Quantitative analysis of ruminal methanogenic microbial populations in beef cattle divergent in phenotypic residual feed intake (RFI) offered contrasting diets

Background Methane (CH4) emissions in cattle are an undesirable end product of rumen methanogenic fermentative activity as they are associated not only with negative environmental impacts but also with reduced host feed efficiency. The aim of this study was to quantify total and specific rumen microbial methanogenic populations in beef cattle divergently selected for residual feed intake (RFI) while offered (i) a low energy high forage (HF) diet followed by (ii) a high energy low forage (LF) diet. Ruminal fluid was collected from 14 high (H) and 14 low (L) RFI animals across both dietary periods. Quantitative real time PCR (qRT-PCR) analysis was conducted to quantify the abundance of total and specific rumen methanogenic microbes. Spearman correlation analysis was used to investigate the association between the relative abundance of methanogens and animal performance, rumen fermentation variables and diet digestibility. Results Abundance of methanogens, did not differ between RFI phenotypes. However, relative abundance of total and specific methanogen species was affected (P < 0.05) by diet type, with greater abundance observed while animals were offered the LF compared to the HF diet. Conclusions These findings suggest that differences in abundance of specific rumen methanogen species may not contribute to variation in CH4 emissions between efficient and inefficient animals, however dietary manipulation can influence the abundance of total and specific methanogen species.


Background
Enteric methane (CH 4 ) emissions from ruminant livestock accounts for approximately 80% of emissions from the agricultural-sector [1]. In the rumen, CH 4 production (methanogenesis) occurs during microbial fermentation of feed by a specific group of microbes known as archaea called methanogens. The majority of CH 4 produced in the rumen is eructed and thus released into the atmosphere. Enteric CH 4 production also represents a significant (2-15%) loss in energy from dietary gross energy intake [2]. Therefore, any reduction in enteric CH 4 emissions would potentially represent both environmental and economic benefits. In beef cattle production, feed efficiency is defined as the efficiency with which dietary substrate is converted into product (e.g. carcass) and is an important determinant of the profitability of meat production [3]. In recent times residual feed intake (RFI) has become the index of choice for measuring feed efficiency [4]. A number of research groups [5,6] including our own [7], have shown that CH 4 produced in the rumen has been shown to be negatively associated with host feed efficiency.
Enteric CH 4 emissions are not only influenced by the quantity of feed consumed by ruminants, but also by its chemical composition [8]. For example forage based diets such as grass are composed of structural carbohydrates such as cellulose and hemicellulose, which produce predominantly acetate and butyrate as fermentation endproducts compared to the propionate dominant fermentation patterns from a cereal based diets. Recently, using clone-sequencing and next generation methanogenspecific tag-encoded pyrosequencing, we showed that specific species of archaea, Methanobrevibacter spp. are the dominant methanogens in the rumen across contrasting diets, with Methanobrevibacter smithii being the most abundant species followed by Methanobrevibacter ruminantium and Methanosphaera stadtmanae [9]. However, particularly when species are present in low abundance, these technologies are not sufficiently accurate to reliably quantify specific methanogens. Quantitative real-time PCR (qRT-PCR) has become a popular method for estimation of methanogen abundance in the ruminant digestive tract [10]. Therefore the objectives of the present study were to quantify the relative abundance of total methanogens and key species viz Methanobrevibacter smithii, M. ruminantium and Methanosphaera stadtmanae in the ruminal fluid of cattle divergent for RFI offered two contrasting diets: a low energy, high forage diet (HF) and a high energy, low forage diet (LF) respectively. Additionally, correlation analysis was used to assess the association between methanogen abundance and animal performance, diet digestibility and rumen fermentation variables.

Materials and methods
All procedures involving animals were approved for the use of live animals in experiments by the Animal Research Ethics Committee, University College Dublin, Belfield, Dublin, Ireland, and were licensed by the Irish government Department of Health and Children, in accordance with the Cruelty to Animals Act (Ireland 1897) and European Community Directive 86/609/EC (http:// ec.europa.eu/food/fs/aw/aw_legislation/scientific/86-609-eec_en.pdf ).

