Search

Objective Our objectives were to determine growth rates, body composition, and pubertal development in replacement gilts fed diets with different ratios of standardized ileal digestible (SID) lysine to ME. Materials and Methods Diets with low, medium, and high ratios of SID lysine to ME (grower: 2.3, 2.6, and 2.8; finisher; 1.7, 1.9, and 2.1 g/Mcal) were fed from 100 to 200 d of age, after which gilts were moved from the gilt development unit to sow farms. Boar exposure and estrus detection began at 160 d of age and continued until first detected estrus. Estimates of BW and body composition were determined at 100, 142, 160, and 200 d of age and at puberty. Results and Discussion Body weights and growth rates were reduced (P Implications and Applications Reducing SID lysine–to–ME ratios in gilt diets can increase the number of gilts within optimal BW range at first estrus, but overall pubertal development is delayed if ratios are reduced below 2.8 and 2.1 g of SID lysine to megacalorie of ME in grower and finisher diets, respectively.

The primary objective of this pilot study was to evaluate the impact of social rank on the well-being of gestating sows housed in a free access stall-pen housing environment. At d 30 post-breeding, 32 multiparous crossbred sows in groups of 4 were allocated to a stall-pen housing environment. Blood samples were taken at gestational d 30 (before mixing) and d 31 (24-h post-mixing), and then again at d 89 and 110; whereas, sow behavior was recorded at gestational d 30, 66, 87, and 102. Social rank was determined based on aggressive encounters, dyadic fighting wins and losses, and displacements between sows by 48-h post-mixing. At d 31 (post-mixing), regardless of social rank, total WBC decreased and, lymphocyte counts increased, but % change was more significant among the subordinates than dominants. The same trend occurred with neutrophil chemotaxis increased more in subordinates, but ConA-induced lymphocyte proliferation increased more in dominants, whereas LPS-induced lymphocyte proliferation was reduced among dominants. Sow behavior was differentially affected by social rank and time-periods or gestational day, with subordinates spending more time sitting and drinking, especially during time-periods 1, 3, and 4. Dominants displayed more oral-nasal-facial behaviors during mid-gestation but more sham-chew during time-period 2, which included feeding time. Social rank also influenced the percentage of time sows spent in either the stall or pen area, with subordinates in stalls and dominants in pen. These data imply that social rank differentially influences physiology and behavior of dry sows housed in a free access stall-pen environment. More specifically, the location of the dominant sow, time of day, and activity may influence when and where the subordinates spend their time within this housing system.

Social conflict is inevitable among group-housed sows and may contribute to poorer welfare among those sows experiencing more social stress. The degree of individual welfare is associated with social position within the group. Therefore, this study examined the effects of social status on behavior, immune, endocrine, and productivity of group-housed pregnant sows fed a diet supplemented with 30% wheat middlings and 15% soybean hulls (MID-SH) or 30% distillers dried grains with solubles and 30% corn germ meal (DDGS-GM) and in pens with individual feeding places made from short (58.4 cm) or long (203.2 cm) barriers. A 2 × 2 factorial design resulted in 4 experimental treatment groups (n = 9 sows/diet-length-block combination): (1) MID-SHshort; (2) MID-SHlong; (3) DDGS-GMshort; (4) DDGS-GMlong. Groups of sows equally representing all diet-length combinations across 4 blocks (n = 36 sows/block) were subjected to a feeding competition test to identify highest (dominant) and lowest (subordinate) ranked sows within each group resulting in 64 sows (n = 16 sows/treatment; n = 32 sows/social status). Data revealed 2- and 3-way interactive effects on aggressive behavior (P < 0.005), postural (P < 0.01), oral (P < 0.0001), and eating (P < 0.005) behaviors, sow mean body weights and gains (P < 0.05) and litter weaning weights (P < 0.05), especially among subordinates in pens with long barriers. Subordinates in pens with long barriers received 21% less aggression and were 73% less likely to be displaced than subordinates in pens with short ones (P < 0.0001). Dietary treatment also influenced some of these measures among the subordinates in pens with long barriers. For example, subordinates in DDGS-GMlong received 64 and 67% less aggression than subordinates in DDGS-GMshort and MID-SHshort (P < 0.005). Eat bouts were greatest among subordinates in MID-SHlong, and sitting and sham-chewing were less. However, those in DDGS-GMlong spent less time standing and laying, and their litters were 15.28 kg heavier (P = 0.01), but overall subordinates fed DDGS-GM diet were lightest and gained less total body weight than those fed MID-SH (P < 0.05). Other measures such as neutrophil-to-lymphocyte ratio were elevated among dominants in MID-SHlong (P < 0.05); whereas, cortisol (P = 0.06) was lowest and glucose (P = 0.09) highest for subordinates in DDGS-GMlong. These data imply that subordinates benefited from being housed in pens with long barriers, but the type of dietary fiber consumed differentially influenced behavioral budget and several sow- or litter-related traits among subordinates in pens with long barriers. In contrast, the subordinates in pens with short barriers had poorer welfare regardless of diet. Collectively, these data imply that social status is a crucial factor contributing to variation in individual well-being among group-housed sows and that sows of different social positions within a group may evoke different biological responses in an attempt to cope.

This review summarizes the effects of ractopamine hydrochloride (RAC) dose (5, 7.5, 10, and 20 mg/kg) on market weight pig welfare indicators. Ractopamine hydrochloride (trade name Paylean) is a β-adrenergic agonist that was initially approved in the U.S. in 1999 at doses of 5 to 20 mg/kg to improve feed efficiency and carcass leanness. However, anecdotal reports suggested that RAC increased the rate of non-ambulatory (fatigued and injured) pigs at U.S. packing plants. This led to the addition of a caution statement to the Paylean label, and a series of research studies investigating the effects of RAC on pig welfare. Early research indicated that: (1) regardless of RAC administration, fatigued (non-ambulatory, non-injured) pigs are in a state of metabolic acidosis; (2) aggressive handling increases stress responsiveness at 20 mg/kg RAC, while 5 mg/kg reduces stress responsiveness to aggressive handling. Given this information, dosage range for Paylean was changed in 2006 to 5 to 10 mg/kg in market weight pigs. Subsequent research on RAC demonstrated that: (1) RAC has minimal effects on mortality, lameness, and home pen behavior; (2) RAC fed pigs demonstrated inconsistent prevalence and intensity of aggressive behaviors; (3) RAC fed pigs may be more difficult to handle at doses above 5 mg/kg; and (4) RAC fed pigs may have increased stress responsiveness and higher rates of non-ambulatory pigs when subjected to aggressive handling, especially when 20 mg/kg of RAC is fed.

Aggression is one of the major welfare concerns among group-housed sows, especially during feeding and regrouping. There are no simple solutions, but any attempt to reduce aggression should be considered. Therefore, the aim was to reduce aggression among group-housed gestating sows by feeding sows different dietary fiber using individual feeding places made from either short- or long-length partitions. Five blocks (n = 36 sows/block) of primiparous and multiparous sows were fed a dietary treatment of either 30% wheat middlings and 15% soybean hulls (MIDD-SY) or 30% distillers dried grains and 30% corn germ meal (DDGS-GM) and housed in pens (9 sows/pen) with individual feeding partitions that were either shoulder (short) or full-body (long) in length. Sow behavior, skin lesions, immune status, and performance were measured. Sow behavior, including aggression and lesion severity scores, were mainly affected by partition length. Aggressive encounters were greater and remained elevated among sows in pens with short partitions until 9 weeks post-grouping but were reduced among sows in pens with long partitions by 3 weeks. During feeding, sows in pens with short ones were more likely to be displaced than were those in pens with long ones. Percentages of time spent lying, standing, eating, and oral&ndash, nasal&ndash, facial behaviors were also differentially influenced by partition length. Dietary fiber differentially influenced immune status and productivity. For example, sows fed MIDD-SY had higher lymphocyte proliferation and increased neutrophils, while those fed DDGS-GM had deeper backfat and weaned heavier piglets. Overall, the length of the feeding partitions influenced the aggressive encounters, other behaviors, and lesion scores, in turn, the fibrous source differentially influenced several immune measures and sow productivity.

