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A review of the nutrition and growth of
suckling pigs by providing
creep-feeding supplements to reduce piglet mortality
and minimize post-weaning syndrome
feuchter57@eudoramail.com
Universidad Autonoma Chapingo
TABLE OF CONTENTS
ABSTRACT
Introduction
Background Information
Rationale and Purpose
Piglet Colostrum and Milk Intake
Colostrum metabolism and fat accretion
Supplementing Baby Pigs
Feed Intake and Milk Production in Sows
Colostrum and Milk Composition
Nutrient Requirements
Requirements for maintenance of energy
Cost of energy for protein and fat deposition
Amino acid requirements
Conclusion
Digestive Enzymes
Physiology
Potential Growth Performance in the Young Pig
Practical targets
Fostering
Feed Processing
Supplementation
Enzyme Additives
Feed Intake
Voluntary feed intake
Water treatment, organic and inorganic acids
and disinfectants
Diseases
Mortality
Feedstuffs
Poultry
Spray Dried Plasma Protein (SDPP)
Milk
Proteins
Fat
Other feedstuffs
Mycotoxins and antinutritional factors
Classification of antinutritional factors
Fermented, Predigested and Home-made Products
Home-made products
Sweeteners
Liquid Feeding
Summary
References
Recommended Reading and Web Sites
Acknowledgments
This compiled project on the nutrition and growth of the suckling piglet provides up-to-date information for the promotion, effects and consequences of using creep-feeding methods and feedstuff ingredients. Although creep-feeding provides a small additional body weight gain 2 lb in lactation and a 4 lb weight gain in the nursery, these weight improvements make an economic difference in posterior growing stages, in the productive efficiency at market time, and providing a faster cash flow as well as global revenue for the swine enterprise.
There is no substitute
for best stockmanship techniques applied in any pork production facility.
Genetics or nutrition will not resolve problems by themselves to ensure profitability.
The use of creep-feeding is an existing m
The objectives
of a creep-feeding systems are to provide better m
There are intrinsic benefits involved in creep-feeding developed techniques for suckling piglets as the result of increased dry matter digestible energy (DE) feed consumption in the transition from suckling ingesta-liquid feeding-slurry-dry feed to weaning time. The early 2-day-old piglet in a liquid-slurry training process for feed consumption maintains intestinal health (villous width and crypt depths), preparing it for a weaning diet while reducing growth check (no feed consumption and lose body weight) after weaning, improving growth rate during the first week after weaning, and providing a three phase feeding preparing the pig to early accept simple diets made of cereal and soybean meal.
There are multiple
feedstuffs and homemade products that can be included in creep-feeding systems
in the same way as preparing food for a human infant 4 months of age. This
is why feeding a suckling piglet is more of an art than a science—to balance
nutrient requirements. The products from the animal slaughter industry (beef,
calf, broiler, layer, pork), dairy factories, egg hatcheries and liquid processing,
fisheries, oilseed extraction, starch, flour, fermentation, snacks and other
industries could be used as components of the creep-feeding diet or as a single
supplement. The main contribution of these supplements is to provide more
nutrients for growth and survivility (energy, protein, vitamins, minerals)
or to complements sow’s milk deficiencies in amino acids (arginine, valine,
tryptophan, lysine, methionine, theronine). However, the selected ingredients
should be palatable, digestible, stimulate feed consumption, and be provided
in a nearly sterile material to reduce scours, minimize digestive disorders,
avoid stomach ulcers, control pathologic diseases, or to stimulate colonization
of beneficial digestive bacteria (bacterioides, streptococci, lactobacillus),
reduce population growth in the intestinal epithelium with bacteria (
A piglet’s genetic growth potential during 21 days of lactation can be 1.3 lb per day but this desired goal is often impaired by many external factors. Creep-feeding helps to overcome or reduce the negative effect of these growth inhibitors. The sow’s metabolic capacity enables production of 50.6 lb of milk per day, but environmental stressors, severe hormonal changes after delivery, reproductive organ reestablishment, lack of appetite or pour nutrition, could reduce her milk yield potential to 10 lb of milk per day or result in agalactia (MMA). Any one genetic breed does not accomplish all the productive characteristics for litter size, survivality, milk production, longevity, birth weight, etc. Variation will be present in all the herds and normal distribution of the birth weight of the piglets requires special attention for the underweight group.
The objective of this creative component research was to provide a usable
document to serve pork producers, swine m
This research
project involves a literature review of different topics related to the nutrition
and growth of the suckling piglet. The nutritional
This article
attempts to incorporate the best scientific principles applying selected published
results for supplementing suckling piglets to enhance weaning weight, and
disseminate practical methods that can be applied to all kinds and sizes of
hog production systems. Experienced nutritionists are the primary researchers
who have extrapolated nutrient requirements from weaning starting diets to
the less mature digestive system of the suckling piglet, thus their recommendations
are not over imposed in this paper. An understanding of this complex phase
requires knowledge in multiple fields such as agronomy, swine nutrition, stockmanship,
farm m
The Journal of Animal Science contains extensive published results that are useful for pig nursery systems. This Journal contains most of the related publications from U.S. researchers in monogastric nutrition, yet many articles are from abroad. This compiled information may assist those involved in swine-related fields by providing nutrient densities of rations in the post-weaning phase to meet pre-weaning nutrient requirements of the piglet.
There is a paucity of objective data available in a compiled format to help producers decide whether an expensive feedstuff is a good nutritional source to improve the welfare of the piglet and sow. There are many external factors involved in the successful use of a particular feed that are not dependent upon the feed itself, nevertheless it is important to know such factors as palatability and digestibility to enhance feed consumption. This research will provide a giant step toward presenting the best alternative choices.
In summary, the scientific knowledge of nutrition using the art of feeds and feeding experiences may contribute to the physiological development and growth rates of the neonate pig. It may reduce morbidity and mortality at this early age of the life cycle of the pig, especially having low birth weights of less than two pounds, yet have good viability to reach market weight. The overall supplementation to the piglets’ diet may ultimately improve reproductive performance of the sow, to reach better efficiency and performance goals in the productive system, and the pig to reach market weight efficiently, which contribute to the overall revenue of the farm. The ultimate decision for the pork producer is to be competitive at home and in the global market.
Supplementing
a suckling pig during the lactation period (before weaning) was a common husbandry
practice during the early 1970s. The lactation period lasted for 42 to 56
days wherein the sow did not have enough milk production and sufficient body
reserves to sustain the fast growing demand of her piglets. During this time
newborn piglets may have had vitamin deficiencies for choline, folic acid
and complex B vitamins, and sows did not have all full functional milking
teats at the end of the lactation period. It was common to observe dams with
broken legs when being relocated from farrowing pens at weaning time because
of calcium and phosphorous depletion from their bone reserves. Some premixes
with vitamins and minerals were not as complete as necessary for the nutritional
requirements for these rotational crossed breeders (e.g., Yorkshire, Landrace,
Duroc, Hampshire). M
In the 1980s, the hog industry turned to rapid growth and use of vegetable byproducts from the oil seed industry, confinement of modern facilities, breed improvement and selection, and intensive production systems that generated a more skillful, technically and scientific way of rearing animals. It was a matter of economic efficiency and space turnover more than the old ways of pork production. The industry changed with the development of rearing and feeding techniques for Specific Pathogen Free (SPF), Minimum Disease (MD), Segregated Early Weaning SEW), Medicated Early Weaning (MEW) and other piglet rearing methods. During this time piglet nutrition research practices focused on feeding methods for post weaning pigs but not on creep feeding or use of other supplementation practices for lactating piglet.
