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ANIMAL PRODUCTION |


* Department of Animal and Food Sciences, Texas Tech University, Lubbock 79409-2141;
and
Pancosma, SA, Geneva, Switzerland; and
and
Prince Agri Products Inc., Quincy, IL 62306
| Abstract |
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Key Words: cattle feed intake morbidity preference sweetener
| INTRODUCTION |
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One strategy by which DMI by stressed calves might be increased is to improve the palatability of the diet. Taste is a key component of the palatability complex. If a calf associates a favorable response (e.g., a sweet taste) with a visit to the feed bunk, DMI might be increased. Research on adding sweeteners or other flavoring agents to the diets of feedlot cattle is limited. Sucrose supplementation of dairy cattle has been investigated, although the intake response to sucrose supplementation has been variable (Nombekela and Murphy, 1995
; Murphy et al., 1997
; Broderick et al., 2000
). A common artificial sweetener for use in human diets is sodium saccharin, which is 300 to 500 times sweeter than sucrose and has been shown to influence dietary preference in rats (Smith and Sclafani, 2002
). In initial research with Sucram (a sodium saccharin-based sweetener), Brown et al. (2004)
fed 0, 97, 194, and 291 mg/kg to stressed calves and observed a 17.2% greater overall DMI (P = 0.04) by calves supplemented with 194 mg of Sucram/kg during a 56-d receiving experiment.
Therefore, the objective of the present studies was to further determine effects of Sucram on health, performance, and dietary preference of feedlot cattle.
| MATERIALS AND METHODS |
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Experiment 1Receiving and Finishing Trial
Cattle.
Two hundred steer calves (British x Continental; average initial BW = 190.4 kg) were shipped 1,588 km from West Point, MS, to the Texas Tech University Burnett Center at New Deal, TX, in mid November. During the 16-h transit, steers lost 5.7% of their preshipment BW of 201.9 kg. Immediately after unloading, the cattle were processed, which included: 1) measurement of individual BW; 2) identification with a uniquely numbered ear tag; 3) vaccination with a modified live virus vaccine (Titanium 5, Agri-Labs, Des Moines, IA) and Clostridium chavoei, C. septicum, C. novyi, sordelli, and C. perfringens type C and D bacterin toxoid (Vision 7 with SPUR, Intervet, Millsboro, DE); 4) treatment with 35 mL of topical moxidectin (Cydectin, Dodge Animal Health, Overland Park, KS); and 5) tipping of horns as needed.
Treatment Assignment, Management, and Weighing Procedures.
The experiment was subdivided into receiving and finishing periods. For the receiving period, 16 soil-surfaced pens were used (4.9 m x 30.5 m; linear bunk space = 4.9 m), with 12 to 13 steers/pen. Treatments were control (no added sweetener) or 200 mg of Sucram/kg (DM basis; Sucram C-150, Pancosma, SA, Geneva, Switzerland; distributed by Prince Agri-Products, Quincy, IL) added to the 65% concentrate receiving diet and 75% concentrate growing diet, both of which were formulated to contain 13.5% CP (Table 1
). Sucram was added in a premix with ground corn at approximately 0.25% of the dietary DM, whereas animals in the control treatment were fed a premix composed of ground corn only (Table 1
). At the time of initial processing, steers were assigned randomly to 1 of 2 pens (the pair of pens constituted a location block), and the 2 treatments were assigned randomly to the pens within each block. Thus, there were 8 pens per treatment (8 location blocks) during the receiving period.
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All cattle were monitored daily for morbidity, and those with signs of BRD (labored breathing, nasal/ ocular discharge, depression, anorexia) were removed from their pen for a more thorough evaluation. When the rectal temperature of a calf that had been pulled from the pen was greater or equal to 39.7°C, the animal was given antimicrobial therapy (according to label directions) and returned to its pen. The first time an animal was treated, it received tilmicosin phosphate (Micotil, Elanco Animal Health, Indianapolis, IN) plus sterile penicillin G benzathine and penicillin G procaine (Aspen Veterinary Resources, Kansas City, MO). Animals that required a second treatment received florfenicol (Nuflor, Schering Plough Animal Health, Union, NJ), and those requiring a third treatment received long-acting oxytetracycline (Maxim 200, Phoenix Pharmaceutical Inc., St. Joseph, MO) plus sulfamethazine boluses (Albon SR, Pfizer, Exton, PA).
