快速生长小母猪较早进行人工授精后对繁殖性能的影响

本试验的目的是研究提早具有较快生长速度(GR)的小母猪的配种时间,是否会降低其头3胎的繁殖性能、提高其1～3胎的淘汰率。试验选用568头Camborough 22小母猪,按配种时的体重和年龄分成3组:第一组(G1组)164头,生长速度高于等于700g/d,配种年龄低于210d;第二组(G2)165头,生长速度高于等于700g/d,配种年龄高于210d;第三组(G3)239头,生长速度低于700g/d,配种年龄高于210d。所有试验小母猪从150d起采取自由采食,并于其第二个或随后的发情期配种。第一胎,G2组小母猪的平均产仔数多于其它组(P<0.05)。然而,在对三胎产仔数进行分析后表明,各组小母猪在总产仔数(分别为11.6、12.3和11.7头)、分娩率(分别为87.1%、88.7%和和89.8%)和淘汰率(分别为30.2%、25.3%和28.2%)上没有显著差异(P>0.05)。因此,日龄在185～210d、体重为127kg的小母猪,可以在其第二个或随后的发情期中给予配种,且配种不会影响其头3胎的生产性能。     

Genetic relationships of body composition, serum leptin, and age at puberty in gilts

Leptin produced by adipocytes acts through leptin receptors in the hypothalamus to control appetite and food intake and thus communicates information about degree of fatness. It is thought that a degree of body fat is required for initiation of puberty and maintenance of reproductive function in mammals. The objective of this study was to determine whether polymorphisms in the leptin (LEP), leptin receptor (LEPR), paired box 5 (PAX5), aldo-keto reductase (AKR), and pro-opiomelanocortin (POMC) genes were associated with age, leptin concentration, backfat as an indicator of body condition, or BW at puberty in 3 lines of gilts and to characterize genetic relationships among these traits. The first 2 lines, born in 2001, were formed by crossing maternal White Cross (Yorkshire x Maternal Landrace) gilts to Duroc (n = 210) or (lean) Landrace (n = 207) boars. The remaining line (n = 507), born in 2002, was formed by crossing progeny of the Duroc- and Landrace-sired lines. At first estrus, age, BW (BWP), and backfat (BFP) at puberty were recorded and blood was collected for leptin assays. Nine SNP were detected in candidate genes/regions: 1 in LEP, 3 in LEPR, 1 in PAX5, 2 in AKR, and 2 in POMC. Animals were genotyped for each of the SNP; genotypes were validated using GenoProb. The association model included fixed effects of farrowing group, covariates of SNP genotypic probabilities (from GenoProb), and random additive polygenic effects to account for genetic similarities between animals not explained by SNP. Variance components for polygenic effects and error were estimated using MTDFREML. Leptin concentrations were logarithmically transformed for data analysis. All 4 traits were moderately to highly heritable (0.38 to 0.48). Age and leptin at puberty had a significant (P < 0.01) genetic correlation at -0.63 +/- 0.097, and the genetic correlation between BWP and age at puberty was 0.65 +/- 0.083 (P < 0.01). Significant additive associations (a; P < 0.05) were detected at PAX5 for age at puberty (a = 3.2 d) and for BFP (a = 0.61 mm). One SNP in LEPR was associated with leptin concentration (a = 0.31 log units; P < 0.05). The associations from PAX5 correspond to a QTL peak for age at puberty detected on SSC1. Although not necessarily the causative mutation, this result implies that a QTL that can decrease age at puberty without increasing BFP and BWP at puberty may exist in this region in commercial pigs.     

