Beneficial Effects of Capparis Spinosa Honey on the Immune Response of Rats Infected with Toxoplasma Gundii.

OBJECTIVES: The Toxoplasma gondii (T. gondii) is an intracellular opportunistic protozoan parasite that infects approximately one-third of the human population worldwide. Honey has long been used for treatment of many diseases in folk medicine. Honey has exhibited significant anthelmintic, nematicidal and anti-protozoal activities.This study was conducted to investigate the immunological patterns in rats infected with T. gondii who were treated orally with supplemented 15% Capparis spinosa honey (Saudi Arabia) for a period of 28 days.
METHODS: Immunoglobulin M, immunoglobulin G, and cytokines were detected by using enzyme-linked immunosorbent assays (ELISAs). In addition, the mortality and the morbidity rates were assessed.
RESULTS: Oral administration of Capparis spinosa honey as a natural food additive was experimentally shown to increase the antibody titer; furthermore, compared with the rats in the control group, the levels of the sera cytokines (IFN-γ, IL-1 and IL-6) were consistently higher at day 7 post-infection in the infected rats treated with oral supplements of Capparis spinosa honey.
CONCLUSION: Orally administered supplements of Capparis spinosa honey increased both the antibody titer and the cytokines (IFN-γ, IL-1 and IL-6) levels in rats infected with T. gondii.

1. Introduction

Toxoplasma gondii (T. gondii) is an intracellular opportunistic protozoan parasite that infects approximately one-third of the human population worldwide [1, 2]. It forms tissue cysts in the brains of warm-blooded animals and manipulates the behavior of infected rodents [3, 4]. Some researchers have reported that urban rats are important for the epidemiology of toxoplasmosis because they act as a source of infection for domestic cats, as well as other carnivores and omnivores, such as dogs and pigs [5-8].

Honey has been used over the past 2,500 years in many civilizations, especially Egypt. It is considered to be an important element in traditional medicines, and scientists have been, and still are, researching its benefits in relation to modern medicine. In folk medicine, honey has long been used for the treatment of patients with many different diseases [9]. The antimicrobial activities of honey against bacteria [10, 11] and fungi [12-19] have been extensively reported. Moreover, honey has exhibited significant anthelmintic activity at concentrations as high as 300 mg/mL [20], as well as nematicidal [21, 22, 23], and anti-protozoal [24] activities. This study was conducted to investigate the beneficial effects of Capparis spinosa honey on the immune response of rats infected with T. gondii.

2. Material and Methods

Fresh Saudi honey samples (1 kg) were kindly provided by Alnahal Aljwal Company, during the 2015 flowering season). The mono floral honey harvested from apiaries (authorized apiary farm of Alnahal Aljwal, Saudi Arabia) is vented as “monofloral”, meaning that the honey must derive from at least 55% of the pollen from a single floral source. The collected honey sample was Shafallah honey (Capparis spinose). The honey samples were collected in sterile universal glass containers and kept at 2 – 8°C until tested. Physiological saline phosphate buffer solution (PBS), pH 7.2, was used for all dilution steps under aseptic conditions.

The study was carried out on 60 males, Albino Wistar rats ranging in weight from 250 to 280 g, which had been obtained from Laboratory Animal House, National Research Center, Egypt. Throughout the study, these animals were housed in standard environmental conditions, a temperature of 24°C and a relative humidity of 50%, with a 12-h:12-h light: dark cycle. They had free access to a standard commercial diet and water.

The T. gondii strain used in the present study, the RH strain, was maintained and secured in the Zoonotic Diseases Department, National Research Center, Egypt. Tachyzoites of T. gondii (RH strain) [25] were maintained in mice by passage every 3 – 4 days. The tachyzoites obtained from the ascitic fluid of the rats were diluted to adjust the tachyzoites count to 103/mL and were used for intraperitoneal acute infection after counting and dilution as necessary [26, 27]. Rats infected with T. gondii were treated orally with supplements of 15% Capparis spinosa honey (Saudi Arabia) for a period of 28 days.

