Effect of fishmeal replacement with spray-dried animal plasma and colistin on intestinal structure,intestinal microbiology,and performance of weanling pigs challenged with Escherichia coli K99

We evaluated spray-dried animal plasma (SDAP) as an alternative to antimicrobial medication with colistin sulfate in weanling pigs challenged with Escherichia coli K99. Forty-eight piglets weaned at 24 d of age were distributed into 12 pens, and each pen was assigned to one of four dietary treatments. All the piglets were given an oral dose of 5 x 10(7) cfu of E. coli K99 at weaning. The dietary treatments followed a factorial arrangement with two levels of SDAP (0 and 7%) and two levels of colistin (0 and 300 mg/kg of diet). The ADG and ADFI were measured on d 7 and 14 of trial. Three piglets from each treatment were killed on d 7 and 14 to remove the small intestine, and to obtain ileal and cecal digestive contents. The inclusion of SDAP improved ADG by 68 g (P < 0.05) and ADFI by 41 g (P < 0.10) in wk 1 of trial. During wk 2, SDAP improved ADG by 41 g (P < 0.10) and gain:feed ratio (G:F) by 25% (P < 0.01). On the other hand, whereas colistin had no effect on performance in wk 1, it improved ADG by 102 g (P < 0.01), ADFI by 62 g (P < 0.01), and G:F by 26% (P < 0.01) in wk 2. Over the 14 d of the trial, ADG was improved by 54 (P < 0.05) and 75 g (P < 0.05), and G:F was improved by 35 (P < 0.05) and 32% (P < 0.05) due to SDAP and colistin, respectively. There was interaction between colistin and SDAP for ADFI in wk 2 and between d 0 to 14 (P < 0.05), which indicates that their effects were not additive. The use of colistin was advantageous in the maintenance of the integrity of the intestinal mucosa of the pigs, as suggested by a small intestine that was 93 g heavier (P < 0.10) and with the tallest villi 106 microm longer (P < 0.10) than in pigs without colistin. The inclusion of SDAP in the diet favored the growth of lactobacilli in the ileum (P < 0.10) and the cecum (P < 0.05), whereas colistin reduced the number of enterococci in the cecum (P < 0.05) and of Escherichia coli both in the ileum and the cecum (P < 0.001). These results suggest that SDAP may be an alternative to medicated feed with antibiotics since it provided a level of protection against an experimental challenge with E. coli K99 similar to that obtained with colistin, an antibiotic of proven efficacy. The current situation in which the use of antimicrobials in animal feeding is being questioned should encourage further investigation into the use of SDAP as a means of preventing disease in pigs at weaning.     

Estimation of the total sulfur amino acid requirement and the effect of betaine in diets deficient in total sulfur amino acids for the weanling pig.

Four experiments were conducted to determine whether betaine (BET) could replace dietary methionine (MET) in diets for weanling pigs. Pigs in each experiment were allotted to treatments on the basis of weight in a randomized complete block design. Each treatment was replicated four (Exp. 4), five (Exp. 1 and 2), or six (Exp. 3) times with five or six pigs per replicate. In Exp. 1, pigs were fed a diet formulated to be deficient in total sulfur amino acids (TSAA) (negative control; NC) or the NC + 0.05 or 0.10% MET or BET during Phase 1 and 0.035 or 0.07% MET or BET during Phase 2. Growth performance was not affected (P > 0.10) by dietary treatments, indicating that the diets were not deficient in TSAA. In Exp. 2, graded levels of TSAA (0.74, 0.79, 0.84, 0.89, or 0.94%) were fed. Overall ADG was increased (0 vs added MET, P < 0.07) in pigs fed TSAA levels of 0.79% or greater, but gain:feed was not affected (P > 0.10) by diet. Overall ADFI was increased (linear, P < 0.08) and plasma urea N (PUN) was decreased (quadratic, P < 0.01) as the level of TSAA was increased. Most of the change in ADG, PUN, and ADFI occurred between 0.74 and 0.84% TSAA. Thus, the 0.74% TSAA diet was used in Exp. 3 as the NC. In Exp. 3, the diets included the following: 1) NC, 2) NC + 0.05% MET, 3) NC + 0.10% MET, 4) NC + 0.039% BET, or 5) NC + 0.078% BET. The addition of MET resulted in increased (linear, P < 0.10) ADG, ADFI, and gain:feed, but MET decreased PUN (linear, P < 0.05). Daily gain, ADFI, and TSAA intake were not different (P > 0.10) between pigs fed 0.05% MET or 0.039% BET, but gain:feed was decreased (P < 0.01) in pigs fed 0.039% BET compared with pigs fed 0.05% MET. In Exp. 4, a 2 x 2 x 2 factorial arrangement of treatments was used (MET, 0 or 0.072%; cystine, 0 or 0.059%; or BET, 0 or 0.057%). Overall ADG and gain:feed were increased (P < 0.10) in pigs fed MET. The intake of TSAA was increased (P < 0.05), and PUN was decreased (P < 0.10) in pigs fed MET or cystine. Overall ADFI was increased in pigs fed BET or MET independently but not affected when BET and MET were fed together (BET x MET, P < 0.10). The addition of BET to TSAA-deficient diets resulted in increased ADG, which was due to an increase in ADFI (TSAA intake). Thus, BET did not spare MET in this experiment.     

