Go to Top Go to Bottom
Anim Biosci > Volume 31(2); 2018 > Article
Nuntapaitoon, Muns, and Tummaruk: Newborn traits associated with pre-weaning growth and survival in piglets

Abstract

Objective

Piglet pre-weaning mortality is an important variable indicating the efficacy of farrowing management and animal well-being during lactation. The present study determined the association of newborn traits measured soon after birth with piglet pre-weaning mortality and growth.

Methods

In total, 805 piglets born from 57 multiparous sows were investigated. Their blood oxygen saturation, blood glucose and rectal temperature at 24 h after birth (RT24h) were monitored. Birth order, sex, skin color, integrity of the umbilical cord, attempts to stand and birth intervention were monitored. Piglets were weighed at day 0, 7, and 21 to evaluate average daily gain (ADG).

Results

Piglet pre-weaning mortality for lactation period was 12.6% and cumulative mortality during the first 7 days of age was 8.6%. A higher proportion of piglets with pale skin color died compared to piglets with normal skin color (26.7% vs 7.7%, p<0.001). A higher (p<0.001) proportion of piglets that attempted to stand after 5 min (38.5%) died compared to piglets that attempted to stand within 1 min (6.3%) after birth. Piglet body weight at birth (BWB), blood glucose and the number of piglets born alive (BA) were correlated with ADG (p<0.05). Piglets with BWB <1.30 kg had higher (p<0.001) mortality rate than piglets with BWB≥1.80 kg (19.0% vs 3.3%) and piglets with BWB 1.30 to 1.79 kg (4.0%). Piglet with RT24h <37.0°C had higher (p<0.001) mortality rate (86.2%) than piglets with RT24h >38.5°C (3.9%).

Conclusion

Low BWB and low RT24h compromise piglet survival during the lactation period in the tropical conditions. Piglets in the litters with a high BA, low BWB and low blood glucose have reduced ADG.

INTRODUCTION

In modern swine industry, producers expect up to 30 pigs weaned per sow per year [1]. However, in practice, a high proportion of piglet mortality occur during pre-weaning period [2]. Thus, factors associated with piglet pre-weaning mortality are becoming a major concern in swine industry worldwide [3]. One of main reason for a high proportion of piglet pre-weaning mortality is the use of high prolific sow genetics, which improved the number of piglets born alive per litter among swine commercial herds worldwide during the past 10 years [1]. Litter size (LS) is an important sow factor related to piglet survival and growth [2]. Nuntapaitoon and Tummaruk [2] demonstrated that piglet pre-weaning mortality in the litter with 13 to 15 littermate pigs (24.1%) was significantly higher than the litter with 1 to 7 (11.9%), 8 to 10 (11.8%), and 11 to 12 (14.6%) littermate pigs, respectively. Large LS also increases the body weight at birth (BWB) variation among the piglets within litter [4]. Hence, the proportion of piglets with low BWB is also increased [5]. Vallet and Miles [6] observed that low BWB piglets had a higher risk of being crushed due to their slower speed of movement and reflexive actions. Intra-partum hypoxia is a main factor influencing piglet vitality as it damages the foetal central nervous system [7]. Thus, several indicators can be used in newborn piglets to evaluate the level of intra-partum hypoxia suffered during the birth process. In addition, piglet vitality determines their capacity to suckle and compete for a teat and is also positively correlated with piglet growth and survival until weaning [8]. One reason for reduced piglet vitality might be related to nutrients and oxygen supplies via umbilical cord from dam to fetus. Blood oxygen, blood glucose concentration, and time to stand after birth have been used as indirect measures of intra-partum hypoxia and neonatal piglet viability [9].
Factors influencing piglet pre-weaning mortality under field conditions include sow factors (e.g., breed, parity, nutritional status, farrowing duration, maternal behavior and LS), piglet factors (e.g., BWB, birth order and sex) and environmental factors (e.g., ambient temperature and stocking density) [2,9]. To our knowledge, most of the studies on risk factors associated with piglet pre-weaning mortality were performed in cold or moderate climates [1012]. Additional information in hot and humid climate countries is required to improve farrowing management and care of newborn piglets. The objective of the present study was to determine the effects of piglet neonatal traits and physiological characteristics measured soon after birth on their pre-weaning survival and growth.

MATERIALS AND METHODS

Animal care

The experiment followed the guidelines documented in The Ethical Principles and Guidelines for the Use of Animals for Scientific Purposes edited by the National Research Council of Thailand, and was approved by the Institutional Animal Care and Use Committee (IACUC) in accordance with the university regulations and policies governing the care and use of experimental animals (approval no. 1431063).

