Research Article

Orally Administered P22 Phage Tailspike Protein Reduces Salmonella Colonization in Chickens: Prospects of a Novel Therapy against Bacterial Infections

  • Shakeeba Waseh,

    Affiliation: Institute for Biological Sciences, National Research Council of Canada, Ottawa, Canada

  • Pejman Hanifi-Moghaddam,

    Affiliation: Institute for Biological Sciences, National Research Council of Canada, Ottawa, Canada

  • Russell Coleman,

    Affiliation: Institute for Biological Sciences, National Research Council of Canada, Ottawa, Canada

  • Michael Masotti,

    Affiliation: Institute for Biological Sciences, National Research Council of Canada, Ottawa, Canada

  • Shannon Ryan,

    Affiliation: Institute for Biological Sciences, National Research Council of Canada, Ottawa, Canada

  • Mary Foss,

    Affiliation: Institute for Biological Sciences, National Research Council of Canada, Ottawa, Canada

  • Roger MacKenzie,

    Affiliations: Institute for Biological Sciences, National Research Council of Canada, Ottawa, Canada, Department of Environmental Biology, Ontario Agricultural College, University of Guelph, Guelph, Canada

  • Matthew Henry,

    Affiliation: Department of Discovery Research, Dow AgroSciences, Indianapolis, Indiana, United States of America

  • Christine M. Szymanski mail, (JT); (CMS)

    Affiliation: Institute for Biological Sciences, National Research Council of Canada, Ottawa, Canada

    Current address: Department of Biological Sciences, University of Alberta, Alberta Ingenuity Centre for Carbohydrate Science, Edmonton, Canada

  • Jamshid Tanha mail (JT); (CMS)

    Affiliations: Institute for Biological Sciences, National Research Council of Canada, Ottawa, Canada, Department of Environmental Biology, Ontario Agricultural College, University of Guelph, Guelph, Canada, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Canada

  • Published: November 22, 2010
  • DOI: 10.1371/journal.pone.0013904


One of the major causes of morbidity and mortality in man and economically important animals is bacterial infections of the gastrointestinal (GI) tract. The emergence of difficult-to-treat infections, primarily caused by antibiotic resistant bacteria, demands for alternatives to antibiotic therapy. Currently, one of the emerging therapeutic alternatives is the use of lytic bacteriophages. In an effort to exploit the target specificity and therapeutic potential of bacteriophages, we examined the utility of bacteriophage tailspike proteins (Tsps). Among the best-characterized Tsps is that from the Podoviridae P22 bacteriophage, which recognizes the lipopolysaccharides of Salmonella enterica serovar Typhimurium. In this study, we utilized a truncated, functionally equivalent version of the P22 tailspike protein, P22sTsp, as a prototype to demonstrate the therapeutic potential of Tsps in the GI tract of chickens. Bacterial agglutination assays showed that P22sTsp was capable of agglutinating S. Typhimurium at levels similar to antibodies and incubating the Tsp with chicken GI fluids showed no proteolytic activity against the Tsp. Testing P22sTsp against the three major GI proteases showed that P22sTsp was resistant to trypsin and partially to chymotrypsin, but sensitive to pepsin. However, in formulated form for oral administration, P22sTsp was resistant to all three proteases. When administered orally to chickens, P22sTsp significantly reduced Salmonella colonization in the gut and its further penetration into internal organs. In in vitro assays, P22sTsp effectively retarded Salmonella motility, a factor implicated in bacterial colonization and invasion, suggesting that the in vivo decolonization ability of P22sTsp may, at least in part, be due to its ability to interfere with motility… Our findings show promise in terms of opening novel Tsp-based oral therapeutic approaches against bacterial infections in production animals and potentially in humans.


Bacterial infections are one of the major causes of morbidity and mortality in both man and economically important animals and impose a huge economical burden in terms of health care cost, lost manpower and contaminated food. Antibiotics are widely used and in some places are the only treatments available. However, due to the emergence of difficult-to-treat infections caused by antibiotic resistant bacteria, there is an urgent need for alternatives. Several other therapeutic approaches involving passive and active immunization, toxin binding agents, lytic bacteriophages, anti-bacterial peptides, phage lytic enzymes and probiotics have been used but they are far from replacing the antibiotic therapy approach [1][9].

Lytic bacteriophages are the natural enemy of their host bacteria and, as such, provide a natural solution for the therapy of bacterial infections. Bacteriophages are also host specific, self-replicating, self limiting and virtually non-toxic. These characteristics have made lytic bacteriophages attractive therapeutic agents to combat bacterial infections. Despite their widely known therapeutic potential, bacteriophages have still not filled the gap of desperately needed alternatives to current antibacterial agents. Antibacterial activities of bacteriophages have been tested in several animal studies but led to, often, mixed outcomes [10][15]. Bacteriophage therapy is associated with drawbacks such as the possibility of showing reduced efficacy under anaerobic conditions in the gut due to bacterial regrowth [16], the emergence of phage-resistant bacteria and the risk of horizontal gene transfer of virulence traits to the bacteria potentially rendering the target organism even more pathogenic [17][19].

To exploit the target specificity and therapeutic potential of bacteriophages without being held back by some of the drawbacks associated with using whole phages, we chose to investigate the utility of bacteriophage tailspike proteins (Tsps). Tsps are components of the tail apparatus of many bacteriophages, and mediate the specific recognition of its bacterial host by binding to surface structures such as polysaccharides [20][27]. Additionally, many Tsps have endoglycosidase activity, hydrolyzing their polysaccharide receptors. Tsps identified to date are homotrimers consisting of an N-terminal capsid-binding domain, a central domain that binds/hydrolyzes the O-antigen region of bacterial surface lipopolysaccharides and a C-terminal region crucial for trimerization. A hallmark of Tsps is their high stability. Tsps, as well as their N-terminal truncated versions, are protease resistance, have excellent thermostability, show resistance to dissociation in high concentrations of urea and SDS, and reversibly unfold in concentrated chemical denaturants [23], [25], [26][29]. One well studied Tsp is that of bacteriophage P22 which is a 215-kDa trimeric protein specifically recognizing several pathogenic Salmonella spp. including S. enterica serovar Typhimurium [30][33]. The shortened version of P22 phage Tsp (P22sTsp) lacking the N-terminal capsid-binding domain exhibits the same native structure, oligosaccharide binding and endorhamnosidase activity as the full-length Tsp [28], [29], [33]. Similar to the full-length Tsp, the shortened P22 Tsp exhibits impressive solubility and stability properties: it is SDS- and trypsin-resistant as well as thermostable at temperatures beyond 80°C [28], [29], [34], [35].