Impact of early postweaning growth rate as affected by diet complexity and space allocation on subsequent growth performance of pigs in a wean-to-finish production system

The objective was to evaluate the effect of restricted early postweaning growth rate due to diet complexity, pen space, or both on subsequent growth to market in a wean-to-finish system. Pigs (n = 1,728) were used in a randomized block design with a 2 x 2 factorial arrangement of treatments: 1) diet complexity (Complex vs Simple) and 2) space allocation (Unrestricted vs Restricted). Treatments were imposed for the first 8 wk after weaning (period 1) and growth was measured from weaning (5.0 +/- 0.01 kg body weight; 15 d of age) to the end of wk 23 postweaning. The Simple diet was based on corn-soybean meal with minimal inclusion of milk products, processed cereals, and animal protein-based ingredients compared to the Complex diet. Floor and feeder-trough spaces were 0.63 m2 and 4 cm and 0.21 m2 and 2 cm per pig for Unrestricted and Restricted space treatments, respectively. From the end of wk 8 to end of wk 23 (period 2), pigs on all treatments had the same floor and feeder spaces and were fed common diets. There was no interaction (P > 0.05) between diet and space treatments. In period 1, Simple diets resulted in similar average daily feed intake (ADFI; 639 vs 650 +/- 5.4 g; P > 0.05), but lower average daily gain (ADG; 408 vs 424 +/- 3.8 g; P < 0.01) and gain:feed ratio (0.64 vs 0.65 +/- 0.002; P < 0.001), and lighter body weight (2.8%; P < 0.01) compared to the Complex diets. In period 2, growth was not affected (P > 0.05) by previous diet complexity, and pig body weight was similar (114.4 vs 114.4 +/- 0.37 kg, P > 0.05) at the end of wk 23. In period 1, pigs with Restricted space had lower ADG (398 vs 434 +/- 3.8 g; P < 0.001), ADFI (621 vs 668 +/- 5.4 g; P < 0.001), and gain:feed ratio (0.64 vs 0.65 +/- 0.002; P < 0.01), and were lighter at the end of wk 8 (6.5%; P < 0.001) than those with Unrestricted space. However, in period 2, pigs with Restricted space had higher (P < 0.01) ADG (3%), ADFI (2%), and gain:feed ratio (3%) than those with Unrestricted space, and body weight was similar (114.5 vs 114.3 +/- 0.37 kg; P > 0.05) at end of wk 23. Carcass backfat and loin-eye depth at market body weight were influenced by neither diet nor space treatment. Using a simple diet program and restricted space allowance immediately postweaning resulted in a lower early growth rate, but had no impact on pig body weight or carcass measures at market.     

Effects of ractopamine on performance and composition of pigs phenotypically sorted into fat and lean groups

Crossbred barrows (n = 144; 80 kg) from four farrowing groups were phenotypically selected into fat (FAT) and lean (LEAN) pens using ultrasound. The difference in 10th-rib fat depth between the LEAN and FAT groups was > or =0.5 cm. Within a farrowing group, pigs were assigned to pens (five pigs per pen and eight pens per phenotype) to equalize pen weight and fat depth. Pigs were fed a corn-soybean meal diet containing 19% CP, 1.0% added animal/vegetable fat, and 1.1% lysine (as-fed basis). Half the pens received 10 ppm (as-fed basis) of ractopamine (RAC) during the 28-d finishing phase. At 7-d intervals, live weight and feed disappearance were recorded to calculate ADG, ADFI, and G:F, and 10th-rib fat depth and LM area were ultrasonically measured to calculate fat-free lean and fat and muscle accretion rates. During the first 7 d on feed, LEAN pigs fed RAC gained less (P < 0.05) than FAT pigs fed RAC or LEAN and FAT pigs fed the control diet (RAC x phenotype; P = 0.02); however, RAC did not (P > 0.25) affect ADG after the second, third, and fourth weeks, or over the entire 28-d feeding period. Although wk-2 and -3 ADG were higher (P < or = 0.03) in LEAN than in FAT pigs, phenotype did not (P = 0.08) affect overall ADG. Dietary RAC decreased (P < or = 0.05) ADFI over the 28-d feeding trial, as well as in wk 2, 3, and 4, but intake was not (P > 0.20) affected by phenotype. Neither RAC nor phenotype affected (P > 0.10) G:F after 7 d on trial; however, RAC improved (P < or = 0.04) wk-3, wk-4, and overall G:F. Lean pigs were more efficient (P < or = 0.05) in wk 2 and 3 and over the duration of the trial than FAT pigs. Ultrasound LM accretion (ULA) was not (P > or = 0.10) affected by RAC; however, LEAN pigs had greater (P < or = 0.02) ULA in wk 2 and 4 than FAT pigs. Although fat depth was lower (P < 0.01) in RAC-fed pigs than pigs fed the control diet, ultrasound fat accretion rate indicated that RAC-pigs deposited less (P = 0.04) fat only during wk 4. In addition, calculated fat-free lean (using ultrasound body fat, ULA, and BW) was increased (P < 0.05) in RAC pigs after 3 and 4 wk of supplementation. In conclusion, RAC enhanced the performance of finishing swine through decreased ADFI and increased G:F, whereas carcass lean was enhanced through decreases in carcass fat and increases in carcass muscling.     

Effects of double stocking and weighing frequency on pig performance in wean-to-finish production systems