Lactation periods
lasted for up to 35 days in the 1980s. The search for the best lactation length
was not defined, therefore tests were carried out for 0, 7, 10, 14, 18, 21,
28 and 35 lactating days to determine the best economical profit and practical
m
With a short
lactation lapse, modern facilities were looking for better weaned pig starting
diets, feed particle size, pellet presentation and extrusion, use of growth
promoters, including artificial amino acids to meet nutritional requirements,
more liable vitamins and digestible mineral sources, and testing probiotics.
Other external aspects of the nutrition system were related to the m
New technological pig farms were changing rapidly but little attention was paid to methods of supplementation of the suckling piglet and appropriate feedstuffs for this early age. During this time, improving this obsolete practice was not considered because it represented an increase in labor demands and a tremendous risk for other diseases and diarrhea. There were too many other demands inside and outside of the production site, than considering the care of the youngest pigs. Pork producer had genetic support from their selected sows to provide enough milk for piglets, a good mothering instinct, resilience to reduce crushing, and excellent farrowing rates.
During the 1990s,
the agro-industry improved the quality of many feedstuffs already existing
in the market and developed new byproducts that had great potential in both
human food and the feed animal industry. At this time the pork industry moved
from family production farms to large corporate production facilities. This
changed the decision making of many activities in the farm, with large purchasing
capacities and computer economic
However, both productive systems involved determining the best economic methods for profitability in this competitive market. Genetic selection for large litter size and short lactation periods did not resolved the litter size at weaning and the low numbers entirely continued to the nursery stages with all the disadvantages of a physiologically immature early weaned piglet. The profitability of the farm did not improve greatly with the advent of new breeds and early weaning practices. The number of pigs per sow per year did not increase considerably and All-In-All-Out systems for early weaning did not work as predicted. During this time, decision making focused on gross important aspects rather than details. The final days of this period fixed lactation length between 18-24 days which represented small lactation weight gains for this growing stage compared with the genetic potential of the lean pig.
During the early
21st century the pig market depends more on international demand
and world market competition. However, large production systems have been
restricted in many countries due to environmental policies and regulations.
The trend toward more natural pig behavior has been appeased by new regulations
for space allowances in the United Kingdom, antibiotic feed additives restrictions
in Sweden, and cage farrowing facilities in the state of Florida USA. These
factors have started to change the outlook of the pig industry worldwide toward
more sustainable methods to produce meat products. Nowadays, to be competitive
and profitable with high quality products, the pork industry must use all
the available factors to reach its goals while avoiding misuse of the technological
opportunities on hand. Several general factors influence the production of
pork meat: nutrition, husbandry, m
Irregardless
of the biological or economic importance of any stage in the life cycle of
the pig, the suckling period is the shortest of all the productive stages.
However, it may be the ignition step for the following growing periods and
the definition of the muscular cell numbers that influence growth rate and,
later on, the reproductive performance and quality of the selected gilt. Thus,
the importance of applying
Despite numerous
available publications with remarkable scientific efforts explaining the importance
of metabolic nutrients for the pre weaning pig, their applied level may be
far from reality. Research results should not only be for the sake of new
knowledge or to understand the stimulus of the feed to the genes’ actions
or how an element affects the mitochondria of the cell. The technology in
this area is advanced but to explain the effect of 50 nutrient components
in the feedstuff in 30 thou
The comparative
nutritional
Only a few research
articles report the digestibility of raw feed materials for neonatal pigs.
In addition, there are a few Extension bulletins for nutrient requirements
of baby pigs, such as the ISU cycle of the pig (176). This is another reason
why the feeding practice of creep feeding has not been adopted in the general
production system. However, there is technical and scientific evidence that
it should be a common m
The main purpose
of this paper is to provide an overview topic of the suckling piglet nutrition
presenting the most relevant and recent published information on baby pig
creep feeding and supplementation. There is a shortage of practical information,
thus the primary objective of the study is provide a review of the information
currently available for the swine nutritionist, stockperson, m
Piglet Colostrum and Milk Intake
Unlike other ungulates, the sow does not lick its newly born piglets or offer them assistance in finding the udders. Some sows will stand several times and sniff their piglets during farrowing (26). This behavior increases the chances for overlaid piglets and, by genetic selection, they may overcome this genetic trait, especially as some breeds have better maternal characteristics than others. The reduction of feed intake 3 days before farrowing induces glucogenesis from fat tissue and stimulates feed intake after delivery.
After birth the piglet will try to find the udder and suck on a teat a soon as possible (<30 minutes), and typically will move along sucking several other different nipples in succession, from 2-13 teats in the first 8 hours (20). These are general considerations that prevail during the first hours of lactation. Competition at the udder affects mortality in smaller piglets of the litter and results in poor growth for many of the survivors. Cross fostering is necessary only when the piglets exceed the number of teats. Split-weaning (SW) is used to achieve a more uniform litter but it does not improve physical conditions for weaning.
The termination of colostrum synthesis occurs 1 hour after the sow releases the placenta, with colostrum ejection every 10-20 minutes. Piglets often consume 5-7% of their body weight in colostrum in the first hour of suckling. The suckling range is 20-92 minutes throughout the day and night, but there is a daylight behavior pattern for most farrowings. An estimation of colostrum and milk intake for the first 2 hours after birth is about 113 grams with consumption of 10-60 g of colostrum per suckling (19). The first day the piglet consumes 280 g/kg body weight (BW)/day of colostrum, but is physically able to consume from 290 to 490 grams per day (2).
When the piglet has sucked all the colostrum from the teat an autocrine mechanism and the withdrawal of progesterone will release synthesis and secretion of milk which reduces the secretion of colostrum. This ensures that, with an extended farrowing period, the last-born piglet obtains colostrum of the same composition and protective capacity as the first-born. The milk ejection reflex of the sow is under tight control, with milk only available to the piglets during a “let-down”, which lasts for about 15-20 seconds per lactation. This control, primarily as a result of oxytocin release, ensures that a dominant piglet does not deprive others of milk. This process maximizes the survival of feral pigs and may be applicable to domestic pigs but not for cows. However, this strategy limits the amount of milk that can be removed by the piglets during suckling, and also limits milk consumption and growth (94).
