Influence of genotype and diet on steer performance, manure odor, and carriage of pathogenic and other fecal bacteria. I. Animal performance

Although Brahman crosses constitute a large portion of US beef cattle, little information is available on their response to diverse feed resources compared with Bos taurus steers. Thus, the objectives were to evaluate genotype and diet effects on steer performance during the growing period and subsequent response to a high grain diet during the finishing period. Fifty-one steers [0 (15), 1/4 (20), 1/2 (7), and 3/4 Brahman (9), with the remaining proportion being MARC III] were allotted to 8 pens. Beginning on December 2, steers were individually fed chopped bromegrass hay (n = 26; DM = 85%, CP = 9.5%, ME = 2.19 Mcal/kg) or a corn silage-based diet (n = 25; DM = 51%, CP = 11.9%, ME = 2.75 Mcal/kg) for 119 d. All steers were then fed a high corn diet (DM = 79%, CP = 11.7%, ME = 3.08 Mcal/kg) to a target BW of 560 kg (176 d). Data were analyzed by ANOVA, with genotype, growing diet, and the 2-way interaction included. The interaction was not significant (P > 0.25). The MARC III and 1/2 Brahman steers weighed more (P < 0.01) than 1/4 or 3/4 Brahman steers initially and at the end of the growing period. Weight of bromegrass-fed (325 kg) steers was less than that of corn silage-fed (384 kg) steers at the end of the growing period. Steer ADG and intake of DM, CP, and ME were less (P = 0.087 to 0.001) for 1/4 and 3/4 Brahman than for 0 or 1/2 Brahman steers during growing, finishing, and total, but efficiency of gain did not differ (P > 0.10). Carcass weight, marbling score, quality grade (P < 0.05), and kidney fat (P = 0.06) differed among genotypes. Daily DMI (6.91 vs. 7.06 kg) was similar, but CP (0.66 vs. 0.84 kg) and ME (15.2 vs. 19.4 Mcal) intake of bromegrass fed was less (P = 0.001) than those of corn silage-fed steers. Values for DMI/gain (22.3 vs. 7.43 kg/kg), CP intake/gain (2.13 vs. 0.88 kg/kg), and ME intake/gain (48.8 vs. 20.4 Mcal/kg) were greater (P < 0.001) in bromegrass-fed than corn silage-fed steers. Over the total study, ADG was lower (0.96 vs. 1.01 kg), and DMI (7.82 vs. 7.19 kg), DMI/gain (8.21 vs. 7.10 kg/kg), and ME intake/gain (22.6 vs. 20.9 Mcal/kg) were greater (P < 0.05) in bromegrass-fed than in corn silage-fed steers. Carcass weight, dressing percent, adjusted backfat, and yield grade (P < 0.05) were greater for corn silage-fed than for bromegrass-fed steers. Feed intake and performance, but not efficiency, differed among these genotypes. Compensatory performance during finishing was insufficient to overcome reduced performance during the growing period.     

Salinomycin and lasalocid effects on growth rate, mineral metabolism and ruminal fermentation in steers

Two experiments were conducted to determine the effects of salinomycin and lasalocid on metabolism and growth of growing steers. In Exp. 1, 80 Angus steers (228 kg) were assigned to the following treatments: 1) control, 2) 50 mg salinomycin.hd-1.d-1, 3) 100 mg salinomycin.hd-1.d-1 and 4) 250 mg lasalocid.hd-1.d-1. Steers were fed corn silage once daily with allotments based on the amount of silage that each pen of five steers would consume in a 24-h period. In addition, .81 kg/hd of a corn-soybean meal supplement was fed daily during the 112-d study. Daily gains were similar across treatments, but feed intake was lower (P less than .05) for steers fed ionophores. Molar proportions of ruminal acetate were lower (P less than .05) in steers fed ionophores at 28 and 90 d. Ruminal propionate was lower (P less than .05) in control steers at 28 d, but values were similar across treatments on d 90. Plasma copper (Cu) was lower (P less than .05) in control steers on both sampling days. In Exp. 2, 16 Hereford steers were allotted to two blocks of eight animals each and assigned to one of three treatments: 1) control (n = 6), 2) 11 mg salinomycin/kg diet (n = 6) and 3) 33 mg lasalocid/kg diet (n = 4). Following a 28-d adjustment period, apparent absorption and retention of macrominerals and nitrogen (N) were determined during a 5-d collection period. Apparent absorption and retention of N did not differ among treatments when data were analyzed using N intake as a covariate.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of diet type and metabolizable energy intake on tympanic temperature of steers fed during summer and winter seasons

