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Applied and Environmental Microbiology, April 2001, p. 1979-1982, Vol. 67, No. 4
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.4.1979-1982.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Inhibition of a Glucose-Limited Sequencing Fed-Batch Culture of
Salmonella enterica Serovar Enteritidis by Volatile Fatty
Acids Representative of the Ceca of Broiler Chickens
Paul W. J. J.
van der
Wielen,1,*
Steef
Biesterveld,2
Len J. A.
Lipman,1 and
Frans
van Knapen1
Centre for Veterinary Public Health and
Environmental Protection, Faculty of Veterinary Medicine, Utrecht
University, Utrecht,1 and Campina
Melkunie, Zaltbommel,2 The Netherlands
Received 2 October 2000/Accepted 5 February 2001
 |
ABSTRACT |
The effects of concentrations of volatile fatty acids on an
anaerobic, glucose-limited, and pH-controlled growing culture of
Salmonella enterica serovar Enteritidis were studied.
Suddenly increasing volatile fatty acids to the concentrations
representative of the ceca of 15-day-old broiler chickens caused
washout of serovar Enteritidis. In contrast, a sudden increase to the
volatile fatty acid concentrations representative of the ceca of
younger broiler chickens caused a reduction in the biomass but not
washout. Gradually increasing volatile fatty acids caused a gradual
decrease in the biomass of serovar Enteritidis. We conclude that the
concentrations of volatile fatty acids present in the ceca of broilers
with a mature microflora can cause washout of serovar Enteritidis in an
in vitro system mimicking cecal ecophysiology.
 |
TEXT |
In recent years, Salmonella
enterica serovar Enteritidis has become the predominant
Salmonella causing human salmonellosis in western countries
such as the United States and The Netherlands (1,
17). The main reservoirs for human serovar Enteritidis infections are poultry and poultry products (17).
Infection of broiler chickens with serovar Enteritidis is age and dose
dependent (7-9). Young broiler chickens are particularly
susceptible to Salmonella infections (3, 6, 9).
Nurmi and Rantale (14) were the first to suggest that this
susceptible period is caused by the lack of a mature microflora in
young broilers. They observed that treating 1-day-old broilers with a
mature cecal microflora from Salmonella-free adult chickens
protected these broilers from colonization with Salmonella
in the ceca (14). The exact mechanism(s) behind reduction
of Salmonella numbers by the mature cecal microflora is not
known. Several mechanisms have been postulated: competition for
nutrients, competition for receptor sites, immunomodulation, production
of antimicrobial substances, or production of volatile fatty acids,
such as acetate, propionate, and butyrate (see reference 5
and references therein). Still more information is needed to evaluate
the relative importance of these mechanisms in reducing Salmonella numbers in the ceca of chickens.
Young broiler chickens (1 to 14 days old) do not contain anaerobic
bacteria as a dominant fraction of their cecal microflora (18). Therefore, the concentrations of acetate,
propionate, and butyrate are low in the ceca during the first week of
life (2, 5, 18). In vivo, it was observed that the
increase in concentrations of acetate, propionate, and butyrate in the ceca is a cause for the decrease in viable counts of members of the
family Enterobacteriaceae in the ceca of broiler chickens (18). The aim of this study is to determine the effects of
mixtures of volatile fatty acids and lactate on serovar Enteritidis
growing under conditions representative of those in the ceca of broilers.
Bacterial strains and culture conditions.
S.
