Combination of an Enzymatically Hydrolyzed Yeast and Yeast Culture with a Direct-fed Microbial in the Feeds of Broiler Chickens

Article information

Asian-Australas J Anim Sci. 2012;25(5):665-673
Publication date (electronic) : 2012 May 01
doi : https://doi.org/10.5713/ajas.2011.11316
1Private practice. Veracruz, Veracruz, México.
2Vi-Cor, 905 S Caroline Ave (50401) PO Box 1483, Mason City, IA. 50402, USA.
*Corresponding Author: S. Gómez. Tel: +52-419-2920033, Fax: +52-419-2920033, E-mail: gomez.sergio@inifap.gob.mx
National Center of Disciplinary Research in Animal Physiology, Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias, Ajuchitlán, Querétaro, CP 76280, México
Received 2011 September 05; Revised 2012 January 09; Accepted 2011 December 07.

Abstract

A balance trial experiment was carried out to evaluate the potential relationship between an enzymatically hydrolyzed yeast (EHY) and yeast culture combined with a live Bacillus subtilis (Bs) on the productive parameters, ileal digestibility, retention of nutrient and energy and villus morphology in broilers. Seventy two 28 d old, Ross B308 male broilers were assigned to a factorial combination of 2 levels of EHY (0 and 1 kg/ton of feed) and 2 levels of Bs (0 and 125 g/ton of feed). The experiment lasted 2 weeks. Several treatment interactions were observed. EHY-fed broilers showed the lowest feed intake and feed conversion ratio whereas Bs-fed broilers showed the highest feed intake and intermediate feed conversion ratio (EHY and BS interaction, p<0.05). Also, EHY-fed broilers had greater ileal digestibility of dry matter (EHY and BS interaction, p<0.01) and energy (EHY and BS interaction, p<0.05) but these responses were counterbalanced by the combination of EHY and Bs. The thickness of the mucosa was similar between the control and EHY-fed broilers, but was lowest when Bs was added alone (EHY and BS interaction, p<0.01). The thickness of the villus was greater in EHY plus Bs-fed broilers, intermediate for the control and lower for Bs or EHY-fed broilers (EHY and BS interaction, p<0.05). The area of the villus was greater in the control and EHY plus Bs-fed broilers (EHY and BS interaction, p<0.05). In addition, EHY-fed broilers showed greater breast yield and nitrogen retention (p<0.01) and ashes digestibility (p<0.05). On the other hand, Bs-fed broilers had greater carcass and breast weight, nitrogen retention, energy excretion and villus height (p<0.05). In summary, EHY and Bs enhanced some growth, carcass and nutrient retention responses, but did not show any synergic relationship in these responses. Opposite to this, the results suggest that the positive effect of EHY on the feed conversion and digestibility of nutrients were counterbalanced by the addition of Bs.

INTRODUCTION

For many years it has been recognized that the use of antibiotics growth promoters (AGP) enhance the efficiency of growth and health of poultry. However, potential dangers associated with the development of resistant pathogenic bacteria after long use of AGP have also been documented, forcing poultry industry to consider other biologically safe alternatives (Ratcliff, 2000; Ferket et al., 2002). Currently, there is considerable evidence showing that the inclusion of mannanoligosaccharide (MOS) in poultry feeds improves the growth and feed conversion ratio, and is considered one of the best options for AGP replacement (Hooge, 2004; Rosen, 2007). Some advantages of MOS over AGP are: i) No withdrawal period required before slaughter; ii) No residual effect on poultry products; and iii) No bacterial mutation which could lead to resistance in pathogenic bacteria.

It is proposed that the benefits of MOS is due to the presence of mannose units that binds potential pathogenic bacteria, particularly those with type 1 fimbria on their surface, blocking their adhesion and colonization of the intestinal cells (Mul and Perry, 1994). It has been suggested that MOS favors the growth of beneficial bacteria such as Lactobacillus which are capable of neutralizing some enterotoxins and inhibiting the growth of pathogenic bacteria like E. coli, Clostridium and Streptococcus by producing organic acids and reducing the intestinal pH (Spring et al., 2000). This can lead to better gut health and increased nutrient availability resulting in enhanced growth and health of poultry (Radecki and Yokoyama, 1991; Stanley et al., 2004). There is also considerable evidence showing that whole cells and several derivatives from yeast such as yeast culture (YC), yeast extracts (YE) and yeast fermentation products, that retain the cell wall components, exert similar beneficial effects as MOS on the growth and feed conversion ratio of poultry (Stanley et al., 2004; Zhang et al., 2005; Gao et al., 2009).

On the other hand, some authors have reported that the combination of an oligosaccharide such as MOS and an appropriate probiotic (symbiotic products) could increase the efficacy above that of both products used separately (Bailey et al., 1991; Fukata et al., 1999; Sun et al., 2004). Bacillus is one of the microorganisms used in broilers as direct-fed microbial (DFM), which also favor the development of Lactobacillus and depresses the growth of pathogenic bacteria such as E. coli, Clostridium, Streptococcus and Salmonella leading to improved growth and feed conversion ratio of poultry. This information suggests that both, MOS and Bacillus, enhance the proliferation of beneficial microbes, and inhibit the multiplication of harmful microbes in the gut.

It is probably that MOS and Bacillus together may increase the digestibility of feeds since the first may increase the disaccharidase activity on the intestinal brush-like border, and the second, may release digestive enzymes during the spore germination (Gedek, 1999). By stimulating the proliferation of Lactobacillus, MOS and Bacillus may also help the digestion process since some research has shown that Lactobacillus increases the level of amylase in the intestine of host chickens, helping the starch digestion (Jin et al., 2000) and is, itself, a good source of digestive enzymes such as amylase, protease and lipase (Panda et al., 2000).