Here, we tested the idea of using bacteriophage Tsps as an alternative to the whole phage approach for oral therapy of bacterial gut infections. The general stability of Tsps and their resistance to proteases makes Tsps - as well as their shortened derivatives - ideal proteins for oral therapeutics as they can better resist the acid-induced denaturation and digestion by proteases in the gastrointestinal (GI) tract. In this study we show that the Salmonella-specific P22sTsp is effective in reducing Salmonella colonization in the gut of chickens and the penetration into internal organs. Our findings show promise in terms of opening novel oral Tsp-based therapeutic approaches against bacterial infections in both man and production animals that provide many advantages over the use of intact bacteriophages including reduced ability of the pathogen to develop resistance and release of harmful bacterial cell components during lysis.


P22sTsp agglutinates Salmonella cells similar to antibodies

The ability of P22sTsp to agglutinate Salmonella cells was assessed in cell micro-agglutination assays. Because P22sTsp is multimeric, it is expected to cross-link and agglutinate the bacterial cells. In micro-agglutination assays, bacteria that are not agglutinated settle to the center of the well forming a dot and those that are agglutinated form a sheet across the well [36] (Figure 1). Micro-agglutination was performed by incubating a constant number of bacterial cells with two-fold dilutions of P22sTsp.


Figure 1. P22sTsp micro-agglutination assay at 4°C.

P22sTsp agglutinates Salmonella effectively as shown by the diffused cell patterns (wells on the left side of the arrow). No agglutination was observed with Staphylococcus aureus (lower panel) at the highest concentration used (cell sediments appear as round dots). MAC: minimum agglutination concentration.


The agglutination ability of P22sTsp was assessed at 4°C and 42°C. At 4°C, the minimum concentration of P22sTsp resulting in detectable cell agglutination (minimum agglutination concentration) was 149 ng/ml (Figure 1). P22sTsp showed slightly better agglutination than the Se155-4 antibody [37], which is specific to the O-antigen of Salmonella enterica serovar Typhimurium (minimum agglutination concentration = 320 ng/ml). The agglutination was specific since P22sTsp did not agglutinate the control organism, Staphylococcus aureus (Figure 1). No agglutination was observed at 42°C (physiological body temperature in chickens) under the examined assay conditions. This can be attributed to the endorhamnosidase activity of P22sTsp interfering with its binding to Salmonella and subsequent agglutination, an activity which is presumably suppressed at 4°C. Consistent with this view, a P22sTsp mutant (D392N; [33]) with wild-type binding affinity and defective endorhamnosidase activity agglutinates Salmonella at 42°C (unpublished results).

P22sTsp is significantly resistant to GI proteases

In the present study, P22sTsp was fed to chickens in order to assess its ability to reduce Salmonella colonization in the gut. The decolonizing efficacy of P22sTsp would depend on its degree of resistance to GI proteases, particularly to trypsin, chymotrypsin and pepsin, the major GI proteases. We, thus, performed a series of GI protease digestion experiments to obtain the resistance profile of P22sTsp. In the first set of experiments, susceptibility of P22sTsp to proteases present in chicken GI fluids was tested. P22sTsp was shown to be completely resistant to GI fluid proteases even after 2 h of incubation at 37°C, whereas a control antibody protein was completely digested (Figure 2A). Also, the antibody control was not digested when incubated with heat-inactivated GI fluid for 2 h at 37°C, demonstrating that the banding pattern was due to proteases in the GI fluids (data not shown). The P22sTsp was also shown to be completely resistant to trypsin (Figure 2B), but somewhat sensitive to chymotrypsin (Figure 2C) and completely sensitive to pepsin digestion (data not shown). However, when 10% bovine serum albumin (BSA) was included in the digestion reactions, chymotrypsin and pepsin did not digest P22sTsp anymore, demonstrating the protective role of BSA against these proteases (Figure 2D). Thus, to diminish the possible adverse effects of variable GI proteases in vivo, the following formulation was chosen for the animal studies: P22sTsp suspended in PBS (pH 7) containing 10% BSA.


Figure 2. Protease resistance profile of P22sTsp.

SDS-PAGE analysis of P22sTsp following treatment with A, chicken GI fluid proteases, B, trypsin, C, chymotrypsin and D, pepsin and chymotrypsin in the presence or absence of 10% BSA. A, Lane 1, molecular weight markers; lane 2, untreated P22sTsp; lanes 3–5, P22sTsp incubated with protease solutions at 37°C for 5 min, 20 min and 2 h, respectively. B, C, Lane 1, molecular weight marker; lane 2, untreated P22sTsp; lane 3, trypsin-treated (B) or chymotrypsin-treated (C) P22sTsp (1 h at 37°C). A control protein (single-domain antibody) incubated with the GI fluid (37°C, 2 h), trypsin or chymotrypsin (37°C, 1 h) showed complete digestion (data not shown). D, All reaction samples, including controls (no proteases) were subjected to a purification step with PureProteome™ Nickel Magnetic Beads prior to their analysis by SDS-PAGE (see Materials and Methods). Digestion reactions were carried out for 0 and 60 min. The positions of the molecular weight markers are indicated on the left of the panel D figures.


P22sTsp reduces Salmonella colonization in the gut and bacterial penetration into internal organs

Next, we set out to investigate, in a series of animal studies, the effect of oral administration of P22sTsp in reducing Salmonella colonization in chicks. Subsequent to Salmonella colonization of the GI tract, the organism has been shown to translocate through the gut into the bloodstream, leading to substantial infection of the liver and spleen [38][41]. Thus, the effect of treatment was assessed by counting the number of viable Salmonella not only in the gut (cecum) but also in the liver and spleen.

For the animal studies, two-day-old chicks were orally infected with Salmonella (104 to 107 colony-forming units (CFU), depending on the experiment) and were subsequently fed with 3 doses of P22sTsp (in PBS/10% BSA). In preliminary experiments two different treatment protocols were tested (Protocol 1 and Protocol 2, Figure 3). The first dose of Tsp in Protocol 1 was given one hour after infection of chicks with Salmonella (107 CFU) and in Protocol 2, the dose was delayed and given at time 18 h post infection. Following the first dose, the second and third doses were given in 24-hour time intervals in both protocols. Chicks were then sacrificed 5 h after receiving the third dose and their Salmonella contents were enumerated in the cecum, liver and spleen.


