African Journal of
Agricultural Research

  • Abbreviation: Afr. J. Agric. Res.
  • Language: English
  • ISSN: 1991-637X
  • DOI: 10.5897/AJAR
  • Start Year: 2006
  • Published Articles: 6859

Full Length Research Paper

Bacteriological quality of drinking water originated from groundwater in Béni-Abbés area (South West Algeria)

BENGARNIA Benmerine*
  • BENGARNIA Benmerine*
  • Laboratory of Applied Microbiology, Department of Biology, Faculty of Nature Sciences and Life, Oran1 University, Ahmed Ben Bella, P. O. Box 16 Es-Senia, Oran 31100, Algeria.
  • Google Scholar
HADADJI Miloud
  • HADADJI Miloud
  • Laboratory of Applied Microbiology, Department of Biology, Faculty of Nature Sciences and Life, Oran1 University, Ahmed Ben Bella, P. O. Box 16 Es-Senia, Oran 31100, Algeria.
  • Google Scholar
RAMDANI Mohammed
  • RAMDANI Mohammed
  • University Mohammed V Agdal, Scientific institute - Rabat, Morocco.
  • Google Scholar
KIHAL Mebrouk
  • KIHAL Mebrouk
  • Laboratory of Applied Microbiology, Department of Biology, Faculty of Nature Sciences and Life, Oran1 University, Ahmed Ben Bella, P. O. Box 16 Es-Senia, Oran 31100, Algeria.
  • Google Scholar


  •  Received: 07 April 2015
  •  Accepted: 18 September 2015
  •  Published: 31 December 2015

 ABSTRACT

The purpose of the present study was to examine the bacteriological quality of the drinking water samples to evaluate the results with the Algeria and international standards for drinking water quality, as well as the identification of the dominant microflora. The water samples (groundwater) are collected monthly from six sites in Béni-Abbés district. Most of the samples have shown the occurrence of Escherichia coli, in addition to Salmonella sp and Clostridium sp. Out of 300 water samples collected, 126 (42%) were contaminated with either one or more than one type of microorganisms: Enterobacter gergoviae detected in 26 samples (11.06%), E. coli in 63 (22.98%), Citrobacter freundii in 16 (6.81%), Vibrio vulnificus in 2 (0.85%), Pseudomonas aeruginosa in 19 samples (8.09%) and Serratia liquefaciens in 22 (9.36%). Clostridium was the common cause of contamination, about 45 (16.60%), and Salmonella sp was detected in 66 (24.25%), Salmonella typhi in 44 samples (18.72%) and Salmonella paratyphi in 13 samples (5.53%). The findings of this study highlight the need for a more stringent self-control of drinking water. In addition, a more systematic surveillance by the official authorities of drinking water is also necessary.
 
Key words: Bacteria, Béni-Abbès, drinking water, groundwater quality, indicators, microbial analysis, Escherichia coli.
 


 INTRODUCTION

Most drinking water in Algerian dry regions comes from groundwater. The quality and purity of this groundwater has direct effect on human health. The use of certain bacteria, as indicators of the potential presence of pathogenic microorganisms in natural and treated waters, is the standard means of assessing the microbiological quality of a water body (Nair et al., 2006). Water scarcity is a major problem in many developing countries. Drinking water is indispensable for human life. However, in many parts of the world, the water is provided only at certain time intervals during the day. Although connected to a supply system, the user still has to store water to have a sufficient amount of water available during the non-supply periods. People can survive days, weeks or months without food, but only about four days without water. The body uses water for digestion, absorption, circulation, transporting nutrients, building tissues, carrying away waste and monitoring body temperature.