If 7-day-old piglets ingest 100, 200 or 300 g of milk intake/kg BW/day their whole body protein synthesis will be 10.7, 16.9 and 20.9 g/d/BW0.75, respectively, and their protein deposition will be 4.5, 14.6 and 19.7 g/d/BW0.75 (82). The more milk consumed, the better the growth rate. Litters of 4 piglets that suckled 1 kg of sow’s milk/pig/day, and milk consumption were 0.7 kg/pig/day in litters of 12 piglets. A litter of 6 pigs may consume 1.3 kg/pig/day, and 0.90 kg/pig/day in litters of 14 (97). There is evidence of piglets consuming 460 g/kg BW in the first 27 hours of life; a sow with a litter of 10 pigs must start producing > 6.4 kg/day of colostum. During the second half of the suckling period, after 7 days of farrowing, the demand is 800-1100 grams of milk/pig/day and at 21 days after birth (at weaning time) the sow’s lactation curve should reach > 20 kg milk/day to supply the energy requirements of 10 pigs per litter (2). A large litter size of >10 pigs will ingest about 10-12 kg of milk per day (97). After the peak of lactation and a plateau period, the milk production slope will eventually decrease even in sows with the highest feed consumption rates (155).
The suckling pig depends on its mother’s milk production for growth and to express its genetic growth potential. If the sow does not achieve genetic milk yield potential either the heaviest piglets in the litter that choose the most productive teats from the dam will reach potential growth. The stronger piglets will retain more teats at the expense of the smaller pigs, and there are many physiological, behavioral and external conditions that will affect complete genetic milk production capacity (167).
Piglets that select the best teats before 3 days of age will remain more dependent on milk and less interested in solid feed (12). In general, a piglet of this age will partition feed nutrients into adipose tissue instead of the more desired economical lean protein muscle accretion; most of the increased protein weight will be on the accelerated growth of the digestive organs. The ingestion of colostrum after birth for 36 hour greatly stimulates growth of all gastrointestinal organs and particularly the small intestine. The leaner Pietrain breeds require more concentrated feed to grow to their genetic potential because their smaller intestinal size reduces its gut capacity to consume feeds. For leaner breeds in general, this early intestinal growth follows a genetic pattern for survivability but it is not a genetic trait that will influence its final lean to fat market ratio.
The gene expression of this early age is not a determinant of the final quality of the end product for meat or reproductive replacement. Appetite and thirst will be satisfied by the sow’s milk production but, in many circumstances, the environmental conditions will not enable them to reach their dam’s milk potential. The desired piglet goal to reach their genetic growth capacity will not be expressed after birth due to the low energy level concentration of the milk colostrum and the small milk production at the beginning of the suckling stimulus. In other instances the sow may be a great milk producer and, if she had farrowed a small litter, the piglet will be constrained by the limitations of its gut capacity and suckling ability. Many internal and external factors are involved in less expression of their genetic potential for the maximum milk production, maximum milk suckling capacity, and maximum growth and survivability (169).
Colostrum metabolism and fat accretion
After suckling, the piglet increases glucose and galactose levels in the plasma from gluconeogenesis of fat-glycerol, lactose, and small contributions of amino acids (62). The levels of lipase from the pancreas are low, but colostrum fat is very digestible because milk provides adequate amounts of carnitine, a substrate required for fat transduction. This enables the liver to oxidize fatty acids. While the new born piglet is very lean and possesses only 10 to 20 g/kg body weight as fat, it increases to 150 to 200 g/kg body fat by 18-21 days of age (62, 66). The body energy reserves are less than 2% body fat content and total body glycogen stores (liver and skeletal muscle) are < 38 g/kg BW. Liver glycogenolysis is active and can utilize 70% of the available glycogen immediately after birth to release blood requirements for glucose. Glucose utilization in neonate piglets is 10g/kg/day (62). Body fat reserves are mobilized at a lower rate and both will be depleted in 24h if the piglet does not consume colostrum. The newborn piglet requires > 14 g/kg BW/d of glucose that must be supplied: 20% from body glycogen, 35% from milk lactose, and 55% from milk fat (16).
A 20-day-old piglet with 4-5 kg body weight can suck 345 g of milk/day/kg BW in natural milking and when fed in a bottle can consume 490 g of milk/day/kg BW. Piglets consume 24% more feed in artificial rearing at days 4 to 28 of age and had growth rates 30% higher than only sow-milked pigs (41). This may be a combined factor in a sow’s low milk capacity or lack of a piglet’s strength to suck. Creep feeding may be beneficial for small piglets or litters with low milk producing sows if the milk replacer is also supplemented after weaning (82). Supplementing the same creep feed after weaning ensures feed consumption for palatability, enzymatic adaptation for the substrate already developing, and reduces post-weaning syndrome and lag stress.
The heaviest pig may consume more than 100 ml of colostrum in the first hour of life whereas the smallest may not ingest colostrum at all. The oral supplementation of the smaller piglets with cow’s colostrum or spray dried blood with immunoglobulin 3 days after birth does not have consistent results; the endocyte closure time of the intestine was not considered in these studies (61). The intestine pinocytosis action has the capacity to absorb colostrum antibodies before intestinal closure at 18 to 36 h of life. Enterocyte cell maturation is completed at 19 days of age, and these mature cells are more capable for digestion (156). Newborn pigs that have fasted respond to an intra-gastric administration of fat, which increases their gluconeogenesis levels and synthesis of glucose (62). This can be a measure to reduce starvation of the neonates.
Feed Intake and Milk Production in Sows
The sow has physical limitations to consume large amounts of feed per day in order to produce more milk. On the contrary the dam is capable of digesting large amounts of feed concentrate, increasing the ingestion of dry matter and protein per day. The sow has the metabolic potential to synthesize 23 kg of milk per day (175). This metabolic potential is impaired by hormonal changes after parturition, the process of uterus involution and protein accretion to regenerate reproductive tissue and low piglet stimulation level at suckling the udder for time expended in fighting, resting or weakness. Transgenic gilts with bovine a-lactalbumin production may increase milk production but time will reveal further results (115). The nutrient content in 7 kg of lactation feed can synthesize 10 kg of milk and this conversion factor produces a shortage of milk supply (41). The lactating sow may need more concentrated diet than the NRC 1998 specifications. Litters of 12 piglets could increase 50.7 kilos of body weight gain in 20 days if the sows are producing milk of 2.9-3.7% protein content. After farrowing, the sows should be fed three times a day and gradually increase feed portions at the rate of feed acceptance and intake. A daily feed rate of controlled quantities will reduce feed spoilage and the likelihood of constipation. This digestive disorder requires higher levels of manganese or other laxative salt or fibrous feed to alleviate this symptom.
Only for high milking sows and large litters (10 piglets), supplementing the sows’ diet with fat, lysine and valine will produce more milk and a positive effect on the weaned weight per litter (95, 125). Excess of valine in the udder cells will be metabolized for energy but will not spare other energy source. Under other conditions increments of the valine content of the lactation feed would not have positive response (155). Sows during 21 days lactating period who received 5.85 kg diet/day with increased valine levels to 1.20% while maintaining the other amino acid levels recommended by the NRC, produced litters with 3 more kilos of weaning weight (61.6 vs. 65.0 kg/litter). The valine content was metabolized in the mammary gland to produce energy in the udder that increased milk urea N (122).