Two studies were carried out in different wean-to-finish barns to determine the effects of double stocking on pig growth performance. In Study 1, pigs (n = 1,560) were used in a randomized complete block design with a 2 x 2 factorial arrangement of treatments: initial stocking treatment (Single [52 pigs/pen] vs Double [104 pigs/pen] stocked for 10 wk after weaning) and weighing frequency (High [12 times during the study] vs Low [3 times]) on pig performance from weaning (5.9+/-0.01 kg BW; 17 d of age) to harvest (114+/-0.67 kg BW). Floor and feeder space per pig were 0.650 m2 and 4 cm and 0.325 m2 and 2 cm for the single- and double-stocked treatments, respectively. In Study 2, pigs (n = 1,458) were used in a randomized complete block design to evaluate two initial stocking treatments (Single [27 pigs] vs Double [54 pigs] stocked for 10 wk after weaning) on pig performance from weaning (4.8+/-0.01 kg BW; 15 d of age) to harvest (24 wk after weaning). Floor and feeder space per pig were 0.640 m2 and 3.4 cm and 0.320 m2 and 1.7 cm for single- and double-stocked pens, respectively. In both studies, double-stocked pigs were split at the end of wk 10 into two equal-sized groups of similar mean BW and CV of BW, and one group was moved to a different pen in the same building. In Study 1, performance was not affected (P > 0.10) by frequency of weighing. For the first 10 wk after weaning, the Double compared to the Single treatment had lower ADG (7.7 and 7.9%, for Studies 1 and 2, respectively; P < 0.001) and lighter pigs at wk 10 (6.8 and 7.3%, respectively; P < 0.001). During the first 10 wk in Study 1, Double compared to the Single pigs had lower ADFI (7%; P < 0.001) but similar gain:feed (P > 0.10). From wk 11 to harvest, pigs on Double and Single treatments had similar (P > 0.10) ADG in both studies and, in Study 1, ADFI was unaffected by initial stocking treatment, but double-stocked pigs had greater gain:feed (4%, P < 0.01). Double-stocked pigs required an additional 2 d to reach a fixed harvest BW (P < 0.05) in Study 1 and were lighter (4%; P < 0.05) at 24 wk after weaning in Study 2. Carcass measures were similar (P > 0.10) for double- and single-stocked pigs. Double-stocked pigs that were moved at the end of 10 wk had growth performance similar (P > 0.10) to those that remained in the original pen. In summary, double stocking reduced growth rate to 10 wk after weaning but subsequently had no effect on growth rate and improved feed efficiency.     

Effect of restricted postweaning growth resulting from reduced floor and feeder-trough space on pig growth performance to slaughter weight in a wean-to-finish production system

The effect of reduced pig growth rate postweaning as a result of restricted floor space and feeder trough space on subsequent growth to slaughter was investigated in a wean-to-finish system. Crossbred pigs (n = 1,728) were used in a randomized block design with a 2 x 2 x 2 factorial arrangement of treatments: 1) floor space (high [0.630 m2/pig] vs. low floor space [0.315 m2/pig]), 2) feeder trough space (unrestricted [4 cm/pig] vs. restricted feeder trough space [2 cm/pig]), and 3) period of imposing floor- and feeder-trough-space treatments (12 vs. 14 wk postweaning). Growth performance was measured from weaning (5.5 +/- 0.01 kg of BW; 17 d of age) to slaughter (the end of wk 25 postweaning). From the end of the treatment period to the end of wk 25, pigs on all treatments had the same floor and feeder trough space. Pigs with low floor space had lower (P < 0.01) ADG, ADFI, and gain:feed ratio than those with high floor space, and were therefore lighter (P < 0.05) at the end of the postweaning treatment period. Pigs given the restricted feeder trough space had lower (P < 0.05) ADFI, similar (P > 0.05) ADG, and higher (P < 0.01) gain:feed ratio than those with unrestricted feeder trough space during the treatment period. Pigs in the 14-wk treatment period had higher (P < 0.01) ADG and ADFI, but lower gain:feed than those in the 12-wk treatment during that period. In the subsequent period, from the end of treatment to wk 25, there was an interaction (P < 0.05) between floor space and treatment period; the difference in ADG and gain:feed for pigs on low vs. high floor space was greater for the 14-wk than the 12-wk treatment period. However, low-floor-space pigs tended (P = 0.06) to be lighter than high-floor-space pigs at the end of wk 25 postweaning. Neither feeder trough space nor treatment period affected pig growth performance during the period from the end of treatment to wk 25. Carcass backfat and longissimus depths at the end of wk 25 were not influenced (P > 0.05) by treatment. In summary, pigs with restricted growth due to low floor space until either 12 or 14 wk postweaning had increased growth and feed efficiency in the subsequent period to wk 25 postweaning, with only a slight effect on BW and no effect on carcass measures.     

Effect of group size on pig performance in a wean-to-finish production system

Crossbred pigs (n = 1,400) were used to evaluate the effect of group size (25 vs 50 vs 100 pigs/pen) in a wean-to-finish production system on growth performance and carcass measures. Pigs were weaned at 17 d (range = 15 to 19) of age with a mean initial BW of 5.9 +/- 0.02 kg and taken to a final mean pen weight of 116 +/- 0.9 kg. A 10-phase dietary regimen was used, and pigs had free access to feed and water. Feeder-trough space (4.3 cm/pig) and floor-area allowance (0.68 m2/pig) were the same for all group sizes. Compared to groups of 25, pigs in groups of 50 and 100 animals were lighter (P < 0.001) at the end of wk 8 after weaning and had lower (3%, P < 0.01) ADG and gain:feed (G/F) but similar (P > 0.05) ADFI during the first 8 wk of the study. At the end of the study, pig weight and the coefficient of variation in pig weight within a pen were similar (P > 0.05) across group sizes. During the period from 8 wk after weaning to the end of the study, pigs in groups of 100 compared to 50 animals had greater (3%, P < 0.01) ADG, and pigs in groups of 25 were intermediate for ADG. Average daily feed intake during this period was similar (P > 0.05) for all group sizes; however, G/F was greater (3%, P < 0.01) for groups of 100 compared to 25 or 50 animals. For the overall study period, ADG, ADFI, and G/F from weaning to slaughter weight were similar across group sizes (P > 0.05; 655, 648, and 658 g; 1,759, 1,755, and 1,759 g; and 0.37, 0.37, and 0.37; for ADG, ADFI, and G/F, respectively, for groups of 25, 50, and 100 pigs, respectively). Mortality was similar (P > 0.05) across group sizes; however, morbidity (pigs removed due to poor health or injury) was higher in groups of 25 pigs compared to the other two group sizes (7.0, 3.5, and 3.9% for groups of 25, 50, and 100, respectively; P < 0.05). Group-size treatment did not affect (P > 0.05) carcass dressing percentage, backfat thickness, or loin-eye depth. In summary, growth performance from weaning to market weight was not affected by group size.     