A summer study and a winter study were conducted using an incomplete factorial structure in a complete randomized design. Within season, the factors studied were 1) type of diet, which included 2 levels of ME, classified as either concentrate (3.04 Mcal of ME/kg) or roughage (2.63 Mcal of ME/kg) diets, and 2) daily ME intakes (MEI) of 11, 18, and 25 Mcal of ME/d for the roughage diets and 18, 25, and 32 Mcal of ME/d for the concentrate diets. In Exp. 1 (summer study), 30 steers (5 steers/treatment combination) were used to collect tympanic temperatures (TT). In Exp. 2 (winter study), 24 steers (4 steers/treatment combination) were used to collect TT. Mean TT was 0.3°C greater for summer than winter (38.9 vs. 38.6°C, respectively; P < 0.05). Steers fed diets based on concentrate tended to display greater TT than steers fed diets based on roughage. Season × diet × hour interactions were found for TT (P = 0.01). In the winter, greater TT (P < 0.05) were found from 0900 to 1400 h when an equal amount of MEI was derived from a concentrate-based vs. roughage-based diet. In cattle fed roughage-based diets during the summer, TT = 38.63 + 0.0114?MEI, whereas for cattle fed concentrate-based diets, TT = 38.69 + 0.0114?MEI. During the winter, for cattle fed a roughage-based diet, TT = 37.65 + 0.0856?MEI - 0.0018?MEI(2), whereas for cattle fed a concentrate-based diet, TT = 35.37 + 0.2635?MEI - 0.0051?MEI(2). In summary, results demonstrate that increases in the energy of the diet resulted in increases in TT. However, the response was dependent on season of the year, with a linear response in TT for summer and a quadratic response during winter.     

Responses to an estrogenic growth promoter in beef steers fed varying nutritional regimens

We investigated the influence of DM and(or) energy intake and dietary CP levels on the performance and nitrogen (N) retention of beef steers with and without growth promoter implants. In Exp. 1, four implanted (Synovex-S, 200 mg of progesterone plus 20 mg of estradiol benzoate) Angus steers and four Angus steers that were not implanted were assigned to concurrent 4 x 4 Latin squares. Initial BW averaged 296 kg. Each square consisted of moderate and moderately high DM intake treatments (4 and 6 kg/d) and low and adequate CP intake treatments (450 and 600 g/d) in a 2 x 2 factorial arrangement. Periods were 2 wk of adaptation, 5 wk of growth, and 1 wk of balance collection. Experiment 2 consisted of two replicates of 32 Hereford steers each (initial BW 324 kg). Each replicate was a 4 x 2 factorial in which steers were individually fed for 63 d. All steers had ad libitum access to a 60% corn-based concentrate diet containing either 7.9, 10.0, 12.1, or 14.6% CP (DM basis), and steers were either implanted or not implanted with Synovex-S. Experiment 3 was similar to Exp. 2 except that all steers (initial BW 315 kg) received a low-protein diet (7.6% CP) with calculated energy densities of either 1.86, 2.04, 2.22, or 2.42 Mcal ME/kg DM, and steers were limited to an equalized DM intake of 9.5 kg daily. In Exp. 1, gains for the low CP, moderate and moderately high DM intakes and the adequate CP, moderate and moderately high DM intakes were 240, 555, 208, and 730 g/d, respectively, for steers not implanted and 333, 643, 488, and 988 g/d, respectively, for implanted steers (SEM = 102 g/d). Respective values for retained N were .13, .18, .16, and .26 g/kg BW.75 and .13, .15, .22, and .29 g/kg BW.75 (SEM = .04 g/kg BW.75). Implant response was greater (CP x implant, P < .01) for both gain and retained N when adequate CP compared to low CP diets were fed. For Exp. 2, the lowest CP diet reduced ADG (.97 vs 1.27 kg/d) and efficiency of gain (100 vs 120 g gain/kg DM). Synovex-S was less effective in improving efficiency for the lowest protein diet than for the other diets (11.7 vs 20.2%). During Exp. 3, neither Synovex-S nor dietary energy influenced gain and efficiency. We concluded that adequate dietary protein is necessary to optimize the response to estrogenic growth promoters and that the low response under inadequate protein and energy intake is not improved by increasing the energy density of the diet.     

Evidence that bovine growth hormone treatment increases the rate of extrathyroidal 5'-monodeiodinase activity in cattle

