1. Introduction
In 2019, there were 43.9 billion pounds of broiler chickens produced, up from 35.5 billion a decade earlier [
1]. Due to the demand for broiler-meat production, the amount of feed needed for production will continue to increase. Feed costs account for more than 60% of the costs involved in poultry production [
2], and the majority of feed costs come from the energy-containing ingredients. Due to this, it is important to have access to updated energy values of the various feed ingredients used in poultry feed, to better meet the requirements of the birds and reduce feed wastage through overfeeding.
In addition to feed costs, infection from the protozoan (
Eimeria species) that causes coccidiosis has had major impacts on commercial poultry production. Broiler chickens are affected by the
Eimeria family of parasitic protozoan pathogen, which can increase mortality and morbidity in the birds with the clinical form of infection [
3]. In both the clinical and sub-clinical forms of coccidiosis, birds may show reduced performance, such as reduced feed intake and body weight gain. They may also show reduced nutrient and energy retention, leading to reduced apparent metabolizable energy (AME) from the diet [
4,
5]. In both cases, there are major economic losses, of which the annual global costs to poultry production have been estimated to be over
$2.2 billion [
6].
Soluble non-starch polysaccharides (NSP) are found in plant-based feed ingredients, and are known to possess antinutritive effects, such as increased digesta viscosity, decreased performance, reduced AME retention, reduced villi size in the small intestine, and sticky droppings [
7,
8,
9,
10,
11,
12,
13]. Corn and wheat are two common energy-containing feed ingredients used in broiler production. Wheat tends to have higher levels of soluble NSP and that may negatively affect the bird’s ability to utilize nutrients and energy in their diet. Carbohydrase enzymes, specifically NSPase, may be supplemented to the diet to counteract some of the antinutritive effects of NSP. There is evidence that soluble NSP can increase Gram-negative bacteria (i.e.,
Escherichia coli) and decrease Gram-positive bacteria (i.e., lactic acid-producing bacteria), but reducing the viscosity through enzyme supplementation may promote an environment less suited for Gram-negative bacterial proliferation [
12].
The fact is, when birds are under coccidia vaccine challenge (CVC) and given a diet high in soluble NSP, both of these may affect the birds’ ability to sequester energy, thereby reducing the AME retention value of the diet or ingredient. Whereas, exogenous enzyme supplementation may improve the nutrient and energy utilization of the diet. Thus, the objectives of this study were to compare the effect of CVC and exogenous enzyme supplementation on AME and AMEn values of CS- and WCS-based diets and wheat in broiler chickens, 7- (day 21; peak-CVC) and 14- (day 28; recovery phase) day post-CVC.
2. Materials and Methods
The management of the birds, experimental procedures, and sample collections for the experiment followed the standard operating procedures for the animal facility, and was reviewed and approved by the University of Kentucky Animal Care and Use Committee (Protocol # 2018-2890).
2.1. Birds and Diets
The experiment used day-old by-product breeder chicks obtained from Cobb Monticello, KY. On day zero, 500 day-old broiler chicks were individually tagged and fed a standard corn-SBM-based broiler starter diet that met or exceeded nutrient and energy requirements from day 0 to 14. Birds were raised in battery cages in an environmentally controlled room with 20 h of light and 4 h of dark. All birds had unrestricted access to feed and water throughout the duration of the experiment. A total of 448 birds were individually weighed and randomized to treatments on day 14 in a completely randomized design. Experimental treatments were arranged in a 2 × 2 × 2 factorial, for a total of eight treatments and seven replicates/treatment, with eight birds per replicate cage. Four birds/cage were sampled on days 21 (the two heaviest and two lightest birds) while the remaining four birds/pen were sampled on day 28. All birds were weighed and euthanized by CO2 asphyxiation prior to sampling on days 21 and 28.
2.2. Coccidia Vaccine Challenge
The reference diet used was a corn-SBM-based diet (CS) in which 30% of the energy yielding portion of the diet (corn, SMB, and soy oil;
Table 1) was replaced with wheat to produce the wheat-corn-SBM-based diet (WCS). Similar ratios of the energy yielding components of the diets were maintained across all the diets used in this study. The exogenous enzyme containing diets were produced from the same basal diet by supplementing a multi-carbohydrase enzyme (Ronozyme
® WX2 and Ronozyme
® VP, DSM Animal Nutrition, Parsippany, NJ, USA) to both the CS and WCS diets (as a ground-corn-based premix,
Table 1). Ronozyme
® WX2 (xylanase) premix was added to the diet to supply 0.1 g/kg of the enzyme/kg of feed, while Ronozyme
® VP (glucanase + pectinase) premix was added to the diet to supply 0.25 g of the enzyme/kg of the diet, as per the manufacturer’s recommendation (DSM, Parsippany, NJ, USA). The diets with enzyme supplementation were produced from the same basal diet as diets without enzyme supplementation.
