1. Introduction
Extensive grazing systems do not always meet the nutrient requirements of the majority of livestock raised on them. Previous studies have successfully incorporated a variety of low-quality raw feed materials, such as cotton seed hulls, taramira oil cake, and sunflower hulls, into complete pelleted diets to fill this nutritional gap, resulting in economic gains for animal producers through improved animal growth rates, ruminal fermentation, and feed efficiency [
1,
2,
3,
4,
5,
6,
7].
The use of natural feed additives in animal rations and the modification of feed formulations to improve the physical and microbiological processes of ruminal fermentation, thereby increasing the supply of volatile fatty acids (VFAs) and essential microbial proteins for ruminant growth [
8,
9], are gaining in popularity. These feed additives also play crucial roles in the regulation of toxic fermentation byproducts in the rumen [
10,
11]. There is a negative relationship between methane production and energy utilization in ruminants; therefore, the use of feed additives to reduce methane production and increase energy utilization is an attractive method of manipulating rumen fermentation [
12,
13].
Yucca is a medicinal plant that was grown originally in Mexico and the southwestern United States. Approximately 10% of the plant mass is dry matter [
14,
15]. Generally recognized as safe (GRAS), the US Food and Drug Administration has allowed the use of numerous YS products, including yucca extract and yucca powder, as additives in the food and drink industry, as well as in livestock and poultry feeds [
16,
17,
18]. The biologically active surfactants in YS have been identified as steroid saponins and glycocomponents [
18,
19]. YS contains a number of polyphenolics which have antioxidant, anti-inflammatory, urease-inhibiting, and antiprotozoal characteristics, as well as properties related to the regulation of lipid metabolism [
18,
20,
21,
22]. Commercially, YS, as a feed additive, is used primarily in controlling environmental ammonia in livestock and poultry facilities in order to reduce odor emissions [
23,
24]. Several studies have indicated that the addition of YS powder to livestock feeds improves productivity and feed efficiency and increases ruminal VFA concentrations, as well as contributing to environmental control, microbial-activity modification, and blood biochemical parameters [
23,
24,
25,
26,
27,
28,
29,
30].
The effects of including dietary YS extract in completed pelleted diets on the productive performance of ruminant animals, particularly growing lambs, are largely unknown, and previous livestock nutrition studies have yielded contradictory results. Therefore, this study sought to determine whether feeding growing lambs on pelleted diets supplemented with varying levels of YS has beneficial effects on productivity, blood metabolic variables, ruminal fermentation, fecal and urine gas emissions, and carcass traits.
2. Materials and Methods
2.1. Experimental Design and Diets
The experiment was undertaken at the Animal Experimental Station, Department of Animal Production, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia, and all procedures in this experiment followed the Animal Welfare Act of Practice for the Care and Use of Animals for Scientific Purposes, with approval from the King Saud University Research Ethics Committee (REC-KSU; Ethics Reference No.: KSU-SE-21-01). Sixty male Awassia lambs initially weighing 26.5, SD ± 2.0 kg, and aged between 3 and 4 months were purchased from the Riyadh livestock market and then transported to the Experimental Station. On the day of arrival, the animals’ weights were recorded and they were ear-tagged and treated against internal and external parasites and vaccinated against the commonest diseases. Animals were given a 14-day adaptation period, and, during this period, they were housed in shaded pens (4.0 m long, 3.0 m wide; 5 lambs in each pen). On the first day of the experiment, the lambs were randomly assigned to one of three treatments (four replicates for each treatment): (1) a complete pelleted diet (without YS supplementation; the basal diet; CON); (2) the basal diet with 300 mg YS/kg DM (YS
300); and (3) the basal diet with 600 mg YS/kg DM (YS
600). The
Yucca schidgera extract BIOPOWDER
®® was provided by Agroin (Ensenada, BC, Mexico). All experimental feeds were formulated according to NRC recommendations [
31] for growing lambs (
Table 1).
2.2. Growth Preformance and Feed Intake
The lambs were weighed on day 1 and then every two weeks in order to determine growth performance (including bodyweight gain and average daily gain). Feed intake was recorded weekly for each pen by calculating the difference between feed offered and feed refused. The feed conversion ratio (FCR) for each lamb was determined by subtracting dry-matter intake consumed from the average daily gain, and then represented as kg of DMI to kg of BW.
2.3. Blood Sample Processing and Analysis
Blood samples from all lambs were taken in the morning before feeding on days 1, 28, 58, and 84. Serum was obtained after the centrifugation of blood samples at 2400× g for 15 min at 4 °C and was then frozen at −20 °C until analysis. Commercial biochemical regents from Randox Laboratories (Antrim, UK) and a microplate reader (Multiskan EX, Thermo Fisher Scientific, Inc., Waltham, MA, USA) were used to determine the concentrations of glucose, total protein, albumin, urea, and creatinine in serum, following the manufacturers’ instructions.
