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PREBIOTICS
• Prebiotic is a selectively fermented ingredient that
allows specific changes, both in the composition and/or
activity in the gastrointestinal microbiota that confers
benefits upon host wellbeing and health (Gibson et al.,
2004).
• Common prebiotics in use include inulins,
fructooligosaccharides (FOS), galacto-oligosaccharides
(GOS), soya-oligosaccharides, xylo-oligosaccharides,
pyrodextrins, isomalto-oligosaccharides and lactulose.
• The majority of studies carried out to date have focused
on inulin, FOS, MOS and GOS (Macfarlane et al., 2008).
Regurgitates crop
contents & feeds
chicks
Reduced flora,
Sterile crops !!
Characteristics of a prebiotic:
Neither hydrolysed nor absorbed.
Selective substrate for one / limited number of
bacteria
Should have known structure
Should be palatable as food ingredient
Mechanism of action of prebiotic:
Modulation of gut microbiota:
- Increases Bifidobacterium and Lactobacilli
- Ferment Non-digestible CHO to SCFA
- Reduce clostridium, Bacteroides, enterococci &
enterobacter sps
Intestinal morphology:
- ↑es no.of epithelial cells
- ↑es length and width of colonic crypts.
- Also alters epithelial cell junction bonding
structures.
- ↑es mucus secretion (Lactococci)
Lowering gut pH:
Inhibits certain growth of pathogens by increasing
the conc. of lactic acid and thereby decreasing pH in
the lower gut.
Phytic acid:
- stimulatory effect on Zinc and iron absorption.
- ↑ed phytate hydrolysis – enhanced breakdown of
phytate.
- SCFA forms soluble ligands with cations to
prevent formation of insoluble mineral phytates.
Preventing colonization:
Gram –Ve bacteria adhere to the intestinal cells of
host with type 1 fimbriae – enables pathogen to
cause disease.
Yeoman et al.(2012)
- Mannose binds the type 1 fimbriae – carry’s
through the git without colonization.
Stimulation of the immune system:
- Beneficial effects on gut associated lymphoid
tissue (GALT) and mucosal immune system (MALT).
- Increase in secretory IgG & IgA
- Butyrate suppresses cytokine induced and
constitutive expression of NFKB in HT29 cell lines.
- Bind to G-coupled receptors on immune cells with
in GALT.
Lipid metabolism:
• Reduction in the activities - hepatic lipogenesis
enzymes;
- FAS,
- Malic enzyme,
- ATP citrate lyase,
- Acetyl -coA carboxylase,
- Glucose -6-phosphate 1-dehydrogenase.
 Fructo-oligosaccharides and manna –
oligosaccharides are most studied prebiotics.
Fructo-oligosaccharides (Inulin):
Short form of oligofructose
Present in Onion, Garlic, Wheat, Chikory
(Cichorium intybus), Jerusalem Artichoke
(Helianthus tuberosus), banana.
Not easily digested due to β (2-1) fructosyl –
fructose units (osidic bond).
Manufacturing procedures of prebiotics:
1. Direct extraction from plants.
2. Controlled enzyamatic hydrolysis of High – DP –
polysaccherides.
3. Enzymatic – catalysed syntesis via microbeal
action of simple sugars.
Chicory plant
Jerusalem
artichoke
- Selectively fermented by Bifidobacteria &
stimulates growth of Bifidobacteria
- ↑es Butyrogenic effect
- Stimulates growth of epithelial cells & mucosa.
Mannanoligosaccharides (MOS):
- Synthesized from cell wall of Saccharomyces
cerevisiae
- Mannose – bind to receptors of bacteria & carried
out.
Galacto-oligosaccharides:
- Produced from lactose.
- 2 – 8 saccheride units with 1 terminal glucose.
- Synthesized by β – galactosidase enzymes.
- 1.) Glucosyltransferases – more yield
2.) Glycohydrolases
Author Methodology Conclusion
Sobolewska
et al.2017
- 5000 eggs were
Injected.
