期刊论文详细信息
BMC Public Health
Detection of Escherichia coli, Salmonella species, and Vibrio cholerae in tap water and bottled drinking water in Isfahan, Iran
Amin Asgarifar4  Ebrahim Rahimi1  Farhad Safarpoor Dehkordi3  Hassan Momtaz2 
[1] Department of Food Hygiene, College of Veterinary Medicine, ShahreKord Branch, Islamic Azad University, ShahreKord, Iran;Department of Microbiology, College of Veterinary Medicine, ShahreKord Branch, Islamic Azad University, P.O. Box: 166, ShahreKord, Iran;Young Researchers Club, Islamic Azad University, ShahreKord Branch, ShahreKord, Iran;Graduated of Veterinary Medicine, College of Veterinary Medicine, ShahreKord Branch, Islamic Azad University, ShahreKord, Iran
关键词: Iran;    PCR;    Water;    Vibrio cholerae;    Salmonella species;    Escherichia coli;   
Others  :  1162126
DOI  :  10.1186/1471-2458-13-556
 received in 2012-07-15, accepted in 2013-05-21,  发布年份 2013
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【 摘 要 】

Background

The quality of drinking water has an important role in human infection and disease. This study was aimed at comparing polymerase chain reaction and culture in detecting Escherichia coli, Salmonella species and Vibrio cholera in tape water and bottled drinking water in various seasons in Isfahan province, Iran.

Methods

A total of 448 water samples from tap water and bottled mineral water were taken over 6 months, from July 2010 to December 2010, and after filtration, samples were examined by culture and polymerase chain reaction methods for detection of Escherichia coli, Salmonella species, and Vibrio cholerae.

Results

The culture method showed that 34 (7.58%), 4 (0.89%) and 3 (0.66%) of all 448 water samples were positive for Escherichia coli, Salmonella species, and Vibrio cholera, respectively. The uidA gene from Escherichia coli, IpaB gene from Salmonella species, and epsM gene from Vibrio cholera were detected in 38 (26.38%), 5 (3.47%), and 3 (2.08%) of 144 tap-water samples, respectively. Escherichia coli was detected in 8 (2.63%) of 304 samples of bottled drinking water from 5 companies. The water of southern part of Isfahan and company 5 had the highest prevalence of bacteria. The Escherichia coli water contamination was significantly higher (P < 0.05) in the hot seasons (July-August) than cold (November-December) seasons and in company 5 than other companies. There were significant differences (P < 0.05) for the prevalence of bacteria between the tap waters of southern part and tap waters of central part of Isfahan.

Conclusions

This study showed that the polymerase chain reaction assays can be an extremely accurate, fast, safe, sensitive and specific approach to monitor drinking water quality from purification facilities and bottled water companies. Also, our study confirmed the presence of Escherichia coli, Salmonella species, and Vibrio cholerae as water-borne pathogens in tap water and bottled drinking water of Isfahan, Iran. The present study showed the important public health problem in Isfahan, Iran.

