A study of Aspergillus niger- hydrolyzed cassava peel meal as a carbohydrate source on the histology of broiler chickens.

The purpose of this study is to investigate the effect of hydrolysed cassava peel inclusion as a replacement for maize in broiler chicken feedstuff on the histology of the internal organs of broiler chickens. Thirty six, two weeks old unsexed broiler chickens were used for the study in a feeding trial of forty two days. The chickens were randomly allocated to six dietary treatments A - F using a completely randomized design. Each treatment group contained two replicates of three broiler chickens. Group A chickens (A1 and A2) were fed with the control diet (0% hydrolyzed cassava peel as main carbon source). Groups B-E (in replicates 1 and 2) were administered with experimental diets containing 25%, 50%, 75%, 100% of hydrolyzed cassava peels respectively replacing maize while group F (F1 and F2) were fed with diet containing 100% unhydrolyzed cassava peels replacing maize as the main carbon source. Feed and water were supplied ad libitum for the six weeks feeding trials period. Vaccine and drugs were administered as at when due. At the end of the third week, two replicate per group were fasted for twelve hours and slaughtered. Samples of liver, kidney and heart were collected and tissue samples were taken for histological examinations. All the chickens in group F that fed on unhydrolyzed cassava peel recorded 100% mortality within the first six days of the feeding trials while those in groups A to E recorded 0% mortality. Histology of the kidney, heart and liver showed increasing mark of coagulative necrosis, degeneration of the hepatocytes and vacuolations due to the shrinking of the hepatocellular and cardiac tissues as the cassava inclusion level increases in feed. It is concluded that birds can be fed with maize replaced with up to 50% hydrolyzed cassava peel in chicken feeds without serious deleterious effects and that the wastes have useful products in animal nutrition. Also, the replacement added economic in chicken production. The hydrolysis has led to a reduction in the potency of cyanide in the peel thereby making it a safe and possible candidate in the production of chicken feeds.

Introduction

The world shortage of cereals global inflationary trends coupled with the use of maize as raw material for ethanol production in the vulnerable bio- fuel industry around the world necessitates the development of livestock feeding systems which are independent of maize and other cereals (Moo-young et al. 1987; Christopher –Berg 2006; Kayode 2009 FIDAAfrique- IFADAfrica 2010). It is for this reason that in Nigeria, recent emphasis is placed on “backward integration” a design by the federal government to encourage industrialists, food scientists, livestock farmers and manufacturers to rely on local sources of raw materials which has previously depended on importation (Sani et al. 1992; Aletor 1990; Kayode 2009; Adeyemo 2003). That food scarcity is a plague in many developing countries of the world, including Nigeria where daily intake of animal protein per caput falls far below the normal intake as recommended by FAO (1986), is not in doubt. To alleviate this situation, it has been realized that broiler production is the fastest and easiest route (Nworgu et al.2000; Dipeolu et al.1996; Larry 1993) since they are prolific, possess a high feed conversion ratio and are accepted by all, irrespective of religion. However, feed cost are presently very high and makes up to 60-70% (Larry 1993) or 70-80% (Oruwari et al.1995) of the total cost of production in Nigeria compared to 50-70% in developed countries (Thackie and Flenscher 1995). This therefore highlights the importance of feed management to broiler producers.

Thus it is necessary to reduce the cost of feeds in order to produce cheaper products without affecting profits. Since energy source constitutes 45-60% of finished feeds for monogastric animals (Steiner et al. 1994) and birds eat to satisfy their energy requirement (Sibbald 1982), cassava peels which is available in large quantity is being investigated to serve as alternative main energy source in broiler feedstuffs (Belewu and Banjo 1999; Hafeni et al. 2013; Sabiiti 2011). Although several authors have reported suboptimal performance or death when monogastrics are fed cassava peel based diets claiming these are due to the cyanide content of the cassava peel. However, little attention has been given to the evaluation of the effects of intake of residual cyanide in processed cassava peel on the histology of internal organs of broiler chickens. This study was therefore designed to address this issue.

Materials and methods

Cassava peel was collected from from five agricultural waste dumpsites in Ilorin metropolis, Kwara state. They were then dried in an oven at 80°C and then ground into very fine powder. The ground powder was dried into constant weight in an oven at 60°C and their proximate analyses determined by AOAC 2000 method. Cyanide content was determined using the modified method of picrate paper kit as developed by Bradbury et al. (1999). The grounded powder was stored in a desiccator until required.

