Effects Of Β-mannanase Supplementation Research Articles

Effects of β-Mannanase Supplementation and Soyhull Inclusion on Production Performance, Economics, Egg Quality, Blood Biochemicals, Nutrient Digestibility, and Intestinal Morphology in Golden Brown Hens (RIR × Fayoumi) during Late Peak Production.

This study investigated the effects of the β-mannanase enzyme and soyhulls on production performance, economics, egg quality, hematology and serum biochemistry, nutrient digestibility, gut morphology, digesta viscosity, and excreta consistency in laying hens during the late peak production phase (37 to 40 weeks of age). Golden brown hens (RIR × Fayoumi; n = 200) were fed a control diet (no soyhulls or enzymes) and diets containing four combinations, i.e., 3% soyhulls with 20 mg/kg β-mannanase (D1), 3% soyhulls with 30 mg/kg β-mannanase (D2), 9% soyhulls with 20 mg/kg β-mannanase (D3), and 9% soyhulls with 30 mg/kg β-mannanase (D4), for four weeks in four replicates of 10 birds each. Overall, a significantly higher (p < 0.05) feed intake, weight gain, feed conversion ratio, and water intake were calculated in the D2 group as compared to the control and remaining combinations of soyhulls and β-mannanase. No mortality was recorded during the entire experiment. Economically, the D1 and D2 groups showed the best results as compared to the D3 and D4 groups. Egg quality parameters like egg weight, shell weight and shell thickness, yolk weight, albumen weight and height, and the Haugh unit remained unchanged (p > 0.05). Similarly, the D2 group showed significantly lower total cholesterol, LDL, and VLDL levels and enhanced gut morphology with greater villus width, height, crypt depth, and surface area across intestinal segments. Crude protein (CP), crude fiber (CF), crude fat, and ash digestibility were higher (p < 0.05) in the D1 and D2 groups compared to the control. Digesta viscosity, excreta consistency, and other egg quality parameters remained unaffected. In conclusion, the dietary inclusion of a combination of 3% soyhulls and 30 mg/kg β-mannanase may have potential benefits for laying hens by improving some production performance and egg quality indicators and economics, lowering blood cholesterol, LDL, and VLDL levels, enhancing nutrient digestibility, and improving gut morphology without affecting egg quality.

Effects of β-mannanase supplementation on productive performance, inflammation, energy metabolism, and cecum microbiota composition of laying hens fed with reduced-energy diets

The objective of this study is to investigate the beneficial effects and underlying mechanism of dietary β-mannanase supplementation on the productive performance of laying hens fed with metabolic energy (ME)-reduced diets. A total of 448 Hy-Line gray laying hens were randomly assigned to seven groups. Each group had 8 replicates with 8 hens. The groups included a control diet (CON) with a ME of 2750 kcal/Kg, diets reduced by 100 kcal/Kg or 200 kcal/Kg ME (ME_100 or ME_200), and diets with 0.15 g/Kg or 0.2 g/Kg β-mannanase (ME_100+β-M_0.15, ME_100+β-M_0.2, ME_200+β-M_0.15, and ME_200+β-M_0.2). The productive performance, egg quality, intestinal morphology, inflammatory response, mRNA expression related to the Nuclear factor kappa B (NF-κB) and AMPK pathway, and cecum microbiome were evaluated in this study. ME-reduced diets negatively impacted the productive performance of laying hens. However, supplementation with β-mannanase improved FCR, decreased ADFI, and restored average egg weight to the level of the CON group. ME-reduced diets increased the levels of interleukin-1β (IL-1β) and IL-6 while decreasing the levels of IL-4 and IL-10 in the jejunum of laying hens. However, dietary β-mannanase supplementation improved jejunum morphology, reduced pro-inflammatory cytokine concentrations, and increased levels of anti-inflammatory factors in laying hens fed with ME-reduced diets. The mRNA levels of IL-6, IFN-γ, TLR4, MyD88, and NF-κB in the jejunum of ME-reduced diets were significantly higher than that in CON, dietary β-mannanase supplementation decreased these genes expression in laying hens fed with ME-reduced diets. Moreover, dietary β-mannanase supplementation also decreased the mRNA levels of AMPKα and AMPKγ, and increased the abundance of mTOR in the jejunum of laying hens fed with ME-reduced diets. Cecum microbiota analysis revealed that dietary β-mannanase increased the abundance of various beneficial bacteria (e.g., g_Pseudoflavonifractor, g_Butyricicoccus, and f_Lactobacillaceae) in laying hens fed with ME-reduced diets. In conclusion, dietary β-mannanase supplementation could improve the productive performance of laying hens fed with a ME-reduced diet by improving intestinal morphology, alleviating intestinal inflammation, changing energy metabolism-related signaling pathways, and increasing cecum-beneficial microbiota.

