Anticoccidial efficacy of Garcinia kola (Heckel H.) against experimental Eimeria tenella infection in chicks

Abstract

There is a need to advance commercial poultry production to cater to the essential protein needs of an ever-increasing population, however, the rampant occurrence of coccidiosis infection poses a threat to this achievement. This study evaluated the in vivo anticoccidial activities of the extracts and fractions of Garcinia kola against experimental Eimeria tenella infection using broiler chickens as experimental subjects. A total of 40 broiler chicks were experimentally infected with E. tenella and assigned randomly into five groups consisting of eight chicks each. Three days post experimental infection groups I and II were administered orally with tween 80 (0.8%) and Amprolium (30 mg/kg) and served as untreated and treated control groups, respectively whereas Groups III, IV, and V were administered orally with crude methanol extract (CME) at doses of 200, 400 and 600 mg/kg, respectively, for five consecutive days. Daily weight gains were recorded and faecal oocysts per gram (OPG) counts were made by the McMaster Egg counting technique. Blood samples from each experimental group were collected on days 0, 3, 6, and 8 for haematological examination. In the acute toxicity studies, the CME of G. kola did not produce any toxic effect or mortality at doses between 10 and 5000 mg/kg. The CME G. kola was then considered safe and the LD₅₀ was assumed to be > 5000 mg/kg. Graded doses of CME of G. kola considerably (P < 0.05) improved body weight gain and decreased OPG in a dose-depended manner. There was also significant improvement in the Packed Cell Volume (PCV), Red Blood Cell (RBC) and White Blood Cell (WBC) counts upon treatment with the graded doses of CME of G. kola. Besides, G. kola significantly decreased histopathological lesions in the caecum. The results of this study indicates that G. kola may provide beneficial effects against E. tenella-induced coccidiosis in broiler chickens.

Introduction

Commercial poultry farming is expanding every day and contributing to the provision of affordable and high-quality protein. However, this sector is confronted with many diseases of which coccidiosis is among the most important (Malik et al. 2016; Shetshak et al. 2021). Coccidiosis is caused by multiple species of the protozoan parasites belonging to the genus Eimeria (Mohiti-Asli and Ghanaatparast-Rashti 2015). Caecal coccidiosis, which is caused by E. tenella, is the most important parasitic disease that requires continuous prophylactic treatment in poultry production (Malik et al. 2016; Habibi et al. 2016). The disease mainly affects young chicks and spreads from one chick to another by contact with infected droppings (Mohiti-Asli and Ghanaatparast-Rashti 2015) resulting in very high infectivity in an intensive husbandry poultry practice (Bindari et al. 2021; Gabriel et al. 2020; Geng et al. 2021; Snyder et al. 2021; Zhou et al. 2020). Infected droppings may contain sporulated oocyst of about seven (7) different species of Eimeria; E. acervulina, E. tenella, E. maxima, E. necatrix, E. brunette, E. mitis, and E. praecox, that invades the cells of the intestinal tract of chickens (Pop et al. 2015). Eimeria parasite generally causes enteritis and diarrhoea resulting in an inability of the birds to absorb dietary nutrients in the gastrointestinal tract. This occurs due to the disruption of the integrity of the intestinal mucosa (Isaac et al. 2017a, b; Qaid et al. 2021; Yan et al. 2021; Yu et al. 2021) leading to low weight gain and feed consumption (Pop et al. 2015), morbidity (Oyegbemi and Adejinmi 2012; Malik et al. 2016), poor feed conversion efficiency and in severe cases, mortality (Pop et al. 2015). In broiler chickens, the most prevalent species of Eimeria are E. tenella, E. acervulina, and E. maxima of which E. tenella is highly pathogenic causing haemorrhagic diarrhoea, a severe reduction in weight, and considerable mortality. E. maxima cause moderate pathogenicity producing lesser economic losses and mortality, whilst E. acervulina is mildly pathogenic, but it is the most common species found in chickens and causes poor feed conversion efficiency and mortality only during heavy infection (McDougald and Fitz-Coy 2008). Coccidial oocysts are easily circulated in the poultry house environment and have such a great reproductive potential, it is not easy to keep chickens free of coccidia especially under the existing intensive rearing conditions (Pop et al. 2015). It has been shown that poultry fed diet containing plant-based bioactive compounds such as green tea extracts or grape seed (proanthocyanidins) have lower small intestinal lesion scores, oocyst output, and mortality as well as improved weight gains and feed conversion ratio than in birds infected with Eimeria infections (Allen and Fetterer 2002; Jang et al. 2007; Naidoo et al. 2008; Wang et al. 2008; Wallace et al. 2010). These plant-derived products exert their anticoccidial activity possibly by protecting infected intestinal tissues from oxidative damage, thereby reducing the severity of coccidiosis (Eckert et al. 2021; Gaboriaud et al. 2021; Hansen et al. 2021; Schneiders et al. 2020). Contemporary science has acknowledged the vast array of compounds produced by plants that possess pharmacological effects and are included in the modern pharmacotherapy (Chabra et al. 2019; Daryani et al. 2015; Yarahmadi et al. 2016). Several studies have been geared towards the evaluation of the anticoccidial activities of natural products such as essential oils and extracts of plants and have been shown to be effective against several species of Eimeria in chickens (Abbas et al. 2012; Zaman et al. 2012; Lamidi et al. 2020). Among these products is artemisinin, a sesquiterpene lactone produced by aerial parts of Artemisia annua (Pop et al. 2015), berberine—a natural plant obtained from the roots of Berberis lyceum (Malik et al. 2016), extracts obtained from the leaves of Vernonia amygdalina and Azadirachta indica (Oyegbemi and Adejinmi 2012) and oregano essential oil (Mohiti-Asli and Ghanaatparast-Rashti 2015) are efficacious against Eimeria parasite in chickens. Garcinia kola Heckel belongs to the Family Clusiaceae or Gluttiferae (Mackeen et al. 2000; Panthong et al. 2007; Okoko 2009; Adesuyi et al. 2012; Abu et al. 2013; Ikpesu 2014). Garcinia kola is an angiospermae that is known in commerce as “bitter kola” (Adesuyi et al. 2012).