Herd and management

The present study was carried out in a 3,500-sows commercial swine herd in the western part of Thailand between June and August 2013. The average ambient temperature during the experimental period ranged from 25.8°C to 30.0°C. The minimum and maximum temperature ranged from 21.1°C to 26.3°C and from 28.1°C to 37.6°C, respectively. The average relative humidity varied from 72.0% to 96.0%. Sows were kept in individual crates (1.2 m2) during gestation in a conventional open-housing system and were provided with fans and individual water sprinklers to reduce the impact of high ambient temperature. During gestation, sows were fed a commercial gestation diet that met or exceed their nutritional requirement estimates (19.7% crude protein, 5.8% fat, 3.8% fibre, and 14.0 metabolizable energy, MJ/kg) [13]. Feed was provided twice a day following a standardised feeding pattern, resulting in an average of 2.5 kg per sow per day. During lactation, sows were fed twice a day with a commercial lactation diet, increasing the daily amount of feed offered, until ad libitum feed was reached after one week of lactation. The animals were received water ad libitum in a continuous water channel. Pregnant sows were moved to the farrowing house about one week before their expected farrowing date. Sows were kept in individual farrowing crates (1.2 m2) placed at the centre of the pens with a space allowance of 4.2 m2. The pens were fully slatted with concrete at the centre for sows and with steel slats at both sides of the farrowing crate for piglets. Each pen was provided with a creep area for piglets (0.60 m2) placed on the floor on one side, covered by a plastic plate and heating lamp during the first week after farrowing. The heating lamp was usually turned on during the night or when the environment temperature fell below 30°C. The temperature in the creep area was between 30°C to 36°C.

Supervision of parturition process

The parturition process was carefully supervised by the first author (M. Nuntapaitoon). Briefly, sows were interfered with as little as possible during parturition, and birth intervention was performed only when dystocia was clearly identified. Dystocia was considered when an interval of >30 min elapsed from the birth of the last piglet, and when the sow showed intermittent straining accompanied by paddling of the legs or when the sow expelled small quantities of foetal fluid together with marked tail switching for >30 min without any piglet being born. Routine procedures performed on piglets included weighing, tail docking, tooth clipping and 1 mL (200 mg) iron supplement administered intramuscularly (Gleptosil, Alstoe Ltd. Animal Health, Leicestershire, England) on the day of birth. Piglets were orally administered a coccidiocide of 20 mg/kg body weight (Baycox [Toltrazuril 5.0% oral suspension], Bayer Inc., Mississauga, ON, Canada) to control neonatal coccidiosis at 3 days of age. In total, 805 piglets born from 57 Landrace×Yorkshire crossbred sows were included. The mean parity was 4.0±1.6 (ranged 2 to 7). Lactation length was on an average of 23.0±2.0 days.

Data collection

The following reproductive variables of the sows were recorded: farrowing duration (i.e., time between the first and last born piglets), total number of piglets born per litter (TB), number of piglets born alive per litter (BA), and mummified foetuses, stillbirths and number of piglets at weaning per litter. The piglets’ heart rate and blood oxygen saturation (SatO2) were monitored within 5 min after birth by using a veterinary pulse oximetry (EDAN VE-H100B Pulse Oximeter, Edan Instrument Inc., San Diego, CA, USA). Thereafter, blood samples for glucose analysis were collected from piglets within 5 to 10 min after birth (i.e., before first suckling). A small amount of blood sample (a mixture of venous and arterial blood) was obtained from the cut umbilical cord. Few drops of blood sample were used to determined blood glucose concentration by using a portable test kit of human glucometer (Accu-Chek Performa, Roche, Mannheim, Germany). Birth order, birth interval (the time elapsed between each piglet born), sex, and time elapsed from birth until first attempts to stand (3 groups: <1 min, 1 to 5 min, and >5 min) were recorded for each piglet. Also, birth assistance was recorded (yes or no) if required by piglets. Skin color of the piglets was recorded at birth and was classified into 2 groups (normal or pale). Integrity of the umbilical cord of each piglet was examined and classified into two groups (intact or broken). Rectal temperature was measured at 24 h after birth (RT24h) with a digital thermometer (Microlife, Microlife AG Swiss Corporation, Widnau, Switzerland, with a display resolution of 0.01°C and ±0.1°C accuracy). All piglets were individually identified by an ear tattoo. Body weight of the piglets was measured immediately at birth. Litters were equalized to 13 or 14 piglets per litter after 24 h and within 48 h after birth. The LS was defined as the number of piglets after cross-fostering. Piglets were weighed again at day 7 and 21 after birth. Mortality rate of the piglets was also determined at day 7 and 21 of lactation. Creep feeding and drinking water were provided to the piglets from 7 days of age until weaning.

