Skip to main content
Brazilian Journal of Microbiology logoLink to Brazilian Journal of Microbiology
. 2010 Sep 1;41(3):694–699. doi: 10.1590/S1517-83822010000300020

Aeromonas Presence in Drinking Water from Collective Reservoirs and Wells in Peri-Urban Area in Brazil

Maria Tereza Pepe Razzolini 1,*, Wanda Maria Risso Günther 1, Solange Martone-Rocha 1, Heloísa Duarte de Luca 1, Maria Regina Alves Cardoso 1
PMCID: PMC3768643  PMID: 24031545

Abstract

Aeromonas genus is considered an emerging pathogen and its presence in drinking water supplies is a reason to public health concern. This study investigated the occurrence of Aeromonas in samples from collective reservoirs and wells used as drinking water sources in a peri-urban area. A total of 35 water samples were collected from collective reservoirs and 32 from wells bimonthly, from September 2007 to September 2008. Aeromonas spp determination was carried out using a Multiple-Tube Technique. Samples were inoculated into alkaline peptone water and the superficial film formed was transferred to blood agar plates amended with ampicillin. Typical Aeromonas colonies were submitted to a biochemical screening and then to biochemical tests for species differentiation. Aeromonas was detected in 13 (19%) of the 69 samples examined (6 from collective reservoirs and 7 from wells). Concentrations of Aeromonas in collective reservoirs ranged from <0.3 to 1.2 x102MPN/100mL and, in wells, from <0.3 to 2.4 x102MPN/100mL. The most frequent specie in the collective reservoir samples was Aeromonas spp (68%), followed by A. encheleia (14%) and A. allosaccharophila (8%) and A. hydrophila (8%). Aeromonas spp (87%) was the most frequent specie isolated from well samples, followed by A. allosacchariphila (8%), A. encheleia (2%) and A. jandaei (5%). These data show the presence and diversity of Aeromonas genus in the samples analyzed and highlight that its presence in drinking water poses a significant public health concern.

Keywords: Aeromonas, peri-urban area, water quality

INTRODUCTION

Aeromonas genus is considered an emerging pathogen (26, 27) and responsible for gastrointestinal disturbances (19), septicemia, endocarditis, conjunctivitis and wound infections (8, 9, 13, 16, 18). These organisms are largely distributed in several water sources such as rivers, lakes, wells, sewage, wastewaters and drinking water supplies (19, 24).

The presence of these organisms in drinking water supplies, including in those chlorinated, is a reason to public health concern due to their capacity to produce toxins (8,20,21), to colonize biofilms (5,20) and to resist to chlorine disinfection (3,24). Ghenghesh et al. (10) analyzed 1000 samples of water collected from wells (980) and miscellaneous sources (120) and Aeromonas species were isolated in 48.7% of them. They carried out Aeromonas speciation in 381 isolated strains and found 225 (59%) A. hydrophila, 103 (27%) A. caviae, 42 (11%) A. sobria and 11 (3%) atypical Aeromonas. Occurrence of Aeromonas hydrophila was detected by Fernández et al. (7) in chlorinated treated water in Argentina when the maintenance disinfection program failed. In the same way, Ivanova et al. (14) isolated Aeromonas from drinking water reservoirs and observed high incidence of A. sobria and A. poppoffi, which are more frequent in water without fecal pollution. Study carried out by Villarruel-López et al. (24) detected Aeromonas in 31% of the samples from drinking water plants in Mexico City. Razzolini et al. (19) detected Aeromonas in chlorinated water reservoirs and drinking water fountains in the city of São Paulo.

In view of this, the objective of this study was to investigate the occurrence of Aeromonas genus in chlorinated water from reservoirs and wells that are used as drinking water sources in a peri-urban area of the Metropolitan Region of São Paulo, Brazil.

MATERIALS AND METHODS

Study area

Three peri-urban areas irregularly established in Protection Water Catchments of Suzano, one of the cities of the Metropolitan Region of São Paulo, were identified.

The population in these areas is about 2,000 inhabitants. Drinking water supply has been done by the transport of treated water in truck-tanks and transference to collective reservoirs with capacity of 5m3. These reservoirs are disposed in public areas and the water withdrawn have been done through hoses, storage in vessels or other recipients such as buckets which are considered inappropriate. The cleaning of the collective reservoirs does not have a fixed frequency and the community is in charge of this task. As water sources are scarce, people look for an alternative water source such as digging well in their backyard. It is important to highlight that the construction of the wells and septic tanks are done without any criterion.