The effects of β-mannanase supplementation on growth performance, digestive enzyme activity, cecal microbial communities, and short-chain fatty acid production in broiler chickens fed diets with different metabolizable energy levels.

This study assessed the effects of β-mannanase (BM) supplementation on growth performance, digestive enzyme activity, cecal microbial communities, and short-chain fatty acid (SCFA) production in broiler chickens fed diets with different metabolizable energy (ME) levels. A total of 1,296 male 1-d-old Cobb 500 broilers were randomly distributed in a 3 × 2 factorial arrangement (3 ME levels × 0 or 200g/ton BM), with 6 replicates per treatment combination. The 3 ME levels were 3,000 (ME1), 2,930 (ME2), and 2,860 (ME3) kcal/kg, respectively, during the 0 to 3 wk-old stages and 3,150 (ME1), 3,080 (ME2), and 3,010 (ME3) kcal/kg, respectively, during the 3 to 6 wk-old stages. Reducing ME levels increased broiler feed intake (P = 0.036) and decreased average daily gain (ADG, P = 0.002) during the entire period. While BM supplementation increased ADG (P = 0.002) and improved the feed conversion ratio (P = 0.001) during the 0 to 3 wk-old stages, with no effect during the 3 to 6 wk-old stages. Overall, reducing ME levels increased pancreatic lipase (P = 0.045) and amylase (P = 0.013) activity and duodenal amylase activity (P = 0.047). Notably, BM supplementation significantly increased pancreatic lipase activity (P = 0.015) and increased lipase (P = 0.029) and amylase (P = 0.025) activities in the jejunal chyme. Although diet or enzyme supplementation did not affect microbial diversity, significant differences in microbial communities were observed. At the genus level, decreasing ME levels significantly affected the average abundances of Tyzzerella (P = 0.028), Candidatus_Bacilloplasma (P = 0.001), Vibrio (P = 0.005), and Anaerotruncus (P = 0.026) among groups, whereas BM supplementation reduced the average abundances of Escherichia-Shigella (P = 0.048) and increased the average abundances of Barnesiella (P = 0.047), Ruminococcus (P = 0.020), Alistipes (P = 0.050), and Lachnospiraceae_unclassified (P = 0.009). SCFA concentrations strongly depended on bacterial community composition, and BM supplementation increased acetic acid (P = 0.004), propionic acid (P = 0.016), and total SCFA concentrations. In conclusion, BM supplementation improved the performance of younger broilers, and both enzyme supplementation and reduced ME levels positively affected digestive enzyme activity and intestinal microflora.

Effects of β-mannanase supplementation on intestinal health and growth of nursery pigs.

