A recombinant chimera comprising the R1 and R2 repeat regions of M. hyopneumoniae P97 and the N-terminal region of A. pleuropneumoniaeApxIII elicits immune responses
© Lee et al.; licensee BioMed Central Ltd. 2014
Received: 23 October 2013
Accepted: 13 February 2014
Published: 18 February 2014
Infection by Mycoplasma hyopneumoniae and Actinobacillus pleuropneumoniae, either alone or together, causes serious respiratory diseases in pigs.
To develop an efficient multi-disease subunit vaccine against these pathogens, we produced a chimeric protein called Ap97, which comprises a deletion derivative of the N-terminal region of the A. pleuropneumoniae ApxIII toxin (ApxN) and the R1 and R2 repeats of M. hyopneumoniae P97 adhesin (P97C), using an E. coli expression system.
The levels of both IgG1 and IgG2a isotypes specific for ApxN and P97C in the sera of Ap97-immunized mice increased, and Ap97 induced the secretion of IL-4 and IFN-γ by mouse splenocytes. Antisera from mice and pigs immunized with Ap97 readily reacted with both native ApxIII and P97 proteins. In addition, immunization with the Ap97 vaccine effectively protected pigs against challenge with both pathogens.
These findings suggest that Ap97 confers immunogenicity, and is an effective vaccine that protects pigs against infection by M. hyopneumoniae and A. pleuropneumoniae.
Actinobacillus pleuropneumoniae is the etiological agent responsible for porcine pleuropneumonia, a contagious and potentially fatal respiratory disease in pigs [1–3]. Based on differences in the capsular polysaccharides, 15 serotypes of A. pleuropneumoniae have been identified to date, which show significant variation with respect to virulence and geographical distribution. Most of those serotypes secrete one or more A. pleuropneumoniae toxin (Apx), identified as ApxI, ApxII, ApxIII, and ApxIV. Apx toxins are major virulence factors of A. pleuropneumoniae and are highly immunogenic. It is well accepted that ApxI and ApxIII are highly toxic for porcine neutrophils and pulmonary alveolar macrophages, and ApxII only moderately so.
A. pleuropneumoniae vaccines include inactivated whole-cell bacterins as well as the more promising subunit vaccines and live attenuated vaccines . Most commercially available vaccines against A. pleuropneumoniae infection comprise inactivated whole-cell bacterins derived from various serotypes of A. pleuropneumoniae. However, bacterins confer only partial protection against homologous serotypes and do not usually protect against challenge with heterologous serotypes [6, 7]. In addition, a large number of mutants were generated and used to produce live attenuated vaccines [8–10]. However, live attenuated vaccines present a number of bio-safety concerns.
Many studies show that subunit vaccines elicit an effective immune response and provide protection against A. pleuropneumoniae infection. Apx proteins have been studied as potential candidates for the development of vaccines against porcine pleuropneumoniae because they are highly immunogenic. Many commercially available A. pleuropneumoniae subunit vaccines contain recombinant Apx proteins . In addition, chimeric proteins containing components of Apx toxin have been produced for vaccine development. Some epitopes of ApxIA were inserted into the B subunit of E. coli heat-labile enterotoxin, and the immunogenicity of the chimeric proteins was analyzed in mice . Recently, ApxIIA fused with the cholera toxin B subunit was expressed in corn as a subunit vaccine candidate .
Mycoplasma hyopneumoniae is the etiological agent responsible for porcine enzootic pneumonia, a chronic non-fatal disease that affects pigs of all ages . Pigs with primary mycoplasmal infection are predisposed to potentially fatal secondary infections by the porcine reproductive and respiratory syndrome virus, Pasteurella multocida, and A. pleuropneumoniae[15–17].
Commonly used vaccines against M. hyopneumoniae comprise inactivated whole-cell bacterins. Although bacterin-based vaccines often reduce the infection level in a herd, protection against clinical pneumonia is usually not complete [18, 19]. In an experimental transmission study, a bacterin vaccine reduced the transmission of M. hyopneumoniae only to a limited extent . Moreover, preparation of bacterin vaccines is not economically advantageous, because in vitro culture of M. hyopneumoniae is time-consuming and requires a rich medium .
P97 adhesin is highly conserved among different strains of M. hyopneumoniae[22, 23]. P97 is essential for the adherence of M. hyopneumoniae to ciliated respiratory epithelial cells. The C-terminus of P97 contains two repeat regions, designated R1 and R2, which play key roles in adherence [24, 25]. Following the discovery of a functional role for the C-terminus of P97, much effort has been made to develop vaccines based on this region, in particular the R1 and R2 repeats.