Animal management
This experiment was conducted as part of a larger study designed to examine the physiological control of energetic efficiency in growing beef heifers [11]. Details of the animal experiment used in this study are as previously described [12]. Dietary ingredients and chemical composition have been previously described in detail [11] and both diets were offered ad libitum. Briefly, individual dry matter intake (DMI) and growth were recorded for 86 yearling Limousin × Friesian heifers offered ad libitum access to a high energy low forage (LF) concentrate based diet over 112 d. The LF diet consisted of 30% corn silage and 70% pelleted concentrate. All animals were subsequently ranked retrospectively on phenotypic RFI. The 14 heifers with the highest (inefficient; high RFI) and 14 heifers with the lowest (efficient; low RFI) RFI coefficients during the study of Kelly et al. [11] were selected for use in the current study. Following initial selection, all 28 animals were re-allocated to a low energy high forage (HF) grass silage diet and individual feed intake recorded for a 44 d period. Following this 44 d period (Period 1) all animals were turned out to pasture for a 56 d dietary "washout" period. Subsequently, all 28 animals were re-housed and re-allocated to a LF concentrate based diet and individual feed intake was recorded for 35 d (Period 2). Individual feed intake and body weight gain were recorded for a further 84 d and RFI was recalculated. All 28 animals remained within their respective RFI groups [13]. The experiment was therefore designed to have two factors (i) RFI phenotype and (ii) diet type.

Rumen sampling and methane measurements
Rumen sampling was performed at the end of both dietary periods. Samples of ruminal fluid were collected using a transesophageal sampling device (FLORA rumen scoop; Guelph, Ontario, Canada) according to manufacturer's instructions. Subsequently, a 20 mL aliquot was transferred using a pipette and sterilized tip into a separate labeled sterilized container, immediately frozen in liquid nitrogen, and stored at −80°C until processing [12].
Methane measurements recorded during the study of Kelly et al. [11] were utilised in the current study (Additional file 1: Table S1). In brief, daily CH 4 emissions were determined using a calibrated tracer (sulphur hexafluoride (SF 6 )) technique [14] during the last 5 d of each dietary period.

DNA extraction from ruminal fluid
A detailed description of the DNA extraction method has been described by Carberry et al. [12]. Total microbial DNA was extracted from the 28 ruminal fluid samples by using a repeated bead beating and column purification method which provides efficient recovery of PCR-quality microbial DNA [12].