Bovine respiratory disease complex (i.e., shipping fever and bacterial bronchopneumonia) is a multifaceted respiratory illness influenced by numerous environmental factors and microorganisms. Bovine respiratory disease (BRD) is just one component of BRD complex. Because BRD is moderately heritable, it may be possible to reduce the incidence of BRD through genetic selection. The objectives of this study were to determine the heritability and associative genetic relationships among immune system traits (i.e., cortisol, total IgG, IgG isotypes, and IL-8) in cattle monitored for BRD incidence. At an average of 83 d after weaning (219 d age and mean = 221.7 kg [SD 4.34]), crossbred Bos taurus steer calves (n = 2,869) were received at a commercial feedlot in southeastern Colorado over a 2-yr period. At receiving, jugular blood samples were collected at 212 (yr 1) and 226 d (yr 2) of age for immune trait analyses. The BRD phenotype was defined as a binomial variable (0 = no and 1 = yes) and compared with immune system traits measured at receiving (prior to illness onset). An animal identified as BRD positive exhibited ≥ 2 clinical signs (i.e., eye or nasal discharge, cough, lethargy, rapid breathing, acute interstitial pneumonia, or acute upper respiratory syndrome and/or a rectal temperature > 39.7°C). Heritability and genetic correlation estimates for categorical variable BRD, cortisol, IgG, IgG1, IgG2, and IL-8 were estimated from a sire model using ASREML. Heritability estimates were low to moderate for BRD (0.17 ± 0.08), cortisol (0.13 ± 0.05), IgG (0.15 ± 0.05), IgG1 (0.11 ± 0.05), IgG2 (0.24 ± 0.06), and IL-8 (0.30 ± 0.06). A moderate negative genetic correlation was determined between BRD and cortisol (rg = −0.19 ± 0.32). Moderate positive correlations were found between BRD with IgG (0.42 ± 0.28), IgG1 (0.36 ± 0.32), and IL-8 (rg = 0.26 ± 0.26). Variation in the BRD phenotype and immune system traits suggested herd health improvement may be achieved through genetic selection.

Limited space allowance within the standard gestation stall is an important welfare concern because it restricts the ability of the sow to make postural adjustments and hinders her ability to perform natural behaviors. Therefore, we evaluated the impacts of increasing stall space and/or providing sows the freedom to access a small pen area on sow well-being using multiple welfare metrics. A total of 96 primi- and multiparous crossbred sows were randomly assigned in groups of 4 sows/treatment across 8 replicates to 1 of 3 stall treatments (TRT): standard stall (CTL; dimensions: 61 by 216 cm), width-adjustable stall (flex stall [FLX]; dimensions: adjustable width of 56 to 79 cm by 216 cm), or an individual walk-in/lock-in stall with access to a small communal open-pen area at the rear of the stall (free-access stall [FAS]; dimensions: 69 by 226 cm). Lesion scores, behavior, and immune and productivity traits were measured at various gestational days throughout the study. Total lesion scores were greatest for sows in FAS and least for sows in FLX ( < 0.001). Higher-parity sows in FAS had the most severe lesion scores (TRT × parity, < 0.0001) and scores were greatest at all gestational days (TRT × day, < 0.05). Regardless of parity, sows in FLX had the least severe scores ( < 0.0001). As pregnancy progressed, lesion scores increased among sows in CTL ( < 0.05). Sow BW and backfat (BF) were greater for sows in FLX and FAS ( < 0.05), and BCS and BF were greater for parity 1 and 2 sows in FAS than the same parity sows in CTL (TRT × parity, < 0.05). Duration and frequency of some postural behaviors and sham chew behavior were affected by TRT ( < 0.05) and time of day (TRT × day, < 0.05). These data indicate that adequate stall space, especially late in gestation, may improve the well-being of higher-parity and heavier-bodied gestating sows as assessed by changes in postural behaviors, lesion severity scores, and other sow traits. Moreover, compromised welfare measures found among sows in various stall environments may be partly attributed to the specific constraints of each stall system such as restricted stall space in CTL, insufficient floor space in the open-pen area of the FAS system, and gate design of the FLX (e.g., direction of bars and feeder space). These results also indicate that parity and gestational day are additional factors that may exacerbate the effects of restricted stall space or insufficient pen space, further compromising sow well-being.

Effects of day of mixing sows after breeding were measured for reproduction and welfare on a commercial research farm. Sows (n = 1,436) were weaned into stalls for breeding, and groups of sows were assigned to 1) no mixing and housed in individual stalls (STL), 2) mixed on d 3 to 7 after breeding (D3), 3) mixed on d 13 to 17 after breeding (D14), or 4) mixed 35 d after breeding (D35). Mixed sows were moved into pens (n = 58 sows/pen) with an electronic sow feeding station and maintained as a static group. In the first 12 d after mixing or movement into STL (period 1), sows were assessed for lameness and lesions every 3 d and then every 2 wk until farrowing (period 2). Cortisol and fights were measured in period 1. Conception rates were reduced (P 0.10) among treatments. Head and body lesion scores declined from period 1 to 2 in all mix groups, whereas vulva lesions increased in the D3 and D35 but did not change in D14 and STL (treatment × period, P < 0.0001). These results suggest STL can improve most measures of welfare compared to mixing in groups. However, when mixing sows, assessments for reproductive performance and welfare may change from gestation to farrowing. The poorest reproductive performance and welfare was observed when sows were mixed 3 to 7 d after breeding. There were few differences between the D14 and D35 treatments in reproduction or welfare, but D14--not D35--differed from STL in weaned sows rebred. Overall, results of this trial suggest that, even though any of the mixing days can result in acceptable measures of reproduction, there are clear effects of day of mixing on fertility and welfare, and special attention should be focused on the long-term reproductive and welfare consequences.

Identifying and optimizing housing and management systems that improve the well-being of the gestating sow is essential to sustaining animal agriculture. Therefore, the impact of 2 floor-space allowances and a high-fiber gestation diet on dry group-housed sows were evaluated using multiple measures of well-being. Groups of 10 multiparous sows/pen (n = 221) were assigned randomly to treatments in a 2 × 2 factorial arrangement to either a corn-soybean meal diet (CTL) or corn-soybean meal diet supplemented with soybean hulls and wheat middlings (FBR), and floor-space allowance of either 1.7 or 2.3 m(2)/sow. Sow BW, backfat (BF), and body condition score (BCS) were all recorded on d 34, 65, 90, and 110 of gestation, whereas skin lesions were scored on d 34, every 2 d for the first 2-wk postmixing, and then biweekly throughout gestation. Blood sample was collected only on d 34 for cortisol (baseline), and samples were collected on d 90 of gestation for other measures including cortisol. Behavior was registered on multiple days throughout gestation. Sows fed FBR and kept at 1.7 m(2) produced heavier litter and weaning weights and greater number of piglets born alive, compared to sows fed FBR but kept at 2.3 m(2) of floor space (diet × floor space, P ≤ 0.04). Sows fed FBR and kept at 1.7 m(2) performed fewer oral-nasal-facial and sham-chew behaviors than sows fed CTL and kept at the same floor space (diet × floor space, P ≤ 0.044). Sows kept at 1.7 m(2) of floor space had a greater (P < 0.05) total lesion severity score than sows kept at 2.3 m(2)/sow, and vulva lesion scores were more (P < 0.02) severe among CTL-fed sows than FBR-fed sows. Parities 2 and 3 sows fed FBR and kept at 1.7 m(2) of floor space were heavier (P < 0.001) than sows fed the same diet but kept at 2.3 m(2). These results indicate that keeping small groups of pregnant sows at a minimum floor-space allowance of 1.7 m(2)/sow and floor feeding these sows a high-fiber diet can improve short-term sow well-being.

Introduction Cattle producers historically have selected for docile temperaments simply for management convenience because calmer animals are conducive to safe environments for their peers as well as their handlers. As many producers would acknowledge, however, there seems to be a relationship between temperament and cattle health, and calmer cattle tend to frequent the working chute for treatment of disease less often.

The effects of room temperature and light intensity before breeding and into early gestation were evaluated on the reproductive performance and well-being of gilts housed individually in crates. In eight replicates, estrus was synchronized in mature gilts (n = 198) and after last feeding of Matrix were randomly assigned to a room temperature of 15°C (COLD), 21°C (NEUTRAL), or 30°C (HOT) and a light intensity of 11 (DIM) or 433 (BRIGHT) lx. Estrous detection was performed daily and gilts inseminated twice. Blood samples were collected before and after breeding for determination of immune measures and cortisol concentrations. Gilt ADFI, BW, and body temperature were measured. On d 30 postbreeding, gilts were slaughtered to recover reproductive tracts to evaluate pregnancy and litter characteristics. There were no temperature × light intensity interactions for any response variable. Reproductive measures of follicle development, expression of estrus, ovulation rate, pregnancy rate (83.2%), litter size (14.3 ± 0.5), and fetal measures were not affected by temperature or lighting (P > 0.10). Gilts in COLD (37.6°C) had a lower (P 0.10) of light or interaction with temperature on other immune cells or measures. These results indicate that temperatures in the range of 15 to 30°C or light intensity at 11 to 433 lx do not impact reproduction during the follicular phase and into early gestation for mature gilts housed in gestation crates. However, room temperature does impact physiological, behavioral, and immune responses of mature gilts and should be considered as a potential factor that may influence gilt well-being during the first 30 d postbreeding.

