Campylobacteriosis is currently the most frequent foodborne zoonosis in many countries. One main source is poultry. The aim of this study was to enhance the knowledge about the potential of bacteriophages in reducing colonization of broilers with Campylobacter , as there are only a few in vivo studies published. Commercial broilers were inoculated with 104 CFU/bird of a Campylobacter jejuni field strain. Groups of 88 birds each were subsequently treated with a single phage or a four-phage cocktail (107 PFU/bird in CaCO3 buffered SM-Buffer). Control birds received the solvent only. Afterwards, subgroups of eleven birds each were examined for their loads with phages and Campylobacter on day 1, 3, 7, 14, 21, 28, 35 and 42 after phage application. The susceptibility of the Campylobacter population to phage infection was determined using ten isolates per bird. In total 4180 re-isolates were examined. The study demonstrated that the deployed phages persisted over the whole investigation period. The Campylobacter load was permanently reduced by the phage-cocktail as well as by the single phage. The reduction was significant between one and four weeks after treatment and reached a maximum of log10 2.8 CFU/g cecal contents. Phage resistance rates of initially up to 43% in the single phage treated group and 24% in the cocktail treated group later stabilized at low levels. The occurrence of phage resistance influenced but did not override the Campylobacter reducing effect. Regarding the reduction potential, the cocktail treatment had only a small advantage over the singe phage treatment directly after phage administration. However, the cocktail moderated and delayed the emergence of phage resistance.
Citation: Fischer S, Kittler S, Klein G, Glünder G (2013) Impact of a Single Phage and a Phage Cocktail Application in Broilers on Reduction of Campylobacter jejuni and Development of Resistance. PLoS ONE 8(10): e78543. doi:10.1371/journal.pone.0078543
Editor: Glenn Francis Browning, The University of Melbourne, United States of America
Received: May 29, 2013; Accepted: September 15, 2013; Published: October 21, 2013
Copyright: © 2013 Fischer et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The work was funded by unrestricted financial recources of the clinic for poultry. The member of the clinic for poultry PD Dr. vet. med. G. Gluender and S. Fischer were involved in all decisions about study design, data collection and analysis, publishing and manuscript preparation.
Competing interests: The authors have declared that no competing interests exist.
Human campylobacteriosis is presently the most frequent foodborne zoonosis in the EU with stable rates of about 53 confirmed cases per 100 000 population and year during 2006-09 . Campylobacteriosis is a diarrheal disease with symptoms of severe abdominal pain, watery and/or bloody diarrhea and fever, after an incubation period of 2–5 days. Usually the disease is self-limiting, but it occasionally results in hospitalization. Antimicrobial therapy is seldom needed. Campylobacter infection has been associated with sequelae such as joint inflammation and Guillain-Barré- and its variant Miller-Fisher-syndrome . The most frequently reported Campylobacter (C.) species are C. jejuni, C. coli and C. lari . Campylobacter spp. can only multiply in warm blooded animals such as poultry, cattle, pigs, wild birds and wild mammals and are excreted into the environment. One main cause of human campylobacteriosis is handling, preparation and consumption of broiler meat, which may account for 20% to 30 percent of human infections with Campylobacter. A total of 50% to 80 percent of human infections are thought to be attributed to chicken farming . A reduction of intestinal colonization of broilers would lead to a considerable decline of human campylobacteriosis . A risk assessment showed that a reduction of log10 2 of Campylobacter counts on broiler carcasses leads to a 30-fold decline in human campylobacteriosis caused by consuming chickens . Currently available conventional pre-harvest strategies to reduce Campylobacter contamination in poultry production are not sufficient . These pre-harvest strategies include the application of on-farm biosecurity measures, the decontamination of litter, and the supplementation of feed with compounds inhibiting Campylobacter and the treatment of drinking water. Moreover, novel strategies, specifically targeting Campylobacter control at pre-harvest level, are in progress, including administration of probiotics, vaccination, antibiotics, changes in feed structure and antimicrobial alternatives, i.e. bacteriophages (phages) and bacteriocins [7,8]. Bacteriophages are ubiquitous in the environment and appear naturally on food for human consumption along with their target bacteria [9–12]. A reduction of Campylobacter counts by an average of log10 2 and a maximum of log10 5 was demonstrated by using phages in several in vivo studies [13–16]. Phages are very specific to their target host having little impact on the remaining microorganisms. Thus, phages are a promising supplementary tool for the production of safe poultry food products .