Quantitative polymerase chain reaction (qRT-PCR) assays
The differences between SYBR green and TaqMan qRT-PCR chemistries have been reviewed [15]. As previously published primers were available for quantification of total methanogens [16] and M. stadtmanae [17] via SYBR green chemistry, we chose to utilise these in our study ( Table 1).
The primers were commercially synthesized (Sigma-Aldrich Ireland Ltd. Dublin, Ireland) and end point PCR was conducted for the validation of the specificity of the primers against target species. For the quantification of M smithii and Methanobrevibcater ruminantium, it was necessary to utilise TaqMan chemistry for these qRT-PCR assays to allow for species specificity. Details of Taq-Man primer and probe sets used in this study, to amplify M smithii and M ruminantium species are listed in Table 2. For the detection of M smithii, primers and a specific FAM labelled probe F were utilised which was designed based on previously published sequences [19]. The same primer set was used in conjunction with a FAM labelled probe designed in the current study to target M ruminantium species. The probe was of the same length as the M smithi probe with the exception of 3 nucleotide changes in the sequence. All primers and probe sets for the TaqMan qRT-PCR assays were generated using the Primer Express algorithm v1.0 from published sequences (National Centre For Biotechnology Information, NCBI: http://www.ncbi.nlm.nih.gov/) and commercially synthesized (Applied Biosystems, Warrington, UK).
DNA was extracted from individual ruminal fluid samples and diluted to a concentration of 100 ng/μL and 1 μL of diluted DNA was used as a template in all PCR reactions. All SYBR PCR amplifications were initially optimised and performed in 0.5 mL tubes in a DNA thermal cycler (Eppendorf Mastercycler®) using the following program: an initial denaturation step of 95°C for 2 min; 30 cycles of 95°C for 30 s, 60°C for 30 s, 72°C for 30 s and a final elongation step of 72°C for 7 min. The PCR reaction solution (50 μL) consisted of 1 × PCR buffer (final concentrations, 16 mmol/L (NH 4 ) 2 SO 4 , 67 mmol/ L Tris-HCl [pH 8.8], 0.01% Tween-20 and 1.5 mmol/L MgCl 2 ), 10 pmol of each primer, a 200 μmol/L concentration of each deoxynucleoside triphosphate, 100 ng of template DNA, and 5.0 U of Taq DNA polymerse (Bioron, Ludwigshafen, Germany) and 40 μL of molecular grade H 2 O. Aliquots of 10 μL PCR products were analysed by electrophoresis on a 2% (w/v) agarose gel to verify the presence and size of the amplicons. Furthermore amplicons were sequenced to confirm their identity. Using BLAST analysis on the NCBI website, all amplicons were confirmed 100% homologous to their target species. Negative controls without template DNA were included in parallel. Specificity of TaqMan assays for the quantification of M smithii and M ruminantium were verified before quantification of ruminal DNA. Each probe was validated by running a non-target clone standard as a negative control. In addition, a 10 fold dilution series starting from 25 ng/μL of clones obtained from our own library [9] and identified as either M smithii or M ruminantium were used as standards and run in triplicate to verify the reproducibility of the TaqMan probe assay. These dilutions were used to calculate PCR efficiencies for each assay. DNA from rumen samples was also diluted and used to calculate PCR efficiencies. For all primer sets, PCR efficiencies were equivalent for both clone libraries and DNA from rumen samples and within the acceptable range to be used to perform qRT-PCR analysis.
The qRT-PCR assays were performed on an ABI 7500 Fast Real-Time PCR system using Fast SYBR® Master Mix (Applied Biosystems, Warrington, UK). Optimization of assay conditions was performed for template DNA concentrations. To reduce inhibition total microbial DNA was diluted to 10 ng/uL. All amplified qRT-PCR reactions were carried out in a 96 well plate format. Non-template controls were included on every plate for each assay to allow screening for possible contamination and primer dimer formation. To minimise variation, all samples included in each analysis were derived from the same extracted DNA batch, prepared under the same conditions and samples were run in triplicate. Efficiency. 3 Primers used for qRT-PCR normalisation. All SYBR green reaction mixtures were prepared in a total volume of 20 μL. The reaction consisted of 1 μL DNA, 10 μL Fast SYBR Green master mix, 1 μL of forward and reverse primers (10 ng of each) and 8 μL nuclease-free H 2 O. Thermal cycling conditions applied to each assay consisted of an initial Taq activation step at 95°C for 15 min followed by 40 cycles of 95°C for 15 s, 60°C for 60 s, followed by an amplicon dissociation stage (95°C for 15 s, 60°C for 1 min, increasing 0.5°C/cycle until 95°C was reached) which confirmed specificity via dissociation curve analysis of PCR end products. Fluorescence detection was also performed at the end of each denaturation and extension step. TaqMan qRT-PCR assays were performed using TaqMan Fast Universal Master Mix (2×) (Applied Biosystems, Warrington, UK) and prepared in a total volume of 20 μL with 1 μL DNA (10 ng/μL), 1 μL 20× TaqMan assay (forward and reverse primer plus probe), 10 μL TaqMan Fast Universal Master Mix (2×) and 8 μL nuclease-free H 2 O. Thermal cycling conditions applied to each TaqMan assay consisted of an initial hold step at 50°C for 2 min and 95°C for 20 s followed by 40 cycles of 95°C for 3 s and 60°C for 30 s.

qRT-PCR data analysis
Real time PCR amplification efficiencies (e) were estimated for all assays using a linear regression of the threshold cycle (Ct) for each dilution versus the log dilution using the formula: e = 5 -1/slope [20] where '5' is the corresponding fold dilution. Efficiencies of the species specific TaqMan probes and primers sets are presented in Tables 1 and 2. Efficiencies for both SYBR green and TaqMan assays ranged from 1.96 to 2.02, close to the theoretical value of 2.0 which is representative of the doubling effect of the target sequence during the qRT-PCR cycle. All primers had PCR efficiencies between 90% and 110% and were therefore acceptable for use in this study.
Inter-plate calibration based on a calibrator sample included on all plates, efficiency correction of the raw cycle threshold (Ct) values and results from triplicate PCR reactions for each target species were averaged and the means calculated using the software package GenEx 5.2.1.3 (MultiD Analyses AB, Gothenburg, Sweden). Within GENEX, the stability of the reference bacterial or methanogen 16S rRNA gene was assessed and assured stable across diet and RFI. Abundance of total methanogens were expressed as a proportion of total estimated rumen bacterial 16S rRNA gene as described previously [21,22] according to the equation: relative quantification = 2 -(Ct target-Ct total bacteria) , where Ct represents threshold cycle. Abundance of specific methanogen species were expressed as a proportion of total estimated methanogen 16S rRNA gene according to the equation: relative quantification = 2 -(Ct target-Ct total methanogens) .