The number of piglets in a litter is determinant for the physiological udder stimulus for milk production level. For 3-4 pigs/litters the expected milk yield would be 4 kg/day. For litters with 5, 6, and 7 pigs, the milk production per litter increases to 5 kg/d. Sows lactating 8,9,10 or 11 piglets produce 8.3 kg of milk/day, whereas for litters with 12 and 13 pigs the sow will produce 9.8 kg of milk per day (126, 134).
Equations for estimating milk production from various authors are as follows:
Milk Yield production = 0.581 Litter Size + 1.81.
MY= 0.796 LS + 2.
MY= 0.689 LS + 5.98. (41, 97).
Another model to predict milk yield production is:
Milk (kg) = (2.50 X ADG) + (80.2 X piglet BW) + 7. Where Y=0.9468x + 0.3888 with a R2=0.8959 for the prediction line and a Y=0.9848x with and R2+0.8944 from the observed data (124).
The determination of milk production to estimate nutrient requirements of lactating sows is represented by the following equation (25):
DM= 0.60 X ADG + 31.7 Eg – 62
E = 4.09 X ADG + 230 Eg – 485
N = 0.027 X ADG + 1.12 Ng – 2.59 ; Where:
Dry Matter (DM) and Nitrogen (N) are in grams/piglet/day;
Energy (E) in kcal/piglet/day;
Average Daily Gain (ADG) in grams/piglet;
Energy in Piglet Weight Gain (Eg) in kcal/gram; and
Nitrogen in Piglet Weight Gain (Ng) in %.
These prediction equations are over 12 liters of milk/day. This is a high metabolic response of the sow because during lactation the animal loses more than 23 kilos of live weight and 8.8 mm back fat over 28 days of lactation, even when consuming more than 5 kilos of feed per day (97). Increasing feed consumption during lactation maintains sow condition scores and increases milk production and piglet growth rate (Table 1.1) (101).
There are different contradictive published results for the curve of lactation in sows that are presented to compare these reports. The peak of lactation is at 10-14 days after farrowing, and it is only sufficient for pigs to attain about 50% of their growth potential (54). Other authors noted that the peak of a sow’s milk production is at 14 to 21 days post farrowing (99). There are genotypic differences among dams and the speed growth rate of a litter pig’s demand for more milk (155). The growth rate of suckling baby pigs is reduced after 8 days on lactation (117). This indicates a shortage in milk production to respond to the growth rate of a fast growing pig.
Table 1.1. Effect of dietary energy intake on sow’s body weight, milk yield and piglet growth during lactation (101)
|
Dietary energy intake (MJ DE/d)
|
||||||
|
|
38.00 |
46.90 |
56.00 |
62.10 |
69.10 |
77.90 |
|
Back fat loss (mm) |
9.8 |
7.7 |
7.1 |
8.1 |
5.8 |
6.5 |
|
Live-weight loss (kg) |
30.9 |
24.0 |
17.5 |
18.8 |
12.0 |
5.0 |
|
Piglet growth (g/d) |
215 |
227 |
237 |
254 |
249 |
267 |
|
Milk yield (kg/d) |
9.18 |
8.91 |
9.80 |
10.25 |
9.95 |
11.45 |
|
N metabolism (g/d) |
|
|
|
|
|
|
|
Milk |
83.7 |
81.9 |
78.3 |
90.8 |
86.5 |
102.9 |
|
Balance |
-25.4 |
-14.3 |
4.5 |
7.8 |
19.3 |
21.7 |
Under different
circumstances based on breed, nutrition, environment and m
Feeding the sow during gestation with extra feed or fat had disappointing results. It did not increase body energy storage in fetal and newborn pigs. The transportation of fatty acids across the placenta was negligible (62). In the occurrence of a positive response after delivery, the milk produced by the sow had more fat content which spared some glycogen in the blood of the piglet and somehow resulted in a more viable neonate pig (19). However, feeding gestating sows with 1, 3 butanediol increased glycogen activity in the liver of the fetus but increased only small amounts of fetal fat reserve (62).
Colostrum and Milk Composition
The release of immunoglobulins (IgG1, IgG2, IgM, IgA) provide antibody protection for the newborn piglet. Other proteins that function as antibodies, cellular elements such as polymorphs and low proportion of macrophages and g-globulins in the milk colostrums also have protective effect. The sow’s milk has higher levels for IgG1 than the other immunoglobulin factors (Table 1.2). There is experimental evidence that stressed sows during gestation do not reduce IgG concentration in the milk. The fetal piglet may receive maternal stress hormones as a flux of corticotrophin (ACTH) causing a reduction in the permeability of the neonatal gut to antibodies. This impairs humoral and cellular immune functions in the suckling pig. The neonates develop their own immunoglobulin synthesis of (IgD and IgE) at an earlier time if colostrum has fewer protective antibodies or if they are passively transmitted in a low rate (139). The antibodies are gamma shaped protein molecules produced in b cells as a primary immune defense. During this adjusting period the piglet is more exposed to diseases while developing synthesis of the immune system. This physiological process increases the risk of diseases. The suckling pig begins synthesizing IgG from 7 days of age but this amount is correlated with the amount absorbed from colostrum (148).
Table 1.2. The protein content of sow’s colostrum and mature milk (22)
|
|
Colostrum1
|
Mature
milk2
|
|
Total
protein (g/100 g milk)
|
15.14
|
5.47
|
|
Casein
(g/100 g milk)
|
1.48
|
2.74
|
|
Whey
(g/100 g milk)
|
14.75
|
2.22
|
|
Serum
albumin (mg/ml milk)
|
15.79
|
4.61
|
|
IgG
|
95.60
|
0.90
|
|
IgA
|
21.20
|
5.30
|
|
IgM
|
9.10
|
1.40
|
|
Lactoferrin
(mg/ml milk)
|
1,200
|
<100
|
1Taken immediately postpartum.
2Classified as milk samples collected between 14 and 21 days postpartum.
These groups of ingested immunoglobulin proteins are absorbed intact and not digested, enhanced by the presence of protease inhibitors already present in colostrum (149). The levels of these maternally derived antibodies are highest at day 1 post-farrowing and then decline to very low levels by the time the pig reaches 3 weeks of age but they will be followed by a transient production of milk immunoglobulin IgA to maintain protection (8).
Sow milk composition changes with the stage of lactation and feed manipulation (155). Total solids, protein, minerals, fat and lactose content result in considerable change but the amino acid build up of the protein will be more stable (Table 1.3 and 1.4).
The presence of free amino acid in milk composition results in a more digestible and efficiently absorbed product (Table 1.5). In whole milk, amino acids found in abundance in whey proteins are cystine, glycine, and threonine which are less digestible than proteins from casein as glutamic acid, proline, and methionine (118). Thus the CP factor 6.38 for nitrogen.
