RÉSUMÉ
The objective was to determine if low- or high-residual feed intake (LRFI or HRFI, n = 24 for each) Hereford × Angus cows on continuously or rotationally grazed rangeland altered their grazing behavior when provided a protein supplement in late autumn. Treatments included continuously grazed, control (CCON, n = 12); continuously grazed, supplemented (CTRT, n = 12); rotationally grazed, control (RCON, n = 12); and rotationally grazed, supplemented pastures (RTRT, n = 12). Cows in each treatment had grazing time (GT), resting time (RT), and walking time (WLK) measured for 2 years with accelerometers. Bite rate (BR) was also measured. Time distributions of GT and RT differed by year (p < 0.05), being influenced by colder temperatures in 2016. Cattle in 2016 spent more time grazing during early morning and late evening (p < 0.05) and rested more during the day (p < 0.05). In 2017, cattle in the CCON treatment walked more (p < 0.05) during early morning time periods than did the CTRT cattle, indicative of search grazing. All supplemented cattle had greater BR (p < 0.05) than control cattle in 2017. Cattle with increased nutritional demands alter grazing behavior in a compensatory fashion when grazing late-season rangelands.
RÉSUMÉ
Bitter taste perception in sheep can lead to avoidance of specific types of forage, such as sagebrush, which is present on many rangeland grazing systems in the Intermountain West. In humans, bitter taste perception is influenced by variation in several TAS2R genes, including more extensively studied TAS2R38 and TAS2R16. We hypothesize that variation in taste receptor genes in sheep is associated with bitter taste. Therefore, the objective of this study was to examine variation in TAS2R genes in relation to consumption of a bitter tasting compound phenylthiocarbamide (PTC) which determines bitter "taster" and "non-taster" status in humans. Rambouillet and Targhee rams (n = 26) were offered various concentrations of PTC solution (0.2-12.29 mM) and water in a side-by-side presentation during two experiments. Blood was collected for DNA isolation and sequencing. Nineteen TAS2R genes were amplified and sequenced with long read Oxford Nanopore MinION technology. A total of 1,049 single nucleotide polymorphisms (SNPs) and 26 haplotypes were identified in these genes. Of these, 24 SNPs and 11 haplotypes were significantly (P < 0.05) associated with PTC consumption in TAS2R3, TAS2R5, TAS2R8, TAS2R9, TAS2R16, TAS2R31-like, TAS2R38, TAS2R39, and TAS2R42-like. Over 50% of the SNPs resulted in a change in amino acid sequence and several resided in potential regulatory regions, which could have downstream functional consequences and influence bitter taste perception in sheep. Further research is needed to validate these associations and elucidate the mechanisms that link variation in TAS2R genes to bitter taste perception in sheep. This may enable producers to select sheep more likely to consume bitter forage such as sagebrush as a flock and rangeland management strategy.
RÉSUMÉ
The objectives were to determine if previously classified, efficient (LRFI, low-residual-feed intake, n = 12 × 2 yr) vs. inefficient (HRFI, high-residual-feed intake, n = 12 × 2 yr) lactating 2-yr-old Hereford × Angus cows differed in grazing behavior, body weight (BW), body condition score (BCS), and calf weaning weight while grazing rugged rangeland pastures. Cows were fitted with grazing halters containing both an accelerometer and a global positioning system (GPS) data logger during June 14 to July 4, 2016, August 2 to 25, 2016, May 23 to June 12, 2017, and August 5 to 28, 2017. GPS data were recorded at 7-min intervals in 2016 and 4-min intervals in 2017 and accelerometer data recorded at 25 times/s. Grazing time (GT), resting, walking, bite rate (BR), daily travel distance (DTD), elevation, and slope were analyzed with a mixed model that included fixed effects of RFI group, day, and RFI group × day and cow within treatment as the random effect. Cow BW, BCS, and calf weaning weight were analyzed by analysis of variance with treatment as the main effect. There were no differences (P > 0.10) due to RFI detected for BW, BCS, or calf weaning weights. During periods of mild heat load (MHL), HRFI cows spent more (P < 0.05) time resting during the day at lower elevations (P < 0.05) than LRFI cows. During a 6-d period in spring with only 2 h MHL, HRFI cows grazed 1.7 h/d longer than LRFI cows (P < 0.05); commencing grazing earlier in the morning and extending the grazing bout later. During the summer with > MHL, LRFI cows grazed more than HRFI cows 18% of the time (P < 0.10). The HRFI cows had greater GT than LRFI cows only 3% of the time (P < 0.10) during summer. There was no difference (P > 0.10) in BR between HRFI and LRFI cattle. The DTD tended (P < 0.10) to be greater for LRFI cattle during summer 2017. Over all sample periods, HRFI had greater walking than LRFI 15% of the time and LRFI exceeded HRFI cattle for walking 3% of the time (P < 0.10). The greater walking for HRFI was assumed to be associated with more search grazing. Metabolic heat load on hot summer days for HRFI cattle is presumed to have contributed to differences observed in grazing behavior. These results suggest that lactating cows with low-RFI phenotypes appear to be better adapted to grazing rugged rangelands in late summer during periods of MHL.