Statistical analysis

All statistical analyses were performed using SAS 9.0 (SAS Inst. Inc., Cary, NC, USA) [14]. Descriptive analysis (mean±standard deviation [SD] median and range) and frequency analysis were obtained for all reproductive parameters. To identify the potential indicators for piglet mortality and piglet average daily weight gain (ADG) at days 7 and 21 of lactation, each recorded factor was individually tested using univariate analyses. Continuous variables indicating the neonatal piglet characters (i.e., TB, BA, LS, birth order, BWB, birth interval, heart rate, SatO2 and blood glucose concentration) were compared between piglets dying and surviving at days 7 and 21 of lactation by using Student’s t test (PROC TTEST). The association between categorical variables (i.e., sex, skin color, attempts to stand, umbilical cord integrity and birth assistance) and the piglet mortality (dead or alive) were analyzed using Chi-square test. The effect of these categorical variables on ADG at days 7 and 21 of lactation was analyzed using the PROC GLM of SAS. Pearson’s correlation was performed to study collinearity among the continuous variables in the univariate models.
For multivariate analyses, generalised linear mixed models (GLMMIX macro) with the dependent variable (mortality) modeled as a binary outcome (dead or alive) was conducted. Factors with significant levels of p<0.10 were included in the final models. Highly correlated variables were not included in the same multivariate analyses models. Then, the final multivariate GLMMIX models for piglet mortality at days 7 and 21 of lactation included BWB of the piglet classes (<1.30, 1.30 to 1.79, and ≥1.80 kg) and RT24h classes (<37.0°C, 37.0°C to 38.5°C, and >38.5°C). The classification of the independent variables was made according to frequency distribution with some minor adjustment based on biological reliability. Similarly, general linear mixed models (PROC MIXED) were conducted to analyze piglet ADG at days 7 and 21 of lactation. The final multivariate MIXED models for piglet ADG at day 7 and 21 included BWB classes (<1.30, 1.30 to 1.79, and ≥1.80 kg), blood glucose concentration classes (≤24 and >24 mg/dL), BA classes (<12, 12 to 14, and ≥15 piglets), sex and attempts to stand (<1, 1 to 5, and >5 min). In all models, sow or litter were introduced as a random effect. Least squares means were obtained from each class of the variables and were compared using Tukey–Kramer adjustment for multiple comparisons. p< 0.05 was regarded to be statistically significance and 0.05<p<0.10 was considered as a tendency for statistically significance. Piglets were defined as experimental units.

RESULTS

Of the 805 piglets, 81 were stillborn (10.1%), 34 were mummified fetuses (4.2%) and 690 were BA (85.7%). Descriptive statistics of newborn piglet traits and piglet performance are presented in Table 1. On average (means±SD), TB, BA, and the number of piglets at weaning were 14.2±3.7, 12.1±3.4, and 11.7±1.7 piglets, respectively. The duration of farrowing averaged 217.8±83.7 min, and the average birth interval between piglets was 16.4±24.1 min. Overall, piglet pre-weaning mortality was 12.6% and cumulative mortality at day 7 was 8.6%.

Univariate analyses

Factors associated with piglet pre-weaning mortality until day 7 after birth

Factors influencing piglet pre-weaning mortality rate until day 7 after birth are presented in Tables 2, 3. Both BWB and RT24h influenced piglet mortality until day 7 after birth (p< 0.001). Piglets that died before day 7 of life had a lower birth interval (9.5 vs 14.9 min, p = 0.005) and were reared in litters with a higher LS (13.7 vs 13.2 piglets, p = 0.038). The total number of piglets born per litter, BA, birth order, heart rate, SatO2, and blood glucose concentration did not influence piglet survival (p>0.05, Table 2). A higher proportion of piglets with pale skin color died compared to piglets with normal skin color (26.7% vs 7.7%; p<0.001, Table 3). A higher proportion of piglets that attempted to stand after 5 min (38.5%) died compared to piglets that attempted to stand within 1 min (6.3%, p<0.001) and within 1 to 5 min (9.2%, p<0.001, Table 3). Birth intervention, sex and umbilical cord integrity had no effect on piglet mortality until day 7 after birth (p>0.05, Table 3).

Factors associated with piglet pre-weaning mortality until day 21 after birth

Factors influencing piglet pre-weaning mortality rate until day 21 after birth are presented in Table 3, 4. Both BWB and RT24h influenced piglet mortality until day 21 after birth (p<0.001). Piglets that died before day 21 of life were born from sows with a higher TB, were reared in litters with a higher LS, and had lower birth intervals (p<0.05, Table 4). Birth order, heart rate, SatO2 and blood glucose concentration did not influence piglet survival (p>0.05, Table 4). A higher proportion of piglets with pale skin color died compared to piglets with normal skin color (36.7% vs 11.5%; p<0.001, Table 3). A higher proportion of piglets that attempted to stand after 5 min (41.0%) died compared to piglets that attempted to stand within 1 min (10.8%, p<0.001) and within 1 to 5 min (10.8%, p<0.001, Table 3). Birth intervention, sex and umbilical cord integrity had no effect on piglet mortality until day 21 after birth (p>0.05, Table 3).