Effects of restricting energy during the gilt developmental period on growth and reproduction of lines differing in lean growth rate: responses in feed intake, growth, and age at puberty

The overall objective was to compare reproductive performance through 4 parities of gilts developed with ad libitum access to feed or with restriction of energy to 75% of ad libitum intake. Effects on growth and pubertal development are reported. The experiment was a 2 × 2 factorial with 661 gilts. One-half of the gilts (n = 330) were allowed ad libitum access to feed from weaning to breeding at 235 d of age (AL), and 331 littermates were developed with ad libitum access to feed to 123 d of age and then restricted to 75% of ad libitum intake to 235 d of age (Res). Diets for gilts on regimen AL were formulated to meet requirements for growth. All nutrients except energy and selenium were increased in the diet fed to gilts on regimen Res so that nutrient intake per unit of BW was expected to be similar to that of gilts on regimen AL. Sires of all gilts were from an industry maternal line. Dams were either an industry Large White-Landrace cross, or Nebraska selection Line 45, producing gilts denoted as LW/LR and L45X, respectively. Traits were recorded every 2 wk. Recording of feed intake and BW began at 53 d of age, and recording of backfat (BF) and LM area (LMA) began at 123 d of age. Estrus detection began at 140 d of age to determine age at puberty (AP). The G:F ratio from 123 to 235 d of age for gilts on the AL regimen was greater (0.269 vs. 0.257, P < 0.01) than for gilts on the Res regimen; the greatest difference occurred in the first 2-wk period following feed restriction. The LW/LR gilts were heavier, had less BF, and had greater LMA than L45X gilts, but interactions with feeding regimen and period of development existed. Feed restriction reduced BW, BF, LMA, and ratio of BF to BW, but had little effect on ratio of LMA to BW. More L45X gilts than LW/LR gilts (98 vs. 93%, P < 0.01) and more gilts developed on regimen AL than regimen Res (98 vs. 91%, P < 0.01) expressed estrus. Mean age at puberty was 178.6 d for LW/LR and 173.0 d for L45X gilts (P < 0.01) and 174.1 d for regimen AL and 177.5 d for regimen Res (P < 0.05). The Res regimen delayed pubertal development. Subsequently, it will be important to determine effects on reproduction through 4 parities.     

同窝公母比例不等对留种母猪受胎率的影响研究

按同窝中公猪所占百分经不同,利用计算机分区统计了31682头留种母猪的受胎率。结果表明,同窝公母比例对母猪受胎率的影响效果明显（P＜0．05）。因此同窝中公猪所占比例高于60％时,该窝母猪不宜作种用。     

Reduction in age of puberty in gilts consuming melatonin during decreasing or increasing daylength

Two experiments were conducted to determine whether oral administration of melatonin alters the onset of puberty in gilts during naturally increasing or decreasing daylength. In Exp. 1, 20 crossbred prepubertal gilts weighing 77.5 +/- .5 kg at 171.8 +/- 1.0 d of age were assigned randomly to receive either a daily oral dose of 3 mg of melatonin (MEL) or ethanol vehicle (ETH) at 1530 from August 31 to December 1, 1987 (decreasing daylength). Gilts were exposed to mature boars for 20 min thrice weekly and blood samples were collected twice weekly. Serum concentrations of progesterone were used to establish age at puberty and length of estrous cycle. In Exp. 2, 20 crossbred prepubertal gilts weighing 67.7 +/- .7 kg at 143.8 +/- 1.1 d of age received either MEL or ETH treatment from February 1 to May 15, 1988 (increasing daylength). Age of puberty was less in gilts that received MEL than in gilts that received ETH in both Exp. 1 (198 +/- 3 vs 228 +/- 7 d; P less than .01) and Exp. 2 (183.8 +/- 2.7 d vs 194.3 +/- 3.3 d; P less than .05). Gilts that received MEL reached puberty at a lighter weight than gilts that received ETH in Exp. 1 (95.6 +/- 2.1 vs 112.4 +/- 3.9 kg; P less than .01) and Exp. 2 (88.1 +/- 1.5 vs 96.0 +/- 1.8 kg; P less than .01). Serum concentrations of LH and FSH, length of estrous cycles, and percentage of muscle of carcasses were similar between MEL and ETH gilts.(ABSTRACT TRUNCATED AT 250 WORDS)     

