Workshop-seminar, 21-24 August 2006, MEKARN-CelAgrid | Workshop on Forages for Pigs and Rabbits |
Contents |
Forage is defined as herbaceous plant material (mainly grasses,
legumes, aquatic plants and leaves from bushes and
trees) eaten by animals, either in fresh or preserved form.
Forages are usually high in the fibrous components of plants (cell
walls), and there are several analytical methods and definitions
for "fiber", the most common being "crude fiber" and "neutral
detergent fiber". Feeding fibrous feeds to pigs generally results
in increased rate of passage of digesta through the gut, and
reduced ileal and total tract nutrient digestibility, although the
effect is very variable and decreases with time of adaptation to
the diet and age. Feeding forages has also been shown to reduce the
incidence of stomach ulcers and diarrhea in growing pigs, although
the presence of anti-nutritional factors in legume leaves and
cassava foliage can reduce performance. Forages can be combined
with energy sources such as cassava root meal or sugar cane juice
that are low in fiber and protein, and as the resulting amino acid
balance is superior to that of conventional diets based on soybeans
and cereals, the overall protein content of the diet can be
reduced. In addition, competition with humans for these grains is
eliminated. Forages can supply all of the protein and a high
proportion of the vitamins and some trace minerals required by
pregnant sows, and their bulkiness helps reduce hunger-related
stress symptoms. There is some evidence that indigenous breeds can
digest and utilize fibrous feeds more efficiently than exotics.
Forages are inexpensive and can be produced on-farm, leading to
increased profitability and
sustainability.
"Fiber" (or "dietary fiber") has been defined as those components of plant cell walls that are resistant to the digestive enzymes of animals, later modified to include all non-starch polysaccharides (NSP) plus lignin. "Crude fiber" (CF) was for a long time the standard measure of fiber, and was determined by acid and alkali hydrolysis as part of the Weende scheme ("Proximate analysis"). However, during the analysis procedure a considerable proportion of the lignin and hemicellulose (supposedly indigestible by non-ruminants) can be dissolved and lost from the residue. What is widely considered to be more accurate measure of plant cell walls was developed by Goering and Van Soest (1970), and includes neutral detergent fiber (NDF) and acid detergent fiber (ADF). NDF includes mainly hemicellulose, cellulose and lignin and gives a reasonably good estimate of the indigestible cell-wall component of plants. However, it does not include some soluble non-starch polysaccharides and pectins. Although CF has been largely replaced by NDF it can still be useful to determine in order to compare results with those from the older literature.
Table 1. Schematic representation of the components of dietary fiber |
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Lignin |
Dietary carbohydrates |
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Dietary fiber (Crude fibre) |
Starch + sugars |
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Lignin |
Non-starch polysaccharides (NSP) |
|
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Neutral detergent fiber (NDF) |
Fructans |
Pectins |
|
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Acid detergent fiber (ADF) |
Hemicellulose |
|
|
||
ADL* |
Cellulose |
|
|
|
|
Lignin |
|
|
|
|
|
*Acid detergent lignin |
Non-starch polysaccharides have been shown to have a considerable effect on gut size and development, particularly the large intestine. For example Jørgensen et al (1996) found that growing pigs fed a high-fiber diet between 45 and 120 kg had a significantly heavier caecum and colon, and the gut contents were also heavier than in pigs fed a low-fiber diet (Table 2).
Table 2. Effect of level of inclusion of dietary fiber on gut characteristics of growing pigs (Jørgensen et al 1996). |
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|
Low-fiber diet |
High-fiber diet |
Body weight (BW), kg |
122 |
129 |
Contents of GI tract, g/kg BW |
29 |
82 |
GI tract, g/kg empty BW |
|
|
Stomach |
5.7 |
7.3 |
Small intestine |
15.6 |
16.2 |
Caecum |
1.6 |
2.8 |
Colon |
8.7 |
17.2 |
Digesta dry weight at ileum, kg/day |
0.270 |
1.073 |
The implications of this are a significantly reduced rate of carcass weight gain, compared to live weight gain on fibrous diets, and reduced dressing percentage. Pluske et al (1998) found that carcass yield was reduced by 0.025 units for each additional gramme of fiber intake, and Len et al (unpublished data) reported that dressing % was over two percentage units lower in pigs given a high-fiber diet containing 300 g/kg NDF compared with those given a low-fiber diet (200 g/kg NDF). Another practical implication of the increased weight of the visceral organs is that they have a high rate of energy expenditure, and the gastrointestinal (GI) tract was reported to account for 25% of whole body maintenance, even though it only represents around 4% of body weight (Yen et al 1989). This finding implies that the poorer feed conversion efficiency found when high fiber diets are fed may be partly a result of increased basal heat production, as well as reduced digestibility of energy and nutrients. This increased basal heat production, in combination with increased heat of fermentation in the large intestine, may also reduce feed intake of fibrous diets if the environmental temperature is high, as is often the case in the tropics.