The usage of phages for farm animals is of particular interest because it may help to reduce the administration of antibiotics. Antibiotic medication only leads to a temporary reduction, but not to an elimination of Campylobacter  and attracts long-lasting public criticism regarding increasing bacterial resistance. Unsurprisingly, after phage treatment, the development of phage resistant Campylobacter strains has been observed. Resistance rates from 2%  up to 13%  have been found. Loc Carrillo et al.  observed that a phage resistant Campylobacter isolate had a significantly reduced ability to colonize the broiler intestine compared to the original susceptible strain. Carvalho et al.  did not observe the same effect. Questions remain concerning the preservation of resistance during further intestinal passage, which may lead to loss of the resistant phenotype. In order to avoid the accumulation of phage resistant Campylobacter strains in the environment Goode et al.  suggested limiting the use of phages to the slaughter house as an epidemiological endpoint. In contrast, Wagenaar et al.  considered the release of phages in the environment to be acceptable and proposed a rotating use of different phages in order to deal with resistance problems.
We tested phage bio-control under controlled conditions in broilers over six weeks with particular regard to the development of resistances against the phages, comparing a four-phage cocktail and a single phage treatment.
Materials and Methods
Ethical statement on bird experiment
This study was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The use of animals in this study was approved by the Animal Welfare Officer of the University of Veterinary Medicine, Foundation, Hannover, whose tasks include the scrutiny of animal welfare, ethics and handling, and then announced to the Lower Saxony State Office for Consumer Protection and Food Safety in accordance with §8a(1,2) of the German Animal Health and Welfare Act. The Lower Saxony State Office for Consumer Protection and Food Safety approved the work on this study under permit number 33.9-42502-05-11A153. The study was notifiable but not subject to approval according to §8(7) Nr. 2 of the German Animal Health and Welfare Act. The accomplishment of the experiment was supervised by a competent person in accordance with the §9 of the German Animal Health and Welfare Act to ensure the compliance of §9 and §9a of the German Animal Health and Welfare Act and all efforts were made to minimize animal suffering.
The phages 1, 2, 5 and 13 (table 1) from the British phage typing scheme were used for this study. Propagation of phages and determining concentration of phage suspensions were performed as previously described . Phage suspensions were stored at 4°C.
|No of Phage strains||Campylobacter strains (NCTC1-No.)|
|Phage||NCTC1||propagation||determination of concentration|
Phage suspensions of each phage were diluted in SM-buffer (5.8g NaCl, 2.0g MgSO4x7H2O, 50ml 1M Tris (Sigma) pH 7.5, 5ml 2% gelatine, filled up with distilled water to 1000ml) to approximately 107 PFU/ml, mixed in equal parts for the cocktail application and supplemented with 33% (w/v) CaCO3 (Roth, 6230.1). Subsequently 1 ml of the suspension was administered directly into the crop of each broiler.
Isolation of phages from cecal contents.
1g of cecal contents was mixed thoroughly 1:10 with the SM- buffer and shaken overnight at 4°C. Chloroform (Sigma-Aldrich, 366919) was added to the sample at a concentration of 5% (v/v), which was then shaken at 300rpm for 15 min and subsequently centrifuged at 13,000 x g for 20 min. The phage containing supernatant was filtered through a 0.22 µm filter (Roth, P668.1) to eliminate bacterial compounds and then serially diluted in the SM- buffer for determining the phage concentration.
All Campylobacter strains were cultured and stored in several aliquots at -70°C to serve as a master seed before studies commenced. Laboratory Campylobacter strains, used for propagating phage strains and determining phage concentration are listed in table 1. Campylobacter jejuni 1474-06 was used as the model field strain for all experiments.
Campylobacter was always cultivated under microaerobic conditions (Oxoid Gas Pak System, Campygen) at 42±0.5°C.
Mc-Farland-Standards (McFSt.) of Campylobacter strains were prepared for propagating phages or determining phage concentrations as well as for susceptibility and resistance testing of Campylobacter isolates. A single colony of the required strain or respective isolate was plated on Mueller-Hinton-Agar (Oxoid) and incubated for 16h. The bacteria were then harvested with a sterile cotton swab, dispensed in 10 mmol MgSO4 solution and adjusted to the McFSt. needed for the particular application in a Densimat (Biomerieux SA France, IDN 013615).
The model organism C. jejuni strain 1474-06 was isolated in an abattoir from poultry pectoral muscles in 2006. This strain is representative for a collection of well characterized Campylobacter field strains and susceptible to all phages used in the United Kingdom Typing Scheme except phage 12 (NCTC12677) .
For inoculation of broilers Campylobacter 1474-06 was propagated in Standard 1 nutrient broth (Merck) for 48h and subsequently diluted to approximately 106 CFU/ml. Reisolation was performed on Karmali Agar (Oxoid). For this, serial dilutions of 1g of cecal contents per broiler were made in phosphate buffered saline (8g NaCl, 2g KH2PO4, 2.9g Na2HPO4, H2O ad 1l, adjusted to pH 7.4 with HCl/NaOH). Aliquots of 100µl were plated on Karmali Agar, from each dilution two separate plates were made. The colonies counted after two days incubation allowed the calculation of the CFU/g cecal contents.