The seeds of G. kola are highly valued ingredients in the African traditional medicine and have been used in many herbal preparations either singly or in combination with other plants (Okunji et al. 2007; Akefe et al. 2019; Isaac et al. 2017a, b). The seeds are consumed as stimulants because on chewing, they produce a bitter astringent and resinous taste, followed by a slight sweetness (Okoko 2009; Adesuyi et al. 2012). Studies have shown that the major phytochemical constituents of this plant include a complex mixture of bioflavonoids—kolaviron (Adedara et al. 2013; Ayepola et al. 2014; Ikpesu 2014), xanthones (Mackeen et al. 2000; Ogbadoyi et al. 2011), triterpenoids (Magadula and Mwanbo 2010), and benzophenones (Okunji et al. 2007; Ikpesu 2014). Other bioactive compounds reported in the plant are tannins, saponins, alkaloids and cardiac glycosides (Adesuyi et al. 2012). The biflavonoids are the most abundant compound in G. kola while kolaflavones are the major components of the kolavirons. In addition, two new chromanols; garcinoic acid and garcinal together with tocotrienol from G. kola have been isolated (Terashima et al. 2002; Ameh et al. 2020).

Extracts of the genus G. kola have been extensively reported to exhibit diverse biological activity like antioxidant, anticarcinogenic, antigenotoxic (Mackeen et al. 2000; Terashima et al. 2002; Adedara et al. 2013), antipyretic, analgesic, and anti-inflammatory (Panthong et al. 2007; Adedara et al. 2013) effects. Studies also revealed the potent antiparasitic activity of Garcinia plant against particularly Trypanosoma brucei (Kubata et al. 2005; Ogbadoyi et al., 2011); ; . Magadula and Mwambo (2010) reported the antimalarial activity of G. kola. Similarly, Ikpesu (2014) demonstrated the restoration of inhibited anticholinesterase activities of G. kola in Clarias gariepinus. However, there are very few or no reports on the effect of G. kola on Eimeria parasites.

Materials and methods

Experimental animals

Sixty day-old broiler chicks were purchased from a reputable commercial hatchery and housed on a deep litter pen. The birds were kept at room temperature with continuous lightning. Chicks were fed with standardized anticoccidial free commercial starter feed. Water and feed were provided ad libitum. Feeders and drinkers were washed on a daily basis to reduce the risk of contamination. Faecal droppings of the chicks were screened for the coccidian parasite using a simple flotation technique as described by (Dryden et al. 2005) before the commencement of experimental infection. Ethical approval for the use of animals for the experiment was obtained from the Ahmadu Bello University Committee on Animal Use and Care (ABUCAUC) Ahmadu Bello University Zaria by submitting an application and a copy of the research proposal (ABUCAUC/2018/009).

Plant materials

Collection and identification

Fresh seeds of G. kola were purchased from Samaru Market in Zaria, Kaduna State Nigeria, and a sample of the seed was sent to the Herbarium, Department of Botany, Faculty of Life Sciences, Ahmadu Bello University Zaria, Nigeria for authentification and identification. The plant was identified and a voucher specimen number 279 was allocated for reference purpose. The husks were removed from the seeds of G. kola and the seeds were grated with stainless steel grater to reduce the particle size. This was done to increase the surface area needed for the sample to dry quickly. The grated plant material was then dried under the shade in open air under room temperature and kept in an airtight polyethene bags until required.

Extraction and concentration

The dried plant material was made pulverized using a mortar and a pestle. One (1) kg of the powdered seeds was exhaustively extracted by hot continuous extraction in a soxhlet apparatus (Redfern et al. 2014) with three liters of methanol (Sigma-Aldrich) as solvent. The liquid extract was concentrated in vacuo at 40 °C in a rotary evaporator (BUCHI Rotavapor™ R-300; Fisher Scientifica).

The crude methanol extract (CME) was serially partitioned with an equal volume of n-hexane, ethyl acetate, and butanol. The fractions were then weighed, labeled, and stored at 4 °C until required.

Phytochemical screening

The extract and fractions of G. kola were evaluated for the presence of carbohydrates, tannins, alkaloids, flavonoids, anthraquinones, steroids/triterpenes, cardiac glycocides, and saponins using standard procedures (Senguttuvan et al. 2014).

Parasite procurement

E. tenella oocysts (Houghton strain) were obtained from the Royal Veterinary College, University London, UK, and maintained in 2.5% potassium dichromate in the refrigerator in the Department of Veterinary Parasitology and Entomology, Faculty of Veterinary Medicine, Ahmadu Bello University, Zaria until when required for the experiment. Oocyst collection, purification, and sporulation were done using the standard procedure as described by Sathyanarayanan and Ortega (2006).

Acute toxicity study

Oral acute toxicity (LD₅₀) of the crude methanol extract (CME) in broiler chickens was performed by the method of Lorke (1983). The animals were deprived of food for 24 h and water for 12 h. The study was carried out in two phases. In the first phase of the trial, three groups of chickens each comprising of 3 animals were administered with 10, 100, and 1000 mg/kg of the extracts orally and examined for mortality within 24 h. In the second phase of the experiment, 4 birds were randomly allocated into 4 groups of 1 chick each and were administered with 2000, 3000, 4000, and 5000 mg/kg respectively. The birds were similarly examined as in the first phase.

Experimental infection

Forty broiler chicks aged 14 days old were infected with the E. tenella oocysts. The sporulated E. tenella oocysts were concentrated by sedimentation via centrifugation (Kumar et al. 2014) and each bird was infected with 0.6 ml of water containing 10,000 oocysts orally using a graduated syringe (Pop et al. 2015).

Experimental Design

Infected chicks were randomly allocated into five groups of eight chicks each.

• Group 1 was given 2% tween 80 (a solvent used to dissolve the extract) and it served as the untreated control.

• Group 2 was administered with amprolium 250® (30 mg/kg) and it served as treated (Standard) control group.

• Groups 3, 4, and 5 were treated with the CME at 200, 400, and 600 mg/kg respectively.

All treatments were administered orally and for 5 consecutive days. The effect of the extract on weight, mortality rate, and infection rate (oocysts per gram of faeces) were evaluated daily throughout the treatment period.

Experimental trial

Droppings from each treatment group were collected and screened for the presence of Eimeria oocysts using a simple floatation technique (Dryden et al. 2005). The oocysts count was determined using the McMaster counting technique as described by Zajac and Conboy (2012).

Three days post-treatment, 2 ml of blood was collected from each chick through the wing vein into a heparinised sample bottle. Birds that survived the period of the experiment were euthanatized by injecting 3 ml of air into the heart (Jaksch 1981) and were grossly examined. Sample of the caecum from a chick in each group was taken and lesions were scored. The caecal samples were then preserved in 10% formalin and processed for histopathological examination (Luna 1968).

Lesion score

The lesions on the caecum were macroscopically evaluated by using the scoring method of Johnson and Reid (1970). Grades from 0 to 4 were allocated to the lesion observed depending on its severity. The scoring was carried out as follows:

• Score of 0 = Absence of any visible gross lesion

• Score of 1 = Few scattered lesions

• Score of 2 = Greater number of discrete lesions involving many areas of the caecum

• Score of 3 = Extensively developed lesions which coalesce and thickening of the intestinal walls

• Score of 4 = Lesions that extensively coalesce with thickening of the intestinal walls and the presence of bloody caecal content.