The negative effects of fiber on diet digestibility and pig growth are well documented, and it is generally accepted that diets containing more than 7-10% of fiber result in decreased growth rates (Kass et al 1980). However, the mechanisms involved and the extent of the reduction in nutrient digestibility and growth performance are complex and depend on a number of factors, including for example the fiber source and composition, level of feed and processing method, and the age and breed of the pig. The mechanisms involved in the decrease in diet digestibility, in addition to the presence of the indigestible components in fibrous forages, include the shielding effect of the plant cell contents by the indigestible cell walls, and increased rates of passage of digesta as a result of its increased bulk and water-holding capacity, and also due to irritation of the gut wall mucosa by VFA produced in the hind-gut. In addition reduced feed and energy intake as a result of the presence of anti-nutritional factors, bulkiness and energy dilution, and possibly also heat stress, can also contribute to reduced daily gains.
Nearly all fiber digestion takes place in the caecum and colon, where bacteria (there are no protozoa in the hind-gut of pigs) break down fermentable carbohydrates (starches, plant cell-wall polysaccharides and host mucopolysaccharides) that have escaped digestion in the stomach and small intestine to produce volatile fatty acids (VFA - mainly acetic, propionic and butyric acids), methane, hydrogen and other gases, and microbial mass (which accounts for around 55% of the faecal DM, more on fibrous diets). VFA from fiber fermentation provide from 5% to 28% of the energy requirements of the growing pig (Kass et al 1980) and the proportion will be even higher for pregnant sows given fibrous diets. However, VFA are not utilized as efficiently as the products of the breakdown of starches and sugars in the small intestine.
Introducing a high-fiber diet initially reduces the microflora of the colon, but then after a few days the number of cellulolytic bacteria increases (Varel 1987). There is also a strong influence of age, and Varel and Pond (1985) calculated that there were 6.7 times more cellulolytic bacteria in the large intestine of mature sows compared to growing pigs when fed the same high fiber diet (containing 40% alfalfa meal) for 3 months, which explains why sows can digest fibrous feeds more efficiently than growing pigs.
Products high in fermentable dietary fiber are receiving considerable attention in view of their potential positive effects on gut health, and therefore as possible replacements for feed antibiotics. For example, swine dysentery ceased to be a problem on farms when maize silage was fed (Prohaska and Lukacs1984), probably because of the lower gut pH and antibacterial effect of increased VFA production on the organism responsible (S.hyodysenteriae). A similar result was reported by May et al (1994) with a different bacterium (Clostridium difficile). However, Pluske et al (1998) found the opposite effect, and reported that a diet that was high in fermentable carbohydrates predisposed pigs to swine dysentery.
There is also some evidence that a high dietary fiber content can prevent the development of gastric lesions. For example, Henry (1970) showed a reduced incidence of stomach lesions when wood cellulose was added to the diet of growing pigs, although Björklund and Pettersson (1976) found the opposite effect when up to 15% of grass or lucerne (alfalfa) meal was included in pig diets.
Conventional concentrates based on cereals and soybean meal are generally imbalanced, in particular with respect to methionine + cystine and threonine. Most green forages are reasonably high in protein and contain concentrations of the essential amino acids that fairly closely match the pig's requirements. This means that if they are combined with an energy source that is extremely low in protein and fiber, such as sugar cane juice, molasses, sugar palm juice or cassava root meal, then the essential amino acid content of the overall diet will still be balanced and the protein content can be reduced by up to 30-35 % (Speer 1990).