Group-housing systems for pregnant sows are considered a welfare-promoting alternative to the individual stall. A major concern associated with pregnant sows housed in group pens is increased aggression at mixing and at feeding, which may cause chronic stress among some of the sows in the group due to low feed intake and social stress. Prolonged activation of the stress axis, based on elevated cortisol levels, may inhibit or impair reproductive success via disruption of the reproductive axis. Mixing sows into groups shortly after insemination evokes a stress response, which may affect fertilization and implantation due to sustained, elevated cortisol levels that disrupt reproductive processes. Yet, most studies reported minimal effects of group housing sows during pregnancy on reproduction or cortisol-related stress response. Differences between housing systems-in terms of group size, floor-space allowance, feeding system, and genetics-could account for these unexpected results. Indeed, interrupted feed intake, especially in early pregnancy, and sustained aggression in late pregnancy are two unfavorable social stresses that deserve special attention in order to achieve good reproductive performance. Unfortunately, most studies do not consider other factors, such as social rank and parity, which may interactively affect reproductive success and aggressive behavior of sows, especially in group-pen systems.

Loss of pigs during or after transport is a welfare concern, but also an economic concern for producers. Transport losses include animals that are dead on arrival (DOA) at the plant, pigs that are injured, and pigs which are not obviously injured but unwilling or unable to walk (non-ambulatory, non-injured or NANI). The objective of this research was to assess the health of non-ambulatory, non-injured (NANI) pigs relative to control pigs at the processing plant by looking at a range of measures, including complete blood chemistry, anatomy, and pathology to determine potential factors associated with pigs going down. Data were collected from NANI and control pigs at five plants in the midwest USA. Feet and legs and internal organs were inspected and the severity of the pathology scored. Alveolar macrophages were collected and counted. Blood was collected for analysis of hematology, blood chemistry and cortisol concentrations. Titers to common porcine respiratory viruses were measured in pigs from one plant. Hoof and pad problems did not differ overall between control and NANI pigs, however the percentage of severe foot problems was greater ( P P P P P

Different floor space allowances for dry, pregnant sows in pens were evaluated to determine the impacts of space on sow performance, productivity, and body lesions during 2 consecutive farrowings. Treatment groups of 5 sows/pen were assigned to 1.4, 2.3, or 3.3 m(2) of floor space/sow or of 5 sows in individual stalls (1.34 m(2)). The experiment consisted of 6 replications (blocks 1 to 6), and within each block measurements were recorded for 2 consecutive pregnancies and farrowings. A total of 152 sows were measured at 1 farrowing, and 65 of those sows were measured at the successive farrowing (n = 217 records). Performance traits were BCS, BW, backfat (BF), days until rebred, and proportion culled. Litter traits were number of piglets born alive, male:female ratio, and proportions of stillborn, mummified, or dead piglets after birth. Litter performance measures were mean piglet BW and gain and litter BW. Lesion scores were assessed for several body regions. There were treatment and parity effects and interactions for several traits. An interaction of space treatment and parity occurred for sow mean BW, d-110 BW, BF, litter size, and litter and piglet BW and gain, with most effects in parity 2, 3, and 4 sows. Space affected sow mean (P < 0.001) and d-110 BW (P < 0.05) and mean BF and adjusted BF (P < 0.001); sows in pens at

Changes in thermal environment can invoke a stress response in pigs, which in turn can potentially impact their immune system and disease susceptibility. We investigated effects of heat stress and social rank on behavior, immune responsiveness, and performance of pigs challenged with porcine reproductive and respiratory syndrome (PRRS) virus. Sixty-four 7-week-old PRRS-naïve pigs were assigned to each of four experimental treatments consisting of a 2 x 2 factorial design: PRRS (PRRS- or PRRS+) and environmental temperature (24 degrees C or 32 degrees C). Blood samples were taken prior to and at days 7 and 14 post-inoculation, and alveolar macrophages were collected via bronchoalveolar lavage at day 14. Total white blood cell counts, natural killer cytotoxicity, macrophage numbers, macrophage subpopulations, and performance measures were all significantly affected by social rank, heat stress, and/or infection status of the pig. Heat stress and PRRS status also significantly influenced the amount of time pigs spent lying with or without contacting another animal. Cortisol and various immune measures were also affected by PRRS status. These results show not only that intranasal inoculation with PRRS virus affects physiological, behavioral, and performance measures in growing pigs, but that social rank influences pigs' immune responsiveness to PRRS as well. Moreover, heat stress does not have additive negative impact on physiological or performance traits in pigs challenged with PRRS virus.

An acute stress response can be provoked by abrupt social, nutritional, and environmental changes associated with weaning, and this may disrupt homeostasis and thus compromise well-being. Manipulating environmental factors, such as photoperiod, might provide a simple way to reduce the physiological consequences that piglets experience due to weaning stress. The objective of this study was to evaluate the impacts of photoperiod manipulation across various weaning ages on leukocyte populations, lymphocyte proliferation, natural killer cytotoxicity (NK), chemotaxis, phagocytosis, and immunoglobulin G, cortisol, and BW of piglets during the nursery phase. Sixty-eight crossbred piglets were obtained from sows kept on a short-day (8 h of light/d) photoperiod from d 90 of gestation until weaning. Piglets were weaned at 14, 21, or 28 d of age and kept on a short or long (16 h of light/d) photoperiod until 10 wk of age. Piglet BW and blood samples were collected at weaning and at 6, 8, and 10 wk of age. Pigs weaned at 28 d had reduced neutrophil counts (P < 0.001), phagocytosis (P < 0.001), and lymphocyte proliferation (P < 0.05) at weaning compared with those weaned at 14 and 21 d. Pigs weaned at 21 d tended to have lower (P = 0.08) lymphocyte counts than did pigs weaned at 14 or 28 d. Pigs weaned at 14 d had reduced (P < 0.01) NK relative to those weaned at 21 or 28 d. Photoperiod also influenced pig BW and immune status. Generally, those pigs on the long-day photoperiod and weaned at 28 d were heavier (P < 0.001) than their counterparts weaned at 14 or 21 d. At 6 wk of age, NK was greater (P = 0.002) in pigs kept on a long day and weaned at 14 or 21 d than in pigs weaned at 28 d. Phagocytosis was less (P = 0.005) at 6 wk of age, but was greater at 8 wk, in piglets kept on the long day and weaned at 28 d than in long-day pigs weaned at 14 or 21 d. These results suggest that photoperiod differentially influences immune responses in piglets weaned at different ages and indicate an inverse relationship between growth and immune status. Here, weaning at 28 d and a long-day photoperiod was the treatment combination that was most physiologically beneficial to piglets, whereas a 14-d weaning and short-day photoperiod was least physiologically beneficial.

Limited space allowance within the standard gestation stall is an important welfare concern because it restricts the ability of the sow to make postural adjustments and hinders her ability to perform natural behaviors. Therefore, we evaluated the impacts of increasing stall space and/or providing sows the freedom to access a small pen area on sow well-being using multiple welfare metrics. A total of 96 primi- and multiparous crossbred sows were randomly assigned in groups of 4 sows/treatment across 8 replicates to 1 of 3 stall treatments (TRT): standard stall (CTL; dimensions: 61 by 216 cm), width-adjustable stall (flex stall [FLX]; dimensions: adjustable width of 56 to 79 cm by 216 cm), or an individual walk-in/lock-in stall with access to a small communal open-pen area at the rear of the stall (free-access stall [FAS]; dimensions: 69 by 226 cm). Lesion scores, behavior, and immune and productivity traits were measured at various gestational days throughout the study. Total lesion scores were greatest for sows in FAS and least for sows in FLX (0.001). Higher-parity sows in FAS had the most severe lesion scores (TRT × parity,0.0001) and scores were greatest at all gestational days (TRT × day,0.05). Regardless of parity, sows in FLX had the least severe scores (0.0001). As pregnancy progressed, lesion scores increased among sows in CTL (0.05). Sow BW and backfat (BF) were greater for sows in FLX and FAS (0.05), and BCS and BF were greater for parity 1 and 2 sows in FAS than the same parity sows in CTL (TRT × parity,0.05). Duration and frequency of some postural behaviors and sham chew behavior were affected by TRT (0.05) and time of day (TRT × day,0.05). These data indicate that adequate stall space, especially late in gestation, may improve the well-being of higher-parity and heavier-bodied gestating sows as assessed by changes in postural behaviors, lesion severity scores, and other sow traits. Moreover, compromised welfare measures found among sows in various stall environments may be partly attributed to the specific constraints of each stall system such as restricted stall space in CTL, insufficient floor space in the open-pen area of the FAS system, and gate design of the FLX (e.g., direction of bars and feeder space). These results also indicate that parity and gestational day are additional factors that may exacerbate the effects of restricted stall space or insufficient pen space, further compromising sow well-being.