A recombinant chimera comprising the R1 region of P97 and E. coli enterotoxin B induced increased humoral and cellular immune responses in mice when compared with the recombinant R1 region alone . Another chimera comprising the R1 region and a domain of Pseudomonas exotoxin A stimulated a higher IgG response to the R1 region than a commercial M. hyopneumoniae vaccine .
Live bacteria harboring vectors encoding either R1, or R1 and R2, have also been evaluated for their potential as vaccines against M. hyopneumoniae infection. Mice that orally ingested Salmonella typhimurium harboring eukaryotic or prokaryotic expression vector encoding the R1 region showed R1-specific Th1 responses . Intranasal and oral immunization of Erysipelothrix rhusiopathiae strains expressing the C-terminal portion of P97, including the R1 and R2 regions, to pigs reduced the severity of pneumonic lung lesions caused by M. hyopneumoniae infection [29, 30]. Adenovirus expressing the C-terminal portion of P97, containing the R1 and R2 regions, also induced protective P97-specific humoral and cellular immune responses in pigs .
There is a high demand for multi-disease vaccines in the swine industry due to the high labor costs incurred by vaccination and because of injection-induced stress in pigs. This is particularly true for preventing M. hyopneumoniae infection and/or secondary infection induced by A. pleuropneumoniae. Therefore, the aim of the present study was to produce a chimeric fusion protein comprising the N-terminal portion of ApxIII and the C-terminal portion of P97 using an E. coli expression system, and to analyze its immunogenicity and protective effects against infection by M. hyopneumoniae and A. pleuropneumoniae.
All chemicals were of reagent grade or higher and were obtained from Sigma-Aldrich (St. Louis, MO), unless otherwise specified.
A. pleuropneumoniae strain 1536 (serotype 2) and M. hyopneumoniae strain J were purchased from the American Type Culture Collection (ATCC, Manassas, VA). A wild-type strain of M. hyopneumoniae was isolated from the lung tissues of pigs suffering from porcine enzootic pneumonia.
The A. pleuropneumoniae strain was cultured in pleuropneumonia-like organism (PPLO) media (BD Biosciences, Sparks, MD) supplemented with 10 μg/ml nicotinamide dinucleotide, 260 μg/ml L-cysteine hydrochloride, 1 mg/ml dextrose, 10 μg/ml L-cysteine dihydrochloride, 0.6 mM glutamine, and 0.1% Tween 80 at 37°C with continuous shaking . For whole-cell lysate preparations, A. pleuropneumoniae was cultured to mid-log phase and collected by centrifugation at 3,000 × g for 10 min. The cell pellet was washed with phosphate buffered saline (PBS, pH 7.4), lysed with lysis buffer (20 mM Tris–HCl (pH 8.0), 0.15 M NaCl, 0.1 M EDTA, 1% SDS) and stored at -70°C until use.
Proteins secreted by A. pleuropneumoniae into the culture media were precipitated by the addition of 0.02% deoxycholic acid (v/v) and 15% trichloroacetic acid (v/v) to the supernatant. Following overnight incubation at 4°C, the precipitate was collected by centrifugation and the pellet was washed with cold ethanol and centrifuged. After aspiration of the supernatant, the pellet was dried and dissolved in PBS.
M. hyopneumoniae strains were cultured to mid-log phase (medium pH range, 6.8–7.2) in ATCC medium 1699 at 37°C with continuous shaking . Cell membranes were isolated by osmotic lysis and sonication. Briefly, the cell pellet was washed with PBS, resuspended in deionized water, and incubated at 37°C for 30 min. The suspensions were disrupted by sonication (thirty 2-s bursts at 200–300 W with a 2-s cooling period between each burst) and then centrifuged at 10,000 × g for 20 min at 4°C. The supernatant was centrifuged at 100,000 × g for 1 h at 4°C to collect the cell membranes . The cell membrane pellet was dissolved in resuspension buffer (10 mM potassium phosphate, 50 mM NaCl, 20% glycerol (v/v)) and stored at -70°C until use.
E. coli DH5α and BL21 (DE3) strains (Stratagene, La Jolla, CA) were used for plasmid DNA amplification and production of recombinant proteins, respectively, and were grown in Luria-Bertani (LB) media at 37°C with continuous shaking.