Porcine colostrum may contain 151 g/kg of protein and is lower in ash content, which is the opposite of that found in many other species (Table 1.6). The liquid form of milk limits protein concentration and its quantity is not a major factor for survival (62). Amino acids participate more on the metabolic energy requirements of the suckling piglet rather than on protein accretion, which is a controversial economic situation when supplementing piglets.
Table 1.3. Average composition (g/kg) of sow colostrum and milk (8, 118)
| Variable |
Colostrum
|
Milk
|
| Dry matter |
215
|
187
|
| Crude protein (N X 6.38) |
105
|
54
|
| Fat |
54
|
71
|
| Lactose |
38
|
54
|
| Gross energy (MJ/kg) |
5.4
|
5.0
|
| Ash (21) |
7
|
9
|
| Essential amino acid (g/16 g N) | ||
| Lysine |
7.32
|
7.33
|
| Methionine+cystine |
3.24
|
3.30
|
| Tryptophan |
1.86
|
1.24
|
| Threonine |
5.46
|
4.52
|
| Leucine |
9.81
|
-
|
| Isoleucine |
3.87
|
3.98
|
| Valine |
5.95
|
5.25
|
| Histidine |
3.17
|
3.23
|
| Phenylalanine |
4.56
|
4.09
|
| Tyrosine |
5.63
|
4.26
|
Table 1.4. Porcine colostrums, milk nitrogen, and amino acid composition (37)
| Variable |
Colostrum
|
Colostrum
|
Milk
|
Milk
|
| Protein (g/L) |
87-155
|
29-55
|
||
| Urea (mmol/L) |
6.04
|
5.18
|
||
| Ammonia (mmol/L) |
2.01
|
1.25
|
||
| Amino acids |
Free*
|
Protein
Bound**
|
Free*
|
Protein
Bound**
|
| Arginine |
25
|
23-50
|
63
|
6-15
|
| Histidine |
1,023
|
14-33
|
538
|
4-12
|
| Isoleucine |
37
|
26-42
|
17
|
9-15
|
| Leucine |
85
|
65-120
|
38
|
20-34
|
| Valine |
64
|
50-81
|
111
|
12-20
|
| Lysine |
30
|
45-77
|
58
|
19-26
|
| Threonine |
40
|
40-88
|
364
|
10-20
|
| Methionine |
12-15
|
21
|
4-7
|
|
| Phenylalanine |
36
|
23-43
|
33
|
7-13
|
| Proline |
50
|
47-142
|
115
|
26-37
|
| Tyrosine |
34
|
25-52
|
63
|
8-15
|
| Cystine |
24
|
11-13
|
218
|
2-3
|
| Glutamine |
108
|
1,929
|
||
| Glutamate |
150
|
78-107
|
905
|
35-56
|
| Alanine |
132
|
42-83
|
659
|
12-22
|
| Aspartate |
38
|
51-108
|
472
|
15-30
|
| Asparagine |
|
201
|
||
| Glycine |
159
|
33-82
|
1,358
|
8-24
|
| Serine |
30
|
49-103
|
376
|
13-26
|
| Citrulline |
46
|
|||
| Ornithine |
43
|
55
|
||
| Taurine |
903
|
1,488
|
*Free, mmol/L: **Protein bound, mmol/L. Glutamic acid, Aspartic acid.
Table 1.5. Porcine colostrum and milk inorganic element composition (mg/L) (37)
| Variable |
Colostrum
|
Milk
|
| Calcium |
900-1519
|
1511-2274
|
| Phosphorus |
900-1579
|
1041-1832
|
| Magnesium |
80-120
|
80-133
|
| Potassium |
1250-1617
|
356-1000
|
| Sodium |
758-820
|
340-542
|
| Chloride |
1200
|
1000
|
| Iron |
2.29-4.68
|
1.33-4.60
|
| Zinc |
9.2-15.98
|
4.94-7.35
|
| Copper |
2.86-3.21
|
1.11-2.01
|
| Manganese |
0.12-0.45
|
0.06-0.38
|
| Selenium |
0.10-0.15
|
0.02-0.03
|
| Chromium |
0.60
|
0.46
|
| Aluminum |
3.5
|
1.8-3.7
|
| Nickel |
0.42
|
0.31
|
| Lead |
0.17
|
0.16
|
| Cadmium |
0.04
|
0.04
|
| Boron |
0.03
|
3.45
|
| Sulfur |
36.1
|
|
| Molybdenum |
0.04
|
0.02-0.10
|
Table 1.6. Composition of mammalian milks at mid-lactation (60)
| Species |
Protein
(g/l)
|
Fat
(g/l)
|
Carbohydrate
(g/l)
|
| Woman |
8
|
41
|
68
|
| Cow |
32
|
37
|
46
|
| Sow |
56
|
83
|
50
|
The protein concentration of sow’s milk does not have an effect for maximum growth rate in suckling pigs. Caseins are nutritional proteins made of amino acids. They are carriers of calcium and may promote non-pathogenic bacteria growth. b-casomorphin and a-casein from casein protein may provide immunologic activity while the whey proteins are protective proteins made of blood serum albumin, a-lactalbumin, b-lactoglobulin, IgG, IgA, IgM, lactoferrin, and other minor proteins such lysozyme, transferrin, Vit. B12-binding protein and the bifidus factor. These whey proteins molecules are absorbed by endocitosis mode of action during the first 1-2 days as explained above.
During the intestine maturation some immunoglobulin molecules will be digested because a-lacatalbumin protein is made of high levels of lysine, cysteine and tryptophan with high digestibility and biological value. The resistance to digestion of IgG is more notorious in the proximal part of the intestine with only 50.7% of the protein molecule being digested and when it passed to the medial part of the gut an additional 47.1% digestion occurs for this IgG protein, upon reaching the terminal part of the intestine the protein molecule had an undigested percentage of 10.1%. In the caecum it was almost fully digested with a remainder of 0.9%; and in the colon was 0.1 %, almost completed digested (100). Under other circumstances, there are some contributions in the amino acid profile of the colostrum composition as immunoglobulins being glucoproteins, but they are not hydrolyzed so they are not digested (22). This protein functions as biding agents for the toxins from bacteria.
The fat content in colostrum varies consistently, from 5% at farrowing time to its highest level of 10% at 72 hours post partum. Afterward, it declines during lactation to an 8% fat content and even lower and its dependent of the caloric density of the diet and feed intake. The composition of milk dry matter content of fat is 400 g/kg during late lactation (Table 1.7 and 1.8). This is direct effect of body fat contribution to the synthesis of milk fatty acids.
Through these tables it is evident that colostrum and milk undergo constant changes during lactation and its composition is highly correlated to metabolic rate, milk synthesis and feed nutrient intake. However, protein composition and microminerals are less manipulated by external factors.