Oocyst decrease ratio (ODR)

Two grams of caecal content of the birds in each group were collected separately and oocysts per gram of content (OPG) was determined using the McMaster’s counting technique as described by Rose and Mockett (1983); Talebi and Mulcahy (2005); Zajac and Conboy (2012). The Oocyst decrease ratio was calculated using the formula below:

$$\text{ODR}=(\text{A}-\text{B})/\text{A}\times 100$$

where A = mean number of oocysts in chicks treated with 2% tween 80; B = mean number of oocysts in chicks treated with the extracts/fractions.

Determination of survivability

Determination of the survivability of chicks as an indication of the anticoccidial activity of the extract of G. kola was evaluated using the “Anticoccidial Index” (ACI) as described by Zhang et al. (2014). The ACI is a measure for assessing the protective effect of a substance against coccidia and was calculated using the formula below:

$$\text{ACI}=\left(\text{survival rate}+\text{relative weight gain}\right)-\left(\text{mean lesion value}+\text{mean oocyst value}\right).$$

The survival rate was estimated by dividing the number of chicks that survived by the number of initial chicks at the start of the experiment. The relative rate of weight gain of the chicks in each group was determined by subtracting the bodyweight of the chicks at the time of challenge with the organism from the bodyweight of the chicks at the end of the experiment. The ACI usually ranges from 0 to 200 (Jeffers 1974; Chapman 1998).

ACI value of:

•  ≥ 180 will be considered high performance

• 160–179 will be considered as effective and

•  < 160 will be considered as ineffective.

Haematology

The blood samples collected during the experimental trial were analysed for haematological parameters such as packed cell volume (PCV), white blood cell (WBC), mean corpuscular haemoglobin concentration (MCHC), mean corpuscular haemoglobin (MCH), and mean corpuscular volume (MCV) using standard procedures (Jain 1986; Campbel 1995; Subhashree et al. 2012).

Statistical analysis

Data obtained from the in vitro and in vivo experimental trials were expressed as mean ± SEM and analysed using one-way analysis of variance (ANOVA), followed by Tukey post hoc test to determine significant difference between groups. Similarly, data obtained from the scoring of caecal lesions from the chicks in different groups were analysed using the Kruskal–Wallis non-parametric test. Graphpad Prism version 5.0 for Windows was used for the analyses (Graphpad software, San Diego, CA, USA). Values of P < 0.05 were considered significant.

Result

Phytochemical Screening of the Seeds of Garcinia kola

Phytochemical screening of the crude methanol extract (CME) and butanol fraction (BTF) revealed the presence of cardiac glycosides, saponins, carbohydrates, steroids/triterpenes, tannins, flavonoids, and alkaloids. The ethyl acetate fraction (EAF) contains all the metabolites except saponins whereas the hexane fraction (HXF) contains only cardiac glycosides, tannins, and steroids/triterpenes (Table 1).

Table 1.

Phytochemical analysis of the seeds of G. kola

Phytoconstituent	Test	CME	BTF	EAF	HXF
Anthraquinones	Bontragers Spp	−	−	−	−
Cardiac Glycosides	Kelle-Killiani	+	+	+	+
Saponins	Frothing	+	+	−	−
Carbohydrates	Molish	+	+	+	−
Steroids/triterpenes	Lieberman-Buchard	+	+	+	+
Tannins	Ferric chloride	+	+	+	+
Flavonoids	Shinoda	+	+	+	−
Alkaloids	Dragendorff	+	+	+	−

Key:+ = Present CME = Crude methanol fraction; −  = Absent; BTF butanol fraction; EAF ethyl acetate fraction; HXF hexane fraction

Acute toxicity studies

There was neither mortality nor any observable toxic effects during the acute toxicity trial. The CME of Garcinia kola was therefore considered acutely safe in broiler chickens and the LD₅₀ was assumed to be > 5000 mg/kg.

Effect of CME of Garcinia Kola H. in broiler chickens experimentally infected with E. tenella (Houghton Strain)

Clinical observations

The observable clinical manifestations of caecal coccidiosis observed in chickens experimentally infected with the Houghton strain of E. tenella in this study were anorexia, ruffled feathers, somnolence, weight loss/emaciation, wet bedding materials, chocolate-brown to bloody faecal droppings (pasty to watery inconsistency; Fig. 1). However, these signs were milder in the treatment groups included mild weight loss, slightly brown faecal droppings, and mild anorexia when compared with the untreated groups of birds.

Fig. 1.

Broiler chicks infected with Eimeria tenella showing chocolate-brown faeces and wet litter material (a), Somnolence (b), and bloody faecal droppings (c)

Mortality rate

There was no mortality observed in all the experimental groups throughout the course of the study.

Effect on weight gain

Days 0–3 (pretreatment), Days 3–6 (3 days in treatment), and Days 6–8 (3-5 days in treatment) were used to evaluate the mean body weight gain. The mean body weight gain of the birds in all the experimental groups in the pretreatment period (Days 0–3: 17 days of age) was observed to be slightly uniform (Table 2).

Table 2.

Mean ± SEM of weight gain in broiler chicks infected with Eimeria tenella oocysts and treated with CME of G. kola

Treatments (mg/kg)	Days				Relative BWG at day 8 of the experiment (%)
	0–3	3–6	6–8	0–8
UC (tween 80)	26.60 ± 11.13a	42.60 ± 10.10a	42.40 ± 10.66a	97 ± 5.86a	0.00
AMP(30)	30.40 ± 11.49a	79.00 ± 10.62a	67.60 ± 09.84a	177 ± 12.99bc	82.47
CME(200)	30.20 ± 14.49a	67.00 ± 16.29a	60.00 ± 10.96a	157.2 ± 31.24b	62.06
CME(400)	31.40 ± 11.86a	60.80 ± 20.23a	66.00 ± 10.41a	158.2 ± 29.70b	63.09
CME(600)	11.40 ± 11.86a	77.80 ± 11.54a	73.80 ± 06.74a	160.4 ± 16.40b	65.36

Values are expressed in Grams (g) as Mean ± SEM (n = 5). Means with different superscript letters (^a−c) in a column differ significantly (p < 0.05). CME: Crude Methanolic Extract, UC: (untreated control), AMP: Amprolium 250® (30 mg/kg). Days 0–3: Pretreatment, Days 3–6: 0–3 days in treatment, Days 6–8: 3–5 days in treatment. BWG: Body Weight Gain (g/bird/day)

The mean body weight values of UC (untreated control) group increased from pretreatment of 372.00 ± 13.44 g to 469.00 ± 18.27 g a day post-treatment (8 days post-infection) with a mean body weight gain of 97 ± 5.86 g. The mean body weight values of AMP (Amprolium) group also increased from 383.2 ± 20.46 g to 569 ± 18.21 g with a mean weight gain of 177 ± 12.99 g. Similarly, the mean body weight values of groups CME_200, CME_400, and CME₆₀₀ (Crude Methanolic Extract in graded dosages) also increased from 388.4 ± 10.02 g to 545.6 ± 35.24 g, 382 ± 18.27 g to 540.2 ± 41.22 g, and 413.4 ± 15.18 g to 573.3 ± 16.65 g at day respective days post infection. The mean weight gains for the CME groups at 200, 400 and 600 mg/kg were 157.2 ± 31.24 g, 158.2 ± 29.7 g, and 160.4 ± 16.64 g respectively (Table 2).

