Colonisation of a Phage Susceptible Campylobacter jejuni Population in Two Phage Positive Broiler Flocks

The pathogens Campylobacter jejuni and Campylobacter coli are commensals in the poultry intestine and campylobacteriosis is one of the most frequent foodborne diseases in developed and developing countries. Phages were identified to be effective in reducing intestinal Campylobacter load and this was evaluated, in the first field trials which were recently carried out. The aim of this study was to further investigate Campylobacter population dynamics during phage application on a commercial broiler farm. This study determines the superiority in colonisation of a Campylobacter type found in a field trial that was susceptible to phages in in vitro tests. The colonisation factors, i.e. motility and gamma glutamyl transferase activity, were increased in this type. The clustering in phylogenetic comparisons of MALDI-TOF spectra did not match the ST, biochemical phenotype and phage susceptibility. Occurrence of Campylobacter jejuni strains and phage susceptibility types with different colonisation potential seem to play a very important role in the success of phage therapy in commercial broiler houses. Thus, mechanisms of both, phage susceptibility and Campylobacter colonisation should be further investigated and considered when composing phage cocktails.


Introduction
Phages are viruses that infect and kill bacteria. Even though they were widely used in the former Soviet Union, their use as antibacterial agents, has raised interest in the western world since antibiotic resistance has become a major problem in treating bacterial infections [1]. More recently, phages have been discussed for application in the food chain to control food-borne pathogens like Campylobacter [2][3][4]. Campylobacter is a Gram negative, motile bacterium and is the most frequent cause of zoonotic infections in developed countries with symptoms of mild diarrhoea, abdominal pain and fever. In 2011, there were 220,209 confirmed cases reported in the EU [5]. In about 1 out of 1000 cases, infections result in serious sequelae such as Guillain Barré Syndrome or Reactive Arthritis [6,7]. Campylobacter is a commensal in birds, and broiler chickens are the main source for human infection [8,9]. Campylobacter jejuni and C. coli are the most frequently isolated species causing human infection. Combating Campylobacter in primary production is considered to be effective for reducing human campylobacteriosis and different experiments have been carried out, confirming the efficacy of phages for reducing Campylobacter load in chicken [10][11][12][13][14]. However, results have been highly variable in the onset and range of reduction and recently first field trials were performed to assess this issue under practical conditions. In two of three field trials a significant reduction was observed, but as in the other studies, the range of reduction varied widely and occurrence of different bacterial phenotypes may have influenced results of these studies [14].
Several studies have reported extensive biodiversity in C. jejuni isolates populating broiler chickens [15][16][17][18] and more than one strain can coexist in one broiler flock at a time [19][20][21][22]. Results indicate that phenotypic differences occur in closely related strains of C. jejuni and might be vital for the ability to colonise [23]. C. jejuni has a largely non-clonal population structure and generates genetic diversity through intra-and interspecies recombination [24]. In contrast to other intestinal pathogens, host factors instead of classical virulence factors seem to play a major role for pathogenesis of human campylobacteriosis [25]. Published studies to date, indicate that intestinal colonisation of chickens and humans is a multifactorial process [26]. The motility, imparted by the polar flagella, seems to play an important role in this process but studies indicate that it is influenced by many metabolic factors [26][27][28][29]. Additionally, motility is considered to be an important pathogenic determinant of C. jejuni [30]. Studies have demonstrated different expression patterns of flagella proteins between a poor and a robust coloniser strain in poultry [31,32]. The genes of proteins involved in the modification of the flagellum are located in hyper variable regions of the C. jejuni genome [33]. While different studies found non-motile mutants exhibiting a decreased ability to enter cultural cells [34,35] other studies have found a number of mutants with measurable defects in interaction with cultural cells that retained full motility [36]. It remains unclear how exactly motility and flagella structure are involved in colonisation of the chicken intestinal tract [30,37,38]. Tests on Campylobacter metabolism revealed wide variability and impact of amino acid catabolism on colonisation of the intestine [39][40][41], which is reasonable when considering that this bacterium uses intermediates of the tricarboxylic acid cycle as an energy source [25]. GGT is an enzyme involved in amino acid catabolism, providing utilisation of glutamine and glutathione and cellular protection against reactive oxygen species [42]. It is reported to be required for persistent colonisation [28]. The presence of the ggt gene was reported to correlate directly with expression of the GGT activity [28,43].
While different studies have investigated the efficacy of applied phages, the development of resistance, and reduced susceptibility in vivo under a controlled environment [4,[10][11][12][13]16,[44][45][46][47][48][49] little is known about the interaction of applied phages with different C. jejuni strains and phenotypes under commercial conditions. It is well known that a diversity of strains occurs in different flocks and slaughter groups [17]. This can result in generation of nonsusceptible isolates [12,32,48] and the modulation of genes and proteins that have an effect on colonisation of susceptible strains [47,50].
Interestingly, results of phage application trials using .3 week old birds by Loc-Carrillo et al. and Scott et al. [11,51] suggested that phage resistant isolates can be generated by chromosomal inversion, but on the other hand express reduced ability to colonise the broiler intestine. However, Carvalho and colleagues who used 1 week old chicks found no differences in the ability of resistant and susceptible phenotypes to colonise the chicken gut [12]. It is worth highlighting that those differences may be associated with the difference in the age of the birds in the trials and the method used to sample the Campylobacter isolates from the birds post treatment.
The present study aims to investigate the bacterial population dynamics of different C. jejuni strains and phenotypes in two phage positive flocks from one farm. Furthermore, it concentrates in investigating two factors which are considered to be important for Campylobacter colonisation in chicken intestine: motility and gamma glutamyl transpeptidase (GGT).

