Salmonella-vectored vaccine delivering three Clostridium perfringens antigens protects poultry against necrotic enteritis

Necrotic enteritis is an economically important poultry disease caused by the bacterium Clostridium perfringens. There are currently no necrotic enteritis vaccines commercially available for use in broiler birds, the most important target population. Salmonella-vectored vaccines represent a convenient and effective option for controlling this disease. We used a single attenuated Salmonella vaccine strain, engineered to lyse within the host, to deliver up to three C. perfringens antigens. Two of the antigens were toxoids, based on C. perfringens α-toxin and NetB toxin. The third antigen was fructose-1,6-bisphosphate aldolase (Fba), a metabolic enzyme with an unknown role in virulence. Oral immunization with a single Salmonella vaccine strain producing either Fba, α-toxoid and NetB toxoid, or all three antigens, was immunogenic, inducing serum, cellular and mucosal responses against Salmonella and the vectored C. perfringens antigens. All three vaccine strains were partially protective against virulent C. perfringens challenge. The strains delivering Fba only or all three antigens provided the best protection. We also demonstrate that both toxins and Fba are present on the C. perfringens cell surface. The presence of Fba on the cell surface suggests that Fba may function as an adhesin.


Introduction
Keeping our food supply safe is one of many challenges facing the agriculture industry. When rearing poultry, maintenance of a healthy flock requires a multi-faceted strategy that includes good husbandry, strong biosecurity practices, proper feed formulation, vaccination, and veterinary care. One element of poultry rearing has been the inclusion of antibiotics in the feed to promote growth. Recent concerns regarding the impact of this practice on increasing antibiotic resistance in human pathogens has led to stricter regulations governing antibiotic use in PLOS

Animal care
All animal experiments were conducted in compliance with and approved by the Arizona State University Institutional Animal Care and Use Committee and the Animal Welfare Act under protocol 16-1480R. Animals were monitored at least twice daily during these experiments. Any animal showing clinical signs were either separated temporarily and monitored closely by the veterinary staff or, if moribund, was humanely euthanized by carbon dioxide inhalation followed by cervical dislocation,

Plasmid constructions
The fba gene, codon-optimized for expression in Salmonella, was synthesized by Genscript (Piscataway, NJ, USA). To construct plasmid pKR023, the fba gene was amplified from plasmid pYA4756 using primers Fba-KpnI-F:  (TGGGGTACCAGATGGCACTGGTTAACGCAAAAG) and 3681-SacII (ATTACCGCGGCTATTAAGCTCTGTTTACTGA) were used to introduce KpnI and SacII sites into pYA3681. The fba gene was cloned into pYA3681, electroporated into Escherichia coli strain MGN055 as described [19], and then subsequently moved into S. Typhimurium strain χ11802. To construct plasmid pYA5130, primers 5023-KpnI-F (CCATGGGGT ACCAGATGAGTATTCAACATTTCCGT) and 5023-SacII (ATTACCGCGGTTACAGATAATATT CGATTTTAATT) were used to amplify the plcC-fba-Gst-netB gene cassette from pYA5023. The purified PCR product was digested with KpnI and SacII. Primers 3681-KpnI and 3681-SacII were used to amplify the plasmid sequences from pYA3681. The purified PCR product was digested with KpnI and SacII. The two fragments were then ligated and electroporated into MGN055. A plasmid of the expected size and DNA sequence was designated pYA5130.
To construct plasmid pKR032, primers netB-EcoRI-F (GATGGGATCCAGCGAACTGAACG) and netB-SalI-R (CTAGTCGACGCTTTTACAGATAATATTC) were used to generate a 900 bp PCR fragment carrying netB. Plasmid pYA5130 was used as the template DNA. The resulting DNA fragment was digested with EcoRI and SalI and ligated to pQE30 cut with the same enzymes to yield plasmid pKR032. A his-tagged Fba protein gene was constructed using primers Fba-KpnI (TGGGGTACCAGATGGCACTGGTTAACGCAAAAG) and Fba-SacII (ATTACCGC GGCTATTAAGCTCTGTTTACTGA) with plasmid pYA4756 as template. The resulting PCR product was digested with restriction enzymes FbaI and SacII. The digested fragment was ligated with plasmid pET30a digested with the same enzymes. The resulting plasmid was designated pYA5107. Construction of both his-tag fusion genes were confirmed by DNA sequence analysis.

