Piglet BW Gain Research Articles

293 The Effect of Creep Feed and Nursery Diet Flavoring on Piglet Lactation and Nursery Performance

Abstract Larger litter sizes in swine production systems and potential milk limitations for piglets have given new opportunities to incorporating creep feeding as a management strategy. Sows (n = 51) and their litters were used to test the effects of creep feed and nursery diets on piglet lactation and nursery growth performance. Ten days before weaning, litters were assigned to one of three creep feeding treatments: 1) Control diet: 2) Control+Flavoring (50 ppm Allium XL, Pancosma): 3) No creep feed. Creep feed was delivered twice/day via one bowl creep feeder/litter. Sows and litters (17/treatment) were allotted to equalize parity (average = 2.8), genetics, number of piglets (average = 10.9), and weaning age (average = 19.1). Litter weights and creep feed intake were recorded on d 0, 4, and 10 (weaning). Post-weaning pigs were allotted to Control or Flavoring (50 ppm Allium XL) diets in a 3x2 factorial arrangement. During nursery there were 10 pens/treatment with 7 or 8 pigs/pen, blocked by initial BW within creep treatment. Nursery treatments were fed in phase 1 (1.13 kg/pig) and 2 (2.27 kg/pig) diets followed by common phase 3 (6.8 kg/pig) and 4 (ad lib to d 35) diets. Weekly pig BW and feed intake were used to calculate nursery pen ADG, ADFI, and G:F. Data were analyzed using GLM procedure of SAS 9.4. Creep feeding treatment during lactation did not affect litter or piglet BW gain pre-weaning. Flavoring did not affect total creep feed intake (control = 114 g/pig vs. flavoring = 110 g/pig). Providing creep feed during lactation increased ADFI on days 2, 3, and 4 post-weaning (P < 0.013). Pigs fed either creep feed increased week 1 nursery ADFI (8.8%; P< 0.02), numerically increased ADG (5.2%), and greater d ay7 BW (P = 0.055). Week 3 ADG (P < 0.05) and ADFI (P < 0.05) were greater for the no creep pigs than pigs fed the control creep feed, flavored creep feed pigs were intermediate. For week 4, ADG, and week 4 and 5 ADFI, pigs previously fed control creep had greater growth performance than pigs previously fed flavored creep with pigs fed no creep being intermediate (P< 0.05). Overall (days 0-35), pigs fed control creep had greater ADG ( P< 0.05) and ADFI (P < 0.05) than flavored creep fed pigs with no creep pigs being intermediate in ADG and greater ADFI than flavored creep fed pigs. Final BW (P < 0.05) was greater for control creep fed pigs than flavored creep fed pigs with no creep pigs being intermediate (23.5 kg, 23.0 kg, 23.3 kg, respectively). Nursery dietary flavoring treatment did not affect post-weaning ADG, ADFI, or G:F at any point during the study (P > 0.12). Lactation creep feeding significantly increases ADFI and ADG during the first week post-weaning, which could improve post-weaning performance and reduce the rate of pigs failing to thrive post-weaning.

Microalgae supplementation to late gestation sows and its effects on the health status of weaned piglets fed diets containing high- or low-quality protein sources

Maternal stress, such as a bacterial infection occurring in late gestation, may predispose offspring to a variety of diseases later in life. It may also alter programming of developing systems within the fetus, such as the hypothalamic-pituitary-adrenal (HPA) axis and immune system. Dietary supplementation during the last trimester of pregnancy with immune-modulating compounds may be a means of reducing potential adverse effects of maternal stress on the developing fetus. Essential omega-3 polyunsaturated fatty acids (n-3 PUFA) such as docosahexanoic acid (DHA) and eicosapentanoic acid are well-known for their immune-modulating and anti-inflammatory properties. Sources of these n-3 PUFA include fish products such as fish oil and microalgae, which may be a suitable alternative to fish-based products. The aim of this study was to determine the effect of supplementing gestating sow diets with n-3 PUFA and inducing an immune stress challenge in late gestation on piglet growth and immune responsiveness when placed on either a high- or low-quality protein diet after weaning. Forty-eight sows were fed gestation diets containing either 3.12% microalgae, 3.1% fish oil or a corn oil control diet containing 1.89% corn oil starting on gestation day (gd) 75. On gd112, half the sows in each treatment were immune stress challenged with bacterial lipopolysaccharide (LPS) endotoxin (10 μg/kg administered i.m). After farrowing, piglet BW gain was monitored weekly during lactation and pigs were weaned at 21 days of age. One week after weaning, four piglets per sow were immune stress challenged with LPS (40 μg/kg administered i.m.). At the same time, four piglets per sow were vaccinated with the novel antigens chicken ovalbumin (OVA) and Candida cellular antigen (CAA) and received booster vaccinations two weeks later. Four weeks after the initial vaccination, a transdermal hypersensitivity immune challenge was performed using the same antigens. Blood samples were also collected to quantify IgG antibody responses to both antigens. PUFA enrichment in sow blood and piglet brain was detected after sows were on feed for 40 days. Piglet growth was increased in pigs fed a high-quality diet in nursery phase 1. Concentrations of the cytokines IL-1ra, IL-6 and IL-10 were elevated in pigs fed a high-quality protein diet following LPS immune challenge. Overall, it appears that in the current study piglet nursery diet quality was more important for determining piglet health and growth than maternal diet and immune stress.

