Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-04T18:03:27.076Z Has data issue: false hasContentIssue false

Effect of feeding Actigen™ to sows during gestation and lactation and on piglet performance

Published online by Cambridge University Press:  27 February 2017

J. Taylor-Pickard*
Affiliation:
Alltech Biotechnology Centre, Sarney, Summer Hill Road, Dunboyne, County Meath, Ireland
T. McArdle
Affiliation:
Alltech Biotechnology Centre, Sarney, Summer Hill Road, Dunboyne, County Meath, Ireland
S. Icely
Affiliation:
Harper Adams University, Edgmond, Shropshire, UK
*
*Corresponding author: [email protected]
Rights & Permissions [Opens in a new window]

Summary

Actigen™ is a second generation, unique bioactive fraction derived from the outer cell wall of a specific strain of yeast, Saccharomyces cerevisiae, where it acts in the gut to bind pathogenic bacteria, preventing disease and competition for nutrients. In the current trial, 260 sows were used and fed either an unsupplemented control diet or one containing Actigen™ at 0.08% of the formulation during gestation, farrowing and lactation, to assess its impact on sow and piglet performance. Results showed significant increases in feed intake for sows fed Actigen™ pre-farrowing, but this was reversed during lactation, leading to a 7 kg saving in feed intake per animal. At birth, piglets weighed 42 g more in litters from Actigen™-fed sows compared to the control group. Weaning weight of the total litter from Actigen™ sows was significantly higher (P< 0.05) by 3.3 kg, although individual piglet weights were the same. Sows showed no significant loss in body weight during the trial, indicating that the improved piglet production was related to improved nutrient availability and perhaps Ig status of piglets due to the addition of Actigen™ in the diet.

Type
Original Research
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © Cambridge University Press and Journal of Applied Animal Nutrition Ltd. 2017

Introduction

Actigen™ (ACT) is a second generation, unique bioactive fraction derived from the outer cell wall of a specific strain of yeast, Saccharomyces cerevisiae, formulated to be used in animal diets. This yeast-derived product has been developed for more than twenty years, with a large body of research demonstrating its mode of action and efficacy in many species, especially where antibiotics have been removed from feeds. The active component attaches to the fibriae present on the surface of pathogenic bacteria, preventing their attachment and colonisation in the gut (Spring et al., Reference Spring, Wenk, Dawson and Newman2000). Its ability to interact with the gut wall and associated immune moieties has been proven to promote immune-competence in young animals, especially when suckling and at weaning (Brennan et al., Reference Brennan, Graugnard, Paul and Xiao2012). In sows, it makes more nutrients available, due to the removal of competition for nutrients by gut microflora, leading to better maintenance of body condition, more piglets born and improved return to service intervals (Miguel et al., Reference Miguel, Rodriguez-Zas, Pettigrew, Lyons and Jacques2002; Le Dividich et al., Reference Le Dividich, Martel-Kennes and Coupel2009; Lazarevic et al., Reference Lazarevic, Spring, Shabanovic, Tokic and Tucker2010).

Commercial trials with gestating and lactating sows have proven that ACT can increase immunoglobulin (Ig) expression in milk (Spring et al., Reference Spring, Geliot and Newman2003) thereby promoting immune protection in young piglets. The prevention of competition for nutrients in sows due to better gut health, as well as immune status, body composition and feeding regime can have a major influence not only on Ig status, but also on colostrum and milk quality, allowing piglets better availability of nutrients from the start of suckling (Fahmy, Reference Fahmy1972; Klobasa et al., Reference Klobasa, Werhan and Butler1987; Goransson, Reference Göransson1990; Zou et al., Reference Zou, McLaren and Hurley1992; Darragh and Moughan, Reference Darragh, Moughan, Moughan and Schrama1998). More efficient digestion with less competition for nutrients is important to maintaining sow condition, allowing her to return to service in a timely manner (Klaver et al., Reference Klaver, van Kempen, de Lange, Verstegen and Boer1981). These changes lead to fewer digestive disorders and diarrhoea at weaning, and better productive performance through to slaughter weight in growing and finishing pigs. In recent trials conducted in 2014 in a commercial pig breeding herd monitored for a 12 month period, ACT supplementation in sow diets prior to parturition gave improved milk Ig levels by 59% and piglet birth weight was increased by 0.19 kg relative to unsupplemented control sows and their litters (McArdle, unpublished).

