The Effect of Chemical Buffering and Microbial Additives on Histomorphometry and Histopathology of the Small and Large Intestine of Lambs Fed High Concentrate Diets

Document Type : Research Articles

Authors

1 Department of Animal Science, Faculty of Animal Science and Food Technology, Agricultural Sciences and Natural Resources University of Khuzestan, Mollasani, Ahvaz, Iran.

2 Ph.D. of Animal Nutrition, Kharazmi Industrial School, of Dezful, Iran

3 Department of Veterinary Medicine, Azad University of Yasoj, Yasij, Iran.

Abstract

Introduction: Intestinal function in nutrient uptake depends on its morphology, and any change in villi structure, as well as changes in the differentiation and development of absorbent cells, can alter digestion and absorption capacity and thus function. Increasing the height and surface of Villus in the gastrointestinal tract of animals consuming high concentrates increases the absorption capacity and in turn, protects the animal from the accumulation of volatile fatty acids and a noticeable decrease in pH. In fact, it helps the lining of the gastrointestinal tract absorb volatile fatty acids faster and stabilize the pH. High starch in diets, followed by a decrease in pH, affects the morphology of the rumen and intestine. Any change in this morphology may predispose the intestines to dysfunction. Megasphaera elsdenii prevents a sharp decrease in ruminal pH due to lactic acid accumulation by consuming lactic acid, and in cases of subacute acidosis by converting lactic acid to propionic acid may provide an opportunity to reduce inflammation and improve energy balance in livestock. Saccharomyces cerevisiae also contributes to the growth and activity of cellulose-degrading bacteria, lactate consuming bacteria, and rumen protozoa and the concomitant use of lactate consuming bacteria with Saccharomyces cerevisiae has been confirmed. Therefore, the aim of this study was to investigate the effect of chemical and microbial buffer additives on histomorphometry and histopathology of the small intestine and large intestine during high concentrate feeding.
 Materials and Methods: Twelve Arabi male sheep at 9 ± 1 months old and initial body weight of 35.95±3.55 kg were used in a completely randomized design with three treatments and four replicates, and the duration of the experiment was 35 days. The experimental treatments consisted of a 1- control diet, 2- control diet + sodium bicarbonate buffer, 3- control diet + Megasphaera elsdenii, and Saccharomyces cerevisiae (bacterial-yeast), which fed ad libitum. At the end of the experiment, the lambs were slaughtered and the small and large intestines were sampled for histomorphometry and histopathology studies. Each sample was placed separately in closed-sealed containers containing 10% formalin, and tissue changes were examined microscopically.
Results and Discussion: No significant difference was observed between the experimental treatments for the tissue indices studied in the duodenum and jejunum. However, the ratio of villus height to crypt depth in the bacterium-yeast recipient treatment was numerically higher than other treatments. In ileum section, villi height, crypt depth and villi area in control treatment 653.33; 506.67; 258.42 compared to buffer treatment 430.00; 328.33; 161.40 and treatment containing bacterial-yeast 445.00; 365.00; 178.04 respectively were significantly higher (P <0.05). In the present experiment, due to the consumption of a diet with high concentrate and possibly increased production of volatile fatty acids in the rumen and their transfer to later parts of the gastrointestinal tract, increased villi height, crypt depth, and villi area in different parts Intestine was observed especially in control treatment; In fact, one of the reasons for increasing the villi height and Villus surface in acidosis, is increased the absorption capacity of volatile fatty acids and help maintain pH of the rumen, Therefore, reducing these indices in chemical buffer and bacterial-yeast treatments can be the result of the positive effects of buffer and microbial additives such as improving the pH of ruminal fluid transferred to different parts of the intestine, as a result of increased activity of cellulolytic bacteria and more acetate production, which has caused relative control of acidosis in the control treatment. Improving the Villus height to crypt depth ratio in the duodenum and jejunum in treatments receiving chemical or microbial additives can be considered as positive results of using pH-adjusting additives in the present experiment. In different parts of the small intestine, in all three treatments, inflammation of the intestinal mucosa was observed in the form of infiltration of mononuclear inflammatory cells, including lymphocytes, plasma cells with different degrees of eosinophils. In the large intestine in the control treatment, hyperemia, the infiltration of inflammatory cells of lymphocytes, plasma cells, and eosinophils in small numbers in Lamina propria and labyrinth of Lieberkohen glands as well as necrosis of the villi was observed. In general, changes in intestinal tissues are to counteract the inflammation caused by acidosis.
Conclusion: In general, although the use of chemical buffering or microbial additives had a positive effect on the histomorphometry of the ileum, but did not have a positive effect on the histopathology of the small and large intestine. It is suggested that the present experiment be examined in the early stages of livestock growth when the microbial flora is not fully established.

