- Research article
- Open Access
Temporal stability of the rumen microbiota in beef cattle, and response to diet and supplements
Animal Microbiome volume 1, Article number: 16 (2019)
Dietary intake is known to be a driver of microbial community dynamics in ruminants. Beef cattle go through a finishing phase that typically includes very high concentrate ratios in their feed, with consequent effects on rumen metabolism including methane production. This longitudinal study was designed to measure dynamics of the rumen microbial community in response to the introduction of high concentrate diets fed to beef cattle during the finishing period.
A cohort of 50 beef steers were fed either of two basal diet formulations consisting of approximately 10:90 or 50:50 forage:concentrate ratios respectively. Nitrate and oil rich supplements were also added either individually or in combination. Digesta samples were taken at time points over ~ 200 days during the finishing period of the cattle to measure the adaptation to the basal diet and long-term stability of the rumen microbiota.
16S rRNA gene amplicon libraries were prepared from 313 rumen digesta samples and analysed at a depth of 20,000 sequences per library. Bray Curtis dissimilarity with analysis of molecular variance (AMOVA) revealed highly significant (p < 0.001) differences in microbiota composition between cattle fed different basal diets, largely driven by reduction of fibre degrading microbial groups and increased relative abundance of an unclassified Gammaproteobacteria OTU in the high concentrate fed animals. Conversely, the forage-based diet was significantly associated with methanogenic archaea. Within basal diet groups, addition of the nitrate and combined supplements had lesser, although still significant, impacts on microbiota dissimilarity compared to pre-treatment time points and controls. Measurements of the response and stability of the microbial community over the time course of the experiment showed continuing adaptation up to 25 days in the high concentrate groups. After this time point, however, no significant variability was detected.
High concentrate diets that are typically fed to finishing beef cattle can have a significant effect on the microbial community in the rumen. Inferred metabolic activity of the different microbial communities associated with each of the respective basal diets explained differences in methane and short chain fatty acid production between cattle. Longitudinal sampling revealed that once adapted to a change in diet, the rumen microbial community remains in a relatively stable alternate state.
As a result of increasing demand for meat and milk, particularly in developing countries, ruminant livestock production is becoming one of the fastest growing agricultural sectors . This trend has led to concerns regarding environmental impact, where livestock farming currently accounts for 44% of the total anthropogenic sources of the greenhouse gas methane (CH4) . Ruminant recovery of energy from the diet, as well as the production of CH4 and N2O, is due to the activity of the rumen microbial community. Therefore, manipulation of the microbiota has the potential to improve the efficiency of animal production, and mitigate greenhouse gas emissions . A practical approach to achieve this is by management of the dietary intake.
The components making up a typical basal diet fed to beef cattle can be categorised into two major feed types. Plant fibre, including straw, hay, and grass or cereal crop silage are classified as forage. A variety of feeds, typically pelleted, and composed of nutrient-rich grains, starch, sugars or protein are classified as concentrates. The different ratios of the two feed types can influence the composition of the rumen microbial community both as a response to the different carbohydrate sources in the diet  and as a result of the changes in interactions between microbial groups . In turn this alters the production rates of microbial metabolic products including short chain fatty acids (SCFA) and methane [6, 7].
Supplements are added to the diet to improve performance or reduce methane production according to key principles. Firstly, they can directly influence growth of key members of the microbial community, either promoting growth of beneficial microbes or inhibiting growth of detrimental microbes. For example, addition of oils can have a defaunating effect, and at high doses can reduce or eliminate ciliate protozoa in the rumen , and vegetable oils and fish oils at doses as low as 1–2% have been found to directly affect the growth of key bacterial species . Nitrate is added as a theoretical ‘sink’ for hydrogen (H2) where it is reduced, typically by Selenomonas spp., to nitrite and ultimately to ammonia . Reduction of ruminal hydrogen in theory limits substrate availability for growth of the methanogenic archaea . Secondly, the supplement can have an effect on metabolite production by inhibiting the activity of key enzymes involved in certain metabolism pathways. Examples are the nitrooxy compounds that inhibit catalysis of the final step of the methanogenesis pathway .
The effect of nitrate and oil/fatty acid supplements on ruminal methane production has not always been reflected by associated changes in the microbial community [13,14,15,16]. The outcomes of these studies are highly dependent on the dose and the chemical composition of the nitrate salt , as well as the choice of methodology, sensitivity of the measurements, the power of the statistical analysis and factoring of variability of responses between individual experimental animals. In studies involving larger cohorts of experimental animals, combined with the appropriate discriminant analysis of metagenome datasets, it has been possible to identify rumen microbe functional biomarkers and inferred taxonomic groups for methane emissions in response to both basal diets and supplements .
Longitudinal experiments have been carried out previously to monitor the development of rumen microbiota during early life [18, 19], to measure the temporal dynamics of the microbiota during colonisation and breakdown of dietary fibre [20,21,22] and the diurnal variability . However, there is a lack of knowledge on the long-term stability and repeatability of measurements of the microbial community during the finishing phase of mature livestock animals.
The aim of the current study was to characterise the rumen microbial community of beef cattle in response to two basal diets comprising different forage:concentrate ratios with addition of high oil and nitrate supplements over the course of the finishing stage of production. Longitudinal sampling enabled the measurement of the temporal dynamics and stability of the microbial community over this period. The most significant discriminant groups of microorganisms responsible for driving changes as a response to diet over time were identified.
16S rRNA gene sequencing of rumen digesta samples was used to assess potential links between basal diet, rumen microbiota composition, and host animal measures such as methane emission and feed efficiency. In total, 313 16S rRNA gene amplicon libraries were sequenced using rumen samples collected during two feed trials carried out over consecutive years (2013 and 2014). 50 finishing beef steers (32 in 2013 and 18 in 2014) were sampled periodically at time points covering the seven-month finishing period when the animals are fed to gain weight and optimise meat and fat composition prior to slaughter. Sampling time points were evenly distributed (approximately one month apart) and covered critical time points listed in Table 1.
