Outdoor sows with nose rings can perform most of their natural behavioural activities except rooting. The prevention of rooting through surgical intervention (nose ringing) may be detrimental to welfare, although the behavioural and welfare consequences of rooting deprivation are not well documented. The present experiment examines exploratory behaviour in unringed, ringed and deringed gilts by repeatedly exposing the gilts to a sandbox supplied with bark chips. Four months prior to the experiment, 16 gilts, eight with nose rings and eight without, were housed in four fields. Over a period of 12 days, the 16 gilts, in pairs from the same field, were walked to the sandbox; each gilt visited the sandbox six times in total. After deringing of the ringed gilts (and a control procedure for the unringed gilts), all of the gilts were exposed to the sandbox twice. During each visit, the exploratory behavioural patterns of rooting, sniffing, manipulating, and chewing were observed using 30 s scan sampling. The ringed gilts showed no rooting behaviour in the sandbox; on the other hand, their mean frequency of chewing behaviour was significantly higher than that of the unringed gilts (19.89 versus 13.54; P < 0.05). When all of the exploratory behavioural patterns were summed, no significant differences were found between ringed and unringed gilts. On the second day after deringing, the previously ringed gilts started to root, and no significant difference in the incidence of rooting behaviour between unringed gilts and newly deringed gilts was found. We discuss whether rooting behaviour can be substituted by chewing in order to explore an environment. Gilts that are prevented from rooting are found to explore as much as rooting gilts, and they achieved an adequate knowledge of the sandbox (as demonstrated by the fact that they did not show increased exploration after deringing), although rooting was the preferred exploratory behaviour. In this study, we did not find serious symptoms of chronically reduced welfare as a result of nose ringing.

Previous research has shown that pre-parturient primiparous pigs (gilts) housed in behaviourally restrictive farrowing crates without straw redirect their nest-building behaviour to non-manipulable substrates such as the bars of the crate. These gilts also show elevated plasma adrenocorticotropic hormone (ACTH) and Cortisol levels, particularly around the peak of nest-building activity, when compared to gilts in larger pens that have been provided with a manipulable substrate (straw). It remains unclear whether these behavioural and physiological responses to crating result from the lack of a suitable nesting substrate or from the restricted space. This study investigated the effects of space (crate [C] versus pen [P] and straw (straw [S] versus no straw [NS]) using a 2 × 2 factorial design. Thirty-four gilts were implanted with an indwelling jugular catheter at around 12 days before parturition. They were moved to one of the four environments five days before parturition, and blood sampling and recording of behaviour were carried out during the pre-parturient period. Penned gilts (P), irrespective of straw availability, spent more time standing and walking and performed more total substrate-directed behaviour than crated (C) gilts. When straw was not available to penned gilts, a large proportion of their substrate-directed behaviour was redirected to the floor. Space also had an effect on ACTH and Cortisol levels across the entire pre-parturient phase, with C gilts having higher levels than P gilts irrespective of straw availability, but particularly so at the peak of nest-building activity. There was no effect of straw on ACTH or Cortisol levels. Overall, it appears that increased space, perhaps through allowing locomotion, increases substrate-directed behaviour of pre-parturient gilts. When space is available but straw is absent, pre-parturient gilts redirect their nest-building behaviour to the floor. The ability to express substrate-directed behaviour as a result of increased space is reflected in lower levels of indicators of physiological stress.

Individual gestation housing of pregnant sows in stalls from four weeks after mating is banned in the EU. Two experiments were conducted to study the effect of two gestation management and housing systems (STALL: gilts housed in stalls and PEN: gilts loose-housed in pens with increased feed ratio) on gilt and piglet performance during lactation. Thirty-seven PEN and 33 STALL gilts were used. Backfat, litter pre-weaning mortality and total feed intake (TFI) during lactation were recorded in gilts. Weight and rectal temperature was recorded in piglets. In Exp 1 the behaviour of a subsample of gilts was videotaped during lactation. In Exp 2 saliva cortisol in gilts, thyroid stimulating hormone (TSH) and T4 hormones in piglet blood were measured. PEN gilts had more backfat when moved to the farrowing stalls. PEN gilts tended to have higher cortisol concentration 24 h after entering the farrowing stall and to spend more time sitting or standing up one day before parturition than STALL gilts. PEN piglets had higher bodyweight (BW) on day 0 (Exp 2) and lower T4 concentration than STALL piglets. However, STALL piglets showed higher rectal temperature 60 min after birth and lower mortality at day 2. In Exp 2, STALL piglets also had higher BW and average daily gain at weaning. During lactation, PEN gilts lost more backfat and weaned less piglets. Gilts loose-housed with increased feed ratio during gestation might be more stressed when housed in farrowing stalls than those kept in stalls during gestation, thus compromising their offsprings’ thermoregulatory capacity and growth however, from our results, it is difficult to differentiate the effect of feed level from the effect of allocation during gestation.