Water can be hard or soft, natural or modified, bottled or tap, carbonated or still (Kendall, 1992). The human bacterial pathogens that can be transmitted by consuming contaminated drinking water, and that present a serious risk of disease, include Salmonella spp. Shigella spp. enterovirulent Escherichia coli, Vibrio cholera, Yersinia enterocolitica, Campylobacter jejuni and Campylobacter coli. After being excreted in faeces from the body of their host, bacterial pathogens gradually lose viability and the ability to cause infection. The rate of decay varies with different bacteria; it is usually exponential, and after a certain period a pathogen will become undetectable. The most common waterborne pathogens are those that are highly infectious or highly resistant to decay outside the body. Pathogens with a low persistence, which do not survive long outside the host, must rapidly find a new host and are more likely to be spread by person-to-person contact or by poor personal or food hygiene than by drinking water (Mc Michael, 2000). Algeria is largest country in Africa and lies mostly in the arid region where water is a scarce commodity, it is considered to be rich in water resources (Kihal et al., 2002). The disease causing organisms called pathogens are discharged along with faecal wastes and are difficult to detect in water supplies. Fortunately, less harmful, easily isolated bacteria called indicator organisms can be used indirectly to detect pathogens. Among these indicators are coliforms bacteria. They live in the intestine of man and other animals and are almost always present, even in healthy people. The presence of coliforms in water is a warning signal that more dangerous bacteria may be present. Diseases resulting from ingestion of pathogens in contaminated water have the greatest public health impact worldwide. Presence of faecal coliforms or E. coli is used as an indicator for the presence of any of the waterborne pathogens (Naresh et al., 2013). The common feature of all routine screening procedures is the primary examination for indicator microorganisms rather than the pathogens. Indicator microorganisms are bacteria such as non-specific coliforms, E. coli and Pseudomonas aeruginosa that are very commonly found in the human or animal gut and which, if detected, may suggest the presence of sewage (Zamberlan et al., 2008; Odonkor and Ampofo, 2013). Indicator organisms are used because even when a person is infected with more pathogenic bacteria, they will still be excreting many millions times more indicator organisms than pathogens. It is therefore reasonable to deduce that if indicator organism levels will be very much lower or absent. World Health Organization (WHO, 1993) recommends that no faecal coliforms will be present in 100 ml of drinking water. Good quality water is odorless, colorless, tasteless and free of faecal contamination and chemicals in harmful amounts. Potable or drinking water can be defined as the  water  delivered  to  the that can be safety used for drinking, cooking and washing (De Zuane, 1997; Ghorbani et al., 2013). The main objective of present study was to identify environmental factors determining total and fecal coliforms and other indicators bacteria levels in drinking water. It was hoped that information from this study might help facilitate source water protection and establish more effective water treatment strategies in Algeria dry zones.


 MATERIALS AND METHODS

Description of the study area

Béni abbes is geographically located between latitudes 30°06’50.4” N and 30°08’34.08” N and between longitudes 2°08’57.12” W and 2°10’48.8” W (Figure 1).

 

 

Sampling

From August 2009 through May 2011, a total of 300 samples of drinking water were collected from different places in Béni-Abbes area. Upon collection, samples, sealed in 1 L to polyethylene terephthalate (PET) bottles, were taken to the microbiological laboratory and stored at refrigeration temperature in the original bottle until tested. All samples were processed within 24 h after collection. The sources were included frame follows: (a) Spring water of Sidi Othman, (b) Municipal well, (c) Ougarta's Foggara, (d) Béni-Abbés, Foggara, (e) Zeghamra's well and (f) Béni-Abbes well. Drinking water samples from different sources in Béni-Abbès town were collected and transported by standard methods as mentioned in APHA (1998) and Al-Toumi, (2007).

 

Bacteriological analysis

All samples were examined for the three widely used bacterial indicators using the relevant ISO (International Organization for Standardization) standards: ISO 9308-2 (1990) for total coliforms and E. coli, and ISO 7899-2 (1998) for Enterococci, as well as ISO 6222 (1999) for total flora at 22 and 36°C. For enumeration of heterotrophic bacteria, the pour plate method was chosen, using 1 ml of mineral water sample and mixing with melted Plate Count Agar (Casein peptone Dextrose Yeast Agar; Merck) tempered at 44°C. Two sets of plates were prepared for all samples. One set was incubated aerobically at 37°C for 24 h and the other set at 22°C for 72 h. All colonies were counted and the results were expressed as colony-forming units (CFU) per milliliter of the water sample.

The predominant microorganisms in drinking water samples were identified using biochemical tests. Isolates of morphologically different colony types were selected from plate count agar and sub cultured. The cultures were then kept in a refrigerator at 4°C until used for further tests. These biochemical tests included: Gram staining, catalase test and oxidase test according to William et al. (2001) and endospore staining, motility test and production of acid from glucose according to Chessbrough (1985) described by Ibrahim et al. (2013).

The Oxidation/Fermentation test was also carried out as described by William et al. (2001). In this test: Hugh and Liefson’s medium was used in two tubes which were inoculated with fresh cultures. One tube was covered with sterile paraffin oil and the other was left open. Incubation was carried out at 37°C for 24 to 72 h. Growth in both tubes was recorded as fermentation metabolism while growth in the open tube only was recorded as oxidative metabolism William et al. (2001).