Belly-nosing in early-weaned piglets is not influenced by diet quality or the presence of milk in the diet

Early weaning of piglets can lead to an increase in belly-nosing and other oral-nasal behavior (nosing, chewing, or sucking other piglets), but the causative factors involved in these behavior patterns are largely unknown. Because these behavior patterns resemble massaging the udder and sucking, they may be associated with feeding. The objectives of this study were to determine any effect of diet quality or the presence of milk in the diet on belly-nosing behavior of piglets weaned at 14 to 18 d. During the first 2 wk after weaning, piglets were fed diets differing in quality and inclusion of milk products. Six replicates of eight piglets per replicate, blocked by initial body weight, (n = 192) were offered one of four dietary treatments: HQM: high quality, high in milk products; HQ: high quality, no milk products; PQ: poor quality, no milk products; HQ+MR: high quality, no milk products (as HQ) sprayed with milk replacer five times daily. Thereafter, the piglets were fed a standard nursery diet. Feed intake was measured daily for wk 1 and again at the end of wk 2. Behavior was recorded every 5 min during two 4-h periods on d 2 to 7, 10, 14, 17 and 21 after weaning. Dietary treatment influenced ADFI and ADG during wk 1. Average daily feed intake (P < 0.05) and ADG (P < 0.05) of piglets on PQ were less than those of piglets on the other treatments. During wk 2, ADFI (P > 0.10) and ADG (P > 0.10) were the same across all treatments. Overall, ADFI was not influenced by the inclusion of milk products in the diet or the addition of milk replacer (P > 0.10); however, ADG was. Piglets on HQM had higher ADG than those on HQ during wk 2 (P < 0.05) and 3 after weaning (P < 0.05). However, milk replacer did not influence ADG (P > 0.10). Although the dietary treatments did affect ADFI and ADG, there were no effects on any behavior pattern recorded, including time spent at the feeder (P > 0.10). Lower weight-for-age piglets performed more oral-nasal behavior, in total, than higher weight-for-age piglets (P < 0.03). Neither feeding a poor-quality diet nor the presence of milk in the diet had an effect on belly-nosing or other oral-nasal behavior patterns during the first 3 wk after weaning. Belly-nosing does not seem to be associated with feeding.     

Effects of feeder-trough space and variation in body weight within a pen of pigs on performance in a wean-to-finish production system

Two studies were carried out with the same group of pigs within a wean-to-finish system. In Study 1 (weaning to wk 8 postweaning), the effect of feeder-trough space in pens that were double-stocked on pig growth was evaluated. In Study 2 (end of wk 8 to 112 +/- 1.5 kg BW), the effect of variation in pig BW within a pen on growth was investigated. In Study 1, a randomized block design was used to compare two feeder-trough space treatments (Double [4 cm/pig] vs Control [2 cm/pig]). Pigs (n = 1,728) were randomly allocated at weaning (5.4 +/- 0.01 kg BW; 16 d of age) to mixed-sex pens (8 pens/treatment) of 108 pigs/pen on the basis of BW. Floor-space (0.30 m2/pig) and drinker allocation (13 pigs/drinker) were the same for both treatments. Two six-place (35 cm/place) feeders were positioned together in the center of each pen and were accessible from both sides. For the Double treatment, both feeders contained feed, whereas for the Control only one feeder contained feed. In Study 2, a randomized block design was used to compare three BW/variation in BW treatments: 1) Heavy BW/Low variation, 2) Light BW/Low variation, and 3) Mixed BW/Normal variation. The double-stocked pens of pigs from within previous feeder-trough space treatment were split into two groups of 54 pigs (equal sex ratio) having either high or low BW variation within pen. Pigs had free access to feed and water throughout the studies. In Study 1, doubling feeder-trough space did not affect (P > 0.05) pig growth from weaning to the end of wk 6. From wk 6 to 8, pigs on the Double treatment compared to the Control treatment had higher (P < 0.05) ADG and were heavier (P < 0.05), but had similar (P > 0.05) ADFI and gain:feed ratio. In Study 2, pen-BW treatment did not impact (P > 0.05) ADG or gain:feed ratio; however, Heavy/Low had greater (P < 0.01) ADFI than Light/Low with Mixed/Normal being intermediate for ADFI. At 112 kg BW, CV of BW within a pen was similar (P > 0.05) across treatments; however, days to market BW was greater (P < 0.001) for Light/Low than Heavy/ Low with Mixed/Normal being intermediate. In summary, increasing feeder-trough space from 2 to 4 cm per pig increased daily gain after wk 6 postweaning in double-stocked pens of pigs; however, sorting pigs on the basis of BW when splitting pens did not impact growth rate or variation in BW within a pen at market BW.     

Utilization of spray-dried blood cells and crystalline isoleucine in nursery pig diets

Three experiments were conducted to evaluate spray-dried blood cells (SDBC) and crystalline isoleucine in nursery pigs. In Exp. 1, 120 pigs were used to evaluate 0, 2, 4, and 6% SDBC (as-fed basis) in a sorghum-based diet. There were six replicates of each treatment and five pigs per pen, with treatments imposed at an initial BW of 9.3 kg and continued for 16 d. Increasing SDBC from 0 to 4% had no effect on ADG, ADFI, and G:F. Pigs fed the 6% SDBC diet had decreased ADG (P < 0.01) and G:F (P = 0.06) compared with pigs fed diets containing 0, 2, or 4% SDBC. In Exp. 2, 936 pigs were used to test diets containing 2.5 or 5% SDBC (as-fed basis) vs. two control diets. There were six replicates of each treatment at industry (20 pigs per pen) and university (six pigs per pen) locations. Treatments were imposed at an initial BW of 5.9 and 8.1 kg at the industry and the university locations, respectively, and continued for 16 d. Little effect on pig performance was noted by supplementing 2.5% SDBC, with or without crystalline Ile, in nursery diets. Pigs fed the 5% SDBC diet without crystalline Ile had decreased ADG (P < 0.01), ADFI (P < or = 0.10), and G:F (P < 0.05) compared with pigs fed the control diets. Supplementation of Ile restored ADG, ADFI, and G:F to levels that were not different from that of pigs fed the control diets. In Exp. 3, 1,050 pigs were used to test diets containing 5, 7.5, or 9% SDBC (as-fed basis) vs. a control diet. There were six replicates of each treatment at the industry (20 pigs per pen) location and five replicates at the university (six pigs per pen) locations. Treatments were imposed at an initial BW of 6.3 and 7.0 kg at the industry and university locations, respectively, and continued for 16 d. Supplementation of 5% SDBC without crystalline Ile decreased ADG and G:F (P < 0.01) compared with pigs fed the control diet, but addition of Ile increased ADG (P < 0.01) to a level not different from that of pigs fed the control diet. The decreased ADG, ADFI, and G:F noted in pigs fed the 7.5% SDBC diet was improved by addition of Ile (P < 0.01), such that ADG and ADFI did not differ from those of pigs fed the control diet. Pigs fed diets containing 9.5% SDBC exhibited decreased ADG, ADFI, and G:F (P < 0.01), all of which were improved by Ile addition (P < 0.01); however, ADG (P < 0.05) and G:F (P = 0.09) remained lower than for pigs fed the control diet. These data indicate that SDBC can be supplemented at relatively high levels to nursery diets, provided that Ile requirements are met.     