Source and maintenance of organisms

Five grams of the freshly obtained peel was taken from the sealed cellophane bags (with which they were collected from source) into sterile universal bottles containing 100 ml of distilled water and shaken thoroughly. The settled supernatants were decanted off into separate test tubes serving as stock solutions. Serial dilutions of the stock were made with 0.1 ml of the aliquot spread on Potato Dextrose Agar (PDA) figures containing 1% streptomycin. (to inhibit bacterial growth). The figures were incubated at room temperature (27 – 31°C) for 48 hours (Lawal et al. 2005; Berghem et al. 1976; Chahal 1992, Bukoye 2001). After incubation, representative fungal colonies were picked from each figure and purified on fresh PDA figures. The purified isolates were transferred to PDA slants incubated at room temperature for 48 hours and stored at 4°C. The isolates were identified according to the scheme of McGinnins (1980).

Screening for cellulose Production

The method of Bisaria and Ghose (1981) was used. Point inoculations of the spores of the isolates were grown on PDA supplemented with Carboxylmethylcellulase (CMC, 2% W/V) medium. The figures were incubated at room temperature (27°C- 32) for 72 hours after which it was stained with 2% Congo red solution for 15 minutes. Excess dye was removed by washing with 1 M NaCl and the figures were fixed with 1 M HCl. The production of extracellular cellulase by the organism was indicated by a zone of clearance around the fungal colonies on the figure. The zone of clearance was measured on each figure and the average determined. Aspergillus niger AC4 showing the biggest zone of clearance was selected for further studies.

Production of crude cellulase

Mineral salts media (MSM) for cultivation of fungal isolates was prepared with compositions as shown below {g/l}. KH2PO 4, 10 g; (NH4)2SO4, 10.5 g; MgSO4.7H2O, 0.3 g; CaCl2, 0.5 g; FeSo4, 0.013 g; MnSO4.H2O 0.04; ZnSO4.7H2O 0.04; Yeast extract 0.5 g; Carbon source 40 g( The carbon sources were delignified cassava peel and carboxylmethylcellulase). One hundred and fifty millilitre of each medium was dispersed into conical flask and sterilized in the autoclave at 121°C for 15 minutes. The final pHs of the medium was adjusted to 5.0 with 0.1 M NaOH and 0.1 M HCl using a pH meter (pyeunicam pH).Spores of 72 hour old cultures of Aspergillus niger AC4 were harvested by washing slants with 10 ml of sterile distilled water. An aliquot of 5 ml of the spore suspension was used to inoculate 150 ml of each of the prepared medium. The culture media were incubated at room temperature (27-32°C) in an orbital shaker (Gallenhamp, England) at 100 rpm for seven days.

Hydrolysis of cassava peel and CMC

The ability of the crude enzyme to hydrolyze cassava peel was studied using the grounded cassava peel sample while commercial carboxymethylcellulase (CMC) was used as the standard. Cellulase activity of the suction culture filtrate was determined colorimetrically by measuring the increase in reducing groups by the hydrolysis of Carboxylmethylcellulase (CMC) substrate and the cassava peel (Ali et al. 1991; Panda 1989). Cultured samples were filtered through whatmann filter paper to remove the mycelia and other particle. The filtrates were used to assay enzymatic activity. The reaction mixture containing 0.5 ml of the enzyme solutions and 1 ml of 2% (w/v) of the carbon sources were incubated at a temperature of 35°C for 20 minutes and the reactions stopped by adding 2.0 ml of DNS Reagent materials (1.0 g of 3,5-dinitrosalicylic acid, 20 ml of NaOH, 30 g of sodium potassium tartarate in 100 ml). The total mixture was then heated for 5 minutes, cooled and 20 ml of distilled water added. The colour intensity was determined at 560 nm using a spectrophotometer (Jenwey 6405 UV/visible). Cassava peel sample was found to have a cellulase activity of 240 U/ml while CMC gave a cellulase activity of 54 U/ml.

Experimental diets

The delignified hydrolyzed cassava peel and other ingredients were used to formulate starter and finisher diets respectively at 25%, 50%, 75% and 100% replacement value for maize to meet the NRC (1984) nutrient requirement of broiler chickens. The feed containing 100% maize was used as control. Soya bean oil was added to obtain equal metabolizable energy.