Statistical analysis
All data were analysed using Statistical Analysis Systems v9.1 2002 (SAS Institute, Cary, NC, USA). Data were examined for normality and homogeneity of variance by histograms, qqplots and formal statistical tests as part of the UNIVARIATE procedure of SAS. Data that were not normally distributed were transformed by raising the variable to the power of lambda. The appropriate lambda value was obtained by conducting a Box-Cox transformation analysis using the TRANSREG procedure in SAS. Delta Ct values for total Methanogens were transformed using a lambda value of −0.5 while M. stadtmanae, M smithii and M ruminantium were transformed using a lambda value of 0.25. The transformed data were used to calculate P-values. However, the corresponding least squares means and standard errors of the nontransformed data are presented in the results for clarity.
A mixed model ANOVA (PROC MIXED) was conducted to determine the effect of RFI phenotype and diet type on the relative abundance of each species of interest. Fixed effects included RFI phenotype (H or l), diet type (LF or HF), and their interaction. The interaction term, if not statistically significant (P > 0.10), was subsequently excluded from the final model. In all analyses the individual animal was denoted as the experimental unit and animal was included as a random effect.
The statistical model used: Y = μ + Ri + Dj + (Rj × Dj) + Ak + εijk, where μ was the overall mean, R i was the fixed effect of RFI phenotype ( I = H to L), D j the fixed effect of diet ( j = LF to HK), R i × D j is the interaction between RFI phenotype and diet type, A k the random effect of animal, and εijk is the associated error. Differences between treatments were determined by F-tests using Type III sums of squares. The PDIFF command incorporating the Tukey test was applied to evaluate pairwise comparisons between treatment means.
Spearman partial correlation analysis (PROC CORR, SAS), was calculated to examine associations amongst physiological data, rumen fermentation variables [23] and measured relative methanogen microbial abundance values using analysis with RFI and dietary treatment included as fixed effects in the analysis. Differences were considered significant where P < 0.05, while tendencies were considered where P < 0.10.

qRT-PCR quantification of methanogens
The relative abundance of total methanogens, Methanosphaera stadtmanae, M smithii and M ruminantium are presented in Table 3. No RFI phenotype × diet interactions (P > 0.05) were observed for any of the methanogens measured, however a tendency (P = 0.08) towards an RFI × diet interaction was observed for the total methanogen population. Additionally, no effect of RFI phenotype was detected for the relative abundance of any of the methanogens analysed (P > 0.05). However, diet type affected (P = 0.03) the relative abundance of the overall methanogen population with a greater relative abundance of total methanogens in cattle offered the LF compared to the HF diet (Table 3). Furthermore, the relative abundance of M. stadtmanae and M. ruminantium was higher (P < 0.001) when animals were offered the LF compared to the HF diet.

