Influence of thermal environment on sows around farrowing and during the lactation period

Our objective was to investigate the effects of floor heating duration (HEAT: 35°c for 12 or 48 h) after birth of first piglet (BFP) under different room temperatures (ROOM: 15°C, 20°C, 25°C) on sows during farrowing and lactation. The study included 8 to 11 repetitions for each combination of ROOM and HEAT. There were no treatment effects on indicators of birth problems (duration of parturition, interbirth intervals, umbilical cord lactate concentration), BW changes of the sow, and litter size and weight until weaning. Sows at 15°C compared with 20°C and 25°C spent more time nest building (P = 0.015). The feed intake was reduced the first 7 d after farrowing in sows at 25°C (P = 0.014); however, both daily feed intake (P = 0.018) and water consumption (P < 0.001) of these warm sows exceeded that at lower temperatures during the last part of the lactation. Sows at 15°C received more medical treatments until weaning at heat = 48 h only (ROOM and HEAT interaction, P = 0.005). Room temperature influenced prefarrowing water consumption (25°C > 20°C and 15°C; P < 0.017), sow surface temperature (15°C < 20°C < 25°C; P < 0.001), respiration rate (25°C > 20°C > 15°C; P < 0.001), and rectal temperature during the first 12 h after bfp (15°C < 25°C; P = 0.009); additionally, long floor heating duration (HEAT = 48 h) increased the respiration rate by 50% d 1 and 2 after bfp (p < 0.001). The proportion of lying time on the unheated slatted floor increased with room temperature (P < 0.001) and, transiently, also for the heat = 48 h treatment 13 to 48 h after BFP (P < 0.001). The majority of piglets (82% to 95%) were born on the heated solid floor, regardless of room temperature (P = 0.46). Sows spent approximately twice as much time standing and walking at 15°C during 13 to 48 h after BFP at HEAT = 12 h only (ROOM and HEAT interaction; P = 0.002). In conclusion, long-term indicators of reduced sow performance were unaffected by room temperature, probably because the farrowing and lactating sows in the current pen design were able to perform thermoregulatory behavior and successfully adapt to room temperatures between 15°C and 25°C.     

Factors affecting the transfer of porcine parvovirus antibodies from sow to piglets

The aim of the study was to investigate the effects of a number of environmental, behavioural and biological factors on passive immunization of piglets as assessed by transfer of porcine parvovirus (PPV) antibodies (ab) from the colostrum of PPV vaccinated mothers to the serum of the piglets. Twenty primiparous sows were housed in pens with peat, straw and branches for nest building. Half the sows were prevented from achieving feedback from a completed farrowing nest by repeated removal of the nest from 10 to 12 h after nest building had begun, whereas the other half kept their nests. Sow serum PPV-ab titres were positively related to colostrum PPV-ab titres at birth of the first piglet (BFP) (P < 0.001). Litter average piglet PPV-ab titre was positively related to both sow serum and colostrum PPV-ab titres (both P < 0.001). In addition, in the individual piglets. PPV-ab titres were reduced as time from BFP to birth and time from birth to first sucking increased and time spent sucking decreased (all P < 0.01). There were no effects of treatment, time spent in lateral recumbency by the sow, number of times the sow stood or piglet weight on day 1 on piglet serum PPV-ab titres. Preventing prolonged farrowing, while at the same time ensuring the piglets' access to the udder, is important for transfer of maternal immunity. Measurements of specific antibodies in sow serum during the periparturient period and in piglet serum at 28 days of age may provide a practical tool for evaluating transfer of maternal immunity from sow to piglets.     