It has been reported that MOS and Bacillus may increase the intestinal absorptive area by increasing the villus height in different portions of the gut (Macari and Maiorka, 2000; Loddi, 2003; Pelicano et al., 2003) resulting in higher nutrient digestion and absorption. It has been reported as well that MOS and Bacillus combined may reduce the depth of the crypt, due to a lower enterocyte replacement rate, and by increasing the villus density in the duodenum (Pelicano et al., 2005b). This suggests that combining MOS and Bacillus may lead to an improvement in health, growth, and digestive processes.

Since there are several sources of MOS, yeast derivatives, and Bacillus (or DFMs) commercially available for broilers, it is important to test the effectiveness of these products against each other or in combination. Therefore, the main issue addressed in the present study was to elucidate if there was any additive or synergistic relationship between a product containing yeast derivatives (Celmanax®) and a product containing a live Bacillus subtilis (GalliPro®) in different digestive responses.

Celmanax® is a trade mark of Vi-Cor® (Mason City, IA, USA) that contains enzymatically hydrolyzed yeast (EHY), YE and YC. Celmanax® also contains yeast mannans and provides the metabolites normally found in YC and can replace yeast-based products in the diet. Heat-tolerant GalliPro® is a registered trademark owned by Chr. Hansen (Hoersholm, Denmark) which is a probiotic feed ingredient, also called DFM. GalliPro® is based on the naturally-occurring superior high activity strain of Bacillus subtilis. Therefore, the present balance experiment was carried out to evaluate the potential relationship between an enzymatically hydrolyzed yeast (EHY) and yeast culture combined with a live Bacillus subtilis (Bs) on the production, ileal digestibility, retention of nutrient and energy, and villus morphology in broilers.

MATERIALS AND METHODS

Birds and treatments

In the experiment, 72 (28 days of age) Ross B308 male broilers individually housed in holding mesh-floored cages with a metal feeder and a cup drinker in a naturally ventilated unit were used. Broilers were randomly allotted to four treatments in a complete randomized design with a factorial combination of 2 levels of EHY (0 and 1 kg/ton of feed) and 2 levels of Bs (0 and 125 g/ton of feed). Monensin (500 g/ton) was added to all diets. Diets were formulated according to the nutrient recommendations of Ross for growing broilers (Table 1).

Diet composition

Management and sampling

Water was provided ad libitum. Broilers were weighed at the beginning and end of the 2 wk trial. Feed was offered ad libitum during the first 10 days. Then feed allowance was limited to 90% of the ad libitum intake during the last four days of the trial and in this period, excreta were totally collected. Feed offered during the excreta collection was added with 0.25% chromic oxide as internal marker for determination of the ileal digestibility of nutrients. On the last day of the trial, all broilers were killed by cervical dislocation. The ileum was excised and its content was collected in polyethylene bags and immediately stored on ice. The ileum was considered the portion of the small intestine limited by the Meckel’s diverticulum and the ileocecal valve. The ileal contents from three broilers per treatment were pooled and each one of these samples was considered one observation. A portion of 5 cm of duodenum was obtained from eight broilers per treatment. The duodenum content was rinsed with 10% formalin and the end points were tied up with silk. Then, 2 ml of formalin were injected to each portion and placed in plastic bottles filled with formalin. Carcass was dissected and its main components (breast, legs and thighs) were rinsed with clean water, dried and weighed.

Laboratory determinations

Excreta and ileal contents were lyophilized and ground using a 2 mm mesh. Determinations of dry matter, ashes, nitrogen, and energy were done in excreta, ileal contents and diets following standard procedures (AOAC, 1992). Chromium was also analyzed in diets and ileal contents. Then, the ileal digestibility and retention of nutrients were estimated. Duodenal portions were fixed in formalin, dehydrated with an alcohol-xylene sequence, and embedded in paraffin. Three pieces of 5-μm slices were prepared and stained with hematoxylin-eosin. Mucosa thickness, villus height and thickness and crypt depth from each slice were measured (μm). The villus area and villi height/crypt depth ratio (VCR) were also estimated. Readings were carried out under light microscope. About 15 measurements were done per bird.

Statistical analysis

Results were subjected to ANOVA by using the GLM procedures (SAS, 1995). For growth performance, carcass measurements, nutrient retention and villi morphology the experimental unit was each broiler, but for the ileal digestibility of nutrients, the experimental unit was a group of three broilers. Percentage results were transformed to arcsine values before analysis.

RESULTS

Growth performance and carcass measurements

The EHY and Bs interaction was significant for feed intake and feed conversion ratio (Table 2). When EHY was added alone, broilers showed the lowest feed intake and feed conversion ratio whereas Bs-fed broilers showed the highest feed intake and intermediate feed conversion ratio (EHY and BS interaction, p<0.05). EHY-fed broilers, either alone or combined with Bs, also showed a greater breast yield (p<0.01).

Productive and carcass measurements in broilers fed an enzymatically hydrolyzed yeast and yeast culture combined with a live Bacillus subtilis

Bs-fed broilers showed a trend for greater weight gain (p<0.10). The carcass and breast weight were improved (p<0.05) and there was a non-significant trend for greater carcass yield (p<0.10) with Bs in comparison to the control group.

Ileal digestibility

The EHY and Bs interaction was significant for the ileal digestibility of dry matter and energy (Table 3). EHY-fed broilers had greater ileal digestibility of dry matter (EHY and BS interaction, p<0.01) and energy (EHY and BS interaction, p<0.05) but these responses were counterbalanced by the combination of EHY and Bs. EHY-fed broilers showed higher (p<0.05) ashes digestibility. There was also a trend (p<0.07) for higher ileal nitrogen digestibility in EHY-fed broilers compared to the control group.