Results previously reported in Troy et al., (2015) and Duthie et al., (2018) [7, 24] from the same animal cohort, found basal diet and, to a lesser extent, nitrate and oil supplements had a significant effect on average methane production across all the animals. The high concentrate diet was associated with significantly lower (p < 0.001) CH4 emissions g per kg Dry Matter Intake (DMI) (Fig. 1), as well as lower molar proportions of acetate (P < 0.001) and butyrate (P < 0.01) and higher molar proportions of propionate (P < 0.001) and valerate (P < 0.05) . Within basal diets, only the combined nitrate and oil supplementation significantly reduced methane production compared to control in the forage fed cattle (Fig. 1). Average residual feed intake (RFI) was lower, (i.e. higher efficiency) in the high concentrate fed animals. However, this was not considered statistically significant.
After quality control and subsampling, 16S rRNA gene sequencing resulted in a total of 6.26 million sequences (randomly subsampled to 20,000 per library) for further analysis, providing > 97% species coverage (Good’s Coverage Index) for each sample. A total of 12,361 OTUs were identified, with over 99% of the sequences contained in the top 2000 OTUs. SILVA 128 SEED reference taxonomy assigned the majority of sequences (39%) to the Bacteroidetes, 30% to Firmicutes, 16% to Gammaproteobacteria, 6% to the Euryarchaeota, 2% Actinobacteria, 2% Spirochaetes 1% Verrucomicrobia and 1% Fibrobacteres, with 3% unclassified phyla (Additional file 1: OTU Table). Mean proportional compositions at the family level for both forage and concentrate-fed animals are shown in Additional file 2: Figure S1.
Average microbial diversity as assessed by calculating the Shannon index for each sample, was significantly lower (p < 0.001) in the cattle fed a high concentrate basal diet (Additional File 2: Figure S2). Furthermore, analysis of molecular variance (AMOVA) applied to the distance matrix used for the non-metric multidimensional scaling plot (NMDS) revealed highly significant clustering of microbial communities by basal diet (p < 0.001) (Fig. 2). Within each of the two basal diet groups, the microbial communities clustered significantly (p < 0.001) following nitrate supplementation compared to all other treatment and control groups. In the forage basal diet groups, combined oil/nitrate supplement samples (2013) clustered separately from the control group only (p < 0.001). In the concentrate fed animals, the oil supplement samples separated from the pre-treatment samples (p < 0.001). There was no significant microbial community dissimilarity between control animals and pre-treatment groups (Additional file 2: Table S3).
Supporting the AMOVA results, significant clustering of the microbial communities of forage and concentrate fed animals were also observed when using parsimony analysis of the microbial community dendrogram (Fig. 3). This clustering was largely driven by an increase in relative abundance of a single species-level operational taxonomic unit (OTU) (OTU00001, assigned to Gammaproteobacteria) in concentrate fed animals, which was also particularly associated with the later time points following the pre-treatment and adaptation periods.
Analysis of similarities (ANOSIM) confirmed the AMOVA results with highest R values associated with comparisons between animals fed different basal diets (p < 0.001). Nitrate (2013 and 2014) and oil (2013 and 2014) supplementation appeared to have relatively lower R values, but nonetheless significant, effects (p < 0.001). The only non-significant treatment was the oil in conjunction with the forage diet when compared to pre-treatment time points. No significant effects or interactions were found as a result of breed or trial year within treatments.
Linear discriminant analysis (LDA) using LEfSe software  identified highly significant OTU biomarkers associated with basal diet groups. With minimum linear discriminant analysis (LDA) effect size set at threshold > 4.0, species level OTUs were assigned to the lowest taxonomic level (using SILVA 128 classification at 100% confidence), with Gammaproteobacteria (class), Prevotella (genus) and Phascolarctobacterium (genus) significantly associated with high concentrate basal diets. OTUs assigned to Methanobrevibacter (genus), Ruminococcacaeae (family), Proteobacteria (phylum) and Lachnospiraceae (family) were significantly associated with forage basal diets (Table 2).
Taxonomic biomarkers were also found to be associated with the animals in the upper quartile of feed efficiency RFI at less stringent effect sizes (LDA > 2.0). These OTUs were low proportional abundance (typically 0.1–0.3% of the total microbial population), however, and were identified as species from the Prevotellaceae, Rikenellaceae and Acidaminococcaceae families.
Next, we carried out a longitudinal analysis, in order to assess the temporal stability of the rumen microbiota. Microbial community alpha diversity appeared to be relatively stable across sampling times during the ~ 200 days from Pre-treatment (TP0) to Slaughter (TP6), with the concentrate fed animals again showing consistently lower rumen microbiota diversity than those on the forage diet (Additional file 2: Figure S3). Clustering by Euclidean distance of average values of observed species richness (SOBS) and Shannon diversity index (H′) across the total time course separated samples by basal diet, with lower microbial community diversity in the high concentrate fed animals compared to the forage group. Within the forage fed animals, average alpha diversity was strongly influenced by trial year, with most animals from 2013 containing significantly lower average species richness and average microbial diversity (Shannon index) from those in the 2014 trial (p < 0.001) (Fig. 4, Additional file 2: Figure S4). However, discriminant analysis (LDA effect size > 4.0) did not reveal any significant OTUs between the 2013 and 2014 forage fed groups.)
Response and adaptation of the microbial community to the basal diets/supplements was measured using the Bray Curtis metric, which measured community dissimilarity relative from the pre-treatment time point as a baseline. Repeated measures ANOVA on these data showed significant community dissimilarity only occurring between Pre-treatment (TP0) and Adaptation (TP1) time points in high concentrate fed cattle. Forage fed cattle from both 2013 and 2014 animal trials did not show significant variability in microbial community composition regardless of additional supplement (Fig. 5). Pairwise Spearman correlations of Bray Curtis values between these time points were all highly significant (p < 0.001) (Additional file 2: Figure S6). Furthermore, the higher average dissimilarity values associated with concentrate diets compared to forage diets in both trial years indicated that the initial addition of concentrates to the diet preceded sweeping changes in microbiota composition. There was no further subsequent significant change in dissimilarity over time points TP1-TP6, however, indicating that the rumen microbiota remained relatively stable after adaptation to a given diet.