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  1. Afzalzadeh, A., Sharifi, S. D., Absalan, M., Khadem, A., & Ghandi, D. (2013). Effect of whole cottonseed feeding on feedlot performance and morphological characteristics of small intestine in Chaal male lambs. Iranian Journal of Animal Science, 43(4), 457-464.‏ (In Persian). https://doi.org/10.22059/ijas.2013.30266
  2. Aschenbach, J. R., Zebeli, Q., Patra, A. K., Greco, G., Amasheh, S., & Penner, G. B., (2019). Symposium review: The importance of the ruminal epithelial barrier for a healthy and productive cow. Journal of Dairy Science, 102(2), 1866-1882. 3168/jds.2018-15243
  3. Attaix, D., & Meslin, J. C. (1991). Changes in small intestinal mucosa morphology and cell renewal in suckling, prolonged-suckling, and weaned lambs. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 261(4), 811-818. 1152/ajpregu.1991.261.4.R811
  4. De Barbieri, I., Hegarty, R. S., Silveira C., Gulino, L. M., Oddy, V. H., Gilbert, R. A., Klieve, A. V., & Ouwerkerk, D. (2015). Programming rumen bacterial communities in newborn Merino lambs. Small Ruminant Research, 129, 48–59. https://doi.org/10.1016/j.smallrumres.2015.05.015.
  5. DeClerck, J. C., Wade, Z. E., Reeves, N. R., Miller, M. F., Johnson, B. J., Ducharme, G. A., & Rathmann, R. J. (2020). Influence of Megasphaera elsdenii and feeding strategies on feedlot performance, compositional growth, and carcass parameters of early weaned, beef calves. Translational Animal Science, 4(2), 863-75. https://doi.org/10.1093/tas/txaa031
  6. Diao, Q., Zhang, R., & Fu, T. (2019). Review of strategies to promote rumen development in calves. Animals, 9(8), 490.‏ 3390/ani9080490
  7. Erdman, R. A., Botts, R. L., Hemken, R.W. & Bull, L.S. (1980). Effect of dietary sodium bicarbonate and magnesium oxide on production and physiology in early lactation. Journal of Dairy Science, 63(6), 923-930. https://doi.org/10.3168/jds.S0022-0302(80)83027-X
  8. Garcia Diaz, T., Ferriani Branco, A., Jacovaci, F. A., Cabreira, C., Jobim Bolson, D. C., & Pratti Daniel, J. L. (2018). Inclusion of live yeast and mannan-oligosaccharides in high grain-based diets for sheep: Ruminal parameters, inflammatory response and rumen morphology. PloS One, 13(2), e0193313. https://doi.org/10.1371/journal.pone.0193313
  9. Jayaraman, S., Thangavel, G., Kurian, H., Mani, R., Mukkalil, R., & Chirakkal, H. (2013). Bacillus subtilis PB6 improves intestinal health of broiler chickens challenged with Clostridium perfringens-induced necrotic enteritis. Poultry Science, 92(2), 370-374. https://doi.org/10.3382/ps.2012-02528
  10. Khorasani,, Chaji, M., & Baghban, F. (2020). Comparison of the effect of sodium bicarbonate buffer with Megasphaera elsdenii as a rumen-consuming acid on growth performance, digestibility, rumen and blood parameters of lambs in high concentrate. Journal of Animal Science Researches, 30(2), 85-99.‏ (In Persian).
  11. Khorasani,, Chaji, M., & Baghban, F. (2021). Effect of chemical buffer and Megasphaera elsdenii-yeast on histomorphometry and histopathology of rumen and liver of Arabian fattening lambs fed with concentrated diets. Animal Production, 23(1), 47-59. (In Persian). https://doi.org/10.22059/jap.2021.307867.623553
  12. Krause, K. M., & Oetzel, G. R. (2006). Understanding and preventing subacute ruminal acidosis in dairy herds: A review. Animal Feed Science and Technology, 126(3-4), 215-236. https://doi.org/10.1016/j.anifeedsci.2005.08.004
  13. Lechartier, C., & Peyraud, J. L. (2011). The effects of starch and rapidly degradable dry matter from concentrate on ruminal digestion in dairy cows fed corn silage-based diets with fixed forage proportion. Journal of Dairy Science, 94(5), 2440-2454. https://doi.org/10.3168/jds.2010-3285
  14. Lei, X., Piao, X., Ru, Y., Zhang, H., Péron, A., & Zhang, H. (2015). Effect of Bacillus amyloliquefaciens-based direct-fed microbial on performance, nutrient utilization, intestinal morphology and cecal microflora in broiler chickens. Asian-Australasian Journal of Animal Sciences, 28(2), 239-246. 5713/ajas.14.0330
