Steam Explosion Pretreatment Changes Ruminal Fermentation in vitro of Corn Stover by Shifting Archaeal and Bacterial Community Structure

Steam explosion is an environment-friendly pretreatment method to improve the subsequent hydrolysis process of lignocellulosic biomass. Steam explosion pretreatment improved ruminal fermentation and changed fermentation pattern of corn stover during ruminal fermentation in vitro. The study gave a comprehensive insight into how stream explosion pretreatment shifted archaeal and bacterial community structure to change ruminal fermentation in vitro of corn stover. Results showed that steam explosion pretreatment dramatically improved the apparent disappearance of dry matter (DM), neutral detergent fiber (NDF), and acid detergent fiber (ADF). Steam explosion pretreatment significantly increased the molar proportion of propionate and decreased the ratio of acetate to propionate. At archaeal level, steam explosion pretreatment significantly increased the relative abundance of Methanobrevibacter, which can effectively remove metabolic hydrogen to keep the fermentation continuing. At bacterial level, the shift in fermentation was achieved by increasing the relative abundance of cellulolytic bacteria and propionate-related bacteria, including Spirochaetes, Elusimicrobia, Fibrobacteres, Prevotella, Treponema, Ruminococcus, and Fibrobacter.


INTRODUCTION
Corn stover is an abundant agricultural residue that can be harvested as a ruminant feedstuff or used to produce biofuel. As a lignocellulosic material, corn stover is mainly composed of three types of polymers: cellulose, hemicellulose, and lignin. These three polymers form a complex network to resist the degradation by microorganisms and enzymes (Malinovsky et al., 2014). Several physical and chemical pretreatment methods have been applied to enhance the utilization of lignocellulosic materials, such as grinding, acid, alkali, enzyme, and steam explosion pretreatment (Schumacher et al., 2014;Schroyen et al., 2015;Bolado-Rodriguez et al., 2016). Although chemical pretreatment methods are useful strategies to improve the utilization of lignocellulosic materials, the chemicals used during processes must be removed and environmental pollution also follows these methods. Compared to chemical pretreatment methods, steam explosion has been recognized as an environment-friendly pretreatment and broadly used for numerous lignocellulosic biomass such as corn stover (Zhao et al., 2018), wheat straw (Ferreira et al., 2013), birch (Vivekanand et al., 2013), and Salix (Horn et al., 2011). Steam explosion is an explosion caused by violent boiling of water into steam, which heats the biomass at high temperature and rapidly drops pressure to disrupt the biomass fibers (Horn et al., 2011). Recent studies have shown that steam explosion can effectively improve digestibility of lignocellulosic biomass (Zhao et al., 2018) and increase the methane (CH 4 ) production during anaerobic digestion (Lizasoain et al., 2017). Steam explosion mainly reduces cellulose degree of polymerization to enhance the digestibility of lignocellulosic biomass (Yu et al., 2015;Jin et al., 2016).
The rumen is a fermentation vat that is home to a vast array of bacteria, protozoa, fungi, and archaea. The structure of ruminal microbiomes is closely related to the process of rumen microbial fermentation. The microorganisms in rumen have been found to be able to effectively ferment lignocellulosic biomass into chemical compounds (Jami et al., 2013;Yue et al., 2013). Volatile fatty acids (VFA) and CH 4 are the two major products in rumen microbial fermentation process. VFA will be subsequently absorbed by ruminants to convert into food products (Jami et al., 2013); While, CH 4 will be released to atmosphere and presents a loss of gross energy intake (2-12%), depending on types of diets (Johnson and Johnson, 1995). In the typical ruminal microbial fermentation process, the formation of acetate and butyrate both result in the release of metabolic hydrogen which must then be re-oxidized to continue the fermentation process (Ungerfeld, 2015). Methanogenic archaea are the only producer of CH 4 in rumen and methanogenesis is the main route to remove metabolic hydrogen which is transferred from bacteria, protozoa, and fungi to archaea (Wolin and Miller, 1997). Steam explosion pretreatment could lead to increased digestibility and metabolic hydrogen production, usually accompanied by CH 4 production. Propionate formation is also considered as an alternative pathway to utilize metabolic hydrogen in rumen (Moss et al., 2000). The strong negative correlation between propionate formation and CH 4 formation has been proved by Pinares-Patino et al. (2003) and Goopy et al. (2006). Ungerfeld (2015) reported that inhibition of methanogenesis increased the propionate production by redirecting the flow of metabolic hydrogen. Zhao et al. (2018) reported that steam explosion pretreatment increased digestibility and fermentation of corn stover by improving ruminal microbial colonization. Du et al. (2019) reported that stream explosion pretreatment significantly altered the fermentation parameters in vitro of wheat straw and decreased the ratio of acetate to propionate by facilitating sugar production and microbial colonization. However, it is unknown whether stream explosion pretreatment shifts the structure of ruminal microbiomes to improve fermentation and change fermentation pattern. The objective of this study was to explore how steam explosion pretreatment shifts archaeal and bacterial community structure to enhance fermentation of corn stover and change ruminal fermentation pattern by building a model of corn stover and steam-exploded corn stover ruminal fermentation in vitro.