Of the OTU biomarkers associated with basal diets (LDA effect size > 4.0), only OTU00001 (derived from an uncultured Gammaproteobacteria lineage) showed significant temporal response to the introduction of the high concentrate diet. The relative abundance of this OTU increased upon addition of concentrates to the diet, and its dominance was maintained throughout the remainder of the experimental period while concentrates were being continually fed to the animals (Fig. 6).
The effects on the rumen microbial community of basal diet, and addition of nitrate and high-oil supplements, was determined with 50 experimental animals consisting of mature beef cattle during the seven-month finishing period.
High concentrate diets were significantly associated with lower methane emissions (g/kg DMI), decrease in acetate and an increase in propionate production. The change in metabolite production was in turn associated with better feed efficiency/lower residual feed intake (RFI). This supported the theory that energy stored in metabolites such as methane may represent a loss to the animal.
The Shannon diversity and species richness of the microbial communities was significantly lower in the concentrate fed compared to the forage fed groups. The effect of microbial community diversity on feed efficiency was previously investigated by Kruger Ben Shabat et al., (2016) , who reported that decreased microbial diversity was associated with a decrease in energy requirements needed for the production of non-relevant metabolites.
The cohort including the forage fed animals were split over two trial years (2013 and 2014), and some apparent differences in microbial diversity were revealed between these two groups, driven in part by a difference in the OTU richness. Analysis of the temporal stability of the microbial community accounted for the difference in baseline diversity as part of the statistical model and revealed a highly significant response over time of the rumen microbial community to the introduction of high concentrate diets compared to the forage fed groups from both trials. This response was followed by relative stability and illustrated in real time the perturbation, and re-stabilisation of the rumen microbial community after a given period of adaptation. Moreover, discriminant analysis provided compelling evidence of the most important microbial groups driving these changes.
Four sequence classification groups accounted for 90% of the total community: The Prevotellacaceae family (39%), sequences derived from uncultured organisms that could only be confidently assigned to the Clostridiales order (29%) and Gammaproteobacteria class (16%), and the archaeal family Methanobacteriaceae (6%). Changes in the relative abundance of these groups likely reflected their substrate preferences and/or tolerance of the environmental conditions  as a result of the different diets provided to the cattle.
Interestingly, the proportional abundance of the family Prevotellaceae relative to the total community did not change in the high concentrate animals. In contrast, the Methanobacteriaceae decreased in favour of increased relative abundance of unclassified Gammaproteobacteria (Additional file 2: Figure S1). This suggests that the growth of the unclassified Clostridiales was less competitive in a low fibre environment, whereas the Prevotellaceae have a greater degree of adaptability to gut conditions .
Hydrogenotrophic Methanobrevibacter spp. were associated with the forage fed animals, and this was reflected in significantly higher methane production (g CH4 /kg DMI) in this group. Reduction of methane emissions relative to dry matter intake (g/kg DMI) is a widely reported effect of increasing percentage of concentrate in the diet formulation, particularly at levels exceeding 80–90% concentrate:forage ratios . This is typically associated with a shift from acetate toward propionate production, as was the case in the present study and previously reported in Troy et al., (2015)  and Duthie et al., (2018) .
A single Proteobacteria OTU (OTU00005) was associated with forage diets. SILVA 128 taxonomy was unable to classify this uncultivated species in more detail. However, an NCBI BLASTn type search and the RDP classifier most closely aligned the representative sequence to a member of the Pasteurellaceae. This family includes rumen isolates Basfia succiniciproducens  and Actinobacillus succinogenes , both characterised as succinate producers with the ability to reduce nitrate. It is possible that the uncharacterised OTUs detected here might have similar functionality. In support of this, LEfSe analysis within diet groups confirmed its association with the nitrate treatment.
The single most abundant OTU, comprising over 10% of total sequence counts, was significantly associated with the high concentrate basal diet. The representative sequence was assigned to the Gammaproteobacteria class using SILVA 128 reference taxonomy, but was not identified as any known cultured isolate. Using the Greengenes reference database, the sequence was mapped to Succinivibrionaceae (71% bootstrap support), while the RDP classifier and an NCBI BLAST type search to mapped it to the genus Frischella (65% bootstrap support and 89% sequence identity respectively) . Phylogenetic analysis (Additional file 2: Figure S5) placed it in a group containing the novel Orbales order isolated from the gut of insects . Examples of rumen Gammaproteobacteria isolates Actinobacillus succinogenes, Basfia succiniciproducens and Mannheimia succiniciproducens [30, 31, 34] are all known for their ability to produce succinate.
Isolates of the succinate-producing Succinivibrionaceae family of microbes have also been characterised from the foregut of the Tammar wallaby, a herbivore known for its unusually low methane emissions . In a previous metagenomic analysis, Succinivibrionaceae were associated with low methane emitting phenotypes in beef cattle . In the present study, detailed taxonomic classification of the Proteobacteria OTU sequences beyond class level was limited by the lack of available references. However, an NCBI BLASTn search of the representative sequences against the total current nucleotide database found many hundreds of highly similar sequences previously recovered from ruminants but not identified. This indicates that this species is likely to be an important and widespread rumen microbiota constituent, and highlights the importance of continuing efforts to culture, isolate and better characterise the rumen microbiota . Cumulatively, the sequence-based data suggest that there are important groups of unclassified Proteobacteria, possibly containing novel taxa that may have a significant role in rumen methane emissions.
Following discriminant analysis, two OTU biomarkers assigned to Prevotella spp. were strongly associated with the high concentrate diet group. Isolates from this genus are known to produce propionate via the succinate pathway , although with low pH conditions some species of Prevotella can be associated with accumulation of succinate . In response to these conditions, a prominent succinate consumer would be expected to thrive. In this study, an uncultured Firmicutes organism strongly associated with the concentrate diets was identified as Phascolarctobacterium (SILVA) or Succiniclasticum (Greengenes/RDP/BLASTn). The type species of this genus, Succiniclasticum ruminis, is known to produce propionate from succinate as the sole mechanism of energy production . Short chain fatty acid analysis, carried out previously, confirmed significantly lower acetate to propionate ratio in concentrate fed animals [7, 24].