Field trials
The farm under investigation in this study was located in the north of Germany. It included 8 sheds in 2 buildings. Each building included two floors and two sheds on each floor. The sheds of the two broiler flocks under investigation were located on different floors of one building. Birds of both flocks were of the same age and housed on the same day. The field trial on this farm was originally part of a larger study by Kittler et al. [14]. Samples were taken from two phage positive flocks: Flock 1, which contained broilers experimentally treated with phage; and flock 2, which contained broilers that had been accidentally crosscontaminated with phage during the phage therapy trial. Application of phages in the field trials described by Kittler et al. [14] was performed according to German law. Formal approval of this study as an animal experiment was according to German law not necessary. However, the study was acknowledged by the Animal Welfare Committee of the University of Veterinary Medicine Hannover (competent ethics committee of the university). In accordance with German law permission to apply bacteriophages as feed additive was given by the competent authority (LAVES Az.: 41.3-63003-13/2011). Studies were performed on the farms R1 and M2. R1 was the farm under investigation in this study and is referred to throughout the manuscript as farm 1. Isolates of M2 (referred to throughout the manuscript as farm 2) were used for comparison of MLST analysis only. The owners gave their consent to participate in the study.

Bacterial isolates
All 668 C. jejuni isolates used in this study were derived from farm 1, during the third phage application field trial described by Kittler et al. [14]. The field trial was carried out in 2012, testing the effect of a phage cocktail to reduce Campylobacter in commercial broiler chickens. Briefly, in each of two broiler chicken flocks 9 individual samples of faeces or caecal content were taken for Campylobacter spp. and phage enumeration. The flocks were naturally colonised by Campylobacter. Samples were taken when birds were 31, 32, 35 and 38 days old.
Depending on the availability of single colonies, up to 100 isolates from each flock and sampling time were collected. If the samples of a sampling time contained less than 100 colonies, all available single colonies were isolated. This altogether resulted in 668 collected isolates from a total of 55 Campylobacter positive samples. Only 15 isolates from flock 1 at day 31 were isolated and .65 isolates for all other samplings. The isolates were stored in skimmed milk as described below. For further examination, isolates were grown in Preston selective broth (Oxoid, Germany) for 48 h under microaerobic conditions and subsequently cultivated on Karmali agar plates (Oxoid, Germany).

Entry of phages
As described in detail by Kittler et al. [14] phages were applied to flock 1 via drinking water after sampling of faeces for Campylobacter and phage detection from 31 day old birds. The phage cocktail consisted of 4 lytic, well characterised phages of the British phage typing scheme (NCTC 12672, 12673, 12674 and 12678). Flock 2 did not receive any phages. However, in flock 2 cross contamination occurred. Phages were found in the samples of this flock four days after phages had been applied in flock 1 [14].

Detection of phages and Campylobacter
All samples were investigated for presence of phages and Campylobacter as previously described [14]. Presumptive Campylobacter colonies were picked from two plates containing ,100 single colonies. They were cultivated on Karmali agar plates for 24 h and stored in skimmed milk at 280uC. Afterwards, they were examined for motility and typical cell morphology under the microscope and for positive catalase and oxidase reaction before storage.