Assessment of lactose level in the mid- to late-nursery phase on performance of weanling pigs

An experiment involving a total of 1,320 crossbred pigs was conducted at 3 universities to assess the effects of various levels of lactose in diets during phase 3 (wk 3 and 4 postweaning) of a 4-phase starter program. Pigs were weaned at 15 to 20 d (6.2-kg initial BW) and allotted to 5 treatments. All pigs were fed a complex phase 1 diet (20% lactose) the first week postweaning followed by a complex phase 2 diet (15% lactose) the second week postweaning. Phase 3 diets containing 0, 2.5, 5.0, 7.5, or 10.0% lactose were fed for wk 3 and 4, and then a common, corn-soybean meal diet was fed for an additional 1 to 2 wk (phase 4). The source of lactose was Dairylac 80, which contains 80% lactose. The phase 1, 2, and 3 diets were prepared at one site. Pigs were weighed, and feed intake was determined at weekly intervals. There were 8 replications at each station for a total of 24 replications per treatment with 5 or 23 pigs per pen. As expected, ADG, DFI, and G:F were not affected (P = 0.10) during the initial 2-wk period when all pigs received the same diet. During wk 3 and 4 (phase 3) when the 5 levels of lactose were fed, ADG and ADFI increased linearly (P < 0.01) with increasing levels of lactose, but G:F was not affected (P = 0.10). Although the quadratic component was not significant, ADG and ADFI reached a numerical plateau at the 7.5% inclusion level of lactose during phase 3. Compared with pigs fed the diet without lactose, the 7.5% level of lactose resulted in 350 g of additional BW gain coupled with 420 g of additional feed consumed per pig during phase 3, and most of the additional BW gain (294 g) was maintained through the end of the 5- to 6-wk study. These results suggest that pigs respond to dietary lactose during the mid to latter phase of the nursery period and that the response was obtained under different management and facility conditions.     

Enzymatically Digested Animal Protein as a Source of Protein for Weanling Pigs

Three experiments were conducted to evaluate the use of an enzymatically digested animal protein (EDAP) as a source of protein for weanling pigs. In each experiment, treatments were replicated with four (Experiments 1 and 2) or seven (Experiment 3) pens of three to five pigs each. Each experiment lasted 3 to 4 wk for the combined Phase I (1.5% Lys in Experiments 1 and 2, 1.6% Lys in Experiment 3) and Phase II (1.3% Lys) periods. In Experiments 1 (6.7 kg; 23 d of age) and 2 (6.1 kg; 22 d of age), pigs were fed one of the following Phase I diets: 1) basal (B) diet containing corn, soybean meal (SBM), whey, fish meal, and blood cells (AP-301 G; American Protein Corporation, Ames, IA); 2) B + 4% spray-dried animal plasma (SDAP); or 3) B + 2% SDAP + 2% EDAP (SDAP + EDAP). In Phase II, the dietary groups from Phase I were divided into two subsequent groups. One group received a diet containing corn, SBM, whey, fish meal, and 2% blood cells, and the second group received the same diet with 2% EDAP, resulting in six treatments for Phase II and overall periods. In Experiment 1, ADG and ADFI were increased (P<0.10) during Phase I for pigs fed SDAP + EDAP, and ADFI was increased (P<0.10) in pigs fed SDAP. In Phase II, the EDAP addition did not affect (P>0.10) ADG, ADFI, or the ratio of gain to feed. Also, Phase I diets did not affect (P>0.10) growth performance during Phase II. Overall, ADG (P<0.10) and ADFI (P<0.04) were increased (P<0.10) in pigs fed SDAP + EDAP during Phase I. In Experiment 2, ADG and the ratio of gain to feed were increased (P<0.10) in pigs fed SDAP + EDAP during Phase I. During Phase II, ADFI was increased in pigs fed SDAP + EDAP or B + SDAP (P<0.01) relative to those fed B only (P<0.003) in Phase I. Also in Phase II, the ratio of gain to feed was increased in pigs fed SDAP + EDAP (P<0.03) relative to those fed B + SDAP. Overall, ADG and the ratio of gain to feed were not affected (P>0.10) by diet, but ADFI was increased (P<0.03) in pigs fed SDAP + EDAP relative to those fed B. In Experiment 3, all pigs (5.7 kg; 17 d of age) were fed a common Phase I diet containing SDAP + EDAP. In Phase II, ADG, ADFI, and the ratio of gain to feed were not affected (P>0.10) by the addition of 2% EDAP or 2% blood cells. In summary, pigs fed SDAP + EDAP perform equally well compared with those fed B + SDAP.     