This study examined the influence of bovine growth hormone (bGH) on liver and kidney thyroxine-5'-monodeiodinase activity (TMA) in growing beef cattle. In a preliminary trial (trial 1), tissue samples were obtained at slaughter from two placebo-injected and two bGH-injected (29.2 IU/day for 14 days before slaughter) Hereford heifers (398 kg avg slaughter wt), with one heifer on each treatment fed at either 1.0 or 2.0 times maintenance energy requirement. In a second trial, tissue and plasma samples were obtained from six placebo-injected and six bGH-injected (29.2 IU/day for 19 days) Hereford steers (331 kg avg slaughter wt) fed at 1.8 times maintenance energy requirement. In a third trial, liver tissue and plasma samples were obtained from 14 Angus X Hereford steers (270 kg avg wt) fed either an 8% protein, 1.96 Mcal-metabolizable energy/kg diet (8 steers) or a 14% protein, 2.67 Mcal-metabolizable energy/kg diet (6 steers) in association with acute administration of bGH. Half the steers in each group were given two injections per steer of either placebo or 37.8 IU bGH at 24-hr intervals and slaughtered 24 hr after the second injection. Units of tissue TMA in all trials were measured at slaughter; one unit defined as 1 ng T3 generated/hr/mg protein during incubation with T4 (1.3 fM). In trial 1, TMA in liver and kidney was 2.86 and 1.21 times greater, respectively, for bGH than for placebo treatments. In trial 2, units of TMA in liver homogenates were higher (P less than .05) for bGH (4.14) than for placebo (2.83) treatments and higher (P less than .02) in liver microsomal preparations for bGH (32.7) than for placebo (27.3) treatments. Units of TMA in kidney homogenates were also higher (P less than .10) for bGH (1.48) than for placebo (.87) treatments and higher (P less than .02) in kidney microsomal preparations for bGH (23.0) than for placebo (16.4) treatments. Following acute injection of bGH (trial 3), units of TMA in liver homogenates were higher (P less than .01) for bGH (2.5) than for placebo (1.8) treatments. Plasma T4 (70.0 vs 73.5 ng/ml) and T3 (1.08 vs 1.18 ng/ml) concentrations appeared slightly higher in bGH-treated steers (trial 2) and increased by 20 and .5 ng/ml, respectively, (P less than .01) within 6 to 12 h after acute injection of bGH (trial 3). Concurrently, plasma TSH concentration increased following acute GH injection (trial 3).(ABSTRACT TRUNCATED AT 400 WORDS)     

Effects of recombinant DNA-derived somatotropin and dietary energy intake on development of beef heifers: II. Concentrations of hormones and metabolites in blood sera

The effects of somatotropin (STH) and energy intake on serum concentrations of glucose (GLU), insulin (INS), nonesterified fatty acids (NEFA), urea nitrogen (UN) and insulin-like growth factor-I (IGF-I) were determined in 40 Angus heifers. At 7 mo (208 +/- 8 d) of age heifers were assigned to four treatment groups: 1) vehicle (V) + high energy (HE; 2.68 Mcal ME/kg DM), 2) recombinant DNA-derived STH (20.6 mg/d; s.c.) + HE, 3) V + low energy (LE; 2.22 Mcal ME/kg DM) or 4) STH + LE. Animals remained on treatments until an average of 15.5 mo of age. Blood samples were taken every 30 min for 4 h at 9, 11, 13 and 15 mo of age to determine circulating concentrations of metabolites and hormones. Serum IGF-I was increased (P less than .01) by STH injections, but this effect appeared to diminish with age (STH x age; P less than .01). Energy intake did not influence IGF-I levels. Somatotropin increased (P less than .01) serum GLU in heifers fed the HE diet but only tended (P = .08) to increase GLU in those fed the LE diet (STH x energy; P = .05). Although STH increased (P less than .01) serum INS in both energy groups, the response in heifers fed the HE diet was greater (P less than .02) than that in heifers fed the LE diet (STH x energy; P less than .05). Heifers fed LE had higher (P less than .01) concentrations of NEFA than heifers fed HE.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of dietary energy level and protein source on site of digestion and duodenal nitrogen and amino acid flows in steers

Six steers (468 kg) with ruminal and duodenal cannulas were fed diets formulated for two levels of energy containing three crude protein (CP) sources in a 6 X 6 Latin square with a 2 X 3 factorial arrangement of treatments. Energy levels were 2.17 and 2.71 Mcal metabolizable energy (ME)/kg dry matter (DM) provided by hay-corn (H) and corn silage-corn (CS) diets, respectively. Soybean mean (SBM), corn gluten meal-urea (CGM) and urea (U) provided 33% of dietary CP in 12% CP diets. Apparent organic matter (OM) digested in the stomach was not affected (P greater than .05) by energy level or CP source, but OM truly digested in the stomach was greater (P less than .05) when steers were fed the CS compared with the H diet. Duodenal flow of non-NH3 N was greater (P less than .05) when steers were fed CS compared with H and when fed SBM or CGM compared with U. Efficiency of bacterial protein synthesis and duodenal bacterial N flow were increased (P less than .05) when steers were fed CS, but non-NH3, nonbacterial N flow to the duodenum was increased (P less than .05) when steers were fed H. When steers were fed CS rather than H, flows (g/d) of bacterial amino acids were greater (P less than .05), but flows of nonbacterial amino acids tended (P less than .08) to be less. Total amino acid flows were not affected (P greater than .05) by energy level. Duodenal flows of total amino acids tended (P less than .06) to be greater when steers were fed CGM compared with SBM or U, due mainly to an increased (P less than .05) flow of nonessential amino acids.     