Comparative study on the relations between backfat thickness in late-pregnant gilts, mammary development and piglet growth.

The potential relation between body condition of gilts in late-pregnancy and litter BW gain as well as mammary development was studied using 2 sets of data. Gilts either from a commercial herd (Part 1, n = 182) or from a series of trials looking at mammary development (Part 2, n = 172) were separated in 3 groups according to backfat thickness (BF) on d 110 of gestation. Group categorization was similar for Parts 1 and 2 of the study and was: low (LOW), 13.6 ± 1.6 mm (mean ± SD); medium (MED), 17.6 ± 1.0 mm (mean ± SD); and high BF (HIGH), 21.8 ± 1.8 mm (mean ± SD) for Part 1, and LOW, 14.2 ± 1.3 mm (mean ± SD); MED, 18.1 ± 1.0 mm (mean ± SD), and HIGH 23.4 ± 2.6 mm (mean ± SD) for Part 2. The effects of BF group on piglet BW gain (Part 1) or on various mammary gland characteristics (Part 2) were determined using ANOVA. Litters from HIGH sows tended to have a greater lactation BW gain than those from LOW sows (P < 0.10). Sows with HIGH BF had more mammary parenchymal tissue and more total protein and total DNA than MED and LOW sows (P < 0.05), which led to greater total protein and total DNA contents (P < 0.05). There were strong positive correlations (P < 0.0001) between parenchymal weight and total protein, total DNA, and total RNA. Results suggest that it is beneficial for primiparous sows to have greater BF (i.e., 20 to 26 mm) at the end of gestation to achieve optimal mammary development and greater litter BW gain in the subsequent lactation.

Impact of sow prepartum behavior on maternal behavior, piglet body weight gain, and mortality in farrowing pens and crates.

In the 24-h period prior to parturition, sows are active and motivated to perform nest-building behavior. The aim of this study was to investigate whether prepartum activity (nesting and postural changes) could predict maternal behavior 24 h postpartum, piglet mortality, and BW gain 24 h postpartum in farrowing pens and crates. Sows were randomly moved either to a farrowing pen ( = 20) or a farrowing crate ( = 18). Prepartum nest-building behavior (PRE-nesting) and prepartum postural changes (prepartum postural changes) were analyzed 24 h before the birth of the first piglet (BFP) and were divided into twelve 2-h intervals. Latency of the first suckling from the litter was observed after the birth of the last piglet. Udder accesses and piglet suckling were noted at 5-min intervals, using 1/0 sampling, during the first 24 h after BFP were counted. Piglet trapping, crushing, and total live-born mortality were measured during the first 72 h after BFP. Piglet BW gain was estimated 24 h after BFP. Increased PRE-nesting observed 2 h before BFP were associated with fewer suckling intervals in crates but not in pens ( < 0.01) as well as an increase in postural changes during parturition ( < 0.001) in both housings. A link between housing and PRE-postural changes was evident. An increase in the number of PRE-postural changes 2 h prior to BFP was associated with lower incidences of udder access in crates but not in pens ( < 0.05). A higher probability of piglet trapping was associated with increased PRE-nesting in the 2 to 4 h before BFP. No significant relationship between either PRE-nesting and postural changes and piglet BW gain and mortality was detected. Our results suggest that increased prepartum activity 2 h before parturition is associated with less suckling and less udder access in farrowing crates but not in farrowing pens. This suggests that the same sow behavior can have different consequences in pens vs. in crates. Future research should focus on nest-building activity, its relationship to endocrine indicators (e.g., oxytocin, cortisol) before parturition, and its potential long-lasting effects on subsequent maternal behaviors and piglet production.