Factors associated with average daily gain until day 7 after birth

Piglet BWB (p<0.001) and blood glucose concentration (p<0.001) positively influenced piglet ADG at day 7 (r = 0.172, p<0.001, Table 5). Piglets born from sows with higher TB and higher BA had a lower ADG at day 7 (p<0.001, Table 5). Piglets without birth intervention had lower growth than piglets with birth intervention (161.1±2.8 vs 182.4±7.7 g/d, p = 0.010, Table 6). Male piglets had higher growth than female piglets (169.1±3.7 vs 157.6±3.9 g/d, p = 0.032, Table 6). Piglets that attempted to stand after 5 min (127.1±13.6 g/d) had lower growth than piglets that attempted to stand within 1 min (165.9±2.9 g/d, p = 0.006) or within 1 to 5 min (156.3±13.6 g/d, p = 0.071, Table 6).

Factors associated with average daily gain until day 21 after birth

Piglet BWB (p<0.001) and blood glucose concentration (p = 0.009) positively influenced piglet ADG at day 21 (r = 0.106, p<0.01, Table 5). Piglets born from sows with higher TB and BA had lower ADG at day 21 (Table 5, p<0.001). Piglets without birth intervention had lower growth than piglets with birth intervention (214.3±2.7 vs 235.1±7.3 g/d, p = 0.008, Table 6). Piglets that attempted to stand after 5 min (190.3±13.1 g/d) had lower growth than piglets that attempted to stand within 1 min (218.0±2.8 g/d, p = 0.039, Table 6).

Multivariate analyses

Average daily gain

The final multi-covariate model for ADG at day 7 included BWB (p<0.001), blood glucose concentration (p< 0.001), BA (p = 0.025), sex (p = 0.087), and attempts to stand (p = 0.093) (Table 7). At day 7, the piglets with BWB<1.30 kg had a lower ADG than the piglets with BWB≥1.80 kg (p<0.001) and the piglets with BWB 1.30 to 1.79 kg (p<0.001, Table 7). The piglets with a blood glucose concentration of ≤24 mg/dL had a lower ADG at day 7 than the piglets with a blood glucose concentration of >24 mg/dL (p<0.001, Table 7). Furthermore, the piglets with a low BA (<12 piglet) had a higher ADG at day 7 than the piglets with 12 to 14 BA (p = 0.087) and the piglets with ≥15 BA (p = 0.030, Table 7). The male piglets tended to have a higher ADG at day 7 than the female piglets (p = 0.087, Table 7). The piglets that stood within 1 min tended to have a higher ADG at day 7 than the piglets that stood after 5 min (p = 0.075, Table 7).
Based on a multivariate statistical model, factors significantly influencing ADG of the piglets at day 21 in the final model included BWB (p<0.001), BA (p<0.001), and blood glucose concentration (p = 0.042). The statistical model revealed that, at day 21, the piglets with a BWB of <1.30 kg had a lower ADG than the piglets with a BWB of ≥1.80 kg (p<0.001) and the piglets with a BWB 1.30 to 1.79 kg (p<0.001) (Table 7). The piglets from litters with a low BA (<12 piglets) had a higher ADG at day 21 than those from litters with a BA of 12 to 14 (p<0.001) and ≥15 (p<0.001). The piglets with a blood glucose concentration of ≤24 mg/dL had a lower ADG at day 21 than the piglets with a blood glucose concentration of >24 mg/dL (p = 0.042). Sex and attempts to stand did not influence ADG of the piglet at day 21 (p>0.10).

Piglet pre-weaning mortality

The final multivariate model for mortality at day 7 included BWB and RT24h (p<0.001). At day 7, the piglets with BWB<1.30 kg had a higher (p<0.001) mortality rate (19.0%) than the piglets with BWB≥1.80 kg (3.3%) and piglets with BWB 1.30 to 1.79 kg (4.0%, Figure 1). The piglets with RT24h < 37.0°C had a higher (p<0.001) mortality rate (86.2%) at day 7 than the piglets with RT24h 37.0°C to 38.5°C (7.3%) and RT24h >38.5°C (3.9%, Figure 2).
Based on a multivariate statistical model, factors influencing piglet mortality at day 21 included BWB (p<0.001) and RT24h (p<0.001). At day 21, the piglets with BWB<1.30 kg had a higher (p<0.001) mortality rate (26.4%) than the piglets with BWB≥1.80 kg (6.0%) and the piglets with BWB 1.30 to 1.79 kg (6.5%, Figure 1). The piglets with RT24h <37.0°C had a higher (p<0.001) mortality rate (89.7%) at day 21 than the piglets with RT24h 37.0°C to 38.5°C (12.9%) and RT24h >38.5°C (7.0%, Figure 2).

