Propolis Inclusion into Broiler Diets Improves the Immunomodulation and Productive Performance After Challenge with Escherichia coli Infection
Propolis Inclusion into Broiler Diets Improves the Immunomodulation and Productive Performance After Challenge with Escherichia coli Infection
Abdulaziz A. Alaqil
Department of Animal and Fish Production, College of Agricultural and Food Sciences, King Faisal University, P.O. Box 420, Al-Ahsa 31982, Saudi Arabia.
Abstract | The infection with avian pathogenic Escherichia coli (EC) causes a great economic loss in the poultry industry. The current study aimed to investigate the effect of propolis (PR) inclusion in the diets of broiler on the immunomodulation and productive performance after challenge with EC infection. Four hundred broiler chickens (Cobb500, 1-d-old) were randomly distributed in equal numbers in 40 battery cages (10 birds per cage). Every ten cages were placed in a room to arrange four experimental room groups identified as C, EC, PR, and PR+EC groups, respectively. From 22-42 d of age, the C and EC groups have received a basal diet with no PR supplements, whereas the PR and PR+EC groups have received PR at 1 g/kg of the basal diet. On day 36 of age, the EC and PR+EC groups were injected with 0.5 mL intraperitoneal (i.p.) suspension contained O157:H7 EC strain (adjusted at 107 CFU/bird), while the C and PR groups were injected i.p. with 0.5 mL saline only. All data were analyzed using one-way analysis of variance and multiple hoc Duncan’s test. The findings of the current investigation displayed a significant (p < 0.05) reduction in the productive performance traits, including the total feed intake, final body weight (FBW), BW gain, and feed conversion ratio in the EC group by approximately 7.7, 22.5, 30.6, and 33.3%, respectively, relative to the group C. The spleen, thymus, and bursa indexes as relative weights of FBW were significantly (p < 0.05) decreased by approximately 16%, 20%, and 35%, respectively, due to EC. Other immunological aspects were significantly (p < 0.05) impaired by EC challenge, recording a reduction of 38% in the total white blood cells counts, 12% in the leukocyte cell viability, 19% in the wattle thickness against phytohemagglutinin injection, 44% in the anti-sheep red blood cells antibody titer, and more than 50% in T- and B-lymphocyte stimulation index, while recording a double increase in the heterophil to lymphocyte ratio. In contrast, the productive traits and immunological aspects were significantly (p < 0.05) augmented by PR supplementation to the broiler diets. Furthermore, PR supplementation successfully restored the broiler production and immune response after challenge with EC infection and elevated (p < 0.05) all PR+EC group measurements relative to the EC group. The results concluded that supplementing dietary with 1 g/kg PR could be implemented as a natural supplement in broiler nutrition to avoid the antibiotic therapies, and simultaneously, maximize the broiler growth and health status, especially under EC challenge.
Keywords | Broiler chickens, Escherichia coli, Immune response, Productive performance, Propolis supplementation
Received | March 29, 2023; Accepted | April 26, 2023; Published | May 23, 2023
*Correspondence | Abdulaziz A. Alaqil, Department of Animal and Fish Production, College of Agricultural and Food Sciences, King Faisal University, P.O. Box 420, Al-Ahsa 31982, Saudi Arabia; Email: email@example.com
Citation | Alaqil AA (2023). Propolis inclusion into broiler diets improves the immunomodulation and productive performance after challenge with Escherichia coli infection. Adv. Anim. Vet. Sci. 11(6):1011-1020.
ISSN (Online) | 2307-8316
Copyright: 2023 by the authors. Licensee ResearchersLinks Ltd, England, UK.
Doubtless broiler production has become a massive branch of the poultry industry and is a main part of people’s food. Some reports predict that the global demand for broiler meats will double within the ongoing thirty years (). Nevertheless, a great economic loss in this sector may occur due to endotoxin stress induced by the infection with Escherichia coli (EC) (; ). Avian pathogenic EC infection impairs the intestinal integrity, deceases the nutrients digestibility (), and increases the mortality rates of broilers (). In addition, broilers infected with EC release some interleukins and cytokines from the immune system to start inflammation and subsequent immune reactions (). Moreover, EC-membranes include lipopolysaccharides (LPS) which increase inflammation, oxidative stress, and immunosuppression in the infected broilers (; ; ). Avian pathogenic EC also depress the antibody- and cell-mediated immunity within broiler chickens ().