Oligonucleotide primers used for PCR
Sequence (5' to 3')
BamHI restriction sequence italicized
XhoI restriction sequence italicized
BamHI restriction sequence italicized
XhoI restriction sequence italicized
NdeI restriction sequence italicized
BamHI restriction sequence italicized
capsular polysaccharide biosynthesis
The pET-Ap97 vector was used to express chimeric protein Ap97, which comprises ApxN and P97C at the N- and C-terminus, respectively. A fragment of the apxIIIA gene was amplified from A. pleuropneumoniae genomic DNA by PCR using primers Ap97-F and Ap97-R (Table 1) and cloned into a pGEM-T Easy vector. The Gly-Ser peptide linker within the chimeric protein was encoded by the sequence 5’-GGATCC-3’ within the Ap97-R primer, or by a BamHI site. The TA-cloned vector was digested with NdeI and BamHI and the insert was ligated into linearized pET-P97C to yield pET-Ap97. The 5’-TAG-3’ nucleotide sequence for a Leu residue was replaced with 5’-CAG-3’ in both Ap97-R and ApxN-R primers (further discussed in the Discussion section).
Expression and purification of recombinant proteins
Each recombinant vector was transformed into E. coli BL21 (DE3) using a heat shock protocol. Selected colonies were cultured at 37°C in LB media supplemented with 100 μg/ml kanamycin. Overnight cultures (diluted 1:100) were grown until mid-log phase as indicated by an A600 between 0.5 and 0.7, at which point protein expression was induced for 4 h by the addition of isopropyl-β-D-thiogalactopyranoside to a final concentration of 1 mM.
Both the P97C and Ap97 proteins were purified from E. coli inclusion bodies. The cells were washed twice with ice-cold PBS (pH 7.4) and then lysed for 30 min in Buffer A (100 mM sodium phosphate, 10 mM Tris–HCl, 100 μg/ml lysozyme and 5 mM phenylmethanesulfonylfluoride (PMSF), pH 8.0). The lysate was centrifuged at 10,000 × g for 20 min, and the resulting pellet was resuspended by incubation for 1 h at room temperature in Buffer B (8 M urea, 10 mM Tris–HCl, 100 mM sodium phosphate and 5 mM PMSF; pH 8.0). The solubilized extracts were then loaded onto a Ni-nitrilotriacetic acid (NTA) column (Qiagen, Chatsworth, CA). The column was washed with Buffer C (8 M urea, 10 mM Tris–HCl, 100 mM sodium phosphate and 5 mM PMSF; pH 6.3) and eluted with Buffers D and E (8 M urea, 10 mM Tris–HCl, 100 mM sodium phosphate and 5 mM PMSF; pH 5.9 and 4.5, respectively) as per the manufacturer’s protocol.
To purify ApxN, the cells were washed with ice-cold PBS, lysed in Buffer F (50 mM sodium phosphate, 300 mM sodium chloride, 10 mM imidazole, 1 mg/ml lysozyme and 5 mM PMSF; pH 8.0) on ice for 30 min and sonicated on ice using six 10-s bursts at 200–300 W with a 10-s cooling period between each burst. The cell debris was pelleted by centrifugation at 10,000 × g for 20 min, and the resulting supernatant was applied to a Ni-NTA column. The column was washed twice with Buffer G (50 mM sodium phosphate, 300 mM sodium chloride, 20 mM imidazole, and 5 mM PMSF; pH 8.0). Proteins bound to the Ni-NTA column were eluted with Buffer H (50 mM sodium phosphate, 300 mM sodium chloride, 250 mM imidazole, and 5 mM PMSF; pH 8.0) as per the manufacturer’s protocol.
Purified proteins were dialyzed for 36 h at 4°C with urea or an imidazole solution diluted serially with PBS containing 150 mM sodium chloride and 5% glycerol. Protein concentrations were determined using a bicinchoninic protein assay kit (Pierce, Rockford, IL).