The lowest mean body weight gain in this study was recorded in the UC (untreated control) group with 97 ± 5.86 g whereas the highest mean body weight recorded was in the AMP (Amprolium) group with 177 ± 12.99 g. However, the mean body weight gains recorded across the three different periods in all the groups were statistically not significant (P > 0.05).

There was a significant difference (P < 0.05) in the overall mean body weight gains obtained in the UC (untreated control) group, the AMP (Amprolium) group, and the CME groups. The overall values of mean body weight obtained in the UC (untreated control) group when computed with the overall values of mean body weight gains obtained in the CME (200, 400, and 600 mg/kg) groups were observed to be statistically not significant (P > 0.05).

Effect on oocysts shedding

The oocyst count per grams of faeces recorded on day 6 post infections for all the groups were 7.7500 ± 0.1216 × 10⁴(UC), 0.8540 ± 0.1104 × 10⁴(AMP; 30 mg/kg), 6.7587 ± 0.5955 × 10⁴(CME; 200 mg/kg), 5.1113 ± 0.1174 × 10⁴(CME; 400 mg/kg) and 3.0947 ± 0.3898 × 10⁴(CME; 600 mg/kg). At the 7th day post infection, the untreated birds treated and those treated with Amprolium (30 mg/kg), and CME (200, 400 and 600 mg/kg) had oocyst count of 10.7267 ± 0.5193 × 10⁴, 0.5193 ± 0.0540 × 10⁴, 4.0993 ± 0.4426 × 10, 3.0600 ± 0.0968 × 10⁴ and 2.6380 ± 0.1961 respectively. Similarly, the oocyst count of birds on the 8th day post infection i.e. a day after treatment were 9.8893 ± 0.0165 × 10⁴, 0.4380 ± 0.0 511 × 10⁴, 2.2413 ± 0.0416 × 10⁴, 2.0673 ± 0.1630 × 10⁴, and 1.9513 ± 0.1681 × 10⁴ in the untreated control group, and birds treated with Amprolium (30 mg/kg), 200, 400 and 600 mg/kg of the CME respectively (Table 3).

Table 3.

The effect of CME of G. kola on oocysts shedding in broiler chicks infected with Eimeria tenella oocysts

Treatments (mg/kg)	Days Postinfection
	6 (× 104)	7 (× 104)	8 (× 104)
UC (tween 80)	7.7500 ± 0.1216a	10.7267 ± 0.5193a	9.8893 ± 0.0165a
AMP (30)	0.8540 ± 0.1104b	0.5193 ± 0.0540b	0.4380 ± 0.0 511b
CME (200)	6.7587 ± 0.5955a	4.0993 ± 0.4426c	2.2413 ± 0.0416c
CME (400)	5.1113 ± 0.1174c	3.0600 ± 0.0968c	2.0673 ± 0.1630c
CME (600)	3.0947 ± 0.3898d	2.6380 ± 0.1961c	1.9513 ± 0.1681c

Values are expressed as Mean ± SEM (n = 3). Means with different superscript letters (^a−d) in a column differ significantly (p < 0.05). CME: Crude Methanolic Extract, UC: Untreated control), AMP: Amprolium 250® (30 mg/kg)

The untreated (UC) group of birds recorded the highest mean oocyst per gram of faeces on both day 6 and 8 post-infection with mean OPG values of 7.7500 ± 0.1216 × 10⁴and 9.8893 ± 0.0165 × 10⁴ respectively. Whereas the least mean oocyst per gram of faeces count on both day 6 and 8 post-infection were recorded in the AMP (Amprolium 30 mg/kg) with mean OPG count of 0.8540 ± 0.1104 × 10⁴ and 0.4380 ± 0.0 511 × 10⁴ respectively (Table 3).

Values of oocyst per gram (OPG) of faeces obtained in the UC group throughout the three days sampling period were statistically significant (p < 0.05) with values obtained in the rest of the groups on days 6, 7, and 8 except for the values obtained on day 6 in the group of birds treated with CME 200 mg/kg. OPG values obtained in the UC (untreated control) throughout the three days sampling period were statistically significant (p < 0.05) with values obtained in the rest of the groups on days 6, 7 and 8. OPG values obtained from the group of birds treated with CME 200 mg/kg also differ significantly with values obtained from the UC (untreated control) and AMP 30 mg/kg group of birds on days 6, 7 and 8 but only differ significantly with values obtained from birds treated with 200 and 600 mg/kg of the CME on day 7. Similarly, OPG values recorded from birds treated with CME 400 mg/kg were statistically significant (p < 0.05) when compared with the rest of the experimental groups only on day 6 and only differ significantly (p < 0.05) with values obtained from the NC and AMP 30 mg/kg groups on day 7 and 8 (Table 3).

Postmortem findings

The observable postmortem findings of caecal coccidiosis observed in chickens experimentally infected with the Houghton strain of E. tenella in this study include: ruffled feathers, emaciation, slightly pale breast muscles, ballooned and distended caecum caeceous materials, chocolate-brown to bloody caecal content (pasty to watery in consistency), and thickened blood-tinged caecal wall. Birds given 0.8% tween 80 (untreated) control group had ballooned and distended caecum with caseous content and thickened walls. The pathologies observed in birds treated with CME (200, 400, and 600 mg/kg) and Amprolium (30 mg/kg) were mild when compared to the birds in the untreated group.

Effect on caecal lesion scoring

The mean lesion score of 1.87 ± 0.34 in the untreated group of birds was recorded. The birds treated with AMP 30 mg/kg and CME (200, 400, and 600 mg/kg) were of mild pathological lesions compared to those obtained in the UC group of birds. The mean lesion scores recorded in the respective groups were 0.63 ± 0.20, 1.67 ± 0.24, 1.13 ± 0.07 and 1.03 ± 0.12 (Table 4).

