The effect of feed intake and body weight on purine derivative excretion and microbial protein supply in sheep.

Urinary excretion of purine derivatives (PD) was used to estimate the microbial N (MN) supply to sheep in three experiments designed to examine the effects of DMI and BW on the efficiency of microbial N supply (EMNS) to the host animal. In Exp. 1, four sheep of about 45 kg BW were given 328, 656, 984, and 1313 g of DM/d of a hay/concentrate diet in a Latin square design. Excretion of PD per kilogram of digestible organic matter intake (DOMI) increased with intake, and EMNS increased from 12.0 to 28.3 g of MN/kg of OM digested in the rumen (DOMR). In Exp. 2, 19 sheep ranging from 22 to 73 kg BW were all offered 820 g of DM/d of the same diet as that fed in Exp. 1. Although DM digestibility was relatively constant, PD excretion varied from 4.5 to 13.5 mmol/d and EMNS from 8 to 36 g of MN/kg of DOMR, both inversely related to animal BW. In Exp. 3, five sheep of 48 to 57 kg BW were given a different diet at 702, 966, or 1,237 g of DM/d. Purine derivative excretion per kilogram of DOMI increased with the DMI:BW ratio. Calculated EMNS ranged from 23 to 35 g of MN/kg of DOMR. Pooled data from all experiments showed EMNS to be related to the DMI:BW ratio. It is suggested that the DMI:BW ratio defines the ruminal digesta passage rate and hence outflow of microbial protein. The results imply that the EMNS for a given diet is not constant, but changes with intake.

Microbial protein synthesis in cattle given roughage-concentrate and all-concentrate diets: the use of 2,6-diaminopimelic acid, 2-aminoethylphosphonic acid and 35S as markers.

Three steers, each fitted with a rumen cannula and a re-entrant cannula in the proximal duodenum, were offered diets consisting of a barley-based concentrate and chopped hay at a daily intake of 61 g/kg live weight0.75 given in three equal meals. The ratio, concentrate: hay was changed from 50:50 to 90:10 and then to 100:0 in successive periods of 12-18 weeks and the flow and composition of digesta at the duodenum was measured over 48-h periods on each dietary treatment. Samples of bacteria and protozoa were separated from rumen contents and the proportions of bacterial and protozoal nitrogen (N) in duodenal digesta were estimated using 2,6-diaminopimelic acid (DAPA) and 2-aminoethylphosphonic acid (AEP) as markers. On separate occasions, radioactive sulphur (35S) was infused into the rumen for 48 h and digesta collected over the final 24 h; the specific radioactivity of S in microbial and digesta fractions was used to estimate the proportions of microbial N. 35S gave reproducible and apparently reliable estimates of microbial protein formation: the proportion of microbial N in digesta was significantly higher (P less than 0.05) for the 50:50 diet than for the other treatments but the energetic efficiency of microbial protein formation did not differ significantly between diets. Estimates of bacterial N based on DAPA concentrations were highly variable and frequently impossibly high. It is suggested that many of the anomalous values were the result of non-representative sampling of the rumen microbial population and that this is particularly likely to occur when conditions within the rumen are unstable. AEP was found to be unsuitable as a marker for rumen protozoa as considerable concentrations of this substance were found also in rumen bacteria.

Methane formation in faunated and ciliate-free cattle and its relationship with rumen volatile fatty acid proportions.

Twelve steers fitted with rumen cannulas were used in three separate experiments to investigate the effects of the presence or absence of rumen ciliate protozoa on methane production. The diet consisted of 850 g barley and 150 g protein supplement/kg, and was given in three feeds daily at a restricted level of 61 g/kg live weight 0.75. Animals were defaunated initially by allowing ad lib. consumption of this diet and were then maintained ciliate-free by isolation or were faunated by inoculation with a mixed ciliate suspension. Samples of rumen fluid were taken routinely for the assessment of microbial populations and for volatile fatty acid (VFA) analysis and energy and nitrogen balances and digestibility measurements were made at intervals while animals were confined in respiration chambers. In each experiment the rumen VFA proportions changed from a high-propionate pattern under ciliate-free conditions to a low-propionate, high-butyrate pattern in the presence of ciliates: differences between treatments were highly significant (P less than 0.001). There were also marked differences between treatments in CH4 production but a reliable comparison was possible only in Expt 3, in which CH4 was significantly higher (P less than 0.001) in the presence of a rumen ciliate population. In Expt 3 the increased loss of energy as CH4 in the faunated animals amounted to 4.8 MJ/100 MJ energy intake. Stoichiometric estimates of CH4 production derived from the observed VFA proportions showed good agreement with CH4 production as measured in respiration chambers. On average, the stoichiometric CH4 values overestimated CH4 production by a factor of 1.08. Highly significant linear relationships (P less than 0.001) were observed between the molar proportion of each major VFA and the quantity of CH4 produced: the proportion of propionic acid was inversely related to CH4 and showed the lowest residual standard deviation of all the relationships examined. The losses of energy in faeces and urine did not differ between treatments hence the increased loss of energy as CH4 in the faunated animals resulted in a significant reduction in the metabolizability of the diet from 0.73 to 0.69 (P less than 0.05). No significant differences were detected between treatments in heat production, apparent digestibility coefficients or N balance. It is suggested that the rumen ciliates, by modifying the rumen VFA proportions, are directly responsible for the increased CH4 production in faunated animals.

2-Aminoethylphosphonic acid concentrations in some rumen ciliate protozoa.

The concentration of 2-aminoethylphosphonic acid has been measured in seven genera of rumen ciliate protozoa. Expressed as milligrams per gram of total nitrogen, 2-aminoethylphosphonic acid concentrations ranged from 17.2 in Ophryoscolex spp. to 72.4 in Eremoplastron spp.