The effect of lean growth rate on puberty attainment in gilts

Two hundred sixteen prepubertal Genex Manor hybrid F1 gilts were used to determine the impact of lean growth rate on sexual development of gilts. This study was composed of two experiments (Exp. 1 and Exp. 2). In Exp. 1, at approximately 96 d of age and 54 kg weight, gilts were allocated with respect to growth rate and litter origin to one of two dietary treatments: 1) a diet formulated to maximize lean growth potential (LP; n = 84) or 2) a diet formulated to produce a lower lean growth rate (LL; n = 84). In Exp. 2, at approximately 88 d of age and 50 kg weight, gilts were allocated with respect to growth rate and litter origin to one of two dietary treatments: 1) a diet formulated to maximize lean growth potential (LP; n = 24) or 2) a diet formulated to restrict lean growth further than was achieved in LL in Exp. 1 (RL; n = 24). All gilts were fed treatment diets for ad libitum consumption and housed in groups of six. Weight, backfat depth and loin depth, and feed intake were measured weekly. Starting at 135 d of age, gilts received 20 min of direct daily exposure to a boar as a pen group for pubertal stimulation. Puberty attainment was determined as the day gilts first exhibited the standing reflex in response to contact with a boar. At pubertal estrus, body weight, backfat depth, and loin depths were recorded. Diet affected (P < or = 0.05) estimated fat-free lean gain (LP, 424 vs LL, 347 g/d, Exp. 1; LP, 397 vs RL, 376 g/d, Exp. 2) during the growth period (start to stimulation). However, age at puberty was not affected by diet (LP, 157.3 vs LL, 157.6, Exp. 1; LP, 166.7 vs RL, 167.3, Exp. 2) or overall lean growth at stimulation (P > or = 0.05 in both experiments), confirming that innate variability in sexual development of commercial genotypes, rather than growth performance, determines onset of sexual maturity. A negative correlation between age at puberty and growth rate from 50 kg until puberty (P < or = 0.05) (LP, r = -0.40, LL, r = -0.36, Exp. 1; LP, r = -0.64, RL, r = -0.48, Exp. 2) was a consequence of reduced lean tissue growth during the stimulation period in later-maturing gilts.     

Effects of adrenalectomy and glucocorticoids on puberty in gilts reared in confinement

The effect of adrenal function and flumethasone (FM, a synthetic glucocorticoid) on induction of puberty in crossbred gilts raised in confinement was examined in two experiments. In Exp. 1, gilts were adrenalectomized (Adx) or subjected to sham adrenalectomy (Sham) between 140 and 160 d of age. Twenty days later indwelling jugular catheters were implanted in Adx, Sham and another group of intact gilts designated as Controls, and the gilts were moved from confinement to outdoor pens and checked daily for estrus with a mature boar. Fewer (P less than .05) Adx (1/11) than Sham (9/14) gilts showed estrus and ovulated by 205 d of age. Response of Control gilts (6/14) was not different from the other groups. Although Adx gilts received 40 mg cortisone acetate and 10 mg deoxycorticosterone acetate daily throughout the experiment, mean plasma glucocorticoids were lower (P less than .05) in Adx (24 +/- 4.7 ng/ml) than in either Sham (47 +/- 8.1 ng/ml) or Control (44 +/- 6.1 ng/ml) gilts. Experiment 2 was conducted to determine whether FM given to Adx gilts immediately after surgery could have inhibited estrus and ovulation. Intact gilts received a total of 27.5 (FM1) or 17.5 (FM2) mg FM over 4 d between 150 and 160 d of age before relocation and boar exposure 20 d later. Control gilts received no injections. Nine of 13 FM-treated but none of the Control gilts showed estrus. It is concluded from these results that the adrenal glands may facilitate the onset of puberty in gilts through increases in glucocorticoid production, but that this is not required for puberty to occur.     