Table 4.

The effect of CME of G. kola on oocysts per gram of caecal content, oocyst decrease ratio (ODR), and caecal lesion score in broiler chicks infected with Eimeria tenella oocysts

Treatments (mg/kg)	Caecal oocysts values		Mean Lesion score
	OPG (n = 3)(× 105)	Oocyst decrease Ratio (%)
UC (tween 80)	2.1441 ± 0.3714a	0	1.87 ± 0.34a
AMP (30)	0.3714 ± 0.0317bc	82.78	0.63 ± 0.20b
CME (200)	0.9609 ± 0.0549bd	55.18	1.67 ± 0.24a
CME (400)	0.6034 ± 0.0333bc	71.86	1.13 ± 0.07a
CME (600)	0.4344 ± 0.0097bc	76.74	1.03 ± 0.12a

Values are expressed in Grams (g) as Mean ± SEM (n = 3). Means with different superscript letters (^a−c) in a column differ significantly (p < 0.05). CME: Crude Methanolic Extract, UC: (untreated control), AMP: Amprolium 250® (30 mg/kg). OPG: Oocysts Per Gram of Caecal Faeces

The mean caecal lesion scores of birds obtained in the untreated control group was not statistically significant (p > 0.05) to those of birds in groups treated with CME at 200, 400, and 600 mg/kg. However, the mean lesion score of birds treated with amprolium differs significantly (p < 0.05) when compared with birds in the other groups (Table 4).

Effect on oocysts per gram (OPG) of caecal content and oocyst decrease ratio (ODR)

UC group recorded the highest mean oocyst per gram of caecal content with mean OPG values of 2.14413 ± 0.3714 × 10⁵ followed by the CME groups with OPG values of 0.43440 ± 0.0097 × 10⁵, 0.60340 ± 0.0333 × 10⁵, and 0.96093 ± 0.0549 × 10⁵ in the 600_, 400, and 200 mg/kg doses respectively. The AMP group had the least mean oocyst per gram (OPG) of caecal content with mean OPG values of 0.37140 ± 0.0317 × 10⁵ (Table 5). The percentage oocyst decrease of the AMP (30 mg/kg) and CME (200, 400, and 600 mg/kg) groups were 82%, 55.18%, 71.86% and 76.74% respectively (Table 4).

Table 5.

The Anticoccidial Activity of CME of G. kola in broiler chicks infected with Eimeria tenella oocysts

Treatment (mg/kg)	SR (%)	RWG (%)	MLS	MOV (× 104)	ACI
UC (tween 80)	100	00.00	1.87 ± 0.34	21.4413 ± 3.7140	0.0
AMP (30)	100	82.47	0.63 ± 0.20	3.7140 ± 0.3170	178*
CME (200)	100	62.06	1.67 ± 0.24	9.6093 ± 0.5485	150
CME (400)	100	63.09	1.13 ± 0.07	6.0340 ± 0.3333	156
CME (600)	100	65.36	1.03 ± 0.12	4.3440 ± 0.0970	160*

SR survival rate; RWG relative weight gain; MLS mean lesion score; MOV mean oocyst value; ACI Anticoccidial Index. Asterisks (*) indicate the level of effectiveness. Interpretation: ACI ≥ 180 (**) was considered of high performance, ACI of 160–179(*) was considered effective, and ACI < 160 was considered ineffective. Crude Methanolic Extract, UC: untreated Control group, AMP: Amprolium 250® (30 mg/kg)

There was a significant difference (P < 0.05) between OPG values of UC group and the rest of the experimental groups. Similarly OPG values recorded in the CME 200 mg/kg group was significant (P < 0.05) statistically when compared with the rest of the experimental groups. OPG values of AMP group were only highly-very significant and very significant with OPG values obtained from the UC and CME 200 mg/kg groups respectively (Table 4). Similarly, OPG values recorded in the CME 400 mg/kg did not differ significantly (P > 0.05) when compared with the AMP (30 mg/kg) and the CME (600 mg/kg) groups.

Anticoccidial index (ACI)

The calculated anti-coccidial index of AMP (30 mg/kg) and the CME at 200, 400, and 600 mg/kg were 178, 150, 156, and 160 respectively The highest ACI was recorded in the AMP (Amprolium 30 mg/kg) group with 178 while the lowest ACI was recorded in the CME 200 mg/kg group with 149 (Table 5).

Haematology

Effect of CME of G. kola on packed cell volume (PCV) of birds infected with E. tenella oocysts

The mean PCV values recorded in this studies decreased from pre-infection values of 33.67 ± 3.18%, 34.67 ± 2.60%, 35.67 ± 1.86%, 33.33 ± 2.91% and 38.00 ± 0.58% to 17.67 ± 0.88%, 34.00 ± 2.08%, 27.00 ± 2.08%, 29.67 ± 1.20% and 34.33 ± 0.67% on the 8 th day post-infection (Table 6). The lowest mean PCV value in this experiment trial was recorded in the UC group (17.67 ± 0.88%) whereas the highest mean PCV value was recorded in the CME 600 group (34.33 ± 0.67%) (Table 6). There was a significant difference (P < 0.05) between the values of PCV counts in the UC group and the rest of the groups of the experimental birds at the end of the experimental trial.

Table 6.

The effect of CME of G. kola on haematological parameters in broiler chicks infected with Eimeria tenella oocysts