Sampling

A total of 35 water samples were collected from collective reservoirs and 32 from wells. The water samples were collected bimonthly from September 2007 to September 2008. The samples were collected according to the APHA Standard Methods (1) in sterile disposable bottles, chilled for transportation and examined within a 24-hour period. Residual chlorine was measured in samples from the collective reservoirs by colorimetric method using Free-chlorine Analyser Policontrol®. Water temperature was taken using mercury column and the pH value using universal paper pH indicator. The occurrence of rainfall in the last 24 hours was recorded.

Aeromonas spp determination was carried out using a Multiple-Tube Technique as recommended by the APHA (1). In brief, serial dilutions were done with sterile 0.85% sodium chloride solution, 1mL of diluted samples were inoculated into alkaline peptone water, pH 8.6, and incubated 24h at 35ºC. The superficial film formed in each tube was transferred to triplicates blood agar plates amended with 10mg/mL ampicillin and incubated for 24h at 35ºC. Typical Aeromonas colonies, with 2-3mm diameter, convex, producing haemolysis or not, were screened for cytochrome oxydase, indole and gas production, lactose acidification and glucose fermentation.

The strains presenting positive results for the Aeromonas genus were submitted to complementary biochemical tests for the determination of the species as follow: nitrate reduction; arginine dihydrolase; lysine and ornithine decarboxylase; growth in peptone broth with 6% NaCl and without sodium chloride; acid production from arabinose, manose, mannitol, sucrose and esculin hydrolysis. Identification to the species level was carried out by comparison of the biochemical results with Table 1. Production of hemolysin was performed in Tryptic Soy Agar (TSA) plates with 5% of sheep blood incubated at 35oC ± 0.5oC for 24 and 48 h.

Table 1.

Biochemical characteristics of different species of Aeromonas

Species NO3 → NO2 D-Glucose, gas Indole Arginine dihydrolase Lysine decarboxylase Ornithine decarboxylase Esculin hydrolysis NaCl tolerance 0% NaCl tolerance 6% Sucrose D-Manitol L-Arabinose Salicin Manose β-hemolysis Resistence to ampicilina
Aeromonas hydrophila + + + + + - + + - + + + + + + +
Aeromonas salmonicida + + + V V - + + - + + + - + V +
Aeromonas media + - + + - - + + - + + + V + V +
Aeromonas encheleia + V + + - - + + - + + - + + V +
Aeromonas allosaccharophila + V + + + - V + - + + V - + V +
Aeromonas eucrenophila + + + + - - + + - V + + + + V +
Aeromonas bestiarium + V + + + - + + - + + + V + V +
Aeromonas caviae + - + + - - + + - + + + + V V +
Aeromonas veronii sobria + V + + + - - + - + + - - + + +
Aeromonas veroniii veronii + + + + - + + + - + + - + + + +
Aeromonas schubertii + - - + + - - + - - - - - + V +
Aeromonas jandaei + + + + + - - + - - + - - + + +
Aeromonas trota + V + + + - - + - V V - - + V -
Aeromonas popoffii + + V + - - - + - - + V - + - +
Aeromonas culicicola + + + + + - - + - + + - - + + +
Aeromonas simiae + - - + + - V + - + - - - + - +
Aeromonas molluscorum + - - + - - + + - + + + + + nd +
Aeromonas sobria + V + - + - - + - + + - - + V V

Source: Pidiyar and col., 2002; Abbott and col., 2003; Harf-Monteil and col., 2004

Note: (+) = .85% of positive strains; (-) = > 85% of negative strains; (V) = 50%; nd = not determined

RESULTS AND DISCUSSION

The presence of Aeromonas was detected in 13 (18.8%) of the 69 samples examined. Aeromonas were found in 6 (17.2%) collective reservoir samples and 7 (21.9%) well samples, as shown in Figure 1.

Figure 1.

Figure 1.

Percentage of positive samples for Aeromonas spp according to the type of source of water.