DISCUSSION

The main objective of this study was to determine the effect of certain newborn piglet traits measured soon after birth on piglet pre-weaning mortality and growth. As expected, BWB and RT24h were the most influential postnatal survival factors at both day 7 and at weaning. Furthermore, BWB, BA and blood glucose concentration significantly influenced piglet growth during the whole lactation period, while sex and time spent attempting to stand had some impact on their growth up to day 7.
In agreement with our results, many studies have identified piglet BWB as the main predictor for both survival and growth during lactation [9,15]. Piglet BWB is positively associated with their physiological maturity and, in turn, correlates with different physical and physiological parameters such as colostrum intake capacity and thermoregulation ability [3]. Small piglets usually have decreased viability and a lower capacity to compete for a teat [16]. Johansen et al [17] found that piglets with a low BWB often have lower ADG in the suckling period. In addition, low BWB piglets are less able to maintain body temperature [18] which leads to starvation, lethargy and increased risk of crushing by the sow. Therefore, lower BWB piglets may also show a low nutritional status and poor passive immunity [19]. In agreement with our results, rectal temperature after birth was identified as an important indicator for piglet survival [9,16], indicating that piglets with low rectal temperature after 24 h might have lower thermoregulation abilities. Thermoregulation is a crucial physiological event for all newborn piglets. The piglets that die during the first days of life are not able to maintain optimal rectal temperature during the first 24 h of life [10]. In the present study, RT24h was significantly associated with mortality rate but was not related with ADG. In contrast, Panzardi et al [9] identified RT24h as an indicator for piglet growth at weaning. Likewise, Pedersen et al [20] found that piglets with low RT24h had low ADG from birth to weaning. One possible explanation might be due to that the piglets with low RT24h may consume less colostrum than the piglets with high RT24h. Thus, growth rate of these piglets might be compromise.
In the current study, BA was observed to influence piglet growth. Likewise, other studies found that BA negatively correlated with the piglet weaning weight [20]. This might be due to the fact that there is also an increase in the number of small piglets in the litter with an increased BA [21]. The present study also demonstrated that BWB of the piglets was significantly decreased when TB increased (Table 5). Competition between littermates might have a negative impact on piglet colostrum intake, especially in the small piglets, resulting in reduced growth during lactation [3]. Moreover, BA was not related with mortality in the present study, whereas in the previous study, there was a positive relationship between the number of piglets in the litter and piglet mortality [2]. Nonetheless, Muns et al [8] and Pedersen et al [20] found a relationship between BA and piglet growth, but not between BA and mortality rate.
In the present study, blood glucose concentration at birth was a significant predictor for piglet ADG at 7 and 21 days of life but not for piglet mortality. Accordingly, studies failed to demonstrate a correlation between blood glucose concentration in newborn piglet and their survival [10,15,16]. However, Panzadi et al [9] found that either too low (24 to 30 mg/dL) or too high (45 to 162 mg/dL) levels of blood glucose in neonatal piglets were associated with an increased pre-weaning mortality. In the present study, piglets with high glucose concentrations at birth might have high energy reserves and, subsequently, enhanced capacity for suckling and growth. This implies that some source of glucose or energy supplementation in neonatal piglets maybe needed to improve the suckling capacity and growth performance in the neonatal piglets.
In the multivariate models for ADG at day 7, time from birth to first attempts to stand was also identified as a predictive factor. In the present study, piglets spending >5 min from birth to first attempts to stand had low ADG. Decaluwé et al [12] also found that piglets spending a long time from birth to suckling had a lower ADG during the lactation period than those spending a short time from birth to suckling. Moreover, neonatal piglets spending a short time from birth to first attempts to stand resulted in a low pre-weaning mortality [9,10]. However, Leenhouwers et al [22] found no relationship between time from birth to first attempts to stand and piglet mortality rate during the first week of lactation. Nonetheless, time elapsed from birth to first suckling significantly influences colostrum intake of the piglets [23]. Therefore, “the time elapsed from birth to first suckling” has been included in a formula for estimating colostrum consumption in piglets [23]. In the present study, piglets spending a short time period from birth to first attempts to stand are probably faster at first suckling, thus increasing their colostrum consumption. The colostrum consumption of the neonatal piglets significantly influence the piglet survival and passive immunity [24]. Therefore, in practice, newborn piglets spending more than 5 min to first attempt to stand need special cares.
In conclusion, low BW B and low RT24h compromise piglet survival during the lactation period in the tropical conditions. In addition, piglets in the litters with a high number of BA and piglets with low BWB and/or low blood glucose concentration have reduced body weight growth during lactation.