Table 1.7. Chemical composition of sow colostrum and milk (22,37)
|
Colostrum
|
|||
| Variable |
During
Parturition
|
24
h after parturition
|
Milk
at 15 days
|
| Dry matter (%) |
23.40
|
22.00
|
19.20
|
| C. P. (Nx6.38) (%) |
13.10
|
9.10
|
5.50
|
| Fat (%) |
5.10
|
6.80
|
8.10
|
| Lactose (%) |
3.80
|
3.90
|
4.80
|
| Energy (kJ/g) |
5.93
|
5.89
|
5.23
|
| Amino acids (g/16g N) | |||
| Arginine |
5.53
|
5.80
|
6.50
|
| Histidine |
2.97
|
2.99
|
2.78
|
| Isoleucine |
3.77
|
3.98
|
3.71
|
| Leucine |
9.85
|
9.40
|
8.36
|
| Lysine |
7.34
|
7.43
|
7.42
|
| Methionine+cystine |
3.40
|
3.02
|
3.34
|
| Phenylalanine |
4.49
|
4.29
|
4.08
|
| Threonine |
5.90
|
5.10
|
5.03
|
| Valine |
6.45
|
6.04
|
5.68
|
| Fatty acids (% total FA) | |||
| C14:0 |
1.90
|
1.80
|
3.40
|
| C16:0 |
23.50
|
22.50
|
38.70
|
| C16:1 |
4.70
|
5.20
|
10.70
|
| C18:0 |
5.30
|
5.80
|
5.50
|
| C18:1 |
38.70
|
42.80
|
23.20
|
| C18:2 |
20.20
|
16.90
|
13.10
|
| C18:3 |
1.60
|
1.30
|
1.10
|
| C20:0 |
0.20
|
0.10
|
0.20
|
| C20:1 |
0.50
|
0.50
|
0.20
|
| C20:2 |
0.50
|
0.50
|
0.20
|
| C20:3 |
0.30
|
0.20
|
0.10
|
| C20:4 |
1.10
|
0.90
|
0.60
|
| Elements | |||
| Ca (%) |
0.066
|
0.103
|
0.146
|
| P (%) |
0.110
|
0.127
|
0.117
|
| Mg (%) |
0.007
|
0.009
|
0.008
|
| K (%) |
0.119
|
0.143
|
0.083
|
| Na (%) |
0.082
|
0.048
|
0.043
|
| Cu (mg/g) |
3.21
|
2.46
|
1.79
|
| Zn (mg/g) |
14.00
|
8.31
|
5.88
|
| Mn (mg/g) |
0.12
|
0.11
|
0.06
|
| Fe (mg/g) |
4.68
|
3.52
|
2.88
|
Table 1.8. Fatty acids (%) in the fat of sow’s colostrum and milk (22, 37)
| Fatty acid |
Colostrum
|
Mature
milk
|
| Butyric Acid (C4:0) |
0
|
0.08
|
| Caproic Acid (C6:0) |
0
|
0.09
|
| Caprylic Acid (C8:0) |
0
|
0.03
|
| Capric Acid (C10:0) |
0
|
0.01
|
| Lauric Acid (C12:0) |
0
|
0.02
|
| Myristic Acid (C14:0) |
3.20
|
3.71
|
| Myristoleic Acid (C14:1) |
0.01
|
0
|
| Pentadecanoic Acid (C15:0) |
0.03
|
0.01
|
| Pentadecenoic Acid (C15:1) |
0.01
|
0
|
| Palmitic Acid (C16:0) |
33.30
|
37.00
|
| Palmitoleic Acid (C16:1) |
5.47
|
9.10
|
| Heptadecanoic Acid (C17:0) |
0.08
|
0.09
|
| Heptadecenoic Acid (C17:1) |
0.13
|
0.14
|
| Stearic Acid (C18:0) |
6.31
|
6.02
|
| Oleic Acid (C18:1) |
37.50
|
33.00
|
| Linoleic Acid ((C18:2) |
12.70
|
8.90
|
| Linolenic Acid (C18:3) |
0.74
|
1.14
|
| Arachidonic Acid (C20:4) |
0.42
|
0.51
|
| Behenic Acid (C22:0) |
0.01
|
0.01
|
| Eicosatric Acid (C20:3)/Erucic Acid (C22:1) |
0.11
|
0.13
|
| Arachidic Acid (C20:0) |
0.12
|
0.15
|
| (C20:1) |
0.30
|
0.16
|
| (C20:2) |
0.30
|
0.16
|
| Erusic Acid (C22:1) |
0.05
|
0.001
|
| Medium chain (%) |
|
0.65
|
| Long chain saturated (%) |
29
|
34
|
| Monounsaturated (%) |
45
|
45
|
| Polyunsaturated (%) |
24
|
20
|
| Cholesterol |
|
0.34
|
| Gross energy (kcal/liter) |
1517
|
1114
|
| Lactose |
40-44
|
50-59
|
| Total lipid |
49-50
|
65-88
|
1Relative percentages of the fatty acid methyl esters.
2Taken immediately postpartum.
3Classified as milk samples collected between 14 and 21 days postpartum.
There are many other components in the sow’s colostrums composition (23, 24, 94, 118, 146), such as:
1. Nutrientsa. Lipids; triacylglycerol, free fatty acids, phospholipids, glycolipids, sphingolipids, sterols, hydrocarbons and fat soluble vitamins);
b. Carbohydrates (lactose, oligosaccharides, galactose, glucose and glycoproteins);
c. Proteins (as1,B, and k-caseins, a-lactalbumin, b-lactoglobulin, lactoferrin, secretory IgA and other immunoglobulins, lysozyme, transferrin, enzymes, hormones and growth factors);
d. Non-protein nitrogenous compounds (urea, creatine, creatine phosphate creatinine, uric acid, amino acids including glutamine, nuclei acids, nucleotides and polyamides); and
e. Water soluble vitamins; f) Macronutrient elements and trace elements (minerals); Copper, zinc, iron and concentrations of some microelements are very low.
2. Hormones (insulin, cortisol, thyroxine);
3. Growth factors (epidermal growth factor, growth hormone receptors (cytokine), growth hormone-binding protein (PRL-BP) (140), transforming growth factor in the small intestine (TGF-B) (73), nerve growth factor, insulin-like growth factors I and II);
4. Cells (neutrophils, lymphocytes, macrophages, eosinophils, epithelial cells, leucocytes); and
5. Other substances (opioid peptides (casomorphins, lactorphins, casoxins, lactoferroxins), bombesin, lactoferrin, neurotensin) present in the colostrum and milk.
Feeding the early gestating sow with extra Fe, Zn, Cu, Se and Cr resulted in better conception rates and fetal survival and colostrum mineral concentration but not on milk mineral concentration, especially for Cu and Fe (68). Piglets reared in the open field did not show iron deficiencies during lactation, because they were licking some soil and the mineral supplement did not come from the milk composition since this mineral is not variable in milk composition (161).
Colostrum has more concentrated energy throughout protein components and milk energy contribution depends on lipid concentration (Table 1.9).