Effect of pre- and post-partum sow activity on maternal behaviour and piglet weight gain 24 h after birth

Within the 24h prior to parturition sows are active and motivated to perform nest-building behaviour. The aim of this study was to investigate: (i) whether pre-partum activity (e.g. nesting and postural changes) could predict maternal behaviour 24h post-partum (pp) and weight gain 24h pp, and (ii) whether post-partum activity (post-partum nesting and postural changes) affect parts of the maternal behaviour 24 pp (e.g. first suckling, udder access, suckling duration) and piglet weight gain 24h pp. Fifteen sows were housed in modified straw-bedded “walk-around” farrowing crates. Pre-partum nesting events and postural changes were recorded 24h before parturition. During parturition the number of nesting behaviour and latency of the first sucking of the whole litter were recorded. Number of postural changes and duration of udder access were recorded 24h after birth of the first piglet (BFP) during three time periods (during parturition, from the end of parturition to 12h after BFP, and 12–24h after BFP). The duration of suckling and sow responsiveness on the playback of piglets’ scream were recorded during two time periods (from the end of parturition to 12h after BFP, and 12–24h after BFP). Piglet BW gain was estimated 24h after BFP. Data were analysed using proc GLM and MIXED and the probability of sow responsiveness using proc GENMOD in SAS. Pre-partum nesting 4h before BFP was related with longer latency of the first sucking (P<0.01), with shorter duration of suckling (P<0.05) and with lower piglet BW gain (P<0.05). More nesting after BFP was associated with a lower probability to react towards the playback of piglets’ screams (P<0.05). However more postural changes after BFP were associated with a higher probability to react towards the playback of piglets’ screams (P<0.05). More postural changes during parturition were related with higher piglet BW gain (P<0.05), but more postural changes during 12–24h after BFP were related with lower piglet BW gain (P<0.01). No other relationships were detected between pre-partum nesting and maternal behaviour within the 24h after BFP. High occurrence of pre-partum nesting 4h before parturition, but not more pre-partum postural changes, may be an early indicator for impaired suckling behaviour and lower weight gain during the first 24h post-partum.

Sow postural changes, responsiveness to piglet screams, and their impact on piglet mortality in pens and crates.

Free farrowing pens (pens) improve the welfare of sows but may increase sow activity and negatively influence piglet production. The aim of this study was to assess the effect of pens and crates on sow postural changes, piglet trapping, sow responses to piglet screams, piglet mortality, and piglet BW gain. It was predicted that provision of greater space (in pens) would increase not only the frequency of sow postural changes and the probability of trappisng but also sow responses to the screams of piglets; thus, the outcome would be no differences in fatal piglet crushing or overall mortality between the housing systems. Sows were randomly moved to either a farrowing pen (n = 20) or farrowing crate (n = 18). Sow behavior was recorded and analyzed for 72 h from the birth of the first piglet (BFP). Sow postural changes included rolling from a ventral to lateral position and vice versa and going from standing to sitting, standing to lying, and sitting to lying. Occurrences of piglet trapping and sow responsiveness to real crushing situations were analyzed. Sow responsiveness was assessed in response to audio playbacks (PB) of piglet screams on d 3 postpartum (48 to 72 h after BFP; PB crush calls) and real piglet crushing during the first 72 h after BFP (real crush calls). Piglet BW gain was estimated 24 h after BFP, piglet BW was recorded at weaning, and piglet crushing and piglet mortality were recorded during the 72 h after BFP. Data were analyzed using PROC MIXED and PROC GENMOD of SAS. Sows in pens showed more postural changes (P = 0.04) and tended to have greater incidences of piglet trapping (P = 0.07) than those in crates. Sow response to PB crush calls was greater in pens (P = 0.04) but did not differ for real crush calls between pens and crates (P = 0.62). There was no effect on the probability of piglet crushing (P = 0.38) and mortality (P = 0.41) during the 72 h after BFP nor in piglet mortality at weaning (P = 0.81) between pens and crates. Piglet BW gain at 24 h after BFP (P = 0.01) and piglet BW at weaning (P = 0.02) were greater in pens. Sows in pens showed more postural changes and tended to trap more piglets; however, the response to real crush calls did not differ between the two housing systems. Despite this, there was no increase in piglet crushing or mortality in pens, which might be influenced by the better piglet body condition observed in pens, which in turn could influence their ability to avoid crushing by the sow.