On d 56, all steers were switched to an 82% concentrate diet (Table 1
). For the finishing period of the experiment, treatments were arranged in a 2 x 2 factorial, with factors being receiving period treatment (control or Sucram) and finishing period treatment (i.e., with or without feeding of Sucram during the finishing period). Based on d-56 BW (e.g., animals of the lightest BW in each treatment group were not used) and health status (e.g., cattle that received 3 treatments for BRD were not used) during the receiving period, 180 animals (an equal number from the 2 receiving treatments) were selected for use in the finishing period. At this time, it was determined that 2 animals to be used in the finishing period were bulls, and they were subsequently surgically castrated. The 180 steers were sorted to 9 BW blocks and assigned to 36 concrete, partially slotted-floor pens (2.9 m x 5.6 m; bunk space = 2.4 m), resulting in 9 pens per each of the following treatments: 1) control during receiving/ control during finishing; 2) control during receiving/ Sucram during finishing; 3) Sucram during receiving/ control during finishing; and 4) Sucram during receiving/Sucram during finishing (Table 1
).
As in the receiving period, Sucram was added in a premix with ground corn at approximately 0.25% of the dietary DM, to supply 200 mg of Sucram/kg (DM basis) in the 82 and 90% concentrate diets (formulated to contain 13% CP; Table 1
). The process of selection and sorting of cattle into treatment groups for the finishing period was accomplished over a 4-d period; thus, steers were weighed and moved to their assigned pens, and the finishing-period dietary treatments began on d 60.
Cattle remained on the 82% concentrate diet for the next 14 d, after which they were switched to the final 90% concentrate diet (Table 1
). Intermediate BW measurements were typically collected on a pen basis at 28-d intervals during the finishing period of the study, except at d 112, when the cattle were reimplanted (Revalor S; 120 mg of trenbolone acetate, 24 mg of estradiol, Intervet), and on the day the cattle were shipped to slaughter, at which time individual BW measurements were obtained.
During the receiving and finishing periods, feed bunks were evaluated visually each day to determine the quantity of feed to offer to each pen. The bunk management approach resulted in 0 to 0.23 kg of feed remaining in the bunks at the time of evaluation. Diets were delivered once daily at approximately 0800 with a Rotomix 84-8 (Rotomix Inc., Dodge City, KS) self-propelled mixer-delivery unit, with the mixer mounted on load cells (scale precision of ± 0.454 kg).
Diet Analyses.
Samples of feed for each treatment were collected weekly from the Rotomix 84-8 mixer-delivery unit throughout the experiment and composited within weigh periods. In addition, at each weigh period (and at d 7 and 14 of the receiving period), feed bunks were swept, and any feed remaining in the bunks was weighed, and its DM content determined. Samples of dietary ingredients were taken every 2 wk during the experiment to measure DM, which was determined by drying samples for approximately 22 h in a forced-air oven at 100°C. Samples of feed delivered to the bunks were analyzed for nutrient content (AOAC, 1990
) in laboratory facilities at Texas Tech University (Table 1
).
Carcass Evaluation.
When approximately 60% of the steers within a given BW block were visually estimated (BW and visual assessment of fatness) to have sufficient finish to grade USDA Choice, all animals in the block were weighed individually and sent via commercial transport to a USDA-inspected slaughter facility (Excel Inc., Plainview, TX) for collection of carcass measurements. Carcass data were collected by personnel of the Cattlemens Carcass Data Service, West Texas A&M University, Canyon. Measurements included HCW, calculated yield grade, quality grade, marbling score, percentage of KPH, LM area, 12th rib fat thickness, and incidence of liver abscesses.