Our findings can be compared with study carried out by Di Bari et al. (6) which detected the presence of Aeromonas in 37% of non treated water samples collected from wells, springs, fountains and mineral waters. Out of 91 samples from wells, 31 (28%) were positive to Aeromonas. Massa et al. (15) isolated Aeromonas in 25% of well water samples in Lecce, Italy. However, other authors, as Ghenghesh et al. (10), found frequency of Aeromonas as high as 48.7% in water samples collected from wells (980) and miscellaneous sources (120).

It was observed that the mean value of residual chlorine in the collective reservoirs did not meet the standard established by the Brazilian drinking water legislation (0.2 mg/L), except in some samples analyzed, but Aeromonas were not isolated. These results reinforce the findings of Brandi et al. (2), Fernández et al. (6) and Villarruel-López et al. (19).

Concentration of Aeromonas in the collective reservoirs ranged from <0.3 to 1.2 x102 MPN/100mL and, in wells, from <0.3 to 2.4 x102 MPN/100mL. Di Bari et al. (5) found in water samples from wells a maximum value of >200 CFU/100mL and <1 CFU/100mL as the minimum value and the geometric mean was 3.9 CFU/100mL. Massa et al. (13), in Italy, reported counts ranging from 26 to 1609 CFU/250mL.

The species identified in the current study are presented in Table 2. Out of 37 isolations from collective reservoirs, Aeromonas spp. (67.6%) were the most frequent followed by Aeromonas encheleia (13.5%) and A. allosaccharophila (8.1%) and A. hydrophila (8.1%).

Table 2.

Frequency of Aeromonas species isolated from samples of the collective reservoirs and wells

Collective reservoirs Wells
Strains (n) % Strains (n) %
Aeromonas spp. 25 67.6 52 86.6
Aeromonas allosaccharophila 3 8.1 5 8.3
Aeromonas bestiarium 1 2.7 nd nd
Aeromonas encheleia 5 13.5 1 1.6
Aeromonas hydrophila 3 8.1 nd nd
Aeromonas jandaei nd nd 2 3.3
Total 37 100 60 100

nd = not detected

A. hydrophila has also been found in drinking water in other studies Havelaar et al. (12), Chauret et al. (5), Sen & Rodgers (21) and Razzolini et al (19). Aeromonas spp. (86.6%) was the most frequent specie isolated from well samples followed by A. allosacchariphila (8.3%). Different results were found by Massa et al. (15) who isolated A. hydrophila, A. sobria and A. caviae from well samples in Italy. Ivanova et al. (14) reported that the most frequent isolation from drinking water samples was A. sobria and Razzolini et al. (19) found A. caviae as the commonest specie in chlorinated drinking water. These findings show the diversity of aeromonads in water sources.

It is worth mentioning that while A. hydrophila, A. bestiarum and A. encheleia occurred only in samples from collective reservoirs, A. jandaei was only isolated from well waters.

The hemolysin production was observed in 39 isolated strains (40.2%), being 21 strains from wells and 18 from collective reservoirs. The species that showed hemolytic activity from collective reservoirs samples were A. encheleia, A. allosaccharophila and Aeromonas sp and from wells samples were Aeromonas sp and A. allosaccharophila. Absence of hemolytic activity in A. hydrophila strains was something unexpected. Production of exotoxin (α and β-hemolysin) is associated with enteric disturbances, as reported by Burke et al (4), Monfort and Baleux (17), Singh and Sanyal (22,23), Pin et al (18), Handfield et al.(11) and Razzolini et al (19). These results highlight the pathogenic potential of Aeromonas species and pose a public health concern. Takahashi et al (25) detected and purified a hemolytic toxin from Aeromonas sobria (ASH), which promotes fluid accumulation in the mouse intestinal loop. This work puts in evidence a novel insight into correlation between ion HCO3-and secretory diarrhea induced by bacterial infections, considering that ASH actively induces the secretion of HCO3-.

The occurrence of Aeromonas genus in stored waters is a human health concern because of its ability to produce toxins, re-growth in low-nutrient environment and survive in chlorinated drinking water. Thus, some authors consider that these organisms should be a sanitary quality indicator (7, 19, 21, 24). Moreover, Aeromonas hydrophila is listed in the first and second Contaminant Candidate List (CCL1 and CCL2) by the US Environmental Protection Agency – USEPA (26), linking these organisms to public health adverse outcomes.