Effects of high fiber intake during late pregnancy on sow physiology, colostrum production, and piglet performance1

Dietary fiber given during pregnancy may influence sow endocrinology and increase piglet BW gain during early lactation. The aim of the current study was to determine whether dietary fiber given to sows during late pregnancy induces endocrine changes that could modulate sow colostrum production and, thus, piglet performance. From d 106 of pregnancy until parturition, 29 Landrace×Large White nulliparous sows were fed gestation diets containing 23.4 [high fiber (HF); n=15] or 13.3% total dietary fiber [low fiber (LF); n=14]. In the HF diet, wheat and barley were partly replaced by soybean hulls, wheat bran, sunflower meal (undecorticated), and sugar beet pulp. After parturition, sows were fed a standard lactation diet. Colostrum production was estimated during 24 h, starting at the onset of parturition (T0) and ending at 24 h after parturition (T24) based on piglet weight gains. Jugular blood samples were collected from sows on d 101 of pregnancy, daily from d 111 of gestation to d 3 of lactation, and then on d 7 and 21 of lactation (d 0 being the day of parturition). Postprandial kinetics of plasma glucose and insulin concentrations were determined on d 112 of pregnancy. The feeding treatment did not influence sow colostrum yield (3.9±0.2 kg) or piglet weight gain during the first day postpartum to d 21 of lactation. Colostrum intake of low birth weight piglets (<900 g) was greater in litters from HF sows than from LF sows (216±24 vs. 137±22 g; P=0.02). Preweaning mortality was lower in HF than LF litters (6.2 vs. 14.7%; P=0.01). Circulating concentrations of progesterone, prolactin, estradiol-17β, and cortisol were not influenced by the treatment. Sows fed the HF diet had greater postprandial insulin concentrations than LF sows (P=0.02) whereas the postprandial glucose peak was similar. At T24, colostrum produced by HF sows contained 29% more lipid than colostrum produced by LF sows (P=0.04). Immunoglobulin A concentrations in colostrum were lower at T0 and T24 (P=0.02) in HF than LF sows (at T0: 8.6±1.1 vs. 11.9±1.1 mg/mL; at T24: 2.5±0.7 vs. 4.8±0.7 mg/mL). In conclusion, dietary fiber in late pregnancy affected sow colostrum composition but not colostrum yield, increased colostrum intake of low birth weight piglets, and decreased preweaning mortality, but these effects were not related to changes in peripartum concentrations of the main hormones involved in lactogenesis.

Piglet behavior as a measure of vitality and its influence on piglet survival and growth during lactation

The aim of the study was to develop a vitality scoring method, based on piglet behavior and relate it to piglet growth and survival. From 21 sows (Sus scrofa), 287 piglets were used. After farrowing (d 0), piglets were weighed and tested for 4 behavioral parameters in a circular enclosure (55 cm diam.): movement capacity (M), udder stimulation (U), number of completed circles around the enclosure (NCC), and screaming (Sc). Piglets were weighed again on d 1, 2, 3, and 17. Piglet rectal temperature (RT) was recorded on d 0, 1, 2, and 3. Farrowing information of the sow was also recorded. Multiple regression analyses for survival and BW gain at weaning as dependent variables were performed. Piglet BW gain at weaning was influenced by BW at birth (P < 0.001), sow parity (P = 0.024), total number of piglets born alive per sow (P < 0.001), and sum of U and NCC parameters (UN; P = 0.023). Piglet survival during lactation was influenced by BW at birth (P = 0.015), UNCC parameter (P = 0.026), and RT on d 3 (P = 0.085). The sum of U and NCC parameters, in combination with BW at birth and information of the sow, might be useful to predict piglet growth survival during lactation, thus becoming a useful tool to improve piglet management during the first days of lactation. In conclusion, UNCC parameter seems to be an easy and useful way to assess piglet vitality for both scientific and commercial purposes.