Growth rate and age at boar exposure as factors influencing gilt puberty

The objective of this study was to verify whether pubertal estrus could be influenced by the growth rate and age of gilts at the onset of boar exposure. Gilts (n = 1486) were evaluated according to two groups of age at boar exposure (A = 130-149 d and B = 150-170 d) and three classes of growth rate (Low = 550–649 g/d; Intermediate = 650–725 g/d and High = 726–830 g/d). Gilts of groups A and B were, respectively, 142.6 ± 4.9 and 157.0 ± 5.1 days of age at the onset of boar exposure. Overall, 85% of gilts showed estrus within 40 days of boar exposure. Within group A gilts a higher (P < 0.05) cumulative percentage of estrus within 20 days of stimulation was observed in High than in Intermediate and Low growth rate gilts (59.7% vs. 48.7% vs. 48.2%; P < 0.05). Nevertheless, within group B there was no difference in the percentage of estrus among growth rate classes (63.8% vs. 67.3% vs. 63.7%, P > 0.05). Within group A, puberty was attained earlier in High than in Low growth rate gilts (159.6 vs. 164.8 days). However, age at puberty was not affected by growth rate, when gilts were exposed to boar in an older age (group B). Overall, age at puberty was positively associated with the age at the onset of boar exposure (r = 0.38; P < 0.0001) and the older the gilts were at boar exposure the lower was the interval (r = - 0.19; P < 0.0001) from stimulation to onset of puberty. In conclusion, successful stimulation of puberty can be obtained through an earlier exposure to boars in high growth rate gilts.     

Effect of diet and exercise on performance, carcass traits and plasma components of growing-finishing barrows

Twenty-four barrows (approximately 25 kg initial wt) were used in each of three 2 X 2 factorially arranged trials to study effects of exercise (not exercised vs walking 30 min/d, 6 d/wk on a treadmill) and diet (low energy vs high energy) on performance during the growing-finishing period. Average daily gain (ADG) of barrows not exercised was greater (P less than .07) than that of those exercised. Barrows fed the high-energy diet had greater (P less than .05) ADG, lower (P less than .01) feed intake and lower (P less than .01) feed-to-gain ratio than barrows fed low-energy diets. In trials 1 and 2, pigs were slaughtered when removed from test and selected carcass measurements and internal organ weights were obtained. Exercise did not significantly affect carcass length, backfat thickness, loin muscle area or lean cuts (as a percentage of off-test weight). Pigs fed the high-energy diet had more (P less than .01) backfat than those fed the low-energy diet. Neither the exercise program nor the diet had a significant effect on organ weights. Pigs not exercised had a higher (P less than .05) plasma albumin-to-globulin ratio and lower (P less than .05) plasma creatinine concentration than did pigs that were exercised. Also, pigs not exercised had slightly higher (P less than .08) plasma albumin and glucose, but lower (P less than .06) plasma globulin levels.(ABSTRACT TRUNCATED AT 250 WORDS)     

Influence of growth rate and exposure to bulls on age at puberty in beef heifers

Two experiments were conducted to test the following hypotheses: 1) exposure of beef heifers to sterile bulls increases the proportion of heifers attaining puberty by 14 mo of age and 2) rate of growth interacts with bull exposure to influence age at puberty in beef heifers. In Exp. I, heifers were assigned to one of two treatments: 1) heifers were exposed to bulls (BE; approximately 70-d period of exposure) or 2) heifers were isolated from bulls (NE) and served as controls. In Exp. II, heifers were assigned to either BE or NE treatments (175-d period of exposure to bulls) and were fed to gain at a moderate (MG; .6 kg/d) or high (HG; .8 kg/d) growth rate. Blood samples were collected twice weekly to determine concentrations of progesterone indicative of onset of corpus luteum function and puberty. In Exp. I a greater (P less than .05) proportion of heifers receiving the BE treatment than of heifers receiving the NE treatment initiated corpus luteum function by 14 mo of age. In Exp. II, there was a bull exposure x growth rate interaction (P less than .05). The effect of bull exposure was greater within the HG groups than within the MG groups. However, heifers fed to attain a moderate or high growth rate and exposed to bulls attained puberty at younger ages than heifers not exposed to bulls and fed to attain a moderate or high growth rate. Mean ages at puberty were 375, 422, 428, and 449 (pooled SEM = 8.6) d for heifers in the BE-HG, BE-MG, NE-HG, and NE-MG groups, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of supplemental manganese on performance of growing-finishing pigs and pork quality during retail display