Immunofluorescence assay
To determine if antibodies against NetB, PlcC, and Fba bound to the bacterial cell surface, we performed an indirect immunofluorescence test. For this assay, we used antibodies raised in rabbits hyperimmunized with rPlcC, rNetB or rFba. The rNetB and rFba proteins were purified from E. coli carrying plasmid pKR032 or pYA5107, respectively. The anti-rPlcC antibody was previously described [10]. Several fresh colonies of C. perfringens from a Trypticase Soy Agar with 5% Sheep Blood plate (BD) were used to inoculate Brain Heart Infusion (BHI) Broth (BD). Cultures were grown anaerobically for 24 h and harvested by centrifugation at 4000 X g for 15 min. Pelleted cells were washed once with PBS and then resuspended with 10% formalin in phosphate buffered saline (PBS) and fixed by overnight incubation at 4˚C with slow rotation. Fixed cells were pelleted, resuspended, and washed twice in PBS. 100μL of fixed cells were pelleted and blocked with 2% BSA for 1 h at room temperature with slow agitation. Cells were pelleted and resuspended in 200 μL of control sera, anti-sera, anti-sera + antigen or control protein, or PBS (no sera control) diluted 1:50 in PBS and incubated overnight at 4˚C with slow rotation. Cells were washed with PBS-0.1% Tween 20 and goat anti-chicken IgG antibody conjugated with fluorescein isothiocyanate (SouthernBiotech, Birmingham, AL) diluted 1:500 in PBS was added. The resulting cell suspension was incubated for 3 h at room temperature with gentle agitation. Cells were washed 3 times with PBS-0.1% Tween 20, resuspended in PBS and mounted for observation under a Leica TCS SP5 confocal microscope.

Synthesis of recombinant antigens in χ11802
To evaluate synthesis of PlcC, Fba and GST-NetB, overnight static cultures of S. Typhimurium χ11802 carrying plasmids pYA5112 (PlcC, GST-NetB), pYA5130 (PlcC, Fba, GST-NetB), pKR029 (Fba) or pYA3681 (empty vector) were inoculated into LB supplemented with 0.1% arabinose and 0.2% mannose and grown to an OD 600 of 0.6. Then, 1 mM isopropyl-β-D-thiogalactopyranoside (IPTG) was added to each culture and induced for an additional 4 h. The final cultures were adjusted to the same density using OD 600 values. Equal volumes of the adjusted samples were centrifuged at 16,000 × g for 5 min and the pellet was resuspended with 100 μL sodium dodecyl sulfate (SDS)-loading buffer (100 mM Tris-HCl, pH6.8; 4% SDS; 0.2% bromophenol blue; 20% glycerol; 200 mM β-mercaptoethanol). Samples were incubated at 100˚C for five minutes to lyse the cells. The whole-cell lysates were subjected to SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and western blot as described using polyclonal rabbit sera raised against the indicated antigens [7].