All procedures for handling the mice used in this study were reviewed and approved by the Institute of Laboratory Animal Resources of Seoul National University and performed in an ethical and humane manner under veterinary supervision. Female Balb/c mice aged 6 to 8 weeks (SLC Japan, Shizuoka, Japan) were divided into groups of five animals and housed in laboratory animal facilities at the College of Veterinary Medicine, Seoul National University. The mice were kept in cages with access to water and food ad libitum for 2 weeks before the first immunization. The mice were anaesthetized with a mixture of 25 mg/kg Zoletil (Virbac, Carros, France) and 10 mg/kg Rompun (Bayer, Seoul, South Korea) and then immunized by subcutaneous administration of 25 μg of immunogen (Ap97, ApxN, or P97C) on Days 0, 14, 28, and 42. PBS-immunized mice were included as negative controls. Immunogens or PBS were administered in complete Freund’s adjuvant on Day 0 and in incomplete Freund’s adjuvant on Days 14, 28, and 42. Freund’s adjuvants are potent oil-based adjuvants that are commonly used in animal research .
Serum samples were obtained by retro-orbital bleeding under anesthesia before immunization on Days 0, 14, 28, and 42. The mice were sacrificed by cardiac puncture 3 weeks after the final immunization (Day 63), and splenectomies were performed to enable the primary culture of splenocytes.
Splenocytes and cytokine analysis
The spleens of mice immunized with Ap97, ApxN, and P97C vaccines were aseptically removed, and single cell suspensions were prepared by passing the organ through a 200-μm nylon mesh sieve. Splenocytes were resuspended in ACK buffer (0.15 M ammonium chloride, 10 mM potassium bicarbonate, and 0.1 mM EDTA, pH 7.4), washed twice with RPMI 1640 media, and cultured in RPMI 1640 media supplemented with 10% fetal bovine serum, 1 mM sodium pyruvate, 2 mM L-glutamine, 100 U/ml penicillin, 100 μg/ml streptomycin and 50 μM β-mercaptoethanol at 37°C under 5% CO2 in a humidified atmosphere. For analysis of cytokine production, splenocytes (4 × 106 cells/ml) were re-stimulated for 72 h with 1.25 μg/ml of Ap97, ApxN, or P97C dissolved in PBS. At the end of re-stimulation, cell culture supernatants were harvested and analyzed for IFN-γ and IL-4 using a bead-based multiplex assay kit (Procarta cytokine assay, Panomics, Fremont, CA), as per the manufacturer’s protocol.
Enzyme-linked immunosorbent assay (ELISA)
The immuno-reactivity of the mouse serum samples against ApxN and P97C was measured using an indirect ELISA. In brief, the wells of a 96-well plate were coated with 0.5 μg of ApxN or P97C in 50 μl of carbonate buffer (pH 9.6) overnight at 4°C. The wells were washed three times with PBS containing 0.05% Tween 20 (PBS-T), blocked with 5% skim milk for 2 h at 37°C, washed with PBS-T, and then incubated with serially diluted serum samples for 2 h at 37°C. The wells were washed and incubated with peroxidase-conjugated anti-mouse IgG, IgG1, or IgG2a (diluted 1:1,000 in PBS-T) for 1 h at 37°C. After washing, the color was developed with o-phenylenediamine (Amresco, Solon, OH) and 3 M HCl was used to stop the reaction. The absorbance was measured at 450 nm in a micro-plate spectrophotometer (Molecular Devices, Sunnyvale, CA). The cut-off values for the assay were calculated as the mean specific optical density (OD) plus three standard deviations (SDs) using serum samples of non-immunized mice (Day 0) assayed at a 1:100 dilution. Titers were established as the reciprocal of the last serum dilution yielding an OD higher than the cut-off.
Gel electrophoresis and western blot analysis
Protein samples were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE; 8–10% acrylamide) using a minigel apparatus (Bio-Rad, Hercules, CA) and stained with Coomassie blue. For western blot analysis, the proteins in the SDS-PAGE gels were transferred to a Protran nitrocellulose membrane (Whatman, Dassel, Germany) in a blotting apparatus (Bio-Rad). The blots were blocked by incubation with 5% skim milk for 1 h and then incubated with antisera from mice or pigs (diluted 1:500) overnight at 4°C. The blots were then incubated with peroxidase-conjugated anti-mouse IgG or anti-pig IgG (MP Biomedicals, Solon, OH) secondary antibodies (diluted 1:5,000) for 1 h and developed with chemiluminescence reagents (Ab Frontier, Seoul, Korea).
Ten 3-week-old male pigs weighing 4–6 kg were obtained from a pathogen-free farm. Pigs were randomly divided into two groups, housed in pens with slatted floors and rubber mats in separate rooms, and provided with water and food ad libitum. Pigs were shown to be free of pathogens by PCR analysis of nasal swabs. A 500-bp fragment of the gene encoding a capsular polysaccharide from A. pleuropneumoniae serotype 2 was amplified using the AppCPS-F and AppCPS-R primers (Table 1), and a 137-bp fragment of the P102 gene from M. hyopneumoniae was amplified using the Mhyop102-F and Mhyop102-R primers.