RÉSUMÉ
Including feed efficiency as a trait for selection has gained interest in the sheep industry because it can result in reduced feed inputs or improve stocking rates, both of which translate into increased profitability for the producer. It is of interest whether the feed efficiency status of a testing population of sheep could be predicted using rumen microbial profiles associated with divergent feed efficiency status in a training population of sheep. Two populations of ewes were fed the same diet, and each group was evaluated for feed efficiency. A total of 20 animals in the testing population were selected for prediction assessment using feed efficiency, including the 6 top-ranked, the 6 bottom-ranked, and 8 middle-ranked ewes stratified over the distribution. Rumen fluid samples were collected and DNA was extracted for sequencing. Using a rumen microbial profile associated with diverging feed efficiency created from the training population, multiple discriminant analyses were performed using the DISCRIM procedure of SAS to determine the probability of correctly identifying lambs in the testing population as low, medium, or high feed efficiency using their microbial profiles. A profile of 6 rumen microbial species were used to correctly (P < 0.001) predict all testing population ewes into their actual feed efficiency status. A regression analysis using the same microbial profile was used to predict feed efficiency values, which were strongly correlated (r = 0.71; P < 0.001) with actual feed efficiency values. These results indicate that specific rumen microbial species may play a role in feed efficiency, and that a microbial profile could be used to rank sheep for feed efficiency.
Sujet(s)
Aliment pour animaux/analyse , Consommation alimentaire , Microbiote , Ovis/microbiologie , Animaux , Régime alimentaire/médecine vétérinaire , Femelle , Phénotype , Rumen/microbiologie , Ovis/physiologieRÉSUMÉ
Mineral intake in grazing cattle is highly variable and research evaluating behavioral aspects of intake are minimal. Development of the GrowSafe System to monitor feed intake allows researchers to record individual feeding behaviors of cattle 24 h per day. In the current experiment conducted during June and July, the GrowSafe System was utilized to evaluate intake behaviors of grazing steers during a short-term free-choice supplementation of either salt-based loose minerals (LM; n = 24; 408 ± 57 kg) or low-moisture molasses-based tub minerals (TUB; n = 24; 396 ± 64 kg). Each treatment was randomized to two of the four irrigated pastures (~5 ha each) consisting of orchard grass (Dactylis glomerat L.), red clover (Trifolium pretense L.), and smooth brome (Bromus inermis). Individual intake was evaluated over three 7-d periods: d - 7 to 0 (adaptation period; AP), d 1 to 7 (period 1; P1), and d 15 to 22 (period 2; P2) of the experiment. The LM mineral mix contained 28% salt during the AP and more salt was added at the initiation of P1 to prevent excessive mineral intake observed during the AP. The LM mineral mix contained 38% salt during P1 and P2. Daily bunk attendance was greater (P < 0.001) for LM (93%) than TUB (67%) steers for the AP. Whereas there was a treatment × period effect (P < 0.001) on daily bunk attendance across P1 (LM: 92%; TUB: 64%) and P2 (LM: 91%; TUB: 82%). Daily mineral intake (as-fed) was greater (P < 0.001) for LM (568 g) than TUB (283 g) during the AP. For P1 and P2, there were no treatment (P = 0.46) and period (P = 0.77) effects on daily mineral intake (LM, 370 g vs. TUB, 343 g), but LM (3.1 visits) had more (P < 0.001) bunk visits per day than TUB (2.0 visits). During the AP, LM (8.5 min) had a greater (P = 0.04) duration of mineral intake per day than TUB (5.6 min); whereas during P1 and P2, TUB (P1 = 8.6; P2 = 12.8 min) had a greater (P ≤ 0.05) duration of mineral intake per day than LM (P1 = 4.9; P2 = 5.7 min). In conclusion, mineral delivery method significantly affected bunk attendance, number of bunk visits per day, and time spent consuming mineral. These results provide additional evidence that mineral type and associated feeding behaviors contribute to the significant variation observed in daily mineral intake in grazing cattle.