Immunization of chickens
Groups of one-day-old Cornish × Rock broiler chickens were purchased from the Murray McMurray Hatchery (Webster City, IA). Chickens were divided into separate pens, with 16-20 chicks per group. On the day of arrival, three chicks were euthanized. Spleen and ceca were collected to confirm their Salmonella-free status. The shipping boxes were also swabbed. Tissues were homogenized in PBS and plated onto Brilliant Green plates for bacterial enumeration. Tissue samples and swabs were also enriched in Rappaport-Vassiliadis medium for 48 h at 37˚C and subsequently plated onto Brilliant Green. No Salmonella were detected in the birds nor in the shipping boxes. The following day (day 0, the birds were 4 days of age), all chicks were orally inoculated with approximately 1 x 10 8 CFU (experiment 1) or 1×10 9 CFU (experiments 2 and 3) of various S. Typhimurium vaccine strains, including the vector-only control strain χ11802(pYA3681), in 100 μL of PBS. Additional groups of control birds were not vaccinated. Thirty minutes later, the chicks were provided with feed and water. The same dose of the same strain was given orally as a boost immunization 14 days later.
We performed three independent experiments, as outlined in Table 2. Intestinal mucosa samples and cellular response data were not collected in experiment 1 and the strain carrying pKR023 was not tested. In experiment 2, all vaccine strains were used and immune response data were collected, but no challenge was performed. In experiment 3, all strains were used and serum, mucosal and cellular response data were collected.

Sample collection for analysis of immune responses
To evaluate mucosal immune responses (experiments 2 and 3), intestinal samples were collected as described previously [20] with some modifications. Three birds from each group were necropsied at 19 (experiment 2) or 21 (experiment 3) days after the 1 st immunization (6 days after the boost). The intestines were opened aseptically and the surface contents were removed gently using a clean paper towel. Then, approximately 3 g of intestinal scrapings were collected using glass slides and resuspended in 30 mL of ice-cold PBS containing Pierce Protease Inhibitor Mini Tablets. After shaking for 1 min, the supernatants were collected by centrifugation at 4000 × g for 20 min at 4˚C to evaluate intestinal IgA, IgY and IgM antibody production. Blood was collected from wing veins of all remaining birds in each group at 21 days after the 1 st immunization to assess the IgY antibody responses to C. perfringens and Salmonella antigens in serum.

Determination of antibody response by enzyme-linked immunosorbent assay (ELISA)
ELISAs were performed in triplicate as described [21] to determine the IgY responses against his-tagged PlcC [10], his-tagged Fba, his-tagged NetB and S. Typhimurium lipopolysaccharide (LPS)(Sigma-Aldrich) in chicken sera and IgA, IgY and IgM responses in intestinal washes. The his-tagged Fba and NetB antigens were purified from E. coli strains carrying pYA5107 or pKR032, respectively, by passage of cell lysates over a metal affinity column. An initial 1:10 dilution of sera and a 1:2 dilution of intestinal washes was made of each sample. Then a 2-fold serial dilutions 7 times from these initial dilutions of sera and intestinal washes was performed and loaded in triplicate on a 96 well Nunc MaxiSorb plate. Biotinylated anti-chicken IgA (Alpha Diagnostic Intl. Inc), IgY (Southern Biotechnology) or IgM (Bioss) antibodies diluted 1:10,000 were used to detect the various antibody isotypes. Cellular proliferation assay. A proliferation assay was performed to evaluate cell-mediated immunity. Twenty-one days post primary immunization, blood and spleens were harvested. Lymphocytes in the blood were harvested using the gentle swirl technique [22] and plated in quadruplicate, in a 96-well plate at 10 5 cells/well in RPMI-1640 without phenol red. Spleens were placed through a 70 μm cell strainer to obtain single cell suspensions. Red blood cells were lysed with Red Blood Cell Lysis solution (eBioscience). Splenocytes were then washed, suspended in RPMI and plated at 10 6 cells/well. Each set of cells was incubated at 37˚C, 5% CO 2 for 72 h with or without 4 μg/ml of either His-Fba, S. Typhimurium LPS, His-NetB, His-PlcC, or 1 μg/ml PMA. Cell proliferation was measured using the Vybrant MTT Cell Proliferation Assay Kit (Molecular Probes). Mean absorbance value of antigen stimulated wells divided by mean absorbance of non-stimulated control wells was used to calculate stimulation index.

