Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 96(2): 169-173, February 2001
Prevalence, Species Differentiation, Haemolytic Activity,
and Antibiotic Susceptibility of Aeromonads in Untreated
Khalifa Sifaw Ghenghesh/+, Abdelmula El-Ghodban*, Rabia Dkakni,
Salaheddin Abeid, Abdurazzaq Altomi, Abdussalam Tarhuni**,
Department of Medical Microbiology, Faculty of Medicine, P.O. Box 80013, Tripoli, Libya *Faculty of Science,
Eotvos Lorand University, Budapest, Hungary **Arab Company of Soft Drinks and Mineral Water,
The use of untreated water for drinking and other activities have been associated with intestinaland extraintestinal infections in humans due to Aeromonas species. In the present study aeromonadswere isolated from 48.7% of 1,000 water samples obtained from wells and other miscellaneous sources. Aeromonas species were detected in 45% of samples tested in spring, 34.5% in summer, 48% in autumnand 60% of samples tested in winter. Speciation of 382 strains resulted in 225 (59%) being A. hydrophila,103 (27%) A. caviae, 42 (11%) A. sobria and 11 (3%) atypical aeromonads. Of 171 Aeromonas strainstested for their haemolytic activity, 53%, 49%, 40% and 37% were positive in this assay using human,horse, sheep and camel erythrocytes respectively. The results obtained indicate that potentiallyenteropathogenic Aeromonas species are commonly present in untreated drinking water obtainedfrom wells in Libya (this may also apply to other neighbouring countries) which may pose a healthproblem to users of such water supplies. In addition, ceftriaxone and ciprofloxacin are suitable drugsthat can be used in the treatment of Aeromonas-associated infections, particularly in theimmunocompromised, resulting from contact with untreated sources of water.
Key words: Aeromonas - water - haemolysin - erythrocytes - antibiotics
Members of the genus Aeromonas are gram-
al. 1983, Janda et al. 1983, George et al. 1985, San-
negative, oxidase-positive, facultative anaerobic,
Joaquin & Picket 1988). Several studies have
rod-shaped bacteria of the family Vibrionaceae.
reported that the drinking of untreated water is the
They occur naturally in fresh water sources and
most probable manner of acquiring these organisms
are established pathogens of fish and amphibians
(Holmberg et al. 1986, Moyer 1987). At least 13
(Hazen et al. 1978, Hazen & Fleirmans 1979,
species are included in the genus Aeromonas at
this time (Janda 1991). Three of these, namely
aeromonads have for some time been recognized
hydrophila, caviae and sobria, are most commonly
as opportunistic pathogens in the immuno-
associated with disease in humans. A number of
compromised (von Graevenitz & Mensch 1968,
virulence factors have been associated with these
Washington 1972). They have been isolated from
organisms and may be responsible for their
skin and soft tissue infections of patients without
enteropathogenicity, these include the production
underlying conditions, but who suffered a trauma
of cytotoxins, enterotoxins and haemolysins
followed by exposure to water (Gold & Salit 1993).
(Gracey et al. 1982, Singh & Sanyal 1992, Majeed &
Furthermore, Aeromonas species have been
Macrae 1994). Burke et al. (1983b) have shown that
implicated as causative agents of diarrhoea in
haemolytic aeromonads are also enterotoxigenic and
children and adults (Burke et al. 1983a, Goodwin et
suggested that the detection of the haemolyticactivity is sufficient to discriminate enterotoxigenicAeromonas species. Although, Aeromonas-associated disease in the very young, the old andthe immunocompromised often requires antimicro-bial therapy, reports on the susceptibility of these
+Corresponding author. Fax: 218-21-333.4474. E-mail:
organisms to antimicrobial agent are rare in our re-
gion. Furthermore, information concerning species
distribution of aeromonads in well water is lacking.
