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Appl Environ Microbiol, May 1998, p. 1822-1824, Vol. 64, No. 5
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Comparison of Free-Living Amoebae in Hot Water Systems of
Hospitals with Isolates from Moist Sanitary Areas by Identifying
Genera and Determining Temperature Tolerance
Ute
Rohr,1,*
Susanne
Weber,1
Rolf
Michel,2
Fidelis
Selenka,1 and
Michael
Wilhelm1
Institut für Hygiene und Mikrobiologie,
Ruhr-Universität Bochum, D-44801 Bochum,1
and
Ernst-Rodenwaldt-Institut, D-56065
Koblenz,2 Germany
Received 11 September 1997/Accepted 16 February 1998
 |
ABSTRACT |
Legionella-contaminated hot water systems and moist sanitary areas
in six hospitals were sampled for amoebae by following a standardized
collection protocol. Genus identifications and temperature tolerance
determinations were made. Amoebae identified as Hartmannella
vermiformis (65%), Echinamoebae spp. (15%),
Saccamoebae spp. (12%), and Vahlkampfia spp.
(9%) were detected in 29 of 56 (52%) hot water samples. Twenty-three
of 49 (47%) swabs obtained from moist areas were amoeba positive. The
following genera were identified: Acanthamoeba (22%),
Naegleria (22%), Vahlkampfia (20%), Hartmannella (15%), and Vanella (7%). The
temperature tolerance of amoebae from hot water systems was strikingly
different from that of amoebae from moist areas. At 44°C on agar,
59% of amoebic isolates sampled from hot water systems showed growth.
The corresponding value for isolates from moist areas was only 17%.
Six Acanthamoeba isolates from the moist areas were
considered potential pathogens. Four Hartmannella and two
Saccamoeba isolates from hot water could be cultured at
53°C.
 |
INTRODUCTION |
Free-living amoebae of the genera
Acanthamoeba, Naegleria, and
Hartmannella have been isolated from various aquatic
habitats in the human environment (2, 5, 14, 20).
Additionally, amoebae have been described as carriers of
meningoencephalitis and keratitis (13, 24).
It has been shown that, in vitro at least, virulent legionella strains
can multiply intracellularly in protozoae after phagocytosis (8,
15, 21). Therefore, it is suggested that the occurrence of
amoebae in aquatic habitats may support legionella growth in these
ecosystems. In particular, hot water systems can provide an
environmental niche for legionellae to multiply to infectious concentrations (7). However, previous reports on isolation of amoebae and legionellae from water samples (1, 10, 16) did not mention sampling procedures in detail. Thus, it remains unclear
if a systemic contamination of hot water systems, local terminal
contamination, or both cold tap water and hot water were investigated.
In our study, collection of water samples was by a standardized
protocol as described by Exner et al. (7) to determine if
amoebae are systemically distributed in hot water systems of hospitals,
as has been reported for legionellae. To evaluate potential pathogenicity, determinations of the temperature tolerance of amoebae
will be presented. Results of comparative investigations will be
reported for moist areas of hospitals. Possible sources of organisms
found in that biotope are the cold or the hot water system. Organisms
in the moist areas colonize at lower temperatures than those in central
areas of hot water systems.
 |
MATERIALS AND METHODS |
Study sites and sample collection.
Six hospitals took part
in this study. Their hot water systems were systemically contaminated
with legionellae. Water samples were collected from 56 hot water taps
by following a collection technique which allows detection of a
systemic contamination as given by Exner et al. (7). Before
sampling, the water was allowed to run for 5 to 10 min until the
temperature was constant. The temperature was recorded, and a sample
volume of 1 liter was collected in sterile glass bottles for
microbiological examination. Forty-nine swabs were taken from moist
environments within sanitary areas, e.g., wall and floor tiles from
bathrooms and showers, the drains of sinks, and water taps. At each
area of investigation one swab was taken. About 50% of these areas had
not been used recently before they were investigated. The water taps
were also part of the hot water sample sites, but the water was not
allowed to run. All samples were tested on the same day.
Recovery, determination, and temperature tolerance of
amoebae.