Challenge with C. perfringens
Chickens were fed an antibiotic-free starter feed containing 21% protein for 20 days, at which time the feed was switched to a high protein (28% protein), wheat-based feed containing 36% fish meal and zinc at 400 ppm (customized by Reedy Fork Farm, NC) to predispose the birds to necrotic enteritis [23,24]. Birds were challenged with virulent C. perfringens strain CP4 [14] in feed from day 28 to day 32 as described [24] with some modifications. Feed was withdrawn on day 27 for 15 h before challenge. On day 28, chickens were orally gavaged with 0.5 mL of an overnight culture of C. perfringens CP4 grown in CMM medium. Immediately after gavage, infected feed was provided thereafter for 5 consecutive days. To prepare infected feed, C. perfringens was grown in CMM medium for 24 h at 37˚C, which then was inoculated into FTG medium at a ratio of 0.3% (v/v) and incubated at 37˚C for 15 h (morning challenge) or 23 h (evening challenge). The C. perfringens culture was mixed with feed at a ratio of 1:1 (v/w). Infected feed was prepared freshly twice daily. All birds were euthanized and necropsied the day following the final challenge (day 33).

Lesion scoring
Protection against C. perfringens challenge was assessed on the basis of gross intestinal lesion scores at necropsy. On day 33, chickens were euthanized with CO 2 and their small intestines (defined here as the section between the gizzard and Meckel's diverticulum) were examined for visible gross lesions. Intestinal lesions were scored as follows: 0 = no gross lesions; 1 = thin or friable wall or diffuse superficial but removable fibrin; 2 = focal necrosis or ulceration, or non-removable fibrin deposit, 1 to 5 foci; 3 = focal necrosis or ulceration, or non-removable fibrin deposit, 6 to 15 foci; 4 = focal necrosis or ulceration, or non-removable fibrin deposit, 16 or more foci; 5 = patches of necrosis 2 to 3 cm long; 6 = diffuse necrosis typical of field cases [24]. We consider scores of 2 or greater to indicate necrotic enteritis [7,25].

Attachment assay
The human colon carcinoma cell line Caco-2 (ATCC #HTB-37) were obtained from the American Type Culture Collection (Manassas, VA) and cultured in Dulbecco's' modified Eagle's medium (DMEM) with 4.5 g/L glucose (Corning, Manassas, VA) containing 4mM Lglutamine, 1% sodium pyruvate, 1% non-essential amino acids (NEEA), 100 U/ml penicillin, 100 μg/ml streptomycin, 20% heat inactivated fetal calf serum. Caco-2 cells were seeded at 5 X 10 5 cells/mL in each well of a 24-well tissue culture plate. Cells were allowed to grow to a confluent monolayer for 48 hours. One hour prior to infection with CP4, media was replaced with antibiotic free DMEM. Then, 1 μg/ml of purified protein (his-FBA or his-PspA) or PBS was added to the Caco-2 monolayer and incubated for 15 min at 37˚C, 5% CO 2 . The bacterial inoculum was prepared as follows. CP4 cultures were grown anaerobically for 24 h in BHI broth inoculated from a fresh blood agar plate. Cultures were pelleted and resuspended in PBS to a target concentration of 5 X 10 5 CFU/ 20 μL. Caco-2 monolayers were infected with an MOI of 1:1 and then centrifuged for 3 min at 240 x g and incubated for 1 hour at 37˚C, 5% CO 2 . Each well was washed twice with PBS to remove non-adherent bacteria. To detach the Caco-2 monolayers, 200 μL/well of 0.25% Trypsin-EDTA was added to each well. Once the monolayer cells detached, 800 μL/well of PBS was added. The trypsinized samples were serially diluted and plated onto blood agar plates for C. perfringens enumeration. All counts were normalized to the inoculum concentration and presented as percentage of the no protein control. This experiment was performed twice using triplicate wells for each treatment.

Statistical analysis
All statistics were carried out using GraphPad Prism 6.0 (Graph-Pad Software, San Diego, CA). Antibody titers and adherence data were analyzed using two-way or one-way ANOVA followed by Tukey's posttest, respectively. Lesion scores were analyzed using a two-tailed Mann-Whitney test. The values were expressed as means ± SEM, and differences were considered significant at P < 0.05.