Figure 3. Schematic overview of the two protocols used for animal studies.

At time point zero, chicks were inoculated with 107 Salmonella. In Protocol 1, chicks were gavaged after inoculation (1 h) with P22sTsp in 10% BSA or with 10% BSA alone. The next two gavages were given at 18 h and 42 h. Chicks were sacrificed at 47 h. In Protocol 2, the first gavage was delayed by 17 h and given at 18 h. The next two gavages were given at 42 h and 66 h. The chicks were subsequently sacrificed at 47 h (Protocol 1) or 71 h (Protocol 2).


P22sTsp treatment of infected animals led to a significant reduction of Salmonella in the cecum, liver and spleen in Protocol 1 (P<0.05) but not in Protocol 2 (Figures 4A and 4B). Infected animals receiving Tsp treatments under Protocol 1 (S.typh.+Tsp/BSA (P1)) and Protocol 2 (S.typh.+Tsp/BSA (P2)) showed at least 100- and 10-fold reduction of bacterial titre in their ceca, respectively (P1 median = 3.3×104 CFU/ml; P2 median = 7.8×105 CFU/ml), compared to control groups which were infected with Salmonella and either treated with BSA alone (S.typh.+BSA) or not treated (S.typh.) (medians: 5.9×106 CFU/ml and 3.2×106 CFU/ml, respectively, Figure 4A).


Figure 4. Effect of orally administered P22sTsp on Salmonella colonization of chick cecum.

Effect of orally administered P22sTsp on Salmonella colonization of chick cecum (A) or liver and spleen (B). Medians are shown as horizontal bars on graph A. The two protocols were compared and for subsequent studies Protocol 1 was used. Chicks not infected with Salmonella Typhimurium (No S.typh.); chicks infected with S. Typhimurium but did not receive any treatment (S.typh.); infected chicks treated with 10% BSA (S.typh.+BSA); infected chicks treated with P22sTsp in 10% BSA according to Protocol 1 (S.typh.+Tsp/BSA (P1)); infected chicks treated with P22sTsp in 10% BSA according to Protocol 2 (S.typh.+Tsp/BSA (P2)). For cecal results, the overall treatment effect was assessed using the Kruskal-Wallis test with Dunnett's post test to correct for the number of comparisons and was significant (P<0.05). For liver and spleen results, all pairs were compared to each other using the chi square test. Not significant (ns).


Examination of bacterial infection in the liver and spleen showed the same overall pattern as those for the cecum (Figures 4A and 4B). Salmonella was detected in the livers and spleens of 65–73% of the control group that was treated with BSA alone (S.typh.+BSA) and 60% of the non-treated control group (S.typh.). Percentages of livers infected were significantly lower for animals that were treated according to Protocol 1 (P<0.0001) but not Protocol 2 compared to the BSA-treated groups (Table 1). However, both protocols were effective in reducing the infection in the spleens of Tsp-treated animals compared to the BSA-treated controls (P<0.0001), with Protocol 1 being more effective than Protocol 2 (P<0.0001; Table 1).


Table 1. Comparative study of two different treatment protocols.


Protocol 1 was then used in all subsequent trials. Two-day-old chicks were divided into two groups, each consisting of 3 cages with 8 chicks (total of 24 per group, Figure 5). Following inoculation with either 104 bacteria (Group 1) or 105 bacteria (Group 2), one cage in each group received BSA (S.typh.+BSA) while the other two received P22sTsp (S.typh.+Tsp/BSA). Ceca of Tsp-treated chicks (S.typh.+Tsp/BSA), from groups 1 and 2, showed a significant reduction of Salmonella counts compared to the BSA-treated cohort (Group 1, p = 0.0007; Group 2, p = 0.003, Figure 5, Table 2). The reduction was 13- and 15-fold for group 1 (medians: 1.5×107 CFU/ml and 1.2×107 CFU/ml, cage 1 and cage 2, respectively) and 13- and 70-fold for group 2 (medians: 6.6×107 CFU/ml and 1.3×107 CFU/ml, cage 1 and cage 2, respectively) when compared to the BSA-treated animals (medians: 2.0×108 CFU/ml and 9.1×108 CFU/ml; group 1 and group 2, respectively). Pooled data from group 1 and group 2 of Tsp-treated animals were compared to pooled data from BSA-treated animals and showed a significant reduction in Salmonella counts in the cecum, liver and spleen (Figure 5, Table 2).


Figure 5. Effect of orally administered P22sTsp on Salmonella colonization of chick cecum, liver and spleen at an inoculation level of 104 (Group 1) and 105 (Group 2) bacteria.

Medians are shown as horizontal bars on the graphs. Protocol 1 was followed. The P22sTsp treatment in each group was done in duplicate (cage 1 and cage 2). Non-inoculated chicks remained pathogen free (n = 9) and are not included in the graph. Infected chicks treated with 10% BSA (S.typh.+BSA); infected chicks treated with P22sTsp in 10% BSA (S.typh.+Tsp/BSA). The data from S.typh.+BSA cohorts of group 1 and group 2 were pooled, since there was no significant difference between the two groups (Mann Whitney two-tailed t-test, cecum: P = 0.32; liver: P = 0.23; spleen: P = 0.5). Pooled data for Tsp-treated animals includes 4 cohorts (2 cages, two groups). For comparison within the groups see Table 2.


Table 2. Effect of P22sTsp on reducing Salmonella colonization in the cecum, liver and spleen of two-day-old chicks.


P22sTsp retards the motility of Salmonella

Bacterial motility is implicated in colonization and invasion of host cells by bacteria [42], [43]. To verify if Tsp treatment of Salmonella would affect bacterial motility, hence its virulence [44], we performed bacterial motility assays. Salmonella cells were applied at the centre of the motility plates with or without P22sTsp throughout the plates and allowed to grow (circles). The diameter of growth was calculated at different time points and used as a measure of motility. The results clearly show that the motility of Salmonella is significantly retarded in the presence of P22sTsp (Figure 6).


Figure 6. P22sTsp reduces Salmonella motility.

The spread of Salmonella representative of its motility on soft agar plates was measured at different time points and used to plot a graph of motility diameter versus incubation time.