Birds in the non-CVC treatments were orally gavaged on day 14 with 0.6 mL of distilled water, whereas CVC birds were orally gavaged with 20× of coccidia vaccine (Coccivac®-B52, Merck Animal Health, Omaha, NE, USA) in 0.6 mL distilled water. The vaccine contained live Eimeria occysts of E. acervulina, E. maxima, E. mivati, and E. tenella. The total collection method was used to determine energy and nitrogen retention, as well as the AME and AME corrected for nitrogen (AMEn). Seventy-two hours before each sampling on day 21 and 28, the excreta collection trays were cleaned, the feed was removed from the feeders and weighed at 0 and 72 h. On days 19, 20, 21, and 26, 27, 28 excreta was quantitatively collected and weighed each morning at the same time before storing at −20 °C, prior to drying in a forced-air oven at 55 °C for six days. Dried excreta samples were weighed and pooled by cage. Dried excreta samples, ingredients (corn, wheat, and SBM), and diets were ground to pass through a 0.5 mm screen using a mill grinder (Wiley Mill Standard Model No. 3, Arthur H. Thomas Co., Philadelphia, PA, USA).
2.3. Histological Analysis
The middle section of the ileum (about an inch) was taken on day 21 to determine the morphometric changes associated with the different treatments, especially the effect of Eimeria species on the ileum. The CVC used in this study is capable of affecting the entire gastrointestinal tract. Sample was taken from the ileum to specifically confirm the effects of the challenge on the gastrointestinal tract of the birds. Samples were processed (stained with haematoxylin and eosin) at the University of Kentucky’s Animal Diagnostics Lab (ADL). Ten villi height and crypt depth measurements were made per slide at 10× (upright clinical microscope, Model Eclipse Ci-E, Nikon Corporation, Tokyo, Japan). Villi height to crypt depth ratio (VHCD) was also determined.
2.4. Viscosity
Jejunal digesta was taken from the two heaviest birds (to have adequate sample quantities)/cage on days 21 and 28 and stored at −20 °C prior to the determination of the digesta viscosity. Digesta from the jejunum was taken for viscosity measurements, because this is the section of the mid-gut where considerable digestion and absorption take place. Approximately 2 g of thawed digesta were centrifuged (11.500× g for 15 min at 20 °C) and the viscosity was determined on 0.5 mL of supernatant using a viscometer (Vibro viscometer, model SV-1 A, A&D Company Limited, Tokyo, Japan) at 40 °C (body temperature of chickens).
2.5. Chemical Analysis
Diets and excreta samples were analyzed for dry matter (DM), gross energy (GE), and nitrogen. The DM (method 934.01) contents of the samples (feed ingredients, diets, and excreta) were determined by drying the samples at 110 °C for 16 h [
14]. Nitrogen (method 990.03) contents of the samples were determined by the combustion method (model FP2000, Leco Corp., St. Joseph, MI, USA) [
15], with EDTA as the internal standard. The GE of the feed ingredients, diets, and excreta samples was analyzed using a bomb calorimeter (Parr adiabatic bomb calorimeter, model 6200, parr instruments, Moline, IL, USA) with benzoic acid as the calibration standard. Feed ingredients were sent to the University of Missouri for proximate composition value determination as shown in
Table 2.
The moisture, crude fat, crude fiber, and ash of corn, wheat, and soybean meal were determined at the University of Missouri Agriculture Experiment Station Chemical Laboratories (Columbia, MO, USA). Crude fat (method 920.39) was determined by ether extraction [
14]. Crude fiber (method 978.10) content was also determined [
14]. The ash (method 942.05) contents of the feed ingredients were also determined [
14]. Proximate analyses of ingredients are contained in
Table 2.
2.6. Calculations and Statistical Analysis
The coefficient of energy and N retention was determined using the equation:
where C is the component being measured (i.e., energy and N).
Apparent metabolizable energy was calculated using the following equation:
where GE is the gross energy of the diet and cEM is the coefficient of energy metabolizability (cEM).
The cEM of the test feed ingredient (wheat) was calculated using the indirect method after correcting for the non-energy yielding portions of the diets [
16].
where EMti is the cEM of the test ingredient, EMtd is the cEM of the test diet, EMrd is the cEM of the reference diet, and FCti/td is the fractional contribution of the test ingredient to the test diet. The caloric value of 8.22 kcal/g was used to correct AME for N to give AMEn [
17].