Characterization of Salmonella vaccine strains
All S. Typhimurium vaccine strains required arabinose for growth (data not shown) and had similar growth characteristics in LB broth (0.1% arabinose, 0.1% mannose) (S1 Fig). Production of PlcC, GST-NetB and Fba by the various Salmonella vaccine strains was assessed by western blot. The strain carrying pYA5130 (plcC fba GST-netB) produced Fba at levels similar to the strain producing Fba alone (Fig 1) and produced GST-NetB at levels similar to the strain carrying pYA5112 (plcC GST-netB). The strain carrying pYA5112 (plcC GST-netB) produced about 8-fold more PlcC than the strain carrying pYA5130 (plcC fba GST-netB) (Fig 1). This is not surprising, as the plcC leader sequence in pYA5112 was modified to increase PlcC synthesis [7], while the plcC gene in pYA5130 does not carry that modification.

Serum antibody responses
In experiment 1, the triple antigen vaccine elicited a significant increase in anti-Fba serum IgY titers when compared to the double-antigen vaccine or vector control (P < 0.0001) (Fig 2A). Modest increases in anti-PlcC and anti-NetB responses were observed, although only the anti-NetB responses elicited by the triple antigen vaccine achieved significance (P < 0.02). In experiments 2 and 3, birds received 10-fold higher vaccine doses. Results from experiments 2 and 3 were similar and the data were combined for analysis. In this case, the anti-Fba serum IgY titers were 14-21-fold greater than controls, which was significant (Fig 2B; P < 0.02). We observed similar, significant increases in anti-NetB titers in birds immunized with Salmonella vaccines producing NetB (P < 0.05). Despite the difference in PlcC production by strains carrying pYA5112 and pYA5130 (Fig 1), the serum responses elicited by the two strains were comparable in both experiments (Fig 2). However, though we observed increased anti-PlcC titers in birds immunized with strains producing PlcC, the increases were not statistically significant. This result is consistent with results from our previous study in which we observed poor seroconversion to PlcC when delivered by the same double antigen strain [7]. The anti-Salmonella LPS titers in immunized birds were 8-32-fold higher than controls (P < 0.0001) (Fig 2B).

Mucosal IgA, IgM and IgY responses
We examined intestinal mucosal responses in experiments 2 and 3 and have combined the data. The vaccine elicited strong, significant mucosal responses to all antigens, including PlcC,  although statistically significant responses against every antigen were not observed for all isotypes (Fig 3). The mucosal IgA responses against PlcC were not significant for either strain delivering PlcC, while mucosal IgM responses elicited by both strains were significant. The anti-PlcC mucosal IgY response was only significant for the strain delivering two antigens.
Birds immunized with the strain delivering only Fba achieved significant anti-Fba mucosal responses across all isotypes (P < 0.02). The anti-Fba IgM and IgA responses were significant in birds immunized with the triple antigen strain. The anti-Fba IgY responses, while elevated, were not significant (P = 0.20). All immunized birds produced elevated anti-NetB responses, although the anti-NetB IgA responses in birds that received the triple antigen strain did not achieve significance (P = 0.08).

Cellular responses
Immunization with the vaccine producing all three antigens elicited strong anti-Fba and anti-PlcC cellular responses in blood lymphocytes and splenocytes (Fig 4). Significant anti-NetB responses were observed in the splenocytes of birds receiving the triple antigen strain  (P < 0.05), but not in lymphocytes. Birds immunized with the strain producing two antigens, PlcC and NetB, produced significant anti-NetB responses in splenocytes (P < 0.005) and significant anti-PlcC responses in lymphocytes (P < 0.05). Birds immunized with the strain producing Fba alone exhibited significant cellular responses in splenocytes (P < 0.0001), while the response in lymphocytes was not significant.