Effects of late introduction of sows to two farrowing environments on the progress of farrowing and maternal behavior

To evaluate the effect of late introduction to farrowing pens on the progress of farrowing and maternal behavior, 20 primiparous and 20 multiparous sows were allocated randomly to 1 of 2 treatments: 1) early introduction to pen (EP, n = 20) and 2) late introduction to pen (LP, n = 20). To evaluate the difference between loose-housed sows and crated sows when introduced late to the farrowing environment, a third treatment was included: late introduction to farrowing crate (LC, n = 20). Sow behavior and piglet birth intervals were recorded using video recordings from 16 h before the birth of the first piglet (BFP) until 48 h after BFP. Behavioral data were analyzed using PROC MIXED in SAS and the percentage of stillborn piglets and the response of the sow to piglet scream were analyzed using PROC GENMOD in SAS. Before farrowing (16 to 3 h before BFP), sows introduced late to pens had more postural changes per hour than sows introduced early to pens (LP = 12.7, EP = 8.9; P = 0.04), whereas there were no differences between sows introduced late to crates and sows introduced late to pens (LC = 14.2, LP = 12.7; P = 0.53). Interbirth interval (P = 0.04), variation in the interbirth interval (P = 0.01), and percentage of stillborn piglets (P = 0.003) were affected by an interaction between parity and treatment. In multiparous sows there were no differences between treatments (P > 0.18) either in the progress of farrowing or in the percentage of stillborn piglets. For primiparous sows, there were no differences (P > 0.22) between sows that were introduced late to pens and sows that were introduced early to pens. Primiparous sows that were introduced late to crates compared with pens had longer interbirth intervals (LC = 29 +/- 4.9 min, LP = 16 +/- 2.9 min; P = 0.02), a greater variation of these intervals (LC = 35 +/- 8.3 min, LP = 16 +/- 3.6 min; P = 0.006), and a greater percentage of stillborn piglets (LC = 21%; 95% confidence interval ranging 14 to 30%, LP = 5%; 95% confidence interval ranging from 2 to 12%; P = 0.004). After farrowing, neither postural changes, time spent in lateral lying, number of near-crushing situations, nor the response to piglet scream test were affected by treatment (P > 0.09). When sows and gilts were introduced late to farrowing pens, neither progress of farrowing nor maternal behavior of importance for piglet crushing was influenced. However, crating primiparous sows that were introduced late to the farrowing environment compared with pen housing had detrimental effects on the progress of farrowing and the percentage of stillborn piglets.     

The induction of parturition in sows using prostaglandin F2auml;

Intramuscular injections (10mg) of prostaglandin F2ä were administered to 19 pregnant sows in one herd on either the 112th or 113th day of gestation and a similar number of untreated sows served as controls. Induced sows for up to 6h after injection generally showed/more walking, drinking defaceating and postural changes. Over the last 20h prepartum they spent more time lying and urinated more frequently. Mean interval from injection to onset of parturition in treated sows was 24.5h and 16 of them commenced farrowing during the working day, compared with 6 in the control group. Induction of parturition did not influence litter size at birth, piglet bodyweights at birth or 14 days of age, the incidence of the mastitis, metrititis agalactae syndrome, re-breeding interval of the sow or size of the subsequent litter at birth. Farrowing time was significantly longer (6.48h v 4.08h) for treated sows and litter pre-weaning mortality was higher but not significantly so. Most piglet deaths in each group resulted from overlaying or starvation but mortality from anaemia and septicaemia occurred only in the treated group. It is considered that the technique could have practical application on well-managed intensive pig units.     

The induction of parturition in sows using prostaglandin F2alpha

Intramuscular injections (10 mg) of prostaglandin F2alpha were administered to 19 pregnant sows in one herd on either the 112th or 113th day of gestation and a similar number of untreated sows served as controls. Induced sows for up to 6h after injection generally showed more walking, drinking defaceating and postural changes. Over the last 20 h prepartum they spent more time lying and urinated more frequently. Mean interval from injection to onset of parturition in treated sows was 24.5 h and 16 of them commenced farrowing during the working day, compared with 6 in the control group. Induction of parturition did not influence litter size at birth, piglet body-weights at birth or 14 days of age, the incidence of the mastitis, metrititis agalactae syndrome, re-breeding interval of the sow or size of the subsequent litter at birth. Farrowing time was significantly longer (6.48 h v 4.08 h) for treated sows and litter pre-weaning mortality was higher but not significantly so. Most piglet deaths in each group resulted from overlaying or starvation but mortality from anaemia and septicaemia occurred only in the treated group. It is considered that the technique could have practical application on well-managed intensive pig units.     