【 授权许可】

   
2013 Momtaz et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Duset AG, da Silva MP, Zietsman I: Coping with hygiene in South Africa, a water scarce country. Int J Environ Health Res 2003, 13:S95-S105.
  • [2]Cherry WB, Hanks JB, Thomason BM, Murlin AM, Biddle JW, Croom JM: Salmonella as an index of pollution of surface waters. Appl Microbiol 1872, 24:334-340.
  • [3]Hunter P: Water-borne disease: epidemiology and ecology. Chichester: Wiley; 1997:384.
  • [4]Momba MN, Malakate VK, Theron J: Abundance of pathogenic Escherichia coli, Salmonella typhimurium and Vibrio cholerae in Nkonkobe drinking water sources. J Water Health 2006, 4:289-296.
  • [5]Momtaz H, Rahimi E, Moshkelani S: Detection of Pseudomonas aeruginosa by PCR in tap-water and bottled mineral water in the Isfahan province of Iran. Water Sci Thechnol Water Supply 2011, 11:642-646.
  • [6]Pegram GC, Rollins N, Espey Q: Estimating the cost of diarrhoea and epidemic dysentery in KwaZulu-Natal and South Africa. Water South Africa 1998, 24:11-20.
  • [7]Al Dahouk S, Tomaso H, Nöckler K, Neubauer H: The detection of Brucella spp. using PCR-ELISA and real-time PCR assays. Clin Lab 2001, 50:387-394.
  • [8]Kong RY, Lee SK, Law TW, Law SH, Wu RS: Rapid detection of six types of bacterial pathogens in marine waters by multiplex PCR. Water Res 2002, 36:2802-2812.
  • [9]Bomfim MR, Barbosa-Stancioli EF, Koury MC: Detection of pathogenic leptospires in urine from naturally infected cattle by nested PCR. Vet J 2008, 178:251-256.
  • [10]Theron J, Cilliers J, Du Preez M, Brözel VS, Venter SN: Detection of toxigenic Vibrio cholerae from environmental water samples by an enrichment broth cultivation-pit-stop semi-nested PCR procedure. J Appl Microbiol 2000, 89:539-546.
  • [11]Ferretti R, Mannazzu I, Cocolin L, Comi G, Clementi F: Twelve-hour PCR-based method for detection of Salmonella spp. in food. Appl Environ Microbiol 2001, 67:977-978.
  • [12]Fratamico PM, DebRoy C, Miyamoto T, Liu Y: PCR detection of enterohemorrhagic Escherichia coli O145 in food by targeting genes in the E. coli O145 O-antigen gene cluster and the shiga toxin 1 and shiga toxin 2 genes. Foodborne Path Dis 2009, 6:605-611.
  • [13]Lotfy NM, Hassanein MA, Abdel-Gawad FKH, El-Taweel GE, Bassem SM: Detection of Salmonella Spp in aquatic insects, fish and water by MPN-PCR. World J Fish Marine Sci 2011, 3:58-66.
  • [14]Daly P, Collier T, Doyle S: PCR-ELISA detection of Escherichia coli in milk. Lett Appl Microbiol 2002, 34:222-226.
  • [15]Perelle S, Dilasser F, Malorny B, Grout J, Hoorfar J, Fach P: Comparison of PCR-ELISA and LightCycler real-time PCR assays for detecting Salmonella spp. in milk and meat samples. Mol Cell Probes 2004, 18:409-420.
  • [16]Albert MJ, Islam D, Nahar S, Qadri F, Falklind S, Weintraub A: Rapid detection of Vibrio cholerae O139 Bengal from stool specimens by PCR. J Clin Microbiol 1997, 35:1633-1635.
  • [17]Chiu CH, Ou JT: Rapid identification of Salmonella serovars in feces by specific detection of virulence genes, invA and spvC, by an enrichment broth culture-multiplex PCR combination assay. J Clin Microbiol 1996, 34:2619-2622.
  • [18]Ramotar K, Waldhart B, Church D, Szumski R, Louie TJ: Direct detection of verotoxin-producing Escherichia coli in stool samples by PCR. J Clin Microbiol 1995, 33:519-524.
  • [19]Tsai YL, Palmer CJ, Sangermano LR: Detection of Escherichia coli in sewage and sludge by polymerase chain reaction. Appl Environ Microbiol 1993, 59:353-357.
  • [20]Fode-Vaughan KA, Maki JS, Benson JA, Collins ML: Direct PCR detection of Escherichia coli O157:H7. Lett Appl Microbiol 2003, 37:239-243.
  • [21]Kerr M, Fitzgerald M, Sheridan JJ, McDowell DA, Blair IS: Survival of Escherichia coli O157:H7 in bottled natural mineral water. J App Microbiol 1999, 87:833-841.