Manipulation of photoperiod may provide a noninvasive, easily implemented, effective method to improve immune status and enhance the efficiency of production. The objective of this study was to evaluate the impact of manipulation of photoperiod on endocrine and immune responses of pregnant sows and their offspring. At d 83 of gestation, sows were moved to gestation stalls and kept on a photoperiod of 12 h of light:12 h of dark until d 90, when sows were assigned to a long day (LD; 16 h of light/d) or a short day (SD; 8 h of light/d) treatment. During farrowing and lactation, one-half of the sows remained on their initial photoperiod (LD:LD or SD:SD), whereas one-half were switched to the opposite treatment (LD:SD or SD:LD). Blood samples were collected from sows at d 0, 7, 14, and 21 posttreatment, 24-h postfarrowing, and the end of lactation (approximately d 21 postfarrowing). Piglets were bled at 7 and 21 d of age for immune measures. Relative to sows on LD, sows on SD had greater concanavalin A- (P = 0.003) and lipopolysaccharide- (P = 0.02) induced proliferative responses at d 7 but reduced responses at d 14. Compared with SD, sows on LD had a greater (P < 0.05) percentage of neutrophils and fewer (P < 0.05) lymphocytes at d 7, resulting in a greater (P = 0.05) neutrophil:lymphocyte ratio. Neutrophil phagocytosis was greater at d 21 in sows kept on LD. Cortisol concentrations tended to be greatest (P = 0.10) in sows on SD:SD at 24-h postfarrowing and throughout lactation. At 7 d of age, piglets on LD:SD had greater (P = 0.001) total white blood cells (WBC) and plasma cortisol (P = 0.001) relative to those on the other photoperiod treatments. Plasma immunoglobulin G was less (P = 0.001) in piglets from sows kept on SD:LD compared with the other photoperiod treatments. Piglets from sows kept on LD:LD tended to have lower total WBC (P = 0.08) at 21 d of age. Piglets from sows kept on SD:SD had greater concanavalin A- (P < 0.001) and lipopolysaccharide-induced (P < or = 0.10) proliferation responses and cortisol (P = 0.05). Phagocytosis was greater (P < 0.003) in piglets from sows that were kept on LD:LD. Cortisol (P = 0.02), WBC (P = 0.003), and immunoglobulin G (P = 0.001) were all influenced by gestational photoperiod treatment. These data indicate that photoperiod influences the immune status and endocrine response of piglets from dams that have been kept on a defined photoperiod. We conclude that photoperiod effects on piglets may be programmed in utero and can last throughout lactation.

Pigs typically experience various environmental stressors, which can negatively affect performance. Cortisol concentrations and various immune and performance measures are influenced by breed, but few data exist describing the impact of breed on stress responsiveness in pigs. The objective of this experiment was to determine if certain physiological responses to chronic stressors differed among 3 breeds and 2 commercial lines of pigs. The pigs were Landrace (n = 36), Meishan (n = 30), Yorkshire (n = 32), or 1 of 2 commercial lines (Line-A and Line-B; both n = 36). All pigs were weaned at 17 to 21 d and kept in a common nursery. At 49 d of age, pigs were assigned to 1 of 2 treatments: stress (heat, crowding, and mixing) or control (no stress treatment). Pigs were allocated to groups of 3 pigs per pen of the same sex. Control pigs were kept with their littermates. At the onset of the experiment, stressed pigs were mixed with 2 unfamiliar pigs once, and heat and crowding stressors were implemented simultaneously for 14 d. Pigs allocated to the stress treatment were video-recorded for 24 h following initiation of mixing to determine social status: dominant, intermediate, or submissive. Blood samples were taken at d 0 (baseline), 1, 7, and 14 to assess cortisol concentrations and immune measures. Breed and treatment affected cortisol, immune, and performance measures, but no significant breed x treatment interactions were found. In general, pigs subjected to the chronic stressor had lower (P < 0.001) BW and ADG (P < 0.001) than did control pigs. Plasma cortisol was lower (P < 0.001) among stressed pigs at d 7 and 14. Regardless of breed, lipopolysaccharide-induced proliferation (P < 0.01) and natural killer (NK; P < 0.005) cytotoxicity were greater in stressed pigs compared with controls. Furthermore, among stressed pigs, dominant pigs had a greater total white blood cell count (P < 0.005), NK (P < 0.05), and phagocytosis (P < 0.05) than the subordinate pigs. The results indicate that pig breed did not influence the physiological responses to the chronic concurrent stressors imposed for 14 d in this study, but social status did influence the immune responsiveness of these pigs to heat, crowding, and mixing.

It was hypothesized in these studies that differences would exist in baseline immune and performance measures among different breeds of pigs, and that these differences would be affected by age of the pig. Baseline immune, plasma cortisol (CORT) concentrations, and performance measures were determined among Berkshire (n = 36), Duroc (n = 18), Meishan (n = 54), Landrace x Yorkshire (White X; n = 36), and Yorkshire (n = 36) pigs at 4, 8, and 12 wk of age. All piglets were weaned at 17 to 21 d of age and moved to a common nursery environment. Total white blood cell (WBC), leukocyte differential, plasma CORT, immunoglobulin G (IgG) concentrations, natural killer cytotoxicity, neutrophil phagocytosis (PHAGO), and chemotaxis (CHTX) were evaluated. At all ages, plasma CORT was greatest in Meishan pigs, and least in York-shires (P < 0.05). Plasma IgG increased with age for all breeds (age: P < 0.01; breed x age: P < 0.005), except that in Meishans, IgG decreased. Natural killer cytotoxicity was greatest (P < 0.05) among Meishan pigs. There were breed x age interactions for neutrophil PHAGO (P < 0.001) and CHTX (P < 0.001). Overall, Yorkshire pigs showed the greatest (P < 0.05) percentage of PHAGO but the least (P < 0.05) CHTX. White X pigs had the greatest (P < 0.05) CHTX response. Berkshire pigs had the greatest (P < 0.001) numbers of neutrophils. At 12 wk of age, Meishan pigs had the least BW gain (P < 0.001), and Durocs had the greatest G:F (P < 0.001). There were no significant sex differences for immune (P ≥ 0.15), performance (P ≥ 0.20), or CORT (P = 0.70) measures. Pig breed and age influenced both baseline immune measures and plasma CORT in growing pigs, suggesting that pig breed and age are important factors influencing the response to various stressors or infectious challenges.

The elevation of central corticotropin releasing factor (CRF) causes an increase in behavioral activity, including increases in overall activity and oral/nasal/facial (ONF) chewing-rooting-rubbing behaviors in the pig and similar behaviors in other species. This study detailed changes in the frequency, duration and sequences of behaviors after central administration of vehicle or porcine CRF (pCRF at 0.5, 5.0, 50 and 150 microg). A sequential analysis described the complex behaviors induced in a dose-dependent fashion by central pCRF. The frequency and duration of ONF behaviors were significantly increased among pigs receiving 50 microg of pCRF. For behaviors such as ONF, 50 microg represented a breakpoint at which the frequency and duration of single behaviors increased. Pigs receiving 50 microg of pCRF were considerably more active and exhibited more ONF behaviors than did pigs receiving lower doses. The highly sensitive sequential analysis revealed that very low doses of central pCRF induced subtle changes in sequences of behaviors. Low doses of central pCRF (0.5 microg) induced fear-related behavioral sequences that included ONF behaviors alternating with periods of inactivity. Central injection of astressin, a CRF receptor antagonist, blocked many, but not all, of CRF-induced behaviors. Compared with saline-injected control pigs, central pCRF increased general activity, ONF, fear-related freezing and sham chewing behaviors. When pCRF was given following astressin, fear-related freezing behaviors were not different compared with pigs receiving saline. However, pigs given astressin plus pCRF showed elevated sham chewing compared with saline-injected control pigs, as did pigs receiving intracerebroventricular (ICV) pCRF. These data indicate that central pCRF activates brain mechanisms associated with hyperactivity, ONF and fear-related behaviors, whereas other behaviors induced by pCRF may be nonspecifically mediated by CRF. Astressin antagonized some, but not all, pCRF-induced behaviors. This model represents the induction of hyperactivity and stereotyped behaviors, which may represent a new model for the study of mania or obsessive-compulsive behaviors.