Two experiments were conducted using 120 pigs to test the hypothesis that supplementation of β-mannanase could reduce digesta viscosity, enhance nutrient digestion, and improve intestinal health and growth of nursery pigs. In experiment 1, 48 crossbred barrows were randomly allotted to four treatments with increasing levels of β-mannanase at 0, 200, 400, and 600 U/kg in feeds. All pigs were euthanized on day 12 to collect jejunal digesta to measure digesta viscosity and ileal digesta to measure apparent ileal digestibility (AID) of dry matter (DM), gross energy (GE), neutral detergent fiber (NDF), and acid detergent fiber (ADF). In experiment 2, 72 nursery pigs were randomly allotted to three treatments with increasing levels of β-mannanase at 0, 400, and 600 U/kg in feeds. Plasma collected on day 9 was used to measure tumor necrosis factor-α (TNF-α), immunoglobulin G (IgG), malondialdehyde (MDA), and protein carbonyl (PC). All pigs were euthanized on day 10 to collect duodenal and jejunal tissues to evaluate the production of TNF-α, IL-6, and MDA, morphology, crypt cell proliferation, and expression of tight junction proteins in the jejunum. Data were analyzed using the MIXED procedure for polynomial contrasts and the NLMIXED procedure for broken-line analysis of SAS. In experiment 1, β-mannanase supplementation tended to have quadratic effects on digesta viscosity (P = 0.085) and AID of GE (P = 0.093) in the pigs. In experiment 2, jejunal digesta viscosity of the pigs was reduced (P < 0.05) when β-mannanase was supplemented at 360 U/kg of feed. β-Mannanase supplementation linearly reduced (P < 0.05) TNF-α, IgG, MDA, and PC in the duodenum, and TNF-α, IgG, and MDA in the jejunum of the pigs. β-Mannanase supplementation linearly increased (P < 0.05) villus height to crypt depth ratio and crypt cell proliferation in the jejunum. β-Mannanase supplementation tended to linearly improve (P = 0.083) expression of zonula occludens-1 in the jejunum. In conclusion, supplementation of β-mannanase at 360 U/kg reduced the digesta viscosity and up to 600 U/kg positively affected intestinal health and growth of pigs by reducing inflammation and oxidative stress whilst enhancing structure and barrier function in the jejunum.

Effect of β-Mannanase Supplementation on Growth Performance, Ileal Digestibility, Carcass Traits, Intestinal Morphology, and Meat Quality in Broilers Fed Low-ME Diets.

Simple Summaryβ-mannans, an example of non-starch polysaccharides, is one of the important anti-nutritional factors found in many leguminous feedstuffs used as raw material in poultry feed formulation. β-mannans bind to nutrients, reduce their bioavailability, and also increase the viscosity of intestinal digesta, which prevents the proper mixing of enzymes with digesta and affects the digestibility of nutrients. All these conditions ultimately reduce the growth performance of poultry birds. So, the objective of present study was to lower the effect of β-mannans by using β-mannanase in broiler diets. Results suggested that β-mannanase supplementation improved the intestinal morphology, which helped to increase the dry matter and crude fiber digestibility in broilers fed low energy diets. In addition, growth performance of broilers was not affected by reducing dietary energy levels with added β-mannanase than the Control group. Similarly, carcass traits were not affected by decreasing dietary energy levels with supplementation of β-mannanase. In conclusion, it could be stated that a low caloric diet with added β-mannanase had no negative effect on growth performance and carcass characteristics; however, it improved the dry matter and crude fiber digestibility.Experiment was designed to analyze the effect of low caloric diets, supplemented with β-mannanase on growth performance, carcass characteristics, nutrient digestibility, and other parameters in broilers. In this study, 400 broiler chicks were randomly divided into four treatments (Cont: without β-mannanase; LM-30, MM-60, and HM-90: supplemented with 200, 400, and 600 mg/kg β-mannanase, respectively). Dietary metabolizable energy (ME) in Cont was standard (starter diet 3100 kcal/kg; finisher diet 3200 kcal/kg) and reduced by 30, 60, and 90 kcal/kg, correspondingly in β-mannanase-supplemented treatments. The results exhibited that growth performance was not affected by reducing dietary energy levels with supplementation of β-mannanase. Ileal digestibility of DM and CF was improved (p < 0.01) by supplementation of β-mannanase at low dietary ME levels. Concerning carcass traits, the relative weight of breast meat, drumstick, and abdominal fat increased (p < 0.05) with β-mannanase supplementation in low-ME diets. Treatment HM-90 showed significantly (p < 0.05) better results regarding villus height and VH:CD. It could be concluded from the present results that supplementation of β-mannanase could improve the nutrient digestibility so that it is possible to reduce the dietary energy level without compromising production performance, carcass trails, and meat quality in broilers.

