Livestock Research for Rural Development 15 (1) 2003 | Citation of this paper |
The potential of sweet potatoes as an
ingredient for broiler chicken feed is not well known in
Increasing the proportion of sweet potato meal in the starter diet negatively influenced weight gain, food intake and food conversion. However, it had no effect on weight gain when included up to 50% in finisher diets. The relative weight of the pancreas, gizzard, intestines and caeca increased with increasing sweet potato meal inclusion. There were no differences in carcass composition among treatment groups. Inclusion of sweet potato meal up to 50 % in finisher diets had no adverse effects on the performance of the broilers.
The recommended level of sweet potato
inclusion in the present study is 50 % in finisher diets and none in starter diets.
Poultry is an important source of protein to the
ever-expanding population in rural areas. The cost of feed has been indicated by farmers in the smallholder sector as the major
constraint in poultry production (Munyawu et al 1998). The
poultry producers have experienced a rise in the cost of production due to the increasing
cost of feed. The cost of the maize ingredient, which makes 65 % of the current poultry
feeds, is very high (Scott 1995; Mutetwa 1996). Maize also
happens to be the staple food in
Maize and sweet potato have comparable metabolizable values of 14.5
and 14.8, respectively (Woolfe 1992).
The digestibility of sweet potato carbohydrate fraction is reported to be above 90 % (Ravindran 1995). However, the level of starch decreases with period
of storage and instead the level of reducing sugars, total sugars and total dextrins
increases (Woolfe 1992). Sweet potatoes have also been reported to exhibit trypsin inhibitor activity
ranging from 20 to 90 % inhibition (Woolfe
1992). However, Ravindran (1995) reported that trypsin
inhibitor levels present in sweet potato tubers are low and should not be a cause for
concern under practical situations. A recent study carried out in
The research was conducted at the University of Zimbabwe, Department of Animal Science bioassay laboratory.
Clean and uncontaminated raw sweet
potatoes were obtained from Murewa communal areas. They were
sliced into chips and dried before milling using a Hippo 1½ hammer miller with no
screen. Maize was purchased from a local farm. The rest of the ingredients were purchased
from a reputable milling company. Manual mixing was employed to prepare the feeds. Sweet
potato flour samples were analysed to determine their proximate composition and gross
energy before inclusion into diets. All the laboratory analyses were carried out in
duplicate following the AOAC (1990) protocol. The five diets were formulated to have
0, 25, 50, 75 and 100 % sweet potato replacement of maize (Tables 1 and 2).
Samples of each formulated diet were analysed to determine their proximate composition
(Table 3).
Table 1. Broiler
starter diets ingredients per tonne of feed. |
|||||
Ingredients,
kg
|
Sweet potato root meal replacing maize, % |
||||
0 |
25 |
50 |
75 |
100 |
|
White maize meal |
620 |
465 |
310 |
155 |
- |
Sweet potato flour |
- |
155 |
310 |
465 |
620 |
Extracted soya meal
|
300 |
300 |
300 |
300 |
300 |
Meat meal |
40 |
40 |
40 |
40 |
40 |
Wheat feed |
20 |
20 |
20 |
20 |
20 |
Limestone |
9 |
9 |
9 |
9 |
9 |
Mono-calcium Phosphate |
4 |
4 |
4 |
4 |
4 |
ıVit./mineral premix |
5 |
5 |
5 |
5 |
5 |
Salt (kg) |
2 |
2 |
2 |
2 |
2 |
ıThe vitamin and mineral
pre-mixes where based on NRC (1984) level of requirement |
Day-old (Cobb 500) broilers were bought from a reputable
breeder. The chicks were placed in an electrically heated wire-floored battery brooder for
six days. The birds received constant illumination and free access to water and feed.
After the six-day brooding period the birds were put on the
experimental diets. A total of 180 birds were randomly distributed among 5 treatments with
9 birds per cage and 4 cages per treatment. The birds were on the experimental starter
diet for 4 weeks and another 4 weeks on the finisher diets.