 


 RESULTS

All the water samples were analysed in Béni-Abbès hospital laboratory. A number of 300 samples were examined in the study. All samples were tested for bacteriological contamination by total aerobic bacteria, indicators groups and potential pathogenic bacteria (Table 1).

 

 

Bacteriological analysis of water

Total plate count

Total plate count for total bacterial count performed for all water samples showed only 58.33% samples were within the WHO (1996) guideline value (<10 cfu/ml). In source wise distribution of samples, 20% of spring water Sidi Othman, 70% of well municipal, 60% of Ougarta's foggara, 40% of Béni-Abbès foggara, 50% of Zeghamra's drilling and 10% of Béni-Abbès drilling samples has exceeded the guideline value.

 

Coliform count

Source wise distribution of coliform count showed that the 30% of spring water Sidi Othman, 50% of well municipal, 50% of Ougarta's foggara, 40% of Béni-Abbès foggara, 40% of Zeghamra's drilling and 20% of Béni-Abbès drilling crossed WHO guideline value (0 cfu/100 ml).

 

Fecal streptococci count

Source wise distribution of faecal streptococci count showed that the 20% of spring water Sidi Othman, 60% of well municipal, 50% of Ougarta's foggara, 40% of Béni-Abbès foggara, 50% of Zeghamra's drilling and 10% of Béni-Abbès drilling.

 

Isolation and identification of bacteria

In this study, 274 isolates of enteric bacteria obtained were identified as E. coli (22.98%), Enterobacter spp (11.06%), Citrobacter spp (6.81%), Pseudomonas aeruginosa (8.09%), Salmonella typhi (18.72%), Salmonella para typhi A (5.53%), Serratia spp (9.36%), Vibrio cholerae (0%) from Vibrio (0.85%) and 16.6% Clostridium (Madigan et al., 1997; Dhanya et al., 2013). Results of the bacteriological analysis of the water sample are presented in Table 3.

The total viable counts for all water samples were quite high ranging from 135 × 103 cfu/ml to 25 × 103 cfu/ml. The Ougarta's foggara sample has the highest microbial load of 135 × 103 while well water far away from refuse site had the least value of 25 × 103cfu/ml (Table 2). The most probable number (MPN) for presumptive total coliform count of the water samples ranged from 1, 6 to140 MPN per 100 ml. Water samples well municipal and Ougarta's foggara (Table 3). Vibrio cholerae count of all water samples not detected but in the well municipal there is a suspected result (Table 3). Salmonella count is detected for samples well municipal and Ougarta's foggara (Table 3). The bacteria isolated from water samples in this work included E. coli, Enterobacter gergoviae, P. aeruginosa, S. typhi, S. para typhi A, Vibrio vulnificus and Clostridium spp. (Table 3). Heterotrophic count measures a range of bacteria that are naturally present in the environment (EPA, 2002). The total bacterial counts for all the water samples were generally high exceeding the limit of 1.0 × 102 cfu/ml which is the standard limit of heterotrophic count for drinking water (EPA, 2002).

 

 

 

The high total heterotrophic count is indicative of the presence of high organic and dissolved salts in the water. The primary sources of these bacteria in water are animal and human wastes. These sources of bacterial contamination include surface runoff, pasture, and other land areas where animal wastes are deposited. Additional sources include seepage or discharge from septic tanks, sewage treatment facilities and natural soil plant bacteria (EPA, 2002). These contaminants are reflected in the highest bacterial load obtained in this study for the Ougarta's foggara water samples.

The microbial count was higher in well municipal water close to refuse disposal site as compared to well water far away but both microbial counts are  lower than that of spring water Sidi Othman. Generally, underground water is believed to be the purest known (Gordan and Gever, 1996; Prescott et al., 2002; Ayoade et al., 2013) because of the purification properties of the soil; however, it can also be contaminated. Ground waters are found to be contaminated due to improper construction, shallowness, animal wastes, proximity to toilet facilities, sewage, refuse dump sites, and various human activities around the well (Bitton, 1994)..The presumed reason for contamination of well water accounts for why the microbial load of well municipal water close to refuse disposal site have higher microbial count than the one far away from refuse disposal site. Environmental Protection Agency (EPA) establishes heterotrophic plate count as a primary standard, which is based on health considerations.

Accordingly, the total coliform count for all samples was exceedingly high the EPA maximum contamination level for coliform bacteria in drinking water of zero total coliform per 100 ml of water (EPA, 2003). The high coliform count obtained in the samples may be an indication that the water sources are faecally contaminated (EPA, 2003; Osuinde and Enuezie, 1999). None of the water samples complies with EPA standard for coliform in water. According to EPA standard, every water sample that has coliform must be analyzed for either fecal coliforms or E. coli (EPA, 2003; Rizvi et al., 2013).