Immunoglobulins in piglets from sows heat-stressed prepartum

Sows were subjected to moderate heat stress in a chamber (32 C) from d 100 of pregnancy until less than 8 h before delivery of first piglet, while control sows were in a thermoneutral chamber (21 C) or farrowing house (22 C). Blood serum and colostrum at parturition of heat-stressed sows and their piglets' serum at birth had elevated cortisol concentrations. Total protein, globulin and immunoglobulin G (IgG) concentrations in sow serum tended to decrease as parturition time was approached; albumin did not change. Total protein and IgG concentrations in colostrum at parturition and in milk 24 and 48 h later tended to be lower in heat-stressed sows. Concentrations of these four protein fractions (total, globulin, IgG and albumin) in piglet serum at birth did not differ among treatment groups, but soon after colostrum ingestion they increased markedly in all groups. Therefore, in all groups total protein remained constant while globulin and IgG decreased. Globulin concentration on d 1 was lowest in piglets from heat-stressed sows, but its rate of decrease after d 1 was not affected by sow treatment. Immunoglobulin G concentration was 11 mg/ml lower, but its rate of decrease through postnatal d 20 was slower in piglets from heat-stressed sows than in those from control sows; a 10-mg/ml difference in IgG concentration on postnatal d 1 has been associated with increased preweaning mortality in piglets. Higher cortisol concentration in serum and lower IgG in colostrum of sows under heat stress was associated in their piglets with higher serum cortisol at birth and lower serum IgG for the first 20 d postnatum.     

Prepartum behavior of gilts in three farrowing environments

To determine effects of the farrowing environment on prepartum behavior, five gilts were monitored continuously for 48 h prior to parturition in each of three farrowing systems: 1) an open farrowing pen (2.1 x 1.5 m); 2) a turn-around farrowing pen, which allowed the gilt to turn around (2.4 m long; 1.8 m wide at back, .6 at front) and 3) a straight farrowing crate (sow zone = .6 x 2.1 m). Videorecords were summarized as three 16-h segments (Period A = 48 to 32 h before the first piglet was delivered, B = 32 to 16 h and C = 16 to 0 h) for analysis of activity over time. In all systems, frequencies of postural changes and oral-nasal activities directed at the floor or wall increased as farrowing was approached, the highest frequencies occurring in Period C. Respective times spent standing, sitting and engaged in oral-nasal activities directed at floor or wall also increased over time. Pawing occurred almost exclusively in Period C. Lying upright (ventral posture) occupied a greater portion of lying time as the gilt's activity increased over time, whereas feeding and drinking behaviors did not change over time. The only behavior affected by the experimental environments was the frequency of 90 degree turns. Gilts in both open and turn-around pens showed an increasing turning frequency over time, and they turned more often in the open pen than in the turn-around pen.(ABSTRACT TRUNCATED AT 250 WORDS)     

