This review examines the role of nutritional strategies to improve lifetime performance in ruminants. Strategies to increase ruminants' productive longevity by means of nutritional interventions provide the opportunity not only to increase their lifetime performances and their welfare, but also to decrease their environmental impact. This paper will also address how such nutritional interventions can increase herd efficiency and farm profitability. The key competencies reviewed in this article are redox balance, skeletal development and health, nutrient utilization and sustainability, which includes rearing ruminants without antibiotics and methane mitigation. While the relationships between these areas are extremely complex, a multidisciplinary approach is needed to develop nutritional strategies that would allow ruminants to become more resilient to the environmental and physiological challenges that they will have to endure during their productive career. As the demand of ruminant products from the rapidly growing human world population is ever-increasing, the aim of this review is to present animal and veterinary scientists as well as nutritionists a multidisciplinary approach towards a sustainable ruminant production, while improving their nutrient utilization, health and welfare, and mitigation of their carbon footprint at the same time.

The advantage of ruminants is their ability to convert fibrous biomass to high quality protein for human nutrition purposes. Rumen fermentation, however, is always associated with the formation of methane - a very effective greenhouse gas. Hindgut fermentation differs from rumen fermentation by a substantially lower methane production and the presence of reductive acetogenesis or dissimilatory sulfate reduction. Sulfate reduction and methanogenesis seem to be mutually exclusive, while methanogenesis and reductive acetogenesis may occur simultaneously in the hindgut. Although acetogenic bacteria have been isolated from the bovine rumen, methanogenesis prevails in the forestomachs. The substitution of acetate for methane as a hydrogen sink in the rumen should increase energy yield for the animal and decrease methane emissions into the environment. Differences in the major hydrogen sinks in both microbial ecosystems are discussed and mainly related to differences in substrate availability and to the absence of protozoa in the hindgut.

A rumen fistulated wether was used for continuous infusion of a 2-bromoethanesulfonic acid (BES) solution (2 g/d in 50 ml of water). The infusion was started after introduction of a pulse dose of BES (2 g) into the rumen. Immediately after introduction of the pulse dose, methane concentration in rumen gases was lowered from about 40 to less than 1%, with concomittant decreases and increases in the molar proportions of acetic and propionic acids respectively in the rumen volatile fatty acids. After 4 days of infusion however, and despite repeated pulse dosage of BES, methanogenesis adapted to BES and methane concentration in rumen gases reached 20%. Addition of BES to incubations of rumen contents with hay resulted in considerable inhibition of methanogenesis. Extra addition of methanol in such incubations increased both acetate and methane production, whereas addition of formate had no effect. In a second experiment using a second rumen fistulated whether, a 4 day control period was followed by 10 days of daily introduction of 11 of cattle cecal contents into the rumen. The cattle cecal contents were collected from slaughterhouse cattle, filtered and kept at -20 degrees C until use. Comparison of in vitro fermentation of thawed with fresh contents showed absence of methanogenesis but not of reductive acetogenesis after freezing and thawing. Evidence for the latter was sought by calculation of metabolic hydrogen recoveries from amounts of end products formed in incubations. In a similar way, evidence for induction of reductive acetogenesis was sought from incubations in vitro, carried out with rumen contents obtained before, during and after introduction of cecal contents into the rumen. No such evidence was obtained.

The effect of varying hay/barley-proportions in the feed ration on biotin metabolism of rumen microbes was studied by means of the rumen simulation technique RUSITEC. The stepwise replacement of hay by barley decreased dietary biotin and the net output of biotin by the microbial metabolism. It is concluded that rumen microbes utilise more and/or synthesize less biotin with increasing proportions of dietary barley. These results indicate that a critical reconsideration of current views with regard to the supply and requirement of the high yielding dairy cow for biotin is necessary.

The aim of this study was to test whether a combination of plant bioactive lipid compounds (also termed ‘essential oils’) and biotin (PBLC+B) could decrease the mobilization of body reserves and ketosis incidence in postpartum dairy cows. We compared non-supplemented control (CON) cows with cows receiving monensin (MON) as a controlled-release capsule at d -21, and with cows receiving PBLC+B from day (d) -21 before calving until calving (Phase 1) and further until d 37 after calving (Phase 2), followed by PBLC+B discontinuation from d 38 to d 58 (Phase 3). The PBLC+B cows had higher body weight and higher back fat thickness than CON cows and lesser body weight change than MON and CON cows in Phase 3. Body condition score was not different among groups. Milk protein concentration tended to be higher on the first herd test day in PBLC+B vs. CON cows. Milk fat concentration tended to be highest in PBLC+B cows throughout Phases 2 and 3, with significantly higher values in PBLC+B vs. MON cows on the second herd test day. Yields of energy-corrected milk were higher in PBLC+B vs. CON and MON cows in Phase 2 and higher in PBLC+B and MON cows vs. CON cows in Phase 3. The incidence of subclinical ketosis was 83%, 61% and 50% in CON, PBLC+B and MON cows, respectively, with lower mean β-hydroxybutyrate values in MON than in PBLC+B cows in Phase 1 prepartum. The serum triglyceride concentration was higher in PBLC+B vs. CON cows on d 37. No differences were observed in serum glucose, urea, non-esterified fatty acids, cholesterol and bilirubin concentrations. Aspartate transaminase and γ-glutamyltranspeptidase but not glutamate dehydrogenase activities tended to be highest in MON and lowest in PBLC+B in Phase 2. We conclude that PBLC+B prevent body weight loss after parturition and are associated with similar ketosis incidence and partly higher yields of energy-corrected milk compared to MON supplementation of dairy cows.