Feed Formulation: C. de Blas and G.G. Mateos
Feed Formulation: C. de Blas and G.G. Mateos
Feed Formulation
C. de Blas and G.G. Mateos
Departamento de Producción Animal, Universidad Politécnica de Madrid,
Ciudad Universitaria, 28040 Madrid, Spain
Introduction
This chapter deals with the nutritive allowances in practical feed formulation
for intensive meat rabbit production. In recent years, performance of
intensively reared rabbits has greatly increased because of improvements in
genetics, management and pathology. Productivity levels, measured as
reproductive yield, milk production or growth rate in the fattening period, are
comparable with those obtained in other intensively farmed domestic species.
However, rabbits are herbivorous animals and require a high dietary fibre
content (about one-third of cell wall constituents on an as-fed basis) to
prevent digestive disorders.
The average composition of commercial feeds in Spain (Table 13.1)
reflects this situation, as they typically contain simultaneously a high
proportion both of fibrous and highly concentrated ingredients. Furthermore,
rabbit diets must be primarily designed to allow a sufficient nutrient intake to
meet their high nutritive requirements per unit of body weight. Therefore,
factors affecting feed consumption, such as nutrient imbalances, raw material
composition and pellet quality, are major concerns in this species.
110
Live weight gain (g day −1)
100
90
80
70
100 150 200 250 300 350
ADF (g kg −1 DM)
Fig. 13.1. Effect of dietary ADF content on average daily gain during the fattening period. 100 =
control diet.
Feed Formulation 243
digestive disorders (Cheeke and Patton, 1980; de Blas et al., 1986) and a
slight decrease in DE intake (Fig. 13.1).
Three long-term studies (> 1 year) conducted with rabbit does have
compared seven diets containing from 162 to 216 g ADF kg–1 and no fat
added (Méndez et al., 1986; Barreto and de Blas, 1993; Cervera et al., 1993).
The results have shown that, over this period, rabbit does are able to maintain
DE intake by increasing consumption when dietary fibre content is increased.
Type of feed had no influence on reproductive performance, but litter weight
at weaning decreased (by about 11%) when dietary ADF content was above
180 g (equivalent to about 10 MJ DE kg–1).
In other work, de Blas et al. (1995) have studied the effect of the
substitution of starch for fibre in rabbit does using isoenergetic diets (10.6 MJ
DE kg–1). Five diets were formulated with increasing levels of neutral
detergent fibre (NDF; from 278 to 371 g kg–1) and ether extract (from 20 to
51 g kg–1) at the expense of the level of starch which decreased from 237 to
117 g kg–1. The type of diet had little effect on DM intake. However, the
regression analyses indicated that dietary levels of NDF, ADF and starch of
around 320, 170 and 180 g kg–1 respectively were optimal for maximal
reproductive performance, growth of young rabbits and feed efficiency (see
Fig. 13.2). The impairment observed in rabbits fed the highest levels of fibre
might be explained by higher fermentation losses in the caecum, together
with an insufficient uptake of glucose from the gut to meet the requirements
for pregnancy and milk lactose synthesis. The negative effects of high starch
concentrations in the diet were related to an increase in mortality through
diarrhoea.
Type of fibre
Several studies have shown that cell wall composition and physical structure
influence feed digestion in isofibrous diets (see Chapter 5).
Lucerne hay is the source of fibre most widely used in rabbit diets,
accounting for around one-third of commercial feeds in Spain (see Table
13.1). Lucerne hay is highly palatable and provides both long and digestible
fibre, which allows an adequate transit time of the digesta and a balanced
caecal flora to be maintained.
Moderate inclusion in the diet (100–150 g kg–1) of fibrous by-products
has little effect on rabbit performance (Motta, 1990; García et al., 1993).
However, an excessive substitution of lucerne hay by highly lignified sources
of fibre leads to a significant impairment both of average daily gain and feed
efficiency (by about 10 and 20%, respectively, in diets with a 50:50 ratio of
lucerne hay and grape marc; Parigi Bini and Chiericato, 1980; Motta, 1990).
A high dietary lignin content depresses energy digestibility and caecal
fermentative activity (García et al., 1996). Therefore, a similar impairment of
244 C. de Blas and G.G. Mateos
Fig. 13.2. Effect of dietary NDF content on performance of rabbit does and feed conversion rate
(base 100 = diet containing 371 g NDF kg–1) (de Blas et al., 1995).
