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Applied and Environmental Microbiology, December 1998, p. 5027-5029, Vol. 64, No. 12
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Occurrence of Male-Specific Bacteriophage in Feral
and Domestic Animal Wastes, Human Feces, and Human-Associated
Wastewaters
Kevin R.
Calci,1,2,*
William
Burkhardt III,1
William D.
Watkins,2 and
Scott R.
Rippey3
U.S. Public Health Service, Food and Drug
Administration, Dauphin Island, Alabama 36528,1
U.S. Public Health Service, Food and Drug Administration,
Washington, D.C. 20204,3 and
Department
of Microbiology, University of Rhode Island, Kingston, Rhode Island
028812
Received 8 June 1998/Accepted 17 September 1998
 |
ABSTRACT |
Male-specific bacteriophage (MSB) densities were determined in
animal and human fecal wastes to assess their potential impact on
aquatic environments. Fecal samples (1,031) from cattle, chickens, dairy cows, dogs, ducks, geese, goats, hogs, horses, seagulls, sheep,
and humans as well as 64 sewerage samples were examined for MSB. All
animal species were found to harbor MSB, although the great majority
excreted these viruses at very low levels. The results from this study
demonstrate that in areas affected by both human and animal
wastes, wastewater treatment plants are the principal
contributors of MSB to fresh, estuarine, and marine waters.
 |
TEXT |
Diseases resulting from the
consumption of molluscan shellfish have been reported in the United
States for many decades (16, 17). In the last two
decades the number of shellfish-associated illnesses due to
enteric viral pathogens, such as the Norwalk and Norwalk-like viruses,
has increased (16, 18). Few municipalities are able to
consistently produce sewage effluents of good virological quality;
thus, shellfish-growing areas continue to be affected by human viral
pathogens (8, 9), with adverse effects on human health.
Total and fecal coliform groups colonize the intestinal tracts of
warm-blooded animals (7), including humans, and have been
employed as indicators of sanitation for many years. These two
bacterial groups are the only microbial indicators accepted by the
National Shellfish Sanitation Program and the Interstate Shellfish
Sanitation Conference to classify the harvest acceptability of
estuarine and marine shellfish-growing waters (23). Many researchers and public health officials have challenged the reliability of coliform bacteria as an indicator of the presence of enteric viral
pathogens (10, 16, 21) for several reasons. Enteric viruses
appear to be more resistant to inactivation by certain environmental
factors (e.g., sunlight and salinity) (1, 12, 19) and to
wastewater treatment, especially chlorine disinfection (6,
14), than bacterial indicators. Molluscan shellfish generally concentrate and retain viruses (including male-specific bacteriophage [MSB]) at higher rates than total and fecal coliform bacteria (2, 3). As a consequence, enteric viruses are a distinct public health hazard that is not reliably indexed by the total or fecal
coliform groups.
In recent years, an MSB group has been suggested as an auxiliary
indicator of fecal coliforms for indexing enteric viral pollution (9, 13, 21). The MSB group was proposed for several reasons. (i) It is more resistant to chlorination and inactivation by
environmental factors than are coliforms (10, 22); (ii) the
method used to enumerate MSB is direct, precise, rapid, facile, and
cost-effective (5, 15); (iii) MSB occurs in high densities
in both treated and untreated sewage effluents (5, 6, 11);
and (iv) it is unlikely to multiply in the estuarine environment
(24).
The application of MSB as an indicator of viral contamination from
human sources is contingent, at least in part, on its ecology, particularly its occurrence in feral and domestic animals
(11). Human enteric viral disease is considered to be
predominantly associated with the ingestion of human-derived
wastes because of the host-specific nature of these enteric pathogens.
Although related viral strains can cause diarrhea in animal species,
data from neither areas of endemicity nor outbreak show zoonotic
transmission as having an important role in human disease (4,
20). To further explore the use of MSB as an indicator of enteric
viral contamination, the contribution of these bacteriophages in both human and animal waste was examined.
Escherichia coli HS(pFamp)RR was used as the host for
bacteriophage enumeration because this strain is relatively resistant to most somatic bacteriophages, and thus more than 95% of the bacteriophages infecting it are male specific (5). Fecal
samples (n = 1,081) were collected from domestic
animals (cattle, chickens, dairy cows, dogs, goats, hogs, horses, and
sheep) and waterfowl (ducks, geese, and seagulls). Fresh fecal samples
were collected from at least five distinct geographical locations, to
include animals representing a variety of habitats and dietary
conditions. The majority of samples (51%) were collected from animals
at farms in Rhode Island. The remainder of the samples were retrieved
from freshwater ponds, the shores of Narragansett Bay, and area
landfills. In most cases, fecal wastes from these animals reach the
aquatic environment as a result of runoff from the land during
rainfall. For each fecal specimen, at least 1 g of freshly voided
feces was collected and placed in a sterile 100-ml specimen container (Falcon, Lincoln Park, N.J.) by using a sterile hardwood tongue depressor. Containers were capped and stored on ice until arrival at
the laboratory. There, 1 g of each fecal sample was transferred into a sterile 50-ml conical screw-cap centrifuge tube (Falcon) and
diluted 1:25 (wt/vol) with tryptone broth. These fecal slurries could
be stored for up to 2 weeks at
80°C. By the direct-plating method,
sample volumes were placed directly in the top agar tube at 48°C, to
which 0.3 ml of a log-phase culture of host strain HS(pFamp)RR and a
supplemental volume of tryptone broth were added, for a total volume of
10 ml. The contents of the tubes were mixed, poured onto prewarmed
bottom agar plates, and distributed evenly over the surface
(5). The remainder of the fecal slurry (21 ml) was utilized
for the enrichment procedure, in which 0.5 ml of a log-phase culture of
HS(pFamp)RR was added, followed by incubation at 35°C for 18 to
24 h. The slurry was then spot tested for the presence of MSB.