The susceptibility of the re-isolated Campylobacter 1474-06 strains for each single phage and for the cocktail was tested as previously described . This test distinguishes between isolates that are as susceptible as the original strain and those, that have reduced susceptibility or are resistant.
Resistance of Campylobacter 1474-06 and re-isolated strains against the phages was examined using the conventional agar overlay plate assay: a suspension of each Campylobacter strain was adjusted to McFSt. 3. NZCYM-overlay-agar (NZCYM broth 22g/l, Roth X974.1, Agar-agar 7g/l, Roth 2266.3) was liquefied in tubes and kept molten at 48±0.5°C in a block heater (Roth, Rotalibo-Block-Heater H250). 100µl of the Campylobacter suspension and 100µl of the test phage-suspension, containing 104 PFU/ml, were added to 5ml NZCYM-overlay-agar, mixed thoroughly and poured into a petri dish containing 20 ml NZCYM-base (NZCYM-broth 22g/l, Agaragar 15 g/l). After the overlay had solidified, plates were inverted and incubated at 42±0.5°C for 24 hours.
Housing and care of laboratory animals
Broilers were used as an animal model, due to the fact that the study was aimed at reducing Campylobacter in commercial broiler production. Each group of birds was placed in separate units of the clinic-affiliated isolation facility as day-old chicks and each was cared for separately by one specialized animal keeper to avoid any environmental and cross contamination. The birds received commercial complete feed and water from the municipal water supply in bell drinkers ad libitum. The broilers were kept on wood shavings approximately 2kg/m2. The temperature was in accordance with commercial rearing conditions. The stocking density was 13 individual birds per square meter at the beginning and reduced by the taking of broilers for necropsy to 1.6 birds/m² at the end of the experiment.
General experimental setup.
92 Commercial broilers per group were housed as day-old chicks. On day six of life, four birds per group were sacrificed in order to confirm the birds were Campylobacter negative via culture. The other birds received 1ml of Campylobacter suspension, adjusted to 104 CFU/ml, directly into the crop. After three days of Campylobacter colonization (day nine of life), each bird of the treatment groups received 1 ml CaCO3-buffered phage suspension, containing 107 PFU/ml, directly into the crop. The phage cocktail was composed of phages 1, 2, 5 and 13 in equal parts. On day 10, 12, 16, 23, 30, 37, 44 and 51 of life, eleven birds per group were sacrificed. Before the dissection the birds were weighed. Ceca were removed aseptically and immediately processed within the clinic-affiliated laboratories. Approximately 1 g of cecal contents from each bird was weighed out twice. The first sample was diluted 1:10 in PBS, the second in SM-buffer then both were mixed thoroughly. Serial dilutions of these suspensions were made in order to determine the concentration of Campylobacter and phages as described above. Single Campylobacter colonies were picked for examination of phage susceptibility.
The treatment group received the buffered phage cocktail. The control group received the buffer suspension only. Ten re-isolated Campylobacter colonies per bird were tested for phage susceptibility. Thus, one hundred colonies from ten birds were investigated at each examination date from the treatment and the control group, respectively. These isolates were identified as belonging to the species C. jejuni by testing one Campylobacter colony from each broiler by PCR . However, testing one colony from one bird cannot confirm that the bird did not harbour other Campylobacter spp.. The PCR was thought as a supplementary tool for controlling the biosecurity measures: If a Campylobacter strain enters a flock, it rapidly spreads across the flock. Therefore, we regarded each group as one unit, which enhanced the significance.
The first treatment group received the buffered phage cocktail. The second treatment group received a buffered suspension, containing phage 1 only. The control group received the phage free buffered suspension medium only. Ten re-isolated Campylobacter colonies per bird were tested for phage resistance as described above. Colonies from the cocktail treated group were tested for resistance against each single phage separately and against the phage cocktail. Colonies from the single phage treated group were tested for resistance against phage 1 and also against the phage cocktail. Colonies from the control group were tested for resistance against the cocktail only.
Data evaluation and figure preparation were performed in Microsoft Excel 2010. Significances were calculated using T-Test and Man-Withney Rank Sum Test in Sigma Stat 3.1.
A susceptibility approximate value, in the following named susceptibility mean (SMean) was calculated for each Campylobacter colony (SMeanC), examined for susceptibility or resistance, in order to allow a broad comparison of the groups with the two different phage treatments as well as susceptibility test procedures. The SMean subserves the analysis of interrelations between the phage susceptibility of the Campylobacter population on the one hand and the colonization level of Campylobacter on the other hand.