Statistical Analyses.
Performance data for the receiving period were analyzed as a randomized complete block design with 2 treatments, whereas finishing-period performance and carcass data were analyzed as a randomized complete block design with a 2 x 2 factorial arrangement of treatments. The MIXED procedure of SAS (SAS Inst. Inc., Cary, NC) was used for these analyses, with block as a random effect. Preliminary analysis of the data indicated significant (P < 0.05) receiving and finishing effects for initial BW during the finishing experiment, which resulted from the blocking of finishing treatments being restricted by receiving-period treatment. Thus, initial BW was used as a covariate in the model for finishing period data. Morbidity data for the receiving period were analyzed using the Glimmix procedure of SAS, assuming a binomial distribution. As with the performance data, treatment was the fixed effect, and block was considered a random effect. The USDA quality grade data (proportion grading below or at and above USDA Choice) also were analyzed with the Glimmix procedure (binomial distribution) using the same model as for the analysis of feedlot performance and other carcass data.
Experiment 2Preference Trial
Cattle.
Two weeks before the beginning of the experiment, 12 steers (British and Continental breeding) with the heaviest BW were selected from a larger group of 81 steers for use in a simultaneously replicated 3 x 3 Latin square dietary preference test. These cattle had been fed a restricted quantity of a 65% concentrate diet for the previous 2 mo. After selection, the steers were housed together in a soil-surfaced pen (4.9 m x 30.5 m) and were transitioned to ad libitum intake by feeding a 75% concentrate diet once daily at 0800 in increasing quantities.
Treatment Assignment.
Eight days before the beginning of the experiment, the cattle (average initial BW = 395.6 ± 6.17 kg) were weighed at 0700 and allocated to pens and dietary treatments. Each Latin square consisted of 3 pens (2 steers/pen) and 3 feeding periods. Each of the 3 feeding periods of the Latin square consisted of a 5-d adaptation period followed by a 5-d data collection period, resulting in a total of 30 d for the experiment. Steers were stratified by BW, with the 6 heaviest animals allocated to the first Latin square and the 6 lightest animals allocated to the second Latin square. Steers in each Latin square were further stratified in descending order by BW and allocated within strata to 1 of 3 pens.
Pens (partially slotted concrete) were 2.9 m wide x 5.6 m long and provided 2.4 m of bunk space/steer. Each feed bunk had a wooden divider at the midpoint, providing 1.2 m of bunk space on either side of the divider.
Treatments consisted of 1) control = a 77.5% concentrate diet delivered daily on both sides of the divider; 2) Sucram = a 77.5% concentrate diet supplemented with 200 mg of Sucram/kg of DM delivered daily on both sides of the bunk divider; and 3) choice = a 77.5% concentrate diet supplemented with or without 200 mg of Sucram/kg of DM delivered daily on either side of the bunk divider (Table 2
). Daily delivery of the Sucram and control diets in the choice treatment were alternated randomly between sides of the bunk divider to prevent positional bias. Sucram was added in a pre-mix with ground corn at approximately 0.50% of the dietary DM to supply 200 mg of Sucram/kg of DM in the complete diet.
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Diet Analyses.
During the data collection period, diet samples (2/period) were collected (from the Rotomix 84-8 mixer-delivery unit) and were analyzed for DM by drying for approximately 22 h in a forced-air oven at 100°C. Samples of dietary ingredients were taken every 2 wk during the experiment to determine DM content. Composite samples of the 2 diets fed during the study were analyzed by SDK Laboratories (Hutchinson, KS) for measurement of CP, ADF, fat, Ca, P, and K (Table 2
).
Statistical Analyses.