The results from both the direct-plating procedures and enrichment
demonstrate the great variability in the occurrence of MSB among animal
species (Fig. 1). Sheep, goats, and
canines had the lowest frequencies of occurrence. Of the 35 canine
fecal specimens examined, none were positive by the direct-plating
procedure, whereas more than 25% of fecal samples examined from
seagulls, hogs, chickens, and horses were positive for MSB by direct
analysis.
Most of the 11 animal species examined in this study shed relatively
low numbers of MSB (Fig. 1). Only four species (chickens, hogs, horses,
and seagulls) were found to excrete a wide range of MSB; in these
species, densities of >104 PFU/g were observed. More than
75% of the horses shed relatively low numbers of MSB (<10 PFU/g of
feces), although a small percentage (8.8%) shed MSB at levels
>103 PFU/g. More than 53% of the chickens shed low
numbers of MSB (<10 PFU/g feces). For both horses and chickens, an
inverse relationship was found between the levels of MSB in feces and
the corresponding percentage of contributing animals. That is, the
greater the number of MSB detected in feces was, the lower the number
of animals found to harbor these increasing densities was. This trend
was not evident for hogs. Instead, about 15% of the hog population shed MSB in log10 ranges between <100 and
>104 PFU/g.
Septic tank samples, obtained from single-family dwellings in southern
Rhode Island, were collected from a septage depth of about 0.5 m.
The samples were placed in sterile screw-cap centrifuge tubes (Falcon)
and held on ice until they were examined. All samples were assayed
within 24 h of collection. MSB was not detected by the
direct-plating procedure in any of the 13 human fecal samples examined
(Table 1) but was found only following
enrichment. These results are consistent with the findings of other
investigators (10). The wastewater from 22 residential
sewage lift stations was examined by the direct-plating method. These
lift stations, which pumped residential wastewater into a main sewerage
system as they filled, each serviced a single-family home. Only two of these stations (9%) were positive for MSB by direct analysis, with
densities of 0.1 × 104 to 2.5 × 104
PFU/100 ml. The wastewater from 17 single-family residential septic
tanks was examined by both direct analysis and the enrichment technique. Fifty-eight percent of the samples were positive for MSB by
direct enumeration. Densities ranged from <0.1 × 106
to 1.0 × 106 PFU/100 ml. Of 11 wastewater samples
collected from main sewer lines, all were positive for MSB by the
direct-plating method. Densities ranged from 4.3 × 103 to 8.7 × 105 PFU/100 ml. Similarly,
high levels of MSB were found in all sewage treatment plant influents
examined from locations around the coastal United States. The locations
were as follows: Maine, Rhode Island, Virginia, South Carolina,
Florida, Alabama, Louisiana, California (n = 4),
Oregon, and Washington (n = 2).
The daily magnitudes of the environmental contributions from animal
sources and wastewater treatment plants are compared in Table
2. The potential contributions of MSB to
the environment from the average animal within each species were
calculated as the product of the mean fecal density of MSB determined
for each species and the per capita fecal output in a 24-h period.
Daily per capita fecal outputs were estimated by us or cited from other sources (7). Though relatively low in MSB density, the daily fecal wastes from a dairy cow are a more significant source of MSB than
the daily wastes from a chicken or bay-associated seagull because of
the cow's comparatively large fecal output per day. Horses and hogs
excrete the highest number of MSB, 1.9 × 107 and
1.1 × 107 PFU/animal/day, respectively. The magnitude
of MSB from human sources was calculated by multiplying the mean
density of MSB for effluents from 14 wastewater treatment plants
located around the coastal United States (3 × 104 per
100 ml) by 1 million gallons/day (1 MGD). Calculations demonstrate that
MSB inputs from animal sources are insignificant compared with those
from wastewater effluents. To equal the MSB levels discharged by a
wastewater treatment plant averaging 1 MGD (1012 PFU/day)
would require the daily fecal contribution of more than 60,000 horses,
100,000 hogs, 180,000 landfill-associated seagulls, or 550,000 dairy
cows. A plant serving a relatively small community of about 10,000 would discharge this volume of wastewater. It is apparent from the
number of inputs that animals are not a significant source of MSB
compared to wastewater treatment plants servicing even relatively small
communities which discharge treated wastes into the aquatic
environment. We found that MSB recovered from waters or shellfish,
excluding those from the most-rural coastal areas, can be presumed to
be of anthropogenic origin. As such, MSB may be a reliable indicator of
enteric viral pathogens in environmental waters and molluscan
shellfish.
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TABLE 2.
Daily per capita MSB loadings for different animal
species and for a hypothetical 1-MGD wastewater treatment plant,
calculated from mean MSB densities determined for respective animal
feces and wastewaters
|
|
While no single water quality indicator can reliably assess both the
bacterial and viral contamination of aquatic environments in all
circumstances, the results of this study strongly support the use of
MSB as the indicator of choice for assessing the potential presence of
human enteric viruses in estuarine and marine environments impacted by
wastewater sources.
 |
FOOTNOTES |
*
Corresponding author. Mailing address: U.S. Food and
Drug Administration, Gulf Coast Seafood Laboratory, P.O. Box 158, Dauphin Island, AL 36528. Phone: (334) 694-4480. Fax: (334) 694-4477. E-mail: KRC{at}VM.CFSAN.FDA.Gov.
 |
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Applied and Environmental Microbiology, December 1998, p. 5027-5029, Vol. 64, No. 12
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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