Twelve 5-year-old beef steers, with an average weight of 2000 lbs., fitted with rumen canulae were used in a 4 × 4 incomplete Latin square design to examine the impact of the direct fed microbial Propionibacterium acidipropionici CP 88 (PA) on rumen fermentation characteristics, in vitro CH4, CO2, and N2 production, and in vivo CH4 and CO2 production. All steers were housed in the same pen equipped with eight GrowSafe feeding stations to monitor individual animal feed intake and one GreenFeed System to estimate individual animal CH4 and CO2 production. Steers were fed a corn-silage-based diet throughout the experiment. Treatments consisted of PA administered at: (1) control (0.0); (2) 1.0 × 108; (3) 1.0 × 109; and (4) 1.0 × 1010 cfu∙animal−1∙day (d)−1. Treatments were administered directly into the rumen as a single bolus dose daily. On day 7 and 14 of each period, rumen fluid was collected from each steer 2 h post treatment administration for VFA analysis and in vitro DM digestibility determination. Following a 14 d washout period, animal treatments were switched and the experiment repeated until the 4 × 4 Latin square was complete. In vivo propionic acid molar proportions and total VFA concentrations were greater (p < 0.05) in steers receiving PA when compared with controls. All other in vivo rumen fermentation characteristics were similar across treatments. In vitro DM disappearance (p < 0.05) and total VFA (p < 0.05) were greater and CH4 lesser (p < 0.04) in fermentation vessels incubated with rumen fluid from animals receiving PA when compared with controls. Dry matter disappearance (p < 0.03) and propionic acid molar proportions increased (p < 0.04) linearly as the dose of PA increased. In vitro total VFA tended (p < 0.08) to increase linearly and CH4 production per unit of DM digested tended (p < 0.09) to decrease quadratically in response to PA dose. All other in vitro rumen fermentation characteristics were similar across treatments. These data indicate that PA impacts in vivo and in vitro rumen fermentation characteristics.

No abstract

The adjusted BPAR rate difference at 3 years posttransplantation was less than 2% (13.6% vs. 11.7%); statistically significant because of the large number of patients included in the analysis, but a difference that may not be clinically meaningful. No differences in graft survival, new-onset diabetes mellitus, or renal function were observed between the treatment groups.

Rumen fluid from three beef steers (480 ± 10 kg), fitted with rumen canulae, were used to investigate the impact of Ca dose and olive meal on in vitro rumen fermentation characteristics. Steers were fed a high concentrate finishing diet for 21d, and rumen fluid was collected from each steer 2h post-feeding. A 2 x 4 factorial arrangement of treatments was used for this experiment. Factors included: 1) 0 or 5% olive meal and 2) Ca dose: 0, 0.02, 0.04, and 0.08% Ca from CaCl2. A McDougall’s buffer-rumen fluid mixture (1:1; 30 mL) was added to conical tubes containing 0.5g of the ground basal diet and incubated at 39°C for 0, 4, 8, and 12h (5 replicates per treatment per time point). After incubation, supernatant was removed for VFA analysis and the remaining digesta was dried to determine DM disappearance (DMD). At 4 and 8h post incubation digestion tubes containing 0.04% Ca had greater (P &lt; 0.001) DMD when compared to all other Ca doses. At 12h post incubation, DMD was greater (P &lt; 0.001) in digestion tubes containing 0.02% and 0.08% Ca compared to all other Ca doses. At 8h post incubation, molar proportions of acetic acid were greater (P &lt; 0.03) in digestion tubes containing olive meal compared to no olive meal and were greater (P &lt; 0.001) in digestion tubes containing 0.08% Ca compared to all other Ca doses. At 12h post incubation, isobutyric acid (P &lt; 0.01) and butyric acid (P &lt; 0.02) were greater in digestion tubes containing 0.02% and 0.04% Ca compared to all other Ca doses. Butyric acid was lesser (P &lt; 0.02) with olive meal inclusion at 12h. Total VFA concentrations were similar across treatments. These data suggest that Ca and olive meal can impact in vitro fermentation characteristics.

The objective of this experiment was to evaluate the effect of Saccharomyces cerevisiae products (NaturSafe) on in-vitro rumen fermentation characteristics and microbial diversity. Three crossbred feedlot steers fitted with rumen cannulae were adjusted to a moderately high-concentrate diet for 28-d. On d-29, 1 L of rumen fluid was collected from each steer and composited. A set of vaccine bottles (n=5/treatment/time + blanks and controls) containing 0.5 g of basal diet plus dietary treatments were filled with 30 ml of rumen fluid-McDougall’s buffer solution (1:1), sealed, and placed in a 39°C water bath. Treatments consisted of 1) Control (no added NaturSafe); 2) NaturSafe-dry (9 g/animal/day equivalent); 3) NaturSafe-dry (12 g/animal/day equivalent); 4) NaturSafe-liquid (14 g/animal/day equivalent); 5) NaturSafe-liquid (21 g/animal/day equivalent); and NaturSafe-liquid (28 g/animal/day equivalent). Samples were collected at 0, 6 and 12 h post-fermentation. No treatment effect on any fermentation parameters was found at 6 h. At 12-h post-incubation, dry matter digestibility (DMD) (P &lt; 0.04) and molar proportions of propionic acid (P &lt; 0.03) were greater for treatments containing NaturSafe compared with control. Molar proportions of acetic acid (P &lt; 0.07), percent CH4 (P &lt; 0.08), and NH3-N (P &lt; 0.06) tended to be lesser and percent CO2 tended (P &lt; 0.07) to be greater for NaturSafe treatments compared with controls. Microbiome 16S rRNA analysis results suggest that microbial communities differed (P &lt; 0.05) between 6 and 12 h post-incubation. Incorporating NaturSafe into fermentation vessels revealed an inverse correlation with NaturSafe concentration and microbial diversity (P = 0.08) and that the overall microbial diversity was altered (P &lt; 0.03) by NaturSafe concentration. The microbial community was not affected by additive type. These data suggest that NaturSafe alters fermentation characteristics and microbial community diversity toward improved rumen efficiency while reducing environmental impact.