Notes

CONFLICT OF INTEREST

We certify that there is no conflict of interest with any financial organization regarding the material discussed in the manuscript.

ACKNOWLEDGMENTS

Financial support for the present study was provided by a grant for International Research Integration: Chula Research Scholar, Ratchadaphiseksomphot Endowment Fund. M. Nuntapaitoon is a grantee of the Research and Researchers for Industries (RRI) Ph.D. program and the Thailand Research Fund, and part of the research grant was supported by the Rachadapisek Sompote Endowment Fund for the 90th Anniversary of Chulalongkorn University. Ramon Muns was supported by the Rachadapisek Sompote Endowment Fund for Postdoctoral Fellowship by Chulalongkorn University.

Figure 1
Percentage of mortality at days 7 and 21 for all piglets classified into low (<1.30 kg, n = 216), medium (1.30 to 1.79 kg, n = 323) and high (≥1.80 kg, n = 151) birth weight categories. A,B,a,b Values with different superscripts within the same day differ significantly (p<0.05).
ajas-31-2-237f1.gif
Figure 2
Percentage of mortality at days 7 and 21 for all piglets classified into low (<37.0°C, n = 29), medium (37.0°C to 38.5°C, n = 248) and high (>38.5°C, n = 413) rectal temperature categories at 24 h after birth. A,B,C,a,b,c Values with different superscripts within the same day differ significantly (p<0.05).
ajas-31-2-237f2.gif
Table 1
Descriptive statistics of 690 piglets evaluated at birth and during the lactation period
Variables N Mean±SD Median Range
Birth weight (kg) 690 1.49±0.38 1.48 0.46 to 2.71
Heart rate (bpm) 685 66.2±33.20 57.0 23.0 to 250
Glucose (mg/dL) 687 49.1±17.72 47.0 11.0 to 159
Oxygen saturation (%) 685 91.2±8.85 92.0 10.0 to 100
Rectal temperature at 24 h (°C) 670 38.7±0.57 38.7 35.5 to 40.3
Weight at day 7 (kg) 632 2.67±0.71 2.7 0.75 to 4.64
Weight at day 21 (kg) 602 6.09±1.51 6.1 1.88 to 10.07
ADG at day 7 (g/d) 632 163.7±67.32 164.6 −7.9 to 340.7
ADG at day 21 (g/d) 602 216.8±63.05 213.3 24.0 to 376.9

SD, standard deviation; ADG, average daily gain.

Table 2
Potential indicators for piglet pre-weaning mortality (means±standard error of the mean) comparing surviving piglets from birth to day 7 of lactation (n = 631) with dying piglets (n = 59)
Variables Surviving Dying p-value
Total number of piglets born per litter 14.9±0.14 15.6±0.43 0.171
Number of piglets born alive per litter 13.0±0.12 13.3±0.45 0.491
Litter size after cross-fostering 13.2±0.07 13.7±0.22 0.038
Birth interval (min) 14.9±0.80 9.5±1.72 0.005
Birth weight (kg) 1.52±0.01 1.11±0.05 <0.001
Birth order 7.5±0.18 8.5±0.59 0.130
Heart rate (bpm) 66.5±1.34 62.5±3.68 0.381
Glucose (mg/dL) 49.3±0.70 47.8±2.69 0.605
Oxygen saturation (%) 91.3±0.36 90.4±0.99 0.458
Rectal temperature at 24 h (°C) 38.7±0.02 38.2±0.14 <0.001
Table 3
Categorical variables influencing piglet pre-weaning mortality at day 7 and 21 after birth
Variables Piglet pre-weaning mortality (%)

Day 7 Day 21
Skin color
 Normal 7.7a 11.5a
 Pale 26.7b 36.7b
Time attempted to stand
 <1 min 6.3a 10.8a
 1 to 5 min 9.2a 10.8a
 >5 min 38.5b 41.0b
Birth intervention
 No 9.0a 13.4a
 Yes 5.1a 6.3a
Sex
 Male 8.0a 13.6a
 Female 9.1a 11.6a
Umbilical cord integrity
 Intact 8.9a 13.0a
 Broken 7.8a 11.9a

a,b Values with different superscripts within the same column within variable differ significantly (p<0.05).

