Effects of feeding the pomegranate pomace silage and dry pomegranate pomace on the intestinal microflora of Mehraban male lambs

Document Type : Research Paper

Authors

1 Department of Animal Science, School of Agriculture, Shiraz University, Shiraz, Iran

2 Department of Food Hygiene and Public Health, School of Veterinary Medicine, Shiraz University, Shiraz, Iran

3 Department of Animal Sciences, School of Agriculture, Shiraz University, Shiraz, Iran

Abstract

Introduction: The antibacterial and antifungal effects of pomegranates peel and seeds is associated with the presence of phenolic compounds (flavonoids and tannin) in them. These effects varies among different types of pomegranate. Aims: The aim of this study to investigate the effects of silage pulp (mixture of seed and pulp) and dry pulp of pomegranate seed on the growing of lactobacillus (profitable) and Escherichia coli (pathogen) bacteria in the digestive tract of fattening lambs. Methods: nine male lamb of Mehraban breed (average weighing of 27.03 ± 3.5 and mean age of 187.8 ± 1.4) were selected and fed on three experimental ration, with the same protein and energy values (including control diet, 27% of pomegranate peel silage and 31% of dried pomegranate seed pulp) for a period of 60 days. To count the microbial flora, one gram fresh samples of ilium and seccum were then collected. The microbial count was performed and reported as CFU (colony forming unit) per each gram of a sample. MRS and MacConky agars were respectively used to enumerate Lactobacillus and Escherchia coli. In a PCR assay a pair of species-specific were also used to confirm the E. coli. Results: The bacterial counts were not affected with the types of diets (p<0.05). A significant lower count of E. coli was shown in the intestinal flora of the lambs fed on the waste pomegranate compared to the control group (p<0.05). No significant difference was observed between the groups fed on the pomegranate silage. Conclusion: A considerable reduction in the E.coli count in the ilium and seccum of the lambs was an interesting findings.
These compounds accumulate in the skin and pomegranate juice and account for 92% of the antioxidant activity of pomegranates (Abid et al. 2017). Total tannins for pomegranate peel and pulp were reported to be 9.73 and 0.66%, respectively (Delavare et al. 2014). The different species of pomegranate have antibacterial and antifungal properties that can influence on a wide range of microorganisms (Carlton et al. 2000). Phenolic compounds in plants and foods by changing the gut microbial population can increase the amount of useful bacteria and reduce harmful bacteria (Katiyar et al. 2002).It has been found that intestinal microflora plays a critical role in the health of the digestive tract and is dependent on the ration as the final source for metabolism of organic compounds. (Choct et al. 1996), To our knowledge, the effects of pomegranate by-products have been investigated on livestock and rumen function, however their effects on the intestinal microflora in ruminants have not been addressed. Therefore due to the high concentration of tannins and phenolic compounds in the pomegranate by-products and their effect on intestinal microflora, the aim of this study was to investigate the effects of pomegranate pomace silage and pomegranate dry pomace on intestinal microflora in Mehraban fattening lambs.
Matherials and methods: Nine Mehraban male lambs (mean weight of 27.03±3.5 kg and mean age of 187.8±1.4 d), were fed on three iso-nitrogenous and iso-caloric experimental diets. Diets were balanced according to NRC (2007) recommendation including control diet, diet contain 27% pomegranate pulp silage and diet contain 31% dry pomegranate seed pulp. All three diets were fed for 60 d after 3 weeks for adaptation in individual pens with free access to salts lick and water. At the end of experiment all lambs were slaughtered and after than for enumeration of intestinal fluoromicrobes, one gram freshly digested specimens of ileum and cecum were collected. Samples were spread on the surface of agar medium. Colonies