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Journal of Animal Health and Production

JAHP_9_2_185-192

 

 

Short Communication

 

Effects of Enzyme in Palm Kernel Meal-Based Diet on Blood, Carcass, and Organ Weights in Weaners Pigs

 

Taiwo K Ojediran1, Raadiyah A Azeez1, Festus A Adejoro2*, Oluwaseun E Areo1, Isiak A Emiola1

1Department of Animal Nutrition and Biotechnology, Ladoke Akintola University of Technology, Ogbomoso, Nigeria; 2Department of Agriculture, Faculty of Natural Sciences, Mangosuthu University of Technology, P.O. Box 12363, Jacobs, 4026, Durban, South Africa.

 

Abstract | Supplementing palm kernel meal (PKM)-based diet with an exogenous enzyme can help to improve the utilization and minimize the negative consequences of the high fibre and antinutritional factors on performance and health of animals. Forty weaned male pigs with an average initial weight of 7.85 ± 0.31 kg were used to determine the effects of supplementing a PKM-based diet with enzyme inclusion, on blood parameters, carcass and organ characteristics. Pigs were allotted to four diets which include the control diet containing 55% PKM while the addition of 1, 2 and 3 g/kg enzyme cocktail was tested in a complete randomized design trial that lasted seven weeks. Feed and water were provided ad-lib and blood sampled via jugular vein after the trial. Pigs fed diets containing high PKM with or without enzyme, did not manifest any significant deviation in their haematology or serum variables. Enzyme inclusions reduce cholesterol concentrations (p<0.05), but no linear or quadratic effect of the enzyme was observed on alkaline phosphatase or creatinine concentration (p>0.05). Eviscerated weight increased (p<0.05) as enzyme inclusion increased but other carcass traits were not affected. Pancreas and empty stomach weights reduced quadratically with enzyme inclusion (p<0.05) and this may ostensibly be due to improved digestive activities of the organs. This study confirms that the inclusion of enzyme in diets containing high proportion of PKM does not have any negative physiological effect on growing pigs.

 

Keywords | Carcass, Digestion, Enzyme, Haematology, High fibre

 

Received | December 29, 2020; Accepted | January 19, 2021; Published | April 25, 2021

*Correspondence | Festus A Adejoro, Department of Agriculture, Faculty of Natural Sciences, Mangosuthu University of Technology, P.O. Box 12363, Jacobs, 4026, Durban, South Africa; Email: adejoro.festus@mut.ac.za

Citation | Ojediran TK, Azeez RA, Adejoro FA, Areo OE, Emiola IA (2021). Effects of enzyme in palm kernel meal-based diet on blood, carcass, and organ weights in weaners pigs. J. Anim. Health Prod. 9(2): 185-192.

DOI | http://dx.doi.org/10.17582/journal.jahp/2021/9.2.185.192

ISSN | 2308-2801

Copyright © 2021 Adejoro et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

 

INTRODUCTION

 

Palm kernel meal (PKM) is an abundant agro-industrial by-product from the oil processing mill with potential nutritive value for livestock feeding. The chemical composition of PKM showed that it has crude protein (CP) concentration of 14–18% and moderate energy value (10.6 MJ/kg DM) (Kim et al., 2016; Sathitkowitchai et al., 2018). These values are dependent on processing techniques which affect the ether extract and crude fibre

 

content (Ojediran et al., 2020). However, PKM has high levels of non-starch polysaccharides (NSP) such as mannan, xylan which limits its utilisation as feed for non-ruminant animals (Adeola and Cowieson, 2011; Sharmila et al., 2014). The cell wall components of PKM consists of 58% mannan, 12% cellulose and 4% xylan (Sathitkowitchai et al., 2018). Furthermore, PKM is coarse-textured, gritty in appearance and high viscosity which tend to decrease nutrient absorption (Ojediran et al., 2020).

 

The β-mannan and non-starch polysaccharide (NSP) present in PKM have anti-nutritional properties that hinder the full utilization of nutrients in pigs (O’Shea et al., 2014; Oladokun et al., 2016). The cell wall of PKM contains (1–4)-linked β-mannose, (1–6)-linked α-galactose (galactomannan) which reduces feed efficiency by 20–30% (Düsterhöft et al., 2006). Despite the limitations to the use of PKM, studies have shown that it can sustain maintenance and moderate growth in pigs and can be used as partial substitute of maize and soybean in pigs and poultry diet (Alshelmani et al., 2017). Previous studies have shown that the feeding value of PKM for monogastric can be improved through solid-state fermentation (Mirnawati et al., 2011; Alshelmani et al., 2017), enzyme supplementation (Kononenko and Gorkovenko, 2011; Ravindran and Son 2011) among others. The addition of enzymes that digest the β-mannan can improve animal weight gain and feed efficiency (Adeola and Cowieson, 2011; Choe et al., 2017). Mannanase enzyme aids in the hydrolysis of linear mannans, resulting in increased digestion of NSPs, improved nutrient utilization and decreased intestinal viscosity of digesta (O’Shea et al., 2014; Ojediran et al., 2020).