Ileal digestibility and retention of nutrients in broilers fed an enzymatically hydrolyzed yeast and yeast culture combined with a live Bacillus subtilis

Nutrient retention

EHY-fed broilers had improved nitrogen retention (p<0.01) and a trend for lower energy excretion (p<0.09; Table 3). Bs-fed broilers showed a positive trend of lower (p<0.07) dry matter and nitrogen excretion and had greater (p<0.05) nitrogen retention and lower (p<0.05) energy excretion compared to the control group.

Villi morphology

The EHY and Bs interaction was significant for several measurements (Table 4). The thickness of the mucosa was similar between the control and EHY-fed broilers, but was lowest when Bs was added alone (EHY and BS interaction, p<0.01). The villus height was similar between the control and EHY-fed broilers, but there was a trend of being lower when Bs was added alone (EHY and BS interaction, p<0.07). The thickness of the villus was greater in EHY plus Bs-fed broilers, intermediate for the control and lower for Bs or EHY-fed broilers (EHY and BS interaction, p<0.05). The area of the villus was greater in the control and EHY plus Bs-fed broilers (EHY and BS interaction, p<0.05).

Histological measurements of the duodenum in broilers fed an enzymatically hydrolyzed yeast and yeast culture combined with a live Bacillus subtilis

EHY-fed broilers showed non-significant trends of higher thickness of the mucosa (p<0.10) and depth of the crypts (p<0.08). Whereas Bs-fed broilers had greater thickness of the mucosa (p<0.01), height of the villi and depth of the crypts (p<0.05).

DISCUSSION

An improved feed conversion ratio shown by EHY-fed broilers is in agreement with previous findings observed in broiler fed diets supplemented with yeast. In a meta-analysis of trials of MOS-fed broilers a positive effect of MOS was observed in 80% of the studies, with an average relative improvement of 1.6 and 1.99% in weight gain and feed conversion ratio, respectively (Hooge, 2004). In this experiment, the feed conversion ratio was improved by 4.4% in EHY-fed broilers. In a recent publication from our laboratory, a 6.9 and 3.8% improvement in weight gain and feed conversion ratio was reported in broilers fed the same EHY product, from 35 to 49 d of age, as that used in the present research (Gomez and Angeles, 2011). Improved growth performance have been reported in broilers fed YC, YC residue, whole cells, cell wall components or a fermentation product from yeast (Stanley et al., 2004; Zhang et al., 2005; Gao et al., 2008, 2009). The greater breast yield in EHY-fed broilers is in agreement to other results observed in broiler fed yeast added diets. Greater weight and yield of the carcass and breast was reported by Gomez and Angeles (2011) in EHY-fed broilers. Clementino dos Santos (2002) reported increased breast yield in MOS-fed broilers. The addition of dried yeast in broilers resulted in higher carcass weight and yield (Adejuno et al., 1999; Onifade et al., 1999; Miazzo et al., 2005). Also, the inclusion of live yeast increased the carcass yield on free-range chicken (Pelicia et al., 2004).

In several studies, substantial improvements in weight gain and feed conversion of broilers supplemented with different types of Bacillus have been observed (Santoso et al., 1995; Gil-Turnes et al., 2007; Opalinzki et al., 2007). In a research including four floor experiments, improvements were also reported in body weight gain and feed conversion ratio in Bs-fed broilers (Hooge et al., 2004). These findings agree with our results since Bs-fed broilers showed better performance and carcass yield compared to the control group. On the other hand, Pelicano et al. (2004; 2005a,b) did not find benefits on the growth performance or carcass yield in broilers fed diets added with different Bacillus.

Based on previous research, an increased digestibility of feeds was expected to be obtained by combining MOS and Bacillus. However, this hypothesis did not hold since only EHY-fed broilers showed an increase, whereas Bs-fed broilers showed lower ileal digestibility of nutrients and energy. In previous research, increased disaccharidase activity on the intestinal brush border, as well as tryptophan absorption through the membranes of the jejunum brush border was reported in MOS-fed broilers (Gedek, 1999; Iji et al., 2001). It has also been suggested that MOS has the capability to decrease intestinal colonization of pathogenic bacteria (improving intestinal health and mucosa integrity) and to reduce competition for nutrients between the host and its microflora allowing more nutrients to be available to the host (Iji and Tivey, 1998; Ferket et al., 2002). Probably, a combination of these factors caused the higher ileal nutrient digestibilities in EHY-fed broilers in the present study. Opposite to these results, in other reports no benefits on starch, protein and fat digestibilities were found in MOS supplemented broilers (Kumprecht and Zobac, 1997; Alves et al., 2003; Yang et al., 2008).

The lack of differences in the ileal digestibility of nutrients between the control group and the Bs-fed broilers was unexpected. One of the suggested modes of actions of Bacillus is the release of some digestive enzymes which help to hydrolyze and assimilate the dietary nutrients (Schallmey et al., 2004; Cepero, 2005; Yamabhai et al., 2008). Breves et al. (2000) reported stimulation of glucose uptake in cells from the jejunum of pigs fed with Bacillus cereus. However, in other studies, it has been reported that dietary Bacillus had no effect on the apparent dry matter, nitrogen and energy digestibility in pigs (Spriet et al., 1987; Kim et al., 1993; Scheuermann, 1993). These results were confirmed by Kornegay and Risley (1996) who evaluated two Bacillus-based products (Bacillus subtilis/Bacillus licheniformis, and Bacillus subtilis/Bacillus licheniformis/ Bacillus pumilus). The lack of effects of Bacillus on the nutrient digestibility in pigs agrees with the findings of the present research in broilers.