		UC (tween 80)	AMP (30)	CME (200)	CME (400)	CME (600)
Day 0	PCV (%)	33.67 ± 3.18a	34.67 ± 2.60a	35.67 ± 1.86a	33.33 ± 2.91a	38.00 ± 0.58a
	WBC (× 109 /L)	13.30 ± 4.01a	11.47 ± 0.81a	13.63 ± 2.38a	14.53 ± 1.07a	13.87 ± 0.70a
	Lymphocytes (× 109 /L)	9.53 ± 2.94a	9.52 ± 1.00a	10.08 ± 1.85a	12.05 ± 0.81a	11.51 ± 0.70a
	Heterophils (× 109 /L)	3.23 ± 1.05a	1.82 ± 0.32a	2.94 ± 0.56a	2.35 ± 0.32a	2.32 ± 0.47a
	Eosinophils (× 109 /L)	0.00 ± 0.00a	0.10 ± 0.10a	0.00 ± 0.00a	0.00 ± 0.00a	0.04 ± 0.04a
	MCHC (g/dL)	33.26 ± 0.04a	33.26 ± 0.04a	32.67 ± 0.57a	33.20 ± 0.02a	33.24 ± 0.05a
	MCH (pg)	20.24 ± 0.04a	19.36 ± 0.64a	20.10 ± 0.38a	20.12 ± 0.15a	19.91 ± 0.71a
	MCV (fL)	60.84 ± 0.07a	59.23 ± 0.95a	60.60 ± 1.17a	60.60 ± 0.49a	59.90 ± 2.23a
Day 3	PCV (%)	34.33 ± 1.20a	37.00 ± 1.16a	35.67 ± 0.33a	34.67 ± 1.76a	35.33 ± 0.88a
	WBC (× 109 /L)	18.27 ± 4.626a	11.87 ± 1.22a	19.77 ± 3.12a	13.27 ± 2.03a	18.47 ± 3.92a
	Lymphocytes (× 109 /L)	14.52 ± 3.76a	9.72 ± 1.33a	15.88 v 2.72a	10.90 ± 10.90a	14.69 ± 3.20a
	Heterophils (× 109 /L)	2.87 ± 0.98a	1.10 ± 0.41a	2.32 ± 0.41a	1.75 ± 0.33a	2.44 ± 0.19a
	Eosinophils (× 109 /L)	0.81 ± 0.05a	0.89 ± 0.28a	1.29 ± 0.19a	0.62 ± 0.11a	1.19 ± 0.71a
	MCHC (g/dL)	33.14 ± 0.15a	33.24 ± 0.06a	33.27 ± 0.06a	33.17 ± 0.03a	33.31 ± 0.12a
	MCH (pg)	19.99 ± 0.45a	22.44 ± 2.46a	20.11 ± 0.11a	20.54 ± 0.36a	20.08 ± 0.28a
	MCV (fL)	60.57 ± 1.27a	67.49 ± 7.38a	60.00 ± 0.30a	61.91 ± 1.14a	60.28 ± 0.80a
Day 6	PCV (%)	27.33 ± 1.74a	33.33 ± 1.76a	29.00 ± 2.89a	29.33 ± 3.18a	32.67 ± 2.40a
	WBC (× 109 /L)	19.33 ± 1.60a	15.33 ± 1.27a	16.40 ± 2.01a	22.10 ± 3.05a	19.63 ± 1.63a
	Lymphocytes (× 109 /L)	17.13 ± 1.35a	12.85 ± 1.25a	13.47 ± 1.51a	18.41 ± 2.70a	16.85 ± 1.29a
	Heterophils (× 109 /L)	1.42 ± 0.54a	1.78 ± 0.25a	2.12 ± 1.07a	3.35 ± 0.97a	2.01 ± 0.62a
	Eosinophils (× 109 /L)	0.73 ± 0.25a	0.49 ± 0.42a	0.54 ± 0.36a	0.35 ± 0.35a	0.27 ± 0.27a
	MCHC (g/dL)	33.29 ± 0.04a	33.40 ± 0.07a	33.22 ± 0.07a	33.19 ± 0.07a	33.26 ± 0.04a
	MCH (pg)	19.78 ± 0.22a	20.23 ± 0.12a	19.96 ± 0.39a	19.55 ± 0.28a	20.40 ± 0.21a
	MCV (fL)	59.41 ± 0.74a	60.58 ± 0.30a	60.08 ± 1.07a	58.89 ± 0.94a	61.35 ± 0.68a
Day 8	PCV (%)	17.67 ± 0.88a	34.00 ± 2.08bc	27.00 ± 2.08b	29.67 ± 1.20bd	34.33 ± 0.67bc
	WBC (× 109 /L)	22.47 ± 2.78a	12.83 ± 0.72b	12.87 ± 2.10b	12.57 ± 1.75b	12.90 ± 0.72b
	Lymphocytes (× 109 /L)	17.85 ± 2.01a	10.65 ± 0.37b	10.57 ± 1.51b	9.48 ± 1.70b	10.68 ± 0.53b
	Heterophils (× 109 /L)	3.45 ± 0.84a	1.87 ± 0.48a	1.73 ± 0.80a	2.48 ± 1.30a	1.762 ± 0.20a
	Eosinophils (× 109 /L)	0.72 ± 0.47a	0.12 ± 0.07a	0.20 ± 0.20a	0.21 ± 0.21a	0.19 ± 0.19a
	MCHC (g/dL)	33.21 ± 0.06a	33.24 ± 0.06a	33.21 ± 0.07a	33.15 ± 0.03a	33.19 ± 0.07a
	MCH (pg)	18.93 ± 0.43a	22.33 ± 2.50a	20.26 ± 0.36a	20.48 ± 0.17a	20.44 ± 0.62a
	MCV (fL)	57.02 ± 1.40a	67.18 ± 7.52a	61.01 ± 1.21a	61.77 ± 0.54a	62.41 ± 5.40a

Values are expressed as Mean ± SEM (n = 3). Means with different superscript letters (^a−c) in a column differ significantly (p < 0.05). CME: Crude Methanolic Extract, UC: (untreated control), AMP: Amprolium 250® (30 mg/kg), PCV (%); Packed cell volume percentage, WBC; White Blood Cell, MCHC; Mean Corpuscular Haemoglobin Concentration, g/dL; Gram Per deciliters, MCH; Mean Corpuscular Haemoglobin, pg; Picogrrams, L; MCV; Mean Corpuscular Volume, fL; fermtoliters, Litter. Day 0: Preinfection, Day 3: 3 days post-infection/pre-treatment Day 6: 3 days in treatment, Day 6: 3 days in treatment, Day 8: A day post-treatment

Effect of CME of G. kola on white blood cells (WBC) of birds infected with E. tenella oocysts

The recorded white blood cell counts prior to experimental infection with E. tenella (Houghton strain) were within the range of 11.47 ± 0.81 × 10⁹ /L to 14.53 ± 1.07 × 10⁹ /L. Shortly after experimental infections, there was a continuous increase in values of WBC in all the experimental groups of birds with a significant increase recorded on day 6 post-infection (Table 6). The UC group recorded the highest mean WBC count of 22.47 ± 2.78 × 10⁹ /L compared to the lower values of WBCs (in a range of 12.57 ± 1.75 to 12.90 ± 0.72) obtained in the AMP (30 mg/kg) and the CME (200, 400 and 600 mg/kg) groups on the 8th day post-infection (a day post-treatment). For the differential WBC (Leucocytes) count, there was lymphocytosis, Heterophilia as well as Eosinophilia. The mean Lymphocyte, mean Heterophil and mean Eosinophil counts obtained from pre-infection to the termination of the experiment are as shown in Table 6.

There was a significant difference (P < 0.05) between the values of WBC and lymphocyte counts in UC group and the rest of the groups of the experimental birds at the end of the experimental trial. While values obtained from the Heterophil as well as the Eosinophil counts were statistically the same (P0.05).