Propolis (PR) is a greenish-brown compound generated by the bees (Apis mellifera) through mixing their own discharges and beeswax with the sap of trees and plants (). PR was known to the ancient communities as a material for healing and fighting the infections (). It contains fundamental nutrients with high amounts of polyphenols and flavonoids that give PR the antioxidant powerful impacts (; ). PR extracts has been also reported to have antimicrobial (), antiapoptotic (), and anti-inflammatory () properties. Particularly, PR has been recently inserted in poultry nutrition for the beneficial effects on the intestinal morphology, antioxidant defense, immune response, and productive performance (; ; ). Furthermore, honeybee products, including PR, improve the poultry performance under stress conditions (; , ).
As far as we know, there is a deficiency of knowledge concerning the potentiality of dietary PR supplementation on poultry species suffering from endotoxin stress induced by EC infection. Hence, the current study was dedicated to explore the possible consequence of PR feeding to ameliorate the deterioration of growth and immune response after EC challenge in broiler chickens.
MATERIALS AND METHODS
The PR was obtained in a yellow-brown powder form a beehives station located in the Agricultural and Veterinary Research center, King Faisal University, Saudi Arabia. Three samples of the PR were analyzed for the basic nutritional composition using the procedures adopted by “Association of Official Analysis Chemists” AOAC (). The PR total polyphenolic and flavonoid contents have been determined following the methods termed in a previous study (). The PR radical scavenging activities have been also detected as described in previous protocols (). The data derived from PR analysis are displayed in and .
Values (% of DM) 1
Dry matter (%)
91.3 ± 5.07
Carbohydrate (g) 1
2.1 ± 0.07
Crude fiber (g) 1
66.8 ± 3.26
Total lipids (g) 1
10.2 ± 1.31
Crude protein (g) 1
3.4 ± 0.18
Total ash (g) 1
1.0 ± 0.04
1Data are mean values analyzed on dry matter basis ± SD of three determinations.
E. coli preparation
The EC strain used in the present study was “O157:H7” that belongs to the Microbiological Resources Center (Cairo, Egypt). The EC strain was grown in a MacConkey broth (Oxoid, Thermo Fisher Scientific Inc., Hampshire, UK) at 37 °C for 24 h. After that, the EC cells were washed and collected by centrifugation, and then homogenized at a concentration of 2 x 107 CFU/mL using a sterile saline solution following the methods illustrated by .
A total of 400 male broiler chickens (Cobb500™, 1-d-old) were purchased from a commercial company (Al Watania Poultry Co., Riyadh, Saudi Arabia). The chicks were arbitrarily distributed at equal numbers in 40 battery cages (10 chicks/cage) measuring 1.25 × 0.90 × 0.60 m3 with a wire floor of 1.5 mm thick. Every ten cages were placed in a room to arrange four experimental room groups, in which all birds were provided with the same nutritional and environmental standards recommended by Cobb500 management guidelines (). Chickens received ad libitum feed and fresh water during the experimentation. Following the implemented EC and PR treatments, the experimental room groups were identified as C, EC, PR, and PR+EC groups. From 22-42 d of age, the C and EC groups received a basal diet free from PR supplements, whereas the PR and PR+EC groups received PR at 1 g/kg of the basal diet. On day 36 of age, the EC and PR+EC groups were injected with a 0.5 mL of intraperitoneal (i.p.) EC suspension (107 CFU/bird), while the C and PR groups were injected i.p. with 0.5 mL saline only. After EC administration, the birds were subjected to frequent observations under constant veterinary supervision. Accordingly, a protocol of euthanasia was directly applied by the veterinarian responsible if any peculiar signs were manifested in the bird due to suffering from EC pathogenic stress.
The bird’s body weights (BW) in each cage were documented on the day 22 and 42 of age to estimate the initial, final (IBW and FBW, respectively), and gain in bird’s BW. We computed the total feed intake (TFI) per bird through subtracting the feed remains from the sum feed provided for each cage in the treatment group. Afterwards, the feed conversion ratio (FCR) was accordingly estimated depending upon the TFI per a unit BWG.
Immune organs indexes
Two birds from each cage in the treatment group were weighed and then slaughtered on the last day of the experimental period (42 d of age). The spleen, bursa, and thymus were directly removed and their weight was assessed. The immune organ indexes were then estimated as their relative weights to the body weights in each treatment group.