In this study we showed that oral administration of Salmonella-specific shortened tailspike protein (P22sTsp) significantly reduced Salmonella infection in chicks. Detailed studies are still required to delineate the mode of action of P22sTsp in reducing Salmonella colonization. However, one mechanism could be through the ability of P22sTsp to retard the motility of Salmonella in vivo, a possibility supported by our in vitro experimental results. This motility-retarding ability of P22sTsps can be attributed to their endorhamnosidase and/or binding activity capable of “modifying” O-antigen, hence, compromising the structure of lipopolysaccharide. This is in line with previous studies showing that (i) motility is a colonization factor for Salmonella which can be retarded by altering the structural integrity of lipopolysaccharides, (ii) the lipopolysaccharide O-antigen of a Salmonella is a significant factor in gastrointestinal colonization of chicks, and (iii) a Salmonella O-antigen-specific antibody inhibited Salmonella enterica serovar Typhimurium motility and entry into epithelial cells [42][48]. Tsp-mediated bacterial agglutination may also have a role in in vivo decolonization, although P22sTsp did not agglutinate Salmonella in vitro at physiological temperature under the conditions we tested [49][51]. Given that bacterial motility and/or cell surface proteins are often required for infection or retention of bacteria, blocking these cell surface binding sites and/or reducing motility of the bacteria will reduce the infectivity of the organism. It is unlikely that the observed therapeutic effect of Tsp is related to a generalized stimulation of the immune system due to endotoxin contamination of Tsp preparations since phage crude lysates were shown not to be toxic in 7-week old chickens [52] and the 2-day old chicks used in the current study would have immature immune systems [53].

If used in oral therapy, an effective decolonizing agent must be somewhat resistant to proteolysis by GI proteases (pepsin, trypsin, chymotrypsin) and able to withstand the low pH of the gastric juice. In vitro digestion studies showed that P22sTsp was sensitive to pepsin and somewhat sensitive to chymotrypsin. To diminish the adverse effect of these enzymes in vivo, the administered P22sTsp was formulated in 10% BSA and PBS (a physiological pH buffer), since our in vitro digestion experiments indicated that 10% BSA protected P22sTsp from digestion by pepsin and chymotrypsin. With that high of a concentration, BSA presents 1000-fold more potential chymotrypsin and pepsin cleavage sites than P22sTsp (Table S1), and thus becomes the target for chymotrypsin and pepsin digestion. These findings are in agreement with previous ones which showed the co-presence of high concentrations of a protein additive (10% BSA in the present case) protects the therapeutic protein from proteolysis [54][57]. Furthermore, the buffering capacity of the formulation (PBS) is also protective as it renders pepsin in the stomach inactive and neutralizes the protein denaturing capability of acidic gastric juice [54], [55], [58], [59]. This may explain why P22sTsp was not digested with the GI fluid which presumably contains pepsin. Formulation of P22sTsp in a higher pH buffer than PBS, e.g., carbonate buffer, or using encapsulation formats should provide P22sTsp with even better protection against the acid-denaturing and peptic environment of the stomach and lead to a more effective therapeutic effect in vivo [55], [59], [60].

From the therapeutic point of view in the context of the GI tract and mucosal surfaces in general, Tsps offer several advantages. Tsps (i) can be expressed in E. coli in high amounts leading to reduced production costs, (ii) maintain their clonal originality during production, as opposed to intact phages which are prone to frequent mutations, (iii) are stable molecules with significant resistance against GI tract major proteases, (iv) reduce pathogen load without lysing bacteria, hence no harmful bacterial products are released, (v) are target specific and should not disturb the gut's normal microflora, (vi) should show reduced emergence of resistance since Tsps do not threaten bacterial viability, (vii) are expected to be nontoxic, as they are regularly consumed in foods as part of phage (usually more than 108 phages per gram of meat) and (viii) are amenable to protein engineering for improved function. For example, Tsps can be engineered to have improved stability, binding and avidity with novel, narrow or broad specificities. They can also be modified to have additional effector functions by means of fusion to toxins. Other novel functions such as agglutination capabilities at physiological temperatures can be imparted on Tsps through mutations that eliminate the enzymatic activity, but retain the binding activity [25], [33].

While the immediate therapeutic inference of the present findings concerns the treatment of chickens for a more economic production of meat [61][64], it has far-reaching implications. One source of human infection with Salmonella is through contaminated meat and therefore Tsp treatment of chickens constitutes a prevention-at-source strategy. The concept of the prevention-at-source strategy is also an attractive one in the case of infections caused by human pathogens such as E. coli O157:H7, a bacterium which is a commensal in cattle and infects humans through contaminated food and water. This prophylactic treatment is more effective and less costly than the downstream treatment of infected individuals. In this regard, incorporation of Tsps into feed and/or water for animals may prove to be a very practical and cost effective preventative measure for both animals and humans. The Tsp therapy approach can be extended to bacterial infections in humans and “production animals” such as cows, pigs, fish and other livestock in general. In humans, in particular, oral therapy with Tsps, may be useful in combating pathogens such as Clostridium difficile or E. coli O157:H7 [65].

Materials and Methods

Cells, phage and P22sTsp

S. enterica serovar Typhimurium (ATCC19585), S. aureus (ATCC12598) and P22 phage (ATCC19585-B1) were purchased from the American Type Culture Collection (Manassas, VA). P22sTsp cloning, expression and preliminary characterization is described in a separate publication. Briefly, the truncated form of the P22 tailspike protein (P22sTsp) [29] spanning amino acid residues 109-666 was cloned and expressed in E. coli. P22sTsp contained an N-terminal His6 tag for purification purposes by immobilized metal affinity chromatography. P22sTsp expression yielded 25–50 mg of purified soluble protein per litre of bacterial culture.

Growth of bacteria

To prepare cells for micro-agglutination assays, a single S. Typhimurium colony from a nutrient agar plate was used to inoculate 15 ml of nutrient broth (NB) and was grown overnight at 37°C with shaking at 250 rpm. The culture was centrifuged, washed with PBS buffer, re-centrifuged and subsequently re-suspended in cold PBS. The cell density was adjusted to an OD600 of 1 (1 OD600 = 1×108 cells/ml) with PBS. S. aureus was grown as described for S. Typhimurium, but in brain heart infusion media.