Effect of CME of G. kola on mean corpuscular haemoglobin concentration (MCHC) of birds infected with E. tenella oocysts

The mean Mean Corpuscular Haemoglobin Concentration (MCHC) values for all the experimental groups of birds recorded a slight increase from pre-infection values of 33.26 ± 0.04 g/dL, 33.26 ± 0.04 g/dL, 32.67 ± 0.57 g/dL, 33.20 ± 0.02 g/dL and 33.24 ± 0.05 g/dL to 33.21 ± 0.0604 g/dL, 33.24 ± 0.0604 g/dL, 33.21 ± 0.0704 g/dL, 33.15 ± 0.0304 g/dL and 33.19 ± 0.0704 g/dL on the 8th day post-infection( a day post treatment) (Table 6).

There was no statistically significant difference (P > 0.05) recorded between all the groups of the experimental birds.

Effect of CME of G. kola on mean corpuscular haemoglobin (MCH) in birds infected with E. tenella oocysts

The Mean Corpuscular Haemoglobin (MCH) values for the AMP (30 mg/kg) and the CME (200, 400 and 600 mg/kg) groups recorded a slight increase from pre-infection values of 19.36 ± 0.64 pg, 20.10 ± 0.38 pg, 20.12 ± 0.15 pg and 19.91 ± 0.71 pg to 22.33 ± 2.50 pg, 20.26 ± 0.36 pg, 20.48 ± 0.17 pg, and 20.44 ± 0.62 pg respectively on the 8th day post-infection (a day post-treatment; Table 6). Whereas the UC group (Table 6) had a decrease in MCH value from pre-infection value of 20.24 ± 0.04 pg to 18.93 ± 0.43 pg on the 8th day post infection (Table 6). The lowest mean MCH value in this experiment trial was recorded in the UC group (18.93 ± 0.43 pg) whereas the highest mean MCH value was recorded in the AMP group (22.33 ± 2.50 pg) (Table 6).

There was no significant difference (P > 0.05) in the values of MCH recorded between all the groups of the experimental birds.

Effect of CME of G. kola on mean corpuscular volume (MCV) of birds infected with E. tenella oocysts

The mean Mean Corpuscular Volume (MCV) values for the AMP and CME (200, 400 and 600 mg/kg) groups recorded a slight increase from pre-infection values of 59.23 ± 0.95 fg, 60.60 ± 1.17 fg, 60.60 ± 0.49 fg and 59.90 ± 2.23 fg to 67.18 ± 7.52 fg, 61.01 ± 1.21 fg, 61.77 ± 0.54 fg, and 62.41 ± 5.40 fg respectively on the 8th day post -infection (a day post treatment) (Table 6). Whereas the UCgroup (Table 6) had a decrease in MCV value from pre-infection value of 60.84 ± 0.07 fg to 57.02 ± 1.40 fg on the 8 th day post infection (Table 6).

The lowest mean MCV value recorded was in the UC group (57.02 ± 1.40 fg) whereas the highest mean MCV value was recorded in the AMP group(67.18 ± 7.52 fg) (Table 6).

There was no significant difference (P > 0.05) in the values of MCV recorded between all the groups of the experimental birds.

Histopathology

Sections of the caeca of the broiler chicks in the untreated control group had multiple invasion of the caecal epithelium by different developmental stages (schizonts, merozoites, microgametes, and macrogametes) of E. tenella. The epithelial surfaces had haemorrhages as well as submucosal oedema. Additionally, there were various necrotic lesions with surrounding diffuse infiltration of inflammatory cells (lymphocytes, plasma cells, eosinophils, and heterophils) (Fig. 2a).

Fig. 2.

Photomicrograph of the cecum of a broiler chick experimentally infected with Eiemeria tenella and treated with a 0.8% tween 80, b Amprolium (30 mg/kg), c Crude methanol extract (200 mg/kg), d Crude methanolic extract (400 mg/kg), e Crude methanol extract (600 mg/kg). Note the developmental stages of Eimeria tenella (arrows), necrotic tissue (N), and diffused mononuclear cells infiltration (C). H and E × 200

In the group treated with amprolium (30 mg/kg), there was mild infiltration of inflammatory cells (lymphocytes, heterophils, and eosinophils). More so, few numbers of developmental stages of E. tenella when compared with findings from the untreated control group were observed (Fig. 2b).

Caeca sections of the broiler chicks treated with CME (200 mg/kg) also had multiple invasion of the caecal epithelium by different developmental stages of E. tenella and diffuse infiltration of inflammatory cells (lymphocytes, plasma cells, eosinophils, and heterophils) (Fig. 2c).

The caecal sections of the chicks in the group treated with CME (400 mg/kg) had a moderate invasion of the epithelial cells by different developmental stages of E. tenella (Houghton strain) and moderate inflammatory cells infiltration (Fig. 2d).

In the group treated with CME (600 mg/kg), there were few numbers of developmental stages of E. tenella with mild infiltration of inflammatory cells (lymphocytes, heterophils, and eosinophils) when compared with the untreated control group (Fig. 2e).

Summarily, in all cases, the intestinal changes observed were associated with the intralesional presence of various developmental stages of E. tenalla with all the described elements fluctuating greatly between experimental groups (Fig. 2a–e). There was a significant reduction in the number of parasites seen as the concentration of the G. kola extract increases.

Discussion

Garcinia kola is well known for its antiprotozoal, antioxidant, antidiabetic antigenotoxic, marked inhibition of gastrointestinal motility, protection against castor oil-induced diarrhoea and hepatoprotective activities (Kerboeuf et al. 2008; Ferreira et al. 2010; Farombi and Owoeye 2011) but less is known about its activity against Eimeria spp.

All birds infected with the Houghton strain of E. tenella showed classical signs of caecal coccidiosis such as droopiness, loss of appetite/weight, and chocolate-brown to bloody faecal droppings. This indicates that the Houghton strain of E. tenella was pathogenic to the experimental broiler chicks. There was however no mortality recorded in the course of the experiment which could be due to the low challenge dose of the parasite used for this experiment. It could as well be due to the low production of chymotrypsin in the younger birds used in the present work, a proteolytic enzyme that contributes immensely to the excystation of sporozoites for epithelial invasion and hence the mild infection observed. Similar observations were made by other workers on E. tenella (Duffy et al. 2005; Song et al. 2009; Gharekhani et al. 2014).