Multi Locus Sequence Typing
A total of 18 selected isolates from the two flocks were characterised by MLST analysis according to the procedure outlined by Dingle et al. [52]. The amplification and sequencing primers were obtained from C. jejuni PubMLST webpage. The seven housekeeping gene loci aspA (aspartase), glnA (glutamine synthetase), gltA (citrate synthase), glyA (serine hydroxyl methyl transferase), pgm (phosphor glucomutase), tkt (transketolase) and uncA (ATP synthase alpha subunit) were used. Sequence files were read, assembled, evaluated, aligned and compared to the reference set of alleles using BioNumerics 7.1 software (Applied Maths, Belgium). The 18 selected isolates were phylogenetically compared to 7 isolates of two other, similarly performed field trials [14] and to 314 strains isolated by members of the FBI-Zoo research network from different sources in Germany 2007-2011 [23]. Table 1 summarises the isolates and applied methods.

GGT activity of Campylobacter isolates
All 668 isolates were tested for GGT activity by using Gamma-Glutamyl-Aminopeptidase Diatabs (Rosco Diagnostica, Taastrup, Denmark) according to the manufacturer's instructions. The test was performed in 48 well microtiter plates. Positive-and negativecontrols were prepared for each assay using the well characterised strains NCTC 12662 and 19660-10 from our laboratory reference stock.

Phage susceptibility of Campylobacter isolates
Susceptibility of Campylobacter isolates to the phages in our cocktail was tested, using a modification of the agar overlay method previously described [53]. Briefly, 100 ml phage test suspension and 100 ml of the respective Campylobacter isolate (McFarland 3, equating log 10 7-9 cfu/ml data not shown,in 10 mmol MgSO 4 ) were added to 5 ml molten NZCYM Overlay agar (0.7% agar agar) and poured on plates of NZCYM base agar (1.5% agar agar). For preparing McFarland 3, Campylobacter was grown on MH blood plates (Oxoid, Germany) for 17 hours. The phage test suspension harboured all four cocktail phages in equal parts at an overall concentration of log 10 4 pfu/ml.

Motility assay of Campylobacter isolates
Motility of all 668 isolates was tested by a method described previously by Gaynor et al. [34] with slight modification. Briefly, 1 ml McFarland 3 suspension of the isolate was stabbed into NZCYM agar plates containing 0.7% agar (Oxoid, Germany). McFarland 3 was prepared as stated above using cultures that had been incubated for 17 h. After 24 h incubation, the diameter of the colonised zone was measured. 41 Representative isolates of all samplings and phenotypic groups were analysed by matrix-assisted laser desorption ionisation-time of flight mass spectrometry (MALDI-TOF MS).

MALDI-TOF analysis
The procedure was adapted from the 'ethanol/formic acid extraction' validated by the manufacturer (Bruker Daltonics GmbH, Germany). Briefly, isolates were cultivated for 17 h and 3-4 colonies were suspended in tubes containing 150 ml bidistilled water and 450 ml absolute ethanol. Subsequently they were stored at 220uC. After thawing they were centrifuged at 20006g, the liquid phase was removed and the pellet was resuspended in 25 ml formic acid (70%), mixed with 50 ml acetonitrile and was centrifuged. 1 ml of the supernatant was placed onto a polished steel MALDI target plate (Bruker Daltonik GmbH, Germany) at four MALDI target positions per strain. After drying at room temperature each sample was overlaid with 1 ml of matrix containing a-cyano-hydroxy-cinnamic acid in 2.5% trifluoroacetic acid and 50% acetonitrile in water (Bruker Daltonik GmbH). They were dried at room temperature and the MALDI-TOF MS measurement was performed using the Bruker Biotyper (Bruker Daltronik GmbH). Raw spectrum data were analysed using Bionumerics Software 7.1.

Biochemical phenotyping
The API Campy test system (Biomerieux, France) was used for biochemical phenotyping of .250 representative isolates of all groups and samplings according to the manufacturer's instructions. Briefly, an overnight culture of each isolate was prepared and suspended in NaCl and AUX medium. Subsequently, microtubes of the API Campy strip were charged and incubated. The reactions were read according to the manufacturer's instructions and analysed using Bionumerics Software 7.1.
Data analysis SAS 9.3 software was used for statistical analysis. For detecting significant differences in Campylobacter counts, the Wilcoxon rank sum test was used. For evaluating susceptibility distribution and GGT activity the Chi-square test or Fisher-Yates-test were used and statistical significant differences in motility were detected using the t-test or Wilcoxon-rank sum-test.
MLST profiles, MALDI-TOF spectra and Biochemical profiles of isolates were compared by using the Minimum Spanning Tree plugin, and the cluster analysis tool of the BioNumerics 7.1 software.