The objective of this study was to determine whether feeding a vitamin E-rich diet would benefit nursery pigs infected with porcine reproductive and respiratory syndrome virus (PRRSV). Sixty-four pigs were subjected to one of four treatment combinations (2 x 2 factorial) of dietary vitamin E (adequate or excess) and PRRSV (medium or inoculation with VR-2385 isolate P-129). Pigs were fed experimental diets during a 3-wk period before inoculation as well as during a 12-d period after inoculation. Growth performance was determined throughout the study, and lipid peroxidation in liver, glutathione peroxidase (GPX) activity in serum, circulating white blood cells, and serum interleukin-1beta (IL-1beta) and interferon-gamma (IFN-gamma) were determined in samples collected from pigs killed 4 or 12 d after inoculation. Infection by PRRSV (P < 0.001) induced a marked decrease in both ADFI and ADG, but neither the main effect of diet nor the diet x PRRSV interaction was significant. Neither diet nor PRRSV affected feed efficiency. At 12 d after inoculation, lipid peroxidation in liver and GPX activity in serum were lower in pigs fed excess vitamin E than in those fed adequate vitamin E (P < 0.01), suggesting that the diet high in vitamin E bolstered the antioxidant status of the pigs. However, PRRSV did not affect lipid peroxidation in liver or serum GPX activity, and the diet x PRRSV interaction was not significant. White blood cell counts were decreased and IFN-gamma, and IL-1beta were increased (P < 0.05) 4 and 12 d after inoculation in PRRSV-infected pigs, but neither diet nor the diet x PRRSV interaction was significant. Collectively, these results indicate that increasing antioxidant defenses by feeding high levels of vitamin E did not ameliorate the effects of PRRSV on decreased growth, leukopenia, and increased serum IL-1beta and IFN-gamma. Thus, feeding nursery pigs a diet high in vitamin E may not be useful for mitigating the acute morbidity effects of PRRSV infection.

Identifying and optimizing housing and management systems that improve the well-being of the gestating sow is essential to sustaining animal agriculture. Therefore, the impact of 2 floor-space allowances and a high-fiber gestation diet on dry group-housed sows were evaluated using multiple measures of well-being. Groups of 10 multiparous sows/pen (n = 221) were assigned randomly to treatments in a 2 × 2 factorial arrangement to either a corn-soybean meal diet (CTL) or corn-soybean meal diet supplemented with soybean hulls and wheat middlings (FBR), and floor-space allowance of either 1.7 or 2.3 m(2)/sow. Sow BW, backfat (BF), and body condition score (BCS) were all recorded on d 34, 65, 90, and 110 of gestation, whereas skin lesions were scored on d 34, every 2 d for the first 2-wk postmixing, and then biweekly throughout gestation. Blood sample was collected only on d 34 for cortisol (baseline), and samples were collected on d 90 of gestation for other measures including cortisol. Behavior was registered on multiple days throughout gestation. Sows fed FBR and kept at 1.7 m(2) produced heavier litter and weaning weights and greater number of piglets born alive, compared to sows fed FBR but kept at 2.3 m(2) of floor space (diet × floor space, P ≤ 0.04). Sows fed FBR and kept at 1.7 m(2) performed fewer oral-nasal-facial and sham-chew behaviors than sows fed CTL and kept at the same floor space (diet × floor space, P ≤ 0.044). Sows kept at 1.7 m(2) of floor space had a greater (P0.05) total lesion severity score than sows kept at 2.3 m(2)/sow, and vulva lesion scores were more (P0.02) severe among CTL-fed sows than FBR-fed sows. Parities 2 and 3 sows fed FBR and kept at 1.7 m(2) of floor space were heavier (P0.001) than sows fed the same diet but kept at 2.3 m(2). These results indicate that keeping small groups of pregnant sows at a minimum floor-space allowance of 1.7 m(2)/sow and floor feeding these sows a high-fiber diet can improve short-term sow well-being.

The effects of room temperature and light intensity before breeding and into early gestation were evaluated on the reproductive performance and well-being of gilts housed individually in crates. In eight replicates, estrus was synchronized in mature gilts (n = 198) and after last feeding of Matrix were randomly assigned to a room temperature of 15°C (COLD), 21°C (NEUTRAL), or 30°C (HOT) and a light intensity of 11 (DIM) or 433 (BRIGHT) lx. Estrous detection was performed daily and gilts inseminated twice. Blood samples were collected before and after breeding for determination of immune measures and cortisol concentrations. Gilt ADFI, BW, and body temperature were measured. On d 30 postbreeding, gilts were slaughtered to recover reproductive tracts to evaluate pregnancy and litter characteristics. There were no temperature × light intensity interactions for any response variable. Reproductive measures of follicle development, expression of estrus, ovulation rate, pregnancy rate (83.2%), litter size (14.3 ± 0.5), and fetal measures were not affected by temperature or lighting (P0.10). Gilts in COLD (37.6°C) had a lower (P0.05) rectal temperature than those in NEUTRAL (38.2°C) and HOT (38.6 ± 0.04°C). Both BW gain and final BW were greater (P0.0001) for gilts kept in HOT than those in NEUTRAL or COLD environments. Cortisol was greater (P0.01) for gilts kept in COLD compared with those kept in the HOT room. Gilts housed in the HOT environment made more postural changes (P0.05) than did those kept in either COLD or NEUTRAL temperatures. Gilts kept in the HOT temperature spent more total time lying and more time lying ventrally compared with those gilts housed in the NEUTRAL or COLD rooms. Total white blood cells and the percentage of neutrophils as well as neutrophil-to-lymphocyte ratio were all influenced (P0.05) by temperature but there was no effect (P0.10) of light or interaction with temperature on other immune cells or measures. These results indicate that temperatures in the range of 15 to 30°C or light intensity at 11 to 433 lx do not impact reproduction during the follicular phase and into early gestation for mature gilts housed in gestation crates. However, room temperature does impact physiological, behavioral, and immune responses of mature gilts and should be considered as a potential factor that may influence gilt well-being during the first 30 d postbreeding.

Different floor space allowances for dry, pregnant sows in pens were evaluated to determine the impacts of space on sow behavior, immune, and cortisol measures. The experiment consisted of 6 replications (blocks 1 to 6; n = 20 sows/group), and within each replicate, physiological measurements were recorded for 2 consecutive pregnancies. A total of 152 sows were measured at 1 gestation, and 65 of those sows were measured at the successive gestation (n = 217). Groups of 5 sows/pen were assigned to 1.4, 2.3, or 3.3 m(2) of floor space/sow or of 5 sows in individual stalls (1.34 m(2)). Behavior measures were stand, sit, lie, walk, drink, oral-nasal-facial (ONF), sham chew, and aggression. Immune traits included both descriptive and functional aspects and cortisol. At d 90 ± 5 of gestation, the occurrence of ONF behaviors increased from 0300 to 1500 h, and lying behavior decreased from 0700 to 1100 h for sows kept at 2.3 m(2). Sows in stalls displayed more (P0.05) ONF from 1500 to 2300 h. Stand, sit, drink, ONF, and sham-chew behaviors were affected by floor space; sows in pens at 2.3 m(2) performed more ONF, and sows at 1.4 m(2) performed more sham chewing (P0.05). Standing (P = 0.05) and drinking (P = 0.06) were increased, but lying (P = 0.06) was reduced for sows in pens at 2.3 or 3.3 m(2). Sitting and drinking were greater but lying was less for sows in stalls compared with sows in pens (P0.01). Immune traits were affected by treatment (P0.05); neutrophils were less and lymphocytes were greater, resulting in a reduced neutrophil:lymphocyte (N:L) ratio (P0.05) for sows in pens at 3.3 m(2). Natural killer cell was greater but lymphocyte proliferation was less for sows in pens at 1.4 m(2) (P0.05). Sows in stalls had greater N:L ratio than sows in pens (P0.05). For sows in pens, linear and quadratic responses were detected for behavior and immune traits. As floor space increased, walking and aggression increased. As floor space decreased, neutrophils, N:L, and natural killer cell increased, but as floor space increased lymphocyte proliferation increased. On the basis of behavioral and physiological responses shown by sows in all 4 environments it is apparent that neither floor space nor stall environment provided adequate or quality of space to improve sow well-being. However, the differential behavioral and physiological mechanisms initiated by sows in response to their specific environment the sows were able to evoke the appropriate response(s) needed to adequately adapt to their environment.

Forty-eight domestic pigs were used to evaluate the effects of heat and social stress on immune indices. Pigs were brought together in groups of three per pen and video-taped for the first 72 h. Video tapes were viewed to determine time spent in aggressive and submissive behaviors. Social status of each pig was determined from outcomes of agonistic interactions. Pens of pigs were housed in either a thermoneural (control, 24 degrees C) or heat-stress (33 degrees C) air temperature. Immune measures were determined from blood samples obtained on d 0, 7, 14, 21, and 28 after grouping. Social status had an effect (P < .05) on lymphocyte proliferation in response to pokeweed mitogen: socially intermediate pigs had a higher proliferative response than socially dominant or subordinate pigs. Many immune measures showed a significant interaction between heat and social stress over days of the study. Generally, socially dominant or submissive pigs had alterations in immune function (elevated numbers of neutrophils, decreased antibody production) compared with socially intermediate pigs. In conclusion, heat and social stress interact in their effect on the pig's immune system. Although one might have predicted immunosuppression among submissive pigs, there also seemed to be immunological costs to dominant pigs as well. These data also have implications in design of stressor research in that social behavior should be measured or controlled.