After a week of acclimatization, both groups of pigs was immunized intramuscularly with either 700 μg of Ap97 adsorbed onto aluminum hydroxide, a standard adjuvant in clinical veterinary vaccines , or 2 ml PBS containing aluminum hydroxide as the negative control (Day 0). A booster was inoculated on Day 14 in a similar manner. Blood samples for immuno-serological analysis were drawn by puncture of the vena cava cranialis on Day 24 after the first immunization, and serum was obtained by centrifugation for 15 min at 1,500 × g. In challenge treatments performed following blood collection, pigs were inoculated with 7 ml culture media containing 2 × 108 colony-forming units of A. pleuropneumoniae and 1.5 × 108 color-changing units of M. hyopneumoniae by intranasal and intratracheal administration, respectively. Clinical signs such as rectal temperature, coughing, dyspenia, tachypnea, depression, and nasal discharge were monitored and recorded 2 weeks after challenge (Day 38). Pigs were euthanized using electric current and complete necroscopies were performed 21 days after challenge (Day 45). The macroscopic lung lesion score was determined as described previously [15, 40].
Statistical analyses were performed using SPSS 15.0 (SPSS, Chicago, IL). Data were expressed as the mean ± SD. The unpaired Student’s t-test was used to compare antibody titers and macroscopic lung lesion scores. The paired Student’s t-test was used to evaluate differences in cytokine production. Data were considered significantly different when P was < 0.05.
Production of recombinant proteins
Immunogenicity of recombinant proteins in mice
Antiserum generated in mice immunized with the Ap97 vaccine was used to test the ability of the chimeric protein to induce the production of antibodies specific for each of its component subunits, ApxN and P97C, as well as to the whole chimeric protein (Figure 2B). Antiserum against the Ap97 vaccine reacted well with ApxN, P97C, and Ap97, demonstrating that immunization with Ap97 induces the production of antibodies that bind to all three recombinant proteins. Thus, Ap97 retained the antigenic characteristics of its two individual components. Antisera from mice immunized with the ApxN and P97C vaccines reacted with Ap97, and with ApxN and P97C, respectively; however, antisera from mice immunized with ApxN did not cross react with P97C and vice versa (Figure 2C and D).
The levels of both the IgG1 and IgG2a isotypes against ApxN and P97C were measured in sera collected 3 weeks after the last immunization (Day 63; Figure 3C and 3D). The levels of both isotypes against ApxN and P97C were higher than those in the corresponding PBS-treated controls (P < 0.01 or P < 0.05), indicating mixed Th1-Th2 responses. However, the mean ratios of IgG2a/IgG1 against ApxN were 7.12 and 9.53 in antisera from mice given the Ap97 and ApxN vaccines, respectively, indicating the predominance of IgG2a production over IgG1 and, thus, a Th1-biased response to ApxN. By contrast, the IgG2a/IgG1 ratios to P97C were 0.78 and 1.68 in the antisera from mice given the Ap97 and P97C vaccines, respectively. This demonstrates that Ap97 and P97C induced relatively balanced IgG2a and IgG1 responses to P97C.
Cytokine secretion induced by recombinant proteins
Reaction of ApxIII and P97 with mouse antisera to the recombinant proteins
Immunogenicity of Ap97 in pigs
Protective efficacy of Ap97 in pigs
Protection of pigs with Ap97 vaccine against A. pleuropneumoniae and M. hyopneumoniae infection
# of pigs with clinical signs / # of pigs challenged
Lung lesion scoreb(Mean ± SD)
A. pleuropneumoniae and M. hyopneumoniae
2.00 ± 0.71*
A. pleuropneumoniae and M. hyopneumoniae
62.30 ± 4.38
There is a high demand for multi-disease and multivalent vaccines in the animal health industry. However, combining vaccine antigens causes a variety of problems, including interference between the various components, antigenic competition, and carrier-specific epitope suppression [42–44]. Thus, combined formulations must be shown to be both safe and effective before licensure. Numerous examples of immunological interference have been observed in laboratory tests and clinical trials . One relevant example involves a study of immunity against A. pleuropneumoniae in swine, in which the protective efficacy of an ApxI/ApxII vaccine was lost when it was supplemented with PalA, an outer membrane protein derived from the pathogen .