  • [22]Ocepek M, Pate M, Kušar D, Hubad B, Avberšek J, Logar K, Lapanje A, Zrimec A: Comparison of DNA extraction methods to detect Salmonella spp. in tap water. Slov Vet Res 2011, 48:93-98.
  • [23]Shanan S, Abd H, Hedenström I, Saeed A, Sandström G: Detection of Vibrio cholerae and Acanthamoeba species from same natural water samples collected from different cholera endemic areas in Sudan. BMC Res Notes 2011, 4:109. BioMed Central Full Text
  • [24]Bourne DE, Coetzee N: An atlas of potentially water related diseases in South Africa. Pretoria: Water Research Commission; 1990.
  • [25]Payment P, Siemiatycki J, Richardson L, Renaud G, Franco E, Prevost M: A prospective epidemiological study of gastrointestinal health effects due to the consumption of drinking water. Int J Environ Health Res 1997, 7:5-31.
  • [26]Amy PS, Hiatt HD: Survival and detection of bacteria in an aquatic environment. Appl Environ Microbiol 1989, 55:788-793.
  • [27]Faruque SM, Albert MJ, Mekalanos JJ: Epidemiology, genetics, and ecology of toxigenic Vibrio cholerae. Microbiol Mol Biol Rev 1998, 62:1301-1314.
  • [28]Martinelli Filho JE, Lopes RM, Rivera ING, Colwell RR: Vibrio cholerae O1 detection in estuarine and coastal zooplankton. J Plankton Res 2011, 33:51-62.
  • [29]World Health Organization (WHO): Guidelines for drinking-water quality. Fourth edition. Switzerland: WHO Library Cataloguing-in-Publication Data; 2011.
  • [30]CAWST: Center for affordable water and sanitation technology. Canada: Introduction to drinking water quality testing a cawst training manual; 2009.
  • [31]Ashbolt NJ, Grabow WOK, Snozzi M: Indicators of microbial water quality. In Water quality: guidelines, standards and health – assessment of risk and risk management for water-related infectious disease. Edited by Fewtrell L, Bartram J. WHO Water Series. London: IWA Publishing; 2001:289-315.
  • [32]Knight IT, Shults S, Kaspar CW, Colwell RR: Direct detection of salmonella spp. In estuaries by using a DNA probe. Appl Environ Microbiol 1990, 56:1059-1066.
  • [33]Heijnen L, Medema G: Quantitative detection of E. coli, E. coli O157 and other shiga toxin producing E. coli in water samples using a culture method combined with real-time PCR. J Water Health 2006, 4:487-498.
  • [34]Lipp EK, Rivera IN, Gil AI, Espeland EM, Choopun N, Louis VR, Russek-Cohen E, Huq A, Colwell RR: Direct detection of Vibrio cholerae and ctxA in Peruvian coastal water and plankton by PCR. Appl Environ Microbiol 2003, 69:3676-3680.
  • [35]Anderson IC, Rhodes MW, Kator HI: Seasonal variation in survival of Escherichia coli exposed in situ in membrane diffusion chambers containing filtered and nonfiltered estuarine water. Appl Environ Microbiol 1983, 45:1877-1883.
  • [36]Heidelberg JF, Heidelberg KB, Colwell RR: Seasonality of Chesapeake Bay bacterioplankton species. Appl Environ Microbiol 2002, 68:5488-5497.
  • [37]Suwandana E, Kawamura K, Tanaka K, Sakuno Y, Raharjo P: Escherichia coli and biophysicochemical relationships of seawater and water pollution index in the Jakarta Bay. Am J Environ Sci 2011, 7:183-194.
  • [38]Abakpa GO, Umoh VJ, Ameh JB: Prevalence OF Salmonella spp in some environmental samples from some households engaged in livestock farming in some parts of Zaria, Nigeria. Continental J Microbiol 2011, 5:6-11.
  • [39]Ahmed W, Neller R, Katouli M: Population similarity of enterococci and Escherichia coil in surface waters: a predictive tool to trace the sources of fecal contamination. J Water Health 2006, 4:347-356.
  • [40]Wilkes G, Edge TA, Gannon VP, Jokinen C, Lyautey E, Neumann NF, Ruecker N, Scott A, Sunohara M, Topp E, Lapen DR: Associations among pathogenic bacteria, parasites, and environmental and land use factors in multiple mixed-use watersheds. Water Res 2011, 45:5807-5825.
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