Many nutritional tables are published worldwide: the National Research Council NRC 1998 (104) in the USA, the Agricultural Research Council (ARC 1981) and British Society of Animal Science in the United Kingdom, in France the Institut National de la Reserche Agronomique (INRA 1984) and Institut Technique du Porc (ITP). The Association Francoise de Zootechnie. Others sources are the Centraal Veevoeder Bureauu (CVB) (www.tessenderlo.com, www.hollandmeat.nl/gb/index.htm) from Netherlands, in Denmark (www.lu,dk), with recent report changes in 2002 for threonine and tryptophan for weaner
Table 1.9. The main components of sow’s colostrum and milk and their relative contribution to gross energy (68)
|
|
Fresh sample |
|
|
|
Variable |
g/kg |
KJ/kg |
% of total gross energy |
|
Colostrum (3 h after farrowing) |
|
||
|
Total crude protein |
175 |
4148 |
56.5 |
|
Total immunoglobulins |
96 |
|
|
|
Pre-albumin+albumin |
47 |
|
|
|
Casein |
32 |
|
|
|
Total lipids |
67 |
2653 |
36.1 |
|
Lactose |
32 |
544 |
7.4 |
|
Total energy |
|
7345 |
100.0 |
|
|
|||
|
Milk (day 7 of lactation) |
|
||
|
Total crude protein |
56 |
1327 |
21.5 |
|
Total immunoglobulins |
20 |
|
|
|
Pre-albumin+albumin |
13 |
|
|
|
Casein |
23 |
|
|
|
Total lipids |
101 |
4000 |
65.0 |
|
Lactose |
49 |
833 |
13.5 |
|
Total energy |
|
6160 |
100.0 |
pigs in www.danskeslagterier.dk.
Lists of tables are provided by the Spanish Foundation for the Development of
Animal of Animal Nutrition (FEDNA). Also AMIpig, AFRC 1991, and in Australia
SCA 1987, AUSPIG and Australian Pork Ltd (PRDC) (48). In addition, C
It is not the
purpose of this paper to
It is important
to consider the size of the animal, its growth rate, feed consumption and feed
concentration to satisfy nutrient requirements. This is accomplished by using
feeding tables along with background information and proper consultation. The
selection of any table is as good as the actual chemical composition
Table 1.10. Amino acid requirements for piglets of different age and weight (g/kg) (50)
|
Pig
weight (kg) or age (weeks)
|
|||||||||
|
NRC
(1988)
|
ARC
(1981) 1
|
|
|||||||
|
Amino acid |
1-5 |
5-10 |
10-20 |
20-50 |
50-110 |
0-32 |
3-82 |
15-50 |
50-90 |
|
Lysine |
14.0 |
11.5 |
9.5 |
7.5 |
6.0 |
15.8 |
13.8 |
11.0 |
7.8 |
|
Arginine |
6.0 |
5.0 |
4.0 |
2.5 |
1.0 |
- |
- |
- |
- |
|
Histidine |
3.6 |
3.1 |
2.5 |
2.2 |
1.8 |
5.2 |
4.5 |
3.6 |
2.6 |
|
Isoleucine |
7.6 |
6.5 |
5.3 |
4.6 |
3.8 |
8.6 |
7.5 |
6.0 |
4.3 |
|
Leucine |
10.0 |
8.5 |
7.0 |
6.0 |
5.0 |
15.8 |
13.8 |
11.0 |
7.8 |
|
Methionine |
|
|
|
|
|
|
|
|
|
|
+cysteine |
6.8 |
5.8 |
4.8 |
4.1 |
3.4 |
7.9 |
6.9 |
5.5 |
3.9 |
|
Phenylalanine |
|
|
|
|
|
|
|
|
|
|
+tyrosine |
11.0 |
9.4 |
7.7 |
6.6 |
5.5 |
15.1 |
13.3 |
10.4 |
7.5 |
|
Threonine |
8.0 |
6.8 |
5.6 |
4.8 |
4.0 |
9.4 |
8.3 |
6.5 |
4.7 |
|
Tryptophan |
2.0 |
1.7 |
1.4 |
1.2 |
1.0 |
2.3 |
2.0 |
1.6 |
1.2 |
|
Valine |
8.0 |
6.8 |
5.6 |
4.8 |
4.0 |
11.0 |
9.7 |
7.7 |
5.5 |
1 Based on the requirements for pigs weighing 15-90 kg on the assumption that the diet contains 13. MJ/kg.
2 Age in weeks: based on the requirements on the assumption that the diet contains 14.1 MJ/kg, which is similar to the energy density recommended by the NRC (1988) for young pigs.
Table 1.11. Total lysine in the diet (grams) for each digestible energy (DEMJ). Ratios (g/MJ) in the diets of growing pigs (3, 138)
|
Protein
deposition
|
Weight
|
Lysine/DE
ratio
|
|
|
|
|
Genotype |
Rate (g/day) |
(kg) |
Castrate |
Gilt |
Boar |
|
Unimproved |
100 |
<25 |
0.78 |
0.80 |
0.83 |
|
25-55 |
0.73 |
0.75 |
0.78 |
||
|
Average |
125 |
<25 |
0.85 |
0.85 |
0.88 |
|
25-55 |
0.78 |
0.80 |
0.83 |
||
|
High |
150 |
<25 |
0.88 |
0.90 |
0.93 |
|
25-55 |
0.83 |
0.85 |
0.88 |
||
|
Hybrid |
175 |
<25 |
1.20 |
1.20 |
1.20 |
|
25-55 |
1.10 |
1.10 |
1.10 |
Table 1.12. Total basis lysine requirements of different classes of weaned pig (3, 138)
| Diet type |
Weight
band (kg)
|
Total
lysine (g/kg)
|
| Pre-starter |
<5
|
17-18
|
|
3-5
|
15
|
|
|
<5
|
16.5-17.5
|
|
| Starter |
5-7
|
15-16
|
|
5-10
|
13.5
|
|
|
5-10
|
14
|
|
|
5-10
|
16.0-16.5
|
|
| Link |
7.0-11.5
|
13.5-14.5
|
|
7-12
|
15-16
|
|
| Early grower |
11.5-23.0
|
12.5-13.5
|
|
10-20
|
11.5
|
|
|
10-25
|
11
|
|
|
10-25
|
15
|
|
| Grower |
15-25
|
10.5
|
|
12-25
|
14-15
|
Different sources from United Kindom, USA and France.
The inclusion of artificial amino acids (lysine, threonine and methionine) in the supplements for baby pigs has been proved to respond in growth rate (160). They do not substitute milk protein but contribute in the balance for the “ideal protein”. In addition, the use of protein sources with high levels of valine and arginine improve growth rate response. The use of these products are determined largely by cost and individual amino acid contribution in the diet. The artificial aminoacid products will no longer be expensive with the construction of the new fermentation plant in the state of Illinois USA in 2004 (Table 1.13).
Table 1.13. Typical inclusion rates of synthetic amino acids in starter feeds (3)
|
Rates
|
Lysine
|
Methionine
|
Threonine
|
Tryptophan
|
|
Kg/Ton
|
2-5
|
0.5-2
|
0.5-1.5
|
0-1
|
Metric units.