No archaea were associated with high concentrate diets above our arbitrarily high LEfSe-based linear discriminant analysis threshold. However, at lower LDA effect size settings, OTUs classified as Methanobrevibacter boviskoreani, a methanogenic archaeal species recently isolated from the rumen of Korean cattle  and Methanomassiliicoccaceae, a methylotrophic methanogen group previously associated with low methane emissions in the rumen , were both significantly associated with high concentrate diets/low methane emissions in the cattle.
Previous comparable analyses of the human gut microbiota have established that, in the absence of major perturbations, the most abundant groups of the microbial community remain in a largely stable state [43, 44]. In contrast, previous longitudinal studies of the rumen microbiota indicate that it can vary significantly over long term seasonal time scales, probably as a result of the changes in grazing quality throughout the year . In the short term, the diurnal variability of the rumen microbial community can overpower both individual and diet effects. The latter effect is typically seen when high concentrate containing rations are provided to the animal once per day . The principle of short-term variability as a result of dietary effect, followed by long term stability was broadly supported in this study. Following the period of adaptation and change, an alternative stable microbial community state was established for the duration of the feed trial. This type of response and single alternative state is one of the models used to describe the variability of community types in response to a change in environment. Other models such as multi-stability or selection of local communities described in the human gut have not been described in the rumen .
Significant changes in the composition of the rumen microbiota can arise as a result of changes in diet promoting increase of the taxa that can best utilise these substrates for metabolism. At the extreme levels of concentrate to forage (90:10) typically provided as a beef cattle finishing diet, reduction of key fibre degraders would be expected . In agreement with this expectation, in the current study LEfSe-based linear discriminant analysis of taxa revealed key fibre-degrading Clostridiales species were most negatively impacted by the dietary change, whereas more generalist taxonomic groups such as Prevotella spp. appeared to be relatively unaffected.
Another mechanism by which dietary changes might change the rumen microbiota is a niche modification effect, whereby the bacteria themselves alter their environment, affecting growth of functionally associated groups . A possible niche modification following dietary change is indicated by the significant increase in proportional abundance of Succiniclasticum, possibly as a result of accumulation of its preferred growth substrate succinate, and a significant decrease in Methanobrevibacter, likely as a result of reduced availability of hydrogen. The dramatic increase of concentrates favoured a single unclassified species (OTU) of Gammaproteobacteria. Linear discriminant analysis identified this OTU as the only taxon significantly associated with the change of the microbiota between TP0 and TP1. As this organism is currently uncultured, it is unknown whether its proportional increase was driven directly by diet effects, or indirectly via niche modification.
Our results build on existing studies emphasizing the importance of diet, and in particular the ratio of concentrate to forage, in driving the composition of the rumen microbiota [4,5,6, 17, 23]. Changes in the ruminal microbiota composition following addition of high concentrate diets and supplements explained many of the phenotypic changes previously reported in the rumen, including methane emissions and SCFA production . Microbial community changes were largely driven by a small number of highly proportionally abundant OTUs, with one identified as an uncultured member of the Gammaproteobacteria of particular significance. As assessed by longitudinal sampling, the change in relative abundance of this and other corresponding taxa was observed during the initial response and the adaptation period. This was followed by a period of relative stability, in respective alternative states corresponding to either the forage or high concentrate diets. This result is reassuring for cross-sectional studies as our results suggest that, once adapted to a dietary intervention, a single sample may be considered reasonably representative of the microbial community during the time course of a typical trial where the animals are fed a consistent diet.
Materials and methods
Digesta samples were taken from a selection of 50 experimental animals that were part of two related trials carried out in consecutive years. The trials investigated the long-term effect of different diets and feed additives on CH4 emissions, performance and feed efficiency in different breeds of beef cattle during the seven-month finishing phase of production.
The first animal trial, carried out between May 2013 and December 2013 and reported in Troy et al., (2015) , involved 32 beef cattle comprising two breeds: crossbred 17 Charolais (CH) and 15 purebred Luing (LU). Over an adaptation period of four weeks, a selection of animals was introduced to the respective diets: 15 to the concentrate-straw based (Concentrate) and 17 to the silage-based (Forage). Individual groups were then allocated to one of three treatments: Control (n = 10), Nitrate (n = 10), or a high oil (Oil) (n = 12) supplement.
The second animal trial, carried out from March 2014 to November 2014 and reported in Duthie et al., (2018)  involved 18 beef cattle comprising two breeds: 10 crossbred Aberdeen Angus (AA) and eight crossbred Limousin (LIM). In this case all animals were given a Silage based diet (Forage) and allocated to one of four treatment groups: Control (n = 4), Nitrate (n = 4), high oil (Oil) (n = 4), or combined nitrate and high oil supplements (n = 6).
Both studies took place at the Beef and Sheep Research Centre, SRUC, Edinburgh, UK. The experimental work was approved by the Animal Experiment Committee of SRUC and was conducted in accordance with the requirements of the UK Animals (Scientific Procedures) Act 1986. Details on the experimental animals, diet formulation, allocation and sampling time points throughout the course of the experiments including sampling timetables can be found in Table 1 and Additional file 2: Tables S1–2.
At each sampling, approximately 50 mL of rumen liquid were taken by inserting a stomach tube (16 × 2700 mm Equivet Stomach Tube, Jørgen Kruuse A/S, Langeskov, Denmark) nasally and aspirating manually. This liquid was filtered through two layers of muslin and 5 mL strained rumen fluid were mixed with 10 ml phosphate buffered saline containing glycerol (30% v/v). These samples were stored at − 20 °C between collection and analysis.
For short chain fatty acid (SCFA) analysis, a 5 ml sample of the filtered liquid was deproteinised by adding 1 mL metaphosphoric acid (215 g/L) and 0.5 mL methylvaleric acid (10 g/L). Measurements were made using HPLC  and expressed as mmol/mol total SCFA.