enterica serovar Enteritidis strain CVI-1 (phage type 4) was
originally isolated from chickens (19). Serovar
Enteritidis was grown in a mineral carbonate-buffered medium. This
medium contained the following (per liter of milli-Q water): 0.3 g
of NH4Cl, 0.5 g of NaCl, 0.2 g of
Na2SO4, 0.4 g of
KH2PO4, 0.67 g of
Na2HPO4, 4 g of NaHCO3, 0.5 g of
yeast extract, 0.5 g of tryptone, 1 ml of Tween 80, 1 mg of
resazurine, 10 ml of trace element solution (15), 10 ml of
vitamin solution (15), and 30 mM glucose. Cecal growth
conditions were mimicked in an in vitro system, which operated as a
sequencing fed-batch reactor. This means that a cycle of 12 h was
repeated continuously in the reactor. During a cycle, the working
volume of the culture vessel (1.5-liter chemostat) increased in 11 h 53 min from 100 to 500 ml. Subsequently, the volume decreased in 7 min to 100 ml. The flow rate of the medium was kept constant at 34.4 ml
h
1. The headspace of the culture vessel was flushed with
a nitrogen-carbon dioxide mixture (80 and 20%, respectively) at a flow
rate of 4.2 liters h
1. The pH was kept constant at
5.8 ± 0.1 with 1 N NaOH and 1 N HCl, and the temperature was
maintained at 41°C. The culture vessel was inoculated with 1 ml of an
overnight-grown culture of serovar Enteritidis. Transient states were
obtained 24 h after glucose became the substrate-limiting nutrient
for serovar Enteritidis (approximately 7 days).
Addition of volatile fatty acids and lactate.
After serovar
Enteritidis reached transient-state conditions, volatile fatty acids
and lactate were administered in two ways. First, volatile fatty acids
and lactate were administered to the medium and culture vessel
simultaneously as sodium salts. This caused a sudden increase in the
concentrations of volatile fatty acids and lactate (Table
1). These concentrations are
representative of those in the ceca of 5-, 8-, and 15-day-old broiler
chickens (18). Second, volatile fatty acids and lactate
were added as sodium salts to the medium vessel every 6 h during a
period of 72 h, resulting in a gradual increase (Fig.
1). The concentrations of volatile fatty
acids and lactate were representative of the ceca of 5-day-old broilers
after 24 h, of 8-day-old broilers after 48 h, of 15-day-old
broilers after 72 h, and of 37-day-old broilers after 96 h
(18). In both types of experiments, the culture vessel was
sampled intensively for 72 h. Thereafter, samples were taken every
24 h just before the volume decreased from 500 to 100 ml.

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FIG. 1.
Gradual increase in acetate, lactate, butyrate, and
propionate concentrations as determined in the culture vessel after
addition of these compounds to the medium vessel every 6 h. This
increase mimicked the increase of volatile fatty acids and lactate in
the ceca of 1- to 37-day-old broiler chickens (18).
Symbols: , acetate; , lactate; , butyrate; , propionate.
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|
The biomass of serovar Enteritidis was estimated by measuring the
optical density at 600 nm (OD
600) and by determining the
total amount of cell protein (
11). Glucose limitation in
the
culture vessel was determined colorimetrically using a glucose
oxidase test (Boehringer Mannheim). The concentrations of glucose,
volatile fatty acids, and lactate were determined by high-performance
liquid chromatography. After the samples were thawed, 990 µl of
sample was acidified with 10 µl of a 25% HCl solution and
subsequently
samples were prepared and measured by high-performance
liquid
chromatography as previously described by van der Wielen et al.
(
18).
Effect of suddenly increasing volatile fatty acids and
lactate.
OD600 and total cell protein measurements
showed similar results (data not shown). Therefore, only
OD600 data are presented as a measure for biomass. If the
concentrations of volatile fatty acids and lactate suddenly
increased to the concentrations measured in the ceca of 5-day-old
broiler chickens, the OD600 remained more or less stable
for 24 h (Fig. 2A). Thereafter,
OD600 decreased until 64 h after which it increased
again. In contrast, a sudden increase to the concentrations in the ceca
of 8-day-old broilers caused an immediate drop in OD600 and
the OD600 decreased to values lower than those in 5-day-old
broilers. After 118 h, the OD600 started to increase
again. Suddenly increasing volatile fatty acid and lactate
concentrations to the concentrations in the ceca of 15-day-old broilers
caused an even more dramatic drop in OD600. After 36 h, the OD600 stabilized at 0.04 and remained at this value
for at least 228 h. During the first 24 h after this sudden increase, the OD600 decreased according to the
theoretically calculated dilution curve. This indicates that these
concentrations of volatile fatty acids and lactate had a bacteriostatic
effect on serovar Enteritidis.