An exploratory study on the effects of a straw dispenser in farrowing crates

The effect of a straw dispenser in farrowing crates was investigated to determine the extent to which the provision of small quantities of straw has an influence on both sows and piglets. Sows and suckling piglets are often housed in barren environments with limited opportunities to show behavior they are highly motivated to perform. Enriching the environment might be a solution; for example, by providing materials that can be manipulated. In this study, 20 sows received a straw dispenser with chopped straw (treatment group) and 20 other sows did not receive any enrichment (control group). The treatment group was split up in 2: in treatment group A, the straw dispenser was placed in front of the sow, above the feed trough; and in treatment group B, the straw dispenser was placed next to the sow. Sows from the treatment groups received the straw dispenser from arrival in the farrowing crate until weaning. The total straw use within the treatment group was very variable but did not differ before and after farrowing. Sows took on average 53.0 g (±8.85) straw from the straw dispenser during the whole period in the farrowing crate. The frequency of undesirable and stereotypical behavior performed by the sows did not differ between treatment and control groups, and the same is seen with nest-building behavior before farrowing. By positioning the dispenser in front of the sow, the frequency of lateral lying increased, which means the udder was exposed more toward the piglets. This was reflected in the higher frequency of udder activity, performed by piglets from this treatment group. By positioning the dispenser next to the sow, sows showed more ventral lying behavior, because of disturbance of lying behavior by piglets. Piglets from this treatment group also showed less udder activity and possibly because of this, more pain-related behavior. These piglets performed more playing behavior in the third week of life compared with other groups, but it cannot be stated with certainty that this is a positive effect. A lower weight gain and weaning weight were seen in piglets within treatment group B. Possible explanations are the higher level of activity among these piglets as the straw dispenser was positioned within their reach or decreased milk consumption because of decreased udder activity and increased ventral lying by the sows. It can be concluded that the straw dispenser has positive effects on the behavior and welfare of sows and piglets, but positioning the straw dispenser in reach of both sow and piglets is not preferred as it is associated with undesirable effects on behavior such as ventral lying in sows and pain-related behaviors in piglets.     

Effects of salinomycin on sow weight change during lactation and on sow reproductive performance

Forty-five gravid cross-bred sows (mean parity 3.3 +/- .3) were randomly allotted to two dietary treatments: corn-soybean mean (CS) or CS plus 60 mg salinomycin per kilogram of diet (CSS). Sows were fed their respective diets through two successive parities with dietary treatment initiated at 100 d postcoitum and continued until weaning of the second successive litter. Therefore, sows fed CSS received salinomycin for 14 d before the first parturition and for approximately 153 d before the second parturition. Daily feed intake was restricted to 2 kg.hd-1.d-1 during gestation and to 3 kg.hd-1.d-1 from weaning to breeding. All sows. had ad libitum access to feed during lactation. Sows were weighed 7 d prior to parturition, at weaning and at breeding. Weaning-to-estrus interval and farrowing interval were recorded for all sows. Litters were weighed at birth and weaning. There were no differences (P greater than .05) between dietary treatments in sow weights before parturition, at weaning or at breeding for either first or second farrowing. The CSS-fed sows lost more weight from weaning to breeding after the first (P less than .03) and second (P less than .05) lactation periods than CS-fed sows. The CSS-fed sows tended to gain more (P = .06) weight during lactation than CS-fed sows. There were no differences (P greater than .05) between treatments in lactation feed intake, weaning-to-estrus interval, farrowing interval, litter size born or weaned, litter weights at birth or at weaning, or in sow culling rate.(ABSTRACT TRUNCATED AT 250 WORDS)     

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

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

Effect of roasted or raw peanut kernels on lactation performance and milk composition of swine

A lactation trial involving 105 sows was conducted to determine the effect of 12% roasted or raw, ground, whole, shelled peanuts on sow weight change during lactation, feed intake, piglet and litter weight gain, milk composition, and days to return to postweaning estrus. The trial was conducted using three sow groups during two farrowing seasons, summer (July to September) and winter (December to February). Diets were based on corn plus soybean meal. Diets contained either 5% animal fat or equivalent added fat from 12% roasted or raw, ground, shelled peanuts. The replacement of animal fat by roasted or raw peanuts had no effect (P greater than .20) on sow weight change, average daily feed intake during lactation or days to estrus postweaning, or on piglet weight gain or survival. Milk composition (percentage fat and protein) was not altered (P greater than .20) by source of fat in the summer; however, in the winter, sows fed roasted peanuts had higher (P less than .05) milk fat and protein percentage at 3 d postfarrowing than other treatment groups. At d 7, sows fed 12% roasted or raw peanuts had higher (P less than .05) milk protein than sows fed 5% animal fat. Sows farrowing in the summer had greater (P less than .01) weight loss and consumed less (P less than .05) feed during lactation than sows farrowing in the winter. Sows farrowed in the summer had larger (P less than .05) litters at birth and 14 d postfarrowing and greater (P less than .10) piglet and litter weight gain postfarrowing than those farrowed in the winter.(ABSTRACT TRUNCATED AT 250 WORDS)     