The neonatal pig is more efficient during the first week of age with a milk metabolizable energy (ME) conversion rate of 17 kJ milk ME/g body weight gain. During this stage the suckling pig is able to consume more that 5 times its ME maintenance. Normally this consumption is 3.3 to 3.8 times MEm and to 2.5 times MEm thereafter, reducing the conversion to 19 kJ milk ME/g BW growth. This rapid change in digestion and efficiency accounts for sudden changes in nutrient requirements and frequent changes in diets producing alternative values in different tests. This means that piglets are able to consume large quantities of digestible milk supplements after birth, and will also continue to suckle their dam at the same rate (167).
It has not been determined if there are consequences due to the reduction of colostrum intake or reduced immunoglobulin protection that may increase piglet morbidity and even mortality with the inclusion of a milk substitute. In addition, there are no studies of supplementing piglets during early lactation to determine if sow’s milk reduces allergic reaction and provides a protective inflammatory factor that reduces allergic reaction from a feed source such as soybean meal. Acclimating pigs to the consumption of viable quantities of solid feed > 15 MJ ME/kg before they are weaned is commensurate with normal growth after weaning (1).
Suckling piglets may have depressed milk ingestion and low creep feed consumption because protein and mineral level in the sow’s milk and the high % CP in the supplement may cause an increase of urinary nitrogen and minerals excretions with a consequent body water loss (162). If the heater lamp raises the temperature in the farrowing creep, it may raise fresh water requirements for neonates. Many farrowing facilities do not provide water for suckling pigs and this depresses milk and total feed dry matter consumption. Neonate piglets can start drinking water after 2 days of age, from 0 to 200 ml/day with an average of 46 ml, but some studies report lesser amounts (104).
The gradual process of weaning by creep feeding provides a transitional training eating period to stimulate free choice feed consumption > 7 g of food/day at 14 days of age and about > 127 g/day at 28 days of age (7). Before weaning at 19-25 days, a lactating sow is able to produce a piglet growing at 300 g BW/day, providing 4.0 MJDE of milk/pig/day, supplementing feed with extra 1.5 MJDE/day containing 19.0 MJDE/kg. In order to support a growth rate of 300 g/day after weaning, the diet should contain > 27.5 MJ DE/kg to sustain a feed intake of 200 grams/day that will provide requirements of 5.5 MJ DE/day (44). Normal (uninterrupted) growth patterns during lactation and after weaning are seen only under the highest standards of husbandry and nutrition practices (168). These accomplishments could be achieved by providing experiences in feed consumption for the piglets and particularly in drinking water before weaning (137).
The second half of lactation after 14 days of age and the immediate post-weaning period are commonly identified as major periods when the deficit in energy intake is the most pronounced. This may cause a slow daily gain rate or even a weight lost with a reduction in muscular cell count. However, a low milk intake during the neonatal period also influences the ability of the piglet to survive and thrive because the low weight piglet is more willing to try creep feeding (2). The major physiological objective of milk and feed consumption during the suckling and weaning phases should be to maximize piglet growth and develop insulation tissue in the endodermis or superficial fat. It is also possible that lipid molecules are carriers of immune factors and precursors of hormonal changes that protect the piglet from diseases and may be a physical barrier for other pathogens. Therefore, because protein deposition increases linearly with energy intake in the suckling pig, maximization of protein deposition also implies maximization of energy intake.
If the piglet gets heavier during the neonatal period it will be fatter, and there is a belief that this will increase back fat thickness affecting carcass composition at slaughter-market time. It is unlikely that the extra fat deposited in the young pig will make a large contribution to the total stored fat in the market pig. There will be too many metabolic and physiological changes before the animal reaches market weight, and this early fat will not be stored in the adipose tissue at the finishing stage. Weaning pigs at 14 days of age have a potential to be fatter at 23 weeks if they had a challenge with post weaning syndrome (PWS) (54). Maybe an effect of extra feed consumed at the end of the finishing period and less protein accretion due to less muscular cells formation in the neonatal piglet increases back fat thickness. This compensatory growth is not always correlated to PWS.
There is little
information in the literature on the estimations of energy cost of maintenance
and growth in the suckling piglet due to the difficulties in determining milk
energy intake precisely. These estimations are also difficult to establish
immediately after weaning because of the usual low intake and the ensuing
negative energy balance during 1-5 days (2). This is a good expl
There is an obvious interest to maximize the efficiency of any diet or to supply the nutrient requirements for every type of breed and age or weight of any pig. The modern nutritionist should also look to animal nutrition and feeding methods used and the importance of considering the effects on the animal welfare, the quality of the product and the impact on the environment (53, 137). Differences in these factors may change the nutrient requirements of the animal to match the market or regulation needs in different parts of the world.
Requirements for maintenance of energy
A summary of values for metabolizable energy requirements for maintenance (MEm) and efficiencies of ME intake for total energy retention (k-g) and for energy retained as protein (k-p) and fat (k-f) is given in Table 1.14. MEm includes the energy cost of basal metabolism, physical activity and thermoregulation. In the suckling pig reported MEm values amounts from 340 kJ ME/kg BW0.75 per day to 470 kJ ME/kg BW0.75 per day. There is small variation in the suckling pig for energy retained and protein accretion compared with the weaning pig range for these concepts. The suckling piglet retains fat from feed to body fat in a 1:1 ratio but not after weaning (19).
In the suckling pig, the energy cost of standing is 0.18 kJ BW0.75 per minute, but in practice the total energy cost of suckling and standing activity is very variable and difficult to assess, especially in outdoor rearing conditions. On the basis that 1g sow’s milk supplies 4.75 kJ ME it is not considered a concentrated feed so the animal have to suck high volumes of milk. The concentrated source of 1g weaning diet supplies >15 kJ ME and the animal needs small amounts to meet maintenance requirements. Sow milk is very digestible (0.99-1.00) because of its high biological value, but values for DE or ME varied widely in relation to its fat content. The fat content in the dry matter of sow milk is about 400 g/kg (44). The true digestibility of sow’s milk reported is 88% for nitrogen, and the average amino acids digestibility is 92%, but for amino acids cystine and threonine the digestibility is 88%
Table 1.14. Summary of the estimated values for maintenance energy requirements (MEm) and for efficiency of metabolizable energy intake for growth (k-g), protein (k-p) and fat (k-f) deposition (19)
|
MEm
|
|
|||
|
(kJ
ME/kg BW0.75)
|
(k-g)
|
(k-p)
|
(k-f)
|
|
| Suckling pig |
340-470
|
0.70-0.73
|
0.56
|
1.0
|
| Weaned range |
420-550
|
0.60-0.79
|
0.50-0.66
|
0.73-0.84
|
and for methionine,
histidine, and glutamic acid is 100%. The average digestibility for all the
amino acids is 92%±4% (118). This is an indication that it is difficult to compare
the digestibility of milk for different herds, because milk composition variability
will affect
Piglets of 3.82 kg body weight digest human milk very well > 90%, but certain amino acids such threonine, valine and phenylalanine are not absorbed as well (98). This paper did not explain the cause and origin of the effect due to the quality properties of the human milk or if it was a deficiency of enzymes in the