The greater nitrogen retention and slightly lower energy excretion in EHY-fed broilers matches other results in broilers and turkeys. In a previous experiment, greater nitrogen retention and AMEn was observed in EHY-fed broilers (Gomez and Angeles, 2011). Broilers fed diets supplemented with dried yeast showed higher apparent retention of dry matter, crude protein, ether extract, crude fibre, hemicellulose, cellulose, and neutral detergent fibre than broilers fed a control diet (Onifade and Babatunde, 1996). In MOS-fed broiler, a trend for improved AME (62 kcal/kg) and NE (38 kcal/kg) was observed compared to broilers fed a control diet (Yang et al., 2008). In turkey poults fed YC, improved gross energy and mineral retention was reported (Bradley and Savage, 1995). In male turkeys, the inclusion of MOS increased the AME by 2.94% (Ferket et al., 2002). However, in other studies no differences were reported on the use of energy and other nutrients in MOS-fed broilers (Hughes, 2003; Yang et al., 2007).

The greater nitrogen retention in Bs-fed broilers and the reduction in the excretion of dry matter and energy agree with a report in broilers in which higher dry matter, crude protein and energy retention were observed in broilers fed Bs (Sen et al., 2011). Similar results were reported in pigs (Scheuermann, 1993), however, Kornegay and Risley (1996) did not find any effect in the nitrogen retention of pigs fed two Bacillus-based products.

Positive responses in the villus height in different portions of the gut (Macari and Maiorka, 2000; Loddi, 2003; Pelicano et al., 2003) have been reported in MOS- or Bacillus-fed broilers which may result in greater nutrient digestion and absorption. Supported in these findings, greater thickness of the mucosa and villus height was presumed by combining EHY and Bs. Opposite to this, in the present research, the thickness of the mucosa and villus height were lowest when Bs was added alone and there was not any difference for the rest of the treatments, including the combination of EHY and Bs. The lack of differences in the thickness of the mucosa and the villus height between the control and EHY-fed broilers fits with a previous report by Ferket et al. (2002) who reported that the addition of MOS did not affect the intestinal mucosa or muscularis tissue mass in turkeys, and reports by others researchers (Santos et al., 2004; Yang et al., 2007) in broilers fed MOS. In disagreement with this, Gao et al. (2008) reported a positive linear effect in the villus height in the duodenum of 42 d old broilers with increasing levels of YC. Whereas Pelicano et al. (2005b) reported lower villus height in the duodenum of 21 d old broilers fed a MOS-based prebiotic.

The thickness and area of the villus were numerically greater when EHY and Bs were supplemented together than when they were added independently; however, since these variables were statistically similar between broilers fed the control and the EHY plus Bs, the physiological meaning of these responses are unknown.

It has been reported that MOS and Bacillus combined may reduce the depth of the crypt, due to a lower enterocyte replacement rate (Pelicano et al., 2005b). Opposite to this, the trend for greater crypt depth in EHY-fed broilers seen in the present research suggests a faster enterocyte turnover rate; however no differences were seen on the VCR. Contrary to this, Gao et al. (2008) found that in broilers fed YC the crypt depth was reduced at a low dose but was increased at higher doses, whereas the VCR showed linear increments as the supplementation of dietary yeast increased. Pelicano et al. (2005b) found a reduction of the crypt depth but no effect on VCR in the duodenum of broilers fed a MOS-based prebiotic. The differences observed in the villi morphology of the duodenum on the studies cited may be attributed to differences on the age of the broilers, length of supplementation, type of yeast and stress conditions.

The reduction of the thickness of the mucosa, villus height and depth of the cryps in Bs-fed broilers in comparison to the rest of the treatments, suggests a reduction on the mucosa proliferation (Table 4). These results are opposite to those reported by Pelicano et al. (2005b) in which the villus height was not affected in the duodenum, but was increased in the jejunum and ileum of Bs-fed broilers from 1 to 21 d of age. Also, the results obtained in the present study are not consistent with other reports in which increased villus height and VCR in the duodenum and ileum were reported in broilers supplemented with Bacillus subtilis (Pelicano et al., 2003, 2005b; Samanya and Yamauchi, 2002; Sen et al., 2011) at 21, 35 and 42 d of age.

It has been suggested that taller villi indicate more mature epithelia and enhanced absorptive function due to increased absorptive area of the villi and increased activity of enzymes secreted from the tips of the villi, resulting in improved digestibility (Hampson, 1986; Cera et al., 1988). The present results indicate that even thought EHY-fed broilers had similar villus height and slightly lower villus area in the duodenum than the control group, the ileal digestibility of dry matter, ashes, nitrogen and energy was higher when EHY was supplemented. In the study of Gao et al. (2008) it was reported that higher Ca and P digestibility was not related to a greater villus height and that in some instances the villus height was even lower compared to the control group in the duodenum, jejunum and ileum of 21 and 42 d old broilers fed YC. These findings agree with results of the present experiment.

Furthermore, several authors have reported that the combination of an oligosaccharide and an appropriate probiotic (symbiotic products) may result in higher efficacy than when both products are fed separately (Bailey et al., 1991; Fukata et al., 1999; Sun et al., 2004). In the current research EHY and Bs enhanced some growth, carcass and nutrient retention responses, but did not show any synergic relationship in these measurements. Opposite to this, it was seen that when EHY was added alone the feed conversion and dry matter, ashes and energy digestibility were enhanced, but when EHY and Bs were added together, the responses were negatively affected. These results suggest that the positive effect of EHY on the feed conversion and digestibility of nutrients was counterbalanced by the addition of Bs. The results also show that the responses on the histological measurements of the duodenum were sometime opposite. However, it is important to point out that the combination of EHY and Bs reduced nitrogen excretion by 12% and increased the nitrogen retention by 48%, compared to the control treatment (Table 3), and even though these differences were not statistically significant, these results suggest a possible additive effect of the products in the nitrogen metabolism. All these issues deserve further clarification.