REVIEWS: Compilation of the Scientific Literature Comparing Housing Systems for Gestating Sows and Gilts Using Measures of Physiology,Behavior, Performance,and Health

The objective of this review was two-fold. First, a series of meta-analyses (analyses of treatment effects across studies) were performed on available data from scientific literature to determine whether sow behavior, performance, or physiology differed for sows in group pens or individual stalls. Second, research publications in areas of performance and health, physiology, and behavior of pregnant gilts and sows in studies that directly compared gestation sow housing systems were summarized. Common systems were stalls, tethers, and various types of group housing systems. Results of meta-analyses showed that the average levels of productivity, oral-nasal-facial behaviors (ONF), and blood cortisol were statistically similar for sows in group pens and stalls. For the review, in some studies, circulating cortisol concentrations were greater among gestating females kept in tethers compared with other systems; however, overall cortisol was not altered by housing system. Immune parameters were largely not influenced by housing system. Housing system did not alter heart rate. Gestation housing system may influence sow behavior including stereotypic ONF, postural locomotory, feeding behaviors, or social behaviors. Overall, total ONF behaviors were comparable between gestation sow housing systems. However, tethered and stalled sows exhibited more stereotypic ONF compared with sows in group or outdoor systems. Compared with group housing, individually confining sows during gestation resulted in postural and movement restrictions. Stall size and design can impact postural adjustments and inter-stall aggression of individually housed sows. Inconsistent performance and health results were found among sow housing studies. Sows in stalls consistently had equal or greater reproductive performance compared with sows in other systems. Farrowing rate for sows in individual stalls was equal to or superior to sows in other systems. Farrowing rate was clearly superior among sows in stalls compared with group systems, where dynamic social groups were employed. However, tethered sows may have reduced litter size and increased piglet birth weight. Sows in group housing systems, particularly electronic sow feeder (ESF) systems, had injury scores greater than sows in either stalls or tethers. Gestation housing system (individual vs group) may impact sow welfare in the farrowing area (using stalls or pens). In conclusion, although individual studies found significant housing system effects, subjected to the overall evidence from adequately designed studies meta-analyses revealed that gestation stalls (non-tethered) or well-managed pens generally (but not in all cases) produced similar states of welfare for pregnant gilts or sows in terms of physiology, behavior, performance, and health.     

Floor heating at farrowing in pens for loose-housed sows

The effects of floor heating at parturition on sow and piglet behaviour in pens were examined in a Danish production herd. A total of 50 gilts and sows were split into two groups; one (n = 25) experienced no treatment; one (n = 25) was exposed to floor heating in the area of the sow around parturition. The sows and piglets were recorded on video 24 h a day for behavioural analyses.Floor heating tended to improve piglet weight at weaning (P = 0.05) but did not affect average daily gain. Piglets in pens with floor heating were more often in proximity of the sow at posture changes than piglets from pens without floor heating on day one postpartum (P = 0.01). Floor heating did not affect duration of parturition or any of the recordings of sow behaviour significantly.     