Crossbred barrows and gilts (n = 168) were used to test the effects of supplemental Mn during the growing-finishing period on performance, pork carcass characteristics, and pork quality during 7 d of retail display. Pigs were blocked by BW and allotted within blocks to pens (5 pigs/pen in blocks 1, 2, 5, and 6, and 4 pigs/pen in blocks 3 and 4). A total of 36 pens was randomly assigned to 1 of 6 dietary treatments, where the basal diets were formulated with (PC) or without (NC) Mn in the mineral premix, and supplemented with 0 or 350 ppm (as-fed basis) of Mn from MnSO4 or a Mn-AA complex (AvMn). Pigs were slaughtered at a commercial pork packing plant when the lightest block of pigs averaged 113.6 kg. During fabrication, boneless pork loins were collected and transported to Oklahoma State University, where 2.5-cm-thick LM chops were packaged in a modified atmosphere (80% O2 and 20% CO2) and subsequently placed in display cases (2 to 4 degrees C) under continuous fluorescent lighting (1,600 lx) for 7 d. Pig performance was not (P > or = 0.44) affected by supplemental Mn; however, during the grower-II phase, pigs fed the basal diets including Mn consumed less (P < 0.02) feed and tended to be more efficient (P < 0.09) than pigs fed the basal diets devoid of Mn. Throughout the entire feeding trial, neither dietary nor supplemental Mn altered (P > or = 0.22) ADG, ADFI, or G:F. Chops from pigs fed the diets supplemented with MnSO4 received greater (P < or = 0.05) lean color scores and had a redder (greater a* and hue angle values), more vivid color than chops from pigs fed the diets supplemented with AvMn. Additionally, LM chops from pigs fed the PC diets supplemented with MnSO4 were darker (lower L* values; P < 0.05) than chops from pigs fed the NC diets or PC diets supplemented with 0 or 350 ppm of AvMn. Even though discoloration scores were similar during the first 4 d of display, chops from pigs fed the PC diets supplemented with MnSO4 were less (P < 0.05) discolored on d 6 and 7 of retail display than chops from pigs fed the PC or NC diets and diets supplemented with AvMn (dietary treatment x display time, P = 0.04). Results of this study indicate that feeding an additional 350 ppm of Mn from MnSO4 above the maintenance requirements of growing-finishing pigs does not beneficially affect live pig performance but may improve pork color and delay discoloration of pork during retail display.     

Longevity, lifetime pig production and productivity, and age at first conception in a cohort of gilts observed over six years on commercial farms.

An observational cohort study was conducted using a producer group of 33 farms selected based on their completeness of reproduction data, including dates of birth, entry to a herd, and removal. Average lifetime pig production and parity at removal in a cohort of 2,265 females born in 1990 were 67.2 pigs born alive and 5.6 parities, respectively. Approximately 90% of farrowings occurred from the second through the fourth year from birth. Farrowing rates between parities of 2 and 4 were higher than other parities, and pigs born alive from parities 3 to 5 were the greatest among parities. The 10th and 90th percentiles of age at first conception were 227 and 322 days. Increasing the age at first mating was associated with low farrowing rate (P<0.01) in parity 0. Older age at first conception was associated with lower parity at removal, shorter reproductive herd life, and fewer lifetime pigs born alive (P< 0.01). Of the 2,265 breeding females, 253 (11.2%) were re-mated at parity 0 and farrowed. These sows with a record re-mating at parity 0 had lower parity at removal, less lifetime pig production and lower lifetime productivity than those with no re-mating at parity 0 (P<0.01). It is recommended that unbred gilts 230 days of age or older should be mated soon.     

大豆黄酮和半胱胺对生长肥育猪生长性能的影响

本试验研究了半胱胺(CS)和大豆黄酮(Da)对杜×长×大生长肥育猪生长性能和胴体性状的影响,结果表明:这两种物质均具有显著促进猪生长作用,且在猪生长期的促生长效果好于肥育期.二者能提高胴体瘦肉率4%以上,脂肪率下降9%.     