Responses to n-3 fatty acid (LCPUFA) supplementation of gestating gilts, and lactating and weaned sows

Feeding n-3 long-chain polyunsaturated fatty acids (LCPUFA) to gilts or sows has shown different responses to litter growth, pre-weaning mortality and subsequent reproductive performance of the sow. Two hypotheses were tested: (1) that feeding a marine oil-based supplement rich in protected n-3 LCPUFAs to gilts in established gestation would improve the growth performance of their litters; and (2) that continued feeding of the supplement during lactation and after weaning would offset the negative effects of lactational catabolism induced, using an established experimental model involving feed restriction of lactating primiparous sows. A total of 117 primiparous sows were pair-matched at day 60 of gestation by weight, and when possible, litter of origin, and were allocated to be either control sows (CON) fed standard gestation and lactation diets, or treated sows (LCPUFA) fed the standard diets supplemented with 84 g/day of a n-3 LCPUFA rich supplement, from day 60 of first gestation, through a 21-day lactation, and until euthanasia at day 30 of their second gestation. All sows were feed restricted during the last 7 days of lactation to induce catabolism, providing a background challenge against which to determine beneficial effects of n-3 LCPUFA supplementation on subsequent reproduction. In the absence of an effect on litter size or birth weight, n-3 LCPUFA tended to improve piglet BW gain from birth until 34 days after weaning (P = 0.06), while increasing pre-weaning mortality (P = 0.05). It did not affect energy utilization by the sow during lactation, thus not improving the catabolic state of the sows. Supplementation from weaning until day 30 of second gestation did not have an effect on embryonic weight, ovulation rate or early embryonic survival, but did increase corpora lutea (CL) weight (P = 0.001). Eicosapentaenoic acid and docosahexaenoic acid (DHA) levels were increased in sow serum and CL (P < 0.001), whereas only DHA levels increased in embryos (P < 0.01). In conclusion, feeding n-3 LCPUFA to gilts tended to improve litter growth, but did not have an effect on overall subsequent reproductive performance.

Production traits of litters in 2 crossbred Duroc pig lines

Genetics of different pig lines affects litter size, birth weight, and neonatal losses. Low birth weight has long been associated with neonatal losses, but piglet body mass index is reported to show stronger correlation with stillbirth. The aim of this study was to investigate differences in litter size, number of stillborn piglets, piglet BW gain, and body mass index between 2 different Duroc crossbred lines. Landrace × Yorkshire sows in 2 farms (n = 89) were divided into 2 groups on each farm. One group of sows on each farm was inseminated with semen from Landrace × Duroc boars (boar group LD, n = 48), and the other was inseminated with semen from purebred Duroc boars (boar group DD, n = 41). Piglets were monitored from birth to weaning at the age of 5 wk. Litter size in boar group LD was larger than in boar group DD (P = 0.03). Number of stillborn piglets in boar group LD tended to be greater than in boar group DD (P = 0.07). Piglets in boar group DD had a greater BW at birth (P = 0.02) and at 3 wk (P = 0.01) than those in boar group LD. Body mass index from birth to weaning was greater in piglets in boar group DD vs. LD (P < 0.01), and both BW and body mass index of liveborn piglets at birth for both groups combined showed a positive correlation with survival at weaning (P < 0.01). In conclusion, breeding for larger litter size in boar group DD may be one approach to increase the number of vigorous piglets in production, but the inverse relationship between litter size and birth weight was more pronounced for this group than for boar group LD (P = 0.03). Further studies of the impact of litter size on BW gain are necessary before a final conclusion can be reached.

Farrowing induction induces transient alterations in prolactin concentrations and colostrum composition in primiparous sows1