Effects of nutrient supply, plasma metabolites, and nutritional status of sows during transition on performance in the next lactation

The aim of the present study was to evaluate the effects of nutrient supply, plasma metabolites, and nutritional status of sows during the transition from gestation to lactation on performance of piglets during the colostral period and throughout lactation. Forty second-parity sows were fed 1 of 4 gestation diets containing a different quantity of dietary fiber (171 to 404 g/kg of DM) from mating until d 108 of gestation. From d 108 of gestation until weaning (d 28 of lactation), sows were fed 1 of 5 lactation diets with a different quantity of dietary fat [3 or 8% with different proportions of medium- (MCFA) and long-chain fatty acids (LCFA)]. Blood was obtained by jugular venipuncture on d 108 and 112 of gestation and on d 1 of lactation, and concentrations of plasma glucose, NEFA, lactate, acetate, propionate, butyrate, and fatty acids were analyzed. Piglet growth and mortality were noted throughout lactation. Piglet mortality during the colostral period (0 to 24 h) was affected by the lactation diets and was positively related to sow backfat (d 108) and plasma lactate (d 112) and negatively related to mean piglet birth weight (P < 0.05). Mean piglet live BW gain (LWG) was recorded in the periods 0 to 24 h, 7 to 10 d, 14 to 17 d, and 17 to 28 d relative to parturition as indirect measures of colostrum yield (0 to 24 h), milk yield in early lactation (d 7 to 10), and at peak lactation (d 14 to 17 and d 17 to 28). Effects of gestation and lactation diets on studied sow traits were tested on selected days during the transition period and the next lactation, and tested statistically on separate days. The LWG in the colostral period was positively correlated with mean piglet birth weight (P < 0.001), plasma concentrations of propionate and MCFA (P < 0.05), and plasma acetate and butyrate (P < 0.1) on d 1 of lactation. The LWG in early lactation was inversely correlated with plasma lactate on d 108 (P < 0.05), plasma glucose on d 112, and backfat thickness on d 108 (P < 0.10). The LWG at peak lactation was positively correlated with MCFA intake of the sow on d 113 to 115 and backfat thickness on d 108 during the transition, and negatively correlated with intake of LCFA and ME intake on d 108 to 112 (P < 0.05). In conclusion, feeding and body condition of sows during the transition from gestation to lactation is important for neonatal piglet survival, lactation performance of sows, and piglet growth during the next lactation.     

Effects of dietary fat and triamcinolone additions during late gestation on the body energy reserves of neonatal pigs

Two trials involving 21 primiparous sows were conducted to evaluate the effects of fat and triamcinolone additions to the diet of late-term, gravid sows on carbohydrate, protein and fat reserves in nursed and fasted neonatal pigs. Beginning 7 d prepartum, sows were fed daily 1.8 kg (6 Mcal metabolizable energy, ME) of a fortified, corn-soybean meal diet that was supplemented with 4 Mcal ME/sow in the form of starch, soybean oil or soybean oil plus 70 mg/sow of triamcinolone, a synthetic glucocorticoid. After parturition, the sows were fed daily 5 kg (15 Mcal ME) of a 14% protein, corn-soybean meal diet. The addition of soybean oil to the diet of sows during late gestation did not influence (P greater than .1) liver glycogen content, serum glucose levels or carcass protein and fat reserves in nursed or fasted pigs from birth to 6, 12, 24 or 48 h of age. The addition of triamcinolone to the sows' prepartum diet increased (P less than .1) fat deposition in the nursed pigs from birth to 48 h of age. Liver glycogen reached minimal levels by 24 h postpartum in both nursed and fasted pigs, regardless of the sows' prepartum treatment. Serum glucose levels were maintained at 80 to 130 mg/dl in the nursed pigs from birth to 48 h of age, but approached hypoglycemic levels (50 mg/dl) by 24 h in the fasted pigs. Nursed pigs deposited 28 g of body protein and 15 g of fat from birth to 48 h of age; whereas, fasted pigs mobilized only minimal quantities (3 g) of body protein and fat.     