To prepare cells for in vivo experiments, a frozen stock of S. Typhimurium was streaked onto a xylose lysine deoxycholate (XLD) plate (Oxoid Company, Nepean, ON, Canada) followed by incubation at 37°C for 18–24 h. Three millilitres of overnight culture (in NB) was started from a single colony of S. Typhimurium on an XLD plate, and grown at 37°C. This culture would typically have an OD600 of approximately 1.4–1.6. A 1:100 dilution of bacterial cells in 2×10 ml NB was made and the cells were grown at 37°C until they reached an OD600 of 0.3–0.5 (~2–3 h). Cells were centrifuged at 12,000 g and re-suspended in PBS to a final OD600 of 1.0. Serial dilutions of the cell culture, on XLD plates, were also performed to confirm the cell density. Cells were immediately used to orally inoculate chicks.

Micro-agglutination assay

S. Typhimurium micro-agglutination assays were performed with P22sTsp or the Se155 IgG control in microtitre plates at 4°C or 42°C [36]. Fifty microlitres of S. Typhimurium or control bacteria (S. aureus) at an OD600 of 1 were added to wells. Subsequently, two-fold serial dilutions of P22sTsp or Se155 IgG in PBS (50 µl) were added to wells. Plates were incubated overnight at 4°C or 42°C. In a micro-agglutination assay, agglutinated cells appear diffused whereas the non-agglutinated ones appear as round dots at the bottom of the wells. The minimum concentration of P22sTsp which resulted in detectable cell agglutination (minimum agglutination concentration) was determined and used as a measure of agglutination potency of P22sTsp.

Preparation of GI fluid protease solution

To prepare the GI fluid protease solution, four chicks were sacrificed and the GI contents were squeezed out of the GI tract and weighed. The appropriate amount of sterile PBS was added to make a 10-fold dilution. The sample was centrifuged at 1000 g for 15 min at 4°C and 1-ml aliquots of the supernatant was transferred to microfuge tubes and spun at maximum speed to pellet down any remaining debris. The supernatants were frozen at −20°C and stored in small aliquots for future digestion experiments.

Protease digestion experiments

Freshly-prepared sequencing grade trypsin or chymotrypsin (Hoffmann-La Roche Ltd., Mississauga, ON, Canada) in 1 mM HCl were used for digestion experiments. One microlitre of 0.012 µg/µl trypsin or chymotrypsin was mixed with 8 µl of 0.3 µg/µl P22sTsp in 100 mM Tris-HCl buffer pH 7.8 (trypsin) or in 50 mM Tris-HCl buffer pH 7.8 plus 20 mM CaCl2 (chymotrypsin). Reactions were carried out in a total volume of 10 µl for up to 1 h at 37°C and stopped by adding 1 µl of 0.1 µg/µl trypsin/chymotrypsin inhibitor (Sigma-Aldrich Canada Ltd.). Following completion of digestion, samples were mixed with SDS-PAGE loading buffer, incubated for 5 min at 95°C and analyzed by PhastSystem SDS-PAGE according to the manufacturer's instructions (GE Healthcare). Pepsin digestion mixtures contained 8 µl of 0.3 µg/µl P22sTsp, 1 µl of 100 mM HCl and 1 µl of 0.012 µg/µl pepsin (Sigma-Aldrich Canada Ltd.). Reactions were carried out at 37°C for up to 1 h and were subsequently analyzed by SDS-PAGE as described above.

To carry out digestion experiments with the GI fluid protease solution, frozen stocks (see above) were thawed, diluted 10-fold, and 30 µl of the diluted samples was mixed with 50 µg of P22sTsp. Reactions were carried out in PBS buffer in a total volume of 80 µl at 37°C for up to 2 h. The reactions were stopped by immediately boiling the samples for 5 min. In protease-negative experiments, 30 µl of inactivated GI fluid was used (inactivated samples were prepared by heating chick intestinal tract fluid at 95°C for 15 min followed by cooling down on ice). In P22sTsp-negative control experiments, P22sTsp was replaced with a control protein. Following completion of the digestions, aliquots were removed and analyzed by SDS-PAGE.

The sensitivity of P22sTsp to chymotrypsin and pepsin in the presence and absence of 10% (w/v) BSA (Fraction V, Minimum 98%, Sigma) was compared. One microlitre of 0.1 µg/µl chymotrypsin, 40 µl of 0.5 µg/µl P22sTsp and 360 µl of 100 mM Tris-HCl buffer pH 7.8 plus 20 mM CaCl2 were combined. For the pepsin digestion experiment, 40 µl of 0.5 µg/µl P22sTsp and 340 µl of PBS were combined. The pH of the reaction mixture was adjusted to 2.0 by adding 20 µl of 1 M HCl followed by the addition of 1 µl of 0.1 µg/µl pepsin. Reactions were carried out in a total volume of 400 µl with or without 10% BSA at 37°C for 1 h and stopped by adding 16 µl of 25x protease inhibitor cocktail (Hoffmann-La Roche Ltd.) to the chymotrypsin digestion or by raising the pH of the reaction mixture to 7–8 with 1 M NaOH for the pepsin digestion. Subsequently, PureProteome™ Nickel Magnetic Beads (Millipore, Billerica, MA) were used to purify His-tagged P22sTsp away from the bulk BSA in the reaction mixtures. The optimal pH for the binding of the nickel beads to the His tag, according to the manufacturer, is 7.5–8.0. After adding 400 µl of the binding buffer (50 mM Tris-HCl/500 mM NaCl/20 mM imidazole pH 7.5) to the 400 µl terminated digestion reactions, including those without 10% BSA, the pH of the reaction mixtures was determined and adjusted to 7.5 to 8.0, if necessary. Fifty microlitres of magnetic beads, equilibrated with the binding buffer, was added to the 800 µl mixture and was incubated for 30 min at 37°C on a desktop rotor. Three consecutive washes were performed with the binding buffer to remove the BSA followed by the elution of nickel-bound P22sTsp with 100 µl of 50 mM Tris-HCl/500 mM NaCl/500 mM imidazole, pH 7.5. Eluted P22sTsp was mixed with SDS-PAGE loading buffer, incubated for 5 min at 95°C and analyzed by SDS-PAGE.

Motility assay

Motility plates (NB plates/0.4% agar with or without 25 µg/ml filter-sterilized P22sTsp) were made the day before their use and left at room temperature. Purified P22sTsp was buffer-exchanged by size exclusion chromatography (Superdex™ 200 column, GE Healthcare) using PBS as the equilibration buffer and then added to the molten motility media just before pouring them into plates (50°C). To perform motility assays, Salmonella cells were grown on NB plates overnight at 37°C (16–18 h). Cells were subsequently suspended in sterile PBS at a cell density of 1 OD600. Employing a 10-µl pipettor, 5 µl of the cell suspension was used to inoculate the centre of the motility plates, lightly piercing the surface of the agar plate with the pipettor tip; the plates were left unmoved until the inoculation spots became dry. The plates were then incubated at 37°C. At different time points, the dimensions of the Salmonella zones of motility were measured. In control experiments, an equal volume of PBS replaced P22sTsp.