Discussion
Efficiency of feed utilisation is a key economically relevant trait to the beef cattle industry worldwide given that feed typically accounts for the greatest single input cost [24]. Improved feed efficiency is not only linked to increased profitability, but also reduces the environmental burden, with efficient animals producing less nutrient excretion [25] and reduced CH 4 emissions [5,6]. As CH 4 is a terminal product of methanogen mediated feed fermentation, recent research has focused on characterising the methanogen population in animals selected for divergent feed efficiency. Studies [17,26,27] have identified both a diet effect and a correlation between host feed efficiency and rumen microbial composition. Methanobrevibacter spp. and Methanosphaera sp. are consistently identified as dominant methanogenic archaea in the rumen irrespective of geographical location or dietary feeding regime [17,[27][28][29][30][31]. Rumen methanogens were previously characterised by our group [9] in cattle divergent for phenotypic RFI and it was reported that Methanosphaera and Methanobrevibacter OTUs were identified as the most dominant methanogens. Therefore, in our study total methanogens and specific ruminal methanogen populations of Methanosphaera, M smithii, and M rumantium were selected for relative qRT-PCR analysis to quantitatively assess whether these populations are associated with variance in feed efficiency and/or dietary energy type in cattle.
There is evidence to suggest that efficient L-RFI animals produce less CH 4 both on a daily basis (g/d) [6,32,33] and as per unit of body weight (g/kg) [23] than their inefficient H-RFI counterparts. However work conducted from our own group examining the effect of phenotypic RFI on CH 4 emissions from the animals utilised in the present study showed no difference in CH 4 between animals ranked as either high or low RFI across the two dietary periods [23]. In our study quantitative analysis showed that the total and specific methanogen communities of animals ranked as either H or L-RFI was not different. This is consistent with previous reports when a low energy feed lot diet was offered [17] and also when the diet was switched from a low to a high energy diet [27]. While there is a sparsity of information in the literature with regard to studies exploring the links between enteric CH 4 emissions and rumen methanogen abundance there is evidence to suggest that CH 4 emissions may be consistent with the population size of methanogens [34,35]. However, since the microbial inhabitants of the rumen function in symbiosis, the metabolic activity and substrate specificity of both the methanogens and the wider rumen microbial community must also be considered. Indeed a growing number of studies have reported Methanogens measured as a proportion of total estimated rumen bacterial 16S rDNA, relative quantification = 2 -(Ct target-Ct total bacteria).
that methanogen abundance does not reflect the amount of enteric CH 4 emissions [35][36][37]. Furthermore, no significant relationship between methanogen abundance and CH 4 production potential in other ecosystems has been reported [38]. Our previous work [9] reported that the rumen appears to harbour a core group of methanogens regardless of host classification for feed efficiency. Therefore, as suggested by the results obtained for total methanogen abundance in our study, the quantity of the total methanogen population may not be indicative of divergence in CH 4 yield between RFI phenotypes. While work from our own group has shown moderate within animal repeatability of RFI while maintained on a constant diet type [13] other recent work has shown that the relative ranking of animals for this trait may change when moved from a low to a high energy diet [39]. This highlights the necessity to investigate both RFI and the rumen microbial community of animals divergent for RFI across different diet types. Previous research has shown that the chemical composition of the diet can have a great effect on the overall rumen bacterial composition in animals divergent for RFI [12]. Despite this, previous reports have suggested that no change in total methanogen abundance of either feed efficient or inefficient cattle divergent for RFI occurs when the diet is changed from a low to high energy diet [27]. Furthermore, it has been suggested that diet has a greater effect on the diversity of the methanogen community rather than total methanogen abundance [17,27]. However, in the current study the abundance of total methanogens was found to be affected by the change in dietary substrate offered. While it was surprising that the relative Spearman correlation coefficient in boldface are different from zero (P < 0.10). 2 Dry matter intake. 3 Methane. 4 Mean live weight. 5 Total volatile fatty acids. 6 Acetate:propionate ratio. 7 Methane energy from gross energy intake. 8 Dry matter digestibility. 9 Organic matter digestibility. 10 Crude protein digestibility. 11 Neutral detergent fiber digestibility. 12 Acid detergent fiber digestibility. 13 Gross energy digestibility. * P < 0.10, ** P < 0.05.
total methanogen abundance was greater when animals were offered the LF compared to the HF diet, this may have arisen due to the nature of the LF diet (30:70 maize silage:concentrate). With the inclusion of 30% forage in this diet hydrogen fermenting bacteria would still have the ability to proliferate, albeit to a lesser extent, thus providing hydrogen for methanogen growth. In addition, on the LF diet, intakes were higher and there was more easily digestible substrate available to support CH 4 emissions and the growth of methanogens. Indeed, overall the CH 4 emissions were higher from animals on the LF diet [23]. Furthermore, decreased rumen pH is often associated with high concentrate diets due to a lowering of the acetate:propionate ratio [40] Decreased ruminal pH can indirectly affect CH 4 synthesis due to its influence on VFA production [5] and directly through inhibition of methanogen activity [41]. However, data from our own laboratory generated from the same pool of animals as the current study showed that although mean ruminal pH for both high and low RFI phenotypes was lower on the LF diet, the pH did not drop below the optimum range for rumen methanogen growth (pH 6.0-7.5) [23]. Therefore, it is hypothesized that methanogen proliferation would not have been inhibited while animals were offered the LF diet in our study. Differences in our findings to that of others could also have arisen due to differences in qRT-PCR quantification methods. Our qRT-PCR results represent the relative abundance of total methanogens to the total bacterial population (relative quantification) while DNA copy number was used to quantify the methanogen population (absolute quantification) in the study by Zhou et al., [27]. While both these methods have been extensively utilised throughout the literature for the quantification of rumen microbiota, it is important to acknowledge that neither method is without its drawbacks [15]. In the current study, quantification using the relative method was favoured due to the implications of quantification of the target in comparison to a standard curve while using absolute quantification [15]. Additionally, host breed genotype has also been shown to influence methanogen diversity in the rumen and therefore could be a contributing factor to the variation across studies [29].