When piglets undergo weaning, their own acquired immunity needs to be robust enough to prevent digestive problems that can reduce growth performance and welfare. Changing from a milk-based to a cereal-based diet resulted in changes in the gut and increased enzyme secretion which can impact digestion and uptake of nutrients. Ensuring the successful transfer of piglets from milk to meal is essential for productive performance, as each extra 100 g in body weight at weaning is considered equivalent to one day less to reach final slaughter weight, saving time, labour and feed costs (Cooper et al., Reference Cooper, Patience, Zijlstra and Rademacher2001). Heavier weaners are considered more efficient at converting feed into gain, and have leaner carcasses at slaughter. Over a twelve month period where a commercial pig breeding herd was monitored, 0.61 more piglets were born per litter, with a 0.5 kg higher average weaning weight at 1.5 days earlier from ACT supplemented sows (Alltech, personal communication). After weaning, time to service was reduced by 0.6 days. Such improvements could have major economic implications for pig producers. Therefore, the objective of the following trial was to evaluate the effect of supplementing ACT in feed throughout the gestation and lactation on both sow and piglet performance.

Materials And Methods

Two hundred and sixty sows and their litters were used in the trial. The sows were crossbred, using JSR Genepacker 90 (LWxLR) and PIC Camborough (LWxLR) xWhite Duroc), with a JSR 900 sire being used for breeding the trial piglets. All pigs were sourced from the Harper Adams University sow herd. PMWS was present in the herd but with low mortality (<3% post-weaning), and the herd was PRRS and enzootic pneumonia positive, and vaccinated accordingly for both.

Sows were allocated to one of two dietary treatments – either a control (unsupplemented) diet or one containing ACT (Alltech Inc. KY) at 0.08% of the total diet formulation. Sows were allocated to diets on the basis of genotype and equalised for parity between treatments. Pens containing eight sows each were allocated to the dietary treatments and these animals remained in the same group throughout gestation. Animals that returned to oestrus and were re-bred stayed within their group but were housed separately when pen mates moved to the farrowing room, which occurred seven to eight days prior to farrowing. Farrowing pens were fully slatted crate systems arranged in two rooms with sows allocated evenly between rooms.

All sows were fed to appetite from previous litter weaning to mating and then restricted to 2.4 kg per day supplied via volumetric dispensers during gestation. Sows received the lactation ration when they entered the farrowing house and were fed 2.5 kg per day until farrowing, whereby the amount rose on the standard Stotfold scale (a standardised feeding strategy for sows) to 11 kg per day depending on litter size. Sows were weighed on entry and exit of the farrowing house. Milk replacer was made available to piglets from birth, and prestarter feed from day 14. Milk replacer was formulated containing whey protein, palm and coconut oil and premix. The prestarter diet main ingredients comprised whey protein, full fat soya, oat flakes, palm oil and wheat with premix to balance. Piglets received 1.3 litres of milk replacer each and were offered 0.85 kg of prestarter diets.

Diets were formulated to meet NRC (2012) requirements and based on commercial (UK) gestation and lactation rations (Table 1). Diets were manufactured by a UK national feed compounder as 3 mm pellets. Milk replacer and piglet feed composition and analyses are shown in Table 2.

Table 1. Diet specifications and nutrient analysis

NB Treatment diets contained 0.08% ACT.

*all as % unless otherwise stated in first column.

