of Lake Ma Vallée.
FIB, HPC and Pseudomonas spp. in surface sediments
The FIB, HPC and Pseudomonas spp. distribution in surface sediments of the bay is presented in Table 3. It shows the higher observed concentrations of bacteria in the surface sediments across the whole bay with an emphasis along the beaches. The concentrations of bacteria in all analysed sediments were observed with significant variations within the analysed samples. The FIB concentration values ranged from 6.6 × 102 to 2.7 × 103 and 9.9 × 102 to 6.3 × 103 CFU g−1, for E. coli and ENT, respectively. The HPC concentration was in order of 108 CFU 100 g−1 for all sampling sites. The concentration of Pseudomonas spp. ranged from 5.6 × 102 to 3.27 × 103 CFU 100 g−1. PCR analysis with specific primers for the general confirmation on the isolated bacterial colonies demonstrated that 92, 100 and 98 % of the isolated bacteria were E. coli, ENT and Pseudomonas spp., respectively. All isolates confirmed as Pseudomonas spp. were further studied for the presence of pathogen P. aeruginosa, and the results revealed their presence in both water and sediment isolated colonies.
In the aquatic environment, sediment may constitute a reservoir of different pollutants including toxic metals and microorganisms. Some studies have assessed the presence of bacterial indicators in the sediments and the water column (Anderson et al. 2005; Davis et al. 2005). The influence of environmental conditions on the persistence and accumulation of microorganisms in sediment is higher when compared with the water column, with a potential risk of pollution for coastal recreational water have been demonstrated (LaLiberte and Grimes 1982; Davies et al. 1995; Evanson and Ambrose 2006). Our recent studies demonstrated that the contrasting freshwater sediments can accumulate great levels of FIB than in overlying water (Haller et al. 2009a, b; Poté et al. 2009a, b, 2012; Thevenon et al. 2012). Other studies demonstrated that FIB can survive longer in sediments than in the water column since sediments provide favourable nutrient conditions (Gerba and McLeod 1976; Laliberte and Grimes 1982), protection from sunlight inactivation (Sinton et al. 1999) and protozoan grazing (Davies and Bavor 2000). The results of this study demonstrate clearly that the sediment of a tropical lake-reservoir may contain FIB (including E. coli and ENT) and Pseudomonas spp. at the levels of 100 to 1,000 times higher than that in the water column. Possible resuspension of FIB and pathogens from the sediments to the water column due to recreational activities or natural turbulence may contribute to potential human health risk (An et al 2002; Craig et al. 2004).
In the river-reservoir Lake Ma Vallée, the concentrations of FIB, HPC and Pseudomonas spp. are significantly higher in sediments than in the water column. The risks associated with swimming in microbiologically polluted lakes or rivers during recreational activities are usually not life threatening but could take a substantial toll in children and immune-compromised individuals (Clark et al. 2003). Because there are no health standards for beach sediments, it is difficult to assess whether the FIB and Pseudomonas spp. levels measured in sediments of Lake Ma Vallée can pose a health risk. But some studies examined whether the bacteria originating (resuspending) from amount of sediment would exceed health standards for water column (Lee et al. 2006; Haller et al. 2009a, b).
Spearman rank order correlation
The Spearman rank order correlation values are presented in Table 4. There is a strong positive correlation (0.762) between the E. coli and OM, which illustrates that increase with OM in the natural water reservoir could also significantly increases the E. coli distribution in the studied samples. The correlation values are also supportive with our previous studies (Haller et al. 2009a, b) which demonstrated that faecal origin bacteria could survive in the sediments for longer time, depending on the availability of organic matter (Table 5). With other parameters analysed, there was no significant values found for the correlation matrix.
Conclusion
The results of this study indicate that Lake Ma Vallée presents the lowest values of faecal indicator bacteria in the water column, suggesting that there are no local permanent sources of contamination in the area. Thus, the Lake can be considered as moderately contaminated by FIB bacteria. On the other hand, the accumulation of FIB and Pseudomonas spp. in the sediments of the lake was observed. This may impact on the potential risks of human infections either by direct uptake or contamination during recreational activities.
To our knowledge, this is the first study to be performed on the assessment of microbial quality in the water column and sediments of Lake Ma Vallée. Under tropical condition, the low concentration of FIB and Pseudomonas spp. in the water column cannot guarantee the sanitary state of the quality of water. Thus, supplementary analyses of both water and sediment, especially on the determination of protozoa and other virus, are needed to assess the microbial quality of water under tropical conditions.
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Acknowledgments
We are grateful to the financial sources: the Swiss National Science Foundation (grant no. 31003A_150163/1) and Forel Institute, University of Geneva. This research presents the results of tripartite collaboration between University of Geneva (Forel Institute), University of Kinshasa and Pedagogic National University of Congo (Democratic Republic of Congo) and Jamal Mohamed College (Affiliated to Bharathidasan University), Tiruchirappalli, Tamil Nadu, India. Naresh Devarajan is a Ph.D. scholar supported by a Swiss Government Scholarships for Foreign Scholars.
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Mwanamoki, P.M., Devarajan, N., Thevenon, F. et al. Assessment of pathogenic bacteria in water and sediment from a water reservoir under tropical conditions (Lake Ma Vallée), Kinshasa Democratic Republic of Congo. Environ Monit Assess 186, 6821–6830 (2014). https://doi.org/10.1007/s10661-014-3891-6
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DOI: https://doi.org/10.1007/s10661-014-3891-6