SMeanC = sum of efficacious phages / sum of phages tested
Campylobacter isolates from trial I were examined for their susceptibility to each single phage and additionally the phage cocktail in the Microplate-Test. Therefore, isolates which were as susceptible as the original strain were entered as “susceptible” into the calculation, whereas reduced susceptible or resistant isolates were not entered. For trial I a SMeanC of “1” was assigned for Camylobacter isolates, which were as susceptible as the original strain to each phage. A SMeanC of “0” was assigned for Campylobacter isolates with reduced susceptibility to each phage.
Accordingly, the SMean was determined for Campylobacter isolates from trial II, which were examined for resistance in the conventional agar overlay plate assay. Here, reduced susceptible isolates were not separately detected and entered as “susceptible” in the calculation. Therefore, an SMeanC of “1” means, that the appropriate isolate has no resistance against any phage and an SMeanC of “0” means, that the isolate is fully resistant to each phage examined.
SMeans, used in this paper, were always calculated for the whole Campylobacter population of each single broiler (SMeanB), whereby the Campylobacter population was represented by ten colonies from each bird examined for susceptibility or resistance.
Therefore, for both trials the general interpretation on bird level of SMeanB of “1” is: no resistance against any phage in any isolate from this bird was found. An SMeanB of “0” means: all ten isolates from this bird showed at least reduced susceptibility or were even resistant to each phage.
Ratio of susceptible and less susceptible/resistant subpopulation.
For each individual bird “B”, the extent of the susceptible Campylobacter subpopulation was calculated, multiplying the Campylobacter load “LB” and the corresponding SMeanB.
extent of susceptible subpopulation (CFU/g) = LB (CFU/g) x SMeanB
The extent of the less susceptible (trial I) or resistant (trial II) Campylobacter subpopulation of any bird was calculated, subtracting its susceptible Campylobacter population from its total Campylobacter load.
extent of resistant subpopulation (CFU/g) = LB (CFU/g) - ( LB (CFU/g) x SMeanB )
Significance of the interpretation of SMean.
As the rate of resistant or less susceptible isolates was unknown when the experiments were planned, we carefully considered the costs and benefits of the amount of isolates for investigations and decided to examine ten isolates per bird: If all ten isolates from one bird are susceptible we can say that this bird harbors less than 20% resistant isolates with a safety level of 90%. Regarding the dissection group as one unit under the same conditions we can approximately say that the group harbored fewer than 2% resistant isolates.
The phage counts in cecal contents were determined for each bird. The rate of phage positive birds from each treatment group and the chronological sequence of the mean phage count from these phage positive birds are shown in Figure 1.
Part A shows the percentage of phage positive birds for each treated group.
Part B shows the mean phage count (log10) of the positive birds for each treated group.
dpa = days post phage application.
All broilers (100%) in trial I were positive for phages in their cecal contents (Figure 1a). In trial II, treated with the same phage cocktail, five broilers tested negative towards the end of the examination period resulting in a carrier rate of 92%. In the group treated with 1 phage in trial II at least one individual was found to be negative for phages at nearly every examination, leading to a rate of 87% phage-positive birds.
The mean phage titers and standard deviations of the phage treated groups during the course of the experimental trials are shown in Figure 1b: Although all groups were inoculated with log10 7.0 PFU per bird, the cocktail treated groups evolved a mean titer of log10 6.1 (trial I) and log10 5.0 (trial II) PFU/g one day after application in contrast to the single phage treated group, which showed a drop to log10 2.7 PFU/g after one day. From day three after phage application onwards the mean phage titers in all three treated groups altered between log10 3.2 and log10 5.2 PFU/g and all groups leveled off at about log10 4 PFU/g towards the end of the examination period.
The phage counts from the cocktail treated group of trial I, amounting to log10 4.9 PFU/g cecal contents in the mean were higher compared to the counts of the cocktail treated group of trial II, which resulted in log10 3.8 PFU/g. The mean phage count of the phage 1 treated group totaled log10 3.4 PFU/g.
The mean phage titer of all phage treated birds was log10 4.05 PFU/g cecal contents. The highest phage count per bird of log10 7.1 PFU/g was found in the single phage treated group. The highest count per bird in the cocktail treated groups accounted for log10 6.7 PFU/g.
Infected control group of trial I.
Phages were isolated from the untreated control group of trial I. The grey line in Figure 2 shows the mean phage counts. The highest count of log10 1.2 PFU/g in the mean value was found in week four (highest count per bird: 1.9 PFU/g ), but did not reach the phage level found in the treatment groups during the investigation period. The mean phage count of the positive birds remained stable at about log10 1 PFU/g, altogether only 32% of all birds were positive. Therefore, the height of the grey line mirrors the proportion of these phage positive birds at the different time points. Once phages were isolated from single birds, the whole group was excluded as control. The control group of trial II could be utilized instead, since the experimental setup was identical in both trials.