The present study was carried out to determine the
Aeromonas in Well Water Khalifa Sifaw Ghenghesh et al.
prevalence, species differentiation, haemolytic ac-
(Bauer et al. 1966). The following antibiotics were
tivity (using four different types of erythrocytes),
tested (Oxoid, UK): ampicillin, ceftriaxone,
and antibiotic susceptibility of Aeromonas strains
ciprofloxacin, cephaloridine, chloramphenicol, gen-
in untreated well water in Tripoli area (population ~
tamicin, kanamycin, nalidixic acid, tetracycline and
MATERIALS AND METHODS Aeromonas species were isolated from 487
From March, 1993 to December, 1994, 1,000
(48.7%) water samples. Speciation of 382 strains
drinking water samples obtained from wells (98%
resulted in 59% being A. hydrophila, 27% A. caviae,
of samples) and other miscellaneous sources of un-
11% A. sobria and 3% atypical aeromonads (Table
treated water were examined. Water samples were
I). Information on the depth of 481 wells was
collected in sterile containers and processed within
available. The wells were divided into three groups
3 h of collection. When it was known, the depth of
according to their depth and aeromonads were
isolated form 56% of 178 wells less than 20 m, 53%of 238 wells 20-30 m and 49% of 65 wells more than
30 m deep. The isolation rates of Aeromonas species
Isolation - For the isolation of aeromonads, 2.5
from the three groups of wells are not statistically
ml of the water samples were added to 25 ml of
significant (P > 0.05). Aeromonads were detected
in 45% of samples tested in spring, 34.5% in summer,
enrichment. After an overnight incubation at 37oC,
48% in autumn and 60% of samples tested in winter
a loopful from the APW was plated onto blood
(Table II). Haemolytic activity of 171 Aeromonas
agar supplemented with 15 mg/l ampicillin and the
strains tested against human, horse, sheep and
plates were incubated at 37oC overnight.
camel erythrocytes is shown in Table III. Regardless
Identification - Identification of Aeromonas
of the erythrocytes used, the results obtained show
species was carried out using API 20E System (Bio-
a statistically significant difference between
Merieux, France) and the following tests:
haemolysin production with A. sobria and A.
production of oxidase, resistance to agent O/129
hydrophila compared with A. caviae strains
(Oxoid, UK), gas production from glucose and
(P<0.001, Chi-square test). Susceptibility testing of
aesculin hydrolysis. Isolates identified as
40 Aeromonas strains (24 A. hydrophila, 12 A.Aeromonas by the API 20E, and which did not
caviae and 4 A. sobria) against antimicrobial agents
produce gas from glucose nor hydrolyse aesculin
resulted in 100% being resistant to ampicillin, 95%
were considered as atypical aeromonads.
to cephaloridine, and 5% to tetracycline. All (100%)
Haemolysin assay - Bacterial strains were
inoculated into 10 ml of brain heart infusion brothsupplemented with 0.3% (wt/vol) yeast extract(Oxoid), and incubated at 37oC with agitation (200rpm) in a waterbath shaker (Karl Kolb, West
Germany) for 48 h. Cell-free supernatants were
Results of speciation of 381 Aeromonas
prepared by centrifugation (4000×g, 30 min) at 4oC
and filtration (0.45 µm membrane filters, Sartorius,
West Germany). Doubling dilutions of the cell-free
supernatant test solutions in phosphate buffered
saline (pH 7.4) were made in microtiter trays. Equal
volumes (100 µl) of a 1% suspension of fresh,
washed (three times) human, horse, sheep or camelerythrocytes was added. Phosphate buffered saline
and broth blanks were included in each tray. Trayswere sealed and incubated for 1 h at 37oC and then
for 1 h at 4oC. Haemolytic activity of cell-free
Seasonal distribution of Aeromonas
supernatants was considered positive if dilutions
of >1:4 of each supernatant yielded 50% haemolysisof the erythrocytes. A total 171 Aeromonas strains
Antibiotic susceptibility tests - The sus-
ceptibility of 40 Aeromonas strains to antimicrobial
agent was determined by the disc diffusion method
Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 96(2), February 2001
Haemolytic activity of Aeromonas species isolated from well water in Tripoli area
% of Aeromonas species showing haemolysis
a: mean value for the sum of all assays
is the predominant species in freshwater and mu-
ciprofloxacin, chloramphenicol, gentamicin, kana-
Using tissue culture and horse erythrocytes, a
statistically significant correlation betweenproduction of cytotoxic haemolysin and the
DISCUSSION
presence of diarrhoea has been reported by Brauer
In the present study, nearly 50% of the untreated
et al. (1985). Although in the present study the
cytotoxic activity of the Aeromonas strains was
Aeromonas species and nearly all of these samples
not determined, the results obtained show that
were obtained from wells. In a study, on the role of
nearly half of our isolates were haemolytic and
Aeromonas species in intestinal infections in the
United States, Holmberg et al. (1986) reported that,
Erythrocytes from small laboratory animals
of 20 patients who could specify their water supply
(mouse, rabbit, guinea pig) have been reported to
in the week before their gastrointestinal illness, 18
be more sensitive than human and sheep erythro-
had obtained their water from private wells and two
cytes in the Aeromonas haemolysis assay
had been drinking untreated spring water.