Effect of select menhaden fish meal in starter diets for pigs

Two trials were conducted to evaluate a select menhaden fish meal (SMFM) as a protein source in starter diets for 390, 3-wk-old weaned pigs. Initial weights averaged 4.8 and 5.5 kg in Trials 1 and 2, and trials were conducted for 5 and 4 wk, respectively. Diets in Trial 1 were formulated by substituting levels of 0, 4, 8, 12, 16 or 20% SMFM for soybean meal plus corn on a protein basis. The 20% fish meal diet contained no soybean meal; all diets contained between 19.8 and 20.2% CP, between 1.34 and 1.40% lysine and 25% dried whey. Replacement of soy protein with fish meal elicited a quadratic improvement (P = .01) in cumulative ADG and average daily feed intake (ADFI) by the end of wk 5. The diet containing 8% SMFM resulted in the maximum observed ADG; however, the maximum ADFI occurred in pigs fed the diet containing 12% SMFM. Breakpoint analysis indicated that 4.5 and 9.3% SMFM maximized ADG and ADFI, respectively. Addition of SMFM did not affect efficiency of feed utilization (F/G). In Trial 2, a 2 X 3 factorial with two levels of dried whey (10 or 20%) and three levels of SMFM (0, 4 or 8%), a SMFM X dried whey interaction (P less than .05) was observed for cumulative ADG and F/G by the of wk 4 with greater benefit from SMFM with 10% than with 20% dried whey.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of dietary spray-dried egg on growth performance and health of weaned pigs

Four experiments were conducted to evaluate the nutrient contributions and physiological health benefits of spray-dried egg (SDE) containing only unfertilized eggs as a protein source in nursery pig diets. In all experiments, all diets were formulated to the same ME and Lys content, and each pen within a block (by BW) housed the same number of barrows and gilts. In Exp. 1 and 2 (168 and 140 pigs, respectively; 5 kg BW; 16 d old; 14 replicates/experiment), conducted at a university farm, treatments were with or without 5% SDE in a nursery control diet, which included antibiotics and zinc oxide. Pigs were fed for 10 d after weaning to measure ADG, ADFI, and G:F. The SDE increased (P < 0.05) ADG (Exp. 1: 243 vs. 204 g/d; Exp. 2: 204 vs. 181 g/d) and ADFI (Exp. 1: 236 vs. 204 g/d; Exp. 2: 263 vs. 253 g/d) compared with the control diet but did not affect G:F. In Exp. 3 (1,008 pigs; 5.2 kg BW; 20 d old; 12 replicates/treatment), conducted at a commercial farm, treatments were in a factorial arrangement of with or without SDE and high or low spray-dried plasma (SDP) in nursery diets, which included antibiotics and zinc oxide. Pigs were fed for 6 wk using a 4-phase feeding program (phases of 1, 1, 2, and 2 wk, respectively) with declining diet complexity to measure ADG, ADFI, G:F, removal rate (mortality plus morbidity), and frequency of medical treatments per pen and day (MED). The diets with the SDE increased (P < 0.05) ADFI during phase 1 only (180 vs. 164 g/d) compared with the diets without the SDE but did not affect growth performance during any other phases. The diets with SDE reduced MED during phase 1 (0.75% vs. 1.35%; P < 0.05) and the overall period (0.84% vs. 1.01%; P = 0.062) compared with the diets without the SDE but did not affect removal rate. In Exp. 4 (160 pigs; 6.7 kg BW; 21 d old; 10 replicates/treatment), conducted at a university farm to determine whether SDE can replace SDP, treatments were in a factorial arrangement of with or without SDP or SDE in nursery diets, which excluded antibiotics and zinc oxide. Pigs were fed for 6 wk using the same schedule used in Exp. 3 to measure ADG, ADFI, and G:F. The diets with SDE increased (P < 0.05) ADFI during phase 1 only (195 vs. 161 g/d) compared with the diets without SDE but did not affect growth performance during any other periods. In conclusion, SDE can be an efficacious protein and energy source in nursery pig diets and improves health and, in some instances, increases growth rate.     

Factors affecting performance response of pigs exposed to different challenge models: a multivariate approach

Factors associated with the severity with which different challenge models (CMs) compromise growth performance in pigs were investigated using hierarchical clustering on principal components (HCPC) analysis. One hundred seventy-eight studies reporting growth performance variables (average daily gain [ADG], average daily feed intake [ADFI], gain:feed [GF], and final body weight [FBW]) of a Control (Ct) vs. a Challenged (Ch) group of pigs using different CMs (enteric [ENT], environmental [ENV], lipopolysaccharide [LPS], respiratory [RES], or sanitary condition [SAN] challenges) were included. Studies were grouped by similarity in performance in three clusters (C1, C2, and C3) by HCPC. The effects of CM, cluster, and sex (males [M], females [F], mixed [Mi]) were investigated. Linear (LRP) and quadratic (QRP) response plateau models were fitted to assess the interrelationships between the change in ADG (∆ADG) and ADFI (∆ADFI) and the duration of challenge. All variables increased from C1 through C3, except for GF, which decreased (P < 0.05). LPS was more detrimental to ADG than ENV, RES, and SAN models (P < 0.05). Furthermore, LPS also lowered GF more than all the other CMs (P < 0.05). The ∆ADG independent of ∆ADFI was significant in LPS and SAN (P < 0.05), showed a trend toward the significance in ENT and RES (P < 0.10), and was not significant in ENV (P > 0.10), while the ∆ADG dependent on ∆ADFI was significant in ENT, ENV, and LPS only (P < 0.05). The critical value of ∆ADFI influencing the ∆ADG was significant in pigs belonging to C1 (P < 0.05) but not C2 or C3 (P > 0.10). The ∆ADG independent of duration post-Ch (irreparable portion of growth) was significant in C1 and C2 pigs, whereas the ∆ADFI independent of duration post-Ch (irreparable portion of feed intake) was significant in C1 pigs only (P < 0.05). Moreover, the time for recovery of ADG and ADFI after Ch was significant in pigs belonging to C1 and C2 (P < 0.05). Control F showed reduced ADG compared with Ct-M, and Ch-F showed reduced ADFI compared with Ch-M (P < 0.05). Moreover, the irreparable portion of ΔADG was 4.8 higher in F (−187.7; P < 0.05) compared with M (−39.1; P < 0.05). There are significant differences in growth performance response to CM based on cluster and sex. Furthermore, bacterial lipopolysaccharide appears to be an appropriate noninfectious model for immune stimulation and growth impairment in pigs.     