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FIG. 2.
Changes in OD600 (A) and glucose
concentration (B) after addition of different concentrations of
volatile fatty acids to the sequencing fed-batch reactor. Symbols
indicate addition of volatile fatty acids mimicking ceca of 5-( ),
8-( ), and 15-day-old ( ) broilers and the gradual increase of
volatile fatty acids as depicted in Fig. 1 ( ).
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|
The increase in glucose concentrations after addition of volatile fatty
acids and lactate as measured in the ceca of 5-day-old
broiler chickens
reached 72% of the glucose concentration in the
medium vessel
(
Sr) (Fig.
2B). This indicates that these
concentrations
of volatile fatty acids and lactate reduced the capacity
of serovar
Enteritidis to metabolize glucose. After 72 h, glucose
concentrations
started to decrease again. Adding volatile fatty acids
and lactate
comparable to the concentrations in the ceca of 8-day-old
broilers
caused an increase of glucose to 91% of
Sr, which was between
the values for the two
other treatments (days 5 and 15). After
120 h, the residual
glucose concentration started to decrease
again. The increase in
glucose concentrations was biggest (100%
of
Sr)
after a sudden increase to the concentrations in the ceca
of 15-day-old
broilers. The glucose concentration remained at
this level for at least
228
h.
The results from these in vitro experiments were compared with
observations made in in vivo studies (
6,
9,
16,
18).
In
very young broiler chickens (less than 8 days old), the concentrations
of volatile fatty acids and lactate are very low in the ceca
(
18).
Infecting 1- and 7-day-old broilers with serovar
Enteridis shows
high numbers of 10
8 and 10
7 per
g of cecal content, respectively. In contrast, broilers infected
at 21 days of age show low numbers of 10
3 per g of cecal content
(
6). This suggests that there might
be an association
between the low concentrations of volatile fatty
acids in the ceca of
young broilers and the high susceptibility
to
Salmonella
colonization in the ceca. The results from our study
show for the first
time that serovar Enteritidis grown under cecal
growth conditions is
very susceptible to a sudden increase in
volatile fatty acid
concentrations as measured in the ceca of
broilers older than 14 days.
Even though other mechanisms proposed
can still play some role in
reducing the number of salmonellae
in the ceca of broilers
(
5), we conclude that the bacteriostatic
effect of
volatile fatty acids is a pivotal mechanism in reducing
the
susceptibility for colonization by
Salmonella as broilers
age.
Effect of gradually increasing volatile fatty acids.
From the
previous experiments, it is clear that serovar Enteritidis could adapt
to day 5 or day 8 concentrations. Therefore, it was studied whether
Salmonella was able to adapt to volatile fatty acids and
lactate when they increased gradually over time. The gradual increase
in concentrations of volatile fatty acids and lactate in the culture
vessel mimicking the cecal ecophysiology caused a gradual reduction of
the OD600 of serovar Enteritidis without any significant
adaptation (Fig. 2A). After 96 h (representing cecal conditions of
37-day-old chickens), OD600 had decreased to 0.028 and
remained at this value for at least 336 h.
Glucose concentrations increased gradually after gradually increasing
concentrations of volatile fatty acids and lactate in
the culture
vessel (Fig.
2B). Glucose concentrations increased
to 24% of
Sr after 24 h, to 77% of
Sr after 48 h, and to 94% of
Sr after 72 h. After 96 h, glucose
reached a concentration of
100% of
Sr and
remained at this value for 336 h. Again, this indicates
that
glucose consumption by serovar Enteritidis could not be
detected.
The gradual increase of volatile fatty acids is faster than was
observed in ceca of broiler chickens during growth (
18).
In contrast, it was observed in studies with competitive exclusion
cultures that 1-day-old broiler chickens receiving a mixture of
cecal
bacterial strains had a very rapid increase in concentrations
of
volatile fatty acids in the ceca (
4,
10,
13). It has
been
proposed that this fast but gradual increase might be responsible
for
the decrease in the numbers of salmonellae (
5).