Experimental birds

A total of thirty two weeks old unsexed broiler chickens with average initial bodyweight of 0.685 ± 0.0027 g were divided into six (6) groups. They were bred and maintained in a six partitioned clean cage, with well-ventilated conditions (temperature 27 ± 5°C; photoperiod: 12 h natural light and 12 h dark; humidity: 45-50%). Cleaning of the cages was done daily. They were kept under this condition for the period of the experiment. The chickens were randomly allocated to six dietary treatments A - F using a completely randomized design. Group A chickens were fed with the control diet (0% hydrolyzed cassava peel as main carbon source). Groups B-E were administered with experimental diets containing 25%, 50%, 75%, 100% of hydrolyzed cassava peels respectively replacing maize as energy source while group F was fed with diet containing 100% unhydrolyzed cassava peels replacing maize as the main carbon source. Feed and water were supplied ad-libitum for the six weeks feeding trials period. Vaccine and drugs were administered as at when due.

Measurements

The study lasted for 42 days. At the end of the third week of the feeding trails, 2 birds per replicate were randomly selected, fasted for 12 hours to empty their gastrointestinal tract, weighed individually, slaughtered, and eviscerated. For histological analysis, tissue samples of each organ were taken, immersed in 10% formolsaline for 72 hours, and processed for paraffin embedding, using ethanol for dehydration and xylene as clearing agent. Sections from each organ were made at a thickness of 4 μm with a Leica rotary microtome, stained with hematoxylin-eosin, and examined by light microscope.

Data analysis

The data obtained were subjected to analysis of variance and the means were compared using the Duncan Multiple range test. A significant level of 0.05 was used. The experiments were all designed as a complete randomized design (CRD).

Result and discussion

Table 1 shows the proximate analysis of the cassava peel used during the period of the experiment. The result showed that cassava peel is very rich in carbohydrate content but very low in protein content as earlier reported by Tewe and Egbunike (2007). It also has a very high digestible energy but low in crude fibre. It has a cyanide content of 0.74 mg/100 g of cassava peel but after hydrolysis by the culture filtrate of the Aspergillus niger AC4, cyanide content reduced to 0.08 mg/100 ml. Table 2 shows the result of the proximate composition of the experimental feeds for each group A- E (Afe to Efe) and feaces from the birds in each group (Afc to Efc) for the five experimental chickens fed 0%, 25%, 50%, 75% and 100% in groups A- E respectively. There is increase in crude protein of faeces compared to the feed because of the presence of uric acid, the excretory product of the chickens that is egested with the faeces while there is a reduction in crude fibre a cellulolytic material because of its hydrolysis by the incorporated cellulase enzyme. There is a reduction in total ash of faeces compared to the feed because the chickens have made use of part of the mineral content of the feed. Crude fat increases because it has become concentrated in faeces since the faeces has absorbed more water as evident by the moisture content of faeces being higher than that of diets. All the chickens in group F that fed on unhydrolyzed cassava peel died within the first six days of the feeding trials. Protein retention of broilers also decreased with increase in cassava inclusion level but was not significantly different until inclusion level beyond 50%. the kidney and liver were moderately damaged such that their functions were hampered and some essential nutrients which should have been used for body building of the chickens were now passed out with the faeces hence the increase in protein content of the faeces compared to diets. This is similar to the result obtained by Muhammad and Oloyede 2009.

Table 1

Proximate analysis of the cassava peel

Carbon source	Dry matter (%)	Crude protein (%)	Carbo - hydrate (%)	Crude fat (%)	Crude fibre (%)	pH	Total ash (%)	Moisture content (%)	Nitrogen free extract (NFE)	Gross energy MJ/Kg	Digestible energy MJ/Kg	Cyanide mg/100 g
Cassava peel	90.94	4.15	93.5	0.84	3.35	5.7	4.37	9.06	67.70	1.65	1.03	0.74

Table 2

Proximate analysis of feeds and faeces ( Fed and egested respectively ) by the experimental chickens

Bird group	Moisture content (%)		Dry matter (%)		Crude protein (%)		Crude fat (%)		Crude fibre (%)		Total ash (%)		Cyanide (mg/100 g)
	Feed (fe)	Faeces (fc)	Feed (fe)	Faeces (fc)	Feed (fe)	Faeces (fc)	Feed (fe)	Faeces (fc)	Feed (fe)	Faeces (fc)	Feed (fe)	Faeces (fc)	Feed (fe)	Faeces (fc)
A	9.37b	11.84a	90.63b	88.16a	17.06d	22.09a	3.67ac	4.24 b	9.95ab	5.04a	25.06a	13.33a	0.08a	0.08a
B	7.74c	11.52a	92.26a	88.48a	15.09c	19.25b	3.24c	4.52b	9.50a	7.60bc	30.24c	14.86b	0.08a	0.08a
C	10.26a	11.20a	89.74ab	88.80a	14.43bc	17.50c	2.15b	3.76ab	9.55a	7.87bc	26.73a	20.96c	0.08a	0.08a
D	9.18b	12.38b	90.82b	87.62b	11.59a	18.59bc	2.67bc	3.78ab	11.19b	6.47b	30.44c	21.24bc	0.08a	0.08a
E	7.82c	11.24a	92.81a	88.76a	13.78b	17.50c	1.35a	3.37a	13.30c	7.92c	29.27b	23.44d	0.08a	0.08a