were counted by ophthalmic count and bacterial count was calculated as CFU/g (number of colonies per gram). The MRS agar and Maconkey (MC) medium were used for identification and enumeration of Lactobacillus spp and Escherichia coli respectively. All samples were incubated at 37ºC for 24 hours. All colonies were enumerated and recorded as CFU/g of culture suspension. For confirmation of Escherichia coli detection on McKonkey agar medium, polymerase change reaction (PCR) was conducted as DNA extraction using commercial kit (Bioneer, Sout Korea), polymerase change reactions, and electrophoresis of PCR products. Detection of molecular bacteria was done using the primers of 23S rRNA gene PCR. The PCR process was initial denaturation at 94 ºC for 2 minutes and totally 35 cycles, denaturation at 94 ºC for 45 seconds, and extension at 72 ºC for 2 minutes. All data was analyzed as a complete randomized design using SPSS software. Significant difference for means was considered at 0.05 level of differences.
Results and discussion: The results of this study showed that in MRS medium either in ilium or cecum, the number of lactobacillus bacteria in all groups were not statistically significant. The mean number of Escherichia coli decreased due to feeding of pomegranate by-products (P<0.05), while the type of pomegranate by-product has not significant effect on number of Escherichia coli. The importance role of gut microflora is well recognized in GIT health, although population of gut microbes has been influenced by diet (Choct et al 1996). In contrast of useful effects of lactobacillus on GIT, Escherichia coli damages the intestine of animals and produces lipopolysaccharide (Munyaka et al. 2012). Tannins are considered as a toxin to microorganisms; these compounds in the soluble environment produce some stable complexes, mainly with protein and to a lesser extent with carbohydrates or some physiological ions elements such as iron and copper (Chung and Chou 1998). The pomegranate peel extract at different levels has antimicrobial effect against microorganisms such as Staphylococcus aureus, Escherichia coli, Candida tropicalis and Candida albicans (Ahmed et al. 2013). The phenolic materials in pomegranate fruit, are responsible for the antimicrobial properties of pomegranates (Seeram et al. 2006). In the present study, reduction of Escherichia coli population in lambs fed pomegranate by-products can be attributed to the adverse effect of phenolic substances in the pomegranate by-products on Escherichia coli population. Several mechanisms have been introduced for antimicrobial properties of phenolic compounds in the pomegranate. Phenolic substances, with high molecular weight proteins, form complexes and by these complexes can react to the some cytoplasmic and membrane enzymes after absorption (Seeram et al. 2006). These complexes can also prevent cell surface receptors from attachment of harmful microorganisms (Cowan 1999). Phenolic compounds can react with the cellular proteins of microorganisms, alter cell wall structure and function (Hugo and Bloomfield 1971), reducing cell wall permeability and reducing substrate transport to cells (Goel et al. 2005). In addition, phenolic compounds can alter or denature some microbial enzymes, and also form complexes with certain nutrients and remove them from microorganisms (Hago and Bloomfield 1971). The decline of Escherichia coli can also be attributed to the increase in the number of Lactobacillus; because by increasing the Lactobacillus and consequently increasing the production of lactic acid and creating an acidic environment, the population of Escherichia coli is reduced due to sensitivity of Escherichia coli to acidic environment (Hammer et al. 1999).
Conclusion: Feeding of the pomegranate pomace silage and dry pomegranate pomace in fattening lambs, decreased the population of Escherichia coli in ileum and cecum, although lactobacillus bacteria was not affected by pomegranate by-products. It seems that the tannins and phenolic compounds present in the pomegranate can effect on Escherichia coli population in ileum and cecum.