In the present study when animals were offered the LF diet overall methanogen abundance was positively associated with acetate and negatively associated with propionate. It is widely accepted that both acetate and butyrate promote CH 4 production, while propionate is considered a rival pathway to methanogenesis [42,43], directly competing with methanogens for available hydrogen during formation [5]. In addition, when total methanogens was correlated with protozoa abundance from our previous study [12] there was strong a positive relationship (data not shown). This positive relationship is compounded by the fact that among H 2 producers, protozoa have a prominent position, which is strengthened by their close physical association with methanogens, which favours H 2 transfer from one to the other [37].
An effect of diet type on the relative abundance of M. stadtmanae was observed in the present study. This result is consistent with the pyrosequencing analysis conducted in our previous study [9] and may be attributed to the difference in the chemical compostion of the diets and also abundance of other rumen microbes. Energy metabolism of M. stadtmanae is more restricted than other methanogenic species, growing only on methanol and H 2 [44]. In the rumen large quantities of methanol are produced via the degradation of pectin by protozoa and other anaerobic bacteria [45]. A HF grass silage based diet is a relatively poor source of dietary pectin, while some constituents of concentrate feeds such as citrus and beet pulp are abundant. We previously reported a tendency towards greater relative abundance of rumen protozoa between the LF and HF dietary periods [12]. Due to the restricted energy metabolism of Methanosphaera, the dietary effect observed on this methanogenic species may have arisen due to the fermentation products produced by other rumen microbial populations. In addition, the fastidious energy requirements of Methanosphaera stadtmanae compared to other methanogens was most likely the causative reason why when animals were offered the LF diet this methanogenic species was negatively correlated with CH 4 .
The effect of diet on the relative abundance of M smithii is most likely due to substrate specificity preference for methanogenesis by this methanogen species. Energy metabolism of M smithii is less restricted than M. stadtmanae in that it can produce CH 4 via CO 2 -H 2 and or formate [45]. In the rumen, formate and hydrogen are the fermentative end products of several types of rumen bacteria and protozoa [46]. We have previously reported a greater abundance of Fibrobacter succinogenes and Prevotella, both of which produce formate as an end product of fermentation [46], in animals offered LF compared with HF diets [12]. This, coupled with the tendency towards greater relative abundance of hydrogen producing rumen protozoa between the LF and HF dietary periods, suggests that the appropriate substrates for M smithii were likely to be in abundance while animals were offered the LF diet. In addition, M smithii also possesses enzymes which have been shown in other methanogens to facilitate utilisation of methanol and ethanol [44,47], which are products of bacterial fermentation. Therefore abundance of these methanogens is most likely affected by both chemical composition of the diet and the availability of appropriate end products produced from rumen microbial fermentation.
The relative abundance of M ruminantium was higher when animals were offered the LF compared to the HF diet. This is in agreement with Zhou et al. [27] who reported a marked shift in the number of M ruminantium when the diet was changed from a low energy to a high energy diet, using PCR-DGGE microbial community analysis. Similar to M smithii, it is believed that formate may also be an important substrate for methanogenesis by M ruminantium [48]. In addition, the genome sequence of this methanogen has revealed an abundance of encoding adhesion proteins [48]. Initial experiments show that some are involved in mediating close assimilations with hydrogen producing bacteria while others synergise association between protozoa and fungi [48]. Although the LF diet offered in the current study would be expected to yield less CH 4 emissions compared to a HF diet, the genomic niche adaptation of M ruminantium may explain the increase in abundance through mutual associations with other rumen microbial populations.

Conclusion
In conclusion, this study is the first to quantify both total and a panel of key candidate rumen methanogens in cattle divergent for phenotypic RFI across two contrasting diets. Quantification of the methanogen community showed that feed efficiency alone had no significant effect on the abundance of total or specific methanogens at the species level. However, our results extend the findings of others by demonstrating that the type of dietary substrate offered greatly influences the abundance of specific methanogen species and in addition the density of total methanogens may also be affected by changes in the diet. It is concluded that diet alone has a greater influence on the relative abundance of specific methanogens at a species level. Future work focused on designing specific qRT-PCR assays which target these rarer, less studied methanogens will provide further insight into the effect of host feed efficiency and diet on the rumen methanogen population. Furthermore, studies investigating the association between CH 4 emissions, rumen methanogen abundance and diet digestibility are required to allow the development of more specific nutritional management strategies to reduce CH 4 emissions without impacting on host health, growth or productivity.

Additional file
Additional file 1: Table S1. Information of tested cattle.