abcdMeans with different superscripts in a column are significantly different (p < 0.05).

Values are means of three replicate determinations.

The photomicrograph of the organs (Kidney, Liver and the Heart) of the control birds and those fed on experimental feeds 0%, 25%, 50%, 75% and 100% for groups A to E respectively are as shown on pages 10–12. Group A chickens were fed control diets while Groups B – E were fed experimental diets respectively. The kidneys of the birds fed with control diet in A were normal with black arrows showing glomerulus and vein as shown on Figure 1 while photomicrographs of Figures 2 and 3 reveals normochromic, mildly degenerated, hypercytic kidney tissues with black arrows showing degenerating glomeruli while white arrows are showing vacuolations due to the shrinking of the internal organelles. Figures 4 and 5 show degenerating glomeruli in hyperchromic, mildly degenerated, hypercytic kidney tissue with white arrows showing more visible vacuolations and black arrows showing degenerating glomeruli. Photomicrograph of the liver in Group A chickens revealed normal hepatocellular tissue with radiating hepatic cords and intact intestinal mucosa, muscle wall and serosa without any visible damage (Figure 6). Figures 7, 8, 9 and 10 however reveal mildly to moderately degenerating hepatocellular tissues with black arrows showing vacuolations while white arrows show the degenerating cells. Figure 11 shows the photomicrograph of the heart of chicken fed control diet A with normal cardiac muscle. Figures 12, 13, 14 and 15 show the photomicrographs of the heart of chickens fed experimental diets in groups B to E respectively revealing normochromic, normocytic tissue (Figures 12 and 13) and hyperchromic mildly degenerated cardiac tissues (Figures 14 and 15). The arrows indicate more visible vacuolations in the heart tissues.

Figure 1

Photomicrograph of kidney of chickens that fed on Hydrolyzed cassava peel at 0% as main energy source.

Figure 2

Photomicrograph of kidney of chickens that fed on Hydrolyzed cassava peel at 25% as main energy source.

Figure 3

Photomicrograph of kidney of chickens that fed on Hydrolyzed cassava peel at 50% as main energy source.

Figure 4

Photomicrograph of kidney of chickens that fed on Hydrolyzed cassava peel at 75% as main energy source.

Figure 5

Photomicrograph of kidney of chickens that fed on Hydrolyzed cassava peel at 100% as main energy source.

Figure 6

Photomicrograph of Liver of chickens that fed on Hydrolyzed cassava peel at 0% as main energy source.

Figure 7

Photomicrograph of Liver of chickens that fed on Hydrolyzed cassava peel at 25% as main energy source.

Figure 8

Photomicrograph of Liver of chickens that fed on Hydrolyzed cassava peel at 50% as main energy source.

Figure 9

Photomicrograph of Liver of chickens that fed on Hydrolyzed cassava peel at 75% as main energy source.

Figure 10

Photomicrograph of Liver of chickens that fed on Hydrolyzed cassava peel at 100% as main energy source.

Figure 11

Photomicrograph of Heart of chickens that fed on Hydrolyzed cassava peel at 0% as main energy source.

Figure 12

Photomicrograph of Heart of chickens that fed on Hydrolyzed cassava peel at 25% as main energy source.

Figure 13

Photomicrograph of Heart of chickens that fed on Hydrolyzed cassava peel at 50% as main energy source.

Figure 14

Photomicrograph of Heart of chickens that fed on Hydrolyzed cassava peel at 75% as main energy source.

Figure 15

Photomicrograph of Heart of chickens that fed on Hydrolyzed cassava peel at 100% as main energy source.

In conclusion, cassava peel which is readily available in large quantity and often treated as waste could be used to replace maize which is in high demand by microbial enzymes to enhance food (protein) production particularly in developing nations like Nigeria. This would strengthen food security and provide needed protein for man.

Compliance with ethical standards

All animal studies have been approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.