Rice mill feed as a replacement for broiler litter in diets for growing beef cattle

The efficacy of replacing broiler litter with rice mill feed was evaluated in four experiments. In Exp. 1, 40 predominantly Angus steers (initial BW = 277+/-18.2 kg) were fed four dietary treatments for 112 d (five steers per pen; two pens per diet). Dietary treatments (DM basis) were as follows: 1) 47% broiler litter:53% corn; 2) 60% rice mill feed:40% corn; 3) 50% rice mill feed:50% corn; and 4) 40% rice mill feed:60% corn. All diets, along with bermudagrass hay, were fed free choice. Daily gains were faster (P < 0.10) for the 50:50 and 40:60 diets (1.26 and 1.30 kg/d, respectively) than for the broiler litter diet (0.89 kg/d). Daily DMI was less (P < 0.10) by steers consuming rice mill feed-based diets than by those consuming broiler litter-based diets. In Exp. 2, 16 Angus x Charolais steers (initial BW = 277+/-22.7 kg) were fed the same four diets used in Exp. 1 while housed in individual metabolism stalls for determination of nutrient digestibility. Daily DMI was not different (P > 0.10) among diets. Nutrient digestibilities did not differ among diets (P > 0.10). In Exp. 3, 40 Continental cross steers (initial BW = 257+/-21.3 kg) were fed one of four dietary treatments for 112 d (five steers per pen; two pens per diet). On a DM basis, diets were as follows: 1) 47% broiler litter:53% soyhulls; 2) 70% rice mill feed:30% soyhulls; 3) 60% rice mill feed:40% soyhulls; and 4) 50% rice mill feed:50% soyhulls. All diets, along with bermudagrass hay, were fed free choice. Daily gains were less (P < 0.05) for the broiler litter diet than for the 60:40 and 50:50 diets (1.05, 1.16, and 1.28 kg/d, respectively), and steers fed the broiler litter diet consumed less DM than did steers fed the varying rice mill feed-based diets (P < 0.10). In Exp. 4, 16 Angus x Charolais steers (initial BW = 292+/-21.1 kg) were fed the same four diets as in Exp. 3 while housed in individual metabolism stalls for determination of nutrient digestibility. Daily DMI was less (P < 0.01) for the broiler litter diet (5.0 kg/d) than for the 70:30, 60:40, and 50:50 diets (7.8, 7.9, and 7.9 kg/ d, respectively). Digestibilities for DM, OM, and ADF did not differ (P > 0.10) among treatments; however, CP digestibility was greatest (P < 0.10) for the 60:40 diet, and NDF digestibility was least (P < 0.10) for the 70:30 diet. Rice mill feed can be used to replace broiler litter to formulate low-cost diets for stocker calves. Soyhulls and corn can be blended with rice mill feed to produce acceptable backgrounding diets for growing beef calves.     

Feed intake and weight gain of growing goats fed diets of various energy and protein levels

Growing goats, 45 Alpine and 45 Nubian, were used in a 3 x 3 factorial arrangement to quantify the influence of dietary energy and protein levels on daily DM intake and nutrient utilization for growth. Goats had ad libitum access to complete mixed diets containing either 2.46, 2.77 or 3.05 Mcal/kg ME plus 11.2, 12.7 or 15.1% CP for 16 wk. Dry matter intake decreased curvilinearly as dietary ME density increased (P less than .001). Dry matter intake increased linearly (P less than .05) as dietary CP level increased during all growth intervals except wk 25 to 28 of age. Average daily gain was 115, 113 and 99 g/d for goats fed diets containing 2.46, 2.77 and 3.05 Mcal/kg ME, respectively. Average daily gain was 104, 106 and 117 g/d for goats fed diets with 11.2, 12.7 and 15.1% CP, respectively. Dry matter intake was higher (P less than .01) for Alpine than for Nubian goats, whereas ADG was similar between breeds. Intake of ME was 248, 260 and 198 kcal/(kg.75.d) for goats fed the low- medium- and high-energy diets, respectively. Intake of CP was 9.1, 10.7 and 13.2 g/(kg.75.d) for goats fed low-, medium- and high-protein diets, respectively. Average requirements for growth derived from regression analysis of all data points were 4.6 kcal ME and .26 g CP/g ADG. The prediction equation for intake of growing goats of 4 to 8 mo of age was: DMI, g/d = 1,749 - 496 DE, kcal/g + 18 live weight, kg + 3 ADG, g/d; r2 = .73 (Sy.x = 127, P less than .0001, n = 90). The requirement of ME for growth was 33% lower than the value recommended in 1981 by the National Research Council.     