An evaluation of reproductive performance, behavior, immunity and ergonomics was conducted for two common sow housing systems: the girth tether and crate. Littermate Yorkshire×Landrace gilts were randomly assigned to either the crate or girth tether system and they remained in that treatment for two consecutive pregnancies and lactations. A total of 171 matings resulted in 141 litters (82.4% farrowing rate). Second parity sows penned in girth tethers had 1.5 fewer piglets born and 1.3 fewer piglets weaned than sows in the crate system ( P P P P P

Cows experience some degree of negative energy balance and immunosuppression around parturition, making them vulnerable to metabolic and infectious diseases. The effect of prepartum feeding of diets to meet (control, 1.34 Mcal/kg of dry matter) or exceed (overfed, 1.62 Mcal/kg of dry matter) dietary energy requirements was evaluated during the entire dry period (∼45 d) on blood polymorphonuclear neutrophil function, blood metabolic and inflammatory indices, and milk production in Holstein cows. By design, dry matter intake in the overfed group (n=9) exceeded energy requirements during the prepartum period (-4 to -1 wk relative to parturition), resulting in greater energy balance when compared with the control group (n=10). Overfed cows were in more negative energy balance during wk 1 after calving than controls. No differences were observed in dry matter intake, milk yield, and milk composition between diets. Although nonesterified fatty acid concentration pre- (0.138 mEq/L) and postpartum (0.421 mEq/L) was not different between diets, blood insulin concentration was greater in overfed cows prepartum (16.7 μIU/mL) compared with controls pre- and postpartum (∼3.25 μIU/mL). Among metabolic indicators, concentrations of urea (4.63 vs. 6.38 mmol/L), creatinine (100 vs. 118 μmol/L), and triacylglycerol (4.0 vs. 8.57 mg/dL) in overfed cows were lower prepartum than controls. Glucose was greater pre- (4.24 vs. 4.00 mmol/L) and postpartum (3.49 vs. 3.30 mmol/L) compared with control cows. Among liver function indicators, the concentration of bilirubin increased by 2 to 6 fold postpartum in control and overfed cows. Phagocytosis capacity of polymorphonuclear neutrophils was lower prepartum in overfed cows (32.7% vs. 46.5%); phagocytosis in the control group remained constant postpartum (50%) but it increased at d 7 in the overfed group to levels similar to controls (48.4%). Regardless of prepartum diet, parturition was characterized by an increase in nonesterified fatty acid and liver triacylglycerol, as well as blood indices of inflammation (ceruloplasmin and haptoglobin), oxidative stress (reactive oxygen metabolites), and liver injury (glutamic oxaloacetic transaminase). Concentrations of the antioxidant and anti-inflammatory compounds vitamin A, vitamin E, and β-carotene decreased after calving. For vitamin A, the decrease was observed in overfed cows (47.3 vs. 27.5 μg/100 mL). Overall, overfeeding energy and higher energy status prepartum led to the surge of insulin and had a transient effect on metabolism postpartum.

Ten multiparous Holstein cows were used to determine the effects of negative energy balance (NEB) on the immune response to a Streptococcus uberis (strain O140J) mastitis challenge during midlactation. Before the study, milk from all quarters of each cow was bacteriologically negative, with a composite somatic cell count of

Different floor space allowances for dry, pregnant sows in pens were evaluated to determine the impacts of space on sow performance, productivity, and body lesions during 2 consecutive farrowings. Treatment groups of 5 sows/pen were assigned to 1.4, 2.3, or 3.3 m(2) of floor space/sow or of 5 sows in individual stalls (1.34 m(2)). The experiment consisted of 6 replications (blocks 1 to 6), and within each block measurements were recorded for 2 consecutive pregnancies and farrowings. A total of 152 sows were measured at 1 farrowing, and 65 of those sows were measured at the successive farrowing (n = 217 records). Performance traits were BCS, BW, backfat (BF), days until rebred, and proportion culled. Litter traits were number of piglets born alive, male:female ratio, and proportions of stillborn, mummified, or dead piglets after birth. Litter performance measures were mean piglet BW and gain and litter BW. Lesion scores were assessed for several body regions. There were treatment and parity effects and interactions for several traits. An interaction of space treatment and parity occurred for sow mean BW, d-110 BW, BF, litter size, and litter and piglet BW and gain, with most effects in parity 2, 3, and 4 sows. Space affected sow mean (P0.001) and d-110 BW (P0.05) and mean BF and adjusted BF (P0.001); sows in pens at/=2.3 m(2) of space had greater (P0.05) BW and BF depth, and primiparous sows had less (P0.05) BW than greater parity sows. Few differences were found for litter traits, except for litter size, litter weaning BW, and pig BW gain. Sows in pens at 3.3 m(2) had the largest (P0.05) litters. Weaning BW was greater (P0.05) for litters born to sows that gestated in stalls. Sow BCS and lesion score were affected by floor space (P0.001) and parity (P0.01); BCS was reduced in sows in pens at 1.4 m(2), and their lesion score was consistently greater (P0.05) than that of other space allowances. Primiparous sows often had the least (P0.05) lesion scores. For sows in pens, linear and quadratic responses were detected for many of the traits assessed. As floor space increased, BW and BF increased (P0.01), but as space decreased, lesion scores increased. Although the effects of gestation system were found and lesion scores often were greater as space decreased, differences in productivity traits were unremarkable with respect to sow welfare or performance compared with industry norms.

An acute stress response can be provoked by abrupt social, nutritional, and environmental changes associated with weaning, and this may disrupt homeostasis and thus compromise well-being. Manipulating environmental factors, such as photoperiod, might provide a simple way to reduce the physiological consequences that piglets experience due to weaning stress. The objective of this study was to evaluate the impacts of photoperiod manipulation across various weaning ages on leukocyte populations, lymphocyte proliferation, natural killer cytotoxicity (NK), chemotaxis, phagocytosis, and immunoglobulin G, cortisol, and BW of piglets during the nursery phase. Sixty-eight crossbred piglets were obtained from sows kept on a short-day (8 h of light/d) photoperiod from d 90 of gestation until weaning. Piglets were weaned at 14, 21, or 28 d of age and kept on a short or long (16 h of light/d) photoperiod until 10 wk of age. Piglet BW and blood samples were collected at weaning and at 6, 8, and 10 wk of age. Pigs weaned at 28 d had reduced neutrophil counts (P0.001), phagocytosis (P0.001), and lymphocyte proliferation (P0.05) at weaning compared with those weaned at 14 and 21 d. Pigs weaned at 21 d tended to have lower (P = 0.08) lymphocyte counts than did pigs weaned at 14 or 28 d. Pigs weaned at 14 d had reduced (P0.01) NK relative to those weaned at 21 or 28 d. Photoperiod also influenced pig BW and immune status. Generally, those pigs on the long-day photoperiod and weaned at 28 d were heavier (P0.001) than their counterparts weaned at 14 or 21 d. At 6 wk of age, NK was greater (P = 0.002) in pigs kept on a long day and weaned at 14 or 21 d than in pigs weaned at 28 d. Phagocytosis was less (P = 0.005) at 6 wk of age, but was greater at 8 wk, in piglets kept on the long day and weaned at 28 d than in long-day pigs weaned at 14 or 21 d. These results suggest that photoperiod differentially influences immune responses in piglets weaned at different ages and indicate an inverse relationship between growth and immune status. Here, weaning at 28 d and a long-day photoperiod was the treatment combination that was most physiologically beneficial to piglets, whereas a 14-d weaning and short-day photoperiod was least physiologically beneficial.

Stress is generally considered to suppress the immune system and may lead to an increase in the occurrence of disease in the presence of a pathogen. The immune system is ordinarily brought back to a baseline response level after immune challenge through homeostatic processes, in part regulated by the hypothalamic-pituitary-axis. Often, findings reported from various studies investigating the effects of stress on the immune system are conflicting and difficult to reconcile into a cohesive and comprehensible set of universally applicable theories. These discrepancies may be partly explained by the types and durations of the stressors, the aspect(s) of immune system measured, genetics, and social status. A particular stressor may enhance cell-mediated immune responses while suppressing humoral responses or vice versa, thus disrupting the balance between these components of the immune system. How farm animals perceive their environment depends not only on traditional environmental stressors (e.g., heat, cold, humidity, pollutants), but also on aspects of their social environment. Dominant animals may have enhanced immune activation, whereas subordinates have suppression of the same immune component in response to the same stressor. This could explain why individual animals within a group respond differently to stressors and disease challenges. A better understanding of the consequences and complex interactions between social and environmental stressors for innate and adaptive immune traits must be developed so we can more fully understand the effects of stress on immunity in livestock. Once these complex relationships are better understood, more effective interventions can be designed to improve animal health and well-being.