Results
A total of 668 C. jejuni isolates were collected from two flocks before and after Campylobacter-phage application on a commercial broiler farm. The isolates were analysed for phage susceptibility, motility and biochemical phenotype. For phylogenetic comparison of selected isolates MLST sequence type (ST) and clonal complex (CC) analysis was carried out.
MLST analyses of 18 selected isolates (9 isolates from each flock of the investigated farm 1, thus including isolates of all samplings) revealed two STs that differed in two of seven MLST loci: 14 isolates belonged to ST 4755, whereas a new ST 6836 was identified for 4 isolates from flock 1 ( Table 2). The new ST differed from ST 4755 in the sequence of aspA and pgm housekeeping genes. Both STs were related, belonging to ST-1034 CC (Fig. 1, farm 1: red isolates). These 18 isolates from farm 1 were compared to 7 isolates from other phage application field trials on a different farm (farm 2) in 2011 and 2012 (Fig. 1, farm 2: yellow and orange isolates) [14]. Results are shown in Fig. 1 A. The STs differed in at least 3 allels. Interestingly, the STs of the 7 isolates from the other field trials were not related to each other and differed in a minimum of 5 allels. The islolates analysed by Gripp et al., deriving from different human, animal, food and environmental sources in Germany from 2007-2011, were used for comparison because they were well characterised and tested for a set of metabolic properties [23]. These properties included metabolic variation, energy harvest and genes proposed to be involved in pathogenesis and metabolism such as motility and presence of the ggt gene. Results of comparing MLST profiles of field trial isolates and the isolates analysed by Gripp et al. are shown in Fig 1 B. The two STs of the investigated farm 1 isolates showed a minimal difference in their allelic profile compared to the ST 1709 isolates analysed by Gripp et al. [23]. The ST 1709 isolates derived from poultry meat in 2008 (Isolate FBI 04313; pubmlst.org) and from a laying hen 2009 (Isolate FBI 04343; pubmlst.org) [23].
The 668 isolates were further examined. Two phenotypes differing in the presence or absence of GGT activity were identified. Results of Campylobacter and phage detection in samples and frequency of GGT activity in both flocks are shown in Table 3. The isolates with GGT activity were significantly more often susceptible to phage infection than isolates displaying no GGT activity (p,0.0001, N = 668, Table 4). However, as displayed in Table 4, 58 isolates did not express these most frequent phenotypic combinations of GGT activity and phage susceptibility (Table 4, no GGT activity and phage susceptibility or GGT activity and no phage susceptibility). These isolates originated from all samplings of the field trial.
In flock 1 a phage cocktail was applied when birds were 31 days old [14]. The results displayed in Table 3 indicate that phages spread rapidly in the flock until they were found in 8 out of 9 samples after four days. Results of Campylobacter detection during the same period (Table 3) showed one positive sample (detection limit 50 cfu/g) when birds were 31 days old before phage application. Results of subsequent testings indicated a rapid spread of Campylobacter until all samples harboured Campylobacter after 10 days, suggesting colonisation occurring despite the presence of phages (Table 3; Flock 1). Distribution of GGT activity among isolates at different times is shown in Table 3. Isolates with GGT activity were isolated mainly after phage application and results indicate a rapid spread and improved colonisation compared to isolates without GGT activity (Table 3; Flock 1). Looking at Fig. 2; A, non-susceptible isolates only were isolated from most samples on the first two samplings, changing over to both, susceptible and non-susceptible isolates, in all samples at the third sampling. Thus, results indicated that the susceptible isolates spread rapidly while non-susceptible isolates  Phage Susceptible Campylobacter Colonisation PLOS ONE | www.plosone.org declined ( Fig. 2; A). As displayed in Table 2, neither GGT activity nor phage susceptibility coincided with a certain MLST profile.
In flock 2, entry of phages occurred due to unintended crosscontamination and horizontal transmission, in contrast to phage application in flock 1 [14]. While no phages were detected from fecal samples tested at day 32, three days later 8 out of 9 samples were tested positively (Table 3; Flock 2). More than 50% of the samples tested positive for Campylobacter when birds were 31 days old and subsequent spreading was observed until all samples were Campylobacter positive 4 days later (detection limit 50 cfu/g).
Isolates with and without GGT activity were present at day 31 in flock 2 but 100% of tested isolates showed GGT activity four days later. However, at the last sampling, isolates without GGT activity reappeared when numbers of Campylobacter were reduced ( Table 3; Flock 1). In this flock most samples harboured both susceptible and non-susceptible isolates at the beginning of observation ( Fig. 2; B), but only susceptible isolates were isolated one day later. However, non-susceptible isolates reappeared six days later, at the last sampling ( Fig. 2; B).
To determine if alteration of susceptibility or GGT activity correlated with changes in motility of the isolates, a motility assay was performed. Results are shown in Figure 3. Isolates with GGT activity showed a significantly higher motility than isolates without GGT activity (p,0.0001). Isolates were ranked in four susceptibility classes and even the lowest susceptibility class with 100 fold reduced susceptibility (1-10 plaques compared to 100-1000 in fully susceptible control) expressed a significantly higher motility compared to the non-susceptible isolates (Fig. 3 B; p = 0.0288 for low susceptibility; p = 0.0060 for medium susceptibility; p,0.0001 for high susceptibility).