Data were analyzed using the GLM procedure of SAS (SAS Inst. Inc. Cary, Cary, NC, 2006). In order to take into consideration the nature of the two groups of the experimental diets (not isonitrogenous), the effects of CVC and enzyme supplementation on DM, N, energy utilization, AME, AMEn, digesta viscosity, and the histology of birds fed CS- and WCS-based diets were evaluated (within each diet group) as a 2 (non-CVC or CVC) × 2 (with or without exogenous enzyme supplementation) factorial arrangement of treatments. The test feed ingredient’s (wheat) AME and AMEn were analyzed as a 2 (non-CVC or CVC) × 2 (with or without exogenous enzyme supplementation) factorial arrangement of treatments. A cage served as the experimental unit, except for jejunal viscosity (two birds/cage) and for histology (one bird/cage), and the number of replicates was seven per treatment, unless otherwise stated. Outliers (data outside mean ± 3 SD) were removed from the data prior to statistical analysis. Where necessary, mean separation was by Tukey’s test and the level of significance was set at p < 0.05. Main and simple effects data were presented.
4. Discussion
The demand for chicken meat will continue to grow, and the need for accurate AMEn of feed ingredients under different production conditions is pressing. While coccidiosis infection still plagues poultry producers, with increased bird mortality and decreased performance, determining the nutrient and energy retention of different feed ingredients in coccidia-challenged birds can further our understanding of how birds utilize different feed ingredients. Different energy-yielding feed ingredients fed to broiler chickens have inherently different properties. There are obvious differences in nutrient and energy values, however there are also physicochemical properties that may change how the birds utilize the nutrients and energy provided by the diet. Wheat contains higher levels of soluble NSP than corn, which has been shown to decrease AMEn and have other antinutritive effects, along with other common feed ingredients (e.g., barley, rye, and triticale) used in poultry production [
11,
18]. Enzyme supplementation has been shown to reduce some of the antinutritive effects of soluble NSP [
9,
19], which may improve the birds’ ability to utilize ingredients high in soluble NSP. Through the various ways AMEn can be reduced or improved, a deeper look into individual ingredients could prove beneficial to the costs associated with feeding broiler chickens.
During the peak of CVC infection (7-day post-challenge; day 21), the two-way interaction of N retention was significantly lower in CVC birds fed the CS-based diets with no enzyme supplementation. Although the effect of exogenous enzyme supplementation to the diets of the unchallenged birds was not significant, exogenous enzyme supplementation improved N retention in CVC birds by 6%. Furthermore, DM and energy utilization, AME, and AMEn were all reduced 7-day post CVC. This observation for CVC birds was an expected result of the challenge and follows in line with the energy retention on day 21. The reduction in the determined energy retention, AME, and AMEn values in the CVC birds showed that the challenge affected the birds’ ability to utilize energy from the diets. Several studies have reported some adverse effects of
Eimeria sp. challenge on the ability of broilers to optimally utilize energy and nutrients in their feed [
20,
21]. These adverse effects include the destruction of intestinal villi, and thickening and shortening of the villi [
22], which leads to a reduction in the surface area available for absorption, as well as a prioritization of gut development, as shown by increased crypt depth [
23]. For the WCS-based diets, the effect of CVC on the birds 7-day post-challenge was similar to what was obtained for birds on the CS-based diets. For both the CS- and WCS-based diets, by day 28 (14-day post-challenge), the birds’ determined energy retention, AME, and AMEn values of the diets were no longer affected by CVC, therefore the pathogenicity of the coccidia infection had decreased, and the birds were already at the recovery phase. It is important to note that unlike under a controlled experimental condition, commercial broiler chickens are raised on the floor, which enables them to be able to recycle oocysts from the litter resulting in sustained compromise to the gastrointestinal tract. Furthermore, the compromised digestive tract presents a perfect environment for secondary bacterial infection to occur [
24,
25,
26].
The determined values of wheat AME and AMEn through the difference method 7-day post-challenge (day 21) for CVC-birds fed CS-based diet resulted in a ~20% decrease in AME (3 379.8 kcal/kg vs 2 718.3 kcal/kg) and AMEn (3 296.6 kcal/kg vs 2 609.6 kcal/kg) when compared with that of the non-CVC birds. This observation, again, confirms the effect that CVC had on the birds’ absorptive capabilities through the damage caused by the infection to the epithelial lining of the small intestine. By day 28 of the study (14-day post-challenge), unlike the significant reduction in wheat’s AME and AMEn, there were no differences in the AME and AMEn of wheat between the CVC and non-CVS birds. This showed that the effects of CVC had significantly reduced, and the birds were able to better utilize the energy in the wheat. The addition of exogenous enzymes to the diet did not improve the AME and AMEn values. One of the reasons for this observation could be because the diets were not formulated to be deficient in energy therefore, may not have revealed the potential benefits to exogenous enzyme supplementation.