Individually measured feed intake characteristics and growth performance of group-housed weanling pigs: effects of sex, initial body weight, and body weight distribution within groups

Feed intake characteristics of 192, 27-d-old weanling pigs housed in groups and given ad libitum access to feed and water were measured individually with the use of computerized feeding stations. The groups were either homogeneous or heterogeneous as to BW distribution; pigs of three defined initial BW classes were used (mean BW of 6.7, 7.9, or 9.3 kg). The effects of BW distribution, BW class, and sex were studied with regard to average performance traits, latency time (interval between weaning and first feed intake), initial feed intake (intake during the first 24 h following first feed intake), and daily increase in feed intake during the interval between first feed intake and the day on which energy intake met or exceeded 1.5 times the maintenance requirement. Homogeneous and heterogeneous groups had similar latency times, initial feed intakes, and daily increases in feed intake. For the period 0 to 34 d after weaning, ADFI and ADG were also similar for homogeneous and heterogeneous groups, but gain:feed ratio was greater (P < 0.05) in the homogeneous groups. Gilts had higher (P < 0.05) initial feed intakes than barrows and also had greater (P < 0.05) ADFI and ADG during the period 0 to 13 d after weaning. Pigs with average BW of 6.7 kg had higher (P < 0.05) initial feed intakes than their counterparts with average BW of 7.9 kg and 9.3 kg, but the daily increase in feed intake was similar for the three groups. The lighter pigs had more daily visits and a lower feed intake per visit and tended to have a shorter postweaning latency to the onset of feeding than the heavier pigs. This study indicates that the high variability in early feeding behavior among group-housed weanling pigs may be related to BW and sex.     

Effect of group size and feeder type on growth performance and feeding patterns in growing pigs

The effects of four group sizes (2, 4, 8, and 12 pigs per pen) and two single-space feeder types (conventional and electronic feed intake recording equipment [FIRE]) on feed intake, growth performance, and feeding patterns were determined in growing pigs over a 4-wk period. A total of 416 hybrid pigs (barrows and gilts) were grown from 26.5 (SD = 1.6) to 47.8 (SD = 2.7) kg BW and given ad libitum access to a corn-soybean meal-based diet (17.4% CP; 0.9% lysine; 3,298 kcal ME/kg). The floor space allowance was 0.9 m2/pig for all treatments. Pigs using the electronic feeders had similar growth rates but lower feed intakes (P < 0.01) and higher gain:feed ratios (P < 0.01) compared to those using the conventional feeders. Barrows compared to gilts had higher growth rates (P < 0.05), numerically higher (P > 0.05) ADFI, and similar feed efficiency and feeding pattern. Feed intakes and growth rates were lowest (P < 0.05) for groups of 12 pigs but gain:feed ratio was not affected by group size. Daily feeder occupation time per pig was lower (P < 0.01) for groups of 12 than for groups of 2 or 4 pigs, and feed consumption rate was higher (P < 0.01) for groups of 12 than for groups of 4 pigs. The proportion of time spent eating was lower (P < 0.01) and the proportion of time spent standing was higher (P < 0.01) for pigs in groups of 12 compared to groups of 2. Correlations between ADG and ADFI and feed intake per visit were 0.29 and 0.30, respectively (P < 0.01), between ADG and ADFI and feed consumption rate were 0.27 and 0.31, respectively (P < 0.01), and between ADFI and feeder occupation time per day were 0.33 (P < 0.01). This study suggests that, in growing pigs given access to a single feeder, changes in feeding behavior with increasing group size were not sufficient to maintain feed intake and growth rate.     

Effects of dietary conjugated linoleic acid in nursery pigs of dirty and clean environments on growth, empty body composition, and immune competence

Early-weaned pigs (n = 64) averaging 5.3 +/- 0.3 kg and distributed into two environments (dirty and clean) were used to evaluate effects of conjugated linoleic acid (CLA) on growth performance, immune competence, and empty body composition. A factorial (2 x 4) arrangement within a split-plot design, with four littermate pigs as the experimental unit for the environment, pig within litter as the experimental unit for dietary treatment, and d-0 body weight used as covariate, were used in data analysis. Diets were formulated to contain CLA at 0, 0.67, 1.33, or 2% and to exceed the NRC (1988) nutrient needs of pigs. Animals were given ad libitum access to feed for 7 wk in three phases (I, 1 to 2; II, 3 to 5; and III, 6 to 7 wk). Within phases, diets were isocaloric and isonitrogenous. In Phase I, as dietary CLA concentration increased, ADG and ADFI decreased linearly (P < 0.05 and P < 0.02, respectively). In Phase II, upon adaptation to dietary CLA supplementation, ADG increased quadratically (603, 623, 622, and 548 g/d; P < 0.01), ADFI decreased linearly (873, 840, 867, and 717 g/d; P < 0.02) and gain:feed ratio tended to increase linearly (691, 742, 715, and 763; P < 0.07). In Phase III, no differences in growth performance were attributed to either dietary or environmental treatments. The poor health status associated with the dirty environment induced a growth suppression; pigs in the clean room had a greater cumulative ADG (P < 0.01) and ADFI (P < 0.01) than pigs in the dirty room. In Phase I, lower plasma urea nitrogen levels observed in pigs found in the dirty room (P < 0.03) indicated a lower protein intake caused by a lower ADFI. The effects of dietary CLA on peripheral phenotypic profiles of lymphoytes did not appear until d 42. However, as indicated by the growth suppression of pigs in the dirty room, the negative effects of the environmental challenge on pig health and growth had already appeared during phase I. On d 42, CLA induced a linear increase in percentages of CD8+ lymphocytes (21.7, 22.3, 28.0, and 32.7%; P < 0.001). These data suggest that a 42-d dietary CLA supplementation preceding a disease challenge could have prevented disease-associated growth suppression. Also, CLA-mediated amelioration of particular infectious diseases will depend on which CD8+ T cell subset (i.e., CD8alphaalpha-immunoregulatory or CD8alphabeta-cytotoxic) is most influenced by dietary CLA supplementation.     