Experimental Design
Corn stover used in present study was harvested in a cornland at Yanqin District Beijing, China. The stover was left and dried in the field after harvest for about 2 months. The full stalk was cut into 50 cm fragments to make it easy to carry. The stover was dried at 65°C for 24 h to obtain air-dried samples. The air-dried corn stover was manually chopped to 3-5 cm fragments by scissors. One 500 g of (dry matter, DM) chopped corn stover samples was milled to pass through a 1 mm sieve using a Wiley mill (Thomas Scientific, Swedesboro, NJ, United States) as the control group fermentation substrate. A 20 L steam explosion reactor connected to a steam generator (QB-200, Hebi Gentle Bioenergy Co. Ltd., China) was used to produce steam-exploded corn stover. Another 500 g of (DM) chopped corn stover samples was accurately weighed, and then atomized evenly 50 g of deionized water on the samples. The samples were sealed in a vacuum bag and infiltrated for about 12 h at room temperature. The steam explosion parameters selected in present study were at 1.5 MPa steam pressure and 10% moisture for 3 min. The steam-exploded corn stover was oven-dried at 65°C for 24 h and then used for the treatment group fermentation substrate. A completely randomized design was applied in an in vitro incubation, and there are two treatments in the current study: CON (the control group fermentation substrate, corn stover) and TRT (the treatment group fermentation substrate, steam-exploded corn stover).
The experimental procedures were approved by the Chinese Academy of Agricultural Sciences Animal Care and Use Committee (Beijing, China). Rumen fluid was collected 2 h before morning feeding from three cannulated lactating Holstein cows fed a total mixed ration (TMR) composed (% DM basis) of corn silage (25%), alfalfa hay (15%), steam-flaked corn (27%), soybean meal (8.5%), cottonseed meal (8.5%), beet pulp (5.5%), distillers dried grains with solubles (7.5%), minerals, and vitamins (3%). The donor cows were fed twice daily at 0500 and 1700 h. Ruminal fluid was filtered through four layers of cheesecloth and immediately brought to the laboratory. Rumen fluid sampled from each of the donor cows was combined on an equal volume basis and diluted with buffer solution (1:2 v/v) formulated as the method of Menke (1988), containing per liter 8.75 g NaHCO 3 , 1.00 g NH 4 HCO 3 , 1.43 g Na 2 HPO 4 , 1.55 g KH 2 PO 4 , 0.15 g MgSO 4 ·7H 2 O, 0.52 g Na 2 S, 0.017 g CaCl·2H 2 O, 0.015 g MnCl 2 ·4H 2 O, 0.002 g CoCl·6H 2 O, 0.012 g FeCl 3 ·6H 2 O, and 1.25 mg resazurin. The preparation process of the mixed liquid is carried out under continuous flushing with carbon dioxide (CO 2 ). The starting pH of the mixed liquid after equilibration under CO 2 is 6.80. The mixed fluid was transferred into 120-ml serum bottles (75 ml/bottle) containing 500 mg of fermentation substrates (CON or TRT) under the continuous flow of CO 2 to remove the air from headspace. In addition, an extra four Frontiers in Microbiology | www.frontiersin.org bottles containing no substrate served as blank for correction of analytes and gases. The serum bottles were immediately sealed with butyl rubber stoppers plus aluminum caps and then connected with vacuumed air bags. The batch fermentation was incubated at 39°C for 72 h with horizontal shaking at 60 rpm. The in vitro batch fermentation was carried out in triplicates and four serum bottles per treatment were arranged in each batch.