Methane emissions were measured during the ‘Chamber’ phase (TP5) of the animal trial with animals housed in closed respiration chambers following adaptation in an open training pen. CH4 concentrations were measured for each chamber by a multi-gas analyser. CH4 production was calculated as the difference between inlet and exhaust gas concentration multiplied by volumetric dry air flow, corrected to standard temperature and pressure (25 °C and 1013 Mbar). Daily CH4 production was calculated as the average of individual values and converted to a mass basis. Feed intake was monitored during this phase and methane emissions calculated per day (g/day) and relative to kg dry matter intake (g/kg DMI).
Feed efficiency was calculated using two metrics: Feed conversion ratio (FCR) was calculated as average dry matter intake (DMI) per day (kg/d)/ average daily gain (ADG).
Residual feed intake (RFI)  was calculated as deviation of actual DMI (kg/d) from DMI predicted based on linear regression of actual DMI on ADG, mid-metabolic body weight (MBW = BW0.75) and FD1 (fat depth at the 12/13th rib at the end of TP4) .
16S rRNA gene amplicon library preparation
DNA was extracted following the protocol based on Yu and Morrison (2004)  by repeated bead-beating followed by precipitation, elution and purification using columns from the QIAamp® DNA Stool Mini Kit, (QIAGEN Ltd., Manchester, UK).
PCR amplification (20 cycles) was carried out in quadruplicate 25 μL reactions using Q5® High-Fidelity DNA polymerase (New England Biolabs Inc.,Hitchin, UK) with universal prokaryotic primers targeting the V4 region of the 16S rRNA gene . Individual samples were identified using unique 12 nucleotide barcodes built into the forward primer. PCR products were cleaned and quantitated using the Qubit high sensitivity dsDNA assay kit (Fisher Scientific UK Ltd., Loughborough, UK). The samples were pooled in equimolar quantities and 80 μL run on a 1% w/v agarose/TBE gel to separate residual primers and dNTPs. The band at the expected size containing the amplicons was cut and purified using a Promega Wizard® SV Gel purification kit (Promega UK, Southampton, UK).
The libraries were quality assessed using an Agilent 2100 Bioanalyzer System (Agilent Technologies. Santa Clara, CA, US) and sequenced by Edinburgh Genomics using Illumina MiSeq v2 250 paired end reagent kits (Illumina UK, Cambridge, UK.). Raw sequence data was uploaded to the European Nucleotide Archive under study accession numbers PRJEB31107 and PRJEB31085.
Sequence data was analysed using mothur 1.39.0  with steps to assemble paired end sequences, remove low quality sequences using both quality control metrics and chimera removal using UCHIME 4.2.40 . Sequence counts in each library were normalised by subsampling to 20,000 sequences per sample.
An operational taxonomic unit (OTU) based approach was selected over phylotyping. This approach better described the microbial community diversity irrespective of whether a taxonomic label could be applied to the representative sequence . This was also important for determination of discriminant taxa where the same phylotype (for example, Prevotella) can be associated with opposing treatment or phenotypic groups .
Sequences were clustered into OTUs using OptiClust  at 97% identity, singletons removed and taxonomic classification of the representative sequences initially using the SILVA 128 SEED reference database . For verification purposes, classifications were subsequently also carried out using the Greengenes (gg_13_8_99)  and Ribosomal Database Project (version 16) reference databases , and NCBI BLASTn against the complete NCBI reference database. OTUs assigned to the Archaea domain were reclassified using the RIM DB taxonomic framework for methanogenic archaea .
Sequence counts in each library were normalised by subsampling to 20,000 sequences per sample prior to statistical analysis. Microbial community data was tested for coverage per sample using Good’s statistic . Microbial community species richness and diversity was summarised using the number of observed OTUs and Shannon diversity index (H′), respectively. Beta diversity was calculated using the Bray Curtis dissimilarity metric.
Significance differences of the beta diversity comparisons were given at values of p < 0.001. The Parsimony test in mothur was used to assess significance in the dendrogram, and analysis of molecular variance (AMOVA) for the distance matrix used to create the nonlinear multidimensional scaling (NMDS) plot of the total sample data.
Taxonomic biomarkers associated with respective treatment groups were determined using Linear Discriminant Analysis (LEfSe)  with a cut off of effect size set at values > 4.0. This was applied to diet, groups, supplement groups and highest and lowest quartile residual feed intake groups.
General statistical analysis was carried out using R version 3.5.1 [25, 64]. Normality of data was determined using quantile-quantile (q-q) plots. The Kruskal-Wallis rank sum test was used to determine significance where data was not normally distributed and Analysis of Variance (ANOVA) was used in instances where data was normally distributed. Repeated measures ANOVA was used for longitudinal data following individual animals over time. The Tukey HSD post hoc test was used to compare multiple treatments. In cases where OTU sequence counts were used for statistical comparison, the data were transformed using square root relative abundance. Correlations were determined using Spearman rank correlation. Significance was given at values of p < 0.05 in the case of phenotype data and p < 0.001 for sequence data.
Availability of data and materials
Sequence data for the 2013 study samples is available from the European Nucleotide Archive under study accession number PRJEB31107, and the data from the 2014 samples under study accession number PRJEB31085.
- 16S rRNA:
16 Svedberg ribosomal ribonucleic acid
Average daily gain
Analysis of molecular variance
Analysis of variance
Basic local alignment search tool
Dry matter intake
Feed conversion ratio
Linear discriminant analysis
Linear discriminant analysis effect size
National center for biotechnology Information
Nonlinear multidimensional scaling
Operational taxonomic unit
Polymerase chain reaction
Ribosomal database project
Residual feed intake
- RIM DB:
Rumen and intestinal methanogen-data base
Short chain fatty acid
Tris borate ethylenediaminetetraacetic acid
Delgado C. Rising demand for meat and milk in developing countries: implications for grasslands – based livestock production. In: McGilloway DA, editor. Grassland: a global resource. The Netherlands: Wageningen Academic Publishers; 2005. p. 29–39.
Gerber PJ, Steinfeld H, Henderson B, Mottet A, Opio C, Dijkman J, Falcucci A, Tempio G. Tackling climate change through livestock – A global assessment of emissions and mitigation opportunities. Rome, Italy: Food and Agriculture Organization of the United Nations (FAO); 2013.