Fat supplementation
The effect of the addition of 30 g of different sources of fat (tallow, lard,
deodorized oleins or sunflower oil) kg–1 in isofibrous diets for fattening
Feed Formulation 245
rabbits has been studied by several authors (Partridge et al., 1986; Santomá et
al., 1987; Fernández and Fraga, 1992). In these studies dietary protein (DP)
content was increased with fat addition to keep the DE:DP ratio as constant as
possible. Results showed that fat inclusion had a positive effect on energy
digestibility (5% on average) and feed efficiency (7%), but not on growth
rate, as feed intake decreased by 6%. No interaction was found between type
and level of supplemental fat. Therefore, the value of fat addition should be
established on an energy–cost basis, taking also into account the effects of fat
quality on carcass and pellet stability (see Chapters 10 and 12).
Several long-term (9–24 months) studies (Fraga et al., 1987; Maertens
and De Groote, 1988a; Barreto and de Blas, 1993; Cervera et al., 1993) have
studied the effect of fat addition in isofibrous diets (200 g ADF kg–1) on
performance of breeding does. Responses were higher for does than in
growing rabbits. The inclusion of 35 g fat kg–1 in diets of does increased DE
intake (by 14.5% on average), which promoted an increase in milk yield, and
litter weight at weaning (by 8.5%). Neither average weight of breeding does
nor fertility or prolificacy was significantly affected by type of diet, although
a trend was found for fat supplementation to lower mortality in litters
containing more than nine pups (Fraga et al., 1987). These results indicate
that the use of fat to increase energy concentration of feeds (over 11–11.5 MJ
DE kg–1) allows maximum milk production and litter growth in highly
productive rabbits, when the remaining constituents of the diet (fibre, protein
and starch) are kept in balance.
67
62
57
52
47
−1
DE)
Fig. 13.3. Effect of the dietary protein/energy ratio on the average growth rate in the fattening
period and content of fat in the empty body of rabbits at 2.25 kg (de Blas et al., 1981; Fraga et al.,
1983).
a decrease in milk production, growth of young rabbits, fertility and weight of
does. An excess of protein content related to energy decreases performance
and increases diarrhoea incidence and environmental pollution.
Table 13.2. Total amino acid requirements of growing-fattening rabbits (g kg–1 as-fed).
Table 13.3. Total amino acid requirements of breeding does (g kg–1 as-fed).
As for other species, there are more available data for growing rabbits
than for breeding does, as well as considerable variation between different
studies. Part of this variation can be explained by differences in the methods
used: purified vs. commercial diets, genetic potential of the animals and
energy concentration of the diets.
Other causes of variability are related to the different availability of the
sources of amino acids used (see Chapter 6). To take into account this effect,
recent studies (Taboada et al., 1994, 1996; de Blas et al., 1996) have
determined the lysine, sulphur and threonine requirements, expressed in
digestible (apparent faecal) instead of crude units. Results are shown in Table
13.4. Optimal values for growth were consistent with those obtained by
Moughan et al. (1988) based on the amino acid composition of the whole
body of 53-day-old rabbits (Table 13.5), although the latter method does not
consider the amino acid requirements for maintenance or the amino acid
248 C. de Blas and G.G. Mateos
Fig. 13.4. Effect of dietary threonine content on feed intake, reproductive performance and feed
efficiency of breeding does (base 100 = diet containing 3.44 g of digestible threonine kg–1) (de Blas
et al., 1996).
Table 13.4. Digestible (faecal apparent) amino acid requirements of rabbits (g kg–1 as-fed basis).
Optimal values
Amino acid Breeding does Fattening rabbits Reference
Lysine 6.4a 6.0 Taboada et al. (1994)
Methionine + cystine 4.9a 4.0 Taboada et al. (1996)
Threonine 4.4a 4.0 de Blas et al. 1996)
a
For maximal milk production. Reproductive performance did not improve above 5.2 g kg–1.
supply by the caecotrophs. The use of digestible amino acids in practical feed
formulation is still limited because of the lack of information on the amino
acid digestibilities for the main ingredients used in rabbit diets.
Table 13.5. Amino acid composition (mg g–1 N) of the whole body of 53-day-old New Zealand
rabbits (Moughan et al., 1988).
used: breeding does, fattening rabbits and a mixed feed for all the animals.
When rabbits are slaughtered at 2.5 kg, more than one fattening feed might be
used. In this case, Maertens and Luzi (1996) proposed decreasing the dietary
protein and amino acid content with age, to reduce N excretion without
altering performance. Several recent studies have studied the possibility of
formulating a special type of feed for starter rabbits (from 21 days of age).
However, the use of such diets is limited because of practical problems of
feed management. Breeding does and starting rabbits are commonly fed from
the same feeder in commercial farms. Therefore, the possibility of using two
different feeds is limited.
Energy concentrations in Table 13.6 have been determined from estimates
based on the optimal proposed levels of carbohydrates and fat. Essential
nutrient recommendations have then been referred to those concentrations.