The bars show the percentage of Campylobacter isolates that were less susceptible to the represented phages. The lines show the corresponding Campylobacter counts and the unwanted phage infection. The detection of phages coincided with loss of phage susceptibility and a decrease of Campylobacter counts in the control group of trial I.
All re-isolated colonies examined by PCR belonged to the species Campylobacter jejuni. The chronological sequence of the mean Campylobacter counts from each group is presented separately for trial I (Figure 3a) and trial II (Figure 3b). The Campylobacter level in the cecal contents from the individual birds of both trials varied considerably from log10 3.4 CFU/g to log10 9.5 CFU/g. Altogether, the mean Campylobacter load of all phage treated birds in this study was log10 5.9 CFU/g cecal contents and is therefore significantly (p<0.001) below the Campylobacter load of the phage free control birds from trial II, which was in mean log10 7.2 CFU/g. Both the cocktail and the single phage treatment resulted in an average reduction of log10 1.3 CFU/g in trial II.
Part A shows the mean Campylobacter counts observed in the groups of trial I.
Part B shows the mean Campylobacter counts observed in the groups of trial II.
dpi = days post Campylobacter-inoculation dpa = days post phage application.
In trial I the phage-treatment led to a significantly (p< 0.001) reduced Campylobacter load up to three days after phage application (Figure 3a). Subsequently, there was no significant difference between the treatment group and the control along with an infection of the control by low numbers of phages and the following decrease of Campylobacter counts in that group (grey and black line in Figure 2). Therefore, only the first measurements are expedient for a solid evaluation of phage treatment efficiency. In trial II, the Campylobacter level of both treated groups is generally below the level of the control, except day three after application of the single phage (Figure 3b). The difference is significant (p< 0.001 - 0.036) from 7 days to 35 days after application for both treatment groups. The largest reduction of log10 2.8 CFU/g cecal contents was measured on day 21.
Resistant and less susceptible Campylobacter subpopulation
Scope of investigations.
A total of 1,540 Campylobacter isolates from trial I were tested for their phage susceptibility to each phage and the phage cocktail. 2,640 isolates from trial II were tested for resistance to the phage cocktail generally and additionally to the individual phages they were subjected to.
Progression of reduced phage susceptibility.
In all phage treated groups a similar course of the emergence of less susceptible or resistant isolates was observed. Generally, phage susceptibility decreased first and subsequently increased towards the end of the investigation period (Figure 4a-c). One day after phage application, there were only slight changes in phage susceptibility of the Campylobacter population in all treated groups. Then, phage susceptibility decreased over two weeks after application of the phage cocktail (Figure 4a+b), but only three days after treatment with the single phage (Figure 4c). Towards the end of examinations, the proportion of the phage susceptible Campylobacter population increased again and reached 98% (cocktail) or 94% (phage 1), respectively.
Part A shows the percentage of isolates from the cocktail treated group of trial I with reduced susceptibility against the individual phages and the cocktail. Data for phage 5 on day 14 after treatment are lacking.
Part B shows the percentage of isolates from the cocktail treated group of trial II that are resistant to infection by the individual phages and the cocktail.
Part C shows the percentage of isolates from the single phage treated group of trial II that are resistant to infection by phage 1 or the cocktail. Resistance for phages 2, 5 and 13 was not separately tested for this group.
In trial I up to ninety percent of the isolates from the cocktail treated group were less susceptible or resistant two weeks after phage application (Figure 4a). For this time point, the results for phage 5 are not given, due to technical faults. The susceptibility for the cocktail followed the same course as observed for the single phages. Only loss of susceptibility for phage 13 started faster and decreased slower.
In the cocktail treated group of trial II (Figure 4b), the course of resistance to phages 1, 2 and 5 was nearly identical and correlated well with the course observed in trial I. Resistance to phage 13 stayed at about 50% towards the end. Resistance to the cocktail was less common than resistance to the individual phages.
In the single phage treated group (Figure 4c) resistance to phage 1 arose earlier reaching 43 %, then dropped back earlier but finally resulted in the same level compared to the cocktail treated groups. Also cross-resistance to the phage cocktail was observed, following a similar trend observed in the cocktail treated groups. From day 21 after phage application the course of resistance to phage 1 and the cocktail were nearly identical in that group.