Cottle DJ, Nolan JV, Wiedemann SG. Ruminant enteric methane mitigation: a review. Anim Prod Sci. 2011;51:491–514.
Belanche A, Doreau M, Edwards JE, Moorby JM, Pinloche E, Newbold CJ. Shifts in the rumen microbiota due to the type of carbohydrate and level of protein ingested by dairy cattle are associated with changes in rumen fermentation. J Nutr. 2012;142(9):1684–92.
Tapio I, Fischer D, Blasco L, Tapio M, Wallace RJ, Bayat AR, Ventto L, Kahala M, Negussie E, Shingfield KJ, Vilkki J. Taxon abundance, diversity, co-occurrence and network analysis of the ruminal microbiota in response to dietary changes in dairy cows. PLoS One. 2017;12(7):e0180260.
Popova M, Martin C, Eugène M, Mialon MM, Doreau M, Morgavi DP. Effect of fibre-and starch-rich finishing diets on methanogenic Archaea diversity and activity in the rumen of feedlot bulls. Anim Feed Sci Technol. 2011;166:113–21.
Troy SM, Duthie CA, Hyslop JJ, Roehe R, Ross DW, Wallace RJ, Waterhouse A, Rooke JA. Effectiveness of nitrate addition and increased oil content as methane mitigation strategies for beef cattle fed two contrasting basal diets. J Anim Sci. 2015;93(4):1815–23.
Newbold CJ, Chamberlain DG. Lipids as rumen defaunating agents. Proc Nutr Soc. 1988;47:154A.
Vargas JE, Andrés S, Snelling TJ, López-Ferreras L, Yáñez-Ruíz DR, García-Estrada C, López S. Effect of Sunflower and Marine Oils on Ruminal Microbiota, In vitro Fermentation and Digesta Fatty Acid Profile. Front Microbiol. 2017;8:1124.
Latham EA, Anderson RC, Pinchak WE, Nisbet DJ. Insights on Alterations to the Rumen Ecosystem by Nitrate and Nitrocompounds. Front Microbiol. 2016;7:228.
Yang C, Rooke JA, Cabeza I, Wallace RJ. Nitrate and Inhibition of Ruminal Methanogenesis: Microbial Ecology, Obstacles, and Opportunities for Lowering Methane Emissions from Ruminant Livestock. Front Microbiol. 2016;7:132.
Duin EC, Wagner T, Shima S, Prakash D, Cronin B, Yáñez-Ruiz DR, Duval S, Rümbeli R, Stemmler RT, Thauer RK, Kindermann M. Mode of action uncovered for the specific reduction of methane emissions from ruminants by the small molecule 3-nitrooxypropanol. Proc Natl Acad Sci U S A. 2016;113(22):6172–7.
Patra AK. The effect of dietary fats on methane emissions, and its other effects on digestibility, rumen fermentation and lactation performance in cattle: A meta-analysis. Livestock Sci. 2013;155:244–54.
Veneman JB, Muetzel S, Hart KJ, Faulkner CL, Moorby JM, Perdok HB, Newbold CJ. Does Dietary Mitigation of Enteric Methane Production Affect Rumen Function and Animal Productivity in Dairy Cows? PLoS One. 2015;10(10):e0140282.
Popova M, McGovern E, McCabe MS, Martin C, Doreau M, Arbre M, Meale SJ, Morgavi DP, Waters SM. The Structural and Functional Capacity of Ruminal and Cecal Microbiota in Growing Cattle Was Unaffected by Dietary Supplementation of Linseed Oil and Nitrate. Front Microbiol. 2017;8:937.
Bayat AR, Tapio I, Vilkki J, Shingfield KJ, Leskinen H. Plant oil supplements reduce methane emissions and improve milk fatty acid composition in dairy cows fed grass silage-based diets without affecting milk yield. J Dairy Sci. 2018;101(2):1136–51.
Auffret MD, Stewart R, Dewhurst RJ, Duthie C-A, Rooke JA, Wallace RJ, Freeman TC, Snelling TJ, Watson M, Roehe R. Identification, comparison and validation of robust rumen microbial biomarkers for methane emissions using diverse Bos taurus breeds and basal diets. Front. Microbiol. 2018;8:2642.
Abecia L, Jiménez E, Martínez-Fernandez G, Martín-García AI, Ramos-Morales E, Pinloche E, Denman SE, Newbold CJ, Yáñez-Ruiz DR. Natural and artificial feeding management before weaning promote different rumen microbial colonization but not differences in gene expression levels at the rumen epithelium of newborn goats. PLoS One. 2017;12(8):e0182235.
Yáñez-Ruiz DR, Abecia L, Newbold CJ. Manipulating rumen microbiome and fermentation through interventions during early life: a review. Front Microbiol. 2015;6:1133.
Huws SA, Edwards JE, Creevey CJ, Rees Stevens P, Lin W, Girdwood SE, et al. Temporal dynamics of the metabolically active rumen bacteria colonising fresh perennial ryegrass. FEMS Microbiol. Ecol. 2016;92:e0149095.
Piao H, Lachman M, Malfatti S, Sczyrba A, Knierim B, Auer M, Tringe SG, Mackie RI, Yeoman CJ, Hess M. Temporal dynamics of fibrolytic and methanogenic rumen microorganisms during in situ incubation of switchgrass determined by 16S rRNA gene profiling. Front Microbiol. 2014;5:307.
Huws SA, Mayorga OL, Theodorou MK, Onime LA, Kim EJ, Cookson AH, Newbold CJ, Kingston-Smith AH. Successional colonization of perennial ryegrass by rumen bacteria. Lett Appl Microbiol. 2013;56(3):186–96.
Shaani Y, Zehavi T, Eyal S, Miron J, Mizrahi I. Microbiome niche modification drives diurnal rumen community assembly, overpowering individual variability and diet effects. ISME J. 2018;12:2446–57.
Duthie CA, Troy SM, Hyslop JJ, Ross DW, Roehe R, Rooke JA. The effect of dietary addition of nitrate or increase in lipid concentrations, alone or in combination, on performance and methane emissions of beef cattle. Animal. 2018;12(2):280–7.