- SYN1 L. salivarius
IBB3154 + Bi2tos, Clasado Ltd.
(2 mg prebiotic
+105 bacteria/egg), and
- SYN2 L. plantarum + lupin
RFOs (2 mg prebiotic
+105 bacteria/egg).
- Control 0.9% Nacl
- Increased the day old bodyweight in
both groups (P<0.05)
- Villi in ileum are wider & deeper crypts
in Syn 2 group than SYN1 in day old.
- On 42nd day no differences b/W 2
groups.
- In jejenum on day 1 wider villi &
deeper crypts were observed in SYN1
group.
- No observable diff in BWG & FCR on
42nd d.
Author Methodology Conclusion
Tavaniello et
al.2018
4 groups injected in ovo with
0.2 mL solution
containing:
1) 3.5 mg/embryo BI (Bi2tos,
transgalactooligosaccharides);
2) 0.88 mg/embryo DN
(DiNovo, extract of Laminaria
spp.);
3)1.9 mg/embryo RFO
(raffinose family
oligosaccharides) and
4) 0.2 mL physiological
saline (C).
- All prebiotics increased breast muscle weight
and yield (P < 0.01).
- Intestinal pH was low in T3 group
- Saturated fatty acid (SFA), polyunsaturated
fatty acid (PUFA) and n-3 fatty acids
contents were higher (P < 0.01), and
monounsaturated fatty acid (MUFA) level
was lower (P < 0.01) in prebiotic groups
compared with C group.
- BWG & carcass yield were higher in T3
group
Author Methodology Conclusion
Naila Chand
et al. 2016
Group A - control; group B
was contaminated with
Eimeria tenella, while groups
C and D were infected with E.
tenella and treated with MOS
(0.8 g/kg feed) and
anticoccidial drug, amprolium
hydrochloride (12 g/
100 l water), respectively.
- BWG were higher in MOS + E.tenella
(2150) vs Amprolium + E.tenella
(2057)
- FI higher in MOS + E.tenella (3279) vs
Amprolium + E.tenella (3171)
- FCR MOS + E.tenella 1.5 vs 1.54
Amprolium + E.tenella
Kim et
al.2011
6 groups
control, avilamycin (6 mg/
kg), 0.25% FOS, 0.5% FOS,
0.025% MOS, and 0.05%
MOS. Each
- Clostridium perfringens and E. coli
decreased with 0.25% FOS, 0.05% MOS, or
avilamycin, and lactobacilli increased in the
0.25% FOS and 0.25% MOS treatment
groups.
- Except for 0.5% FOS group bwg were higher
in all other groups.
- No diff in FI & FCR.
Conclusion:
Supplementation of prebiotics have beneficial
effects
- At 0.25% of FOS & MOS have more pronounced
effects
- Increases the intestinal beneficial bacteria like
Lactobacilli & Bifidobacteria increases epithelial
cells.
- Increases immunity
- Reduces the colonisation of pathogenic bacteria &
improves meat quality.
References:
1) Sobolewska, A., Bogucka, J., Dankowiakowska, A., Elminowska-
Wenda, G., Stadnicka, K., & Bednarczyk, M. (2017). The impact of
synbiotic administration through in ovo technology on the
microstructure of a broiler chicken small intestine tissue on the 1
st and 42 nd day of rearing. Journal of animal science and
biotechnology, 8(1), 61.
2) Tavaniello, S., Maiorano, G., Stadnicka, K., Mucci, R., Bogucka, J.,
& Bednarczyk, M. (2018). Prebiotics offered to broiler chicken
exert positive effect on meat quality traits irrespective of delivery
route. Poultry Science.
3) Kim, G. B., Seo, Y. M., Kim, C. H., & Paik, I. K. (2011). Effect of
dietary prebiotic supplementation on the performance, intestinal
microflora, and immune response of broilers. Poultry
Science, 90(1), 75-82.
4. Mirza, R. A. (2018). Probiotics and Prebiotics
for the Health of Poultry. In Probiotics and
Prebiotics in Animal Health and Food Safety (pp.
