Oral immunization with an attenuated Salmonella Gallinarum mutant as a fowl typhoid vaccine with a live adjuvant strain secreting the B subunit of Escherichia coliheat-labile enterotoxin
© Jeon et al.; licensee BioMed Central Ltd. 2013
Received: 11 January 2013
Accepted: 4 May 2013
Published: 6 May 2013
The Salmonella Gallinarum (SG) lon/cpxR deletion mutant JOL916 was developed as a live vaccine candidate for fowl typhoid (FT), and a SG mutant secreting an Escherichia coli heat-labile enterotoxin B subunit (LTB), designated JOL1229, was recently constructed as an adjuvant strain for oral vaccination against FT. In this study, we evaluated the immunogenicity and protective properties of the SG mutant JOL916 and the LTB adjuvant strain JOL1229 in order to establish a prime and boost immunization strategy for each strain. In addition, we compared the increase in body weight, the immunogenicity, the egg production rates, and the bacteriological egg contamination of these strains with those of SG 9R, a widely used commercial vaccine.
Plasma IgG, intestinal secretory IgA (sIgA), and cell-mediated responses were significantly induced after a boost inoculation with a mixture of JOL916 and JOL1229, and significant reductions in the mortality of chickens challenged with a wild-type SG strain were observed in the immunized groups. There were no significant differences in increases in body weight, cell-mediated immune responses, or systemic IgG responses between our vaccine mixture and the SG 9R vaccine groups. However, there was a significant elevation in intestinal sIgA in chickens immunized with our mixture at 3 weeks post-prime-immunization and at 3 weeks post-boost-immunization, while sIgA levels in SG 9R-immunized chickens were not significantly elevated compared to the control. In addition, the SG strain was not detected in the eggs of chickens immunized with our mixture.
Our results suggest that immunization with the LTB-adjuvant strain JOL1229 can significantly increase the immune response, and provide efficient protection against FT with no side effects on body weight, egg production, or egg contamination.
Fowl typhoid (FT) is a severe septicemic bacterial disease in poultry caused by Salmonella enterica serovar Gallinarum biovar Gallinarum (SG), which can be horizontally or vertically transmitted [1, 2]. Due to a variety of factors, both the morbidity and mortality of FT are highly variable, and a recent study reported mortality rates in excess of 60% in experimentally infected chickens . Although strong eradication programs have largely or completely controlled the disease in North America and several European countries, SG is still of considerable economic importance in many countries throughout South America, Africa, and Asia . Attenuated rough strains of SG strain 9 (SG 9R) have been used as live vaccines for chickens since the 1950s . SG 9R strain has been still accepted as the most effective live vaccine against FT infection in endemic countries [5, 6]. Unfortunately, invasive administration of the 9R vaccine using syringes is both uneconomical and labor intensive.
Recently, an SG mutant, JOL916 was constructed as a live vaccine candidate for FT by deleting the lon and cpxR genes, which are related to the host-pathogen interaction . An attenuated SG strain, JOL1229, which secretes Escherichia coli heat-labile enterotoxin B subunit (LTB), was also constructed as an adjuvant strain for oral vaccination against FT . A non-toxic LTB binds to the monosialotetrahexosylganglioside (GM1) ganglioside receptors of target cells, and induces the cell to take up the whole toxin, which allows for the utilization of LTB as an adjuvant for foreign antigens . LTB acts on modulating cell-mediated immune responses (Th1) and humoral immune responses (Th2) . Oral immunization with a mixture of four parts JOL916 and one part JOL1229 was reported to enhance the immune response and provide efficient protection against FT in 6-week-old chickens . In order to maintain immunogenicity till the egg laying period in inoculated chickens, it will be necessary to optimize this novel oral immunization strategy through a prime-boost strategy using the LTB adjuvant strain. In the present study, we aimed to establish prime and boost immunization strategies using the SG mutant JOL916 and the LTB adjuvant strain JOL1229, and we examined both the immune responses and protection efficacy. In addition, changes in body weight, immunogenicity, egg production rates, and bacteriological contamination after immunization with the JOL916-JOL1229 mixture were compared with a SG 9R-immunized group.