Table 2. Analysis of milk replacer and prestarter diets for piglets

All piglets were tagged and individually weighed at birth and at approximately three days of age and at weaning. Any cross fostering was done within the first 24 hours within treatments and recorded for each piglet. Feed intake was measured on a daily basis and averaged per sow when group-housed, or expressed on an individual basis in the farrowing house. During lactation, weekly feed intakes were calculated at seven day intervals. The actual duration of gestation was calculated for each sow, and no farrowing was induced. The weaning to first service and effective service intervals were recorded post-weaning. Total piglets born, numbers alive, stillborn, mummified, fostered, joint ill incidence and all health treatments and mortality were recorded. Pigs were observed daily for signs of ill health. Sick animals were treated as necessary and recorded by ear tag including the reason for treatment, medication received, date and duration of treatment. For welfare reasons, sick piglets were removed and the weight recorded. Mortality was recorded on an individual piglet basis.

The trial was run according to Harper Adams University standards of ethical treatment of animals. Data was analysed using the GLM procedure of UNISTAT release 5.5 (London, UK), with confidence limits sets at 95% (P < 0.05).

Results

At the start of the trial, there were no significant differences between the control group or ACT-fed groups of sows. From entry into crates until farrowing, feed intake was higher for the sows fed ACT (P = 0.0014), however intake was significantly lower for the sows fed ACT during the first two weeks post-farrowing (data not shown), leading to an overall decrease in total feed consumed for the ACT group (P = 0.0128; Table 3).

Table 3. Performance of sows fed control or ACT-supplemented feeds during gestation and lactation

1Sows house 7-8 days pre farrowing. Means with different superscripts vary significantly (P < 0.05). 2Although offered on the Stotfold scale for intake, sows were allowed to eat to their biological requirement.

Piglets from sows fed ACT were significantly heavier at birth (P = 0.0009) compared to those from the control group. Sows fed ACT had more piglets at day three and weaning (Table 4), with the ACT sow litters being younger and more numerous (P < 0.05) compared to the control. Litter weight at weaning was significantly higher (P = 0.0395) and the piglets were 0.6 days younger in litters from sows fed ACT versus the control group.

Table 4. Effects of ACT fed to sows on piglet litters

Means with different superscripts vary significantly (P < 0.05).

Discussion

Feeding ACT to sows during gestation and lactation had various benefits, including reduced feed costs due to decreased feed intake post-farrowing. The piglets from the ACT supplemented group were heavier at birth and weaning, more numerous and attained weaning at a younger age compared to the control group. As the ACT supplemented sows consumed less feed during lactation, this suggested that milk production and quality was enhanced by supplementary ACT, despite intakes being significantly lower, and hence sows were using feed more efficiently without loss in body weight. This is in agreement with the published work of Miguel et al. (Reference Miguel, Rodriguez-Zas, Pettigrew, Lyons and Jacques2002) and Lazarevic et al. (Reference Lazarevic, Spring, Shabanovic, Tokic and Tucker2010) who reported that ACT supplements made more nutrients available to the sow, by promoting correct gut microflora, promoting body weight and reproductive performance. Although not measured in this trial, it may be assumed (based on previous data) that the sows fed ACT would have had higher levels of Ig in their colostrum and increased milk nutrient profiles, both of which would have improved piglet health, viability and growth. Maintaining sow body weight, achieving heavier piglets at weaning, requiring less time to attain weaning and reduced wean to oestrus intervals are all important to the economics of pig production. Time, labour and feed costs are saved by weaning piglets earlier. In addition, heavier piglets at weaning have been shown to need less time to reach target slaughter weights - which has been calculated at one day saved for each 100 g higher weaning weight (Cooper et al., Reference Cooper, Patience, Zijlstra and Rademacher2001). In the case of this trial, nearly half a day was saved.

Conclusions

The trial demonstrated various economic and performance benefits for sows and their piglets when gestation and lactation diets were supplemented with ACT. Such improvements in performance and reductions in feed costs demonstrated a net improvement of £22 per sow (at current pricing on trial date) per year, which amounted to 3.8:1 return on investment in the breeding herd. This was attributed to the combination of performance factors that were enhanced by feeding ACT. Economics of pig production, and benefits in early piglet growth are typically carried over throughout the growing period until slaughter weight, and it would be expected that pigs from dams fed ACT would have higher subsequent growth rates and higher carcass yields at slaughter.