Animal studies

Leghorn chicks were obtained from the Canadian Food Inspection Agency one day after hatch. The animals were maintained and used in accordance with the recommendations of the Canadian Council on Animal Care Guide to the Care and Use of Experimental Animals. The experimental procedures were approved by the institutional animal care committee (Protocol Number 2004-20). One-day-old chicks were provided with feed and water ad libitum and cared for in accordance to the approved guidelines of the Canadian Council for Animal Care. For determining the presence of endogenous Salmonella, cloacal swabs were taken from 10% of the chicks, selected at random, with calcium alginate swabs (Fisher Scientific, Ottawa, ON, Canada). XLD plates were streaked with the swabs and incubated at 37°C overnight. The presence of Salmonella was identified as black colonies on the red/pink XLD plate.

Infection of 2-day-old chicks was done by oral gavaging the animals with 104–107 Salmonella/300 µl PBS. Subsequently, chicks were gavaged a total of 3 doses of P22sTsp (30 µg/300 µl) in 10% BSA or with 10% BSA alone. The 3 oral doses were given at 1 h, 18 h and 42 h (Protocol 1) or at 18 h, 42 h and 66 h (Protocol 2) post-infection and the chicks were subsequently sacrificed at 47 h (Protocol 1) or 71 h (Protocol 2). Following sacrifice, the cecal materials, livers and spleens were collected and processed for determination of Salmonella titre as described below.

Cecal material.

The cecal samples were weighed (≤0.2 g), diluted in PBS (10−1 dilution) and vortexed. Further serial dilutions up to 10−6 were performed in 200 µl of PBS in 96-well microtitre plates using a multi-channel pipettor. Starting from the highest dilution, 50 µl was plated on XLD plates. The plates were allowed to dry and subsequently incubated at 37°C overnight. The bacterial counts from the serial dilutions were determined the next day.

Liver and spleen.

To homogenize samples, two Bio 101 ¼” ceramic beads (Qbiogene, Carlsbad, CA) were placed in 2-ml screw cap tubes (Diamed, Mississauga, ON, Canada). Sterile PBS was added to spleen samples (600 µl) or liver samples (800 µl, which were cut from the right front lobe of liver) and kept on ice prior to placing them in the Fastprep Instrument (Qbiogene). Fifty microlitres of the homogenized samples, which resulted in countable colonies, were plated on XLD plates. Plates were incubated overnight at 37°C and the bacterial counts were determined in the morning. Any infected liver with lower than 24 bacteria (2 times the 1/12 dilution factor) or infected spleen with a bacterial count lower than 32 (2 times the 1/16 dilution factor) was below the detection limit of this method.


We assumed a non-Gaussian distribution of the data and therefore used non-parametric tests. To compare 3 or more unpaired groups, the Kruskal-Wallis test with Dunnett's post test was performed to correct for the number of comparisons. Medians of two unpaired groups were compared using the two-tailed non-parametric t-test (Mann-Whitney test). The chi square test was used to compare the pairs. P values less than 0.05 were considered significant. All analyses were performed using GraphPad Prism version 4.02 for Windows (GraphPad Software, San Diego, CA; “”).

Supporting Information

Table S1.

Theoretical number of cleavage sites for P22sTsp and BSA.


(0.03 MB DOC)


We thank Sonia Leclerc for DNA sequencing and Tom Devecseri for preparing publication quality figures. We would also like to thank Marc Lamoureux, Nathalie Gaudette, Ryan Walton, Anna Cunningham, Kevin Smit and Tassnim Moradipour for assistance with the chicken studies and Tsp purifications. CMS is an Alberta Ingenuity Scholar. This is National Research Council of Canada Publication 50007.

Author Contributions

Conceived and designed the experiments: RC RM MH CMS JT. Performed the experiments: SW PHM MM SR MF. Analyzed the data: SW PHM JT. Contributed reagents/materials/analysis tools: RC MM SR MF. Wrote the paper: SW PHM JT. Supervision: JT. Responsible for animal study: RC.