The results indicate that EHY-fed broilers had improved feed conversion ratio, breast yield, ileal digestibility of dry matter, ashes, nitrogen and energy, and nitrogen retention even though they had similar histological duodenal measurements than the control group. The inclusion of Bs improved the feed intake, weight gain, carcass weight and yield, the retention of nitrogen and caused a thinning of the duodenal mucosa. EHY and Bs enhanced some growth, carcass and nutrient retention responses, but did not show any synergic relationship in these responses.

References

Adejuno D, Onifade O, Olutunde O, Shanni-Awal A, Babatunde D, Odu O, Ademola S, Adebesi Q. 1999. The effect of concentration, age and duration of feeding supplemental yeast (Levucel, SBTM in a high-fiber diet on the performance of broiler chicken. In : Abs. de la 88th. Annual Meeting of the Poultry Science Association, Inc.. p. 52.
Alves A, Guedes CM, Gomes MJ, Mourao JL, Pinheiro VC. 2003. Digstibility and gut development of broiler chickens fed Bio-MOS versus control. Report For Alltech Biotechnology Universidade de Tras-os-Montes e Alto Douro. Vila Real, Portugal:
AOAC. 2002. Official methods of analysis 17th edth ed. Association of Official Analytical Chemists. Arlington, VA:
Bailey JS, Blankenship LC, Cox NA. 1991;Effect of fructooligosaccharide on Salmonella colonization of the chicken intestine. Poult Sci 70:2433–2438.
Bradley GL, Savage TF. 1995;The effect of autoclaving a yeast culture of Saccharomyces cerevisiae on turkey poult performance and the retention of gross energy, and selected minerals. Anim Feed Sci Technol 55:1–7.
Breves G, Walter C, Burmester M, Schröder B. 2000;In vitro studies on the effects of Saccharomyces boulardii and Bacillus cereus var. toyoi on nutrient transport in pig jejunum. J Anim Physiol Anim Nutr 84:9–20.
Cepero BR. 2005. Retirada de los antibióticos promotores de crecimiento en la unión europea: causas y consecuencias. In : XII Congreso bienal de la Asociación Mexicana de Especialistas en Nutrición Animal. Puerto Vallarta, Jal. p. 1–49.
Cera KR, Mahan DC, Cross RF, Reinhart GA, Whitmoyer RE. 1988;Effect of age, weaning and posweaning diet on small intestinal growth and jejunal morphology in young swine. J Anim Sci 66:574–584.
Clementino Dos Santos E, Soares Teixeira A, Gilberto Bertechini A, Tadeu R, de Freitas Fonseca, Borges Rodregues P, Souza Dias E, Torres DM, Vieira Santos A, Giacometi RA. 2002;Effect of growth beneficial additives on broiler carcass yield. Proc Braz Soc Anim Prod :5.
Ferket PR, Parks CW, Grimes JL. 2002. Benefits of dietary antibiotic and mannan oligosaccharide supplementation for poultry. p. 22. In : Proc. Multi-State Poult. Feed. Nutr. Conf.. Indianapolis, Indiana USA; May 14–16;
Fukata T, Sasai K, Miyamoto T, Baba E. 1999;Inhibitory effects of competitive exclusion and fructooligosaccharide, singly and in combination, on Salmonella colonization of chicks. J Food Prot 62:229–233.
Gao J, Zhang HJ, Yu SH, Wu SG, Yoon I, Quigley J, Gao YP, Qi GH. 2008;Effects of yeast culture in broiler diets on performance and immunomodulatory functions. Poult Sci 87:1377–1384.
Gao J, Zhang HJ, Wu SG, Yu SH, Yoon I, Moore D, Gao YP, Yan HJ, Qi GH. 2009;Effect of Saccharomyces cerevisiae fermentation product on immune functions of broilers challenged with Eimeria tenella. Poult Sci 88:2141–2151.
Gedek BR. 1999. Mode of actions of probiotics in chickens. In : Proc. XII Eur. Symp. on Poultry Nutrition. Veldhoven, The Netherlands. p. 83–90.
Gil-Turnes C, Conceição FR, Gil de los Santos JR. 2007;Bacillus cereus var. toyoi improves feed efficiency and health in animals. Int J Prob Preb 2:21–28.
Gomez S, de Angeles ML. 2011;Effects of an enzymatically hydrolyzed yeast and yeast culture combined with flavomycin and monensin on finishing broiler chickens. Int J Poult Sci 10:433–439.
Hampson DJ. 1986;Alterations in piglet small intestinal structure at weaning. Res Vet Sci 40:32–40.
Hooge DM. 2004;Meta-analysis of broiler chicken pen trials evaluating dietary mannan oligosaccharide, 1993–2003. Int J Poult Sci 3:163–174.
Hughes RJ. 2003. Variation in the digestion of energy by broiler chickens. PhD Diss. Univ. Adelaide; Australia:
Iji PA, Tivey DR. 1998;Natural and synthetic oligosaccharides in broiler chicken diets. Poult Sci 2:129–143.
Iji PA, Saki AA, Tivey DR. 2001;Intestinal structure and function of broiler chickens on diets supplemented with a mannan oligosaccharide. J Sci Food Agric 81:1186–1192.
Jin LZ, Ho YW, Abdullah N, Jalaludin S. 2000;Digestive and bacterial enzyme activities in broilers fed diets supplemented with Lactobacillus cultures. Poult Sci 79:886–891.
Kim IH, Hancock JD, Hines RH, Risley CR. 1993. Effects of cellulase and bacterial feed additives on the nutritional value of sorghum grain for finishing pigs. Kansas Agric Exp Sta Rep Prog No. 695 p. 144.
Kornegay ET, Risley CR. 1996;Nutrient digestibilities of a corn-soybean meal diet as influenced by Bacillus products fed to finishing swine. J Anim Sci 74:799–805.
Kumprecht I, Zobac F. 1997;The effect of mannan oligosaccharides in feed mixtures on the performance of broilers. Zivocisna Vyroba 42:117–124.
Loddi MM. 2003. Probióticos, prebióticos e acidificante orgânico em dietas para frangos de corte [tese] Jaboticabal: FCAV, UNESP;
Macari M, Maiorka A. 2000. Função gastrintestinal e seu impacto no rendimento avícola. Anais da Conferência Apinco de Ciência e Tecnologia Avícolas Campinas: FACTA. 2p. 161–174.
Miazzo RD, Peralta MF, Picco M. 2005;Performance productiva y calidad de la canal en broilers que recibieron levadura de cerveza (S. cerevisiae) (Productive performance and carcass quality in broilers fed yeast (S. cerevisiae)). Revista electrónica de veterinaria REDVET 6:1–9. http:www.veterinaria.org/revistas/redvet.