Hothorn T, Bretz F, Westfall P. Simultaneous Inference in General Parametric Models. Biometrical J. 2008;50(3):346–63.
Kruger Ben Shabat SK, Sasson G, Doron-Faigenboim A, Durman T, Yaacoby S, Berg Miller ME, White BA, Shterzer N, Mizrahi I. Specific microbiome dependent mechanisms underlie the energy harvest efficiency of ruminants. ISME J. 2016;10:2958–72.
Henderson G, Cox F, Ganesh S, Jonker A, Young W, RMG Collaborators, Janssen PH. Rumen microbial community composition varies with diet and host, but a core microbiome is found across a wide geographical range. Sci Rep. 2015;5:14567.
Duncan SH, Louis P, Thomson JM, Flint HJ. The role of pH in determining the species composition of the human colonic microbiota. Environ Microbiol. 2009;11(8):2112–22.
Martin C, Morgavi DP, Doreau M. Methane mitigation in ruminants: from microbe to the farm scale. Animal. 2010;4(3):351–65.
Kuhnert P, Scholten E, Haefner S, Mayor D, Frey J. Basfia succiniciproducens gen. Nov., sp. nov., a new member of the family Pasteurellaceae isolated from bovine rumen. Int J Syst Evol Microbiol. 2010;60(Pt 1):44–50.
Guettler MV, Rumler D, Jain MK. Actinobacillus succinogenes sp. nov., a novel succinic-acid-producing strain from the bovine rumen. Int J Syst Bacteriol. 1999;49:207–16.
Engel P, Kwong WK, Moran NA. Frischella perrara gen. Nov., sp. nov., a gammaproteobacterium isolated from the gut of the honeybee, Apis mellifera. Int J Syst Evol Microbiol. 2013;63(Pt 10):3646–51.
Kwong WK, Moran NA. Cultivation and characterization of the gut symbionts of honey bees and bumble bees: description of Snodgrassella alvi gen. Nov., sp. nov., a member of the family Neisseriaceae of the Betaproteobacteria, and Gilliamella apicola gen. Nov., sp. nov., a member of Orbaceae fam. Nov., Orbales ord. Nov., a sister taxon to the order ‘Enterobacteriales’ of the Gammaproteobacteria. Int J Syst Evol Microbiol. 2013;63(Pt 6):2008–18.
Lee PC, Lee SY, Hong SH, Chang HN. Isolation and characterization of a new succinic acid-producing bacterium, Mannheimia succiniciproducens MBEL55E, from bovine rumen. Appl Microbiol Biotechnol. 2002;58:663–8.
Pope PB, Smith W, Denman SE, Tringe SG, Barry K, Hugenholtz P, McSweeney CS, McHardy AC, Morrison M. Isolation of Succinivibrionaceae implicated in low methane emissions from Tammar wallabies. Science. 2011;333(6042):646–8.
Wallace RJ, Rooke J, McKain N, Duthie C-A, Hyslop JJ, Ross DW, et al. The rumen microbial metagenome associated with high methane production in cattle. BMC Genomics. 2015;16:839.
Seshadri R, Leahy SC, Attwood GT, Teh KH, Lambie SC, Cookson AL, Eloe-Fadrosh EA, Pavlopoulos GA, Hadjithomas M, Varghese NJ, Paez-Espino D, Hungate1000 project collaborators, Perry R, Henderson G, Creevey CJ, Terrapon N, Lapebie P, Drula E, Lombard V, Rubin E, Kyrpides NC, Henrissat B, Woyke T, Ivanova NN, Kelly WJ. Cultivation and sequencing of rumen microbiome members from the Hungate1000 Collection. Nat Biotechnol. 2018;36(4):359–67.
Reichardt N, Duncan SH, Young P, Belenguer A, McWilliam Leitch C, Scott KP, et al. Phylogenetic distribution of three pathways for propionate production within the human gut microbiota. ISME J. 2014;8:1323–35.
Louis P, Flint HJ. (2017) Formation of propionate and butyrate by the human colonic microbiota. Environ Microbiol. 2017;19(1):29–41.
van Gylswyk NO. Succiniclasticum ruminis gen. Nov., sp. nov., a ruminal bacterium converting succinate to propionate as the sole energy-yielding mechanism. Int J Syst Bacteriol. 1995;45(2):297–300.
Lee JH, Kumar S, Lee GH, Chang DH, Rhee MS, Yoon MH, Kim BC. Methanobrevibacter boviskoreani sp. nov., isolated from the rumen of Korean native cattle. Int J Syst Evol Microbiol. 2013;63(Pt 11):4196–201.
Poulsen M, Schwab C, Jensen BB, Engberg RM, Spang A, Canibe N, Højberg O, Milinovich G, Fragner L, Schleper C, Weckwerth W, Lund P, Schramm A, Urich T. Methylotrophic methanogenic Thermoplasmata implicated in reduced methane emissions from bovine rumen. Nat Commun. 2013;4:1428.
Schloissnig S, Arumugam M, Sunagawa S, Mitreva M, Tap J, Zhu A, Waller A, Mende DR, Kultima JR, Martin J, et al. Genomic variation landscape of the human gut microbiome. Nature. 2013;493:45–50.
Faith JJ, Guruge JL, Charbonneau M, Subramanian S, Seedorf H, Goodman AL, Clemente JC, Knight R, Heath AC, Leibel RL, et al. The long-term stability of the human gut microbiota. Science. 2013;341:1237439.
Noel SJ, Attwood GT, Rakonjac J, Moon CD, Waghorn GC, Janssen PH. Seasonal changes in the digesta-adherent rumen bacterial communities of dairy cattle grazing pasture. PLOS ONE. 2017;12(3):e0173819.
Gonze D, Lahti L, Raes J, Faust K. (2017) Multi-stability and the origin of microbial community types. ISME J. 2017;11(10):2159–66.
Fernando SC, Purvis HT 2nd, Najar FZ, Sukharnikov LO, Krehbiel CR, Nagaraja TG, Roe BA, Desilva U. Rumen microbial population dynamics during adaptation to a high-grain diet. Appl Environ Microbiol. 2010;76(22):7482–90.