Female Hy-Line Brown layer chickens were used in this study. Chickens were provided with ad libitum access to water and antibiotic-free feed. Animal experiments were conducted with the approval of the Chonbuk National University Animal Ethics Committee in accordance with the guidelines of the Korean Council on Animal Care (CBU 2011–0017).
JOL916, an SG mutant with the lon and cpxR genes deleted, was used as the live vaccine strain , and JOL1229, which carries a recombinant Asd+ plasmid harboring the eltB gene expressing LTB protein, was used as the live adjuvant strain . For comparative study with a commercial SG vaccine, the Nobilis® SG9R vaccine (Intervet International, Boxmeer, The Netherlands) was used. The wild-type SG strain JOL420, provided by the Animal, Plant, and Fisheries Quarantine and Inspection Agency of Korea, was used for the challenge inoculation to induce acute systemic FT.
Immunization, mortality, and gross lesions in the internal organs of chickens after challenge in experiment 1
Experiment 2: For the comparison of the safety and efficacy of our SG vaccine candidate with the commercial vaccine SG 9R, thirty-six chickens were divided into three groups. Group I chickens were orally primed and boosted with 200 μl of bacterial suspension containing 1 × 108 CFU of a mixture consisting of four parts JOL916 (0.8 × 108 CFU) and one part JOL1229 (0.2 × 108 CFU) at 6 and 16 weeks of age. Group II chickens were primed and boosted with 200 μl of bacterial suspension containing 2 × 107 CFU of SG 9R at 6 and 16 weeks of age. Group III chickens were inoculated with 200 μl of PBS at 6 and 16 weeks of age as the control group. For the bacteriological examination of eggs, eggs were collected daily for the four weeks (from 18 to 21 weeks of age) following the first egg laid by each chicken, and were examined for SG. Egg production of all hens was monitored for four weeks (from 22 to 25 weeks of age).
Cell-mediated immune response
A lymphocyte proliferation assay (LPA) was performed in experiment 1 and 2 using specific antigens prepared from wild-type SG as previously described . Peripheral blood samples were aseptically collected from five randomly selected birds per group, for three weeks after prime and boost immunization. Peripheral blood mononuclear cells (PBMCs) were separated using the Histopaque®-1077 (Sigma-Aldrich, St. Louis, MO, USA) according to the product information. Lymphocyte proliferation activity was measured using adenosine triphosphate (ATP) bioluminescence as a marker of cell viability using a ViaLight® Plus (Lonza Rockland, ME, USA). The blastogenic response of the assay was expressed as the mean stimulation index (SI), which was calculated by dividing the mean OD value of the culture stimulated with the antigen by the mean OD value of the non-stimulated culture .
Humoral immune responses
Indirect enzyme-linked immunosorbent assay (ELISA) was performed using an outer membrane protein (OMP) fraction extracted from the wild-type SG strain, JOL420 . Plasma samples were separated by centrifugation of wing vein peripheral blood to determine plasma immunoglobulin G (IgG) concentrations. Intestinal lavage samples were collected using pilocarpine-based lavage method . All plasma and intestinal lavage samples were collected biweekly in experiment 1. In addition, all plasma and intestinal lavage samples were collected at 0, 3, 8 wppi and 3 wpbi in experiment 2. Evaluation of plasma IgG and intestinal secretory immunoglobulin A (sIgA) concentrations was performed as previously described  using chicken IgG and IgA ELISA Quantitation Kits (Bethyl Laboratories, TX, USA) according to the product information. Microlon® ELISA plate wells (Greiner Bio-One GmbH, Frickenhausen, Germany) were coated with 100 μl of OMP at a concentration of 0.2 mg/ml. Wells were reacted with plasma and intestinal lavage samples at dilutions of 1:250 and 1:100, respectively, for 1 hr, followed by reaction with HRP-conjugated goat anti-chicken IgG and IgA at dilutions of 1:100,000 and 1:60,000, respectively, for 1 hr.
Chickens in all experiment 1 groups were orally challenged with 200 μl of bacterial suspension containing 1 × 106 CFU of the wild-type SG strain JOL420, at 4 weeks post-boost-immunization (wpbi). Mortality was assessed daily for 14 days post challenge. All remaining animals were euthanized on 14 days post-challenge (dpc) for postmortem examination. Gross lesions in the livers and spleens were observed and scored as previously described .