Effects of cold environment and intake level on the energetic efficiency of feedlot steers.

The effects of cold climatic conditions on energy partitioning were investigated with 49 Hereford-type steers fed an all-concentrate, barley-based diet in a 2 x 3 factorial comparative slaughter trial. Steers (seven per treatment) were kept either indoors or outdoors (n = 2) and fed at 50, 65, or 80 g of DM/kg of BW.75 (n = 3) for up to 106 d. Mean temperatures were 16.9 +/- 2.7 degrees C and -7.6 +/- 6.8 degrees C in indoor and outdoor locations, respectively. Steers housed indoors grew 49% faster (P less than .001) and had 51% better gain: feed ratios (P less than .05) than those kept outdoors. Outdoor steers retained 65% less (P less than .001) energy. Estimated fasting heat production in the outdoor steers was 18% higher (P less than .01) and efficiency of ME use for maintenance 14% lower (P less than .01) than in the indoor steers, which resulted in an estimated increase of 41% in the ME requirements for maintenance in the outdoor steers. The NEg content of the diet was decreased from 1.29 Mcal/kg in the indoor steers to .76 Mcal/kg in the outdoor steers. Outdoor steers deposited 21% of their energy as protein, whereas indoor steers deposited only 14% of their energy as protein, which could explain the low NEg value of the diet in the cold environment. It was concluded that the main factors contributing to reduced energetic efficiency in the cold were an increased maintenance requirement and a greater proportion of the dietary energy retained as protein.     

Effects of energy and lasalocid on productivity of first-calf heifers

One hundred forty-three crossbred, fall-calving first-calf heifers were used to determine the effects of two levels of energy and two levels of lasalocid on cow-calf productivity. Diets fed for approximately 110 d prepartum were calculated to provide a daily intake of 15.3 (LE) or 18.0 (HE) Mcal ME; diets fed for approximately 130 d postpartum were calculated to provide a daily intake of 17.8 (LE) or 21.0 (HE) Mcal ME. Two supplements were fed with each energy level to provide a calculated 0 (C) or 200 mg.hd-1.d-1 lasalocid (L). Heifers fed HE gained .06 kg more (P = .08) per day prepartum than LE heifers. There was an interaction (P less than .05) between treatment and prepartum days on trial for heifer weight approximately 2 wk prepartum and body condition at calving. Energy had no effect on heifer weight at 2 wk prepartum or condition score at calving when estimated and compared at 90 d on trial. However, regression estimates for 130 d on trial showed that HE heifers would have been 19 kg heavier (P less than .001) and would have had .4 unit higher condition score (P less than .01) than LE heifers. Energy and lasalocid had no effect (P greater than .05) on hip height or pelvic area at calving or on calf birth weight, calving ease score or gestation length. Cows fed HE weighed 17 kg more (P less than .05) and had .5 unit higher (P less than .001) condition score than LE cows at approximately 130 d postpartum. Lasalocid had little effect on postpartum changes in weight or body condition. Lasalocid supplementation to the LE diet tended to increase milk production and calf weight, whereas supplementation to the HE diet did not. Feeding the LE diet decreased (P less than .05) cycling activity by 18 percentage points and decreased (P less than .01) overall pregnancy rate by 25 percentage points. Lasalocid had no influence on reproductive performance.     

Growth, carcass quality, and protein and energy metabolism in beef cattle with different growth potentials and residual feed intakes

Twenty-four beef steers (predominantly Angus x Hereford, 14 to 18 mo of age, 403 +/- 3 kg of BW), were housed and fed in individual pens for about 122 d. Twelve steers came from a herd that had been selected for growth (high growth; HG) and the other 12 from a herd with no selection program (low growth; LG). Another 6 steers (3 from each group) were slaughtered at the beginning to obtain the initial composition. All steers were fed the same corn-based diet (3.06 Mcal of ME/kg of DM, 13.6% CP) on an ad libitum basis. Two weeks before slaughter, total urine was collected for 5 d for estimation of 3-methylhistidine excretion and myofibrillar protein breakdown rates. Compared with LG steers, HG steers had less initial BW but greater final BW, DMI (7.52 vs. 6.37 kg/d), ADG (1.33 vs. 0.853 kg/d), G:F (0.176 vs. 0.133 kg/kg), ME intake (0.233 vs. 0.201 Mcal x kg of BW(0.75) x d(-1)), and retained energy (RE; 0.0711 vs. 0.0558 Mcal x kg of BW(0.75) x d(-1)); gained more fat (676 vs. 475 g/d); and tended to gain more whole body protein (100 vs. 72 g/d), with no difference in residual feed intake (RFI). Estimated net energetic efficiency of gain (k(g)) and ME for maintenance (ME(m)) did not differ between the 2 groups, averaging 0.62 and 0.114, respectively. The HG steers had greater HCW (350 vs. 329 kg), backfat (16.1 vs. 11.6 mm), and yield grades (3.53 vs. 2.80), with a similar dressing percent, KPH fat, LM area, and marbling score. Skeletal muscle protein gain (70.2 vs. 57.6 g/d) and fractional protein accretion rate (0.242 vs. 0.197%/d) tended to be greater in HG than in LG steers. Steers were classified into low (-0.367 kg/d) and high (0.380 kg/d) RFI classes. Compared with the high RFI steers, low RFI steers consumed less DM (6.61 vs. 7.52 kg/d) and ME (0.206 vs. 0.234 Mcal x kg of BW(0.75) x d(-1)) and tended to gain less fat (494 vs. 719 g/d), but were similar for initial and final BW, ADG, G:F, protein gain, HCW, dressing percent, backfat, KPH fat, LM area, marbling score, and yield grade, as well as for all observations related to myofibrillar protein metabolism. Residual feed intake may be positively [corrected] correlated with ME for maintenance. The maintenance energy requirement increased by 0.0166 Mcal x kg(-0.75) x d(-1) for each percentage increase in fractional protein degradation rate, confirming the importance of this process in the energy economy of the animal.     