Nine hundred milliliters of each water sample was
filtered through a cellulose nitrate filter (0.45-µm pore diameter;
Sartorius, Göttingen, Germany) with a weak vacuum (flow rate, 1.3 ml/min). The filters were inverted on nonnutrient agar plates (NN-A)
according to the method of Page (18), seeded with living
Enterobacter amnigenus, and incubated at 30°C. After 3 to
4 days the membranes were removed and the plates were incubated for a
further 1 to 2 weeks. Swabs were stroked on NN-A within an area 4 by 4 cm in size and incubated at 30°C for up to 2 weeks.
Amoebic isolates were identified by the morphologic criteria described
by Page and Siemensa (19) and characterized with regard to
their temperature tolerance (6). All plates were incubated
in two independent series for 3 days at different temperatures and then
examined for growth. Growth means that a clear migration of
trophozoites on the agar surface can be seen and that their isolates
can be cultured again. Fifty percent of the amoebic isolates were
tested again for temperature tolerance after 3 months of stock
culturing on NN-A at 30°C. These isolates showed the same results
when the temperature tolerance experiment was repeated.
 |
RESULTS |
Amoeba detection frequency.
Amoebae were detected in 29 of 56 (52%) hot water samples and on 23 of 49 (47%) swabs obtained from
moist areas.
Temperatures of water samples which were cultured for amoeba recovery
ranged from 24.7 to 59.5°C (mean, 45.8°C; median, 47.3°C; 95th
percentile, 57.3°C). Amoeba isolation frequencies from water samples
with different temperature ranges were 73% (40 to 44.9°C), 43% (45 to 49.9°C), 57% (50 to 54.9°C), and 57% (55 to 59.9°C) (Fig.
1). Even at temperatures between 55 and
60°C, four of seven samples were amoeba carriers.

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FIG. 1.
Systemic distribution of amoebae in hot water systems
from six different hospitals in relation to the water temperature range
(900-ml samples were used). The total number of water samples
investigated was 56.
|
|
Amoeba determination.
Morphologic characterization of the
isolates showed that Hartmanella vermiformis was the
dominant species systemically distributed in the hot water systems.
From a total of 34 isolates, the following organisms were identified:
Hartmannella vermiformis (65%), Echinamoeba spp.
(15%), Saccamoeba spp. (12%), and Vahlkampfia
spp. (9%). H. vermiformis is shown in Fig.
2.

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FIG. 2.
Three trophozoites and one cyst (C) of H. vermiformis (05101). N, nucleus; pV, pulsating vacuole. Arrowheads
indicate pseudopodiae formed by the hyaline zone. Magnification,
×1,200.
|
|
In swabs taken from moist areas, a greater variety of species was
present. From the 41 isolates, organisms of six different
genera were
identified:
Acanthamoeba spp. groups II and III (22%),
Naegleria spp. (22%),
Vahlkampfia spp. (20%),
H. vermiformis (15%),
unidentified amoebae (10%),
Vannella spp. (7%), and unidentified
miniamoebae (5%).
Temperature tolerance of the amoebic isolates.
All amoebic
isolates from both biotopes were able to be cultured at room
temperature and at 30°C on NN-A. Temperature tolerance of amoebae
revealed striking differences between both biotopes studied. At 44°C
on agar, 59% of amoebic isolates from hot water systems (total
n = 34) showed growth (Hartmannella, 41%;
Saccamoeba, 12%; Vahlkampfia, 6%). The
corresponding value for the amoebic isolates from the moist areas
(total n = 41) was only 17%. The distribution of
genera was as follows: Vahlkampfia, 7%;
Hartmannella, 5%; Acanthamoeba, 2%; and
unidentified amoebae, 2%.
Six strains were able to grow at 53°C on NN-A. These thermotolerant
amoebae belonged to the genera
Hartmannella
(
n = 4) and
Saccamoeba (
n = 2) and have been isolated from a total of six
hot water samples with
temperatures between 46.5 and 55.7°C.
Six of nine
Acanthamoeba isolates from the moist areas were
able to grow at 40°C, and one of them even grew at 44°C. None
of
the
Naegleria isolates from the moist areas could be
cultured
at 42 or 44°C.
 |
DISCUSSION |
In our investigations the most common amoeba systemically
distributed in hot water systems was H. vermiformis (65%).