Observation of general condition and body weight after immunization
In experiment 2, general body condition, clinical symptoms, and mortality were observed daily from 6 to 25 weeks of age, for 19 weeks after prime-immunization. In addition, the body weights of all chickens were recorded at 5, 9, 13, 17, and 21 weeks of age.
Egg production and bacteriological examination of eggs after immunization
Primers used in this study
Primer sequence (5’- 3’)
Alvarez et al. (2004)
Kang et al. (2011)
Jeon et al. (2012)
Jeon et al. (2012)
Hur and Lee (2011)
Statistical analyses were performed with SPSS 16.0 (SPSS Inc., Chicago, IL, USA). All results are expressed as means ± standard error of the mean (SEM), unless otherwise specified. Comparisons between the immunized and control groups were made using the Mann–Whitney U test. The chi-square test was performed for significant differences of mortality post-challenge between the immunized and control groups. Statistical significance was identified as p-value < 0.05.
General condition and immune responses
Protection efficacy against virulent challenge
Chickens from each group were orally challenged with 1 × 106 CFU of virulent wild-type SG JOL420 at 4 wpbi. Chickens in all immunized groups were markedly protected against FT (p < 0.05) (Table 1). The mortality rates in Groups A, B, and C were 10%, 10%, and 70%, respectively. On 14 dpc, all surviving chickens were sacrificed for postmortem examination. The control group demonstrated severe pathological gross lesion scores of 2.1 ± 1.4, 2.1 ± 1.4, 2.1 ±1.4 and 2.3 ±1.3 for liver enlargement, liver necrotic foci, spleen enlargement and spleen necrotic foci, respectively (Table 1). However, lesion scores in all of the immunized groups were significantly lower than those of the control group (p < 0.05 or p < 0.01) (Table 1).
General condition and body weight increase after immunization
Immune responses induced by the JOL916-JOL1229 mixture compared with those induced by a commercial vaccine
SG-antigen-specific immune responses after prime -boost immunization in experiment 2
Plasma IgG (μg/ml)
Intestinal sIgA (μg/ml)
Egg production after immunization
Egg production rate in the immunized and unimmunized groups in experiment 2
Week of age
Isolation of the vaccine strain from egg contents after immunization
In experiment 2, eggs from the immunized chickens with our vaccine strains were collected daily from 18 to 21 weeks of age, and examined for detection of Salmonella. Over the four weeks of the experiment, our vaccine strains were not detected in any eggs from the immunized chickens.
The prime-boost immunization strategy can elicit long-lasting humoral, mucosal, and cellular responses against a variety of antigens . In the present study, we evaluated protection efficacy and immune responses in layer chickens, which had been immunized with a double immunization in order to optimize the efficacy of the vaccine. In the first experiment, group A chickens were primed and boosted with a mixture consisting of JOL916 and JOL1229, and group B chickens were primed with the same mixture and boosted with JOL916 alone. Both immunized groups showed a significant increase in the intestinal sIgA levels after prime and boost immunization, and this result indicates that the oral immunizations can stimulate antigen-specific mucosal immunity (p < 0.05) (Figure 1B). The mucosal immune defense is largely mediated by sIgA antibodies, which are the first line of defense against microorganisms and operate through immune exclusion [20, 21]. Mucosal immunizations such as oral inoculations can be an effective means of inducing sIgA, as well as systemic antibodies and cell-mediated immune responses . Plasma IgG antibody levels in the immunized groups were also significantly increased compared to those in the control group (p < 0.05) (Figure 1A). Systemic antibodies clear Salmonella from the blood, and also promote phagocytosis of Salmonella by opsonization method [23, 24]. Significant cell-mediated immune responses were shown by LPA in both immunized groups compared to the control group at 3 wppi and 3 wpbi (p < 0.05) (Figure 2). It is widely accepted that enhancement of cellular immunity is crucial for protection against a primary Salmonella infection . In addition, Th1-dominated cell-mediated responses are likely to be more important in the clearance of SG, which is believed to survive and multiply within macrophages [3, 26]. All immunological data indicate that oral immunization with the LTB strain with a prime-boost strategy can effectively enhance and extend considerable levels of acquired immunity, including the mucosal immune responses.