Characterization of biological types of cattle (cycle III). IV. Postweaning growth and feed efficiency

Postweaning growth and feed efficiency data were analyzed on 769 F1 crossbred steers out of Angus and Hereford dams and sired by Pinzgauer, Tarentaise, Brahman, Sahiwal, Hereford and Angus sires. Breed groups were fed in replicated pens and slaughtered serially at three different dates in each of 2 yr. Quadratic regressions of pen mean weight on days fed and of cumulative metabolizable energy consumption (ME) on days fed were used to estimate gain, ME consumption and efficiency (Mcal ME/kg gain) over time (0 to 213 d on feed) and weight (250 to 470 kg) intervals, and from d 0 to a small degree of marbling (corresponds to USDA low Choice quality grade) and an 18.9% fat trim end point. Brahman-sired crosses were significantly heavier at weaning than all other breed groups. However, during the postweaning period, which included winter months, and while being fed a moderately high concentrate diet, average daily gain of Brahman-sired crosses tended to be less than Angus- or Hereford-, Tarentaise- and Pinzgauer-sired crosses and that of Sahiwal-sired crosses was significantly less than all other breed groups. Differences among breed groups were not significant for feed efficiency in the time constant interval from 0 to 213 d. In a weight interval from 250 to 470 kg, only Sahiwal-sired crosses differed significantly, requiring more Mcal ME/kg gain than other breed groups. Hereford-Angus crosses were more efficient than all other breed groups (P less than .05) to the marbling end point and to the 18.9% fat trim end point, primarily because of fewer days on feed and thus less net energy required for maintenance. Pinzgauer-sired crosses were significantly more efficient than Tarentaise-, Brahman- and Sahiwal-sired crosses to the marbling end point (P less than .05).     

Effects of ruminal and postruminal infusion of starch hydrolysate or glucose on the microbial ecology of the gastrointestinal tract in growing steers

Forty crossbred steers were used to determine the effects of carbohydrate supply site on the indigenous bacteria of the gastrointestinal tract. Steers were fitted with ruminal and abomasal infusion catheters and assigned randomly to one of eight groups in a complete randomized block design. The experimental period was 36 d. Treatments included: 1) a pelleted basal diet fed at 0.163 Mcal ME x (kg BW(0.75)) x 1 x d(-1) (LE); 2) the basal diet fed at 0.215 Mcal ME x (kg BW(0.75)) (-1) x d(-1) (HE); 3) the basal diet fed at 0.163 Mcal ME x (kg BW(0.75))(-1) x d(-1) with ruminal infusion of starch hydrolysate (SH) (RSH); 4) the basal diet fed at 0.163 Mcal ME x (kg BW(0.75))(-1) x d(-1) with abomasal infusion of SH (ASH); and 5) the basal diet fed at 0.163 Mcal ME x (kg BW(0.75))(-1) x d(-1) with abomasal infusion of glucose (AG). The total volume ofinfusate (5 kg x site(-1) x d(-1)) was equalized across treatments and infusion sites by infusion of water. Glucose and SH were infused at rates of 14.35 and 12.64 g x (kg BW(0.75)) x d(-1), respectively. Ruminal, cecal, and fecal samples were obtained on d 36. Ruminal pH was low (5.79) in LE steers and unaffected (P > 0.10) by increased energy intake or carbohydrate infusion. Cecal and fecal pH were 6.93 and 7.00, respectively, for LE steers. Increasing energy intake (P < 0.10) and the rate of carbohydrate infusion (P < 0.01) significantly decreased cecal and fecal pH compared with LE. Ruminal counts of anaerobic bacteria in LE steers were 8.99 log10 cells/g and abomasal carbohydrate infusion had no affect (P > 0.10) on these numbers. However, ASH and AG steers had approximately 1.5 log10 cells/g more (P < 0.01) cecal and fecal anaerobic populations. Ruminal, cecal, and fecal aerobic bacterial counts were 40, 22, and 23%, respectively, lower than anaerobic counts. Generally, aerobic counts responded similarly to the anaerobic counts. Less than 1% of the anaerobic bacteria enumerated in the rumen, cecum, and feces were coliforms, and 97% of the coliforms were Escherichia coli. Carbohydrate infusions resulted in only numerical increases in fecal coliform and E. coli concentrations (P > 0.10). Fecal E. coli were highly acid sensitive in all steers, with less than 1% surviving a 1-h exposure to low pH (2.0). This suggests that cecal or fecal pH is not a good indicator of acid resistance, and it supports the concept that there are other factors that may induce acid resistance.     