Leukocyte’s count, differentiation, and viability
On the last experimental day (42nd day of age), blood samples have been obtained from the brachial vein of two birds per cage in the treatment group and transferred into heparinized tubes. After gently vortexed, a drop from the fresh sample (approximately 10 µL) was used to estimate the total white blood cells (TWBC) count using hemocytometer slide and the brilliant cresyl blue stain, according to previous methods (). Another drop from the fresh blood sample (about 10 µL) was dispersed on a glass slide, and the leukocyte cells were differentiated utilizing Hema-3 stain solutions to finally determine the heterophils/lymphocytes (H/L) ratio (). The rest of the sample was assigned to determine the leucocyte cell viability (LCV) following the protocols given in . In brief, the blood sample was admixed with an equivalent volume of separation medium and centrifuged to later separate the layered peripheral blood mononuclear cells (PBMC). The PBMC were washed and then incubated with tetrazolium salt (MTT) in a microplate. The incubation medium was removed after centrifuging, and an acidified isopropyl alcohol solution was added to raise a specific color of formazan, which can be estimated at 570 nm by means of an automated ELISA reader.
On the 42nd day of age, two heparinized blood samples were obtained from each cage of the treatment groups. The stimulation index of B- and T- cells (BSI and TSI, respectively) was evaluated following the methodology detailed in a previous work (). In brief, The PBMC was separated, washed, as previously mentioned, and then incubated with trypan blue stain to detect and fix the viable lymphocytes concentration at 106 cells/mL in a microwell-plate. After that, B- and T-cells in each sample were induced via incubation with Lipopolysaccharide or Concanavalin-A mitogen, respectively, at 42 ºC for 48 h, and then incubated for additional 4 h after supplementing with MTT solution. Finally, the samples were complemented with sodium dodecyl sulfates to deposit a color that can be scanned at 570 nm by means of ELISA microplate reader.
Humoral and cell-mediated immune assay
The anti-sheep red blood cells antibody (Anti-SRBC AB) titer, as a proxy for the broiler humoral immune response (), was measured. On the 35th day of age, two birds from each cage in the treatment groups were treated with SRBC (1 mL of 5%) via an intravenous injection. One week later, blood samples have been obtained from these birds and the sera were obtained by centrifuging (400x g, 4°C, 10 min). The sera samples were diluted with saline solution in dual serial orders in microplate wells, and then a constant volume of 2% SRBC suspension was supplemented to all wells. The samples were then allowed for agglutination overnight. The AB titer was referred as log2 transformation of the inversed value of the last diluting with positive agglutination. Alternatively, two birds from each cage of the treatment groups were appointed for the examination of the cell-mediated immune response following a previous work (). Simply, a specific area of the bird wattle was marked and then intradermally injected with a mitogenic phytohemagglutinin (PHA) (Thermo Fisher Scientific). After swelling reaction appeared in the marked area at least 24 h post-injection, the wattle thickness increase was estimated through a positive reaction to the PHA-wattle immune assay.
Data were subjected to one-way analysis of variance (ANOVA) and General Linear Model (GLM) analyses (). The obtained results were represented as mean ± standard error (SE). The observations number per treatment group denotes the experimental unit for each accomplished test (n= 20 for the immunological factors, and n= 10 for the productive performance traits). The post hoc Duncan’s test was adopted to separate the mean differences at a significant level less than 5%.
RESULTS AND DISCUSSION
The EC infection of broiler chickens was frequently induced by the exposure of the birds to stress factors or contaminated materials with a pathogenic strain of EC (). According to our previous study (), the PR supplementation at 0.1% (1 g/kg as fed) was recommended to advance the performance of broilers. The current study examined the possible impact of PR supplementation to broiler foods on their immunological and growth performance after challenge with EC infection.
As shown in , EC challenge cause a significant (p < 0.05) lowering the immune-organs weight by approximately 16%, 20%, and 35% in the spleen, thymus, and bursa indexes, respectively, in comparison with the control. Conversely, PR supplementation maintained the spleen and bursa weights at normal indexes of the control, and it significantly (p < 0.05) elevated the thymus index relative to the control. Moreover, PR supplementation significantly (p < 0.05) ameliorated the reduction of the immune-organs indexes persuaded via the EC infection within the broilers. These results could be attributed to the trophic effects of bee products on these tissues in birds (; ). The integrity of such lymphoid immune organs in birds is essential to establish the first defense line against infectious pathogens ().