  1. 1. Berchieri A Jr, Lovell MA, Barrow PA (1991) The activity in the chicken alimentary tract of bacteriophages lytic for Salmonella typhimurium. Res Microbiol 142: 541–549.
  2. 2. Lyerly DM, Bostwick EF, Binion SB, Wilkins TD (1991) Passive immunization of hamsters against disease caused by Clostridium difficile by use of bovine immunoglobulin G concentrate. Infect Immun 59: 2215–2218.
  3. 3. Barrow P, Lovell M, Berchieri A Jr (1998) Use of lytic bacteriophage for control of experimental Escherichia coli septicemia and meningitis in chickens and calves. Clin Diagn Lab Immunol 5: 294–298.
  4. 4. Kurtz CB, Cannon EP, Brezzani A, Pitruzzello M, Dinardo C, et al. (2001) GT160-246, a toxin binding polymer for treatment of Clostridium difficile colitis. Antimicrob Agents Chemother 45: 2340–2347.
  5. 5. Boman HG (2003) Antibacterial peptides: basic facts and emerging concepts. J Intern Med 254: 197–215.
  6. 6. Fischetti VA (2005) Bacteriophage lytic enzymes: novel anti-infectives. Trends Microbiol 13: 491–496.
  7. 7. Marco ML, Pavan S, Kleerebezem M (2006) Towards understanding molecular modes of probiotic action. Curr Opin Biotechnol 17: 204–210.
  8. 8. Parisien A, Allain B, Zhang J, Mandeville R, Lan CQ (2008) Novel alternatives to antibiotics: bacteriophages, bacterial cell wall hydrolases, and antimicrobial peptides. J Appl Microbiol 104: 1–13.
  9. 9. Wang W, Wang EQ, Balthasar JP (2008) Monoclonal antibody pharmacokinetics and pharmacodynamics. Clin Pharmacol Ther 84: 548–558.
  10. 10. Smith HW, Huggins MB, Shaw KM (1987) The control of experimental Escherichia coli diarrhoea in calves by means of bacteriophages. J Gen Microbiol 133: 1111–1126.
  11. 11. Barrow PA, Soothill JS (1997) Bacteriophage therapy and prophylaxis: rediscovery and renewed assessment of potential. Trends Microbiol 5: 268–271.
  12. 12. Alisky J, Iczkowski K, Rapoport A, Troitsky N (1998) Bacteriophages show promise as antimicrobial agents. J Infect 36: 5–15.
  13. 13. Loc Carrillo C, Atterbury RJ, El-Shibiny A, Connerton PL, Dillon E, et al. (2005) Bacteriophage therapy to reduce Campylobacter jejuni colonization of broiler chickens. Appl Environ Microbiol 71: 6554–6563.
  14. 14. Huff WE, Huff GR, Rath NC, Donoghue AM (2006) Evaluation of the influence of bacteriophage titer on the treatment of colibacillosis in broiler chickens. Poult Sci 85: 1373–1377.
  15. 15. Atterbury RJ, Van Bergen MAP, Ortiz F, Lovell MA, Harris JA, et al. (2007) Bacteriophage therapy to reduce Salmonella colonization of broiler chickens. Appl Environ Microbiol 73: 4543–4549.
  16. 16. Tanji Y, Shimada T, Fukudomi H, Miyanaga K, Nakai Y, et al. (2005) Therapeutic use of phage cocktail for controlling Escherichia coli O157:H7 in gastrointestinal tract of mice. J Biosci Bioeng 100: 280–287.
  17. 17. Brüssow H, Canchaya C, Hardt W-D (2004) Phages and the evolution of bacterial pathogens: from genomic rearrangements to lysogenic conversion. Microbiol Mol Biol Rev 68: 560–602.
  18. 18. Clark JR, March JB (2006) Bacteriophages and biotechnology: vaccines, gene therapy and antibacterials. Trends Biotechnol 24: 212–218.
  19. 19. Kropinski AM (2006) Phage therapy - everything old is new again. Can J Infect Dis Med Microbiol 17: 297–306.
  20. 20. Steinbacher S, Baxa U, Miller S, Weintraub A, Seckler R, et al. (1996) Crystal structure of phage P22 tailspike protein complexed with Salmonella sp. O-antigen receptors. Proc Natl Acad Sci U S A 93: 10584–10588.
  21. 21. Steinbacher S, Miller S, Baxa U, Budisa N, Weintraub A, et al. (1997) Phage P22 tailspike protein: crystal structure of the head-binding domain at 2.3 Å, fully refined structure of the endorhamnosidase at 1.56 Å resolution, and the molecular basis of O-antigen recognition and cleavage. J Mol Biol 267: 865–880.
  22. 22. Steinbacher S, Miller S, Baxa U, Weintraub A, Seckler R (1997) Interaction of Salmonella phage P22 with its O-antigen receptor studied by X-ray crystallography. Biol Chem 378: 337–343.
  23. 23. Freiberg A, Morona R, Van Den Bosch L, Jung C, Behlke J, et al. (2003) The tailspike protein of Shigella phage Sf6. A structural homolog of Salmonella phage P22 tailspike protein without sequence similarity in the beta-helix domain. J Biol Chem 278: 1542–1548.
  24. 24. Barbirz S, Müller JJ, Uetrecht C, Clark AJ, Heinemann U, et al. (2008) Crystal structure of Escherichia coli phage HK620 tailspike: podoviral tailspike endoglycosidase modules are evolutionarily related. Mol Microbiol 69: 303–316.
  25. 25. Müller JJ, Barbirz S, Heinle K, Freiberg A, Seckler R, et al. (2008) An intersubunit active site between supercoiled parallel beta helices in the trimeric tailspike endorhamnosidase of Shigella flexneri phage Sf6. Structure 16: 766–775.
  26. 26. Walter M, Fiedler C, Grassl R, Biebl M, Rachel R, et al. (2008) Structure of the receptor-binding protein of bacteriophage Det7: a podoviral tailspike in a myovirus. J Virol 82: 2265–2273.
  27. 27. Barbirz S, Becker M, Freiberg A, Seckler R (2009) Phage tailspike proteins with beta-solenoid fold as thermostable carbohydrate binding materials. Macromol Biosci 9: 169–173.
  28. 28. Danner M, Fuchs A, Miller S, Seckler R (1993) Folding and assembly of phage P22 tailspike endorhamnosidase lacking the N-terminal, head-binding domain. Eur J Biochem 215: 653–661.
  29. 29. Miller S, Schuler B, Seckler R (1998) Phage P22 tailspike protein: Removal of head-binding domain unmasks effects of folding mutations on native-state thermal stability. Protein Sci 7: 2223–2232.
  30. 30. Israel JV, Anderson TF, Levine M (1967) In vitro morphogenesis of phage P22 from heads and base-plate parts. Proc Natl Acad Sci U S A 57: 284–291.
  31. 31. Iwashita S, Kanegasaki S (1976) Enzymic and molecular properties of base-plate parts of bacteriophage P22. Eur J Biochem 65: 87–94.
  32. 32. Israel V (1978) A model for the adsorption of phage P22 to Salmonella typhimurium. J Gen Virol 40: 669–673.
  33. 33. Baxa U, Steinbacher S, Miller S, Weintraub A, Huber R, et al. (1996) Interactions of phage P22 tails with their cellular receptor, Salmonella O-antigen polysaccharide. Biophys J 71: 2040–2048.
  34. 34. Chen B, King J (1991) Thermal unfolding pathway for the thermostable P22 tailspike endorhamnosidase. Biochemistry 30: 6260–6269.