Discussion
In this study the dynamics of Campylobacter colonisation in presence of phages in two broiler flocks was investigated. MLST, MALDI-TOF and biochemical analysis, phage susceptibility and motility as well as GGT activity were examined.
The results of the present study indicate that a phage susceptible C. jejuni subpopulation with increased motility and GGT activity could overgrow a non-susceptible subpopulation in the presence of phages. Susceptibility of the isolates was only tested in vitro. Even though we used standard test methods for phage susceptibility, we cannot rule out that differences between in vitro and in vivo susceptibility existed. A reduced ability of phages to kill in-vitrosusceptible Campylobacter in vivo was reported in another study [11]. Nevertheless, phage replication occurred during the trials and is a sign of sufficient concentrations of susceptible Campylobacter. According to pharmacokinetic experimental and modelling approaches of Cairns et al. [46] minimum concentrations of approx. log 10 4 cfu/g of non-culturable Campylobacter isolates must have been present, if phages did not replicate in the susceptible Campylobacter that were isolated. Reappearance of non-susceptible isolates in flock 2 occurred when phages reached high concentrations and Campylobacter counts were reduced in this flock [14]. Even though no significant Campylobacter reduction occurred in flock 1, phage replication up to a mean of log 10 5 pfu/g caecal content was observed [14]. These findings suggest that Campylobacter may have been under selective pressure of phage induced lysis in this trial. These results support the findings of Loc Carrillo et al. and Scott et al. [11,47,51] who found that a resistant phenotype had fitness costs and was rapidly dominated by a susceptible phenotype in vivo. Scott et al. [47] found dominance of the susceptible strain only when phages were absent, which is in contrast to our findings (Table 3). However, Scott et al. [47] found a horizontal gene transfer of .112 kb to be responsible for change of MLST ST and loss of susceptibility while the metabolic features of the dominant strain remained unclear. Nonetheless, in vivo experiments might not reflect conditions in commercial broiler houses.
MLST analysis of the 18 selected isolates found presence of STs 4755 and 6836. Both STs belonged to the ST-1034 CC. They differ in the loci aspA and pgm and are closely related to each other. Previously published Campylobacter isolates from poultry sources were found to differ in only one allele compared to each of these STs [23], demonstrating that the isolates of the investigated field  trail were closely related to different isolates from other poultry sources. Isolates from other field trials revealed unrelated STs (Fig. 1). This finding is in accordance with Bull et al. [54] who found unrelated STs being present in one flock. Different susceptibility classes and GGT activity were found for isolates having the same ST (Table 2). These results are in contrast to Scott et al. [47] who found resistance to be associated with change of MLST locus pgm allelic profile. All 668 isolates were tested for phage susceptibility and were subdivided into four levels of susceptibility: Non-susceptible, low susceptible, medium susceptible and high susceptible correspondent to the number of observed plaques (10 and 100 fold reduced for medium and low susceptibility compared to control NCTC 12662). In both flocks an increase of phage susceptible isolates was observed during the trial. When numbers of Campylobacter were reduced in flock 2 [14], non-susceptible isolates reappeared (Fig. 2). GGT activity was found to be correlated with phage susceptibility (p,0.0001, Table 4). Due to the fact that some isolates displayed phage susceptibility but no GGT activity or vice versa (Table 4), results indicate that there is no direct link between susceptibility and GGT activity. It is more likely that the GGT active phenotype is linked to other mechanisms which determine phage resistance. We explicitly looked for new STs among the isolates that displayed unusual GGT-phage susceptibility phenotypes (Table 4). These isolates are thus overrepresented in Table 2. However, they displayed the same STs as the frequent phenotypes did. As they occurred in low numbers in all samplings, they do not seem to play a major role in the population dynamics of this field trial. In order to detect additional strains or subtype-clusters we