The influence of virginiamycin on digestion and ruminal parameters under feedlot conditions.

This experiment aimed to assess the impact of virginiamycin on in vitro gas production dynamics, rumen kinetics, and nutrient digestibility in beef steers fed a grain-based diet. Nine ruminally cannulated British-crossbred steers (596 ±â€…49 kg) were assigned to this experiment. Animals were housed in three pens (n = 3/pen) equipped with a Calan gate feed system and water troughs. Pens were enrolled in a 3 × 3 Latin square design containing three periods of 16 d, and a 5-d washout interval between periods. Dietary treatments consisted of virginiamycin (VM) administration at 0 (VM0), 180 (VM180), or 240 mg/d (VM240). During days 15 and 16 of each period, about 600 mL of rumen fluid and urine samples were collected before (0 h), and at 4, 8, 12, and 16 h after the morning feed (0730 hours), rumen inoculum was used to take pH and redox potential measurements immediately after collection using a portable pH and redox meter, and subsamples were taken for volatile fatty acids (VFA) and NH3-N analyses, and urine samples were composited daily and analyzed for creatinine and purine derivatives (PD) content to estimate microbial crude protein flow. During the 4-h post-morning feed rumen collection, rumen inoculum was utilized to perform in vitro gas production measurements. Fecal samples were collected on day 16 of each period to estimate nutrient digestibility using acid detergent insoluble ash as an internal marker. Animals were considered the experimental unit for the statistical analyses, and periods and squares were included as random variables. The total and rate of gas production were similar among treatments (P ≥ 0.17). The second-pool (i.e., fiber) gas production increased linearly as VM inclusion increased (P = 0.01), with VM240 being greater compared to VM180 and VM0 (7.84, 6.94, and 6.89 mL, respectively). Ruminal pH linearly increased as VM increased, with VM240 being greater than VM0 and VM180 intermediate (5.90, 5.82, and 5.86, respectively; P = 0.03). The VFA concentrations did not differ (P ≥ 0.13), but the acetate-to-propionate ratio was the highest in VM240 (P = 0.005). Branched-chain VFA increased (P ≤ 0.03) while lactate concentrations decreased (P = 0.005) linearly with VM. The ruminal NH3-N concentration was the lowest in the VM0 (P = 0.006). The estimated absorbed PD, purine derivative to creatinine index, and microbial N flow increased linearly with VM (P ≤ 0.07). The provision of VM influenced rumen dynamics in a dose-dependent manner.

The influence of extended supplementation of quebracho extract to beef steers consuming a hay diet on digestion, ruminal, and blood parameters.

The addition of natural plant secondary compounds to ruminant feed has been extensively studied because of their ability to modify digestive and metabolic functions, resulting in a potential reduction in greenhouse gas emissions, among other benefits. Condensed tannin (CT) supplementation may alter ruminal fermentation and mitigate methane (CH4) emissions. This study's objective was to determine the effect of quebracho CT extract [QT; Schinopsis quebracho-colorado (Schltdl.) F.A. Barkley & T. Meyer] within a roughage-based diet on ruminal digestibility and kinetic parameters by using the in situ and in vitro gas production techniques, in addition to blood urea nitrogen (BUN) and ruminal (volatile fatty acid [VFA], NH3-N, and protozoa count) parameters. Twenty rumen-cannulated steers were randomly assigned to four dietary treatments: QT at 0%, 1%, 2%, and 3% of dry matter (DM; QT0: 0% CT, QT1: 0.70% CT, QT2: 1.41% CT, and QT3: 2.13% CT). The in situ DM digestibility increased linearly (P = 0.048) as QT inclusion increased, whereas in situ neutral detergent fiber digestibility (NDFD) was not altered among treatments (P = 0.980). Neither total VFA concentration nor acetate-to-propionate ratio differed among dietary treatments (P = 0.470 and P = 0.873, respectively). However, QT3 had lower isovalerate and isobutyrate concentrations compared with QT0 (P ≤ 0.025). Ruminal NH3 and BUN tended to decline (P ≤ 0.075) in a linear fashion as QT inclusion increased, suggesting decreased deamination of feed protein. Ruminal protozoa count was reduced in quadratic fashion (P = 0.005) as QT inclusion increased, where QT1 and QT2 were lower compared with QT0 and QT3. Urinary N excretion tended to reduce in a linear fashion (P = 0.080) as QT increased. There was a treatment (TRT) × Day interaction for in vitro total gas production and fractional rate of gas production (P = 0.013 and P = 0.007, respectively), and in vitro NDFD tended to be greater for QT treatments compared with no QT inclusion (P = 0.077). There was a TRT × Day interaction (P = 0.001) on CH4 production, with QT3 having less CH4 production relative to QT0 on day 0 and QT2 on days 7 and 28. Feeding QT up to 3% of the dietary DM in a roughage-based diet did not sacrifice the overall DM digestibility and ruminal parameters over time. Still, it is unclear why QT2 did not follow the same pattern as in vitro gas parameters. Detailed evaluations of amino acid degradation might be required to fully define CT influences on ruminal fermentation parameters and CH4 production.

Comparison of in situ techniques to evaluate the recovery of indigestible components and the accuracy of digestibility estimates.

Indigestible components, including indigestible dry matter (iDM) and indigestible neutral detergent fiber (iNDF), play an integral role as internal markers for determining ruminal kinetics and digestibility estimations. However, the accuracy of internal markers is dependent upon the incubation technique utilized as bag type (BT) and incubation length (IL) can be significant sources of error. Previous studies have primarily focused on iDM and iNDF as digestibility markers, but few studies have compared digestibility estimates to those of acid detergent insoluble ash (ADIA). Therefore, our objective was to investigate the effect of BT (F57, F58, and Dacron) and IL (288 and 576 h) on iDM and iNDF residues, DM and NDF digestibilities, and fecal recoveries when using in situ incubations. Additionally, we evaluated the accuracy of digestibility estimates when using iDM, iNDF, and ADIA. For iDM and iNDF, feed residues demonstrated a BT × IL interaction (P < 0.01). However, fecal residues were only influenced by the main effects of BT and IL (P < 0.01), with the F58 BT and 288-h IL having the greatest residues for both iDM and iNDF. The variation in residues was greatly reduced when using iNDF compared with iDM. Fecal recovery estimates most closely approximated 100% recovery when utilizing ADIA and iDM using the F57 × 576 h incubation method (P < 0.01), although recovery was overestimated for all incubation combinations. Fecal NDF recovery estimates better represented the excretion profiles when the F57 × 576 h combination was used with iDM as the internal marker (P < 0.01). Estimates of DM and NDF digestibility were the most accurate when utilizing ADIA (P < 0.01) relative to all other treatments. Our results indicate that the proper methodological application is specific to the purpose of the inferences. When evaluating fecal recoveries and digestibility, ADIA or iDM with F57 at 576-h in situ incubation provides the greatest accuracy.