Effects of recombinant DNA-derived somatotropin and dietary energy intake on development of beef heifers: I. Growth and puberty

The effects of dietary energy intake and somatotropin (STH) on growth and puberty were studied in 40 Angus heifers. At an average age of 7 mo (208 +/- 8 d), heifers were assigned to four treatment groups: 1) vehicle (V) + high energy (HE; 2.68 Mcal ME/kg DM), 2) recombinant DNA-derived STH (20.6 mg/d; s.c.) + HE, 3) V + low energy (LE; 2.22 Mcal ME/kg DM) or 4) STH + LE. Animals remained on treatments until 15.5 mo of age. Body weights (BW), hip heights (HH) and areas of pelvic openings (PA) were measured every 28 d and backfat thicknesses (BF) were measured every 56 d. Plasma progesterone was measured in blood samples taken three times per week beginning at 9 mo of age to determine age at first ovulation. Heifers fed HE were heavier (P less than .01), gained faster (P less than .01) and had greater BF (P less than .01) than those fed LE. Animals treated with STH gained faster (P less than .01) and were heavier (P less than .05) between 12 and 15 mo of age than V-treated heifers. Heifers treated with STH also had less BF (P less than .05) and a tendency for a greater (P = .08) increase in HH than in V-treated heifers. Somatotropin interacted with energy (P less than .05) and age (P less than .01) to influence PA. Somatotropin increased (P less than .01) PA in heifers fed the HE diet but not in those fed the LE diet.(ABSTRACT TRUNCATED AT 250 WORDS)     

Influence of oscillating dietary crude protein concentration on performance, acid-base balance, and nitrogen excretion of steers

Decreasing dietary N inputs into beef cattle feeding operations could potentially decrease environmental concerns relating to air and water quality. Previous studies with sheep suggest that oscillating dietary CP concentrations may improve N use efficiency and thereby decrease dietary N requirements. Therefore, two studies were conducted to determine the effects of oscillating dietary CP concentrations on performance, acid-base balance, and manure characteristics of steers fed high-concentrate diets. Steers were fed to a constant backfat thickness in both studies. In the first trial, 92 steers (mean BW = 408 +/- 2.8 kg; four pens/treatment) were fed the following diets: 1) constant 12% CP, 2) constant 14% CP, and 3) 10 and 14% CP oscillated at 2-d intervals. Steer performance and carcass characteristics were measured. In the second trial, 27 steers were individually fed the same three experimental dietary regimens (nine steers/treatment). Animal performance, arterial acid-base balance, plasma metabolites, and fecal characteristics were measured. In both trials, steers fed the 14% CP diet tended (P < 0.10) to have greater ADG and gain:feed than steers fed the 12% CP diet. Steers fed the oscillating CP regimen had intermediate performance. In Trial 1, steers fed the 14% CP diet tended (P = 0.09) to have smaller longissimus area and higher quality grades than steers fed the oscillating CP regimen. Protein retentions (g/d) calculated from NRC (2000) equations were greater (P = 0.04) for steers fed the 14% CP diet than steers fed the 12% CP diet. Steers fed the oscillating CP regimen tended (P = 0.08) to have greater calculated protein retention (g/d) than steers fed the 12% CP diet. Steers fed the 14% CP diet had greater (P < 0.05) calculated urinary N excretion than steers fed the 12% CP or oscillating CP regimens. Venous plasma concentrations of urea N were greater (P < 0.001) in steers fed the 14% CP diet than in steers fed the 12% CP diet; steers fed the oscillating CP regimen were intermediate but fluctuated over days. Based on arterial blood gas concentrations, acid-base balance was not significantly affected by dietary CP regimen. Results of these trials suggest that the CP requirement of steers in these studies was greater than 12% of the diet DM, and/or that the degradable CP requirement was greater than 6.3% of diet DM. However, the effects of oscillating dietary CP were minimal.     

Net energy of ensiled wet corn gluten feed in corn silage diets for finishing steers.