2.4. Rumen Fermentation Profiles
Before the morning feeding, samples of rumen fluid (50 mL) from 15 lambs in each treatment were collected using an oral stomach tube on day 70 for evaluation of the ruminal fermentation profiles. The samples were analyzed for pH values, strained through four layers of cheesecloth, transferred into plastic tubes, acidified with 2 mL of concentrated sulfuric acid, and then frozen at −20 °C for further analysis. The ruminal fluid samples were then thawed and analyzed for ammonia (using a TECO Diagnostics kit) and volatile fatty acid (VFA) proportions and totals, including acetic, propionic, butyric, isobutyric, valeric, and isovaleric acids, as described by [
32], using 2-ethylbutyric acid as an internal standard and a gas chromatograph–mass spectrometer (7010C Triple Quadrupole GC/MS, Agilent Technologies, Palo Alto, CA, USA). The total volatile fatty acid concentrations were expressed as concentrations mol/l (mM), while individual VFA proportions were expressed as molar percentages of total molar VFAs (% mol).
2.5. Fecal and Urinary Odor Evaluation
On day 90, seven lambs from each treatment were removed into metabolism cages (7 days) for the digestibility trial. During the collection period (3 days), urine and feces from each animal were measured daily. Representative samples of the collected urine and feces were used for the evaluation of fecal and urinary odor emissions. Fecal (150 g) and urine (150 mL) samples were mixed in 3 L plastic boxes, and then the mixtures of feces and urine were kept at room temperature for 0, 12, and 24 h to ferment and produce odor gases. After each fermentation period, the total ammonia, hydrogen sulfide, and acetic acid contents in the mixtures were quantified using colorimetric gas detector tubes (model: Gv100s Gas Detection System, Gas Tec, Wangara, WS, Australia) and a gas chromatograph–mass spectrometer (7010C Triple Quadrupole GC/MS, Agilent Technologies, Palo Alto, CA, USA), following a methodology described by [
33].
2.6. Carcass Traits and Meat Quality
At the end of the experiment (day 84), 12 lambs from each treatment were slaughtered after 16 h of feed deprivation. With the live bodyweights obtained, hot carcasses and different organs were weighed immediately after slaughtering and then stored at 4 for 24 h. The carcasses were weighed again the next day for evaluation of the cold carcasses, and the percentages of dressing and chilling losses for each carcass were recorded. The right side of each carcass was separated to measure the pH value, back-fat thickness, the area of the longissimus thoracis muscle, and meat color value. Samples of muscles (about 300 g) were taken for the determination of water-holding capacity (WHC) [
34], cooking loss (CL) [
35], and myofibril fragmentation index (MFI) [
36], while meat hardness, cohesiveness, chewiness, and springiness were measured using a texture analyzer (TA; HD, Stable Micro Systems, Surrey, UK) with a compression-plate attachment.
2.7. Statistical Analyses
All data were analyzed using a complete randomized design with general linear model procedures of statistical analysis software (SAS Institute Inc., Cary, NC, USA). The statistical model included the level of yucca, the collection day, and the interaction of treatment and day as fixed effects, with animal within treatment (with the exception of using pens for feed intake data) as a random effect. Carcass and meat quality characteristics, ruminal fluid fermentation, and fecal–urinary odor emissions data were entered into the GLM model in SAS. Data are reported with the least-square means (±SEs), and differences between them were considered significant at p ≤ 0.05.
4. Discussion
In Saudi Arabia, sheep production is a primary livestock industry in the agricultural sector. It plays a critical role in social and economic sustainability. According to [
37], the sheep population in Saudi Arabia was estimated to be approximately 17.5 million head, representing approximately 70% of the total livestock population [
37]. Under extensive grazing systems, sheep often do not receive their required nutrients because of shortages in natural resources, and this can cause reductions in the productive efficiency of flocks. Providing a range of feedstuffs, in particular forage, required by feeding ruminants is currently a major challenge facing the livestock industry in Saudi Arabia because of high feed prices.
According to [
38], Awassi lambs fed complete pelleted diets had 10 and 21% higher ADGs and feed efficiencies, respectively, when compared to those fed on grain barley and alfalfa hay. Previous research found that feeding lambs a complete pelleted diet resulted in an increase in the color of ruminal tissue (L* value from 50.66 to 29.11) and a reduction in the pH values of ruminal fluid from 6.05 to 5.27 [
39,
40].