 

The use of an enzyme to improve the digestibility of NSPs and other antinutritional factors in feed could enhance, not just the growth performance of the pigs, but also the health and immune status of the animals as reflected in haematology and serum biochemical parameters (Ao et al., 2011; Stephenson et al., 2014; Zuo et al., 2015). Furthermore, feeding high fibre feeds like PKM to pigs can have confounding effects on body weight as compared to carcass weight because of enlarge digestive organs causing higher relative organ weights (Agyekum et al., 2012). However, there are limited studies on the effect of a cocktail of enzymes on the blood parameters, carcass traits and relative organ weight in growing pigs. Beside the effect of fibre on nutrient digestion, the impact of enzyme inclusion on the overall physiology of the animals consuming high fibre diets may provide further justification for increasing the use of it in pig production systems. Therefore, the objective of this study was to evaluate the effect of a cocktail of different enzymes, supplemented to a PKM-based diet, on the haematology and serum biochemical parameters, as well as carcass characteristics and organ weights of weaned piglets.

 

MATERIALS AND METHODS

 

Ethics statements

Animal care and all experimental procedures were approved by the Research Ethics Committee of the Ladoke Akintola University of Technology with approval number: LAUTECH/EC/2019/09/011.

 

Animals and Experimental Design

The trial was conducted at the Piggery section of the Research Farm of the University and located on latitude 8 10.398’N and longitude 4 16.272’E. Forty (40) male weaner pigs (Large white x Landrace) with an average initial body weight of 7.85 ± 0.31 kg were grouped by weight and from each group, randomly assigned to one of four dietary treatments in a 7-week trial with 10 pigs per treatment allocated to individual pens. The dietary treatments include a control diet which contained PKM, and with 1, 2, 3 g/kg enzyme supplementation (Table 1). The enzyme source is Polyzyme, a commercial enzyme product containing a proprietary cocktail of mannanase, xylanase, cellulase, glucanase, phytase, amylase, pectinase, lipase, galactosidase, and protease enzymes (Zeus Biotech Company, Mysore-Karnataka, India). The powdered product was incorporated at the dosage of 2 g/kg feed DM, into the complete ration with a vertical mixer, and weekly batches of each feed was produced and fed to the respective animals, all through the trial. All the pigs were housed in concrete floor pens of 2 m2/pen, 1.5 m walls and iron roofing. Pigs were adapted to the respective diets for seven days, in two equal instalments daily using one-sided plastic feeders at 08h00 and 14h00. Thereafter, both feed and water were provided ad libitum throughout the trial period which lasted additional seven weeks.

 

Table 1: Ingredient and Chemical Composition of Experimental Diet (g/kg DM)

 

Ingredients Diet
Maize 150
Fish meal 30
Full fat Soya 90
Palm kernel meal 550
Wheat offal 150
Bone meal 15
Limestone 10

1premix

2.5

Salt

2.5
Total 1000
Nutrient composition (g/kg)
Crude Protein 199
Ether Extract 63.5
Crude Fibre 87
ME (MJ/kg) 11.4
Calcium 9.5

2Lysine (%)

0.87

2Methionine (%)

0.4


1supplied the following (per kg feed): vitamin A, 12 500 IU; vitamin D3, 5 000 IU; vitamin E, 40 mg; vitamin K3, 2 mg; vitamin B1, 3 mg; vitamin B2, 5.5 mg; niacin, 55 mg; calcium pantothenate, 11.5 mg; vitamin B6, 5 mg; vitamin B12, 25 mg; folic acid, 1 mg; biotin, 50 mg; choline chloride, 500 mg; manganese, 300 mg; iron, 120 mg; zinc, 80 mg; copper, 85 mg; iodine, 1.5 mg; cobalt, 3 mg; selenium, 1.2 mg; anti-oxidant, 120 mg. 2Calculated composition.

 

Data Collection

At the end of the 7-week feeding period, 5 mL blood samples were collected via the jugular vein into both EDTA vacuum tubes and plain vacutainer tubes. Six animals were randomly sampled per treatment, tubes kept in a cooler box immediately after collection and then analysed for haematological and serum biochemical variables as described in Ojediran et al. (2019a). Thereafter, all the pigs were transferred to the slaughterhouse and slaughtered using conventional procedures. After evisceration, the primal cuts and organs were weighed and expressed in relation (percentage) to the live weight of the respective animal.