The effect of dietary PR supplementations on the H/L ratio, TWBC, and LCV of EC-infected broilers is shown in . The results of EC-infected broilers exhibited a significant (p < 0.05) decrease in the LCV and TWBC
by 12% and 38%, respectively, and a significant (p < 0.05) double increase in the H/L ratio in comparison with the control broilers. The low TWBC and LCV values in the infected birds may be due to the negative impact of EC on the spleen which is responsible for leucopoiesis or leukocyte generation (). It also may be attributed to the suppressive effect of stress on the lymphocyte and monocyte contents in the blood (). In addition, exposure of birds to stress may cause leukocyte destruction and removing them by the bone marrow (). The increased H/L ratio within the infected birds is an indication of suffering stress (). In contrast, PR treatment caused as significant (p < 0.05) enhancement in the TWBC by 13% and the LCV by 18%, in comparison with the control. In the EC-infected broilers, PR supplementation significantly (p < 0.05) alleviated reduction of the TWBC and LCV, while reduced the H/L ratio increasing. Similar positive results were obtained for the effect of PR administration on the leukocytes count and viability of EC-infected laying hens in a previous study (). Furthermore, it was reported that PR has a strong bactericidal activity through increasing the membrane permeability and decreasing the motility of bacteria; hence it can reduce the harmful effect of EC on blood cells ().
The dietary PR supplementations consequence on the T- and B-lymphocyte stimulation indexes of EC-infected broilers is presented in . The T- and B-cells lymphocyte proliferation was significantly (p < 0.05) suppressed by 70% and 50%, respectively, in the EC group compared to the control group. These findings agree with those attained in previous studies (, ), which affirmed a depressive effect of EC on splenocyte proliferation in birds. In a recent report, such adverse impact for EC on lymphocyte proliferation in broilers has been documented (). It was reported that body cells apoptosis, DNA-damage, and dysfunction may be associated with the EC infection (; ). Additionally, endotoxins released by EC infection produced excessive reactive oxygen species (ROS) and inflammatory cytokines that lead to T- and B-cells lymphoproliferative defects (; ). On the other hand, as shown in , treatment with PR caused a significant (p < 0.05) enhancement in the TSI by 42% and the BSI by 14%, compared to the control. Moreover, PR supplementation into the EC-infected broilers’ diets significantly (p < 0.05) alleviated the reduction in the TSI and BSI and normalized them again to similar values to the control. The analysis of PR () evidenced the occurrence of elevated flavonoids and polyphenols contents. These compounds can potentially relieve ROS and inflammation and, subsequently, stimulate T- and B-lymphocyte proliferation (). Furthermore, the sustainable effect of PR on the thymus (T-cell generator) and bursa (B-cell generator), as presented in , can in turn activate the lymphocyte T- and B- cells proliferation, respectively ().
In the current investigation, we evaluated the dietary PR supplementations effect on the humoral and cellular-mediated immuno-measurements of EC-infected broilers, and the results are shown in . EC infection induced a significant (p < 0.05) lowering in the anti-SRBC-Ab titer and the PHA-wattle thickness by approximately 44% and 19%, respectively, relative to the control broilers. Alternatively, PR supplementation significantly (p < 0.05) increased the anti-SRBC-Ab titer by 16% and the PHA-wattle thickness by 22%, compared to the control. Moreover, PR supplementation caused a significant (p < 0.05) increase in the anti-SRBC-Ab titer and PHA-wattle thickness within the EC-infected broilers, in comparison with those infected with EC but did not have SP supplements. The harmful effect of EC on the LCV and lymphocyte proliferation can directly cause a disturbance in humoral and cellular immune responses (). These researchers also attribute the immunosuppressive impact of EC to the over-expression of forkhead box family (FOXO) proteins, which are transcription factors involved in immune cell apoptosis, proliferation inhibition, and antibody hypo-production in infected birds (; ). In consistent with the current study findings, the humeral and cellular immune parameters in different poultry species were substantially improved by adding bee products, including PR, into the diets (; ). Moreover, findings suggested that PR supplementation successfully managed to normalize the humoral and cellular immune measurements in EC-infected birds. These positive effect of PR in both EC-infected and non-infected birds can be ascribed to the PR antioxidant potentialities, evidenced by high flavonoid and polyphenol contents (). It was suggested that these antioxidant compounds can multiplicate lymphocyte numbers among the other leukocyte components (), inhibit prostaglandin formation (), encourage interleukins releasing (), and reduce FOXO expression (). These events, in turn, participate in increasing the LCV, T- and B-cells mitogenesis, and antibody production ().