127-154). Springer, Cham.

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Benefits of Prebiotics for Poultry Health and Performance

  • 2. • Prebiotic is a selectively fermented ingredient that allows specific changes, both in the composition and/or activity in the gastrointestinal microbiota that confers benefits upon host wellbeing and health (Gibson et al., 2004). • Common prebiotics in use include inulins, fructooligosaccharides (FOS), galacto-oligosaccharides (GOS), soya-oligosaccharides, xylo-oligosaccharides, pyrodextrins, isomalto-oligosaccharides and lactulose. • The majority of studies carried out to date have focused on inulin, FOS, MOS and GOS (Macfarlane et al., 2008).
  • 3. Regurgitates crop contents & feeds chicks Reduced flora, Sterile crops !!
  • 4. Characteristics of a prebiotic: Neither hydrolysed nor absorbed. Selective substrate for one / limited number of bacteria Should have known structure Should be palatable as food ingredient
  • 5. Mechanism of action of prebiotic: Modulation of gut microbiota: - Increases Bifidobacterium and Lactobacilli - Ferment Non-digestible CHO to SCFA - Reduce clostridium, Bacteroides, enterococci & enterobacter sps
  • 6. Intestinal morphology: - ↑es no.of epithelial cells - ↑es length and width of colonic crypts. - Also alters epithelial cell junction bonding structures. - ↑es mucus secretion (Lactococci) Lowering gut pH: Inhibits certain growth of pathogens by increasing the conc. of lactic acid and thereby decreasing pH in the lower gut.
  • 7. Phytic acid: - stimulatory effect on Zinc and iron absorption. - ↑ed phytate hydrolysis – enhanced breakdown of phytate. - SCFA forms soluble ligands with cations to prevent formation of insoluble mineral phytates. Preventing colonization: Gram –Ve bacteria adhere to the intestinal cells of host with type 1 fimbriae – enables pathogen to cause disease. Yeoman et al.(2012)
  • 8.
  • 9. - Mannose binds the type 1 fimbriae – carry’s through the git without colonization. Stimulation of the immune system: - Beneficial effects on gut associated lymphoid tissue (GALT) and mucosal immune system (MALT). - Increase in secretory IgG & IgA - Butyrate suppresses cytokine induced and constitutive expression of NFKB in HT29 cell lines. - Bind to G-coupled receptors on immune cells with in GALT.
  • 10. Lipid metabolism: • Reduction in the activities - hepatic lipogenesis enzymes; - FAS, - Malic enzyme, - ATP citrate lyase, - Acetyl -coA carboxylase, - Glucose -6-phosphate 1-dehydrogenase.
  • 11.  Fructo-oligosaccharides and manna – oligosaccharides are most studied prebiotics. Fructo-oligosaccharides (Inulin): Short form of oligofructose Present in Onion, Garlic, Wheat, Chikory (Cichorium intybus), Jerusalem Artichoke (Helianthus tuberosus), banana. Not easily digested due to β (2-1) fructosyl – fructose units (osidic bond).
  • 12. Manufacturing procedures of prebiotics: 1. Direct extraction from plants. 2. Controlled enzyamatic hydrolysis of High – DP – polysaccherides. 3. Enzymatic – catalysed syntesis via microbeal action of simple sugars.
  • 14. - Selectively fermented by Bifidobacteria & stimulates growth of Bifidobacteria - ↑es Butyrogenic effect - Stimulates growth of epithelial cells & mucosa.
  • 15. Mannanoligosaccharides (MOS): - Synthesized from cell wall of Saccharomyces cerevisiae - Mannose – bind to receptors of bacteria & carried out.
  • 16.