Table 4
Potential indicators for piglet pre-weaning mortality (means±standard error of the mean) comparing surviving piglets from birth to day 21 of lactation (n = 603) with dying piglets (n = 87)
Variables Surviving Dying p-value
Total number of piglets born per litter 14.9±0.14 15.9±0.33 0.010
Number of piglets born alive per litter 12.9±0.12 13.7±0.32 0.028
Litter size after cross-fostering 13.2±0.07 13.6±0.18 0.042
Birth interval (min) 15.2±0.83 9.3±1.37 <0.001
Birth weight (kg) 1.53±0.01 1.16±0.05 <0.001
Birth order 7.5±0.19 8.1±0.45 0.319
Heart rate (bpm) 66.9±1.39 61.4±2.71 0.076
Glucose (mg/dL) 49.5±0.71 46.6±2.13 0.156
Oxygen saturation (%) 91.2±0.37 91.3±0.80 0.872
Rectal temperature at 24 h (°C) 38.7±0.02 38.3±0.10 <0.001
Table 5
Pearson’s correlations among the most significant potential predictor measured during farrowing and soon after birth and average daily gain (ADG) of the piglets from birth until 7 and 21 days of age
TB BA BI BWB HR GLU
BA 0.798*** - - - - -
BI −0.138*** −0.128*** - - - -
BWB −0.309*** −0.348*** 0.180*** - - -
HR −0.092* −0.077* - - - -
SatO2 - - - - −0.179*** -
GLU −0.118** −0.136*** 0.146*** 0.187*** - -
RT24h - - - 0.128*** - -
ADG7 −0.272*** −0.283*** - 0.430*** - 0.172***
ADG21 −0.197*** −0.284*** - 0.431*** - 0.106**

TB, total number of piglets born per litter; BA, number of piglets born alive per litter; BI, birth interval; BWB, birth weight; HR, heart rate; GLU, blood glucose concentration; SatO2, blood oxygen saturation; RT24h, rectal temperature at 24 h after birth; ADG7, average daily gain from birth until day 7; ADG21, average daily gain from birth until day 21.

Significance levels:

* p<0.05,

** p<0.01,

*** p<0.001.

Table 6
Categorical variables influencing average daily gain (means±standard error of the mean) at day 7 and 21 after birth from univariate analyses
Variables Average daily gain (g/d)

Day 7 Day 21
Skin color
 Normal 163.6±2.7a 217.0±2.6a
 Pale 164.4±14.4a 210.6±14.5a
Time attempted to stand
 <1 min 165.9±2.8a 218.0±2.8a
 1 to 5 min 156.3±8.7ab 215.9±8.3ab
 >5 min 127.1±13.7b 190.3±13.1b
Birth intervention
 No 161.1±2.8a 214.3±2.7a
 Yes 182.4±7.7b 235.1±7.3b
Sex
 Male 169.1±3.7a 219.1±3.6a
 Female 157.6±3.9b 214.4±3.7a
Umbilical cord integrity
 Intact 160.4±3.2a 215.6±3.1a
 Broken 170.6±4.7a 219.4±4.5a

a,b Values with different superscripts within the same column within variable differ significantly (p<0.05).

Table 7
Predictive factors included in the final models for average daily gain (least square means±standard error of the mean) from birth until 7 and 21 days of life from multivariate analyses
Variables Average daily gain (g/d)

Day 7 Day 21
Number of piglets born alive per litter, piglets
 <12 150.6±11.09aA 226.8±9.88a
 12 to 14 126.4±11.39abB 190.6±9.60b
 ≥15 121.3±11.16b 192.8±9.94b
Birth weight (kg)
 <1.30 88.9±9.72c 165.5±9.01c
 1.30 to 1.79 145.3±9.52b 210.5±8.45b
 ≥1.80 164.2±10.59a 234.2±9.40a
Glucose (mg/dL)
 ≤24 107.8±15.32b 190.3±15.95b
 >24 157.8±6.16a 220.6±4.99a
Sex
 Male 136.5±9.45A NS
 Female 129.1±9.53B NS
Attempt to stand (min)
 <1 141.8±8.27A NS
 1 to 5 140.2±10.78AB NS
 >5 116.4±13.87B NS

a,b,c Values with different small superscripts within the same column differ significantly (p<0.001).

A,B Values with different capital superscripts within the same column tended to be differences (0.05<p<0.10).

NS, the variables were not significant (p>0.01) and were not included in the final models.

REFERENCES

1. Knox R. Getting to 30 pigs weaned/sow/year. In : Proceedings of London Swine Conference; 2005; London, UK. p. 47–59.

2. Nuntapaitoon M, Tummaruk P. Piglets pre-weaning mortality in a commercial swine herd in Thailand. Trop Anim Health Prod 2015; 47:1539–46.
crossref pmid
3. Muns R, Nuntapaitoon M, Tummaruk P. Non-infectious causes of pre-weaning mortality in piglets. Livest Sci 2016; 184:46–57.
crossref
4. Shankar BP, Madhusudhan HS, Harish DB. Pre-weaning mortality in pig-causes and management. Vet World 2009; 2:236–9.