Administration
of different defined bacterial mixtures to 1-day-old
broilers
showed that cecal propionate concentrations in 3-day-old
broilers
correlated negatively with the numbers of salmonellae in the
ceca
of 10-day-old broilers (
12). However, these
researchers do not
conclude that propionate caused the reduction in
Salmonella. Propionate
may be an indication that the cecal
bacterial strains applied
have become established in the ceca at 3 days
of age but that
these bacteria inhibit
Salmonella by other
mechanisms (
12).
Here, we report in an in vitro model that
a fast gradual increase
in concentrations of volatile fatty acids and
lactate causes very
low biomass of serovar Enteritidis. In contrast, a
sudden increase
to concentrations mimicking those in the ceca of
5-day-old broilers
resulted in adaptation of serovar Enteritidis. This
could be an
indication that the slow gradual increase in volatile fatty
acids,
as observed in the ceca of nontreated broilers, does not cause
a
significant reduction in the biomass of serovar Enteritidis.
Therefore,
the results of our experiments fully support the hypothesis
that a
rapid gradual increase in volatile fatty acids is the most
important
reason for lower numbers of salmonellae in the ceca
of broilers treated
with competitive exclusion cultures (
4,
10,
12,
13). This
result is important not only for understanding
the mechanism(s) behind
Salmonella reduction in the ceca of older
broilers or
broilers treated with competitive exclusion cultures
but also for
selection of cecal bacterial strains in competitive
exclusion
mixtures.
 |
ACKNOWLEDGMENTS |
We thank Amos Zhao for providing us with the strain of S. enterica serovar Enteritidis and David Keuzenkamp, Otto van de
Beek, and Peter Scherpenisse for technical assistance.
 |
FOOTNOTES |
*
Corresponding author. Mailing address: CVVM,
Faculty of Veterinary Medicine, Utrecht University, P.O. Box 80175, 3508 TD Utrecht, The Netherlands. Phone: 31 30 253 33 79. Fax: 31 30 253 23 65. E-mail: wielen{at}vvdo.vet.uu.nl.
 |
REFERENCES |
| 1.
|
Angulo, F. J., and D. L. Swerdlow.
1999.
Epidemiology of human Salmonella enterica serovar Enteritidis infections in the United States, p. 33-41.
In
A. M. Saeed (ed.), Salmonella enterica serovar Enteritidis in humans and animals. Iowa State University Press, Ames.
|
| 2.
|
Barnes, E. M.,
C. S. Impey, and B. J. H. Stevens.
1979.
Factors affecting the incidence and anti-Salmonella activity of the anaerobic cecal flora of the young chick.
J. Hyg.
82:263-283.
|
| 3.
|
Cooper, G. L.,
L. M. Venables,
M. J. Woodward, and C. E. Hormaeche.
1994.
Invasiveness and persistence of Salmonella enteritidis, Salmonella typhimurium, and a genetically defined S. enteritidis aroA strain in young chickens.
Infect. Immun.
62:4739-4746[Abstract/Free Full Text].
|
| 4.
|
Corrier, D. E.,
A. Hinton, Jr.,
R. L. Ziprin,
R. C. Beier, and J. R. DeLoach.
1991.
Effect of dietary lactose and anaerobic cultures of cecal flora on Salmonella colonization of broiler chicks, p. 299-308.
In
L. C. Blankenship (ed.), Colonization control of human bacterial enteropathogens in poultry. Academic Press, New York, N.Y.
|
| 5.
|
Corrier, D. E.,
A. Hinton, Jr.,
R. L. Ziprin, and J. R. DeLoach.
1990.
Effect of dietary lactose on Salmonella colonization of market-age broiler chickens.
Avian Dis.
34:668-676[CrossRef][Medline].
|
| 6.
|
Duchet-Suchaux, M.,
P. Lechopier,
J. Marly,
P. Bernardet,
R. Delaunay, and P. Pardon.
1995.
Quantification of experimental Salmonella enteritidis carrier state in B13 leghorn chicks.
Avian Dis.
39:796-803[CrossRef][Medline].
|
| 7.
|
Gast, R. K.