The first 160 residues of the ApxIII N-terminus are involved in its cytotoxicity and pro-apoptotic activity, and convalescent serum collected from a pig infected with A. pleuropneumoniae reacted with the N-terminus . Based upon these findings, the region encompassing residues 21–131 of ApxIII was used to construct Ap97. In preliminary studies, the first 20 residues of ApxIII were also included, but the expression efficiency was very low (data not shown). This could be due to the inclusion of two under-represented Arg codons (AGG and AGA) at residues 14 and 20, respectively. In E. coli, AUA (Ile), CUA (Leu), and AGA, AGG, or CGA (Arg), represent less than 8% of their corresponding population of codons . Another rarely-observed codon, CUA, at residue 124 of ApxIII was replaced with CUG using an Ap97-R primer that contains a single base substitution (Table 1). This was also the case for the expression of ApxN.
The expression of recombinant proteins, especially chimeric proteins, can result in aberrant tertiary folding of the expressed protein; correct folding is critical for maintaining the antigenic characteristics. It was not established whether or not both components of Ap97 protein possessed the correct tertiary structure. However, Ap97 retained the antigenic properties of its two component proteins, ApxN and P97C (Figure 2), and antisera from mice and pigs immunized with Ap97 readily reacted with native ApxIII and P97 from A. pleuropneumoniae and M. hyopneumoniae, respectively (Figures 5, 6, 7). In addition, immunization with the Ap97 vaccine induced humoral and cellular immune responses in mice (Figures 3 and 4), and pigs immunized with the Ap97 vaccine were protected against challenge by A. pleuropneumoniae and M. hyopneumoniae (Table 2). These findings suggest that Ap97 contains antigenic epitopes similar to those of native ApxIII and P97.
IL-4 activates B cells and induces class switching to the IgG1 isotype (a Th2 type immune response), while IFN-γ induces IgG2a responses (Th1 type) [48, 49]. A Th1 antibody response is involved in protection from infection, while a Th2 response is helpful for clearing the infection. Thus, an ideal vaccine should enhance Th1 responses while concomitantly maintaining Th2 responses. Ap97 induced secretion of both Th1 and Th2 cytokines by splenocytes (Figure 4). Along with an increase in cytokine levels, the levels of both the IgG1 and IgG2a isotypes specific for ApxN and P97C were also increased in the sera of Ap97-immunized mice (Figure 3). These indicate that Ap97 induced a mixed Th1-Th2 response. P97C induced balanced IgG1 and IgG2 responses in mice (Figure 3). By contrast, ApxN induced IgG2a more than IgG1, indicating a Th1-biased response to ApxN. This difference in the responses elicited by the two components of Ap97 is interesting; however, the underlying mechanism is unclear. Previous studies indicate that the pattern of IgG isotypes induced by protein vaccines depends on the adjuvants and protein antigens used [50–52].
Of the three recombinant proteins, Ap97 induced the greatest concentrations of IFN-γ and IL-4 in the culture media of re-stimulated splenocytes (Figure 4). Notably, the concentration of IFN-γ in the media from Ap97-stimulated cells was a bit higher than the sum of the cytokine concentrations in the media from ApxN and P97C-stimulated cells. This was also the case for IL-4. These suggest that both components of Ap97 do not interfere each other on cytokine induction.
The membrane fraction of M. hyopneumoniae contained not only P97 but different-sized proteins, which were recognized by serum from a pig artificially infected with M. hyopneumoniae as well as antisera from mice immunized with the Ap97 and P97C vaccines (Figure 6). Based on previous studies that identified different-sized cleavage products of P97, the non-97 kDa proteins may represent cleavage products of P97 [22, 27, 53].
The chimeric protein, Ap97, was both immunogenic and effective as a vaccine under the conditions of these experiments. To the best of our knowledge, this is the first study to demonstrate the prevention of infection by A. pleuropneumoniae and M. hyopneumoniae using a multi-disease subunit vaccine. The only previous report related to multi-disease vaccination against these two pathogens was based on immunization with a live attenuated strain of A. pleuropneumoniae, which was engineered to express M. hyopneumoniae P36 . While the results of this study are limited to two proteins derived from these pathogens, it will be interesting to evaluate the potential of other proteins derived from these microorganisms, especially ApxI, ApxII, and ApxIV toxins from various A. pleuropneumoniae serotypes, to contribute to the development of safer and more effective multi-disease vaccines.
This work was supported by the Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries.
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