RÉSUMÉ
Ruminant animals have a symbiotic relationship with the microorganisms in their rumens. In this relationship, rumen microbes efficiently degrade complex plant-derived compounds into smaller digestible compounds, a process that is very likely associated with host animal feed efficiency. The resulting simpler metabolites can then be absorbed by the host and converted into other compounds by host enzymes. We used a microbial community metabolic network inferred from shotgun metagenomics data to assess how this metabolic system differs between animals that are able to turn ingested feedstuffs into body mass with high efficiency and those that are not. We conducted shotgun sequencing of microbial DNA from the rumen contents of 16 sheep that differed in their residual feed intake (RFI), a measure of feed efficiency. Metagenomic reads from each sheep were mapped onto a database-derived microbial metabolic network, which was linked to the sheep metabolic network by interface metabolites (metabolites transferred from microbes to host). No single enzyme was identified as being significantly different in abundance between the low and high RFI animals (P > 0.05, Wilcoxon test). However, when we analyzed the metabolic network as a whole, we found several differences between efficient and inefficient animals. Microbes from low RFI (efficient) animals use a suite of enzymes closer in network space to the host's reactions than those of the high RFI (inefficient) animals. Similarly, low RFI animals have microbial metabolic networks that, on average, contain reactions using shorter carbon chains than do those of high RFI animals, potentially allowing the host animals to extract metabolites more efficiently. Finally, the efficient animals possess community networks with greater Shannon diversity among their enzymes than do inefficient ones. Thus, our system approach to the ruminal microbiome identified differences attributable to feed efficiency in the structure of the microbes' community metabolic network that were undetected at the level of individual microbial taxa or reactions.
Sujet(s)
Aliment pour animaux/analyse , Microbiome gastro-intestinal , Voies et réseaux métaboliques , Métagénomique , Ovis/physiologie , Animaux , Femelle , Rumen/métabolisme , Rumen/microbiologie , Ovis/microbiologieRÉSUMÉ
BACKGROUND: Grazing mammals rely on their ruminal microbial symbionts to convert plant structural biomass into metabolites they can assimilate. To explore how this complex metabolic system adapts to the host animal's diet, we inferred a microbiome-level metabolic network from shotgun metagenomic data. RESULTS: Using comparative genomics, we then linked this microbial network to that of the host animal using a set of interface metabolites likely to be transferred to the host. When the host sheep were fed a grain-based diet, the induced microbial metabolic network showed several critical differences from those seen on the evolved forage-based diet. Grain-based (e.g., concentrate) diets tend to be dominated by a smaller set of reactions that employ metabolites that are nearer in network space to the host's metabolism. In addition, these reactions are more central in the network and employ substrates with shorter carbon backbones. Despite this apparent lower complexity, the concentrate-associated metabolic networks are actually more dissimilar from each other than are those of forage-fed animals. Because both groups of animals were initially fed on a forage diet, we propose that the diet switch drove the appearance of a number of different microbial networks, including a degenerate network characterized by an inefficient use of dietary nutrients. We used network simulations to show that such disparate networks are not an unexpected result of a diet shift. CONCLUSION: We argue that network approaches, particularly those that link the microbial network with that of the host, illuminate aspects of the structure of the microbiome not seen from a strictly taxonomic perspective. In particular, different diets induce predictable and significant differences in the enzymes used by the microbiome. Nonetheless, there are clearly a number of microbiomes of differing structure that show similar functional properties. Changes such as a diet shift uncover more of this type of diversity.
Sujet(s)
Régime alimentaire , Microbiome gastro-intestinal/physiologie , Voies et réseaux métaboliques , Métagénomique , Rumen/microbiologie , Ovis/microbiologie , Aliment pour animaux/analyse , Animaux , Digestion/physiologie , Grains comestibles , Comportement alimentaire , Rumen/physiologie , Ovis/physiologieRÉSUMÉ
We surveyed the ruminal metagenomes of 16 sheep under two different diets using Illumina pair-end DNA sequencing of raw microbial DNA extracted from rumen samples. The resulting sequence data were bioinformatically mapped to known prokaryotic 16S rDNA sequences to identify the taxa present in the samples and then analysed for the presence of potentially new taxa. Strikingly, the majority of the microbial individuals found did not map to known taxa from 16S sequence databases. We used a novel statistical modelling approach to compare the taxonomic distributions between animals fed a forage-based diet and those fed concentrated grains. With this model, we found significant differences between the two groups both in the dominant taxa present in the rumen and in the overall shape of the taxa abundance curves. In general, forage-fed animals have a more diverse microbial ecosystem, whereas the concentrate-fed animals have ruminal systems more heavily dominated by a few taxa. As expected, organisms from methanogenic groups are more prevalent in forage-fed animals. Finally, all of these differences appear to be grounded in an underlying common input of new microbial individuals into the rumen environment, with common organisms from one feed group being present in the other, but at much lower abundance.