  15. Li, G. H., Ling, B. M., Qu, M. R., You, J. M., & Song, X. Z. (2011). Effects of several oligosaccharides on ruminal fermentation in sheep: an in vitroRevue de Medecine Veterinaire, 162, 192-197.
  16. Malekkhahi, M., Tahmasbi, A. M., Naserian, A. A., Danesh-Mesgaran, M., Kleen, J. L., Al-Zahal, O., & Ghaffari, M. H. (2016). Effects of supplementation of active dried yeast and malate during sub-acute ruminal acidosis on rumen fermentation, microbial population, selected blood metabolites, and milk production in dairy cows. Animal Feed Science and Technology, 213, 29-43. https://doi.org/10.1016/j.anifeedsci.2015.12.018
  17. Mashayekhi, R., Erfani-majd, N., Sari, M., & Rezaei, M. (2020). Investigating the effects of slow-release urea and molasses on histomorphometric tissue of rumen and abomasum and rumen fermentation parameters of fattening lamb. Iranian Veterinary Journal, 16(1), 82-93. (In Persian). 10.22055/IVJ.2019.151750.2077
  18. Mohammadabadi, T., Bakhtiari, M. A., & Alimirzaei, P. (2018). Isolation and identification of lactate-producing and utilizing bacteria from the rumen of najdi goats. Indian Journal of Small Ruminants, 24(2), 276-280. 5958/0973-9718.2018.00056.9
  19. NRC. (2007). Nutrient Requirements of Small Ruminants: Sheep, Goats, Cervids and New World Camelids. National Academy Press Washington DC.
  20. Odongo, N. E., AlZahal, O., Lindinger, M. I., Duffield, T. F., Valdes, E. V., Terrell, S. P., & McBride, B. W. (2006). Effects of mild heat stress and grain challenge on acid-base balance and rumen tissue histology in lambs. Journal of Animal Science, 84(2), 447-455. 2527/2006.842447x
  21. Pinloche, E., McEwan, N., Marden, J. P., Bayourthe, C., Auclair, E., & Newbold, C. J. (2013). The effects of a probiotic yeast on the bacterial diversity and population structure in the rumen of cattle. PloS One, 8(7), e67824.
  22. Prabhu, R., Altman, E., & Eiteman, M. A. (2012). Lactate and acrylate metabolism by Megasphaera elsdenii under batch and steady-state conditions. Applied and Environmental Microbiology, 78, 8564-8570. https://doi.org/10.1371/journal.pone.0067824
  23. Rose, B. D. (1989). Clinical physiology of acid-base and electrolyte disorders, 3rd Mc Grow Hill Inc. Singapore, 261-268: 478- 501
  24. Sedighi, R., & Alipour, D. (2019). Assessment of probiotic effects of isolated Megasphaera elsdenii strains in Mehraban sheep and Holstein lactating cows. Animal Feed Science and Technology, 248, 126-131. https://doi.org/10.1016/j.anifeedsci.2019.01.007
  25. Steele, M. A., Penner, G. B., & Chaucheyras-Durand, F. (2016). Development and physiology of the rumen and the lower gut: Targets for improving gut health. Journal of Dairy Science, 99(6), 4955-4966.‏ 3168/jds.2015-10351
  26. Stone, W.C. (2004). Nutritional approaches to minimize subacute ruminal acidosis and laminitis in dairy cattle. Journal of Dairy Science, 87, 13–26. https://doi.org/10.3168/jds.S0022-0302(04)70057-0
  27. Strusińska, D., Minakowski, D., Bomba, G., Otrocka-Domagała, I., Wiśniewska, M., & Tywończuk, J. (2009). Effect of whole cereal grains contained in the ration on calf performance and selected morphometric parameters of the rumen and small intestine. Czech Journal of Animal Science, 54(12), 540-551. 17221/133/2009-CJAS
  28. Vi, R. B., McLeod, K. R., Klotz, J. L., & Heitmann, N. (2004). Rumen development, intestinal growth and hepatic metabolism in the pre-and postweaning ruminant. Journal of Dairy Science, 87, 55-65. https://doi.org/10.3168/jds.S0022-0302(04)70061-2
  29. Wang, Y. H., Xu, M., Wang, F. N., Yu, Z. P., Yao, J. H., Zan, L. S., & Yang, F. X. (2009). Effect of dietary starch on rumen and small intestine morphology and digesta pH in goats. Livestock Science, 122(1), 48-52. https://doi.org/10.1016/j.livsci.2008.07.024
  30. Yáñez-Ruiz, D. R., Macías, B., Pinloche, E., & Newbold, C. J. (2010). The persistence of bacterial and methanogenic archaeal communities residing in the rumen of young lambs. FEMS Microbiology Ecology, 72(2), 272–278. 1111/j.1574-6941.2010.00852.x

 

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