The AME and AMEn of wheat determined in the non-CVC birds without exogenous enzyme supplementation were 3368.9 kcal/kg and 3290.4 kcal/kg, respectively, 7-day post challenge and 3438 and 3353, respectively, 14-day post-challenge. The same treatment group on day 28 was similar for AME and AMEn with a slight increase of around 60 kcal/kg. The reported AMEn of hard red wheat is 2900 kcal/kg [
18]. The determined AMEn values for 21 and 28 day were around 400 kcal/kg higher than those reported by [
18], however a study using birds of similar age determined the AMEn of wheat to be 3372 kcal/kg using the regression method [
27]. The relatively higher AME values could be due to differences in the cultivar (or improvement in seed breeding) of wheat used or an improvement in the efficiency with which modern day broilers are able to utilize feed ingredients.
Jejunal digesta viscosity of birds fed CS-based diets decreased by 11% as a result of CVC, while it decreased by 5% as a result of enzyme supplementation. For birds on WCS-based diets, interaction between CVC and enzyme supplementation resulted in non-CVC birds fed diets without enzyme supplementation having the highest viscosity, while the combination on CVC and enzyme supplementation resulted in the lowest viscosity. This was expected because both the CVC and enzyme supplementation individually reduced jejunal viscosity. Irrespective of the state of challenge (CVC or non-CVC), enzyme supplementation significantly reduced jejunal digesta viscosity. Lazaro [
28] showed a similar trend in the decreased viscosity through exogenous supplementation of a carbohydrase blend in the diet. Interestingly, the significant effect of CVC and enzyme supplementation in reducing digesta viscosity in birds on CS-based diets 7-day post-challenge disappeared 14-day post challenge. However, this effect persisted in birds on WCS-based diets 14-day post challenge, in which case, CVC and enzyme supplementation reduced jejunal digesta viscosity by 8 and 16%, respectively. This reduction in jejunal digesta viscosity indicates that during the recovery phase (14-day post-CVC), enzyme supplementation to the WCS-based diets further reduced digesta viscosity (16% vs. about 0% for CS-based diet). The interaction between CVC and enzyme showed that the supplementation of exogenous enzymes significantly reduced jejunal digesta viscosity (7-day post- challenge) when added to a WCS-based diet, but no interaction was observed when for both CS- and WCS-based diets 14-day post challenge. The presence of an appropriate substrate is key to the effect of enzyme supplementation in this study. This is evidence for the efficacy of the Ronozyme
® enzyme in reducing viscosity in diets high in NSP. Lazaro [
28] reported a similar trend in the decreased viscosity through exogenous supplementation of a carbohydrase blend in the diet. Exogenous xylanase supplementation was also shown to significantly reduce jejunal and ileal digesta viscosity in broilers fed wheat-based diets [
29,
30].
For birds on a CS-based diet 7-day post-CVC, no significant interaction between CVC and enzyme supplementation was observed for villi height, crypt depth, and the ratio between villi height and crypt depth. Despite the lack of significant interaction, CVC resulted in shorter villi, deeper crypt depth, and smaller villi height to crypt depth ratio. Similar trends were observed for the villi height and crypt depth of CVC-birds fed a WCS-based diet. Based on this observation, it is clear that the
Eimeria infection led to significant damage of the villi, and thus leading to decreased surface area for absorption. The two
Eimeria species that target the ileum of chickens contained in the Coccivac
®-B52 used in this study are
E. acervulina and
E. maxima, with
E. maxima being the most pathogenic of the two [
3]. Although the data are not presented, we know that
E. acervulina and
E. mivati are found to infect the duodenum, and
E. maxima also infects the jejunum of the SI [
31], which may have further led to reduced nutrient and energy utilization [
10]. At 7-day post challenge for bids fed a WCS-based diet, ileal VH:CD showed a two-way interaction. There was no difference in VH:CD for CVC birds, with or without enzyme supplementation, and non-CVC birds without enzyme supplementation. However, enzyme supplementation to the WCS-based diet in the absence of CVC resulted in higher VH:CD compared to the other treatments. This increase was driven mostly by a reduction in crypt depth (118.5 vs average of 168 µm). This increase in VH:CD as a result of enzyme supplementation would suggest that the enzymes increased the ileum’s surface area for absorption in the small intestine. Despite this observation, performance parameters, nutrient and energy retention, AME, and AMEn did not significantly increase with the increased absorptive capabilities in the ileum during the two-week period of this study. Future studies may explore the long-term effects of CVC on performance when birds are fed a WCS-based diet without mixed carbohydrase enzyme supplementation.