Performance responses of broilers and pigs fed diets with β-mannanase

ABSTRACT This study was developed using meta-analysis to evaluate the effect of β-mannanase on both poultry and pig performance. Two databases were constructed using information from previous studies that evaluated the β-mannanase supplementation in diets for broilers (30 papers; 19,643 birds) and pigs (20 papers; 5,319 animals). The meta-analysis followed three sequential analyses: graphical, correlation, and variance-covariance. The effect of β-mannanase supplementation on performance considerably varied in both databases. Data analysis considering the study effect showed that β-mannanase supplementation did [...]

Effects of β-mannanase supplementation on the intestinal microbiota composition of broiler chickens challenged with a coccidiosis vaccine

The objective of this study was to evaluate the diversity and composition of the ileal and cecal microbiota of broiler chickens supplemented with β-mannanase and subjected or not to a coccidiosis challenge. The treatments were: unsupplemented and unchallenged control; unsupplemented and challenged control; supplemented and unchallenged; supplemented and challenged. The enzyme was included in the feed throughout the entire experimental period at 400 mg/kg. The challenge consisted of 20x the recommended dose of a commercial coccidiosis vaccine applied on d14. Ileal and cecal microbiota were analyzed on d21 and 42 through 16S rRNA sequencing. On d21, Chao index decreased because of the challenge when compared to the unchallenged control treatment, but the supplementation of β-mannanase reverted this effect in both cecal and small intestinal microbiota. On d21, the cecal microbiota was dominated by members of the family Ruminococcaceae and Lachnospiraceae, followed by the genera Faecalibacterium and Bacteroides, and the order Clostridiales. The family Ruminococcaceae was increased (P ≤ 0.05) in the cecal microbiota of β-mannanase supplemented broiler chickens when compared to the unsupplemented. Overall, β-mannanase modulated the microbiota, leading to an increase of beneficial groups, such as Lactobacillus, Ruminococcaceae, and Akkermansia, and reduction of Bacteroides that is related to poor feed efficiency in broiler chickens.

Effects of β-mannanase supplementation on growth performance, nutrient digestibility, and nitrogen utilization of Korean native goat (Capra hircus coreanae)

The use of agricultural by-products possessing high β-mannan content as an animal feed ingredient has become increasingly important in achieving cost-effective agriculture. Recent studies showed improvement in growth performance from a diet containing high β-mannan concentrations by the addition of β-mannanase in monogastric animals. Few studies, however, have been conducted to examine the value of β-mannanase supplementation in ruminant diets. In the present study, the effects of β-mannanase supplementation on growth performance, nutrient digestibility, and nitrogen (N) utilization were investigated in growing Korean native goats (Capra hircus coreanae). Twelve Korean native goats (13±1.9kg) were divided into three groups and randomly allocated into one of the following treatments: (1) control (CON), (2) 0.1% β-mannanase supplementation (TRT1), or (3) 0.3% β-mannanase supplementation (TRT2) in a concentrate mix based on dry matter (DM). Diets composed of 40% of tall fescue hay and 60% of each concentrate mix were formulated to meet the National Research Council requirements for indigenous goats. No difference was observed among treatments in terms of DM intake and highest DM and organic matter digestibility (P<0.05) were observed in goats fed CON. However, β-mannanase supplementation significantly increased the average daily gain (P<0.05) and improved feed conversion ratio (P<0.05) as well as N retention (P<0.05). The N intake (P<0.05) and biological value (P<0.10) increased linearly by increasing the dosage of supplementation of β-mannnase. No difference was observed between the two levels of β-mannanase supplementation. In conclusion, β-mannanase supplementation may promote growth and feed efficiency in ruminant animals receiving feedstuffs with high β-mannan concentrations.