 

Statistical analysis

All data were subjected to the Proc Mixed procedure of SAS (Statistical Analysis System, version 9.4., SAS Institute Inc., Carry, NC, USA). The model statement included dietary treatment as a fixed effect, animals as random effect as shown:

yijk = μ + Ai + Tj + εij

 

where yijk = individual observation; μ = overall mean; Ai = animal effect (random); Tj = treatment effect (fixed), and εij =random error. Single degree of freedom contrast was used to compare i) control versus average of enzyme-treated diets, ii) the linear effect of increasing enzyme inclusion, iii) the quadratic effect of increasing enzyme inclusion.

 

RESULTS

 

Table 2 showed that the red blood cell (RBC), mean corpuscular haemoglobin concentration (MCHC), and lymphocyte counts in pigs were not affected by enzyme inclusion in the palm kernel meal-based diet (p>0.05). In contrast, enzyme supplementation in the diets affected the haemoglobin (Hb), haematocrit (HCT), total white blood cell (WBC), mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH) and platelet count in the pigs (p<0.05). While there was lower HCT and Hb concentration in enzyme supplemented animals, their WBC and platelet counts were higher (p<0.05). There was a linear increase in WBC count with increasing enzyme inclusion while platelet counts increased both linearly and quadratically with increasing inclusion levels (p<0.05).

 

Comparing pigs in the control diets versus the average of the enzyme supplemented pigs, albumin, total protein, urea, and creatinine concentration was not affected by enzyme inclusion (p>0.05) (Table 3). However, globulin, cholesterol, triglyceride, and glucose concentration were affected by enzyme supplementation of the palm kernel meal-based diet (p<0.05). A quadratic increase in globulin, total protein and cholesterol concentration in pigs was associated with increasing enzyme inclusion while a linear increase, as well as quadratic increase in glucose and creatinine concentration, was associated with increasing enzyme inclusion in the pig diets (p<0.05). Furthermore, alkaline phosphatase (ALP) concentrations were neither affected by the average effects nor by the increasing inclusion levels of enzyme supplementation in the pig diets (p>0.05).

 

Table 4 shows the carcass characteristics of weaner pigs fed PK-based diet with or without enzyme supplementation. The bled weight, eviscerated weight, head, jowl, loin, picnic shoulder, buston butt and belly were not different between animals on the control diet and the average of the enzyme-supplemented diets (P >0.05). Ham, spare rib and trotters were different between animals on the control diet and the average of the enzyme supplemented group (p<0.05). Furthermore, increasing inclusion levels of enzyme linearly reduced carcass weight but linearly increased ham weight (p<0.05).

 

The spleen and kidney weights were not different in the pigs across the dietary treatments (p>0.05) (Table 5). However, Liver weight was lower in the enzyme supplemented pigs compared to the control group (p<0.05). Pancreas weight was equally lower in enzyme supplemented pigs and increasing inclusion levels resulted in a linear and quadratic decrease in pancreas weight. Empty stomach weight and lung weight were not affected by diet differences. There was a linear and quadratic change in heart weight across the enzyme inclusion levels.

 

DISCUSSION

 

Previous data published showed that there were no significant differences among the pigs in terms of Average daily intake, average daily gain (ADG) and feed conversion ratio (FCR) (P >0.05). Average daily intake ranged from 620- 800 g/d while ADG ranged between 240- 290 g/d (Ojediran et al., 2020). Haematological values are of diagnostic importance in practical husbandry, which is in response to the environment and dietary changes and reveal adverse conditions even when without obvious signs of ill health (Eze et al., 2010). The result of the effect of the experimental diets on haematological parameters indicates that the experimental diets had no detrimental effects on the health status of the weaner pigs as most of the parameters measured were within the reference values prescribed by Mitruka and Rawnsley (1977) as well as Thorn, (2000). Abnormal deviations in haematological variables in pigs are thought to be due to malnutrition or dietary influence

 

Table 2: Haematological Parameters of Weaner Pigs Fed Palm Kernel Meal-Based Diet, with Graded Levels of Enzyme Supplementation

 

Parameters Enzyme supplementation (g/kg Diet) SEM

1Contrast P-values

  Control (0) 1 2 3   C vs Enzy

EnzyL

EnzyQ

Red blood cell (×106/µl)

7.58 7.20 7.07 7.20 0.11 0.144 0.249 0.319
Haemoglobin (g/dl) 10.3 9.40 8.85 9.90 0.15 <0.01 0.04 <0.01
Haematocrit (%) 46.0 43.3 40.7 44.4 0.65 0.025 0.147 0.016

White blood cells (×103/µl)

17.3 20.0 21.5 21.8 0.60 0.01 <0.01 0.266
Mean corpuscular volume (fl) 60.8 60.4 57.6 61.6 0.40 0.125 0.906 <0.01