Morphometric analysis of proinflammatory cytokines in mammary glands of sows suggests an association between clinical mastitis and local production of IL-1beta, IL-6 and TNF-alpha

Twelve healthy primiparous sows received intramammary inoculation with Escherichia coli (serotype O127) during the 24-h period preceding parturition. Mammary gland biopsy samples were taken immediately before inoculation (0 h) and from the inoculated and the contralateral non-inoculated glands 24 h after inoculation. The analyses of interleukin-1 beta (IL-1beta), IL-6, IL-8, and tumor necrosis factor alpha (TNF-alpha) by immunohistochemistry revealed that the production of these proinflammatory cytokines significantly increased in the inoculated mammary glands of sows that developed clinical signs of mastitis (affected group, n=4) 24 h after inoculation. This was also true for IL-8 in the inoculated mammary glands of sows that did not develop clinical signs of mastitis (nonaffected group, n=8). Sows that developed clinical signs of mastitis displayed significantly lower constitutive production of IL-1beta than did sows that remained clinically healthy. The data indicate that the development of clinical symptoms of coliform mastitis in the sow is associated with a locally increased proinflammatory cytokine production in response to intramammary E. coli infection.     

Selective protein loss in lactating sows is associated with reduced litter growth and ovarian function

This study was designed to test the degree of protein loss that may be sustained by lactating sows before milk biosynthesis and ovarian function will be impaired. First-parity Camborough x Canabrid sows were allocated to receive isocaloric diets (61 +/- 2.0 MJ of ME/d) and one of three levels of protein intake in lactation: 1) 878 g of CP and 50 g of lysine/d (n = 8), 2) 647 g of CP and 35 g of lysine/d (n = 7), or 3) 491 g of CP and 24 g of lysine/d (n = 10). Every 5 d during a 23-d lactation, sow live weight, backfat depth, and litter weight were recorded, and a preprandial blood sample was collected. Milk samples were collected on d 10 and 20 of lactation. Sows were slaughtered on the day of weaning, and liver and ovarian variables were measured. Lower dietary protein intakes elicited progressively larger live weight losses during lactation (-13, -17, and -28 +/- 2.3 kg; P < 0.001), but similar and minimal backfat losses (-1.3 +/- 0.29 mm). Approximately 7, 9, and 16% of the calculated body protein mass at parturition was mobilized by d 23. Lactation performance did not differ among treatments until d 20, at which time approximately 5, 6, and 12% of the calculated protein mass at parturition had been lost. The milk protein concentration on d 20 of lactation reflected the amount of body protein lost, and was lowest (P < 0.05) in sows that lost the most protein. After d 20, piglet growth rate decreased (P < 0.05) in a manner related to the amount of body protein lost. At weaning, ovarian function was suppressed in sows that had mobilized the most body protein; they had fewer medium-sized follicles (> 4 mm; P < 0.05), their follicles contained less (P < 0.01) follicular fluid, and had lower estradiol (P < 0.05) and IGF-I (P < 0.10) contents. Culture media containing 10% pooled follicular fluid (vol/vol) from high-protein-loss sows were less able to support nuclear and cytoplasmic maturation of oocytes in vitro, evidenced by more oocytes arrested at metaphase I (P < 0.05) and showing limited cumulus cell expansion (P < 0.06). Plasma insulin and IGF-I concentrations did not seem to be related to the observed differences in animal performance. Our data suggest that no decline in lactational performance or ovarian function when a sow loses approximately 9 to 12% of its parturition protein mass. However, progressively larger decreases in animal performance are associated with a loss of larger amounts of body protein mass at parturition.     