looked for clustering of isolates using BioNumerics 7.1 analysis for MALDI-TOF raw spectra and ApiCampy phenotypes. Isolates from all samplings and all possible GGT-phage susceptibility phenotypes were included in these tests. The typing methods applied were performed consecutively, i.e. when MLST and ApiCampy did not reveal enough detail, MALDI-TOF was additionally applied. Thus the isolates selected for each test varied slightly. Clustering by ApiCampy was not reliable as was indicated by branch quality error flags (data not shown). The cluster analysis of raw spectra using peak based pearsson correlation indicated two reliable clusters (Fig. S1). However, they included different STs and all combinations of GGT-phage susceptibility phenotypes (Fig. S1).
These results suggest that no additional strain or subtype was isolated. In recent studies GGT was found to be important for the colonisation of chickens and was associated with severe human cases [28,55,56]. To investigate further reasons for the superiority in colonisation of the phage susceptible GGT positive phenotype, we investigated motility of all isolates. Motility is considered to be important for Campylobacter colonisation [25,27]. An increased motility of the susceptible phenotype was found (Fig. 3), which could explain why susceptible C. jejuni isolates replaced nonsusceptible isolates in the presence of phages, since GGT activity and increased motility might promote colonisation potential of this predominant phenotype. Thus, the results of previous in vivo studies were confirmed which found reduced motility of phage resistant phenotypes [51,57] and sensitive revertants overgrowing the resistant phenotype [47]. In contrast, Carvalho at al. [12] found no differences in colonisation potential of resistant and susceptible isolates. Different mechanisms have been reported that influence phage susceptibility of Campylobacter. These mechanisms can cause reversible or non-reversible genetic or metabolic changes and can thus lead to alteration in genotype or phenotype [16,47,48,50,51,57,58]. While some of these alterations might be reflected in MLST allelic profile, others might not [55,59]. MLST STs and phage susceptibility did not coincide in our trial, thus demonstrating that the mechanism responsible for change of the MLST housekeeping genes pgm and AspA did not influence susceptibility of the isolates. In contrast, the presence of susceptible and non-susceptible isolates of both STs implies that other, very variable mechanisms might be responsible for the change of susceptibility and correlation with motility and GGT activity. Possible interpretations of this phenomenon include phase variation and pleiotropic effects as reported for other phageresistant bacteria [60][61][62][63]. Structural features such as the flagellum and CPS are known to undergo phase variation [50,64] and might contain receptor molecules necessary for phage adsorption [65]. Thus, in our study phase variation might have occurred and might have had pleiotropic effects on GGT activity. Furthermore, two separate mechanisms might have mediated resistance to different cocktail phages and have had effects on different metabolic features of the isolates. Further research is needed for a better understanding of underlying mechanisms.
Despite successful colonisation of the susceptible phenotype, Kittler et al. [14] demonstrated reduction of Campylobacter concentration in chicken caeca of the second flock. Reduced numbers of Campylobacter in phage positive flocks were also reported previously by Atterbury et al. [45] in an epidemiological investigation. Figure S1 Dendrogram of MALDI-TOF mass spectra and MLST sequence and phenotypes of Campylobacter jejuni isolates. Sequence and phenotypes of isolates are not consistent with clustering of mass spectra. The dendrogram was generated using peak based pearsson correlation and UPGMA algorithm in BioNumerics 7.1. Error flags indicate branch quality by standard deviation associated with each cluster. Error flags which don't overlap indicate consistent clustering (green error flags). While overlapping error flags indicate non-consistent clusters (red error flags). Triangles display GGT activity (white triangle: no GGT activity, black triangle: GGT activity). Hexagons display phage susceptibility (white hexagon: non susceptible, black hexagon: susceptible). * Test result with low sensitivity: no distinct GGT phenotype. n.d. ST of this isolate was not tested. (TIF)