However, DE content of fattening feeds can vary from 9.7 to more than
11.5 MJ kg–1 with no effects on rabbit performance. Changes in DE concen-
tration with respect to the values given in this table should be accompanied by
proportional parallel corrections in the contents of essential nutrients.
Minimal levels of fibre and maximum levels of starch are more critical
than maximum levels of fibre and minimum of starch, as they affect not only
performance but also mortality.
Recommendations for type of fibre include an optimal concentration for
lignin and a minimum level for long fibre particles. Both restrictions should
be followed simultaneously, as some highly lignified by-products can have an
insufficient content of long fibre.
Only the better established amino acid requirements are presented in
Table 13.6. Dietary tryptophan content can be estimated at 0.18–0.20 of the
optimal lysine concentration. For other essential amino acids, the ideal
protein pattern (Table 13.5) can be followed.
250 C. de Blas and G.G. Mateos
Table 13.6. Nutrient requirements of intensively reared rabbits as concentration kg–1 corrected to a
dry matter content of 900 g kg–1.
Table 13.7. Trace element and vitamin requirements of intensively reared rabbits as concentration
kg–1 corrected to a dry matter content of 900 g kg–1.
References
Adamson, I. and Fisher, H. (1973) Amino acid requirements of the growing rabbit: an
estimate of quantitative needs. Journal of Nutrition 103, 1306–1310.
Barreto, G. and de Blas, C. (1993) Effect of dietary fibre and fat content on the
reproductive performance of rabbit does bred at two remating times during two
seasons. World Rabbit Science 1, 77–81.
Berchiche, M. and Lebas, F. (1994) Supplémentation en méthionine d’un aliment à
base de feverole: effets sur la croissance, le rendement à l’abattage et la
composition de la carcasse chez du lapin. World Rabbit Science 2, 135–140.
de Blas, C., Pérez, E., Fraga, M.J., Rodríguez, M. and Gálvez, J. (1981) Effect of diet
on feed intake and growth of rabbits from weaning to slaughter at different ages
and weights. Journal of Animal Science 52, 1225–1232.
de Blas, C., Santomá, G., Carabaño, R. and Fraga, M.J. (1986) Fiber and starch levels
in fattening rabbit diets. Journal of Animal Science 63, 1897–1904.
de Blas, C., Taboada, E., Mateos, G.G., Nicodemus, N. and Méndez, J. (1995) Effect
of substitution of starch for fiber and fat in isoenergetic diets on nutrient
digestibility and reproductive performance of rabbits. Journal of Animal Science
73, 1131–1137.
252 C. de Blas and G.G. Mateos
de Blas, C., Taboada, E., Nicodemus, N., Campos, R. and Méndez, J. (1996) The
response of highly productive rabbits to dietary threonine content for reproduc-
tion and growth. In: Lebas, F. (ed.) Proceedings of the 6th World Rabbit
Congress, Toulouse. Association Française de Cuniculture, Lempdes, pp. 139–144.
Cervera, C., Fernández, J., Viudes, P. and Blas, E. (1993) Effect of remating interval
and diet on performance of female rabbits and their litters. Animal Production
56, 399–405.
Cheeke, P.R. and Patton, N.M. (1980) Carbohydrate overload of the hindgut. A
probable cause of enteritis. Journal of Applied Rabbit Research 3, 20–23.
Colin, M. (1975) Effets sur la croissance du lapin de la supplémentation en L-lysine et
en DL-méthionine de régimes végétaux simplifiés. Annales de Zootechnie 24,
465–474.
Colin, M. (1978) Effets d’une supplémentation en méthionine ou en cystine de
régimes carencés en acides aminés soufrés sur les performances de croissance du
lapin. Annales de Zootechnie 27, 9–16.
Colin, M. and Allain, D. (1978) Etude du besoin en lysine du lapin en croissance en
relation avec la concentration énérgetique de l’aliment. Annales de Zootechnie
27, 17–31.
Davidson, J. and Spreadbury, D. (1975) Nutrition of the New Zealand White rabbit.
Proceedings of the Nutrition Society 34, 75–83.
Fernández, C. and Fraga, M.J. (1992) The effect of source and inclusion level of fat
on growth performance. In: Cheeke, P.R. (ed.) Proceedings of the 5th World
Rabbit Congress. Oregon State University, Corvallis, Oregon, pp. 1071–1078.
Fraga, M.J., de Blas, C., Pérez, E., Rodríguez, J.M., Pérez, C. and Gálvez, J. (1983)
Effects of diet on chemical composition of rabbits slaughtered at fixed body
weights. Journal of Animal Science 56, 1097–1104.