For each day of the three 5-d measurement periods, DMI on both sides of the feed bunk was calculated. Dietary preference within the choice treatment was calculated as Sucram diet DMI minus control diet DMI. For control and Sucram treatments, dietary preference was calculated based on orientation (left or right) of Sucram and control diets in the choice treatment for a given day. A positive value indicated a preference for Sucram over the control diet in the choice treatment or, or a preference for the same side of the bunk as the Sucram diet (applied to the choice treatment) in the control and Sucram treatments. A negative value indicates a preference for the control diet in the choice treatment or the same side of the bunk as the control diet (applied to the choice treatment) in the control and Sucram treatments.
The daily DMI differences and DMI for each treatment were subsequently analyzed as a simultaneously replicated Latin square with repeated measures using the MIXED procedure of SAS. The model included fixed effects of treatment, day, and treatment x day, and the random effects of square, period, and pen nested within square. The repeated term was day, and the subject of the repeated measure was defined as pen nested within square x period combinations. The variance-covariance structure of the repeated measures was evaluated with unstructured, autoregressive, and compound symmetry covariance structures, with homogeneous or heterogeneous variance. Based on Akaike and Schwarzs Bayesian information criteria, the unstructured covariance structure was found to provide the best fit for the DMI differences, whereas the autoregressive heterogeneous structure provided the best fit for the daily DMI data. Pairwise differences among preference estimates for the 3 treatments were evaluated using the PDIFF option of the MIXED procedure.
| RESULTS AND DISCUSSION |
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The trend observed for increased DMI during the second half (d 29 to 56) of the receiving period coincided with the change from a 65 to 75% concentrate diet. Galyean and Defoor (2003)
reported that dietary roughage NDF is a reasonably good predictor of effects of roughage source on DMI by feedlot cattle. Different percent concentrate diets may differ in sensory properties such as appearance, odor, taste and texture, as well as the metabolic and physical feedback mechanisms controlling feed intake. Nonetheless, further research would be required to determine whether an interaction exists between dietary roughage concentration and Sucram in receiving and growing diets. Another possible reason for the tendency for a greater response in DMI to Sucram during the second half of the receiving period could be that high levels of morbidity (59.7 vs. 58.0% for control and Sucram, respectively) combined with environmental, physical, and psychological stressors, decreased DMI in both treatment groups early in the receiving period. Proinflammatory cytokines associated with the immune response to infection may decrease feed intake (Broussard et al., 2001
; Johnson and Finck, 2001
). The multifactorial control of feed intake makes it difficult to delineate factors regulating DMI of the diets fed in the receiving period of our study.
Experiment 1Finishing Period
Simple-effect means for performance data for the finishing period are shown in Table 5
, and carcass data are presented in Table 6
. Probability values are shown for the main effects of receiving-period treatment, finishing-period treatment, and the receiving x finishing interaction.
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A trend for a receiving x finishing interaction (P = 0.08) was detected for DMI during the finishing period. Essentially, this interaction was the result of greater DMI by cattle fed Sucram in both the receiving and finishing periods than by cattle in the other 3 treatment groups. Indeed, adding Sucram at 200 mg/kg of the dietary DM to the finishing diet of cattle that had been fed the control diet during the receiving period had no effect on DMI compared with cattle that never received Sucram. Cattle fed Sucram during the receiving period and then switched to the control diet during the finishing period consumed the least DM during most of the cumulative periods of finishing, which also contributed to the receiving x finishing interaction. Reasons for the differential effects of Sucram on DMI by cattle during the receiving and finishing periods are unclear, but this finding may imply that cattle fed Sucram during receiving became accustomed to it and removal during the finishing period tended to decrease DMI.
The NRC (1996)
provides equations that allow calculation of dietary NEm and NEg concentrations based on performance data. Basically, this approach involves solving for the NEm and NEg values that would be required to yield the observed performance data. For these calculations, the average initial and final shrunk (multiplied by 0.96) BW and the d 0 to end DMI shown in Table 6
were used, with shrunk ADG calculated from the BW data and an average days on feed of 186.2. The resulting performance-based dietary NEm concentrations (Mcal/kg of DM) were 2.27, 2.28, 2.27, and 2.26 for the control receiving/control finishing, control receiving/Sucram finishing, Sucram receiving/ control finishing, and Sucram receiving/Sucram finishing treatments, respectively. Similarly, the performance-based dietary NEg concentrations were 1.58, 1.59, 1.58, and 1.57 Mcal/kg of DM, respectively, for the 4 treatment combinations. Performance-based values were approximately 5 to 7% greater than values based on NRC (1996)
tabular data for the feedstuffs used in the diets (Table 1
), but calculated NE values obviously differed little among treatments.