Mean corpuscular haemoglobin (pg)

13.6 13.2 12.6 13.8 0.14 0.09 0.877 <0.01
Mean corpuscular haemoglobin concentration (g/dl) 22.4 21.8 21.8 22.3 0.11 0.15 0.879 0.039

Platelets (×103/µl)

235 348 423 363 21.1 <0.01 <0.01 0.065

Lymphocytes (×103/µl)

10.2 11.8 11.7 10.5 0.29 0.115 0.01 0.233
Red cell distribution width _SD (fl) 45.7 44.1 37.5 43.0 0.85 0.01 0.01 0.01
RDW_CV (%) 21.3 20.8 17.7 19.9 0.39 0.01 0.01

0.03


1Contrast analysis across treatments: C vs. Enzy, control diet vs. average of enzyme treated diets; EnzyL, linear effect of enzyme levels; EnzyQ, quadratic effect of enzyme levels. SEM, standard error of means.

 

Table 3: Serum Biochemistry Parameters of Weaner Pigs Fed PKM-Based Diet and with Increasing Levels of Enzyme Supplementation

 

Parameters

Enzyme supplementation (g/kg Diet)

SEM

1Contrast P-values

  Control (0) 1 2 3   C vs Enzy

EnzyL

EnzyQ

Albumin (g/dl) 2.71 2.65 2.81 2.36 0.06 0.531 0.123 0.083
Globulin (g/dl) 0.91 1.21 1.97 1.07 0.13 0.01 0.06 <0.01
Total protein (g/dl) 3.62 3.85 4.78 3.43 0.17 0.08 0.483 <0.01
Cholesterol (mg/dl) 170 109 160 144 6.21 <0.01 0.552 0.015
Alkaline phosphatase (U/L) 29.1 27.9 31.6 29.6 0.72 0.698 0.703 0.319
Urea (mg/dl) 7.31 11.3 6.77 7.07 0.66 0.452 0.313 0.162
Triglyceride (mg/dl) 341 298 192 260 22.3 0.04 0.056 0.129
Glucose (mg/dl) 156 84.0 163 171 8.47 0.024 <0.01 <0.01
Creatinine(mg/dl) 0.77 0.72 0.79 0.95 0.11 0.103 <0.01

0.01


1Contrast analysis across treatments: C vs. Enzy, control diet vs. average of enzyme treated diets; EnzyL, linear effect of enzyme levels; EnzyQ, quadratic effect of enzyme levels. SEM, standard error of means.

 

Table 4: Carcass Characteristics of Weaner Pigs Fed PKM-Based Diet and with Increasing Levels of Enzyme Supplementation

 

Parameters (%) Enzyme supplementation (g/kg Diet) SEM

1Contrast P-value

  Control (0) 1 2 3   C vs Enzy

EnzyL

EnzyQ

Bled weight 94.70 95.59 94.64 96.64 0.26 0.103 <0.01 0.01
Eviscerated weight 69.72 70.40 71.05 71.11 0.25 0.44 0.011 0.387
Carcass weight 53.34 52.49 52.82 51.91 0.30 0.055 0.039 0.445
Head 8.34 8.37 7.38 8.97 0.22 0.295 0.225 0.702
Jowl 2.62 1.91 4.44 3.00 0.28 0.61 0.219 0.289
Loin 12.60 10.91 11.53 10.09 0.27 0.682 0.021 0.363
Ham 14.03 12.93 13.28 13.98 0.17 <0.01 <0.01 0.818
Picnic shoulder 9.52 11.52 10.03 8.21 0.32 0.117 0.421 0.024
Buston butt 10.70 10.47 10.18 10.71 0.11 0.341 0.01 <0.01
Spare rib 3.10 2.22 2.73 5.06 0.38 0.047 0.32 0.003
Belly 3.19 2.69 2.95 2.56 0.10 0.768 0.046 0.035
Trotters 1.76 1.38 1.82 1.70 0.06 0.047 0.062

0.81


1Contrast analysis across treatments: C vs. Enzy, control diet vs. average of enzyme treated diets; EnzyL, linear effect of enzyme levels; EnzyQ, quadratic effect of enzyme levels. SEM, standard error of means.