The broiler’s productive performance results, as influenced by PR supplementing and EC challenge, are presented in . A significant (p < 0.05) depression of 7.7% was recorded in FI of the EC-infected birds in comparison with the control birds. This feed intake reduction could be explained by the deleterious effects of oxidative stress and inflammatory cytokines on the EC-infected chickens’ tissues (; ). It was reported that feed depression in the birds adversely affect the other productive aspects (). EC challenge in the current investigation also induced a substantial reduction of 22.5% and 30.6% in the FBW and BWG, respectively, and elevated the FI per kg weight gain by 33.3% relative to the EC-noninfected broilers. Similarly, other works found a reduction in FI, FBW, and BWG by approximately 7-42%, 20-33%, and 16-55%, respectively, along with an elevation in FCR by 9-29% within the EC-infected broilers relative to noninfected ones (; ; ). It is known that lipopolysaccharides (LPS) are existed on the outer membrane of EC (). LPS generate excessive quantity of inflammatory cytokines and reactive oxygen/nitrogen species, which subsequently harm wide target-cells in the infected birds and induce abnormal function (; ). The antioxidant defense system failure to overcome with these harmful products lead to cell damage and directly lower the performance (). These events can partially explain the immunomodulation impairment and the poor growth performance in broilers challenged with EC.
On the other hand, the productive performance was improved by PR supplementing within both the PR and PR+EC broiler groups (). Our findings and results from former investigations (; ) ascribed the PR application as a potential natural feed supplement to promote broiler growth. The feed consumption was significantly (p < 0.05) elevated by 7-8% in both the PR and PR+EC broiler groups, in comparison with the control group. This could be attributed to the palatability of broilers to some PR components such as wax, vanillin, resin, and honey (). Moreover, the significant (p < 0.05) enhancement obtained in the FBW and BWG (rising by 4% and 6%, respectively) of the PR group, in comparison with the control group, can be owed to the contribution of PR to add nutritional values of protein, lipid, and carbohydrate to the diets of the broilers. These results were also evidenced in similar studies on turkey poults (), laying hens (), and Japanese quail (; ). Furthermore, the PR positive impact on broiler performance under EC infection could be, in some extent, modulated by its antimicrobial activity against various pathogenic microorganisms in the chicken gastrointestinal tract (). Also, it was reported that PR supplementation to infected/stressed animals improved the intestinal absorption and digestibility through supporting villi structure and epithelium tight and gap junctions (; ; ; ).
CONCLUSIONS and Recommendations
The results of the present study introduced a firm argument for the deleterious consequences of E. coli infection regarding the immune status and the productive performance of broiler chickens. However, propolis inclusion into the broiler diets at 1 g/kg improved the immune response and enhanced the feed consumption and the other growth aspects. Moreover, PR can successfully restore the immunomodulation and growth performance after deterioration effects caused by EC infection. Therefore, this study features the implementation of PR as a natural supplement in poultry nutrition to avoid antibiotic therapies, and concomitantly, maximize the broiler growth and health status, especially under the EC-infection challenge.
A great economic loss in the poultry industry may occur due to exposure to endotoxin stress persuaded by the avian pathogenic Escherichia coli (EC) infection, and sometimes, intermittent courses of antibiotic therapy are implemented although its compromising impacts on animal and human health. Recently, feeding with natural products as an alternative strategy to the antibiotic therapies have been widely encouraged for improving the performance and health of poultry during intensive production systems. This study investigates the prospective impacts of dietary propolis (PR) supplementing on the immunomodulation and growth performance of EC-infected broiler chickens. Our findings exhibited that addition of PR to broiler diets can cope with the EC harmful consequences on immune response and productive performance.
Abdulaziz A. Alaqil contributed to the conceptualization, investigation, data collection, analysis, writing-original draft, reviewing, and approving the current version of the manuscript.
The present animal study protocol has been approved by the research ethical commission of King Faisal University, Saudi Arabia (Ref. No. KFU-REC-2022-MAR-EA000545).
Conflict of interest
The authors have declared no conflict of interest.
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