(Handfield et al. 1996). However, if the haemolysin
Aeromonas species were reported to be isolated
assay is to be used routinely in clinical laboratories
in higher numbers during the summer (Ljungh &
to detect enteropathogenic aeromonads, small ani-
Wadstrom 1985). Also Aeromonas-associated
mals are not a practical source of erythrocytes to
diarrhoea was found to be high during the summer
be used in such an assay. Our findings and those
months (Burke et al. 1984, Agger et al. 1985). In the
of others (Monfort & Baleux 1991) support the use
present work, isolation rates of aeromonads were
of human or horse erythrocytes in the haemolysin
highest in the months of winter and lowest in
assay and show that this simple assay can be eas-
summer. Although there is no clear explanation to
ily used to assist in the detection of pathogenic
our findings, we can speculate this is may be due
strains of Aeromonas species isolated from un-
to the relatively mild winter and hot summer seasons
treated water sources. Although camel erythrocytes
in our region. Pathak et al. (1988), studying the
have not been reported previously to detect
seasonal distribution of aeromonads in river water,
haemolytic aeromonads, they are not recommended
for use in Aeromonas haemolysis assay.
We found no differences in the isolation rates
In addition to drinking untreated water that con-
of Aeromonas species in the water samples
tains Aeromonas species, the taking of antibiotics
obtained from wells with different depths. However,
such as ampicillin to which these organisms are
it is worth mentioning that one strain (A. caviae)
resistant, may be a predisposing factor for the de-
was isolated from a water sample obtained from a
velopment of gastroenteritis (Holmberg et al. 1986,
Moyer 1987). Antibiotic-resistant strains of
There is little information available about
Aeromonas have been isolated from aquatic envi-
species distribution in aquatic environment (Araujo
ronments and this resistance is principally plasmid
Boira 1996). In the present study, A. hydrophila
mediated (Hedges et al. 1985, Borrego et al. 1991).
was the most common species representing nearly
Similar to other reports (Altwegg & Geiss 1989) all
60% of the aeromonads identified to the species
our isolates were resistant to ampicillin and 95% to
level. These results are consistent with the findings
cephaloridine. All were susceptible to ceftriaxone,
of others (Krovacek et al. 1992, Hanninen et al. 1997,
cholramphenicol, ciprofloxacin and gentamicin.
Kuhn et al. 1997) whoreported that A. hydrophila
Although the isolates were also susceptible to
Aeromonas in Well Water Khalifa Sifaw Ghenghesh et al.
trimethoprim-sulphamethoxazole and nalidixic acid,
Burke V, Gracey M, Robinson J, Peck D, Beaman J,
recently we isolated aeromonads from children with
Bundell C 1983a. The microbiology of children
diarrhoea and from chicken carcases that were
gastroenteritis: Aeromonas species and other
highly resistant to trimethoprim-sulphamethoxazole
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Burke V, Robinson J, Beaman J, Gracey M, Lesmana M,
and nalidixic acid respectively (Ghenghesh et al.
Rockhill R, Echeverria P, Janda JM 1983b. Correla-
1998). Because of the isolation of multiple-resis-
tion of enterotoxicity with biotype in Aeromonas
tant Aeromonas species (including to trimethoprim-
spp. J Clin Microbiol18: 1196-1200.
sulphamethoxazole and nalidixic acid) from
Burke V, Robinson J, Gracey M, Peterson D, Patridge
freshwater in other parts of the world (Borrego et
K 1984. Isolation of Aeromonas hydrophila from a
al. 1991), our findings warrant the need to take
metropolitan water supply: seasonal correlation with
proper measures to prevent the introduction of
clinical isolates. Appl Environ Microbiol48: 361-
aeromonads, that are resistant to these drugs, to
George WL, Nakata MM, Thompson J, White ML
1985. Aeromonas related diarrhoea in adults. Arch
In Libya, as it is in other developing countries,
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Ghenghesh KS, Abeid S, Dkakni R, Tawil A, Elkot R
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1998. Susceptibility of Aeromonas species isolated
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in Libya to antimicrobial agents. Second International
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