The phage infected control group of trial I showed a similar emergence of a less susceptible Campylobacter subpopulation as seen in the treatment group (bars in Figure 2). In contrast, only loss of susceptibility for phages 1, 2 and 5 was observed, phage 13 remained fully efficacious with all examined isolates. The highest occurrence of less susceptible isolates was approximately 70%. The following decline of the less susceptible part of the Campylobacter population was lower as observed in the treatment group. The emergence of a less susceptible subpopulation correlated with the detection of phages and the decline of the Campylobacter counts in that group.
Total resistance to the single phages and the phage cocktail, considering the different treatments.
Table 2 shows for each group how many Campylobacter isolates were less susceptible (trial I) or resistant (trial II) in total for the several phages during the investigation period.
|trial||group||phage 1||phage 2||phage 5||phage 13||cocktail|
Loss of susceptibility or increase of resistance was the most pronounced for phage 13 and the least pronounced for phage 5, regarding the individual phages; the cocktail was generally less affected.
The phages which infected the control group of trial I induced a stronger loss of susceptibility for phages 1, 2 and 5 than the experimentally administered phage cocktail, but no loss of susceptibility for phage 13.
The cocktail treatment in trial II induced marginally more resistance to phage 1 and the cocktail than treatment with only phage 1 did.
Only two out of 880 Campylobacter isolates from the phage free control group of trial II showed spontaneous resistance to the phage cocktail. Both were isolated from one bird.
Impact on Campylobacter colonization level
All birds from the treated groups were categorized into four groups, depending on the amount of phage resistant Campylobacter isolates in their ceca (measured as SMean).
Comparison of the mean Campylobacter level of i) treated birds harboring a pure susceptible Campylobacter population ii) treated birds harboring resistant isolates and iii) untreated birds.
For the birds harbouring resistant isolates (ii) two mean counts were calculated: the mean of the Campylobacter counts, including the resistant isolates and the mean of the Campylobacter counts after deducting the resistant subpopulation.
A good correlation (Figure 5) exists between the proportion of the resistant Campylobacter subpopulation, measured as “Susceptibility Mean” (SMean), and the Campylobacter colonization level. Birds whose Campylobacter population was categorized into the lowest susceptible group of SMean=0 were colonized the most at log10 7.5 CFU/g on average. The Campylobacter colonization level decreased continuously with rising susceptibility and reached log10 5.6 CFU/g at an SMean of 1.
Therefore, the Campylobacter colonization level in phage treated birds, harboring a resistant or less susceptible Campylobacter subpopulation, was higher (log10 6.16 CFU/g cecal contents on average; Figure 6) compared to the level of phage treated birds harboring a pure susceptible Campylobacter population (log10 5.56 CFU/g cecal contents), but did not reach the colonization level of the phage free control birds (log10 7.15 CFU/g cecal contents). After deducting the subpopulation showing resistance or reduced susceptibility, a colonization level of log10 5.65 CFU/g for the susceptible Campylobacter subpopulation of mixed colonized birds resulted. Therefore, the mean colonization level, reached by a susceptible Campylobacter population was about log10 5.61 CFU/g. The mean increase caused by the Campylobacter subpopulation showing resistance or reduced susceptibility was estimated to be about log10 0.51 CFU/g.
Current framework conditions
Neither the overall prevalence of Campylobacter in chicken retail products, nor the number of reported poultry meat consumption-related human campylobacteriosis cases have been reduced in recent years [23,24]. It is difficult to keep broiler farms free from Campylobacter colonization because small numbers of the ubiquitous and well adapted bacteria suffice to colonize the birds´ intestine . Campylobacter enters the food chain continuously on a farm level and survives all stages from ´farm to fork` [5,26,27]. Therefore, all stages from enhanced prevention measures at farm level to improved consumer information have been considered and evaluated for their suitability as critical control points to reduce the risk of human campylobacteriosis [4–7,28–31]. Reduction of contamination at broiler farms is considered to be efficient, but a major decrease of infections at a farm level is not expected in the short term  as there is still no effective, reliable and practical intervention measure available to prevent or to reduce Campylobacter colonization in poultry [6,32]. Three general strategies have been proposed to control Campylobacter in poultry at farm level: i) reduction of environmental exposure, ii) an increase in poultry’s host resistance to reduce Campylobacter carriage in the gut, and iii) the use of antimicrobial alternatives to reduce and even eradicate Campylobacter from colonized chickens . Regarding the growing number of organic and free range flocks having a very high risk of becoming Campylobacter positive by contamination with bacteria from the environment , the bacterial load reducing measures including bacteriophages are becoming increasingly important.