 

Table 5: Organ Weight of Weaner Pigs Fed Palm Kernel Meal-Based Diet with or without Enzyme Supplementation

 

Parameters (%) Enzyme supplementation (g/kg DM) SEM

1Contrast P-values

  0 1 2 3 C vs Enzy

EnzyQ

EnzyL

Spleen 0.12 0.12 0.13 0.13 0.00 0.186 0.773 0.097
Kidney 0.43 0.44 0.39 0.40 0.01 0.443 0.377 0.504
Liver 2.88 2.59 2.71 3.01 0.04 0.028 <0.01 0.848
Pancreas 0.23 0.23 0.24 0.19 0.01 0.01 <0.01 <0.01
Empty stomach 1.29 1.28 1.33 1.17 0.09 0.27 0.762 0.024
Lungs 0.92 1.30 0.95 0.87 0.19 0.424 0.917 0.019
Heart 0.45 0.43 0.41 0.45 0.07 0.022 0.01 <0.01


1Contrast analysis across treatments: C vs. Enzy, control diet vs. average of enzyme treated diets; EnzyL, linear effect of enzyme levels; EnzyQ, quadratic effect of enzyme levels. SEM, standard error of means.

 

(Yan et al., 2012; Dlamini et al., 2017; Min et al., 2019). In a similar study, the inclusion of enzyme in the pig diets did not have any negative effect on the metabolic processes of the growing and fattening pig youngsters but rather, there was increased haemoglobin concentration in pigs supplemented with endoxylanase enzyme in a high NSP-triticale diet (Kononenko and Gorkovenko, 2011).

 

Only a slight increase in WBC count was observed in animals supplemented with the enzyme. Although Akintunde et al. (2011) observed that supplementing a diet containing 30% PKM inclusion had no effect on the haematological parameters such as Hgb, RBC, WBC, MCV, MCH and MCHC, however, the current study observed marked differences in only RBC and WBC. Overall, the result of the current study showed that the pigs were not anaemic nor their immunity compromised. Low and high WBC beyond the normal ranges is indicative of impaired immune function (Akanmu et al., 2020). While exogenous enzymes function primarily to complement the activities of digestive enzymes, the gut microbiota has been known to affect the integrity of the intestinal barrier against colonization by pathogens (Jandhyala et al., 2015), and via anti-inflammatory immune enhancement (Wu and Wu, 2012). For example, dietary probiotics resulted in increased production of immunoglobins and act as an immune adjuvant in pigs (Naqid et al., 2015).

 

Multi Enzyme product containing xylanases did not affect blood profile and carcass characteristics in finishing pigs in the study reported by Min et al. (2019). However, enzyme supplementation in the current study seemed to reduce blood cholesterol concentration, and this is similar to the observation of Józefiak et al. (2011) who reported reduced cholesterol concentration in broilers. Furthermore, Kilic et al. (2006), reported that enzyme supplementation significantly reduced abdominal fat deposition in broilers. Increased fibre digestibility through enzyme supplementation may have modulated the synthesis of cholesterol and other fats in the enzyme supplemented pigs. Increased metabolic activity by visceral organs has been associated with increased cellular turnover and may affect haematological parameters of the pigs (Adejoro et al., 2013). Some antinutritional factors are known to irritate the gut, and this may be easily detected from serum biochemical parameters (Eze et al., 2010; Adejoro et al., 2013; Alshelmani et al., 2017). Elevated creatinine concentration is an indication of muscular wastage (Akanmu et al., 2020). Although slightly higher at 0.3 g/kg enzyme inclusion, creatinine concentration was within the normal range as described by Thorn, (2000).

 

The result of the eviscerated weight in this study also shows that the enzyme supplemented groups recorded significantly higher eviscerated weight than the control group. The higher eviscerated weight in the treated groups agrees with the findings of Wang et al. (2011) with keratinase enzyme. In contrast, O’Shea et al. (2014) and Choe et al. (2017) did not observe any improvement in pig carcass traits as a result of enzyme supplementation. Ojediran et al. (2019b) attributed changes in carcass characteristics like jowl, loin ham, picnic shoulder and belly to feed utilization. Nkosi et al. (2020) reported that enzyme supplementation did not affect most of the carcass characteristics and the current study agrees with this.

 

Supplementation of enzyme to high fibre diet did not affect relative organ weight as observed in the current study and that is consistent with the observation of Agyekum et al. (2012) in crossbred pigs fed distillers dried grains (DDGS). It appears that the metabolic strain on the digestive process associated with high fibre diet was not ameliorated by enzyme supplementation which aimed to improve fibre digestion. Furthermore, O’Shea et al. (2014) noted that the addition of protease to the diets of growing pigs did not affect carcass characteristics (carcass weight, back fat, lean meat, and dressing percentage) and this is consistent with the present study.