Hormonal changes involved in the farrowing process partly control the initiation of lactation. Inducing farrowing by injection of PG may alter the normal prepartum hormonal cascade. The aim of the study was to investigate the consequences of farrowing induction on colostrum yield and composition, as well as newborn piglet growth. Gilts were treated with 2 mg of alfaprostol on d 113 of gestation (induced farrowing, IF, n = 9) or were injected with 1 mL of a saline solution (natural farrowing, NF, n = 11). Colostrum production was estimated during 24 h, starting at the onset of parturition, based on piglet BW gains. Colostrum samples were collected during the 36 h after the onset of parturition. Blood samples were collected from sows as of d 112 of pregnancy until d 2 postpartum (d 0 being the day of parturition). Piglet blood samples were obtained at birth, on d 1, and on d 21. Litter size and litter weight at birth did not differ between groups (P > 0.10). Farrowing induction did not influence (P > 0.10) colostrum yield (3.96 ± 0.20 kg) or piglet BW gain during d 1 postpartum (116 ± 8 g). At the onset of farrowing (T0), lactose content in colostrum was greater in IF sows than in NF sows (P < 0.05), whereas colostrum ash and protein contents were less (P < 0.05) in IF sows. Concentrations of IgG in colostrum were similar in both groups of sows, whereas concentrations of IgA at T0 were less in IF than in NF sows (P < 0.01). Overall, endocrine changes in blood from d -2 until d 2 (cortisol, prolactin, progesterone, and estradiol-17β) were not altered by farrowing induction (P > 0.10), but 1 h after the injection of alfaprostol, IF sows had greater circulating concentrations of prolactin (P < 0.01) and cortisol (P < 0.10) than NF sows. The greater concentration of lactose in colostrum from IF sows could be attributed to this transient increase in prolactin and cortisol. At birth, concentrations of white blood cells were less in piglets born from IF sows (P < 0.01). On d 1 and 21, piglets from IF sows had similar IgG concentrations in plasma to piglets from NF sows (P > 0.1). In conclusion, farrowing induction at 113 d of pregnancy induced transient hormonal changes in sows and alterations in colostrum composition, without significantly affecting colostrum yield. It also modified some hematological variables of piglets at birth.

The effect of nesting material on the nest-building and maternal behavior of domestic sows and piglet production1

Nest building is an important part of maternal behavior in domestic pigs. The aim of the study was to assess the effect of nesting material sawdust vs. straw on sow behavior 24 h before and after birth of the first piglet (BFP) and piglet production. Sows, housed in farrowing crates, were randomly divided into 2 treatments: sawdust (n = 12) and straw (n = 13). Sawdust and straw were provided during the pre- and parturient period; after parturition, straw was given to both experimental groups. The prepartum nesting period (the time interval between the first and last nest-building records, including all other activity and resting before BFP), the nesting records (number of nesting records), nesting duration (duration of all nesting records), the start and termination of nesting, and the frequency of prepartum postural changes were collected 24 h before BFP. After BFP, number of nesting records and time to first sucking of the litter were collected. Frequency of postural changes and duration of udder access were collected 24 h after BFP during 3 time periods (during parturition, from the end of parturition to 12 h after BFP, and 12 to 24 h after BFP) and the frequency of nursing during 2 time periods (from the end of parturition to 12 h after BFP, and 12 to 24 h after BFP). Piglet BW gain and mortality were estimated 24 h after BFP. Data were analyzed using PROC MIXED and the probability of the piglet mortality using PROC GENMOD in SAS. Nesting material did not affect (P > 0.10) most of sow prepartum nesting behavior and had no effect (P > 0.10) on the prepartum frequency of postural changes. Sows from the sawdust treatment had a longer nesting period (P < 0.05), and nest building tended to start sooner (P < 0.10) than in the straw treatment. Nesting material had only a small effect on later maternal behavior. Sows from the straw treatment tended to have more nesting records after BFP (P < 0.10). The frequency of postural changes was affected by the interaction (P < 0.01) between treatments and time period: sow from the straw treatment had more postural changes during parturition compared with other time periods and sawdust treatment. No effect (P > 0.10) of the nesting material on piglet BW gain and mortality was found. The results suggest that sawdust compared with straw as nesting material provided to sows before and through parturition does not negatively affect maternal behavior during the 24 h before and after parturition or piglet production. Therefore, sawdust can be recommended as a suitable nesting material for farrowing sows when straw is not available.

Effect of dietary supplementation of n-3 fatty acids and elevated concentrations of dietary protein on the performance of sows