5. Campos PHRF, Silva BAN, Donzele JL, Oliveira RFM, Knol EF. Effects of sow nutrition during gestation on within-litter birth weight variation: a review. Animal 2012; 6:797–806.
crossref pmid
6. Vallet JL, Miles JR. Comparison of myelination between large and small pig fetuses during late gestation. Anim Reprod Sci 2012; 132:50–7.
crossref pmid
7. Herpin P, Le Dividich J, Hulin JC, et al. Effect of the level of asphyxia during delivery on viability at birth and early postnatal vitality of newborn pigs. J Anim Sci 1996; 74:2067–75.
crossref pmid
8. Muns R, Manzanilla EG, Sol C, Manteca X, Gasa J. Piglet behaviour as a measure of vitality and its influence on piglet survival and growth during lactation. J Anim Sci 2013; 91:1838–43.
crossref pmid
9. Panzardi A, Bernardi ML, Mellagi AP, et al. Newborn piglet traits associated with survival and growth performance until weaning. Prev Vet Med 2013; 110:206–13.
crossref pmid
10. Baxter EM, Jarvis S, D’Eath RB, et al. Investigating the behavioural and physiological indicators of neonatal survival in pigs. Theriogenology 2008; 69:773–83.
crossref pmid
11. Pedersen LJ, Malmkvist J, Kammersgaard T, Jørgensen E. Avoiding hypothermia in neonatal pigs: effect of duration of floor heating at different room temperatures. J Anim Sci 2013; 91:425–32.
crossref pmid
12. Decaluwé R, Maes D, Wuyts B, et al. Piglets’colostrum intake associates with daily weight gain and survival until weaning. Livest Sci 2014; 162:185–92.
crossref
13. Committee on Nutrient Requirements of Swine, National Research Council. Nutrient requirements of swine. 11th edWashington, DC, USA: National Academy Press; 2012.

14. SAS Institute Inc. SAS User’s guide. Statistics version 9.0. Cary, NC, USA: SAS Institute Inc; 1996.

15. Rootwelt V, Reksen O, Farstad W, Framstad T. Postpartum deaths: piglet, placental, and umbilical characteristics. J Anim Sci 2013; 91:2647–56.
crossref pmid
16. Tuchscherer M, Puppe B, Tuchscherer A, Tiemann U. Early identification of neonates at risk: traits of newborn piglets with respect to survival. Theriogenology 2000; 54:371–88.
crossref pmid
17. Johansen M, Alban L, Kjærsgård HD, Bæbo P. Factors associated with sucking piglet average daily gain. Prev Vet Med 2004; 63:91–102.
crossref pmid
18. Theil PK, Nielsen MO, Sørensen MT, Lauridsen C. Lactation, milk and suckling. Bach KKE, Kjeldsen NJ, Poulsen HD, Jensen BB, editorsNutritional physiology of pigs. Copenhagen, Denmark: Pig Research Centre; 2012. p. 49

19. Quiniou N, Dagorn J, Gaudré D. Variation of piglets’ birth weight and consequences on subsequent performance. Livest Prod Sci 2002; 78:63–70.
crossref
20. Pedersen LJ, Schild SLA, Malmkvist J. The influence of the thermal environment and other early life events on growth rate of piglets during lactation. Animal 2015; 9:1529–35.
crossref pmid
21. Quesnel H, Brossard L, Valancogne A, Quiniou N. Influence of some sow characteristics on within-litter variation of piglet birth weight. Animal 2008; 2:1842–9.
crossref pmid
22. Leenhouwers JI, de Almeida CA, Knol EF, van der Lende T. Progress of farrowing and early postnatal pig behavior in relation to genetic merit for pig survival. J Anim Sci 2001; 79:1416–22.
crossref pmid
23. Devillers N, van Milgen J, Prunier A, Le Dividich J. Estimation of colostrum intake in the neonatal pig. Anim Sci 2004; 78:305–13.
crossref
24. Devillers N, Le Dividich J, Prunier A. Influence of colostrum intake on piglet survival and immunity. Animal 2011; 5:1605–12.
crossref pmid


Editorial Office
Asian-Australasian Association of Animal Production Societies(AAAP)
Room 708 Sammo Sporex, 23, Sillim-ro 59-gil, Gwanak-gu, Seoul 08776, Korea   
TEL : +82-2-888-6558    FAX : +82-2-888-6559   
E-mail : editor@animbiosci.org               

Copyright © 2024 by Asian-Australasian Association of Animal Production Societies.

Developed in M2PI

Close layer
prev next