Effects of a novel carbohydrate and protein source on sow performance during lactation

Ninety-one primiparous and multiparous sows and their pigs were used to evaluate the effects of a novel carbohydrate- and protein-based feed ingredient (Nutri-Pal, NP) on sow and litter performance during lactation. Nutri-Pal is a feed supplement for sows that consists of a blend of milk chocolate, brewer's yeast, whey products, and glucooligosaccharides. The dietary treatments consisted of a corn-soybean meal control and a corn-soybean meal plus 5% NP fed from d 110 of gestation to weaning. The diets were formulated to be equal in total Lys and ME. Sows were allotted to treatment based on parity, body weight, and the date of d 110 of gestation. There were 46 and 45 sows per treatment over four farrowing groups. Litters were standardized to 10 pigs and weighed within 1 d of farrowing, and all sows weaned at least 8 pigs at an average age of 21 d. Sows were weighed on d 110 of gestation, d 1 postfarrowing, and at weaning. Sows were fed three times daily during lactation. Sows were checked twice daily after weaning for signs of estrus. The weaning weight of sows fed NP was increased (P < 0.10) compared with those fed the control diet. Sows fed the control diet tended (P = 0.11) to lose more weight per day from d 110 of gestation to weaning than the sows fed NP. Otherwise, sow response variables (sow weight on d 110 of gestation and d 1 postfarrowing, d 110 of gestation to d 1 postfarrowing and lactation weight change per day, d 110 of gestation to d 1 postfarrowing, lactation, and total feed intake, days to estrus, pigs born alive or dead, and litter and average pig birth weight) were not affected (P > 0.10) by diet. There were no effects (P > 0.10) of diet on litter performance response variables (pigs weaned, litter and average pig weaning weight and gain, and survival percent). The NP feed ingredient had minor effects on sow productivity, but it did not affect litter productivity indices.     

Effects of dietary additions of 1,3-butanediol or lard for sows on survival of neonatal pigs

In nine trials, 278 late-term gravid sows were fed isocaloric amounts (8,500 kcal metabolizable energy (ME)/d) of a fortified, corn-soybean meal based diet in which 20% of their daily ME intake was supplied by corn starch, 1,3-butanediol or lard from about d 106 of gestation to parturition. After parturition, the sow's daily ME intake was increased to 18,000 kcal. Sows fed starch and lard remained on their respective diets for the duration of a 28-d lactation; whereas, those initially fed butanediol were switched to the starch diet after parturition. Number of pigs born per litter, average pig birth weight and incidence of stillbirths were not influenced (P greater than .30) by the prepartum diet of the sow. However, the inclusion of isocaloric levels of butanediol for starch in the preparatum diet and lard for starch in the pre- and postpartum diets increased the number of pigs weaned per litter by .45 (P less than .13) and .16 pigs (8.25, 7.96 vs 7.80) and improved the survival rate of pigs from birth to weaning by 4.3 (P less than .13) and 2.7 percentage units (84.5, 82.8 vs 80.1%), respectively. Average pig weights at 28 d of age for litters of sows fed butanediol prepartally were similar to those of sows fed starch, but were less (P less than .01) than those of sows fed lard throughout lactation.     

Effects of sarcoptic mange on lactating swine and growing pigs

The impact of Sarcoptic mange on sows and on performance of their offspring from birth to slaughter was determined. Sows naturally infested with Sarcoptic mange were paired, mated to the same boar, and assigned randomly to treated or control farrowing groups. Treated sows received ivermectin s.c. at 300 micrograms/kg body weight; control sows received the vehicle s.c. Sow performance was evaluated via sow feed consumption, litter size, litter birth weights, litter weaning weights and piglet death loss from birth to weaning. Seven replicates (farrowing groups), each with six sow pairs, were included in the trial. Offspring from treated and control sows, 35 head/group, were fed to slaughter weights. Untreated sows had litters that weighed 4.14 kg less than ivermectin-treated sow litters at 21 d (P less than .07). Treated sows consumed 1.95 kg less feed per weaned piglet and .13 kg less feed per kilogram of weaned piglet (P less than .05). Piglets from treated sows were 5.79 kg/head heavier at slaughter (P less than .05) and had a .05 kg/d superior average daily gain (P less than .05).