 

The mechanism of action of exogenous enzymes on the gastrointestinal tract (GIT) and the physiological effect on pigs when consuming PKM-based diets alone or in combination with enzymes are not well understood. Previous studies showed that high fibre diets increased organ weight in pigs (Nyachoti et al., 2000; Unigwe et al., 2017). It has been noted that feeding high fibre diets like PKM to pigs may affect gastrointestinal tract activity due to gut weight and gut fill, thereby confounding bodyweight changes as against carcass weight at slaughtering (Njoku et al., 2015). The study by Agyekum et al. (2012) observed that gut mass and digestive organs such as liver, pancreas and spleen were larger in pigs consuming DDGS diets without enzyme. The implication of this is the increase of energy requirement for maintenance in the animal. High fibre diets increase secretion of digestive fluids for the breakdown of fibre (Wenk, 2001) and the enlargement of the digestive organs. Any exogenous factor that aids fibre digestion will be savings on energy cost and the secretory activities of the organs and GIT to break down these high-fibre diets (Zamora et al., 2011; Agyekum et al., 2012). This, along with the improved feed utilisation may justify the inclusion of enzyme in pig diets containing high fibre concentration.

 

CONCLUSION

 

Weaned pigs fed PKM-based diet supplemented with enzyme did not manifest any significant change in haematological or serum biochemical variables. Furthermore, carcass characteristics and organ weights did not follow any specific pattern but a tendency for increase in eviscerated weight and reduced empty stomach weight was observed. This justifies the inclusion of enzyme up to 3% dietary inclusion in pig diets containing a high proportion of PKM.

 

CONFLICT OF INTEREST

 

All the authors declare that there are no conflicts of interest in carrying out this study.

 

ACKNOWLEDGEMENTS

 

The authors are grateful to the respective Universities for providing the needed institutional support to carry out this investigation.

 

authors contribution

 

Conceptualization: TKO, RAA. Methodology: TKO,RAA, IAE. Data acquisition and analysis: RAA, FAA, OEA. Writing and editing: RAA, FAA. Project Supervision: TKO, IAE.

 

REFERENCES

 

