Strategies to Optimize Gastrointestinal Functionality in Piglets

In Brief
 
  • Optimizing piglets’ gut function is key to minimizing post-weaning transient diarrhea and helping to avoid antibiotic usage
  • A dual strategy can help optimize gut function: supporting gastrointestinal functionality and creating a less favorable environment for pathogens. 

For producers to raise healthy pigs and to avoid the use of antibiotics, it is critical the piglet has optimal gastrointestinal functionality. However, around weaning there are significant challenges that make this goal difficult to achieve. Optimal gastrointestinal functionality is a situation where the welfare, health and performance of the pig is not constrained by intestinal dysfunction (Celi et al., 2017).  To achieve optimal gastrointestinal functionality, there has to be effective digestion and absorption of the feed which requires a normal and stable microbiota, appropriate structure and function of the mucosa and a balanced immune system.

Supporting the piglet at weaning starts with supporting the gut. The gut provides three important functions: it regulates nutrient and fluid uptake, it plays a role in the immune system, and it provides a barrier to the external environment. In nature, the piglet is weaned over many weeks in a gradual, prolonged process which permits full development of these functions. However, in commercial production, the weaning process is an abrupt one-day event which brings many challenges to the three essential functions of the gut, culminating in the most commonly reported problem in weaned pigs globally of post-weaning diarrhea, sometimes resulting from leaky gut syndrome. 

Leaky gut syndrome

Leaky gut syndrome is characterized by hyper-permeability of the intestinal epithelium.  A failure in tight-junction functionality results in an increase in paracellular transfer of deleterious compounds (such as bacteria and undigested nutrients) from the intestinal lumen. These deleterious compounds activate the NFkB pro-inflammatory cytokine cascade causing an increased production of reactive oxygen species such as peroxides to fight the microbes but which can also cause collateral damage to cells. Pathogens, such as enterotoxigenic E. coli (ETEC) are then able to adhere to the intestinal cells and produce toxins that induce a loss of water and electrolytes from the cells resulting in diarrhea (Gresse et al., 2017). In addition to diarrhea, the other outcomes of the enteric infection such as reduced feed intake, weight loss, fever, poor feed efficiency and lack of uniformity are easily seen by the producer.  What is not easily seen though is the underlying increased production of pro-inflammatory cytokines and acute phase proteins that the enteric infection triggers.  The production of these compounds significantly modifies qualitatively and quantitatively the requirement for specific nutrients such as amino acids, vitamins, minerals, antioxidants and lipids.

The severity of leaky gut syndrome is impacted by direct and indirect factors. The direct factors include allergens and antigens that activate the pro-inflammatory cytokine cascade that cause gut inflammation.  Allergens can originate from feed and the most prevalent in piglet diets originate from soybean meal. Antigens can also originate from feed and include components such as mycotoxins, but can also originate in the gut lumen from cellular debris (peptidoglycans) originating from cell walls of dead gram-positive bacteria (McCormack et al., 2020).

The indirect factors contributing to the severity of leaky gut syndrome are the facilitators of a gut environment that supports the growth of pathogens both in terms of the substrates they need to grow and the environment in which they live in. 

The dual strategy to reduce leaky gut syndrome are outlined in Figure 1.  

Strategies to support optimum gastrointestinal functionality

  1. Deactivate glycinin with a targeted protease. A major and common allergen found in many swine feeds are the soybean proteins of glycinin and B-conglycinin.  These two proteins typically account for about 75% of the protein fraction of soybeans or 25-35% of the seed weight (Hammond et al., 2016). These soy allergens increase the permeability of the intestine which induces a local immune response leading to sensitization, resulting in impaired gut homeostasis and functionality. Using a targeted protease to deactivate glycinin has shown to decrease pro-inflammatory cytokines in plasma and reduce the permeability of the jejunal barrier (Park et al., 2020).
  2. Deactivate mycotoxins. Mycotoxins, particularly compounds such as deoxynivalenol and fumonisins are also known to disrupt tight junction protein function and further facilitate absorption of other mycotoxins and compounds from the gut. Effective deactivation of mycotoxins has shown to improve weight gain of piglets and prevent intestinal histology damage (Maching, 2015).

Strategies to create a less favorable gut environment for pathogens

  1. Use enzymes to mitigate E. coli risk and improve nutrient digestibility. In addition to the allergens, soybean meal also contains protease inhibitors which interfere with the activity of trypsin and or chymotrypsin, essential endogenous enzymes for protein digestion. While heat treatment during soybean meal production can mitigate some of the protease inhibitor effects, if destruction of the protease inhibitors is not complete, the undigested protein in the diet can be fermented in the hindgut and lead to the production of toxic nitrogen containing metabolites and diarrhea (Jha and Berrocoso, 2016). The presence of viscous fiber has also been shown to support the growth of gram-negative bacteria which are known to have negative effects on gastrointestinal functionality and overall health of the pig (Hopwood et al., 2004). Use of enzymes targeting the soluble non-starch polysaccharide component of the diet have been shown to reduce the viscosity of the digesta and mitigate the risk of pathogenic E. coli growth and lead to improved nutrient digestibility and animal performance as seen by average daily gain improvements and reductions in watery diarrhea (Kim et al., 2011).
  2. Deactivating the antinutrient effect of phytate. Dietary phytic acid is known to bind nutrients and enzymes in the stomach and small intestine which can decrease digestibility and increase nutrient flow to the hindgut (Woyengo and Nyachoti, 2013).  Furthermore, the high negative charge density of phytic acid results in strong complexing of cations such as iron as well as calcium, zinc and magnesium (Humer et al., 2014) and therefore may provide a valuable source of iron for supporting pathogen growth in the hindgut. Use of phytases to hydrolyze phytic acid and therefore reduce the negative effects of phytic acid on nutrient flow to the hindgut and mineral binding has been shown to be an effective strategy (Lee and Stahl, 2001). 
  3. Change the pH of the digesta. Changing the pH environment of the digesta to favor inhibition rather than proliferation is another effective strategy to reduce pathogen growth. Using an ultra-pure benzoic acid to reduce the pH of the digesta to 5.5 has been shown to effectively reduce the growth of E. coli compared to other acids. Furthermore, when ultra-pure benzoic acid was added to piglet diets, a significant and dose dependent response on the pH of the digesta in the stomach and small intestine was observed (Knarreborg et al., 2002).