Many of the green forages in the tropics that are potentially valuable sources of protein and trace nutrients contain anti-nutritional factors that can depress pig performance, such as cyanogenic glycosides, trypsin inhibitors, mimosine, goitrogens, oxalic acid, tannins and saponins. However many of these can be inactivated to a greater or lesser extent by various processing methods, such as heat treatment, sun-drying and ensiling
Early experiments with green forages suggested that, for example, providing alfalfa meal in the diets of pregnant sows resulted in improved breeding efficiency and fertility, as well as improved viability of the piglets farrowed. The increased litter size in sows given alfalfa or grass meal was found to be due to increased ovulation rate (Teague 1955) and/or pre-natal survival (Mazilis 1962). As the exact mechanisms could not be established it was concluded that green forages provided unknown factors that positively influenced ovulation rates. However, it is more likely that the control diets were deficient in vitamin A or its precursors (carotenes). This is likely to be a particular problem in hot, humid tropical environments, where deterioration of vitamin A in premixes can occur quite rapidly. Although green forages can thus play an important role in ensuring an adequate supply of vitamin A precursors there is also evidence that inclusion of some forages inhibits the absorption of minerals such as calcium, phosphorus and copper. There is also evidence that in addition to the positive effects on fertility through the supply of vitamin A precursors and possible unidentified factors, fibrous feeds as such can improve reproductive performance, as reviewed by Reese (1997) (Table 3).
Table 3. Effect of fibrous diets supplied during gestation on the reproductive performance of sows (Reese 1997) |
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Fibre effect |
|
Sow traits |
|
|
Gestation weight gain, kg |
-2.7 |
21 |
Lactation weight loss, kg |
-1.3 |
18 |
Lactation feed intake, kg/day |
+0.27 |
17 |
Litter traits |
|
|
Number of piglets born alive |
+0.3 |
24 |
Number of piglets weaned |
+0.3 |
24 |
Average piglet birth weight, g |
-91 |
24 |
Average piglet weaning weight, g |
+409 |
24 |
Feed allowances for pregnant sows are severely restricted in order to prevent over-fatness, possible problems with mastitis around farrowing and depressed appetite in lactation. The degree of restriction means that when sows are fed cereal-based concentrates the daily DM intake in gestation is usually only around 50% of ad libitum intake, which results in hunger-related stress symptoms. Feeding bulky diets high in fiber to pregnant sows has been shown to reduce stereotypic behaviour (eg. Robert et al 1997) and aggression, increase the time spent eating and chewing, and reduce feeding competition in group-housed sows.
Ninh Thi Len et al (2006) found that when given
high-fiber diets, dry matter and nutrient intakes were
significantly higher for Mong Cai (MC) growing pigs than for
Landrace x Yorkshire (LY) when expressed as a proportion of
metabolic BW. The probable explanation for this is that the
capacity of the gastrointestinal tract of the MC is higher than
that of LY, which would be of particular importance in the case of
high fiber diets. Results in a previous study also showed that an
indigenous pig (Chinese Meishan) had a higher capacity of the
gastrointestinal tract than an improved breed (Fevrier et al 1992).
There is considerable evidence that indigenous breeds and
their crosses with exotics can also digest high-fiber diets
more efficiently than exotic breeds (Kanengoni et al 2002; Ndindana et al 2002; Fevrier et al 1992). Recently, Khieu Borin et al (2005) showed
that MC pigs were more efficient in digesting dietary fiber
fractions than improved pigs, and Ninh Thi Len et al (2006)
also found that MC growing pigs digested organic matter, energy and
other dietary components more efficiently than LY. In contrast, a
study carried out with an indigenous Cuban breed was unable to confirm
any breed differences in terms of diet digestibility (Ly et al 1998).
In spite of the disadvantages and problems mentioned above associated with feeding forages to growing pigs they have a number of important advantages, in that they are an inexpensive source of protein, can be grown at small-farm level, and are often by-products or co-products of multipurpose crops and trees. Feeding locally produced green forages to growing pigs and sows will in most cases significantly increase the sustainability, stability and profitability of the farming system.
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