Manipulation of photoperiod may provide a noninvasive, easily implemented, effective method to improve immune status and enhance the efficiency of production. The objective of this study was to evaluate the impact of manipulation of photoperiod on endocrine and immune responses of pregnant sows and their offspring. At d 83 of gestation, sows were moved to gestation stalls and kept on a photoperiod of 12 h of light:12 h of dark until d 90, when sows were assigned to a long day (LD; 16 h of light/d) or a short day (SD; 8 h of light/d) treatment. During farrowing and lactation, one-half of the sows remained on their initial photoperiod (LD:LD or SD:SD), whereas one-half were switched to the opposite treatment (LD:SD or SD:LD). Blood samples were collected from sows at d 0, 7, 14, and 21 posttreatment, 24-h postfarrowing, and the end of lactation (approximately d 21 postfarrowing). Piglets were bled at 7 and 21 d of age for immune measures. Relative to sows on LD, sows on SD had greater concanavalin A- (P = 0.003) and lipopolysaccharide- (P = 0.02) induced proliferative responses at d 7 but reduced responses at d 14. Compared with SD, sows on LD had a greater (P0.05) percentage of neutrophils and fewer (P0.05) lymphocytes at d 7, resulting in a greater (P = 0.05) neutrophil:lymphocyte ratio. Neutrophil phagocytosis was greater at d 21 in sows kept on LD. Cortisol concentrations tended to be greatest (P = 0.10) in sows on SD:SD at 24-h postfarrowing and throughout lactation. At 7 d of age, piglets on LD:SD had greater (P = 0.001) total white blood cells (WBC) and plasma cortisol (P = 0.001) relative to those on the other photoperiod treatments. Plasma immunoglobulin G was less (P = 0.001) in piglets from sows kept on SD:LD compared with the other photoperiod treatments. Piglets from sows kept on LD:LD tended to have lower total WBC (P = 0.08) at 21 d of age. Piglets from sows kept on SD:SD had greater concanavalin A- (P0.001) and lipopolysaccharide-induced (Por = 0.10) proliferation responses and cortisol (P = 0.05). Phagocytosis was greater (P0.003) in piglets from sows that were kept on LD:LD. Cortisol (P = 0.02), WBC (P = 0.003), and immunoglobulin G (P = 0.001) were all influenced by gestational photoperiod treatment. These data indicate that photoperiod influences the immune status and endocrine response of piglets from dams that have been kept on a defined photoperiod. We conclude that photoperiod effects on piglets may be programmed in utero and can last throughout lactation.

Pigs typically experience various environmental stressors, which can negatively affect performance. Cortisol concentrations and various immune and performance measures are influenced by breed, but few data exist describing the impact of breed on stress responsiveness in pigs. The objective of this experiment was to determine if certain physiological responses to chronic stressors differed among 3 breeds and 2 commercial lines of pigs. The pigs were Landrace (n = 36), Meishan (n = 30), Yorkshire (n = 32), or 1 of 2 commercial lines (Line-A and Line-B; both n = 36). All pigs were weaned at 17 to 21 d and kept in a common nursery. At 49 d of age, pigs were assigned to 1 of 2 treatments: stress (heat, crowding, and mixing) or control (no stress treatment). Pigs were allocated to groups of 3 pigs per pen of the same sex. Control pigs were kept with their littermates. At the onset of the experiment, stressed pigs were mixed with 2 unfamiliar pigs once, and heat and crowding stressors were implemented simultaneously for 14 d. Pigs allocated to the stress treatment were video-recorded for 24 h following initiation of mixing to determine social status: dominant, intermediate, or submissive. Blood samples were taken at d 0 (baseline), 1, 7, and 14 to assess cortisol concentrations and immune measures. Breed and treatment affected cortisol, immune, and performance measures, but no significant breed x treatment interactions were found. In general, pigs subjected to the chronic stressor had lower (P0.001) BW and ADG (P0.001) than did control pigs. Plasma cortisol was lower (P0.001) among stressed pigs at d 7 and 14. Regardless of breed, lipopolysaccharide-induced proliferation (P0.01) and natural killer (NK; P0.005) cytotoxicity were greater in stressed pigs compared with controls. Furthermore, among stressed pigs, dominant pigs had a greater total white blood cell count (P0.005), NK (P0.05), and phagocytosis (P0.05) than the subordinate pigs. The results indicate that pig breed did not influence the physiological responses to the chronic concurrent stressors imposed for 14 d in this study, but social status did influence the immune responsiveness of these pigs to heat, crowding, and mixing.

It was hypothesized in these studies that differences would exist in baseline immune and performance measures among different breeds of pigs, and that these differences would be affected by age of the pig. Baseline immune, plasma cortisol (CORT) concentrations, and performance measures were determined among Berkshire (n = 36), Duroc (n = 18), Meishan (n = 54), Landrace x Yorkshire (White X; n = 36), and Yorkshire (n = 36) pigs at 4, 8, and 12 wk of age. All piglets were weaned at 17 to 21 d of age and moved to a common nursery environment. Total white blood cell (WBC), leukocyte differential, plasma CORT, immunoglobulin G (IgG) concentrations, natural killer cytotoxicity, neutrophil phagocytosis (PHAGO), and chemotaxis (CHTX) were evaluated. At all ages, plasma CORT was greatest in Meishan pigs, and least in Yorkshires (P0.05). Plasma IgG increased with age for all breeds (age: P0.01; breed x age: P0.005), except that in Meishans, IgG decreased. Natural killer cytotoxicity was greatest (P0.05) among Meishan pigs. There were breed x age interactions for neutrophil PHAGO (P0.001) and CHTX (P0.001). Overall, Yorkshire pigs showed the greatest (P0.05) percentage of PHAGO but the least (P0.05) CHTX. White X pigs had the greatest (P0.05) CHTX response. Berkshire pigs had the greatest (P0.001) numbers of neutrophils. At 12 wk of age, Meishan pigs had the least BW gain (P0.001), and Durocs had the greatest G:F (P0.001). There were no significant sex differences for immune (Por = 0.15), performance (Por = 0.20), or CORT (P = 0.70) measures. Pig breed and age influenced both baseline immune measures and plasma CORT in growing pigs, suggesting that pig breed and age are important factors influencing the response to various stressors or infectious challenges.

Recent studies suggest that exposure of cattle to photoperiod can influence immune function. The objective of this study was to determine whether treatment of cows with short day photoperiod (SDPP; 8 h light: 16 h darkness) during the dry period alters immune function, relative to cows subjected to a long day photoperiod (LDPP; 16 h light: 8 h darkness). Multiparous Holstein cows (n = 39) were dried 62 d before calving and exposed to photoperiod treatment until parturition; thereafter, cows were exposed to natural photoperiod. General health was monitored weekly during the dry period and cellular immune function was examined monthly during the dry period and at calving. Concentrations of prolactin and cortisol were measured from 10 d before calving to 2 d after calving. The periparturient prolactin surge in plasma was greater in LDPP cows (54.6 ng/ mL) than SDPP (22.4 ng/mL). Relative to LDPP cows, neutrophil chemotaxis and lymphocyte proliferation were enhanced in SDPP cows during the dry period. Neutrophil chemotaxis averaged 142.5 and 178.8 cells/ well during the dry period for LDPP and SDPP, respectively. Lymphocyte proliferation during the dry period averaged 197.6 and 326.5% for LDPP and SDPP cows, respectively. Physiological characteristics of the cows were not affected by treatment during the dry period. However, differences between treatments were observed within 2 d of parturition. Potential implications of photoperiod management for cow health and well-being merit further investigation.

Recent evidence suggests that photoperiod influences immune function. Interestingly, photoperiod has profound effects on concentrations of prolactin (PRL), a hormone also known to be involved in fluctuations of the immune system. However, the impact of photoperiod on PRL receptor (PRL-R) expression is poorly understood, particularly in tIssues of the immune system. Two experiments were performed to increase the general understanding of how photoperiod interacts with the immune system. Our first objective was to determine the effects of photoperiod on PRL-R mRNA expression and cellular immune function. Lymphocytes were isolated from blood collected from calves (n=10) and PRL-R mRNA expression of both long and short forms was quantified using real-time PCR. Lymphocytes expressed PRL-R mRNA, suggesting that PRL could act directly on these cells. To determine the relationship between photoperiod and PRL-R mRNA expression in other tIssues, hepatic and mammary biopsies were collected after calves were exposed to long days (LDPP; 16 h light:8 h darkness) or short days (SDPP; 8 h light:16 h darkness). Relative to LDPP, SDPP decreased circulating PRL, but increased expression of both forms of PRL-R mRNA in liver, mammary gland and lymphocytes. Short days also increased lymphocyte proliferation compared with long days. Reversal of photoperiodic treatments reversed the effects on circulating PRL, PRL-R mRNA expression and lymphocyte proliferation. Our second objective was to manipulate PRL concentration in photoperiod-treated animals, using bromocriptine. Concentrations of PRL in LDPP animals injected daily with bromocriptine for 1 week were decreased compared with LDPP controls, to a level similar to SDPP animals. Receptor expression was increased in LDPP+bromocriptine-treated animals relative to LDPP controls, as was lymphocyte proliferation. Overall, our results indicate that photoperiodic effects on PRL-R mRNA expression were inverse to those on circulating PRL, with short days stimulating expression of both forms of PRL-R mRNA. Expression of PRL-R mRNA changed in the same direction as lymphocyte proliferation with regard to photoperiod treatment, suggesting a link between photoperiodic effects on PRL sensitivity and immune function. Thus, PRL signaling may mediate photoperiodic effects on immune function.