Mul AJ, Perry FG. 1994. The role of fructo-oligosaccharides in animal nutrition. Recent Advances in Animal Nutrition In : Garnsworthy PC, Cole DJA, eds. Nottingham University Press. Nottingham, UK: p. 57–79.
Onifade A, Odunsi A, Babatunde G, Olonede S, Muma E. 1999;Comparison of the supplemental effects of Saccharomyces cerevisiae and antibiotics in low protein and high fibre diet fed to broiler chickens. Arch Tiernahr 52:29–39.
Onifade AA, Babatunde GM. 1996;Supplemental value of dried yeast in a high-fibre diet for broiler chicks. Anim Feed Sci Technol 62:91–96.
Opalinski M, Maiorka A, Dahlke F, Cunha F, Vargas FSC, Cardozo E. 2007;On the use of a probiotic (Bacillus subtilis- strain DSM 17299) as growth promoter in broiler diets. Rev Bras Cienc Avic 9:99–103.
Panda AK, Rama Rao SV, Raju MVLN, Sharma SR. 2006;Dietary supplementacion of lactobacillus sporogenes on performance and serum biochemico-lipid profile of broiler chickens. J Poult Sci 43:235–240.
Pelicano ERL, Souza PA, Souza HBA, Oba A, Norkus EA, Kodawara LM, Lima TMA. 2003;Morfometria e ultra-estrutura da mucosa intestinal de frangos de corte alimentados com dietas contendo diferentes probióticos. Rev Port Ciênc Vet 98:124–134.
Pelicano ERL, Souza PA, Souza HBA, Oba A, Leonel FR, Zeola NMBL, Boiago MM. 2004;Productive traits of broiler chickens fed diets containing different growth promoters. Braz J Poult Sci 6:177–182.
Pelicano ERL, Souza PA, Souza HBA, Oba A, Boiago MM, Zeola NMBL, Scatolini AM, Bertanha VA, Lima TMA. 2005a;Carcass and cut yields and meat qualitative traits of broilers fed diets containing probiotics and prebiotics. Braz J Poult Sci 7:169–175.
Pelicano ERL, Souza PA, Souza HBA, Figueiredo DF, Boiago MM, Carvalho SR, Bordon VF. 2005b;Intestinal mucosa development in broiler chickens fed natural growth promoters. Rev Bras Cienc Avic 7:221–1229.
Pelicia K, Mendes AA, Saldanha ESPB, Pizzolante CC, Takahashi SE, Moreira J, Garcia RG, Quinteiro RR, Paz ICLA, Komiyama CM. 2004;Use of prebiotics and probiotics of bacterial and yeast origin for free-range broiler chickens. Braz J Poult Sci 6:163–169.
Radecki SV, Yokoyama MT. 1991. Intestinal bacteria and their influence on swine nutrition. Swine Nutrition In : Miller ER, Duane EU, Lewis AJ, eds. Boston: p. 439–447.
Ratcliff J. 2000. Antibiotic bans- a European perspective. p. 135–152. In : Proceedings of the 47th Maryland Nutrition Conference for Feed Manufacturers; March 22–24;
Rosen GD. 2007;Holo-analysis of the efficacy of Bio-Mos®in broiler nutrition. Br Poult Sci 48:21–26.
Samanya M, Yamauchi K. 2002;Histological alterations of intestinal villi in chickens fed dried Bacillus subtilis var. natto. Comp Biochem Physiol 133:95–104.
Santoso U, Tanaka K, Ohtani S. 1995;Effect of dried Bacillus subtilis culture on growth and lipogenic enzyme activity in female chicks. Br J Nutr 74:523–529.
SAS Institute. 1999. SAS/STAT User’s Guide, version 8 4th Editionth ed. SAS Institute Inc. Cary, NC, USA:
Schallmey M, Singh A, Ward OP. 2004;Developments in the use of Bacillus species for industrial production. Can J Microbiol 50:1–17.
Scheuermann SE. 1993;Effect of the probiotic Paciflor (CIP 5832) on energy and protein metabolism in growing pigs. Anim Feed Sci Technol 41:181.
Sen SLI, Kim JS, Kim KH, Kim YW, Khong Chou, Lohakare JD, Kim EK, Kim HS, Kwon IK, Chae BJ. 2011;Effect of Supplementation of Bacillus subtilis LS 1-2 grown on citrus-juice waste and corn-soybean meal substrate on growth performance, nutrient retention, caecal microbiology and small intestinal morphology of broilers. Asian-Aust J Anim Sci 24:1120–1127.
Spriet SM, Decuypere JA, Henderickx HK. 1987;Effect of Bacillus toyoi (Toyocerin) on the gastrointestinal microflora, concentration of some bacterial metabolites, digestibility of the nutrients and the small intestinal mean retention time in pigs. Meded Fac Landbouwkd Rijksuniv Gent 52:1673.
Spring P, Wenk C, Dawson KA, Newman KE. 2000;The effects of dietary mannanoligosaccharides on cecal parameters and the concentrations of enteric bacteria in the ceca of salmonella-challenged broiler chicks. Poult Sci 79:205–211.
Stanley VG, Winsman M, Dunkley C, Ogunleye T, Daley M, Krueger WF, Sefton AE, Hinton A Jr. 2004;The impact of yeast culture residue on the suppression of dietary aflatoxin on the performance of broiler breeder hens. J Appl Poult Res 13:533–539.
Sun X, Novak C, McElroy A, Sefton T. 2004. The use of a drug free feeding program to maintain performance of broiler chickens from 0 to 49 days of age. In : Proc. XXII World’s Poultry Congress. Istanbul. CD-Rom.
Yamabhai M, Emrat S, Sukasem S, Pesatcha P, Jaruseranee N, Buranabanyat B. 2008;Secretion of recombinant Bacillus hydrolytic enzymes using Escherichia coli expression systems. J Biotechnol 133:50–57.
Yang Y, Iji PA, Kocher A, Mikkelsen LL, Choct M. 2007;Effects of mannanoligosaccharide on growth performance, the development of gut microflora, and gut function of broiler chickens raised on new litter. J Appl Poult Res 16:280–288.
Yang Y, Iji PA, Kocher A, Thompson E, Mikkelsen LL, Choct M. 2008;Effects of mannanoligosaccharide in broiler chicken diets on growth performance, energy utilisation, nutrient digestibility and intestinal microflora. Br Poult Sci 49:186–94.
Yang Y, Iji PA, Choct M. 2009;Dietary modulation of gut microflora in broiler chickens: a review of the role of six kinds of alternatives to in-feed antibiotics. World’s Poult Sci J 65:97–114.
Zhang AW, Lee BD, Lee SK, Lee KW, An GH, Song KB, Lee CH. 2005;Effects of yeast (Saccharomyces cerevisiae) cell components on growth performance, meat quality, and ileal mucosa development of broiler chicks. Poult Sci 84:1015–1021.