Saponins, a group of secondary compounds in plants, are able to alter rumen fermentation characteristics and encourage animal productivity [
41]. Several studies have indicated that yucca saponins increased productive indicators, such as growth rate, meat, and milk production, in sheep when they were fed roughage diets [
42,
43]. A study reported in [
25] observed that growing lambs fed a diet supplemented with YS at levels between 40 and 60 mg YS/kg DM had higher growth rates [
25]. This is in agreement with the results obtained in our study: YS improved bodyweight, ADG, and feed efficiency ratio, in particular at 0 and 300 mg YS/kg DM. YS
0 and YS
300 generally performed better than YS
600. Overall, lambs treated with YS
300 had a higher final bodyweight (3.4%), ADG (6.6%), and feed efficiency (6.17%) in comparison with YS
600 lambs.
Serum concentrations of total protein, albumin, and creatine were not affected by yucca supplementation in this study, and were all within the reference ranges reported in [
44]. These results are consistent with those of previous studies [
45,
46,
47] showing that neither the levels nor saponins of yucca supplementation affected total protein, albumin, and creatine levels in ruminants. A reduction in serum urea concentration was associated with the highest level of yucca supplementation (YS
600) in our study, and the mean urea concentration was within the normal range for sheep (3.67–9.28 mM) [
48]. Previous studies have indicated that yucca extract components might modify kidney function by increasing the rate of urea clearance and lowering blood urea concentrations [
26].
In the current study, there was no response to the addition of yucca in terms of total VFA concentrations or in the proportions of the majority of individual VFAs in ruminal fluids. This is consistent with the results of previous studies, which indicated that dietary yucca supplementation had no beneficial effects on the VFA profiles of ruminant animals [
49,
50]. The authors of [
51] suggested that saponins supplemented at higher concentrations might adversely affect rumen fermentation. Conversely, a report by [
52] observed increases in gas and VFA production in dairy cattle fed a concentrate diet supplemented with yucca.
Reductions of 5.0 and 18.5% in ruminal ammonia concentrations were observed in lambs fed diets supplemented with 300 and 600 mg YS/kg DM, respectively, compared to those fed the CON diet (without yucca) in the current study. The complete pelleted diets of 300 and 600 mg YS/kg DM produced less ammonia compared with the control diet. The mechanism by which ammonia concentration is affected by the addition of YS could be attributed to an increase in ruminal nitrogen, as metabolic pathways (protein digestibility) and the involvement of saponins appeared to assist in reducing ammonia production in the rumen when yucca was added to the diets, while rumen ammonia concentration increases as a result of proteolysis in protein bacteria due to increases in rumen bacterial digestion by protozoa [
50,
53]. Thus, a reduction in ammonia production in the rumen could be attributed to the antiprotozoal activity utilized by saponins [
53,
54]. Similar findings have been reported in several previous studies [
26,
27,
55].
Yucca has important applications in ruminant nutrition and plays an important role in the regulation of fecal and urinary odor emissions, this being one of the main reasons for adding it to ruminant diets. This role is related to its involvement in various physiological functions, including the improvement of ruminal fermentation characteristics and microbiome responses and alterations to digestion and metabolic pathways, and the high-value compounds present in yucca (e.g., steroid saponins, glycocomponents, phenolics, and several enzymes). For example, yucca plays beneficial roles in enhancing nitrogen utilization through digestion, absorption, and metabolic and excretion processes in ruminants and poultry [
56,
57,
58]. These roles could be attributed to the reductions in the concentration of ammonia in fecal and urinary odor emissions that were observed in the current study when lambs were fed complete pelleted diets supplemented with yucca at a level of 600 mg/kg. Meanwhile, the release of fecal and urinary odors with the YS addition in the current study would have been due to the increase in acetic acid, which is involved in the regulation of a variety of enzymes; these include mono-oxygenases and the enzymatic family of aminotransferases. These enzymes are mainly responsible for the conversion of tryptophan in the diet into acetic acid [
58].
Differences in carcass characteristics and meat quality between the dietary treatments showed that feeding lambs the 300 mg YS/kg DM yucca diet increased slaughter weight, hot-carcass yield percentage, and shoulder wholesale cut weight. The dressing percentage increased with the 600 mg YS/kg DM yucca diet, and chilling loss was reduced with the CON diet. In general, the meat samples from the yucca-supplemented groups were harder, springier, and chewier. The results obtained here are in disagreement with those obtained by the authors of [
59], the latter reporting insignificant differences in the weights of parts of the carcass, meat, fat, and bones of lambs fed YS extracts at incremental levels from 0 to 400 mg YS/kg DM. In broilers fed with YS (100 mg YS/kg DM) supplements, the authors of [
60] reported positive improvements in live weight and carcass characteristics, such as carcass yield, dressing percentage, and breast. Similarly, these results were confirmed by previous research, which found that YS supplementation of broilers improved evisceration weight and yield of breast and thigh meat [
61,
62]. The mechanism by which the carcass and meat quality characteristics are affected positively by the addition of YS into livestock diets could be attributed to the improvements in gut histomorphology and nutrient absorption and utilization caused by steroid saponins [
60].