Other bacteria isolated from all water samples such as P. aeuruginosa (Shittu et al., 2008). Enterobacter aerognes isolated from the water samples are examples of non-fecal coliforms and can be found in vegetation and soil which serves as sources by which the pathogens enters the water (Schlegel, 2002). The British Standard Institute (BSI, 1993) specified that counts greater than 104 are considered unsatisfactory for Enterobacter spp described by Shittu et al. (2008); Manjula et al. (2011).


 DISCUSSION

The main objective of this study was evaluation of quality of drinking water from different sources of Béni-Abbès town. The coliform count has been used extensively as a basis for regulating the microbial quality of drinking-water. In this study, both regulatory parameters were excessively as the WHO guideline values. Study results clearly indicated that most of the natural water sources are less contaminated. The detection of pathogenic enteric bacteria in different sources of drinking water in Béni-Abbès water also reveals the alarming situation for water borne epidemics in water.

Kehr and Butterfield (1943) showed the coliform test to be a useful indicator of S. enterica serovar Typhi. The authors concluded that the presence of even moderate numbers of coliforms presented a high risk, citing an outbreak in Detroit, Michigan, where mean coliform counts in the water supply of only 3 and 10 colony forming units in every 100 ml of water on two successive days were the indicator for an outbreak of waterborne typhoid. Kehr and Butterfield (1943) also noted the much greater risk of gastroenteritis associated with this low coliform count: for the eight cases of typhoid recorded in this outbreak, there were 45 000 cases of gastroenteritis.

Water supply of only 3 and 10 colony forming units in every 100 ml of water on two successive days was the indicator for an outbreak of waterborne typhoid. Kehr and Butterfield (1943) also noted the much greater risk of gastroenteritis associated with this low coliform count: for the eight cases of typhoid recorded in this outbreak, there were 45 000 cases of gastroenteritis.

Water quality indicates that pollution of the water is increasing alarmingly and that it has created serious threat to human health and environment. Bacteriological pollution   of  water  supplies  may  be  either  due  to  the failure of the disinfections of the raw water at the treatment plant or to the infiltration of contaminated water (sewage) through cross connection and leakage points. The results emphasize the importance of adopting appropriate routinely monitoring system in order to prevent or to diminish the chances of contamination of this water source.


 CONFLICT OF INTEREST

The authors have not declared any conflict of interest.



 REFERENCES

Al-Toumi AS (2007). Manual of Bacteriological Examination of Drinking Water English Ed. Biotechnology Research Centre. P 65.

 

American Public Health Association (APHA) (1998). Standards Methods for the Examination of Water and Wastewater. 20th edition, American Public Health Association, Washington, D.C.

 
 

Ayoade F, Fayemi SO, Daramola GG, A Osho, Oyejide NE, Adenodi SA, Anazodo KO (2013). Effectiveness of storage as a point-of-use means of improving the bacteriological quality of drinking water. Int. J. Biol. Chem. Sci. 7(1):96-106.
Crossref

 
 

Bitton G (1994). Waste Water Microbiology. Gainesville, New York Wiley- Liss. P 118.

 
 

BSI, British Standards Institute (1993). Microbiological examination of food and animal feeding stuff. Enumeration of Enterobacteriaceae. London. BSI (5763: Part 10:1993(ISO 7402:1993).

 
 

Chessbrough M (1985). Medical Laboratory Manual for Tropical Countries. Microbiology II:248-264.

 
 

De Zuane J (1997). Hand book of drinking water quality. 2nd Ed. John Wiley and Sons, Inc. New York USA J.

 
 

Dhanya VC, Anitha J, Dhanashree B (2013). Bacteriological Screening of Water in Mangalore, India. Brit. Microbiol. Res. J. 3(1):84-95.
Crossref

 
 

EPA (2002). US Environment Protection Agency, Safe Drinking Water Act Ammendment http:// www. epa. gov/safe water /mcl. Html

 
 

EPA (2003). US Environmental Protection Agency Safe Drinking Water Act. EPA 816 – F – 03 –016.

 
 

Ghorbani J, Moradianfard S, Reisi P, Shehni GM (2013). Survey of heterotrophic bacteria population changes in Kerman drinking water distribution system and GIS zoning. Eur. J. Exp. Biol. 3(2):476-483.

 
 

Gordan MF, Gever JG (1996). Water supply and Waste Removal in: Waste supply and Waste Removal In: Waste Engineering Vol. John Wiley and Sons, pp. 220-236.