Rooke JA, Borman AJ, Armstrong DG. The effect of inoculation with Lactobacillus plantarum on fermentation in laboratory silos of herbage low in water-soluble carbohydrate. Grass and Forage Science. 1990;45:143–52.
Koch RM, Swiger LA, Chambers D, Gregory KE. Efficiency of feed use in beef cattle. J Anim Sci. 1963;22:486–94.
Basarab JA, Price MA, Aalhus JL, Okine EK, Snelling WM, Lyle KL. Residual feed intake and body composition in young growing cattle. Canadian Journal of Animal Science. 2003;83:189–204.
Yu Z, Morrison M. Improved extraction of PCR-quality community DNA from digesta and fecal samples. Biotechniques. 2004;36(5):808–12.
Thompson LR, Sanders JG, McDonald D, Amir A, Ladau J, Locey KJ, Prill RJ, Tripathi A, Gibbons SM, Ackermann G, Navas-Molina JA, Janssen S, Kopylova E, Vázquez-Baeza Y, González A, Morton JT, Mirarab S, Zech Xu Z, Jiang L, Haroon MF, Kanbar J, Zhu Q, Jin Song S, Kosciolek T, Bokulich NA, Lefler J, Brislawn CJ, Humphrey G, Owens SM, Hampton-Marcell J, Berg-Lyons D, McKenzie V, Fierer N, Fuhrman JA, Clauset A, Stevens RL, Shade A, Pollard KS, Goodwin KD, Jansson JK, Gilbert JA, Knight R. Earth Microbiome Project Consortium.. A communal catalogue reveals Earth’s multiscale microbial diversity. Nature. 2017;551:457–63.
Schloss PD, Westcott SL, Ryabin T, Hall JR, Hartmann M, Hollister EB, Lesniewski RA, Oakley BB, Parks DH, Robinson CJ, Sahl JW, Stres B, Thallinger GG, Van Horn DJ, Weber CF. Introducing mothur: Open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol. 2009;75(23):7537–41.
Edgar RC, Haas BJ, Clemente JC, Quince C. Knight R UCHIME improves sensitivity and speed of chimera detection. Bioinformatics. 2011;27(16):2194–200.
Schloss PD, Westcott SL. Assessing and improving methods used in operational taxonomic unit-based approaches for 16S rRNA gene sequence analysis. Appl Environ Microbiol. 2011;77(10):3219–26.
Tapio I, Snelling TJ, Strozzi F, Wallace RJ. The ruminal microbiome associated with methane emissions from ruminant livestock. J. Anim. Sci. Biotechnol. 2017;8:7.
Westcott SL, Schloss PD. OptiClust, an Improved Method for Assigning Amplicon-Based Sequence Data to Operational Taxonomic Units. mSphere. 2017;2(2):e00073–17.
Yilmaz P, Parfrey LW, Yarza P, Gerken J, Pruesse E, Quast C, Schweer T, Peplies J, Ludwig W, Glöckner FO. The SILVA and “All-species Living Tree Project (LTP)” taxonomic frameworks. Nucl Acids Res. 2014;42:D643–8.
DeSantis TZ, Hugenholtz P, Larsen N, Rojas M, Brodie EL, Keller K, Huber T, Dalevi D, Hu P, Andersen GL. Greengenes, a chimera-checked 16S rRNA gene database and workbench compatible with ARB. Appl Environ Microbiol. 2006;72(7):5069–72.
Cole JR, Wang Q, Fish JA, Chai B, McGarrell DM, Sun Y, Brown CT, Porras-Alfaro A, Kuske CR, Tiedje JM. Ribosomal Database Project: data and tools for high throughput rRNA analysis. Nucl Acids Res. 2014;42:D633–42.
Seedorf H, Kittelmann S, Henderson G, Janssen PH. RIM-DB: a taxonomic framework for community structure analysis of methanogenic archaea from the rumen and other intestinal environments. Peer J. 2014;2:e494.
Good IJ. The Population Frequencies of Species and the Estimation of Population Parameters. Biometrika. 1953;40(3–4):237–64.
Segata N, Izard J, Waldron L, Gevers D, Miropolsky L, Garrett WS, Huttenhower C. Metagenomic biomarker discovery and explanation. Genome Biol. 2011;12(6):R60.
R Core Team (2018). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL https://www.R-project.org/.
Sampling of ruminal digesta was carried out at Scotland’s Rural College (SRUC) by Laura Nicoll, Lesley Deans and Claire Broadbent.
Sequencing using Illumina MiSeq was carried out by Edinburgh Genomics, The University of Edinburgh. Edinburgh Genomics is partly supported through core grants from NERC (R8/H10/56), MRC (MR/K001744/1) and BBSRC (BB/J004243/1).
Data were processed using the Maxwell High Performance Computing Cluster of the University of Aberdeen IT Service (www.abdn.ac.uk/staffnet/research/hpc.php), provided by Dell Inc. and supported by Alces Software.
This work was funded by the Rural and Environment Science and Analytical Services Division (RESAS) of the Scottish Government as a collaborative HEI project between The University of Aberdeen, The Roslin Institute, and Scotland’s Rural College (SRUC). The funding body had no role in the design of the study or collection, analysis, or interpretation of data or in writing the manuscript.
Ethics approval and consent to participate
Digesta sampling was conducted at Scotland’s Rural College (SRUC) Beef and Sheep Research Centre in Edinburgh in 2013 and in 2014. The experimental protocol was approved by SRUC’s Animal Welfare and Ethical Review Body, the Animal Experiments Committee, and was conducted in accordance with the requirements of the United Kingdom Animals (Scientific Procedures) Act, 1986.
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Snelling, T.J., Auffret, M.D., Duthie, C. et al. Temporal stability of the rumen microbiota in beef cattle, and response to diet and supplements. anim microbiome 1, 16 (2019) doi:10.1186/s42523-019-0018-y
- Concentrate diet
- Forage diet
- Nitrate supplementation
- Oil supplementation
- Temporal stability