The findings of this investigation confirm the presence of Aeromonas genus in drinking water samples from collective reservoirs and wells in the study area. As Aeromonas is considered an emerging pathogen and can cause health disturbances, including serious illnesses, its presence in drinking water poses a significant public health concern.

ACKNOWLEDGEMENTS

We would like to thank FAPESP – Fundação de Amparo à Pesquisa do Estado de São Paulo for the financial support and technical trainee scholarship. The authors were partially supported by the CNPq (scholarship 303049/2007-3 to M.R.A.C. and 305071/2008-4 to W.M.R.G.).

REFERENCES

  • 1.American Public Health Association (1998). Standard Methods for the Examination of Water and Wastewater 20th edition, American Water Works Association, Water Environ. Res, Washington, DC. [Google Scholar]
  • 2.Brandi, G.; Siste, M.; Giardini, F.; Schiavano, G.F.; Albano, A. (1999). Survival ability of cytotoxic strains of motile Aeromonas spp. in different types of water. Lett. Appl. Microbiol. , 29, 211-215. [DOI] [PubMed] [Google Scholar]
  • 3.Burke, V.; Robinson, J.; Cooper, M.; Beaman, J.; Partridge, K. (1984). Isolation of Aeromonas hydrophila from a metropolitan water supply:seasonal correlation with clinical isolates. Appl. Environ. Microbiol, 48(2), 361-366. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Burke, V., Robinson, J., Cooper, M., Beaman, J., Partridge, K., Peterson, D. & Gracey, M.(1984) Biotyping and virulence factors in clinical and environmental isolates of Aeromonas species. Appl. Environ. Microbiol, 47(5):1146-49. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Chauret, C.; Volk,C.; Creason, R.; Jarosh, J.; Robinson, J. (2001). Warner,C. Detection of Aeromonas hydrophila in a drinking water distribution system: a field and a pilot study. Can. J. Microbiol, 47, 782-786. [PubMed] [Google Scholar]
  • 6.Di Bari, M.; Hachich, E.M.; Melo, A.M.J.; Sato, M.I.Z. (2007) Aeromonas spp and microbial indicators in raw drinking water sources. Braz. J. Microbiol, 38(3), 516-521. [Google Scholar]
  • 7.Fernandez, M.C.; Giampaolo, B.N.; Ibañez, S.B.; Guagliardo, M.V.; Esnaola, M.M.; Conca, L.; Valdivia, P.; Stagnaro, S.M.; Chiale, C.; Frade H. (2000). Aeromonas hydrophila and its relation drinking water indicators of microbiological quality in Argentine. Genetica, 108, 35-40. [DOI] [PubMed] [Google Scholar]
  • 8.Figueras, M.J.; Suarez-Franquet, A.; Chacón, M.R.; Soler, L.; Navarro, M.; Alejandre, C.; Grasa, B.; Martinez-Murcia, J.; Guarro, J. (2005). First record f the rare species Aeromonas culicicola from drinking water supply. Appl. Environ. Microbiol, 77(1), 538-541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Freitas, A.C.; Milhomem, A.M.; Nunes, M.; Ricciardi, I.D. (1993). Virulence factors produced by Aeromonas hydrophila strains isolated from a different sources. Rev. Microbiol., 24(3), 168-174. [Google Scholar]
  • 10.Ghegehnsh, K.S.; El-Ghodban, A.; Dkakni, R.; Abeid, S.; Altomi, A.; Tarhuni, A.; Maialigeti, K. (2001). Prevalence, species differentiation, hemolytic activity and antibiotic susceptibility of aeromonads in untreated well water. Mem Inst. Oswaldo Cruz, 96(2), 169-173. [DOI] [PubMed] [Google Scholar]
  • 11.Handfield, M., Simard, A., Couillard, M. & Letarte R (1996) Aeromonas hydrophila isolated from food and drinking water: hemagglutination, haemolysis and cytotoxicity for a human intestinal cell line (HT-29). Appl Environ Microbiol, 62(9):3459-61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Havelaar, A.H.; Schets F.M.; Sifhout A.V.; Jansen W.H.; Wieten G.; Kooji D.V.D. (1992). Typing of Aeromonas strains from patients with diarrhea and from drinking water. J. Appl. Bacteriol, 72, 435-444. [DOI] [PubMed] [Google Scholar]