Table 2. Broiler finisher diets ingredients per tonne of feed |
|||||
Ingredients, kg |
Sweet potato root meal replacing maize, % |
||||
0 |
25 |
50 |
75 |
100 |
|
White maize Meal |
650 |
487.5 |
325 |
162.5 |
- |
Sweet potato flour |
- |
162.5 |
325 |
487.5 |
620 |
Extracted soya meal |
270 |
270 |
270 |
270 |
270 |
Meat meal |
40 |
40 |
40 |
40 |
40 |
Wheat feed |
20 |
20 |
20 |
20 |
20 |
Limestone |
9 |
9 |
9 |
9 |
9 |
Mono-calcium Phosphate |
4 |
4 |
4 |
4 |
4 |
ıVit./mineral premix |
5 |
5 |
5 |
5 |
5 |
Salt (kg) |
2 |
2 |
2 |
2 |
2 |
ıThe vitamin and mineral pre-mixes where based on NRC (1984) level of requirement |
Table 3: Proximate composition of diets, % # |
|||||
Sweet potato root meal replacing maize, % |
|||||
0 |
25 |
50 |
75 |
100 |
|
Starter
diets
|
|||||
Crude protein |
22.8 |
22.1 |
22.3 |
21.7 |
21.5 |
Ether extract |
1.9 |
1.6 |
1.5 |
0.69 |
0.66 |
Ash |
2.8 |
2.8 |
2.6 |
2.6 |
2.5 |
Crude fibre |
2.94 |
3.0 |
3.0 |
3.11 |
3.4 |
*ME (MJ/kg) |
10.9 |
10.6 |
10.8 |
10.7 |
10.3 |
Finisher diets |
|||||
Crude protein |
18.8 |
18.2 |
18.1 |
17.8 |
17.9 |
Ether extract |
3.3 |
2.8 |
2.6 |
1.9 |
1.9 |
Ash |
3.0 |
2.7 |
2.8 |
2.8 |
2.6 |
Crude fibre |
3.5 |
3.3 |
3.2 |
3.2 |
3.1 |
*ME, MJ/kg |
10.3 |
10.6 |
10.3 |
11.2 |
10.5 |
#Air-dry basis * ME: Metabolisable
energy (Derived from Macdonald et al 1995) |
Measurements
Records on feed intake and live weight
were taken weekly. Relative weight of the gizzard, pancreas and gastrointestinal tract
segments (intestines and caecum) to mass of broilers were
measured and calculated at slaughter. At the
termination of the experiment a bird from each cage was sacrificed by cervical
dislocation. The birds were cut along the midline and half of the sample from each bird
was ground in a mincer (Kusina
1988) to determine crude protein, ether extract, ash, calcium and phosphorous following
AOAC protocol (1990).
All data were subject to analysis of variance and means were
separated using Dunnetts test (SAS 2000). The effects of
sweet potato meal sweet potato meal on the variables measured were analysed using the
General Linear Models of SAS (2000). Data were analysed as a completely randomized design
and were presented as the means of each group and pooled standard error.
Feed intake, live weight gains, mortality and
feed conversion ratio are summarized in Table 4. The inclusion of sweet potato had a
negative effect (P<0.05) on performance of birds. There was a significant decline in
weight gain of birds with increase in inclusion rate of sweet potato meal during the
starter phase. There was a numerical decline in feed intake although no significant
difference up to 75% maize replacement rate. There was no difference (P<0.05) in feed
conversion of birds up to 50% maize replacement but it continued to deteriorate with
increase in inclusion of sweet potato meal.
Inclusion of sweet potato meal negatively
affected growth rate and feed conversion of birds during the finishing phase. Feed intake
of birds on the finisher diet was lower (P<0.05) than the control at maize replacement
rates at and above 75%. Mortality increased with increase in sweet potato maize
replacement level in the diets beyond the 25% level. Inclusion of sweet potato had an
effect (P<0.05) on the size of digestive organs (Table 5). The relative weights of the
pancreas, intestines and caeca were significantly higher
(P<0.05) for birds on and above 50% maize replacement rate. There was an increase in
size of the pancreas with increase in sweet potato concentration of the diet. There was no
difference (P>0.05) in relative weight of the gizzard across diets. The length of the
intestines was significantly shorter among birds on diets with 75% and 100% maize
replacement by sweet potato. Birds on diets containing 50% maize replacement by sweet
potato passed watery droplets. Inclusion of sweet potato in the diets had no effect (P>0.05) on
carcass quality of broilers at eight weeks of age.
Table 4: Performance traits of broiler chickens fed diets with varying levels of sweet potato meal |
||||||
Sweet
potato maize
replacement, % |
||||||
0% |
25% |
50% |
75% |
100% |
SEM |
|
Starter phase (1-4 wk) |
||||||
Weight gain (g) |
575a |
462b |
377c |
290d |
238e |
18 |
Feed intake (g) |
1151a |
1056a |
972ab |
917ab |
707b |
72 |
Feed conversion |
1.95a |
2.38ab |
2.58ab |
3.16b |
3.00b |
0.21 |
Finisher phase (4-8 wk) |
||||||
Weight gain (g) |
1309a |
1123a |
1030a |
675b |
396b |
65 |
Feed intake (g) |
3243a |
3523a |
3211ab |
2379c |
2659bc |
128 |
Feed conversion |
2.52a |
3.16a |
3.13a |
3.74a |
6.62b |
0.54 |
Mortality (%) |
2.9 |
2.1 |
6.1 |
8.3 |
11.1 |
- |
abcd Means in the same row bearing a different letter differ at P < 0.05 |
The CP, EE and CF content of sweet potato meal were slightly lower in this
study compared to the values reported by Ravindran and Blair
(1991). The variation can be attributed to differences in varieties, geographical areas
and the conditions under which the plant was grown. The ash content of the sweet potato
meal used in this study was similar to that reported by Ravindran
and Blair (1991). The starter and finisher diets had crude protein contents, which were
within the recommended range (NRC 1984). The energy content was similar across treatment
diets. This means that maize and sweet potato are similar in energy content, an
observation also made by Ravindran and Blair (1991).