Protection studies
Protection against challenge was assessed by scoring intestinal lesions using a 6 point scoring system [24]. In experiment 1, birds immunized with either the double antigen strain or the triple antigen strain had significantly lower lesion scores than birds in the control groups (Table 3). There was no statistical difference between the average lesion scores for the triple antigen and double antigen strain groups (P = 0.25) in this experiment.
In experiment 3, we included a strain producing only Fba in addition to the strains evaluated in experiment 1. Chickens immunized with any strain carrying C. perfringens antigens had significantly lower lesion scores than non-vaccinated or Salmonella only controls (Table 4), indicating protection against C. perfringens challenge. As in the previous experiment, there were no statistical differences between the double antigen and triple antigen groups (P = 0.19). However, there was a significant difference in lesion scores between the Table 3. Intestinal lesion scores from Experiment 1.

Group
Number of birds with the indicated score Av. Fba-only group and the double antigen group (P = 0.01), indicating that Fba is contributing to protection against C. perfringens challenge.

Plc, NetB and Fba are displayed on the surface of C. perfringens
Opsonophagocytosis is mediated by antibodies that bind to the surface of pathogenic bacteria, promoting killing of invading pathogens. Since NetB and Fba are secreted, it is likely that they might also be present, at least transiently, on the cell surface. In addition to toxin neutralization in the case of NetB [8], this would provide a possible mechanism for how immune responses against these antigens may facilitate protection.
To evaluate the potential of rabbit antisera raised against rPlcC, rNetB and rFba to bind directly to C. perfringens, we used an immunofluorescence assay. Previous work showed that anti-PlcC antibodies bind to the surface of C. perfringens [10]. We confirmed this observation. Rabbit antibodies raised against rPlcC bound to challenge strain CP4 and another NE strain, JGS4143 (Fig 5). Binding was dependent on the presence of α-toxin, as no fluorescence was observed when we probed JGS5388, a Δplc derivative of JGS4143. In addition, when purified rPlcC was mixed with the antisera prior to incubation with CP4, immunofluorescence was drastically reduced, indicating that fluorescence was mediated by anti-α-toxin-specific antibodies present in the serum. When we probed wild-type C. perfringens strains CP4 and JGS4143 with anti-NetB antisera, we observed immunofluorescence. We also observed immunofluorescence using Δplc strain JGS5388. However, no immunofluorescence was observed using the naturally occurring NetBstrain JGS4043 or when we mixed purified rNetB with the anti-NetB antisera prior to incubation with CP4 (Fig 5, right column). Interestingly, Fba appears to be present on the cell surface as well, since we observed immunofluorescence of all strains when probed with anti-Fba antisera. Fluorescence was lost when the sera was pre-incubated with purified rFba (Fig 5, right column). Incubation of C. perfringens with pre-immune sera or the secondary antibody alone did not result in immunofluorescence (S2 Fig). As an additional control, we incubated purified rFba with the anti-NetB antisera and rNetB with the anti-Fba antisera prior to probing C. perfringens CP4. These incubations did not diminish immunofluorescence (S2 Fig), indicating that protein-specific titration of each antibody was required to prevent its binding to C. perfringens. This result supports our interpretation that NetB and Fba are displayed on the surface of C. perfringens.

Fba facilitates adherence to eukaryotic cells
The presence of Fba on the C. perfringens cell surface raises the possibility that it plays a role in attachment to the host epithelium. To investigate the possible role of Fba in adherence, we examined the effect of pre-incubating Caco-2 cells with Fba prior to performing an attachment assay. As a control, we included wells in which the Streptococcus pneumoniae protein PspA was substituted for Fba. Prior addition of Fba to the wells resulted in a significant reduction in adherence (P < 0.037) (Fig 6). The irrelevant S. pneumoniae protein PspA had no effect. These results suggest a possible role for Fba in adherence to intestinal epithelial cells.