All the birds infected with E. tenella had some levels of weight loss with the least and highest being observed in the group treated with amprolium (standard drug) and the untreated control group respectively. The observed decrease in weight could be associated with the changes in the intestinal villi as a result of damage caused by the invasion and the multiplication of the parasite, thus impairing normal absorption of nutrients (Shaban 2012). The weight gain observed in all the birds treated with the CME of G. kola was similar to that observed in the group treated with amprolium. This could be attributed to the fact that both amprolium and the plant extract might have altered the microenvironment of the host digestive tract that is necessary to stimulate the excystation of the oocyst resulting in the release of sporozoites that invade and destroy cells in the intestinal mucosa (Dalloul and Lillehoj 2005; Jatau et al. 2014).

It was observed that birds treated with CME and amprolium had significantly (p < 0.05) lower oocysts/gram of faeces and shedding of the Eimeria oocyst when compared to birds in the group administered with 0.8% tween 80 (untreated control) at 6 days post-infection. Artemisinin, a sesquiterpene lactone derivative of Artemesia annua, and the extracts of the fruits/leaves of Azadirachta indica and Vernonia amygdalina were shown to have a similar effect on oocysts of E. tenella. This was attributed to the protective effects of these plant materials on the intestinal mucosa against the Eimeria organism (Abbas et al. 2006; Oyegbemi et al., 2012; Pop et al. 2015). Similarly, findings from this study on oocyst decrease ratio (ODR) correlates with that of faecal oocysts shedding in the treated birds.

The postmortem findings observed in the present study were relatively mild and correlates with the observed gross lesion scores as well as the histopathological findings. The findings of the present study were in agreement with the study of Jatau et al. (2014) and this was possibly attributed to the mild nature of the infection. The lesions and the histopathological lesions with the number of parasites observed at histological examination correlate also with the macroscopic lesion score and the oocysts counts for all birds (Pop et al. 2015). The lesion observed in all the birds could be associated with the damages caused by the replicating effect of developmental stages of the Eimeria parasites which might have possibly resulted in inflammatory reactions as well as secondary bacterial infection (Jatau et al. 2014). Perhaps this is due to the observed cellular infiltration.

The PCV values obtained in this study significantly (p < 0.05) decreased in the untreated group on the 8th day postinfection with only a slight decrease in PVC in the groups treated with the extract of G. kola and amprolium. These findings also correlate with the slightly pale breast muscles, chocolate-brown to bloody caecal content (pasty to watery in consistency), thickened blood-tinged caecal wall observed at postmortem. All these alterations observed could be a result of the damages to the gastrointestinal tract caused by the offending parasites leading to loss of blood and fluids in faeces (Irizaary-Rovira 2004; Ogbe et al. 2010).

Three days post-infection, leucocytosis was seen in all the birds. This is observed for up to 6 days post-infection. However, birds in the treated groups showed a decrease in the levels of white blood cells when compared to birds in the untreated control group. This is indicative that peripheral blood leucocytes were likely mobilized in response to the invasive activities of the offending organism (E. tenella) in the gastrointestinal tract (Rose et al. 1979; Ricklefs and Sheldon 2007).

The differential WBC counts in this study, showed mild lymphocytosis, heterophilia as well as eosinophilia in all the birds infected with E.tenalla. The mild lymphocytosis observed was consistent in birds treated with CME but it was more pronounced on the 6th day of infection. Values of lymphocytes count increased continuously in the untreated group up till day 8 of the experiment (end of the experiment). This is contrary to the observable decrease in the WBC counts obtained in the group treated with amprolium and CME. The increase in lymphocyte count may be attributed to their response to the inflammatory reactions caused by E. tenella in the caecum (Irizaary-Rovira 2004). Although the mechanism of action of the anti-inflammatory activity of Garcinia plants as reported by Panthong et al. (2007) is not quite clear, the reduction in lymphocyte counts seen in the group of birds treated with G. kola extract may be related to its possible inhibitory effect on inflammation.

Heterophil count in birds normally increases with acute or chronic inflammatory disease conditions (Irizaary-Rovira 2004) as is the case in this study. They contain basophilic granules that contribute to the first line of defense against bacterial infections. This might be the possible reason relating to the high heterophil count recorded in the infected/untreated group on the 8th day post-infection.

Eosinophilia in birds rarely occurs but may be associated with parasitism as is the case in this study. This was noticed on the 3rd day of experimental infection and the eosinophil values decreased upon treatment with the experimental plant extract and amprolium but remain consistently high in the untreated control group.

The Mean Corpuscular Haemoglobin Concentration (MCHC), Mean Corpuscular Haemoglobin (MCH), and Mean Corpuscular Volume (MCV) values obtained in this study showed slight alterations from the pre-infection values. The MCHC values recorded across all the experimental groups showed a slight observable decrease from the values obtained a day prior to experimental infection. This could possibly be due to the low-grade infection with E.tenella as well as the Packed Cell Volume values recorded in this study.

The MCH values, on the other hand, increased slightly on the 8th day post-infection from pre-infection values in the groups of birds treated with amprolium and G. kola extract. On the contrary, the values of MCH obtained in the untreated group decreased from those obtained before the experimental infection. Values of MCV in the untreated group decreased considerably compared to the slight increase recorded in the group of birds treated with amprolium and CME.

Flavonoids such kolaviron (a biflavonoid of G. kola) are well known for their antioxidant effect due to their redox properties. Some flavonoids act on host-parasite interactions, and others disturb the development or metabolism of protozoan parasites (Fotie 2008; Kerboeuf et al. 2008; Akefe et al. 2020). This could likely be the explanation regarding the increased weight gain, reduced rate of oocysts shedding, high oocyst decrease ratio, and the reduction in both gross and histopathological lesions, which also correlates with the haematological findings of this study.

The Anticoccidial Index (ACI), which is a measure for assessing the protective effect of a substance. It was used here to demonstrate the overall anticoccidial activity of CME of G. kola. In this study, birds treated with CME (600 mg/kg) had an ACI of 160 which compares very well with the group treated with amprolium (ACI = 178). It is possible from the study that higher doses of the extract could have an improved aniticoccidial effect by increasing the ACI values.

Conclusions

The present study demonstrated the anticoccidial potential of the crude methanol extract (CME) of Garcinia kola in broilers experimentally infected with E. tenella. The administration of graded doses of Garcinia kola in broiler chicks infected with E. tenella improved the body weight gain, haematological parameters, anticoccidial index, and in addition, decreased the rate of oocysts shedding, and histological lesions. This study therefore highlights the beneficial effects of administering G. kola in the treatment and control of E. tenella-associated coccidiosis infection in chickens. This is the first report on the anticoccidial activities of G. kola, however, further investigation to identify the active principle responsible for the anticoccidial activities of G. kola is required.

Declarations

Conflict of interest

All authors declare that they have no conflict of interest.