  • Adejoro FA, Ijadunola TI, Odetola OM, Omoniyi BA (2013). Effect of sun-dried, soaked and cooked wild cocoyam (Colocasia esculenta) meal on the growth performance and carcass characteristics of broilers. Livest. Res. Rural Dev. 25: 1-7.
  • Adeola O, Cowieson AJ (2011). Board-invited review: opportunities and challenges in using exogenous enzymes to improve nonruminant animal production. J. Anim. Sci. 89: 3189–3218. https://doi.org/10.2527/jas.2010-3715
  • Agyekum AK, Slominski BA, Nyachoti CM (2012). Organ weight, intestinal morphology, and fasting whole-body oxygen consumption in growing pigs fed diets containing distillers dried grains with solubles alone or in combination with a multienzyme supplement.  J. Anim. Sci 90(9): 3032-3040. Doi:10.2527/jas.2011-4380. https://doi.org/10.2527/jas.2011-4380
  • Akanmu AM, Hassen A, Adejoro FA (2020). Haematology and Serum Biochemical Indices of Lambs Supplemented with Moringa oleifera, Jatropha curcas and Aloe vera Leaf Extract as Anti-Methanogenic Additives. Antibiot. 9(9): 601. https://doi.org/10.3390/antibiotics9090601
  • Akintunde AO, Omole CA, Sokunbi OA, Lawal TT, Alaba O (2011). Response of growing pigs to diet physical form and Allzyme® SSF supplementation in a palm kernel meal-based diet. Anim. Prod. 13 (2): 69-75.
  • Alshelmani MI, Loh TC, Foo HL, Sazili AQ, Lau WH (2017). Effect of feeding different levels of palm kernel cake fermented by Paenibacillus polymyxa ATCC 842 on broiler growth performance, blood biochemistry, carcass characteristics, and meat quality. Anim. Prod. Sci. 57: 839-848. https://doi.org/10.1071/AN15359
  • Ao, X, Zhou TX, Meng QW, Lee JH, Jang HD, Cho JH, Kim IH (2011). Effects of a carbohydrase cocktail supplementation on the growth performance, nutrient digestibility, blood profiles and meat quality in finishing pigs fed palm kernel meal. Livest. Sci. 137: 238–243. https://doi.org/10.1016/j.livsci.2010.11.014
  • Choe J, Kim KS, Kim HB, Park S, Kim J, Kim S, Kim B, Cho SH, Cho JY, Park IH, Cho JH, Song M (2017). Effect of protease on growth performance and carcass characteristics of growing-finishing pigs. S. Afri. J. Anim. Sci. 47(5): 697-703. https://doi.org/10.4314/sajas.v47i5.13
  • Dlamini ZC, Langa RLS, Aiyegoro OA, Okoh AI (2017). Effects of probiotics on growth performance, blood parameters, and antibody stimulation in piglets. South African J. Anim. Sci. 47(6): 766–775. https://doi.org/10.4314/sajas.v47i6.4
  • Düsterhöft M, Posthumus A, Voragen AGJ (2006). Non-starch polysaccharides from sunflower (Helianthus annuus) meal and palm-kernel (Elaeis guineensis) meal-investigation of the structure of major polysaccharides E-M. J. Sci. Food Agric. 59(2):151–160. https://doi.org/10.1002/jsfa.2740590204
  • Eze JI, Onunkwo JI, Shoyinka SVO, Chah FK, Ngene AA, Okolinta N, Nwanta JA, Onyenwe IW (2010). Haematological profiles of Pigs raised under intensive management system in South-Eastern Nigeria. Nigerian Vet. J. 31 (2):115-123. https://doi.org/10.4314/nvj.v31i2.68958
  • Jandhyala SM, Talukdar R, Subramanyam C, Vuyyuru H, Sasikala M, Reddy DN (2015). Role of the normal gut microbiota. World. J. Gastroenterol. 21:8787-8803. https://doi.org/10.3748/wjg.v21.i29.8787
  • Józefiak D, Ptak A, Kaczmarek S, Maćkowiak P, Engberg RM (2011). Exogenous supplementation of carbohydrases lowers serum insulin and cholesterol and improves the nutritive value of full-fat rapeseed in chickens. J. Anim. Feed Sci. 20(1): 107-117. https://doi.org/10.22358/jafs/66162/2011
  • Kilic U, Saricicek BZ, Garipoglu AV (2006). Effect of enzyme supplementation to the rations in which soybean meal replaced by Canola meal on performances of broilers. Asian J. Anim. Vet. Adv. 1(1): 76-81. https://doi.org/10.3923/ajava.2006.76.81
  • Kim S, Kim B, Kim Y, Jung S, Kim Y, Park J, Song M, Oh S (2016). Value of palm kernel co-products in swine diets. Korean J. Agric. Sci. 43(5): 761-768. https://doi.org/10.7744/kjoas.20160079
  • Kononenko SI, Gorkovenko LG (2011). Broad spectrum enzymatic agent ronozyme wx in pig feeding. Scientific Papers: Series D, Animal Science-The International Session of Scientific Communications of the Faculty of Animal Science. 54.
  • Min Y, Choi Y, Choe J, Kim Y, Jeong Y, Kim D, Kim J, Jung H, Song M (2019). Effects of dietary mixture of protease and probiotics on growth performance, blood constituents, and carcass characteristics of growing-finishing pigs. J. Anim. Sci. Technol. 61(5): 272. https://doi.org/10.5187/jast.2019.61.5.272
  • Mirnawati YR, Marlida Y, Kompiang P (2011). Evaluation of palm kernel cake fermented by Aspergillus niger as substitute for soybean meal protein in the diet of broiler. Int. J. Poult. Sci. 10: 537–541. https://doi.org/10.3923/ijps.2011.537.541
  • Mitruka BM, Rawnsley HM (1977). Chemical biochemical and haematological reference values in normal experimental animals. Masson, New York. Masson publishing: 287-380.
  • Naqid IA, Owen JP, Maddison BC, Gardner DS, Foster N, Tchórzewska MA, La Ragione RM (2015). Prebiotic and probiotic agents enhance antibody-based immune responses to Salmonella Typhimurium infection in pigs. Anim. Feed. Sci. Technol. 201: 57-65. https://doi.org/10.1016/j.anifeedsci.2014.12.005