Sample Collection and Analysis
The 100-ml calibrated glass syringes (Häberle Labortechnik, Lonsee-Ettlenschieß, Germany) were used to measure the total gas production of each air bag. The pH of incubations was measured using a SevenGo ™ portable pH meter (Mettler Toledo, Switzerland). The pre-weighed nylon bags (8 cm × 12 cm, 42 μm) were used to filter the whole biomass material of each bottle. Then, the nylon bags were washed with cold running water until the effluent ran clear. Afterwards, the nylon bags were dried at 55°C for 48 h for analysis of the apparent disappearance of DM, neutral detergent fiber (NDF), and acid detergent fiber (ADF). The filtrate samples (2.5 ml) from each bottle were individually collected for determining VFA profiles, and another 2.5 ml of filtrate sample was collected for microbial analysis. The samples for VFA profiles were frozen at −20°C and the samples for microbial analysis were frozen immediately in liquid nitrogen. The ANKOM A200 fiber analyzer (ANKOM Technology, Macedon, NY, United States) was used to measure the contents of NDF and ADF according to the approach described by Van Soest et al. (1991). Sodium sulfite and α-amylase were used for the analysis of NDF. The concentrations of CH 4 and hydrogen (H 2 ) were determined using a gas chromatograph (7890B, Agilent Technologies, United States) fitted with a thermal conductivity detector and a packed column (Porapak Q, Agilent Technologies, United States). The VFA concentrations were analyzed by a gas chromatograph (7890B, Agilent Technologies, United States) equipped with a flame ionization detector and a capillary column (30 m × 0.250 mm × 0.25 μm; BD-FFAP, Agilent Technologies, United States). More detail methods were described by Wang et al. (2018).

DNA Extraction, Microbial 16S RNA Genes Amplification and Sequencing
Microbial DNA was extracted using an E.Z.N.ATM Mag-Bind Soil DNA kit (Omega, Norcross, Georgia, United States), in accordance with the manufacturer's instructions. The quality and concentration of the extracted DNA were assessed by 1% agarose gel electrophoresis and a Qubit 3.0 spectrometer (Invitrogen, United States), respectively. This method gave DNA yields sufficient for analysis (averaging 35 ng/μl), but kit-based assays may yield non-representative taxonomic sampling (Henderson et al., 2013).

Sequencing Data Processing and Analysis
Sequencing reads were matched to different samples in accordance with the unique barcode of different samples, and then pair-end reads were merged using FLASH (Magoč and Salzberg, 2011). The quality of these merged reads was controlled by using PRINSEQ (Schmieder and Edwards, 2011). Then, the barcode and primers were removed, and UCHIME was used to filter out PCR chimeras to get clean sequences (Edgar et al., 2011). After filtration, the average length of all the clean reads was 416 and 379 bp, and the average sequencing depth was ca. 58,574 and 61,208 clean reads for bacterial and archaeal community analysis, respectively. After removal of singletons, operational taxonomic units (OTU) were clustered at 97% sequence identity using UPARSE (Edgar et al., 2011). The taxonomic classification of the sequences was carried out using the ribosomal database project (RDP) classifier at the bootstrap cutoff of 80%, as suggested by the RDP. The alpha diversity indices including Simpson, Shannon, Chao1, Coverage, and ACE were calculated through the QIIME 2 software package. The principal coordinate analysis (PCoA) was conducted by the weighted UniFrac distance (Lozupone et al., 2007), and the significant difference between treatments was assessed by an analysis of similarity (ANOSIM) in QIIME with 999 permutations (R Core Team, 2013). The extended error bar plot was performed to visualize the difference in relative abundance of bacteria and archaea by bioinformatics software (STAMP; Parks et al., 2014).

Statistical Analysis
Data were analyzed using PROC MIXED of SAS (version 9.4; SAS Institute Inc., Cary, NC). Spearman's rank correlations between the relative abundance of microbial genera and fermentation variables were analyzed using the PROC CORR procedure of SAS (version 9.4; SAS Institute Inc., Cary, NC). p < 0.05 was considered statistically significant.