The experiments were performed according to the Guidelines for the Care and Use of Laboratory Animals, and Ethical Approval for this research was granted by the Committee, National Research Centre, Egypt. The experimental design was as follows: The rats were divided into six groups of 10 rats per group (Table 1). The healthy control group was treated with saline solution (group 1). The groups two and five were treated for 28 days with oral supplements of 15% Capparis spinosa honey (Saudi Arabia), groups 4 and six (Drug group treated with the standard treatment with sulfadiazine (tablet: 500 mg) + pyrimethamine drug (tablet: 25 mg) as the treatment of choice for toxoplasmosis [28] while groups 3 (infected control group), 5 and six (infected group treated with the standard treatment) were infected with toxoplasma. The rats in all groups were monitored for mortality daily, and at days 7, 14 and 28, some rats were sacrificed, and their weights were measured.

Table 1

Groupings of the rats used in this study and the treatment for each group

Group Name	No. of animals	Treatment
		Saline	Honey	Toxoplasma	Sulfadiazine + Pyrimethamine	Toxoplasma + Honey	Toxoplasma + Sulfadiazine + Pyrimethamine
Healthy Control	10	+	−	−	−	−	−
Honey Control	10	−	+	−	−	−	−
Toxoplasma (Infected Control)	10	−	−	+	−	−	−
Sulfadiazine + Pyrimethamine (Standard Treatment Control)	10	−	−	−	+	−	−
Toxoplasma + Honey (Infected, Treated with Honey)	10	−	−	+	−	+	−
Toxoplasma + Sulfadiazine + Pyrimethamine (Infected, Treated with Standard Treatment)	10	−	−	+	−	−	+

Blood samples were collected via the tail vein into heparinized capillary tubes, and the serum portion was separated by centrifugation at 3,500 rpm and was then kept in a deep freeze at − 70°C until the IgM and the IgG levels were determined at days 7, 14 and 28 by using enzyme-linked immunosorbent assays (ELISAs) [29]. Complexes including antigen and antibody couples were tracked. All control and infected rats were examined for infections by using ELISA kits designed in our laboratory. Toxoplasma lysate antigen (TLA) was prepared from tachyzoites of the T. gondii RH strain [30]. The RH strain (about 2 × 109 tachyzoites) harvested in PBS was filtered and centrifuged at 750 g three times for 15 min each time. The pellet was solubilized by adding distilled water, after which the solution was supplemented with the protease inhibitor, 5-mM phenylmethylsulphonyl fluoride. The suspension was freeze-thawed five times. The protein content of TLA was determined using the Bradford method [31], after which the TLA was stored at − 20°C until used.

The ELISAs were carried out using a procedure described by Ref [32]. Ninety-six-well, flat-bottom microtiter plates were coated overnight at 4°C with a 10-μg/mL solution of TLA in carbonate buffer, pH 9.6 (100 μL per well). Plates were washed with phosphate buffered saline Tween (PBST) (PBS, pH 7.4, containing 0.05% Tween 20) for three times for 3 min each time. The ELISA plate was blocked for 1 h by using 100 μL of 3% skim milk powder in PBS 0.05% Tween 20 and washed. Sera samples diluted in 3% skim milk in PBS were added to a volume of 100 μL and at a concentration of 1: 100. After the plate had been washed, it was incubated with peroxidase labelled rabbit anti-rat IgG (Sigma-Aldrich Company, St. Louis, MO, USA) diluted 1: 10,000 in PBST plus 3% skim milk and incubated for 1 h at 37°C. Finally, the enzymatic activity was revealed using the substrate tetramethylbenzidine (Sigma). After 20 min of incubation at room temperature, the reaction was stopped by adding 50 μL of H2SO4 (1.25 M), and the optical density (OD) was measured at 450 nm by using an ELISA reader. A sample was considered positive when the mean OD for infected rats was higher than the mean of control rats by three standard deviations (cut-off). Titer was defined as the reciprocal of the highest dilution that produced OD readings of more than 0.1 OD unit above background. The absorbance was measured at 405 nm, and an IgG anti-Toxoplasma level < 15 UI/mL was reported as negative while a level ≥15 UI/mL was reported as positive. In regard to IgM, levels lower than 1 UI/mL were reported as negative, and levels equal to or higher than 1 UI/mL were reported as positive.