  • 13.Hiransuthikul, N.; Tantisiriwat, W.; Lertutsahakul, K.; Vibhagool, A.; Boonma, P. (2005). Skin and soft-tissue infections among tsunami survivors in southern Thailand. Clin. Infec.t Dis., 41, 93-96. [DOI] [PubMed] [Google Scholar]
  • 14.Ivanova, E.P.; Zhukova, N.V.; Gorshkova, N.V.; Chaikina, E.L. (2001). Characterization of Aeromonas and Vibrio species isolated from a drinking water reservoir. J. Appl. Microbiol, 90, 919-927. [DOI] [PubMed] [Google Scholar]
  • 15.Massa, S.; Altieri, C.; D’Angela, A.A.A. (2001). The occurrence of Aeromonas spp in natural water and well water. Intern. J. Food Microbiol, 63, 169-173. [DOI] [PubMed] [Google Scholar]
  • 16.Merino, S.; Rubiers, X.; Knochel, S.; Tomás, J.M. (1995). Emerging pathogens: Aeromonas sp. Intern. J. Food Microbiol, 28, 157-168. [DOI] [PubMed] [Google Scholar]
  • 17.Monfort, M. & Baleux, B.(1991) Haemolysin ocurrence among Aeromonas hydrophila, Aeromonas caviae and Aeromonas sobria strains isolated from different aquatic ecosystems. Res Microbiol, 142: 95-102. [DOI] [PubMed] [Google Scholar]
  • 18.Pin, C.; Marín, M.L.; Selgas, D.; Tormo, M.L.G.J.; Casas, C. (1995). Differences in production of several extracellular virulence factors in clinical and food Aeromonas spp. strains. J. Appl. Bacteriol, 78, 175-179. [DOI] [PubMed] [Google Scholar]
  • 19.Razzolini, M.T.P.; Bari, M.; Sanchez, P.S.; Sato, M.I.Z. (2008). Aeromonas detection and their toxins in drinking water from reservoirs and drinking fountains. J. Water Health, 6(1), 117-123. [DOI] [PubMed] [Google Scholar]
  • 20.Scoaris, D.O.; Colacite, J.; Nakamura, C.V.; Nakamura, T.U.; Abreu Filho, B.A.; Dias Filho, B.P. (2008). Virulence and antibiotic susceptibility of Aeromonas spp. Isolated from drinking water. Antonie van Leeuwenhoek, 93, 111-122. [DOI] [PubMed] [Google Scholar]
  • 21.Sen, K.; Rodgers, M. (2004). Distribution of six virulence factors in Aeromonas species isolated from US drinking water utilities: a PCR identification. J. Appl. Microbiol, 97 (5), 1077-1086. [DOI] [PubMed] [Google Scholar]
  • 22.Singh, D.V. & Sanyal, S.C. (1992) Haemolysin and enterotoxin production by Aeromonas caviae isolated from diarrhoeal patients, fish and environment J. Diarrhoeal Dis. Res, 10(1):16-20, 1992. [PubMed] [Google Scholar]
  • 23.Singh, D.V. & Sanyal, S.C. (1992) Enterotoxicity of clinical and environmental isolates of Aeromonas sp. J. Med Microbiol, 26: 269-72. [DOI] [PubMed] [Google Scholar]
  • 24.Villarruel-Lopez, A.; Fernandez-Rendon, E.; Mota-de-la-Garza, L.; Ortigoza-Ferado, J. (2005). Presence of Aeromonas spp. in water from drinking-water-and wastewater-treatment plants in México City. Water Environ. Res, 77 (7), 3074-3079. [DOI] [PubMed] [Google Scholar]
  • 25.Takahashi, A., Nakano, M., Okamoto, K., Fijii, Y., Mawatari, K., Harada, N. & Nakaya, Y. (2006). Aeromonas sobria hemolysin causes diarrhea by increasing secretion of HCO3- FEMS Microbiol. Lett, 258:92-95. [DOI] [PubMed] [Google Scholar]
  • 26.USEPA (2006). Environmental Protection Agency. Aeromonas: Human Health Criteria Document. Washington DC. [Google Scholar]
  • 27.World (2004) World Health Organization. In Guidelines for Drinking-water Quality, 3rd edition, Recommendations, Geneve. [Google Scholar]

Articles from Brazilian Journal of Microbiology are provided here courtesy of Brazilian Society of Microbiology

RESOURCES