Phages are found in high numbers, provided that their hosts occur, in seawater as well as on food . Just a few studies have evaluated the natural incidence of Campylobacter phages in poultry and on poultry products. Phages could be isolated from 3% up to 51% of the samples examined, whereby free range husbandries were more frequently affected compared to indoor systems [10,12,35–38]. A wide range of bacteriophage titers from log10 1.5 to log10 6.9 PFU/g cecal contents of the individual birds were recovered in these studies [10,12]. Also, several studies concerning the experimental phage treatment of Campylobacter in broilers and considering the phage titers were conducted [13–16]. All the treatments of Campylobacter colonized chickens resulted in the bacteriophages persisting and replicating in the chickens` intestinal tract. Wagenaar et al.  found opposing highs and lows of Campylobacter and phage counts after several repeated phage applications and interpreted this as alternating shifts in amplification of bacteria and phages. The mean phage counts of Campylobacter colonized birds ranged from log10 5 to log10 8 PFU/g faeces, whereby the counts tended to decrease after the end of the treatment. Loc Carillo et al.  recovered phage titers ranging from log10 3.2 to log10 6.5 PFU/g cecal contents which did not correlate with simple dilutions of the different input doses (log10 5, 7 and 9 PFU/bird), implying that viral replication occurred within 24 h of administration. El Shibiny et al.  likewise found that irrespective of the initial phage dose administered, the mean phage counts stabilized at certain levels between log10 4 and log10 5.9 PFU/g intestinal contents depending on the intestinal segment. Carvalho et al.  found different mean phage counts after administering the same phage cocktail to Campylobacter jejuni (log10 5.3 PFU/g feces) and to Campylobacter coli (log10 3.4 PFU/g feces) colonized birds. Nevertheless, these phage counts remained constant throughout the experimental period of seven days within both groups. The mean phage titers, obtained in our experiments ranging from log10 2.7 PFU/g to log10 6.1 PFU/g are in accordance with previously reported phage counts of naturally occurring and experimentally administered phages in the birds´ intestine. We also found the bacteriophages replicating and existing at stable levels at about log10 4 PFU/g over the whole investigation period of six weeks (Figure 1), which is in accordance with other studies [13–16]. It seems that the present Campylobacter and phage strain combinations result in a clear natural balance. In contrast to the previously reported initial high phage titers, we found a remarkably low level of phage 1 one day after application. This might be explained by a low pH tolerance of the phage, which has been reported for several other phages [14,39]. Furthermore, this could also explain why the phages did not reach the intestine of some birds and why the phages excreted by the phage positive birds did not suffice to allow self-treatment after orally intaking of excrements over at least six weeks.
Campylobacter load and reduction
The considerable variation of Campylobacter titers from the individual birds was previously described . Different studies revealed the effect of phages on the Campylobacter counts in chickens [10–16,41]. The presence of phages in various commercial flocks resulted in an on average statistically significant log10 1.8 CFU/g lower Campylobacter load compared to the phage free flocks in that study . Different treatment designs including water and feed treatment, different dosages, preventive and therapeutic applications, single and repeated administration, using different phage and Campylobacter strains have been tested for their potential to reduce Campylobacter in chickens. These studies are inter alia reviewed by Connerton et al. . Reductions of the Campylobacter load up to log10 5.6 CFU/g intestinal contents have been found. Preventive gavage of phages delayed the colonization of Campylobacter. Uptake of phages incorporated in feed resulted in earlier reduction of Campylobacter compared to oral gavage. Several times a prominent initial drop of the Campylobacter load, followed by a re-increase of the Campylobacter level, resulting in a poor reduction level compared to the controls, was detected [15,16]. Therefore, a treatment of the flocks shortly before slaughter has been suggested . In contrast to that, our results show an initial low reduction, followed by a four-week period of significant reduction and ending again with low reduction levels (Figure 3b). Therefore, an adequate timeframe of between one and four weeks before slaughter would be reasonable. Nevertheless, the treatment shortly before slaughter would be more practical, since Campylobacter can enter the flock towards the very end of fattening. An early phage gavage would then be useless, since phages can only persist and replicate in the intestine in presence of their host .
Phage cocktails were assembled in order to enlarge the host range. In addition, we looked for benefits of the cocktail concerning the reduction potential and emergence of resistance. In trial II the cocktail administration resulted in a basic reduction, whereas the administration of the single phage could not maintain the usually observed reduction on day three after treatment (Figure 3b). This coincided with the early short term emergence of the highest resistance rate of the Campylobacter population (Figure 4c, phage 1 bar). The combination with three further phages resulted in a delayed and lower emergence of isolates resistant to the applied cocktail (Figure 4b, cocktail bar). Here, we compare resistance to phage 1 in the single phage group and resistance to the cocktail in the cocktail group since the resistance to the entity of the applied and therapeutically active phages is decisive for the efficiency of the treatment.
Impact of phage resistance on Campylobacter colonization level.