Blood samples were obtained from anesthetized animals. Serum samples were stored at − 70°C until analyzed. Sera were diluted 1/10 in PBS; then, the tumor necrosis factor (TNF)-α, IL1β and IL6 levels were measured at 7 and 28 days by using the ELISA technique as described in Ref [33]. ELISA reagent kits (Lucerne Chem AG, Lucerne, Switzerland) were used according to the manufacturer’s instructions. All measurements were performed in triplicate. Experiments were repeated three times, with 3 animals per group. The concentrations of cytokines were determined spectrophotometrically. The absorbance was read at 450 nm. A standard curve was constructed by using cytokine standards. The cytokine concentrations in unknown samples were calculated according to the standard curve, and the absorbance readings were converted to pg/mL based upon the standard curves obtained using recombinant cytokine in each assay.

The results obtained in the present study are represented as means ± standard errors of the mean (SEM) and were analyzed using the analysis of variance (ANOVA). Samples were compared using the unpaired Student’s t-test (two-tailed) for unpaired samples with equal variance, as calculated using Excel (Microsoft, Seattle, WA). The significance of any difference between means at P < 0.05 was calculated using the Duncan Multiple Range Test [34].

3. Results

Rat serum immunoglobulin M and G at days 7, 14 and 28 under this experiment was determine by ELISA assy. Reciprocal titers were determined in sera collected from all groups of control rats and from all rats infected with T. gondii and treated with oral supplements of 15% Capparis spinosa honey or with the standard treatment illustrated in (Fig. 1). Antibody responses after intraperitoneal infection with T. gondii reached their maximum levels, in particular in the groups infected with T. gondii which represented significant increases, at day 7 (IgM-specific antibody) and at day 28 (IgG-specific antibody) post infection, as detected by using ELISAs (Fig. 1). The immune status of honey normal group showed rising its level while the group infected and treated with honey showed rising titer. While group treated with sulfa showed reduction of the antibody level.

Figure 1

Serum immunoglobulin levels in the control and the treated groups.

Rat serum samples for determining the cytokine levels by using ELISAs were obtained from the rats in the healthy, the infected, the honey, and the standard treatment control group, as well as from infected rats treated either with honey or the standard treatment of sulfadiazine + pyrimethamine. The results are presented in Fig. 2. After infection with T. gondii, the rats in the infected control group showed significantly elevated levels of TNF-α, IL-1β and IL-6 levels. compared to the rats in the healthy control group. Administration of honey to the infected rats significantly reduced the TNF-α, IL-1β and IL-6 levels. Values in Fig. 2 are presented as means ± SEMs (P < 0.05).

Figure 2

Levels of cytokines level in the control and the treated groups.

4. Discussion

T. gondii is an opportunistic intracellular parasite pathogen that infects approximately one-third of the human population worldwide [1]. The rat model was chosen for this research because the natural resistance of this species to toxoplasma infection is similar to that observed in humans [35]. Antibody responses after intraperitoneal infection reached their maximum levels in the infected controls at day 7 (IgM) and at day 28 (IgG) post infection, as detected by using ELISAs (Fig. 1). During the course of acute and chronic toxoplasma infection in mice, the serum levels have been found to be elevated [36, 37]. The IgM- and the IgG-specific antibodies of rats infected with T. gondii, but not treated, were increased significantly, as were those of the infected rats treated orally with supplemented of 15% Capparis spinosa honey, compared to the values for rats in the healthy control and the honey control groups. Previous findings were observed by. [38] Who reported a rise in IgM first, followed by the IgA response [38]. A contrary to the findings of others, observed simultaneous rises in the IgM and the IgA responses [39]. The results obtained so far show that for orally-induced infection, the IgM and the IgA responses appear concomitantly, with less than a one-day lag between them [40].

A variety of biologically active compounds, such as flavonoids, vitamins, antioxidants and hydrogen peroxides, are present in honey [41]. Muhammad et al [42] found that consumption of honey daily had both positive and negative effect on male Wister albino rat. The major components of honey, chrysin, and other flavonoids exerted beneficial effects [43, 44]. The synergistic effects of the wide range of compounds present in honey are due to the antioxidant activity [16], hepatocytes protection [45], and anti-inflammatory activity [46]. Administration of honey to rats significantly reduced the TNF-α, IL-1β and IL-6 levels in rats infected with T. gondii. All kinds of honey significantly increased the TNF-α, IL-1β and IL-6 releases from MM6 cells (human monocytes) when compared with untreated and artificial-honey-treated cells (P < 0.001). Jelly bush honey significantly induced the maximal release of each cytokine compared with manuka, pasture, or artificial honey (P < 0.001). These results suggest that the effect of honey on wound healing may in part be related to the stimulation of inflammatory cytokines from monocytic cells [58].