Fraga, M.J., Lorente, M., Carabaño, R. and de Blas, C. (1987) Effect of diet and of
remating interval on milk production and milk composition of the doe rabbit.
Animal Production 48, 459–466.
Fraga, M.J., Pérez, P., Carabaño, R. and de Blas, C. (1991) Effect of type of fiber on
the rate of passage and on the contribution of soft faeces to nutrient intake of
finishing rabbits. Journal of Animal Science 69, 1566–1574.
García, G., Gálvez, J.F. and de Blas, C. (1992) Substitution of barley grain by
sugar-beet pulp in diets for finishing rabbits. 2. Effect on growth performance.
Journal of Applied Rabbit Research 15, 1017–1024.
García, G., Gálvez, J. and de Blas, C. (1993) Effect of substitution of sugarbeet pulp
for barley in diets for finishing rabbits on growth performance and on energy and
nitrogen efficiency. Journal of Animal Science 71, 1823–1830.
García, J., Carabaño, R., Pérez, L. and de Blas, C. (1996) Effect of type of fibre on
neutral detergent fibre digestion and caecal traits in rabbits. In: Lebas, F. (ed.)
Proceedings of the 6th World Rabbit Congress, Toulouse. Association Française
de Cuniculture, Lempdes, pp. 175–180.
Maertens, L. and De Groote, G. (1988a) The influence of the dietary energy content
on the performance of post-partum breeding does. In: Proceedings of the 4th World
Rabbit Congress, Budapest. Sandar Holdas, Hercegalom, Hungary, pp. 42–52.
Maertens, L. and De Groote, G. (1988b) The effect of the dietary protein:energy ratio
and the lysine content on the breeding results of does. Archiv für Geflügelkunde
52, 89–95.
Feed Formulation 253
Maertens, L. and Luzi, F. (1996) Effect of dietary protein dilution on the performance
and N excretion of growing rabbits. In: Lebas, F. (ed.) Proceedings of the 6th
World Rabbit Congress, Toulouse. Association Française de Cuniculture,
Lempdes, pp. 237–242.
Méndez, J., de Blas, C. and Fraga, M.J. (1986) The effects of diet and remating
interval after parturition on the reproductive performance of the commercial doe
rabbit. Journal of Animal Science 86, 1624–1634.
Motta, W. (1990) Efectos de la sustitución parcial de heno de alfalfa por orujo de uva
o pulpa de remolacha sobre la utilización de la dieta y los rendimientos
productivos en conejos en crecimiento. PhD Thesis, Universidad Politécnica de
Madrid, Spain.
Moughan, P.J., Schultze, W.H. and Smith, W.C. (1988) Amino acid requirements of
the growing meat rabbit. 1. The amino acid composition of rabbit whole body
tissue – a theoretical estimate of ideal amino acid balance. Animal Production
47, 297–301.
Parigi Bini, R. and Chiericato, G.M. (1980) Utilization of various fruit pomaces
products by growing rabbits. In: Camps, J. (ed.) Proceedings of the 2nd World
Rabbit Congress, Barcelona. WRSA, pp. 204–213.
Partridge, G.G., Findlay, M. and Fordyce, R.A. (1986) Fat supplementation of diets
for growing rabbits. Animal Feed Science and Technology 16, 109–117.
Partridge, G.G., Garthwaite, P.H. and Findlay, M. (1989) Protein and energy retention
by growing rabbits offered diets with increasing proportions of fibre. Journal of
Agricultural Science 112, 171–178.
Santomá, G., de Blas, C., Carabaño, R. and Fraga, M.J. (1987) The effects of different
fats and their inclusion level in diets for growing rabbits. Animal Production 45,
291–300.
Santomá, G., de Blas, C., Carabaño, R. and Fraga, M.J. (1989) Nutrition of rabbits.
In: Haresign, W. and Cole, D.J.A. (eds) Recent Advances in Animal Nutrition.
Butterworths, London, pp. 109–138.
Spreadbury, D. (1978) A study of the protein and amino acid requirements of the
growing New Zealand White rabbit with emphasis on lysine and
sulphur-containing amino acids. British Journal of Nutrition 39, 601–603.
Taboada, E., Méndez, J., Mateos, G.G. and de Blas, C. (1994) The response of highly
productive rabbits to dietary lysine content. Livestock Production Science 40,
329–337.
Taboada, E., Méndez, J. and de Blas, C. (1996) The response of highly productive
rabbits to dietary sulphur amino acid content for reproduction and growth.
Reproduction, Nutrition and Development 36, 191–203.
Xiccato, G. (1996) Nutrition of lactating does. In: Lebas, F. (ed.) Proceedings of the
6th World Rabbit Congress, Toulouse. Association Française de Cuniculture,
Lempdes, pp. 29–50.