These results confirm those of other investigations with various water samples from plumbing systems of hospitals (1, 22). Breiman et al. (1) reports that about 71% of the amoeba isolates
from drinking water and cooling tower water were of the genus
Hartmannella. Besides Hartmannella, both Breiman
et al. (1) and Sanden et al. (22) found
Acanthamoeba and Vahlkampfia. We also cultured Vahlkampfia from our water samples, but we found no trace of
Acanthamoeba. Both Breiman et al. and Sanden et al. (1,
22) probably worked with cold water or mixed water samples,
whereas we followed the criteria for the detection of systemic hot
water contamination (7). It is strongly suggested that our
sample technique detects mainly microorganisms distributed in the
central areas of hot water systems. Thus, it is not surprising that our
results are only partly in line with other observations (1,
22). The fact that the majority of our samples had temperatures
above 45°C supports the conclusion that only organisms with high
temperature tolerance may survive. Acanthamoeba and
Naegleria show a relatively low temperature tolerance.
Strains from these genera which are able to grow at 45°C have rarely
been found (3, 6). Our study confirms these reports. We
frequently found these genera colonizing moist areas at room
temperature but not the hot water system. It is possible that they
colonize hot water systems with lower temperatures, cold water systems,
or only the pipes near the outlets.
Up to now no pathogenic potential has been described for the genera we
isolated from the hot water systems (Hartmannellae, Echinamoebae, Saccamoebae, and
Vahlkampfia). The barrier of pathogenicity is apparently not
related to temperature, as has been described for the genera
Acanthamoeba and Naegleria (9).
Therefore, our results indicate that there was no danger of infection
via the amoebae present in the investigated hot water. On the other
hand, in moist environments within sanitary areas we found six
Acanthamoeba strains which must be regarded as potential
pathogens because they can grow at 42°C (4). We found
these strains colonizing drains, the wall and floor tiles from
bathrooms, and shower heads. Although no epidemiological correlation
exists, from a hygienic point of view infections may be possible by the
inhalation of amoeba-contaminated aerolized water (water spray). None
of the Naegleria isolates from the moist areas showed
potential pathogenicity (9, 11).
Nevertheless, it should be noted that we have isolated
Hartmannella and Saccamoeba strains with extreme
temperature tolerance from hot water systems. To our knowledge, it has
not been reported in previous studies that amoebae have been cultured
at 53°C on NN-A. As a rule, investigations of the temperature
tolerance of Hartmannella and other possible apathogenic
forms have not been carried out. Only Griffin (9) reported
such an investigation. In his study Hartmannella growth was
detectable on agar up to 40°C. Kuchta et al. (12) also
recognized that H. vermiformis shows a high temperature
tolerance in water culture at 55°C in vitro.
The aim of our investigation was to detect amoebae in aquatic habitats
where legionellae were known to be systemically distributed (7). Acanthamoeba and Naegleria did
not colonize these central areas of the investigated hot water systems
at temperatures between 40 and 60°C. Nevertheless, they are often
used as host organisms for legionellae in vitro (15, 17). If
amoebae really support survival and growth of legionellae in hot water
systems, they probably belong to hartmannellae and other
thermoresistant forms. Our results are in agreement with those of other
investigations (22, 23). A growth-supporting effect of
H. vermiformis on legionellae in tap water in vitro has been
described by Wadowsky et al. (23). Sanden et al.
(22) found that a correlation exists between the occurrence
of H. vermiformis and Legionella pneumophila (serogroup 1) in the water systems of hospitals.
 |
FOOTNOTES |
*
Corresponding author. Mailing address: Institut
für Hygiene und Mikrobiologie, Ruhr-Universität
Bochum, Universitätsstr. 150, D-44801 Bochum, Germany. Phone:
49234/700-2365. Fax: 49234/709-4199. E-mail:
rohr{at}hygiene.ruhr-uni-bochum.de.
 |
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Appl Environ Microbiol, May 1998, p. 1822-1824, Vol. 64, No. 5
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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