1999.
Applying experimental infection models to understand the pathogenesis, detection, and control of Salmonella enterica serovar Enteritidis in poultry, p. 233-243.
In
A. M. Saeed (ed.), Salmonella enterica serovar Enteritidis in humans and animals. Iowa State University Press, Ames.
|
| 8.
|
Gast, R. K., and S. T. Benson.
1996.
Intestinal colonization and organ invasion in chicks experimentally infected with Salmonella enteritidis phage type 4 and other phage types isolated from poultry in the United States.
Avian Dis.
40:853-857[CrossRef][Medline].
|
| 9.
|
Gorham, S. L.,
K. Kadavil,
H. Lambert,
E. Vaughan,
B. Pert, and J. Abel.
1991.
Persistence of Salmonella enteritidis in young chickens.
Avian Pathol.
20:433-437[Medline].
|
| 10.
|
Hume, M. E.,
D. E. Corrier,
D. J. Nisbet, and J. R. DeLoach.
1996.
Reduction of Salmonella crop and cecal colonization by a characterized competitive exclusion culture in broilers during grow-out.
J. Food Prot.
59:688-693.
|
| 11.
|
Lowry, O. H.,
N. H. Rosebrough,
A. L. Farr, and R. J. Randall.
1951.
Protein measurement with the Folin phenol reagent.
J. Biol. Chem.
193:265-275[Free Full Text].
|
| 12.
|
Nisbet, D. J.,
D. E. Corrier,
S. C. Ricke,
M. E. Hume,
J. A. Byrd II, and J. R. DeLoach.
1996.
Cecal propionic acid as a biological indicator of the early establishment of a microbial ecosystem inhibitory to Salmonella in chicks.
Anaerobe
2:345-350[CrossRef].
|
| 13.
|
Nisbet, D. J.,
S. C. Ricke,
C. M. Scanlan,
D. E. Corrier,
A. G. Hollister, and J. R. DeLoach.
1994.
Inoculation of broiler chicks with a continuous-flow derived bacterial culture facilitates early cecal bacterial colonization and increases resistance to Salmonella typhimurium.
J. Food Prot.
57:12-15.
|
| 14.
|
Nurmi, E., and M. Rantale.
1973.
New aspects of Salmonella infection in broiler production.
Nature
241:210-211[CrossRef][Medline].
|
| 15.
|
Otto, R.,
B. Ten Brink,
H. Veldkamp, and W. N. Koning.
1983.
The relation between growth rate and electrochemical proton gradient of Streptococcus cremoris.
FEMS Microbiol. Lett.
16:69-74.
|
| 16.
|
Sadler, W. W.,
J. R. Brownell, and M. J. Fanelli.
1969.
Influence of age and inoculum level on shed pattern of Salmonella typhimurium in chickens.
Avian Dis.
13:793-803[CrossRef][Medline].
|
| 17.
|
van de Giessen, A. W.,
W. J. van Leeuwen, and W. van Pelt.
1999.
Salmonella enterica serovar Enteritidis in the Netherlands: epidemiology, prevention and control, p. 71-80.
In
A. M. Saeed (ed.), Salmonella enterica serovar Enteritidis in humans and animals. Iowa State University Press, Ames.
|
| 18.
|
van der Wielen, P. W. J. J.,
S. Biesterveld,
S. Notermans,
H. Hofstra,
B. A. P. Urlings, and F. van Knapen.
2000.
Role of volatile fatty acids in development of the cecal microflora in broiler chickens during growth.
Appl. Environ. Microbiol.
66:2536-2540[Abstract/Free Full Text].
|
| 19.
|
van Zijderveld, F. G.,
A. M. van Zijderveld-van Bemmel, and J. Anakotta.
1992.
Comparison of four different enzyme-linked immunosorbent assays for serological diagnosis of Salmonella enteritidis infections in experimentally infected chicken.
J. Clin. Microbiol.
30:2560-2566[Abstract/Free Full Text].
|
Applied and Environmental Microbiology, April 2001, p. 1979-1982, Vol. 67, No. 4
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.4.1979-1982.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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