Resistances are seen as a possible obstacle for short- and long-term phage treatment efficiency. When phages were previously used to reduce Campylobacter counts in the intestine of poultry, phage resistant Campylobacter isolates were observed. Resistance rates from 2%  up to 13%  were reported. Even the impact of resistant Campylobacter isolates to the following phage treatment was examined. Loc Carrillo et al.  found a significantly reduced capability of a phage resistant isolate to colonize the broiler intestine compared to the susceptible original strain, whereas Carvalho et al.  could not confirm such a difference in comparable studies. The findings of investigations concerning the preservation of resistance during a further intestinal passage differ highly. The percentage of isolates, which lost their resistant phenotype, was specified by the mentioned authors as being between 54% and 97%. In order to avoid an accumulation of phage resistant Campylobacter strains in the farm environment it has been proposed to limit the use of phages to the abattoirs .
It seems that the phages used in this study kept the colonization level of the susceptible Campylobacter 1474-06 population at approximately 5.6 CFU/g (Figure 6). Once resistant subpopulations occurred they were not subjected to the reduction by phages and increased the total Campylobacter load without reaching the colonization level of the phage free control birds when considering the trials as a whole. However, the greater amount of the resistant Campylobacter population of some birds correlated with higher Campylobacter loads (Figure 5). The inability of the resistant subpopulation to maintain the colonization level of the control birds over time might be due to a reduced colonization capability of the resistant isolates, which is described as accompanying resistance .
Regarding these findings and especially the increase and decrease of the phage resistant subpopulation, we assume that the previously described different outcomes not only depend on different phage-bacteria combinations but also on the different time points of investigations (Figure 4). Furthermore, our findings suggest that long term efficiency is not seriously compromised by the emergence of resistance. Therefore, we agree with Wagenaar et al. , who consider the release of phages into the environment to be acceptable. Nevertheless, this must be validated for more phage bacteria combinations, considering additionally the resistance mechanisms in order to develop well designed phage bio-control strategies for the enhancement of food safety.
Cross-resistances in the single phage treated group.
In the single phage treated group first resistance to the deployed phage arose, followed by resistance to the whole phage cocktail (Figure 4c). Therefore, it seems that different resistance mechanisms occurred, first a phage 1 specific mechanism and afterwards a more basic mechanism, perhaps changing the structure required for phage bacteria interaction, resulting in cross resistance to the three other phages tested. The resistance mechanism should be specified in further studies. At the moment, this underlines the importance of well-founded knowledge about phage bacteria interactions in order to combine different acting phages to wide ranging and resistance avoiding cocktails.
Spontaneous resistance in the control group of trial II.
Spontaneous resistance of Campylobacter 1474-06 to the four phages in vitro was not observed in already published examinations . Nevertheless, after colonization in the broiler gut two spontaneous resistant isolates were recovered (table 2). Carvalho et al.  observed 6% resistant Campylobacter jejuni isolates from untreated chickens inoculated with a susceptible Campylobacter strain as well. The amount of bacteria and the multiplication frequency is considerably higher in the gut environment compared to the in vitro environment. Therefore, it was not surprising that the naturally occurring resistant strains  were recovered from the cecal and not from the in vitro samples.
Infected control group
This group was included in this paper despite infection in order to offer the data from a fresh natural phage infection. We assumed an infection by one or more unknown phages from the environment due to the different susceptibility pattern: Significant lower phage levels compared to the treatment groups were found, which may be the strongest indication for an infection by an unknown phage. Furthermore, no loss of susceptibility for phage 13 was observed, in contrast to development of cross-resistance to all phages, including phage 13 in the single phage treated group of trial II. Therefore, an infection by phage 1 is unlikely, but we cannot obviously rule out that phages 2, 5 or 13 were transferred.
Bacteriophages are able to reduce the Campylobacter load in chicken sustainably. We could show for the first time that resistances of Campylobacter against phages stabilized at a low level after an initial increase, which could be moderated and delayed by the use of more than one phage. Considering our own and previously described findings [10–16] we believe that phage bio-control could play a promising role in combating Campylobacter at farm level and thus in reducing human campylobacteriosis. Intelligent combinations of different phages could contribute to the success of phage bio-control by reaching a broad host range and keeping resistances under control. For this, further studies are required in order to gain sufficient knowledge of phage-bacteria interactions of all phages intended for future commercial use.
The phages were kindly supplied by Lohmann Animal Health Company, Cuxhaven, Germany. We would like to thank Hilke Bartels and Sonja Bernhard for their excellent technical assistance and advice.
Conceived and designed the experiments: SF SK GK GG. Performed the experiments: SF. Analyzed the data: SF. Contributed reagents/materials/analysis tools: SF. Wrote the manuscript: SF. Supervised animal experiments: GG. Supervised manuscript preparation: GK GG.
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