Two trials were conducted to determine the NE value of ensiled wet corn gluten feed (WCGF) in corn silage finishing diets for beef cattle. In Trial 1, 96 Angus-crossbred yearling steers were fed corn silage-based diets containing 0, 20, 40, or 60% ensiled WCGF. Increased dietary WCGF resulted in improved DMI (linear, P less than .05), ADG (linear; P less than .05), and feed/gain (linear, P less than .05). Levels of WCGF had no (P greater than .05) effect on fat thickness, marbling, quality grade, carcass protein, and carcass fat. In Trial 2, four Angus-crossbred yearling steers were used in a 4 x 4 Latin square design to determine the effect of feeding 0, 20, 40, or 60% WCGF on DE and ME values. Level of WCGF had no (P greater than .05) effect on dietary DE and ME values. Regression equations were developed for predicting NEm (Y = 1.51 + .0009X; R2 = .22) and NEg (Y = 1.04 + .0028X; R2 = .35) in which Y = predicted diet NE values in megacalories/kilogram and X = percentage of dietary WCGF. The NEg value increased .06 Mcal/kg for each 20% increase in WCGF. Predicted NEm and NEg values for WCGF are 1.60 and 1.32 Mcal/kg, respectively.     

Influence of breed and diet on growth, nutrient digestibility, body composition and plasma hormones of Brangus and Angus steers

Two split-plot designed experiments were conducted to determine the effects of breed (Angus, A, or Brangus, B) and diet (fescue hay, FH; corn silage, CS; or concentrate) on composition and rate of growth, diet digestibility and plasma hormones of steers. In Exp. 1, 10 steers (five of each breed) were fed a CS-based diet followed by a FH-based diet for two consecutive 60-d periods. Both breeds had lower (P less than .01) DM intake and digestibility when fed FH than when fed CS diets. The B steers had higher (P less than .01) plasma insulin concentrations than A steers when fed the CS diet. In Exp. 2, during two consecutive years, 10 steers previously fed CS- and FH-based diets were finished with a corn silage-whole shelled corn-based diet. During yr 1, A steers had higher (P less than .01) DM intake and plasma triiodothyronine (T3) and thyroxine (T4) concentrations (P less than .05) than B steers did. Although final weights were similar (P greater than .10), A steers had heavier (P less than .05) carcass weights than B steers did. During yr 2, A steers had higher (P less than .07) DM and starch digestibilities and higher (P less than .01) plasma T4 concentrations than B steers did. The greater (P less than .01) energetic efficiency of A steers was attributed to the greater rates of fat deposition during yr 2. Regardless of type of diet fed, A steers were more efficient at depositing energy. Higher circulating T4 concentrations of A than B steers may explain some of the physiological differences between these breeds.     

Effects of lysine:calorie ratio on growth performance of 10- to 25-kilogram pigs

Crossbred barrows (n = 336 Newsham Hybrids) initially 9.9 kg and 31+/-2 d of age were used to evaluate the effects of energy density and lysine:calorie ratio on growth performance. Pigs were allotted by initial weight in a 3 x 4 factorial arrangement of treatments in a randomized complete block design with six replicate pens per treatment. Each pen had four or five pigs with an equal number of pigs per pen within replicate. Pigs were fed increasing dietary energy densities (3.25, 3.38, and 3.51 Mcal ME/kg) and lysine:calorie ratios (3.00, 3.45, 3.90, and 4.35 g lysine/Mcal ME). Energy density was changed by levels of choice white grease (0, 3, and 6%), and lysine:calorie ratio was changed by altering the corn:soybean meal ratio. Over the 21-d trial, an energy density x lysine:calorie ratio interaction was observed for ADG (P < .05). Pigs fed diets containing 3.25 or 3.51 Mcal ME/kg had increasing ADG with increasing lysine:calorie ratio, whereas ADG of pigs fed 3.38 Mcal ME/kg was not affected by lysine:calorie ratio. Feed efficiency (gain:feed ratio) increased and ADFI decreased as lysine:calorie ratio increased (linear, P < .01) and as energy density increased (quadratic, P < .01 and .10, respectively). On d 21, two pigs per pen were scanned ultrasonically for backfat depth. An energy density x lysine:calorie ratio interaction (P < .06) was observed. Pigs fed diets containing 3.25 and 3.38 Mcal ME/kg had decreasing fat depth as lysine:calorie ratio increased; however, backfat depth was not affected by lysine:calorie ratio and was greatest for pigs fed 3.51 Mcal ME/kg. These results suggest that 10- to 25-kg pigs fed diets containing 3.38 Mcal ME/kg had maximum feed efficiency and that they required at least 4.35 g lysine/Mcal ME. However, pigs fed 3.51 Mcal ME/kg had increased fat depth regardless of calorie:lysine ratio.