Keywords


Abid M, Yaich H, Cheikhrouhou S, Khemakhem I, Bouaziz M, Attia H and Ayadi MA, 2017. Antioxidant properties and phenolic profile characterization by LC-MS/MS of selected Tunisian pomegranate peels. Journal of Food Science and Technology 54:2890-2901.
Adams LS, Zhang Y, Seeram NP, Heber D and Chen S, 2010. Pomegranate ellagitannin-derived compounds exhibit antiproliferative and antiaromatase activity in breast cancer cells in vitro. Cancer Prevention Research 3:108-113.
Ahmed SA, Abood NH and Al-Janabi AA, 2013. Antimicrobial effect of pomegranate peel extract on some pathogenic microorganisms. Engineering and Technology Journal 31:316-324.‏
Ahmet D, Duman A, Ozgen M, Dayisoylu K, Erbil N and Durgac C, 2009. Antimicrobial activity of six pomegranate (Punica granatum L.) varieties and their relation to some of their pomological and phytonutrient characteristics. Molecules 14:1808-1817.‏
Carlton PS, Kresty LA and Stoner GD, 2000. Failure of dietary lyophilized strawberries to inhibit 4-(methylnitrosamino)-1- (3-pyridyl)-1-butanone-and benzo [a] pyrene-induced lung tumorigenesis in strain A/J mice. Cancer Letters 159:113-7.
Caterina MJ, Schumacher MA, Tominaga M, Rosen TA, Levine JD and Julius D, 1997. The capsaicin receptor: A heat activated ion channel in the pain pathway. Nature 389:816-824.
Choct M, Hughes RJ, Wang J, Bedford MR, Morgan AJ and Annison G, 1996. Increased small intestinal fermentation is partly responsible for the anti‐nutritive activity of non‐starch polysaccharides in chickens. British Poultry Science 37:609-621.
Chung KT, Lu Z and Chou MW, 1998. Mechanism of inhibition of tannic acid and related compounds on the growth of intestinal bacteria. Food Chemical Toxicology 36:1053-1060.
Cowan MM, 1999. Plant products as antimicrobial agents. Clinical Microbiology Reviews 12:564-572.
Delavar MH, Tahmasbi MA, Danesh-Mesgaran M and Valizadeh R, 2014. In vitro rumen fermentation and gas production: Influence of different byproduct feedstuffs. Annual Research and Review in Biology 4:1121-1128.
Ebrahimi B, Taghizadeh A and Mehmannavaz Y, 2013. Ruminal degradation of pomegranate pomace using nylon bags technique. European Journal of Experimental Biology 3:260-262.
Estabraghi E, Sadeghpour M and Mehrabani A, 1397. Study of Pomegranate Hydromethanol Extract on Staphylococcus Aureus and Escherichia Coli by Microplate in Laboratory Conditions. Tehran Paramedical Journal 12: 183-192.
Goel G, Puniya AK, Aguilar CN and Singh K, 2005. Interaction of gut microflora with tannins in feeds. Naturwissenschaften 92:497-503.
Hammer KA, Carson CF and Riley TV, 1999. Antimicrobial activity of essential oils and other plant extracts. Journal of Applied Microbiology 86:985-990.
Hugo WB and Bloomfield SF, 1971. Studies on the mode of action of the phenolic antibacterial agent fentichlor against Staphylococcus aureus and Escherichia coli. 3. The effect of fentichlor on the metabolic activities of Staphylococcus aureus and Escherichia coli. Journal of Applied Bacteriology 34:579-591.
Katiyar SK, 2002. Treatment of silymarin, a plant flavonoid, prevents ultraviolet light induced immune suppression and oxidative stress in mouse skin. International Journal of Oncology 21:1213-1222.
Klaver FAM and Van der Meer R, 1993. The assumed assimilation of cholesterol by lactobacilli and Bifidobacterium bifidum is due to their bile salt deconjugating activity. Applied Environmental Microbiology 59:1120-1124.
Lei XJ, Yun HM and Kim IH, 2018. Effects of dietary supplementation of natural and fermented herbs on growth performance, nutrient digestibility, blood parameters, meat quality and fatty acid composition in growing-finishing pigs. Italian Journal of Animal Science 17:984-993.‏
Lilly DM and Stillwell RH, 1965. Probiotic: growth promoting factors produced by microorganism. Science 12:747-478
Munyaka PM, Tactacan G, Jing MKO, House JD and Rodriguez-Lecompte JC, 2012. Immunomodulation in young laying hens by dietary folic acid and acute immune responses after challenge with Escherichia coli lipopolysaccharide. Journal of Poultry Science 91:2454–2463.
National Research Council. NRC, 2007. Nutrient requirements of small ruminants: sheep, goats, cervids, and new world camelids. National Academy of Science, Washington DC. PP. 10036-10070.
 Nayebpor M, Farhomand P and Hashemi A, 2007. Effect of different levels of direct fed microbial (Primalac) on the growth performance and humoral immune response in broiler chickens. Journal of Animal Advances 6:1308-1313.
Riffon R, Sayasith K, Khalil H and Dubreuil P, 2001. Development of a rapid and sensitive test for identification of major pathogens in bovine mastitis by PCR. Journal of Clinical Microbiology 39:2584-2589.
Seeram NP, Schulman RN and Heber D, 2006. Pomegranates: Ancient roots to modern medicine. Medicinal and aromatic plants - Industrial profiles. Chemical Rubber Company Press Taylor and Francis Group.
Simitzis PE, 2017. Enrichment of animal diets with essential oils—A great perspective on improving animal performance and quality characteristics of the derived products. Medicines 35:1-21.
 Tongnuanchan P and Benjakul S, 2014. Essential oils: extraction, bioactivities, and their uses for food preservation. Journal of Food Science 7:1231-1249.