Article information Continued

Table 1

Diet composition

Ingredients %
Ground sorghum 58.74
Soybean meal 17.78
Canola meal 10.00
Corn gluten meal 5.00
Soybean oil 4.17
Calcium phosphate 1.64
Calcium carbonate 1.10
Premix1 0.70
Salt 0.33
Sodium bicarbonate 0.26
Lysine-HCl 0.22
DL-methionine 0.06
Calculated content of nutrients
 ME (Kcal/kg) 3,150
 CP (%) 20.5
 Digestible lysine (%) 0.95
 Calcium (%) 0.85
 Available phosphorus (%) 0.42
1

Each kg provides: 6,500 IU of vitamin A; 2,000 IPU of vitamin D3; 15 IU of vitamin E; 1.5 mg of vitamin K; 1.5 mg of thiamine; 5 mg of riboflavin; 35 mg of niacin; 3.5 mg of pyridoxine; 10 mg of pantothenic acid; 1,500 mg of choline; 0.6 mg of folic acid; 0.15 mg of biotin; 0.15 mg of vitamin B12; 100 mg of Mn; 100 mg of Zn; 50 mg of Fe; 10 mg of Cu; 1 mg of I.

Table 2

Productive and carcass measurements in broilers fed an enzymatically hydrolyzed yeast and yeast culture combined with a live Bacillus subtilis

Main effects Interaction p-value

EHY1 EHY0 SEM




EHY0 EHY1 SEMa Bs0 Bs125 SEM Bs0 Bs125 Bs0 Bs125 EHY Bs Interaction
Productive measurements
 Feed intake (g/d) 130.7 129.0 0.89 126.5 133.2 0.86 128.7b 132.8c 124.4d 133.7c 1.26 0.18 <0.01 <0.05
 Weight gain (g/d) 77.0 79.1 0.97 76.7 79.4 0.95 74.9 79.0 78.4 79.8 1.37 0.12 <0.10 0.32
 Feed conversion ratio 0.59 0.62 0.022 0.61 0.60 0.028 1.73b 1.69b 1.59c 1.68b 0.03 <0.05 0.49 <0.05
Weight of the carcass and its components (g)
 Carcass 1,130 1,149 15.31 1,112e 1,167f 15.53 1,099 1,161 1,126 1,172 21.65 0.38 <0.05 0.73
 Breast 430 446 6.30 429e 447f 6.39 415 445 443 449 8.91 0.08 <0.05 0.21
 Legs 193 197 3.25 190 199 3.29 190 195 190 203 4.59 0.41 0.06 0.37
 Thighs 315 320 5.08 312 323 5.15 307 323 317 323 7.18 0.46 0.13 0.53
Yield of the carcass and its components (%)
 Carcass 52.4 53.1 0.43 52.2 53.3 0.44 52.1 52.6 52.4 53.9 0.61 0.20 0.10 0.40
 Breast 19.9g 20.6h 0.18 20.1 20.4 0.18 19.6 20.1 20.6 20.6 0.25 <0.01 0.29 0.36
 Legs 8.9 9.0 0.13 8.9 9.0 0.14 9.1 8.8 8.8 9.3 0.19 0.63 0.44 0.16
 Thighs 14.5 14.8 0.17 14.5 14.8 0.18 14.4 14.6 14.7 15 0.25 0.23 0.32 0.74

EHY0 = 0 kg/ton and EHY1 = 1 kg/ton of an enzymatically hydrolyzed yeast and yeast culture.