Live weight gain and feed conversion were negatively associated with replacement rate of maize by sweet potato meal (Figures 1 and 2).
Figure 1: Effect on weight gain of broilers of replacing maize by sweet potato root meal
Figure 2: Effect on conversion of broilers of replacing maize by sweet potato root meal
The decrease in weight gain with an increase in
level of sweet potato in the starter diet could have been a result of decrease in feed
intake of birds on 100% sweet potato meal and poor nutrient utilisation
by birds on 75% and 100% maize replacement by sweet potato meal. A decrease in feed intake
of birds with increasing levels of sweet potato concurred with observations made by Tewe (1991). Feed intakes of birds on 25%, 50% and 75% maize
replacement levels were lower than intake of birds on the control diet, which could have
been a reflection of poor palatability and acceptability of sweet potato to broilers
according to Banser et al (2000). Feed
conversion ratio deteriorated with increasing level of sweet potato flour in the diet
which agrees with the report of Tewe (1991). The decrease in
the efficiency of utilization of feed was attributed by Agwunobi
(1999) and Tewe (1991) to the increased rate of passage. Tewe (1991) reported that sweet potato tuber was not efficiently utilised by young chicks of less than two weeks of age. Ravindran (1995) attributed this to the presence of anti-nutritional factors like trypsin
inhibitors in sweet potatoes.
Table 5: Carcass composition and internal organ characteristics (CDM = cold dressed mass) of birds fed diets with varying levels of sweet potato meal |
||||||
|
Sweet potato maize replacement, % |
|||||
0% |
25% |
50% |
75% |
100% |
SEM |
|
As % of fresh weight |
|
|
|
|
|
|
Dry matter |
35.0 |
33.9 |
32.9 |
33.6 |
33.1 |
0.77 |
Crude protein |
22.7 |
22.0 |
21.5 |
21.0 |
20.8 |
1.08 |
Ether extract |
10.6 |
10.4 |
9.85 |
9.77 |
8.74 |
0.52 |
Ash |
3.19 |
3.27 |
3.43 |
3.64 |
4.01 |
0.28 |
Calcium |
0.73 |
0.77 |
0.81 |
0.84 |
0.85 |
0.13 |
Phosphorous |
0.28 |
0.28 |
0.28 |
0.29 |
0.32 |
0.04 |
Internal organs, g/100g CDM |
|
|
|
|
||
CDM |
1670a |
1280b |
1140bc |
880cd |
760d |
60 |
Pancreas |
0.27a |
0.45ab |
0.46b |
0.61bc |
0.79c |
0.04 |
Gizzard |
3.87 |
4.30 |
3.91 |
4.29 |
4.59 |
0.46 |
Caeca |
0.50c |
0.72bc |
0.84abc |
1.05ab |
1.13a |
0.08 |
Intestines |
|
|
|
|
|
|
Length (m) |
1.97a |
1.86a |
1.66ab |
1.40b |
1.62b |
0.06 |
Weight, g/100g CDM |
1.90a |
2.47a |
3.39a |
3.82b |
3.94b |
0.45 |
abcd Means in the same row bearing a different letter differ at P < 0.05. |
A similar trend for reduced live weight gain
with increasing level of sweet potato meal was observed during the finisher phase (Figure
1). The degree of recovery of birds on the 50% maize replacement level
suggests that the birds had undergone a period of compensatory growth after digestive
tract adaptations had occurred (Banser et al 2000). The lower
feed intake at 75% maize replacement, could be due to smaller
gut size at the start of the finisher phase since there is a physical limit to the gastro
intestinal tract capacity resulting in reduced feed intake. The feed conversion
ratio at 100% maize replacement was pooer than the control, which is consistent with other
reports (Tewe 1991; Agwunobi
1999). The feed conversion was generally poorer for birds on the finisher diets compared
to those on the starter diets, which is a normal phenomenon according to Mutetwa (1996). From Figure
2 it
can be deduced that broiler chickens fed on sweet potato meal grew less rapidly than those
on a diet containing maize. Birds fed a diet containing 50% of maize replaced by sweet
potato showed a tendency to select against the sweet potato component, and this was
associated with a much higher feed wastage due to the jerky movement
of the head when selecting the feed. This resulted in an over estimate of the amount of
feed consumed. Selection against sweet potato was made easier due to the differences in
particle size of the sweet potato and maize meals. The lower resistance of sweet potato to
grinding, as compared to maize, resulted in a smaller particle size of the sweet potato
meal.