The aim of this investigation was to determine whether murine models of inflammatory, neuropathic and cancer pain are each characterized by a unique set of neurochemical changes in the spinal cord and sensory neurons. All models were generated in C3H/HeJ mice and hyperalgesia and allodynia behaviorally characterized. A variety of neurochemical markers that have been implicated in the generation and maintenance of chronic pain were then examined in spinal cord and primary afferent neurons.Three days after injection of complete Freund's adjuvant into the hindpaw (a model of persistent inflammatory pain) increases in substance P, calcitonin gene-related peptide, protein kinase C gamma, and substance P receptor were observed in the spinal cord. Following sciatic nerve transection or L5 spinal nerve ligation (a model of persistent neuropathic pain) significant decreases in substance P and calcitonin gene-related peptide and increases in galanin and neuropeptide Y were observed in both primary afferent neurons and the spinal cord. In contrast, in a model of cancer pain induced by injection of osteolytic sarcoma cells into the femur, there were no detectable changes in any of these markers in either primary afferent neurons or the spinal cord. However, in this cancer-pain model, changes including massive astrocyte hypertrophy without neuronal loss, increase in the neuronal expression of c-Fos, and increase in the number of dynorphin-immunoreactive neurons were observed in the spinal cord, ipsilateral to the limb with cancer. These results indicate that a unique set of neurochemical changes occur with inflammatory, neuropathic and cancer pain in C3H/HeJ mice and further suggest that cancer induces a unique persistent pain state. Determining whether these neurochemical changes are involved in the generation and maintenance of each type of persistent pain may provide insight into the mechanisms that underlie each of these pain states.

Publisher Summary This chapter discusses the cellular and neurochemical remodeling of the spinal cord in bone cancer pain. To determine the neurochemical mechanisms that give rise to cancer pain, a model of bone cancer pain that shares many similarities with human cancer bone pain is developed. Following development of the model, the chapter characterized the extent of cancer-induced bone destruction, the sensory innervation of the bone, and the animal behavior indicative of pain, and the neurochemical changes that occur in the spinal cord and primary afferent neurons that may be involved in the generation and maintenance of cancer pain. The unique neurochemical reorganization of the spinal cord in bone cancer is mirrored by the clinical experience that analgesics that are efficacious in the relief of inflammatory or neuropathic pain are frequently ineffective at relieving advanced bone cancer pain. Understanding the distinct neurochemical events that are involved in the generation and maintenance of different persistent pain states should provide a mechanistic approach for understanding and developing novel therapies for unique persistent pain states such as cancer pain.

The cancer-related event that is most disruptive to the cancer patient's quality of life is pain. To begin to define the mechanisms that give rise to cancer pain, we examined the neurochemical changes that occur in the spinal cord and associated dorsal root ganglia in a murine model of bone cancer. Twenty-one days after intramedullary injection of osteolytic sarcoma cells into the femur, there was extensive bone destruction and invasion of the tumor into the periosteum, similar to that found in patients with osteolytic bone cancer. In the spinal cord, ipsilateral to the cancerous bone, there was a massive astrocyte hypertrophy without neuronal loss, an expression of dynorphin and c-Fos protein in neurons in the deep laminae of the dorsal horn. Additionally, normally non-noxious palpation of the bone with cancer induced behaviors indicative of pain, the internalization of the substance P receptor, and c-Fos expression in lamina I neurons. The alterations in the neurochemistry of the spinal cord and the sensitization of primary afferents were positively correlated with the extent of bone destruction and the growth of the tumor. This “neurochemical signature” of bone cancer pain appears unique when compared to changes that occur in persistent inflammatory or neuropathic pain states. Understanding the mechanisms by which the cancer cells induce this neurochemical reorganization may provide insight into peripheral factors that drive spinal cord plasticity and in the development of more effective treatments for cancer pain.

The effects of intracerebroventricular (icv) administration of porcine corticotropin-releasing hormone (pCRH) and cortisol on the immune system and behavior were examined in domestic pigs. In Experiment 1, 50 micrograms of pCRH in 200 microliters of saline or 200 microliters of vehicle was administered i.c.v. at 0600 h. Blood samples were obtained at 0600 (prior to injection), 0700, and 0800 h. Plasma cortisol concentrations were higher at 1 and 2 h after pCRH than after saline. Generally, pCRH failed to effect NK cytotoxicity or lymphocyte proliferation in response to phytohemagluttin (PHA). However, 1 h postinjection, pigs administered pCRH i.c.v. had marginally lower NK activity than control pigs. Pigs injected with pCRH had substantially lower neutrophil chemotaxis (CHTX) than the control pigs at 1 and 2 h postinjection. As blood cortisol concentration increased, neutrophil CHTX decreased. Pigs injected i.c.v. with pCRH had higher neutrophil numbers and neutrophil:lymphocyte ratios than control pigs. Percentage of lymphocytes was higher among control than treated pigs. Central pCRH increased overall activity, particularly walking, standing, licking, rooting, and increased activity-related sequences (e.g., sit, walk and stand, walk), but reduced complex oral/nasal sequences (e.g., root, lick). In Experiment 2, pigs were injected i.c.v. with 10 micrograms of cortisol in 200 microliters of saline or with vehicle at 0600 h. Administration of cortisol failed to effect NK cytotoxicity, lymphocyte proliferation, CHTX, or leukocyte distribution. Pigs given cortisol had no apparent change in behavior. These data indicate leukocyte distribution and specific neutrophil function in pigs were significantly modulated by stress-related hormones of the hypothalamic-pituitary-adrenal axis and complexity of behavioral sequences (pigs repeating certain behavioral sequences) associated with increased activity was reduced. Oral/nasal stereotypies (as seen among confined sows) were not elevated among pigs given i.c.v. pCRH. CRH given by i.c.v. administration may serve as a better model for acute rather than chronic stress.

Porcine natural killer (NK) cell cytotoxicity, plasma cortisol, total white blood cells (WBC), neutrophil:lymphocyte ratio (N:L), and circulating blood leukocytes were examined from pigs injected i.v. with either saline, ACTH, cortisol, or treated with metyrapone. Plasma cortisol increased (P.05) after ACTH and cortisol treatments and decreased (P.05) after metyrapone treatment; thus, treatments had the intended effects on in vivo cortisol concentrations. In Exp. 1, pigs were injected with either saline or ACTH at 0600 after the initial blood samples were taken (time 0). The ACTH had no effect (P.10) on NK cytotoxicity. Pigs injected i.v. with ACTH had fewer lymphocytes and more neutrophils (P.05) than control pigs. The N:L ratio was greater (P.05) among ACTH-injected than among control pigs. In Exp. 2, pigs were injected i.v. with either saline or 40 or 400 micrograms of cortisol at 0600 after the initial blood samples were obtained (time 0). Cortisol at 40 micrograms had no effect (P.10) on NK cytotoxicity. However, a 400-micrograms bolus of cortisol reduced (P.05) NK cytotoxicity (control = 39.5, cortisol = 28.3% cytotoxicity, SEM = 3.7). Each dose of cortisol reduced (P.05) circulating blood lymphocyte numbers. In Exp. 3, pigs were fed 1 g of metyrapone or no metyrapone the night before sampling. Blood samples were obtained at 0600, 0700, and 0800. Metyrapone reduced (P.05) NK cytotoxicity (control = 28.6, metyrapone = 11.8%, SEM = 1.9). Pigs treated with metyrapone had greater (P.05) numbers of neutrophils than control pigs. Numbers of lymphocytes were greater (P.05) among control than among treated pigs. Pigs treated with metyrapone had a greater (P.05) N:L ratio than control pigs. In conclusion, normal physiological concentrations or moderately increased blood cortisol concentrations did not influence NK activity, although leukocyte distributions were changed. We conclude that greatly increased or greatly decreased circulating concentrations of cortisol reduced NK cytotoxicity.