DDGS对生长育成猪的生产性能及胴体品质的影响

本试验旨在研究DDGS对生长育成猪的生产性能和胴体品质的影响。432头体重为29.8±0.2kg的育成猪被随机分成1-9个日粮组,分别为对照组（D0）,D15-0wk,D15-3wk,D15-6wk,D15-9wk,D30-0wk,D30-3wk,D30-6wk和D30-9wk,其中D0、D15和D30分别代表DDGS在猪日粮中的百分含量;0wk、3wk、6wk和9wk代表在屠宰0、3、6和9周前分别取消DDGS在猪日粮的添加时间。结果显示,当生长育成猪日粮中的DDGS含量为15%或30%时,不管屠宰前是否取消DDGS的添加,除了D30-0wk处理组的猪的ADG比对照组（D0）稍降外（0.87：0.92kg/d;P〈0.05）,其他处理组猪的ADG、ADFI和G：F均没有显著差异（P=0.76）。DDGS的不同含量或屠宰前取消DDGS的添加时间（0周、3周、6周和9周）对猪胴体质量、背最长肌（LM）猪肉品质、背脂和腹脂颜色评分分数没有显著影响（背脂,P=0.47;腹脂,P=0.17）。相对对照组,D30-0wk组的腹部猪肉嫩度稍低（P=0.04）,其他处理组猪的腹部猪肉嫩度与对照组的差别均不大（P=0.26）。当增加猪日粮中的DDGS含量时,腹脂的亚油酸含量（C18：2;P〈0.001）和碘值（IV;P〈0.001）有所增加。当猪日粮中含有15%DDGS时,在屠宰前的0～9周取消DDGS添加可以线性的降低猪腹脂的C18：2含量和腹脂碘值（屠宰前的第0-、3-、6-和9周的腹脂C18：2含量分别为：14.6%、13.3%、12.6%、10.9%;P=0.001;碘值分别为：67.3、64.4、64.1和62.7）;而当猪的日粮中含有30%DDGS时,在屠宰前0～9周取消DDGS的添加也可以线性的降低猪腹脂的C18：2含量和腹脂碘值（屠宰前的第0-、3-、6-和9周的腹脂C18：2含量分别为：17.3%、16.1%、14.2%和12.4%;P〈0.001;碘值分别为：71.2、68.2、64.5和62.7）。总体来看,当在生长育肥猪中添加高达30%DDGS对猪的生产性能有极小影响,且在屠宰前的3周取消在猪日粮中的DDGS的添加可以降低猪腹脂的C18：2含量和碘值。     

Genetic analysis of age at first service, return rate, litter size, and weaning-to-first service interval of gilts and sows

The aim of this study was to estimate genetic parameters of seven traits related to sow reproductive performance. Data on all Norwegian Landrace pigs (NL) born in nucleus herds and raised in nucleus or multiplying herds from 1990 to 2000 were extracted from the Norwegian national recording scheme. Reproductive traits investigated were age at first service (AFS), return rate in gilts (RRg), age at first farrowing (AFF), live-born piglets in the first litter (NBA1), interval from weaning to first service after first litter (WTS1), return rate after first litter (RR1), live-born piglets in the second litter (NBA2), and interval from weaning to first service after second litter (WTS2). After editing, the data set comprised 12,583 to 56,042 records, depending on the trait. A mixed linear and a joint linear threshold animal model were used to estimate (co)variance components. A full Bayesian approach via Gibbs sampling was adopted. The statistical model used for analysis included contemporary groups of herd-year (-season), purebred or crossbred litter, single or double insemination, mating type, parity in which the animal was born, a regression on lactation length, and an additive genetic effect. Neither the estimated heritabilities nor the genetic correlations differed much between the two approaches, but there was a tendency for higher genetic correlations using the joint linear threshold model approach. Average heritabilities were as follows: AFS = 0.31; RRg = 0.03; RR1 = 0.02; NBA1 = 0.12; NBA2 = 0.14; WTS1 = 0.08; and WTS2 = 0.03. The highest genetic correlations were estimated between NBA1 and NBA2 (r(g) = 0.95), RR1 and WTS1 (r(g) = 0.93), and between WTS1 and WTS2 (r(g) = 0.78). The estimated genetic correlation between NBA and WTS were close to zero. Selection for increased NBA will slightly increase AFS and reduce the probability of a return. Selection for decreased AFS will have a favorable effect on WTS intervals; however, selection for decreased AFS seems to have an unfavorable effect on return rate both on gilts and sows. Conversely, selection for decreased WTS intervals will reduce the probability of a return. Potential selection candidates to include in a multivariate fertility index are AFS, NBA, and WTS1. Due to the low heritability and low, but favorable, genetic correlations to NBA and WTS, RR is not recommended as a selection candidate.