Generally, oral tolerance has been defined as the specific suppression of cell-mediated and/or humoral immune responses to antigens by prior oral administration of the antigen . Oral administration of antigens with recombinant enterotoxin B subunits such as LTB and cholera toxin B subunit (CTB) has been found to induce tolerance to the same antigens when subsequently inoculated . In the experiment 1, chickens in groups A and B were both orally inoculated with a JOL916-JOL1229 mixture at 6 weeks of age. Group A chickens were orally boosted with the same mixture, while group B chickens were orally boosted with JOL916 alone at 16 weeks of age. Prime and boost immunizations offered significant protection efficacy against a wild-type SG challenge (p < 0.05), while 70% mortality was observed in the unimmunized control group (Table 1). In addition, the gross lesion scores of internal organs in the immunized groups were significantly lower than those of the control group (p < 0.05) (Table 1). Very mild or no gross lesions in the liver and spleen in the immunized groups may indicate that the acquired immunity successfully controlled FT infection after the booster inoculation. In addition, there were no statistically significant differences in the protection efficacy or immune responses between groups A and B (Figures 1 and 2, and Table 2), which suggests that oral tolerance may not be induced by boost inoculation with the LTB adjuvant strain. It is possible that the time interval (10 weeks) between the prime and boost inoculations can be a factor in the evasion of an oral tolerance event.
In the experiment 2, we compared the immunogenicity, body weight, and egg production rates of the chickens immunized with the JOL916-JOL1229 mixture to those immunized with SG 9R, a commercial SG vaccine. The cell-mediated immune responses and the systemic IgG responses were significantly increased in both immunized groups compared to the control group (p < 0.05 or p < 0.01) (Table 3). However, the sIgA concentrations of the chickens immunized with SG 9R were not significantly elevated compared to the control group (Table 3), while a significant elevation in intestinal sIgA in chickens immunized with our mixture was observed at 3 wppi and 3 wpbi (p < 0.05). The body weights of all immunized chickens were monitored for 16 weeks (5 to 21 weeks of age) after vaccination. There were no significant differences in body weight gain among the groups (Figure 3). The egg production rate after vaccination was also examined in the immunized groups and control group for four weeks (22 to 25 weeks of age). There was no statistical difference in number of eggs laid by the double immunized chickens with our vaccine mixture, with SG 9R strain, and the unimmunized chickens (Table 4). These data suggest that both immunized groups showed similar results in the body weight gain, egg production rates and systemic IgG immune response. However, immunization with only JOL916-JOL1229 mixture showed enhanced intestinal sIgA immune response, which may be important to mediate antibody-dependent T-cell-mediated cytotoxicity against Salmonella.
In FT infection, chickens may infect their own, as well as succeeding generations through egg transmission . In the present study, bacteriological examination of the total content of the eggs was performed to determine the safety of the JOL916-JOL1229 mixture. The SG mutant and/or LTB adjuvant strains were not detected in any egg of the immunized chickens during four weeks (18 to 21 weeks of age), which suggests that immunization with the JOL916-JOL1229 mixture does not cause bacterial contamination of the ovum.
In conclusion, data from both the experiments indicate that the immunizations with the JOL916-JOL1229 can be safe; and can induce acquired immunity including enhanced mucosal immunity. Furthermore, double immunization with the JOL916-JOL1229 may trigger elevated levels of immune responses to optimize the protection efficacy against FT infection in hens.
Brilliant Green Agar
Buffered peptone water
Cholera toxin B subunit
Enzyme-linked immunosorbent assay
lymphocyte proliferation assay
Escherichia coli heat-labile enterotoxin A subunit
Escherichia coli heat-labile enterotoxin B subunit
Outer membrane protein
Peripheral blood mononuclear cells
Standard error of the mean
Salmonella enterica serovar Gallinarum biovar Gallinarum
- SG 9R:
Attenuated rough strains of Salmonella Gallinarum strain 9
Secretory Immunoglobulin A
This work was supported by Mid-career Researcher Program through an NRF grant funded by the MEST (No. 2012R1A2A4A01002318) in the Republic of Korea.
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