Milk production by the sow is a major factor limiting the growth and survival of her litter. Understanding the process of morphogenesis of the sow’s mammary gland and the factors that regulate mammary development are important for designing successful management tools that may enhance milk production. Primordia of the mammary glands are first observable in the porcine embryo at approximately 23 days of gestation. The glands then progress through a series of morphologically distinct developmental stages such that, at birth, each mammary gland is composed of the teat, an organized fat pad and two separate lactiferous ducts each with a few ducts branching into the fat pad. The glands continue to grow slowly until about 90 days of age when the rate of growth increases significantly. The increased rate of mammary gland growth coincides with the appearance of large ovarian follicles and an increase in circulating estrogen. After puberty, the continued growth of the gland and elongation and branching of the duct system into the fat pad takes place in response to the elevated levels of estrogen occurring as part of the estrous cycles. After conception, parenchymal mass of each gland increases slowly during early pregnancy and then grows increasingly rapidly during the final trimester. This growth is in response to estrogen, progesterone, prolactin and relaxin. Lobuloalveolar development occurs primarily during late pregnancy. By parturition, the fat pad of the mammary gland has been replaced by colostrum-secreting epithelial cells that line the lumen of the alveoli, lobules and small ducts. All mammary glands develop during pregnancy, however, the extent of development is dependent on the location of the mammary gland on the sow’s underline. The mammary glands undergo significant functional differentiation immediately before and after farrowing with the formation of colostrum and the transition through the stages of lactogenesis. Further growth of the glands during lactation is stimulated by milk removal. Individual glands may grow or transiently regress in response to the intensity of suckling during the initial days postpartum. Attempts to enhance milk production by manipulation of mammary development at stages before lactation generally have met with limited success. A more in depth understanding of the processes regulating porcine mammary gland morphogenesis at all stages of development is needed to make further progress.

Estrus synchronization is important for optimal management of gilt reproduction in pig farms. Hormonal treatments, such as synthetic progestogens, are used on a routine basis, but there is a growing demand for non-hormonal alternative breeding tools. Before puberty, gilts exhibit a ‘waiting period,’ related to the ovarian development and gonadotrophin secretions, during which external stimulations, such as boar exposure, could induce and synchronize first ovulation. Practical non-invasive tools for identification of this period in farms are lacking. During this period, urinary oestrone levels are high, but urine sampling is difficult in group-housed females. The aim of this work was to search for specific biomarkers of the ‘waiting period’ in saliva and urine. In total, nine 144- to 147-day-old Large White gilts were subjected to trans-abdominal ultrasonography three times a week for 5 weeks until puberty detection (week –5 to week –1 before puberty). Urine and saliva samples were collected for oestrone assay to detect the ‘waiting period’ and for metabolome analysis using 1H-nuclear magnetic resonance spectroscopy to detect potential biomarkers of the ‘waiting period.’ Gilts were slaughtered 7 days after puberty detection for puberty confirmation. Results were consistent with ultrasonography data for six gilts. Urine and saliva samples from these six gilts were analyzed. Urinary estrone concentration significantly increased 2 weeks before puberty detection. Metabolome analysis of urine samples allowed the identification of 78 spectral bins, among them, 42 low-molecular-weight metabolites were identified. Metabolome analysis of salivary samples allowed the identification of 59 spectral bins, among them, 23 low-molecular-weight metabolites were detected and 17 were identified. No potential biomarker was identified in urinary samples. In saliva, butyrate and 2HOvalerate, 5.79 ppm (putatively uridine), formate, malonate and propionate could be biomarker candidates to ascertain the pre-puberty period in gilt reproduction. These results confirm that non-invasive salivary samples could allow the identification of the physiological status of the gilts and presumably the optimal time for application of the boar effect. This could contribute to synchronize puberty onset and hence to develop non-hormonal breeding tools.

Nutrients are essential for the health and survival of human beings and animals. Also, they play a major role in enhancing reproductive efficiency. The aim of the current study was to investigate the effects of sodium butyrate (SB) on reproductive performance and colostrum composition in gilts. A total of 40 Large White×Landrace replacement gilts (at the age of 160 to 175 days) were fed either a standard diet (control group, n=20) or standard diet top dressed with encapsulated SB at the level of 500 mg/kg (SB group, n=20) from 1 month before mating to 7 days after farrowing. The rate of gilts regular return to estrus after insemination was lower in SB group than the control group. The total number of piglets born (P=0.179) and the litter weight at birth (P=0.063) did not differ between the two treatment groups. However, the mean BW at day 7 tended to be greater in SB group (P=0.051) and average daily gain of piglets was greater (P=0.011) compared with control group. Colostrum samples were collected at parturition and the concentrations of total protein (P=0.197), cholesterol (P=0.161) and lactose (P=0.923) were not influenced by SB supplementation. However, compared with control gilts, colostrum from SB-treated gilts contained lower triglyceride (P=0.050). Moreover, colostrum concentrations of prolactin (P=0.005) and leptin (P=0.006) were significantly lower in SB group. No significant differences were noted for the colostral concentrations of cortisol (P=0.899), thyroxine (P=0.891) or triiodothyronine (P=0.194). The concentration of lipopolysaccharide in colostrum was not influenced by SB supplementation (P=0.972). However, colostrum from SB-treated gilts had significantly lower tumor necrosis factor α (TNFα) (P=0.030) and higher immunoglobulin A (IgA) (P=0.042). Collectively, SB supplementation could reduce the rate of gilts return to estrus, alter the composition of colostrum and enhance the growth rate of piglets. Moreover, SB could alter the immune function of newborn piglets through decreased production of TNFα and increased IgA concentration in colostrum.

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