The carcass measurements of HCW, KPH percent, and fat thickness were largely unaffected by receiving and finishing period treatments (Table 6
). Dressing percent was greater (P = 0.11) for cattle fed the control diet during the finishing period. A receiving x finishing interaction existed for USDA yield grade (P = 0.09). This interaction reflected decreased yield grade for cattle fed the control receiving/Sucram finishing combination compared with those fed the control receiving/ control finishing combination. Decreased yield grade also was observed in cattle fed the Sucram receiving/ control finishing combination vs. the Sucram receiving/Sucram finishing combination.
Marbling score was increased (P = 0.04) for cattle fed the control diet vs. those fed Sucram during the receiving period (Table 6
). The increased marbling score of cattle fed the control diet during the receiving period, however, did not produce changes in quality grade; the percentage of carcasses grading USDA Choice or Prime did not differ among treatments. Reasons for the increased marbling score of cattle fed the control diet during the receiving period are not readily apparent. Occurrence of abscessed livers was typical for cattle at the Texas Tech University Burnett Center, and these data were not analyzed statistically because of the low rates in various abscess categories.
Drager et al. (2004)
studied the effect of Sucram (0 or 198.4 mg/kg of DM), on finishing period performance and carcass characteristics in heavy crossbred steers (486 kg of average BW; 39 steers; 3 pens/treatment). Feedlot performance and carcass characteristics (P > 0.22) were not influenced by the inclusion of Sucram, a finding that is similar to our results. For the overall feeding period, effects of adding Sucram to the diet were small, but it is noteworthy that interactions with receiving-period treatment affected finishing-period DMI. Thus, the optimal duration of feeding Sucram in beef cattle diets needs further study; however, our data suggest that benefits seem greater early in the feeding process (the receiving period) than later (the finishing period).
Experiment 2Preference Trial
Results of Exp. 2 are shown in Table 7
. Overall, the effects of treatment (P = 0.22) and day (P = 0.33) were not significant, but a significant treatment x day interaction (P = 0.03) was detected for preference. Thus, differences among the least squares means on individual days were examined. As expected, dietary preference where no diet choice was offered (control and Sucram treatments; same diet on both sides of the bunk divider) was largely not different (P = 0.79 to 0.96). Nonetheless, on d 2, animals fed the control treatment had a greater dietary preference (P = 0.01) than those in the Sucram or choice treatments (i.e., the difference in DMI between the 2 sides of the bunk was greatest for the control treatment). Reasons for this response are unknown. A difference in dietary preference was detected on d 1 (P = 0.01) and d 3 (P = 0.02) of the 5-d period for control vs. choice and Sucram vs. choice comparisons, with cattle provided the choice treatment consuming 0.49 and 1.72 kg of DM more of the Sucram diet than the control diet, respectively. This effect, however, was not consistently present across days (Table 7
). Daily DMI intake variation by steers fed these concentrate-based diets ad libitum may have contributed to the inconsistency of these observations. Average DMI did not differ among treatments (P = 0.81; Table 7
).
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| IMPLICATIONS |
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| Footnotes |
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3 Present address: Eli Lilly, Monterrey, Mexico. ![]()
2 Corresponding author: joe.mcmeniman{at}ttu.edu
Received for publication February 17, 2006. Accepted for publication May 6, 2006.
| LITERATURE CITED |
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and leptin: Two players in an animals metabolic and immunologic responses to infection. J. Anim. Sci. 79(Suppl. E):E118E127.
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