Effect of chromium picolinate and chromium propionate on glucose and insulin kinetics of growing barrows and on growth and carcass traits of growing-finishing barrows

Two experiments were conducted to determine the effects of dietary Cr tripicolinate (CrPic) or Cr propionate (CrProp) on growth, carcass traits, plasma metabolites, glucose tolerance, and insulin sensitivity in pigs. In Exp. 1, 36 barrows (12 per treatment; initial and final BW were 20 and 38 kg) were allotted to the following treatments: 1) corn-soybean meal basal diet (control), 2) as 1 + 200 ppb Cr as CrPic, or 3) as 1 + 200 ppb Cr as CrProp. Growth performance data were collected for 28 d, and then 23 pigs (seven, eight, and eight pigs for treatments 1, 2, and 3, respectively) were fitted with jugular catheters and a glucose tolerance test (500 mg glucose/kg BW) and an insulin challenge test (0.1 IU of porcine insulin/kg BW) were conducted. Both CrPic and CrProp decreased (P < 0.05) ADG and ADFI but did not affect gain:feed (P > 0.10). Fasting plasma glucose, total cholesterol, urea N, insulin, and high-density lipoprotein cholesterol:total cholesterol concentrations were not affected (P > 0.10) by either Cr source. Pigs fed CrPic had lower (P < 0.02) fasting plasma NEFA concentrations than control pigs, but plasma NEFA concentrations of pigs fed CrProp were not affected (P > 0.10). During the glucose tolerance test, glucose and insulin kinetics were not affected by treatment (P > 0.10). During the insulin challenge test, glucose clearance was increased (P < 0.01) in pigs fed CrProp but not affected (P > 0.10) in pigs fed CrPic. Glucose half-life was decreased (P < 0.03) in pigs fed CrPic or CrProp, but insulin kinetics were not affected (P > 0.10). In Exp. 2, 48 barrows (four replicates of four pigs per replicate; initial and final BW were 23 and 115 kg) were allotted to the same dietary treatments in a growing-finishing study. Average daily gain, ADFI, and gain:feed were not affected (P > 0.10) by treatments. Carcass length tended (P = 0.10) to be greater in pigs fed CrPic than in pigs fed CrProp, but other carcass measurements were not affected (P > 0.10). Glucose kinetics from the insulin challenge test indicate that both CrPic and CrProp increase insulin sensitivity and that both Cr sources are bioavailable.     

Effects of fish oil supplementation on the performance and the immunological, adrenal, and somatotropic responses of weaned pigs after an Escherichia coli lipopolysaccharide challenge

Seventy-two crossbred pigs (7.58 +/- 0.30 kg BW) weaned at 28 +/- 3 d of age were used to investigate the effects of fish oil supplementation on pig performance and on immunological, adrenal, and somatotropic responses following an Escherichia coli lipopolysaccharide (LPS) challenge in a 2 x 2 factorial design. The main factors consisted of diet (7% corn oil [CO] or 7% fish oil [FO]) and immunological challenge (LPS or saline). On d 14 and 21, pigs were injected intraperitoneally with either 200 microg/kg BW of LPS or an equivalent amount of sterile saline. Blood samples were collected 3 h after injection for analysis of interleukin-1beta (IL-1beta), prostaglandin E2 (PGE2), cortisol, growth hormone (GH), and insulin-like growth factor (IGF)-I. On d 2 after LPS challenge, peripheral blood lymphocyte proliferation (PBLP) was determined. Lipopolysaccharide challenge decreased ADG (487 vs. 586 g; P < 0.05) and ADFI (as-fed, 776 vs. 920 g; P < 0.05) from d 14 to 21 and ADG (587 vs. 652 g; P < 0.10) from d 21 to 28. Fish oil improved ADG (554 vs. 520 g; P < 0.10) and ADFI (891 vs. 805 g; P < 0.10) from d 14 to 21. On d 14, LPS challenge x diet interactions were observed for IL-1beta (P < 0.10), PGE2 (P < 0.001), and cortisol (P < 0.05) such that these measurements responded to the LPS challenge to a lesser extent (IL-1beta: 93 vs. 114 pg/mL, P < 0.05; PGE2: 536 vs. 1,285 pg/mL, P < 0.001; cortisol: 143 vs. 206 ng/mL, P < 0.05) in pigs receiving the FO diet than in pigs fed the CO diet. In contrast, among LPS-treated pigs, pigs fed the FO diet had higher IGF-I (155 vs. 101 ng/mL; P < 0.10) than those fed the CO diet. On d 21 among LPS-treated pigs, pigs fed FO had lower IL-1beta (70 vs. 84 pg/mL; P < 0.10) and cortisol (153 vs. 205 ng/mL; P < 0.05) than those fed CO. Pigs fed FO had lower PGE2 (331 vs. 444 pg/mL; P < 0.05) and higher IGF-I (202 vs. 171 ng/mL; P < 0.10) compared with those fed CO. Lipopolysaccharide challenge decreased GH (0.27 vs. 0.33 ng/mL; P < 0.05) on d 14, whereas it had no effect on GH on d 21. During both LPS challenge periods, the challenge increased PBLP when these cells were incubated with 8 (1.46 vs. 1.32; P < 0.10) or 16 microg/mL (1.46 vs. 1.30; P < 0.05) of concanavalin A. Fish oil had no effect on PBLP. These results suggest that FO alters the release of proinflammatory cytokines, which might lead to improved pig performance during an immunological challenge.