A study was conducted to determine the effect of dietary supplementation of n-3 fatty acids (O3FA) with or without elevated concentrations of protein on the performance of sows during the first and the subsequent parity. Sixty-four pregnant gilts with BW of 195.0 +/- 2.1 kg and backfat (BF) thickness of 12.9 +/- 0.2 mm were assigned to 4 dietary treatments from d 60 of gestation (late gestation) to d 21 of lactation. Dietary treatments were 1) a control diet; 2) a high-protein diet (HP); 3) the control diet + 0.2% O3FA (O3); and 4) the HP diet + 0.2% O3FA (HPO3). For the control and O3 treatments, CP contents were 12.3% for late gestation and 17.9% for lactation, and for the HP and HPO3 treatments, CP contents were 18.4% for late gestation and 19.5% for lactation. On d 60 and 110 of gestation and after farrowing (within 12 h postfarrowing), on d 10 and 21 of lactation, BW, BF thickness, and blood samples were obtained. The total number of piglets and the number of piglets born alive and their birth weights were measured within 12 h postfarrowing. Colostrum and milk samples were obtained on d 2 and 21 of lactation, respectively. All piglets were weaned at 21 d. The wean-to-estrus interval and ADFI were recorded. The same measurements were obtained from the control and O3 groups during the subsequent parity. Dietary treatment did not affect BW, BF thickness, ADFI, and the wean-to-estrus interval of sows during their first reproductive cycle. Supplementation of O3FA increased both eicosapentaenoic acid and docosahexaenoic acid contents (P < 0.05) in colostrum and mature milk. First-parity litter size and piglet birth weight did not differ among treatment groups. Piglet BW was greater (P < 0.05) for the O3 group compared with both the control and HPO3 groups at d 10 and 21 of lactation. The same pattern was also noted for overall piglet BW gain. Both piglet and litter characteristics of the HP group did not differ from those of other groups throughout lactation. During the subsequent parity, both total and live piglet birth weights tended (P < 0.07) to be greater for the O3 group than for the control group. Compared with the control group, piglet BW and BW gain in the O3 group showed a pattern similar to the previous parity. Results indicated that O3FA alone during lactation improved the growth of nursing piglets, regardless of parity. However, the O3FA diet, with or without elevated protein, did not affect first-parity gestation performance, although O3FA alone may have improved piglet birth weight in the subsequent litter.

Effects of suckling intensity on milk yield and piglet growth from lactation-enhanced gilts1

The effects of suckling intensity on milk yield and piglet growth were determined when lactation capacity of the sow was enhanced through overexpression of a mammary-specific transgene, bovine alpha-lactalbumin. Lactational response to increased suckling stimulation was determined by fostering litters of the same age (d 1) or 7 d older (d 7) than the day of lactation to sows nontransgenic (control) or transgenic (TG) for bovine alpha-lactalbumin. Twenty first-parity gilts were allocated to 4 treatments dependent on gilt genotype and age of litter fostered (control d 1, control d 7, TG d 1, and TG d 7). Litters were standardized to 10 piglets within 24 h postpartum, and nonbirth piglets were fostered to gilts with an equal litter BW within age groups at 36 h postpartum. Milk yield was determined by the weigh-suckle-weigh method on d 6, 9, 12, 15, and 18 of lactation. Mean daily milk yield was greater (P = 0.031) for TG gilts compared with control gilts and tended to be greater (P = 0.056) for all gilts with d-7 piglets compared with those with d-1 piglets. Daily milk yield of TG d 7 gilts increased rapidly to peak at d 9 and was greater than milk yield of all control gilts at d 9 (P < 0.01), 12 (P < 0.02), and 15 (P < 0.02). Mean daily milk yield of TG d 7 gilts was 2.1 kg greater (P = 0.002) than for control d 7 gilts and 2.0 kg greater (P = 0.004) than for TG d 1 gilts. Daily milk yield of control d 1 gilts was not different from that of TG d 1 gilts (P = 0.49) or control d 7 gilts (P = 0.63). Piglet BW gain between d 3 and 6 was greater (P < 0.01) in the TG d 7 group than for all other groups and was greater (P < 0.05) than the control groups between d 6 and 9. No difference was found when comparing accumulated BW gain of the piglets between the day of age at foster (d 1 vs. 7; P = 0.606) or between the control d 1 and control d 7 groups (P = 0.759). Accumulated BW gain of piglets suckling TG d 7 gilts from d 3 through 9 was greater (P < 0.02) than that of the other groups and continued to be greater (P < 0.05) than that of either of the control groups through d 15. However, by d 15, accumulated BW gain of piglets suckling TG d 1 gilts was no longer different (P = 0.40) from that of the TG d 7 group and was greater (P < 0.05) than that of the control d 1 group. The enhanced lactation potential of these TG gilts synergized with suckling intensity to stimulate increased milk production during early lactation, resulting in increased piglet growth.