  35. 35. Kreisberg JF, Betts SD, Haase-Pettingell C, King J (2002) The interdigitated beta-helix domain of the P22 tailspike protein acts as a molecular clamp in trimer stabilization. Protein Sci 11: 820–830.
  36. 36. Ryan S, Kell AJ, van Faassen H, Tay L-L, Simard B, et al. (2009) Single-domain antibody-Nanoparticles: promising architectures for increased Staphylococcus aureus detection specificity and sensitivity. Bioconjug Chem 20: 1966–1974.
  37. 37. Sigurskjold BW, Altman E, Bundle DR (1991) Sensitive titration microcalorimetric study of the binding of Salmonella O-antigenic oligosaccharides by a monoclonal antibody. Eur J Biochem 197: 239–246.
  38. 38. Carter PB, Collins FM (1974) The route of enteric infection in normal mice. J Exp Med 139: 1189–1203.
  39. 39. Barrow , PA , Huggins , MB , Lovell MA (1994) Host specificity of Salmonella infection in chickens and mice is expressed in vivo primarily at the level of the reticuloendothelial system. Infect Immun 62: 4602–4610.
  40. 40. Shea JE, Beuzon CR, Gleeson C, Mundy R, Holden DW (1999) Influence of the Salmonella typhimurium pathogenicity island 2 type III secretion system on bacterial growth in the mouse. Infect Immun 67: 213–219.
  41. 41. Kramer J, Visscher AH, Wagenaar JA, Boonstra-Blom AG, Jeurissen SHM (2001) Characterization of the innate and adaptive immunity to Salmonella enteritidis PT1 infection in four broiler lines. Vet Immunol Immunopathol 79: 219–233.
  42. 42. Siitonen A, Nurminen M (1992) Bacterial motility is a colonization factor in experimental urinary tract infection. Infect Immun 60: 3918–3920.
  43. 43. Forbes SJ, Eschmann M, Mantis NJ (2008) Inhibition of Salmonella enterica serovar Typhimurium motility and entry into epithelial cells by a protective antilipopolysaccharide monoclonal immunoglobulin A antibody. Infect Immun 76: 4137–4144.
  44. 44. Toguchi A, Siano M, Burkart M, Harshey RM (1990) Genetics of swarming motility in Salmonella enterica serovar Typhimurium: critical role for lipopolysaccharide. J Bacteriol 182: 6308–6321.
  45. 45. Nevola JJ, Stocker BA, Laux DC, Cohen PS (1985) Colonization of the mouse intestine by an avirulent Salmonella typhimurium strain and its lipopolysaccharide-defective mutants. Infect Immun 50: 152–159.
  46. 46. Craven SE, Cox NA, Bailey JS, Stern NJ, Meinersmann RJ, et al. (1993) Characterization of Salmonella california and S. typhimurium strains with reduced ability to colonize the intestinal tract of broiler chicks. Avian Dis 37: 339–348.
  47. 47. Craven SE (1994) Altered colonizing ability for the ceca of broiler chicks by lipopolysaccharide-deficient mutants of Salmonella typhimurium. Avian Dis 38: 401–408.
  48. 48. Carroll P, La Ragione RM, Sayers AR, Woodward MJ (2004) The O-antigen of Salmonella enterica serotype Enteritidis PT4: a significant factor in gastrointestinal colonisation of young but not newly hatched chicks. Vet Microbiol 102: 73–85.
  49. 49. Ma JK, Hunjan M, Smith R, Kelly C, Lehner T (1990) An investigation into the mechanism of protection by local passive immunization with monoclonal antibodies against Streptococcus mutans. Infect Immun 58: 3407–3414.
  50. 50. Duchet-Suchaux M, Menanteau P, van Zijderveld FG (1992) Passive protection of suckling infant mice against F41-positive enterotoxigenic Escherichia coli strains by intravenous inoculation of the dams with monoclonal antibodies against F41. Infect Immun 60: 2828–2834.
  51. 51. de Geus B, Harmsen M, van Zijderveld F (1998) Prevention of diarrhoea using pathogen specific monoclonal antibodies in an experimental enterotoxigenic E. coli infection in germfree piglets. Vet Q 20: Suppl 3S87–S89.
  52. 52. Oliveira A, Sereno R, Nicolau A, Azeredo J (2009) In vivo toxicity study of phage lysate in chickens. Br Poult Sci 50: 558–563.
  53. 53. Bar-Shira E, Friedman A (2006) Development and adaptations of innate immunity in the gastrointestinal tract of the newly hatched chick. Dev Comp Immunol 30: 930–941.
  54. 54. Schmidt P, Wiedemann V, Kühlmann R, Wanke R, Linckh E, et al. (1989) Chicken egg antibodies for prophylaxis and therapy of infectious intestinal diseases. II. In vitro studies on gastric and enteric digestion of egg yolk antibodies specific against pathogenic Escherichia coli strains. Zentralbl Veterinarmed B 36: 619–628.
  55. 55. Wiedemann V, Kühlmann R, Schmidt P, Erhardt W, Lösch U (1990) Chicken egg antibodies for prophylaxis and therapy of infectious intestinal diseases. III. In vivo tenacity test in piglets with artificial jejunal fistula. Zentralbl Veterinarmed B 37: 163–172.
  56. 56. Morgavi DP, Newbold CJ, Beever DE, Wallace RJ (2000) Stability and stabilization of potential feed additive enzymes in rumen fluid. Enzyme Microb Technol 26: 171–177.
  57. 57. Harmsen MM, van Solt CB, Hoogendoorn A, van Zijderveld FG, Niewold TA, et al. (2005) Escherichia coli F4 fimbriae specific llama single-domain antibody fragments effectively inhibit bacterial adhesion in vitro but poorly protect against diarrhoea. Vet Microbiol 111: 89–98.
  58. 58. Northrop JH (1920) The influence of hydrogen ion concentration on the inactivation of pepsin solutions. J Gen Physiol 2: 465–470.
  59. 59. Worledge KL, Godiska R, Barrett TA, Kink JA (2000) Oral administration of avian tumor necrosis factor antibodies effectively treats experimental colitis in rats. Dig Dis Sci 45: 2298–2305.
  60. 60. Shimizu M, Miwa Y, Hashimoto K, Goto A (1993) Encapsulation of chicken egg yolk immunoglobulin G (IgY) by liposomes. Biosci Biotechnol Biochem 57: 1445–1449.
  61. 61. Bryan FL, Doyle MP (1995) Health risks and consequences of Salmonella and Campylobacter jejuni in raw poultry. J Food Prot 58: 326–344.
  62. 62. Kaiser MG, Lamont SJ (2001) Genetic line differences in survival and pathogen load in young layer chicks after Salmonella enterica serovar Enteritidis exposure. Poult Sci 80: 1105–1108.
  63. 63. Khan MI, Fadl AA, Venkitanarayanan KS (2003) Reducing colonization of Salmonella Enteritidis in chicken by targeting outer membrane proteins. J Appl Microbiol 95: 142–145.
  64. 64. Bjerrum L, Pedersen AB, Engberg RM (2005) The influence of whole wheat feeding on Salmonella infection and gut flora composition in broilers. Avian Dis 49: 9–15.
  65. 65. Marcos LA, DuPont HL (2007) Advances in defining etiology and new therapeutic approaches in acute diarrhea. J Infect 55: 385–393.