  • 17. Galacto-oligosaccharides: - Produced from lactose. - 2 – 8 saccheride units with 1 terminal glucose. - Synthesized by β – galactosidase enzymes. - 1.) Glucosyltransferases – more yield 2.) Glycohydrolases
  • 18. Author Methodology Conclusion Sobolewska et al.2017 - 5000 eggs were Injected. - SYN1 L. salivarius IBB3154 + Bi2tos, Clasado Ltd. (2 mg prebiotic +105 bacteria/egg), and - SYN2 L. plantarum + lupin RFOs (2 mg prebiotic +105 bacteria/egg). - Control 0.9% Nacl - Increased the day old bodyweight in both groups (P<0.05) - Villi in ileum are wider & deeper crypts in Syn 2 group than SYN1 in day old. - On 42nd day no differences b/W 2 groups. - In jejenum on day 1 wider villi & deeper crypts were observed in SYN1 group. - No observable diff in BWG & FCR on 42nd d.
  • 19. Author Methodology Conclusion Tavaniello et al.2018 4 groups injected in ovo with 0.2 mL solution containing: 1) 3.5 mg/embryo BI (Bi2tos, transgalactooligosaccharides); 2) 0.88 mg/embryo DN (DiNovo, extract of Laminaria spp.); 3)1.9 mg/embryo RFO (raffinose family oligosaccharides) and 4) 0.2 mL physiological saline (C). - All prebiotics increased breast muscle weight and yield (P < 0.01). - Intestinal pH was low in T3 group - Saturated fatty acid (SFA), polyunsaturated fatty acid (PUFA) and n-3 fatty acids contents were higher (P < 0.01), and monounsaturated fatty acid (MUFA) level was lower (P < 0.01) in prebiotic groups compared with C group. - BWG & carcass yield were higher in T3 group
  • 20. Author Methodology Conclusion Naila Chand et al. 2016 Group A - control; group B was contaminated with Eimeria tenella, while groups C and D were infected with E. tenella and treated with MOS (0.8 g/kg feed) and anticoccidial drug, amprolium hydrochloride (12 g/ 100 l water), respectively. - BWG were higher in MOS + E.tenella (2150) vs Amprolium + E.tenella (2057) - FI higher in MOS + E.tenella (3279) vs Amprolium + E.tenella (3171) - FCR MOS + E.tenella 1.5 vs 1.54 Amprolium + E.tenella Kim et al.2011 6 groups control, avilamycin (6 mg/ kg), 0.25% FOS, 0.5% FOS, 0.025% MOS, and 0.05% MOS. Each - Clostridium perfringens and E. coli decreased with 0.25% FOS, 0.05% MOS, or avilamycin, and lactobacilli increased in the 0.25% FOS and 0.25% MOS treatment groups. - Except for 0.5% FOS group bwg were higher in all other groups. - No diff in FI & FCR.
  • 21. Conclusion: Supplementation of prebiotics have beneficial effects - At 0.25% of FOS & MOS have more pronounced effects - Increases the intestinal beneficial bacteria like Lactobacilli & Bifidobacteria increases epithelial cells. - Increases immunity - Reduces the colonisation of pathogenic bacteria & improves meat quality.
  • 22. References: 1) Sobolewska, A., Bogucka, J., Dankowiakowska, A., Elminowska- Wenda, G., Stadnicka, K., & Bednarczyk, M. (2017). The impact of synbiotic administration through in ovo technology on the microstructure of a broiler chicken small intestine tissue on the 1 st and 42 nd day of rearing. Journal of animal science and biotechnology, 8(1), 61. 2) Tavaniello, S., Maiorano, G., Stadnicka, K., Mucci, R., Bogucka, J., & Bednarczyk, M. (2018). Prebiotics offered to broiler chicken exert positive effect on meat quality traits irrespective of delivery route. Poultry Science. 3) Kim, G. B., Seo, Y. M., Kim, C. H., & Paik, I. K. (2011). Effect of dietary prebiotic supplementation on the performance, intestinal microflora, and immune response of broilers. Poultry Science, 90(1), 75-82.
  • 23. 4. Mirza, R. A. (2018). Probiotics and Prebiotics for the Health of Poultry. In Probiotics and Prebiotics in Animal Health and Food Safety (pp. 127-154). Springer, Cham.