The depression in weight gain of birds given
sweet potato meal was associated with changes in the relative weight of the organs, which
implies an involvement of anti-nutritional factors. The results from this study clearly
showed that there was pancreatic hypertrophy, which was observed to increase with
increasing levels of sweet potato in the diets. Pancreatic hypertrophy is caused by the
presence of trypsin inhibitors in the diet (Nishino et al
2001). This has frequently been observed in rats (Nishino et al 2001) and chicks (Viveros
et al 2001). The increase in size of the pancreas can be used as a crude indicator of trypsin inhibitor levels in a feed. Suppression of trypsin in the intestine increases pancreatic secretion of the
enzymes through a feedback mechanism, which is mediated by cholecystokinin
(CCK) and, consequently induces pancreatic hypertrophy and hyperplasia (Nishino et al 2001).
CCK induces gut motility. The plasma levels of
CCK are ultimately affected and there is an increase in gut motility. Increased motility
is likely to increase the muscle mass of the intestines, caeca
and rates of passage. Gut motility affects rate of passage, which ultimately affects
utilization of nutrients. Therefore a sequence of events that are triggered by trypsin inhibitor results in poor nutrient utilization through
increase in passage rates and loss of endogenous and exogenous nitrogen. Trypsin inhibitors increase the loss of endogenous proteins such as
digestive enzymes, which can be rich in essential amino acids (Viveros
et al 2001).
The increase in the weight and length of the
lower parts of the guts can be attributed to the bulkiness of the diets with sweet potato
as a direct substitute of maize. Bulkiness of a diet results in the bird taking in a large
volume of the feed in order to satisfy its nutrient requirements ultimately exerting a
pressure, which stretches the intestines (Hetland and Svihus 2001). The increase in the weight of digestive organs of
birds can be attributed, to some extent, to the presence of a high concentration of
indigestible materials in the intestine of the animal (Viveros
et al 2001).
Mortality was high among birds on a diet with 100% replacement of maize by sweet potato . This could have been due to
a sudden change of diet, which stressed the birds. Of the total mortalities, 84.7% occurred
during the first week of feeding the experimental diets. Birds
that died had watery and whitish diarrhoea, The high soluble
sugar content of sweet potato might have been the cause of the gastrointestinal disorders
in the poultry. However,
Tewe (1991) and Ravindran and Sivakanesan
(1996) showed that the level of sweet
potato meal in broiler diets had no effect on mortality rate in their studies. Post-mortem results revealed that the birds in the present
experiment had an erosion of the gizzard,
this is when the cuticle of the gizzard separates from the mucosa.
The results showed that the level of sweet potato
meal inclusion into broiler diets had no effect on the chemical composition of the
carcass at eight weeks of age. However, Woolfe (1992) observed that the
fat content of broilers fed with sweet potato meal was significantly lower than that of
those fed with maize meal at 10 weeks of age. The difference in these findings may
be due to differences in age since older animals deposit more fat
compared to young animals (Kusina 1988). However, in this
study there was a tendency for a decline in fat content as
the level of sweet potato meal in the diet increased.
The addition of sweet potato meal in broiler starter diets had a negative effect on the performance of the birds. However, sweet potato could be included in broiler finisher diets at 50 % maize replacement without adversely affecting productivity. The above recommendation has been made, assuming that the farmer has the sweet potato at their disposal.
Future studies should also explore the possibility of increasing the maize replacement level beyond 50 % through pelleting the sweet potato diets to reduce selection against the sweet potato ingredient.
There is also a need to investigate the optimum storage conditions that will reduce the level of soluble sugars in sweet potato containing diets since these have been reported to cause gastrointestinal disorders.
Additional studies are necessary in order to
determine the role of trypsin inhibitors in sweet potatoes on the bioavailability of
nutrients and also the best processing methods to deactivate these. Crop breeders are
encouraged to start a sweet potato variety selection programme for varieties with low
trypsin inhibitory activity, which could be used for animal
feed.
Mr T
Rukuni, the director of Development Technology Centre (DTC), is gratefully
acknowledged for facilitating the financing of this study. The technical assistance
of Mr Karosi and Mr Sena is
gratefully acknowledged.
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Received 7 June 2002, accepted 6 September 2002