Discussion
Fba is an enzyme of the Embden-Meyerhof-Parnas glycolytic pathway that converts D-fructose-1,6-bisphosphate into D-glyceraldehyde-3-phosphate and dihydroxyacetone phosphate [26]. In C. perfringens, it also plays a role in the catabolism of myo-inositol [27] and is negatively regulated by the VirR/VirS two component system that also regulates production of a number of virulence factors including α-toxin [28] and NetB [29]. An enzyme important in central metabolism may seem to be an unusual choice for inclusion in a vaccine. However, in several organisms, Fba is recognized as a "moonlighting protein", one that can perform two or more autonomous functions [26]. Fba has been shown to serve as an adhesin in a number of dissimilar bacterial pathogens, including S. pneumoniae [30], Mycobacterium tuberculosis [31] and Neisseria meningitidis [32]. Our immunofluorescence data shows that a protein crossreactive with anti-Fba antisera is present on the surface of C. perfringens (Fig 5), a result consistent with a possible role for Fba as an adhesin in this organism. Our tissue culture results support this as well, as adherence to Caco-2 cells is inhibited in the presence of rFba (Fig 6). However, the importance of this finding will need to be confirmed using a chicken epithelial cell line and more detailed analysis.
As a vaccine, immunization with the appropriate homologous Fba is partially protective against infection with S. pneumoniae [33], S. pyogenes [34] and the fish pathogen, Edwardsiella tarda [35]. In C. perfringens, Fba was previously identified as one of several secreted proteins recognized by sera taken from chickens with acquired immunity to necrotic enteritis [12]. In an initial assessment of its vaccine potential, chickens given a single intramuscular injection with recombinant Fba were well protected against a mild C. perfringens challenge [13]. Protection against a more severe challenge required multiple injections. Fba delivered by a non-lysis attenuated S. Typhimurium vaccine was also found to elicit partially protective immunity [36], although protection was not as effective as when it was delivered by intramuscular injection. In the current study, Fba delivered by an attenuated lysis S. Typhimurium strain elicited the strongest protection in our challenge model, significantly better than the vaccine delivering the two toxoid antigens (Table 4). It is possible that, despite the careful strain design to prevent loss of immunogenicity due to antigen load, there is some stress on the vaccine strain delivering the two toxoid antigens, leading to lower immune responses against each antigen. However, in the triple antigen strain, this deficiency appears to be offset by the combined protective efficacy provided by each antigen. Although immunization with the strain delivering Fba alone yielded the lowest lesion scores, it is likely that the triple antigen strain will provide the broadest protection. This question will be examined in future experiments.
It is of interest that, in this study, we achieved anti-Fba serum IgY titers similar to the serum titers observed when Fba was delivered by a non-lysis strain [36]. Conversely, delivery by lysis strain elicited much greater mucosal responses, indicating that mucosal immunity is more important than humoral immunity for protection against challenge.
Previous work demonstrated that anti-PlcC antibodies bound to the surface of C. perfringens, indicating the presence of α-toxin [10]. We extended those observations to confirm that antibody binding did not occur in a Δplc mutant and that binding is reduced by incubation of antisera with purified PlcC (Fig 5). Our data also indicate that NetB toxin is present on the surface of C. perfringens. The presence of all three antigens on the cell surface suggests that the anti-C. perfringens mucosal antibodies elicited by our vaccine may bind directly to C. perfringens, facilitating opsonization and/or inhibiting toxin secretion. If, as our data suggest, Fba serves as an adhesin for C. perfringens, anti-Fba antibodies bound to C. perfringens cells may serve to prevent close contact of the bacterium with the host epithelium, an important step in pathogenesis [37,38]. In addition, anti-PlcC antibodies were previously shown to inhibit C. perfringens growth directly, suggesting another mechanism for the action of these antibodies.
This work highlights the potential for a Salmonella-vectored vaccine to control NE. Our findings show that the Salmonella lysis vector strain χ11802 was capable of delivering up to three antigens simultaneously, generating humoral, cellular and mucosal responses against all antigens. In particular, this strain is able to generate strong mucosal responses as shown here and in a previous study [7]. Our results also support the idea that intestinal mucosal responses are an effective deterrent against lesion formation caused by C. perfringens.