Bs0 = 0 g/ton and Bs125 = 125 g/ton of Bacillus subtilis.

a

SEM = Standard error of the mean.

b,h

Within a row, means without a common superscript letter differ (p<0.05).

Table 3

Ileal digestibility and retention of nutrients in broilers fed an enzymatically hydrolyzed yeast and yeast culture combined with a live Bacillus subtilis

Main effects Interaction p-value

EHY0 EHY1 SEM




EHY0 EHY1 SEMa Bs0 Bs125 SEM Bs0 Bs125 Bs0 Bs125 EHY Bs Interaction
Ileal digestibility (%)
Dry matter 76.6 78.5 0.78 78.9 76.7 0.73 76.0b 77.2b 81.0c 75.9b 1.11 0.20 0.10 <0.01
Ashes 68.8d 71.8e 0.75 71.2 69.4 0.76 68.8 68.8 73.6 70.0 1.07 <0.05 0.10 0.10
Nitrogen 84.0 85.7 0.62 85.3 84.4 0.62 84.7 83.3 86.0 85.5 0.62 0.07 0.31 0.63
Energy 79.0 80.7 0.78 80.8 79.0 0.71 78.4f 79.6f 83.1g 78.3f 1.10 0.14 0.13 <0.05
Retention of nutrients
 Dry matter
 Intake 89.8 89.8 - 89.8 89.8 - 89.8 89.8 89.8 89.8 -
 Excretion 37.5 36.2 0.71 37.9 35.9 0.72 38.3 36.8 37.4 34.9 1.01 0.20 0.07 0.63
 Retention 58.2 60.0 0.88 58.1 60.2 0.91 57.4 59.1 58.8 61.3 1.29 0.15 0.13 0.78
Ashes
 Intake 5.8 5.8 - 5.7 5.9 - 5.7 6.0 5.8 5.9 -
 Excretion 5.0 4.8 0.16 4.9 4.9 0.17 4.9 5.0 5.0 4.7 0.23 0.66 0.68 0.46
 Retention 14.9 20.0 2.78 16.4 18.4 2.9 13.6 16.1 19.2 20.8 4.10 0.21 0.62 0.91
Nitrogen
 Intake 2.9 3.0 - 2.9 3.1 - 2.8 3.1 3.0 3.1 -
 Excretion 2.0 1.9 0.05 2.0 1.8 0.05 2.0 1.9 2.0 1.8 0.07 0.13 0.07 0.35
 Retention 32.4h 40.4i 1.7 33.3j 39.4k 1.77 29.4 35.4 37.3 43.5 2.51 <0.01 <0.05 0.99
Energy
 Intake 418.7 417.8 - 420.0 416.5 - 419.3 418.1 420.7 414.9 -
 Excretion 138.8 132.2 2.57 139.3j 131.7k 2.61 143.0 134.6 135.7 128.8 3.64 0.09 <0.05 0.85
 AMEn 2,724 2,755 22.44 2,726 2,753 23.45 2,695 2,753 2,756 2,753 31.70 0.35 0.40 0.35

EHY0 = 0 kg/ton and EHY1 = 1 kg/ton of an enzymatically hydrolyzed yeast and yeast culture.

Bs0 = 0 g/ton and Bs125 = 125 g/ton of Bacillus subtilis.

a

SEM = Standard error of the mean.

b,k

Within a row, means without a common superscript letter differ (p<0.05).

Table 4

Histological measurements of the duodenum in broilers fed an enzymatically hydrolyzed yeast and yeast culture combined with a live Bacillus subtilis

Main effects Interaction p-value

EHY0 EHY1 SEM




EHY0 EHY1 SEMa Bs0 Bs125 SEM Bs0 Bs125 Bs0 Bs125 EHY Bs Interaction
Thickness of the mucosa (mm) 161.1 166.4 2.32 168.8 158.8 2.38 171.2b 151.0c 166.3b 166.5b 3.28 0.10 <0.01 <0.01
Height of villi (mm) 146.4 151.5 2.67 153.0d 144.8e 2.63 154.0 138.7 152.0 150.9 3.78 0.19 <0.05 0.07
Thickness of villi (mm) 15.3 15.4 0.22 15.1 15.6 0.25 15.3fg 15.2fg 14.8g 15.9f 0.32 0.60 0.12 0.05
Area of villi (mm2) 1,114 1,165 26.87 1,152 1,127 28.68 1,175f 1,052g 1,128g 1,202f 38.00 0.19 0.53 <0.05
Depth of crypt (mm) 9.3 10.0 0.28 10.0d 9.2e 0.25 9.6 8.9 10.4 9.5 0.39 0.08 <0.05 0.83
VCR 15.8 15.2 0.53 15.3 15.7 0.58 16 15.5 14.6 15.8 0.75 0.88 0.69 0.57

EHY0 = 0 kg/ton and EHY1 = 1 kg/ton of an enzymatically hydrolyzed yeast and yeast culture.

Bs0 = 0 g/ton and Bs125 = 125 g/ton of Bacillus subtilis.

a

SEM = Standard error of the mean.

b,g

Within a row, means without a common superscript letter differ (p<0.05).