Conclusion

Reducing the need for medications post-weaning relies on supporting the piglet gut that causes diarrhea and supporting optimum gastrointestinal functionality. The achievement of this objective requires a multifaceted approach that is not dependent on a single product strategy, but encompasses a comprehensive nutrition approach. In contrast, to tackle this challenge, success lies in the use of tailormade solutions that support a normal gut environment that is not favorable for pathogen growth.

References

  1. P.Celi, A.J.Cowieson, F.Fru-Nji, R.E.Steinert, A.-M.Kluenter, V.Verlhac. Gastrointestinal functionality in animal nutrition and health: New opportunities for sustainable animal production. Animal Feed Science and Technology, Volume 234, December 2017, Pages 88-100
  2. Gresse R, Chaucheyras-Durand F, Fleury MA, Van de Wiele T, Forano E, Blanquet-Diot S. Gut Microbiota Dysbiosis in Postweaning Piglets: Understanding the Keys to Health. Trends Microbiol. 2017 Oct;25(10):851-873. doi: 10.1016/j.tim.2017.05.004. Epub 2017 Jun 8. PMID: 28602521.
  3. Ursula M McCormack, Mikkel Klausen, Lisa A Laprade, Sonja Christian, Carsten Østergaard Frederiksen, Maria C Walsh, Tsungcheng Tsai, Charles V Maxwell, Casey L Bradley. The effect of a microbial Muramidase on peptidoglycan content in the gut of swine using in-vitro and in-vivo measures, Journal of Animal Science, Volume 98, Issue Supplement_3, November 2020, Pages 79–80, https://doi.org/10.1093/jas/skaa054.142
  4. E.G. Hammond, L.A. Johnson and P.A. Murphy. In Chapter “Soybean: Grading and Marketing”, pages 25-28 of the ‘Encyclopedia of Food Grains’ 2nd Edition (2016) edited by Colin Wrigley, Harold Corke, Koushik Seetharaman and Jon Faubion. Elsevier.
  5. Sangwoo Park, Jung Wook Lee, Aaron J Cowieson, Guenter Pappenberger, Tofuko Awori Woyengo. Soybean meal allergenic protein degradation and gut health of piglets fed protease-supplemented diets.  Journal of Animal Science, Volume 98, Issue 10, October 2020, skaa308, https://doi.org/10.1093/jas/skaa308
  6. Maching, S. Effects of Mycofix Plus 5.E on performance and intestinal histology of pigs fed diets naturally contaminated with DOPN, ZEN and FUM. Trial Report, MPL 5E_S_EN_AT06-0915
  7. Wolf, A., Underhill, D. Peptidoglycan recognition by the innate immune system. Nat Rev Immunol 18, 243–254 (2018). https://doi.org/10.1038/nri.2017.136
  8. Rajesh Jha and Julio F.D.Berrocoso. Dietary fiber and protein fermentation in the intestine of swine and their interactive effects on gut health and on the environment: A review. Animal Feed Science and Technology.  Volume 212, February 2016, Pages 18-26 https://doi.org/10.1016/j.anifeedsci.2015.12.002
  9. Deborah E Hopwood, David W Pethick, John R Pluske, David J Hampson. Addition of pearl barley to a rice-based diet for newly weaned piglets increases the viscosity of the intestinal contents, reduces starch digestibility and exacerbates post-weaning colibacillosis. Br J Nutr. 2004 Sep;92(3):419-27. doi: 10.1079/bjn20041206.
  10. Woyengo, T. A. and Nyachoti, C. M. Review: Anti-nutritional effects of phytic acid in diets for pigs and poultry – current knowledge and directions for future research. Can. J. Anim. Sci. 2013: 93: 9–21.
  11. E. Humer, C. Schwarz, K. Schedle. Phytate in pig and poultry nutrition. Journal of Animal Physiology and Animal Nutrition. 2014: https://doi.org/10.1111/jpn.12258
  12. Lei, X. G. and Stahl, C. H. Biotechnological development of effective phytases for mineral nutrition and environmental protection. Applied Microbiology & Biotechnology. Oct 2001, Vol. 57 Issue 4, p474-481.
  13. Knarreborg, A.; Miquel, N.; Granli, T.; Jensen, B. B. Establishment and application of an in vitro methodology to study the effects of organic acids on coliform and lactic acid bacteria in the proximal part of the gastrointestinal tract of piglets. Animal Feed Science and Technology 99, 131–140 (2002).

Published on

18 July 2022

Tags

Share

You are being redirected.

We detected that you are visitng this page from United States. Therefore we are redirecting you to the localized version.