Acknowledgements

The authors would like to thank Alltech Inc. for their financial support of this project.

Declaration of Interest

Dr. Jules Taylor-Pickard and Mr. Terry McArdle are employees of Alltech Biotechnology Centre, Ireland.

References

Brennan, K.M., Graugnard, D.E., Paul, M. and Xiao, R. (2012) Effect of maternal Actigen supplementation during gestation and lactation on piglet gut development and gene expression. Journal of Animal Science, 90: 390, 2012Google Scholar
Cooper, D.R., Patience, J.F., Zijlstra, R.T. and Rademacher, M. (2001) Effect of nutrient intake in lactation on sow performance: Determining the threonine requirementof the high producing lactating sow. Journal of Animal Science, 79: 23782387 Google Scholar
Darragh, A.J. and Moughan, P.J. (1998) The Composition of Colostrum and Milk. In: The Lactating Sow (Eds: Moughan, Verstegen and Schrama, ) Wageningen Press, Wageningen, Netherlands pp. 321 Google Scholar
Fahmy, M.H. (1972) Comparative study of colostrum and milk composition of seven breeds of swine. Canadian Journal of Animal Science, 52: 621627 CrossRefGoogle Scholar
Göransson, L. (1990) The effect of late pregnancy feed allowance on the composition of the sow's colostrum and milk (sic). Acta Veterinaria Scandinavia, 31: 109115 Google Scholar
Klaver, J., van Kempen, G.J.M., de Lange, P.G.B., Verstegen, M.W.A. and Boer, H. (1981) Milk composition and daily yield of different milk components as affected by sow condition and lactation/feeding regimen. Journal of Animal Science, 52: 10911097 Google Scholar
Klobasa, F., Werhan, E. and Butler, J.E. (1987) Composition of sow milk during lactation. Journal of Animal Science, 64: 14581466 Google Scholar
Lazarevic, M., Spring, P., Shabanovic, M., Tokic, V. and Tucker, L.A. (2010) Effect of gut active carbohydrates on plasma IgG concentrations in piglets and calves. Animal, 4: 938943.Google Scholar
Le Dividich, J., Martel-Kennes, Y. and Coupel, A. (2009) Bio-Mos in diets for sows: effects on piglet performance. Journees Recherche Porcine, 41: 249250 Google Scholar
Miguel, J.C., Rodriguez-Zas, S.L. and Pettigrew, J.E. (2002) Practical responses to Bio-Mos in nursery pigs: a meta-analyses. In: Nutritional biotechnology in the feed and food industry. (Eds: Lyons, and Jacques, ) Nottingham University Press, UK.Google Scholar
National Research Council (2012) Nutrient Requirements of Swine.Google Scholar
Spring, P., Geliot, P. and Newman, K.E. (2003) Effect of dietary mannan oligosaccharide in sow diets on performance of sows and nursing piglets. Proceedings of the 9th Symposium on Vitamins and Additives in Nutrition of Man and Animals. Jena/Thurinigia, Germany.Google Scholar
Spring, P., Wenk, C., Dawson, K.A. and Newman, K.E. (2000) The effects of dietary mannanoligosaccharides on cecal parameters and the concentrations of enteric bacteria in the ceca of salmonella-challenged broiler chicks. Poultry Science, 79: 205211.Google Scholar
Zou, S., McLaren, D.G. and Hurley, W.L. (1992) Pig colostrum and milk composition: comparisons between Chinese Meishan and US breeds. Livestock Production Science, 30: 115127.CrossRefGoogle Scholar
Figure 0

Table 1. Diet specifications and nutrient analysis

Figure 1

Table 2. Analysis of milk replacer and prestarter diets for piglets

Figure 2

Table 3. Performance of sows fed control or ACT-supplemented feeds during gestation and lactation

Figure 3

Table 4. Effects of ACT fed to sows on piglet litters