 
 

Ibrahim TA, Akenroye O, Opawale BO (2013). A Survey of Physicochemical and Bacteriological Quality of Pipe-Borne Water Used for Drinking in Rufus Giwa Polytechnic, Owo Ondo State, Nigeria. Greener J. Sci. Eng. Technol. Res. 3(6):181-185.

 
 

ISO 6222 (1999). Water quality - Enumeration of culturable microorganisms -Colony count by inoculation in a nutrient agar culture medium.International Organization for Standardization, Geneva, Switzerland.

 
 

ISO 7899-1 (1998). Water quality - Detection and enumeration of intestinal enterococci in surface and waste water - Part 1: Miniaturized method (Most Probable Number) by inoculation in liquid medium. International Organization for Standardization, Geneva, Switzerland.

 
 

ISO 9308-2 (1990). Water quality - Detection and enumeration of coliform organisms, thermotolerant coliform organisms and presumptive Escherichia coli - Part 2: Multiple tube (most probable number) method. International Organization for Standardization, Geneva, Switzerland.

 
 

Kehr RW, Butterfield CT (1943). Notes on the relation between coliforms and enteric pathogens. Public Health Report, Washington. 58:589-607.
Crossref

 
 

Kendall P (1992). Newsletter in Drinking water quality and health, Colorado State University.

 
 

Kihal M, Boutiba Z, Henni DE, Al-Aboudi AK (2002). Microbiological quality of drinking water at arid zones in Adrar south Algeria. J. Alg. Rég. Arid. 1:26-30.

 
 

Madigan MT, Martinko JM, Parker J (1997). Biology of Microorganisms. 8th Ed Brock Prentice Hall International Inc. P. 986.

 
 

Manjula AV, Shankar GK, Metgaud PS (2011). Bacteriological Analysis of drinking water samples. J. Biosci. Tech. 2(1):220-222.

 
 

Mc Michael AJ (2000). The urban environment and health in a world of increasing globalisation; issues for developing countries. Bull. World Health Org. 78:117-126.

 
 

Nair GA, Bohjuari JA, Al-Mariami MA, Attia FA, El-Toumi FF (2006). Groundwater quality of north-east Libya. J. Environ. Biol. 27:695-700.

 
 

Naresh K, Ankusha S, Priya S (2013). To study the Physico-Chemical properties and Bacteriological examination of Hot Spring water from Vashisht region in Distt. Kullu of HP, India. Int. Res. J. Environ. Sci. 2(8):28-31.

 
 

Odonkor ST, Ampofo JK (2013). Escherichia coli as an indicator of bacteriological quality of water: an overview Licensee PAGE Press. Italy Microbiology Research 4:e2 doi:10.4081/mr.2013.e2
Crossref

 
 

Osuinde MI, Eneuzie NR (1999). Bacteriological analysis of ground water. Nig. J. Microbiol. 13:47-54.

 
 

Prescott LM, Harley JP, Klein DA (2002). Microorganisms in aquatic environments In Microbiology 5th edition, Mc Gram – Hill Companies Inc. New York, pp. 632-663.

 
 

Rizvi R, Kamble LH, Kadam AS (2013). Heterotrophic plate count Bacteria in drinking water supply of a selected area of Nanded City. Sci. Res. Rep. 3(1):66-68.

 
 

Schlegel HG (2002). General Microbiology. 7th. Ed. Cambridge. University Press. P. 480.

 
 

Shittu OB, Olaitan JO, Amusa TS (2008). Physico-Chemical and Bacteriological analyses of Water Used for Drinking and Swimming Purposes in Abeokuta. Nigeria. Afr. J. Biomed. Res. 1(11):285-290.

 
 

WHO (1993). Guidelines for Drinking Water Quality, Volume I, II and III, World Health Organizations, Geneva.

 
 

WHO (1996). Guidelines for Drinking Water Quality 2nd edition. Volume II, Health criteria and other supporting information. World Health Organizations, Geneva.

 
 

William AS, Harriet R, Bruce DF (2001). Lippincott's illustrated Reviews. Microbiology, pp. 22-23, 26-27, 102-103.

 
 

Zamberlan da SME, Getirana RS, Guilhermetti M, Camargo I, Filho E, Harue E, Ueda-Nakamura T, Nakamurac CV, Dias FBP (2008). Comparison of the bacteriological quality of tap water and bottled mineral water. Int. J. Hyg. Environ. Health 211:504-509.
Crossref

 
 

 




          */?>