  • Njoku CP, Adeyemi OA, Sogunle OM, Aina ABJ (2015). Growth performance, carcass yield and organ weight of growing pigs fed different levels of feed. Slovak J. Anim. Sci. 48 (1):16–22.
  • Nkosi BD, Seshoka ML, Fourie PJ, Kanengoni AT, Malebana IMM, Thomas RS (2020). Dietary enzyme addition on the growth performance and carcass characteristics of pigs fed diets containing avocado oil cake silage. Trop. Anim. Health Prod. 52:2945-2953. https://doi.org/10.1007/s11250-020-02312-8
  • Nyachoti CM, de Lange CFM, McBride BW, Leeson S, Schulze H (2000). Dietary influence on organ size and in vitro oxygen consumption by visceral organs of growing pigs. Livest. Prod. Sci. 65:229–237. https://doi.org/10.1016/S0301-6226(00)00157-3
  • Ojediran TK, Ajayi AF, Emiola IA (2019a). Effects of processing methods and levels of inclusion of Jatropha curcas kernel meal on performance, organ characteristics, haematology and serum chemistry of finisher broiler chickens. J. Agric. Sci. 64(1): 69-83. https://doi.org/10.2298/JAS1901069O
  • Ojediran TK, Bamigboye DO, Olonade GO, Ajayi AF, Emiola IA (2019b). Growth response, cost benefit, carcass characteristics and organoleptic properties of pigs fed biscuit dough as a replacement for maize. Acta fytotechn et zootechn. 22(2): 58–63. https://doi.org/10.15414/afz.2019.22.02.58-63
  • Ojediran TK, Olayiwola S, Adeyeye M, Ajayi AF, Emiola IA (2020). Effects of Palm Kernel Meal-Based Diet with or without Enzyme Supplementation on Growth Performance, Economic Benefits and Villi Morphometry of Weaned Pigs. Pol. J. Natur. Sc., 35(2): 129–139.
  • Oladokun AA, Wahab A, Rahman N, Suparjo M (2016). Prospects of maximizing palm kernel cake utilization for livestock in Malaysia: A review. J. Biol. Agric. Healthcare. 6(13): 65–69.
  • O’Shea CJ, McAlpine PO, Solan P, Curran T, Varley PF, Walsh AM, Doherty JVO (2014). The effects of protease and xylanase enzymes on growth performance, nutrient digestibility, and manure odour in grower-finisher pigs. Anim. Feed Sci. Technol. 89: 88-97. https://doi.org/10.1016/j.anifeedsci.2013.11.012
  • Ravindran V, Son JH (2011). Feed enzyme technology: present status and feed developments. Recent Pat. Food Nutr. Agric. 3:102–109. https://doi.org/10.2174/2212798411103020102
  • Sathitkowitchai W, Nitisinprasert S, Keawsompong S (2018). Improving palm kernel cake nutrition using enzymatic hydrolysis optimized by Taguchi method. 3 Biotech. 8(10), 407. https://doi.org/10.1007/s13205-018-1433-6
  • Sharmila A, Alimon AR, Azhar K, Noor HM, Samsudin AA (2014). Improving nutritional values of palm kernel cake (PKC) as poultry feeds. Rev. Mal. J. Anim. Sci. 17(1): 1–18.
  • Stephenson EW, DeRouchey JW, Escobar J, Woodworth J, Tokach MD, Goodband RD, Dritz. SS (2014). Effects of a novel protease enzyme (CIBENZA DP100) on finishing pig growth performance and carcass characteristics. Kans Agric. Exp. Stn. Res. Rep. 69–76. https://doi.org/10.4148/2378-5977.6912
  • Thorn CE (2000). Normal haematology of the pig. In: Chalm’s veterinary haematology. Ed. B.F. Feldman, J.G. Zinkl, N.C. Jain, 5th edition, Blackwell Publishing, Narayana Press, Denmark, pp. 1085–1095.
  • Unigwe CR, Raji AM, Ajayi JO, Popoola, Balogun FA, Adekunle FO (2017). Carcass, organ weights and histo-morphology of internal organs of sows fed fermented and enzyme-supplemented cassava peels meal (CPM) based diets. J. Plant Anim. Sci. 2(1), 026-036.
  • Wang D, Zeng Z, Piao X, Li P, Xue L, Zhang Q, Han X, Zhang H, Dong B, Kim SW (2011). Effects of keratinase supplementation of corn-soybean meal-based diets on apparent ileal amino acid digestibility in growing pigs and serum amino acids, cytokines, immunoglobulin levels and loin muscle area in nursery pigs. Arch. Anim. Nutr. 65: 290-302. https://doi.org/10.1080/1745039X.2011.586140
  • Wenk C (2001). The role of dietary fibre in the digestive physiology of the pig. Anim. Feed. Sci. Technol. 90:21–33. https://doi.org/10.1016/S0377-8401(01)00194-8
  • Wu HJ, and Wu E (2012). The role of gut microbiota in immune homeostasis and autoimmunity. J. Gut. Microbes. 3: 4-14. https://doi.org/10.4161/gmic.19320
  • Yan L, Meng QW, Kim IH (2012). Effects of fermented garlic powder supplementation on growth performance, nutrient digestibility, blood characteristics and meat quality in growing-finishing pigs. Anim. Sci. J. 85(5):411-417. https://doi.org/10.1111/j.1740-0929.2011.00973.x
  • Zamora V, Figueroa JL, Reyna L, Cordero JL, Sanchez-Torres MT, Martinez M (2011). Growth performance, carcass characteristics and plasma urea nitrogen concentration of nursery pigs fed low-protein diets supplemented with glucomannans or protease. J. Appl. Anim. Res. 39:53-6. https://doi.org/10.1080/09712119.2011.565217
  • Zuo J, Ling B, Long L, Li T, Lahaye L, Yang C, Feng D (2015). Effect of dietary supplementation with protease on growth performance, nutrient digestibility, intestinal morphology, digestive enzymes, and gene expression of weaned piglets. Anim. Nutr. 1: 276-282. https://doi.org/10.1016/j.aninu.2015.10.003
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    Journal of Animal Health and Production

    October

    Vol. 11, Iss. 3, Pages 234-329

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