ELISAs were used to measure the serum cytokine levels for the infected and the non-infected rats in the control groups and for the infected rats treated either with honey or the standard treatment of sulfadiazine combined with pyrimethamine, and the results are shown in Fig. 2. From this figure, the serum cytokine levels of rats after infection with T. gondii showed significantly elevated levels of TNF-α, IL-1β and IL-6 levels compared to those of rats in the healthy, honey, standard treatment, and infected control groups. Moreover, administration of honey to rats significantly reduced the TNF-α, IL-1β and IL-6 levels compared to the values for the infected rats. The values represent means ± SEMs (P < 0.05). IL-lβ is important in the induction and the propagation of the inflammatory response and is intimately involved in the regulation of the acute phase response [36]. IL-6 levels may be intimately involved in the pathogenesis of T. gondii infection or be associated with an acute phase response [47, 48].

Neutrophils and inflammatory monocytes are important for the control of toxoplasmosis in the mouse [49]. In comparison to the serum cytokines of the rats in the healthy and the honey control groups, those of the control infected with T. gondii were increased significantly, as were those of infected rats treated with an oral supplement of 15% Capparis spinosa honey. Infected rats treated with a honey, supplement showed significantly increased cytokine levels compared with the levels in the healthy, the honey, and the standard treatment control groups. Infection with T. gondii is characterized by the development of acute hyperinflammation and lethal ileitis [50]. The primary function of the innate immune system is the detection of pathogens and the rapid activation of host defense mechanisms [51, 52]. The effects of honey chrysin and other flavonoids mediated the stimulation of TNF-α release, inhibited lipoprotein oxidation, and induced apoptosis [43, 44].

The authors of Ref [53] stated that macrophages could be able to limit parasite replication and produce cytokines that contributed to immunity, making them important regulatory and effector cells during toxoplasma infection. Neutrophils influence the T-cell response by enhancing the functions of dendritic cells [54] or inflammatory monocytes [55]. Infection of mice by using intraperitoneal (i.p.) inoculation with low amounts of a highly virulent strain of T. gondii or with a high inoculum of low-virulence strains resulted in the recruitment of neutrophils to the peritoneal cavity [56].

TNF-α and IL-1β have roles in the pathogenesis of many inflammatory diseases. IL-6 is considered to be an anti-inflammatory cytokine that inhibits the generation of TNF-α and augments the actions of acute-phase proteins and immunoglobulins [57]. Tonks et al [58] stated that TNF-α was a pleiotropic, pro-inflammatory cytokine, with the ability to affect almost every tissue and organ system. Both TNF-α and IL-1β stimulate the release of growth factors; these, in particular, PDGF and TGF-b, are chemotactic for monocytes and fibroblasts and maintain the activity of these cells [59].

Cytokines have been shown to play an important role in the pathogenesis of toxoplasmosis. The induction of inflammatory cytokine (IL-12, TNF-α, and IFN-γ) responses is a key event in the initiation of immunity to T. gondii [60]. Moreover, this pro-inflammatory context may lead to a modulation of immune responses, either directed against a parasite or unrelated antigens that develop in the host concomitantly with the infection. Early stimulation of macrophages also plays an important role in directing cell- mediated immunity because IL-12 promotes Th1-type acquired immunity, which is essential for controlling toxoplasma infection. A balance between IL-12 and IL-10 is, thus, essential for controlling toxoplasma infection [61]. IL-4 is secreted by type-2 lymphocytes. IL-4 alone does not appear to influence the intracellular growth of toxoplasma in vitro [62]. Pro-inflammatory mediators, such as IL-1β, IL-6 and TNF-α, may also act as amplification signals for immune cells [63]. The anti-inflammatory action of honey has been assessed [64], and cytokines have been found to be regulatory proteins that normally function as part of a complex interactive network [65].

5. Conculsion

The experimental observations made during this research clearly demonstrate that the oral administration of honey (Capparis spinosa) as a natural food additive increased the antibody titer and the levels of sera cytokines (IFN-γ, IL-1 and IL-6) in rats infected with T. gondii.