Changes in Ruminal Fermentation in vitro in Response to Steam Explosion Pretreatment
Data of substrate apparent disappearance, the molar proportion of VFA, and CH 4 and H 2 production are presented in Table 1.
Based on the previous studies on in vitro forage fiber digestion, we terminated the incubation process at 72 h (Cross et al., 1974;Zhao et al., 2018). Steam explosion pretreatment dramatically improved the apparent disappearance of DM, NDF, and ADF. This was similar to the previous study, which reported that the improvement in digestibility of the steam-exploded corn stover was consistent with the enhanced colonization of microorganism (Zhao et al., 2018). Some other studies also reported that steam explosion pretreatment can enhance the degradability of lignocellulosic biomass by increasing porosity (Dan et al., 2017) and reducing degree of polymerization (Jin et al., 2016). In response to the improved DM degradability, the concentration of total VFA was significantly increased, which was similar to the previous studies (Zhao et al., 2018;Du et al., 2019). Steam explosion pretreatment increased the release of sugars from corn stover to improve the production of VFA (Zhao et al., 2018;Du et al., 2019). Steam explosion pretreatment changed the fermentation pattern and promoted a shift in the fermentation pattern toward a higher molar proportion of propionate in the present study. Du et al. (2019) also reported that steam explosion pretreatment increased the molar proportion of propionate. Fermentation of nonstructural carbohydrates (i.e., sugars, starches, organic acids, and other reserve carbohydrates), compared to fermentation of structural carbohydrates (i.e., cellulose, hemicellulose, and lignin), increased amounts of propionate and decreased the ratio of acetate and propionate (Dijkstra, 1994). Therefore, the higher molar proportion of propionate should be attributed to more soluble nonstructural carbohydrates released from steam explosion pretreatment. Zhao et al. (2018) and Du et al. (2019) both reported that steam explosion pretreatment increased the release of soluble nonstructural carbohydrates. Corresponded with the increased total VFA concentration and the higher molar proportion of propionate, the pH of TRT was significantly decreased compared with CON. Previous studies also reported that increases in total VFA concentrations and the molar proportion of propionate were associated with the decrease in pH due to containing more soluble nonstructural carbohydrates in diets (Penner and Oba, 2009;Song et al., 2018).
Total gas production and CH 4 production from TRT were both higher than that from CON, but the increases were both statistically insignificant. The results are not consistent from previous studies (Lizasoain et al., 2017;Mulat et al., 2018), which reported that steam explosion pretreatment significantly increased the total gas production and CH 4 production. Steam explosion pretreatment improved the digestibility of corn stover and more readily fermentable substrates should produce more gas. While the lack of significant increase in total gas production and CH 4 production in the present study might be attributed to the limited number of substrates initially added in the in vitro incubation. In addition, the anaerobic digestion inoculum used in the present study is rumen fluid, which is home to a vast array of ciliate protozoa, fungi, bacteria, and archaea. The compositions and interactions of different microbes are more complex than those used in the previous studies (Lizasoain et al., 2017;Mulat et al., 2018). In the present study, the formation of propionate might be served as an alternative to H 2 formation and then reduce the utilization of H 2 in methanogenesis, shifting H 2 flow from CH 4 to propionate production. Zhang et al. (2016) reported that propionate accumulation led to lower CH 4 production of microwave pretreatment food waste compared to microwave pretreatment sewage sludge. Therefore, the higher proportion of propionate or the changed fermentation pattern may limit the significant increase in CH 4 production in the present study. In the present study, there was a 24% increase in DM disappearance from the TRT fermentation compared to the CON fermentation (from 61.9 to 76.7%), but only a 4.6% increase in VFA production (from 62.8 to 65.7 mM), and increases in gas production were not significant. Much more DM disappeared than was recovered in VFA production. The reason may be due to sugars being released, and not being fermented to VFA. Zhao et al. (2018) and Du et al. (2019) reported that the concentration of reducing sugar, xylose, and fructose in steam explosion group increased after the 72 h of incubation. The chemical composition of corn stover and steam-exploded corn stover was shown in Supplementary Material.

Changes in Archaeal Community Structure in Response to Steam Explosion Pretreatment
After merging and quality control, a total of 1,637,655 sequences from 24 samples were generated, and 1,572,671 high-quality sequences were acquired, with an average read length of 379 bp. After chimera removal, OTUs were obtained from the remaining 1,468,988 sequences, with 97% sequence similarity. After filtering, the remaining 24,035 OTUs were used for subsequent analysis. At archaeal phylum level, Euryarchaeota and Thaumarchaeota represented the archaeal community, where Euryarchaeota represented on average 99.99%. At archaeal genus level, Methanobrevibacter (38.53%), Methanomassiliicoccus (34.79%), Methanomicrobium (25.36%), and Methanosphaera (0.31%, Figure 1A) were the four predominant genera. Methanobrevibacter was recognized to be the most common genus in rumen (Janssen and Kirs, 2008;Danielsson et al., 2017). Methanomassiliicoccus has a high relative abundance similar to Methanobrevibacter in the present study. Alpha archaeal diversity was presented in Table 2. No significant differences were observed between treatments based on the alpha diversity indices of Chao1, ACE, Shannon, and Simpson, showing that the archaeal community richness and diversity were not affected by steam explosion pretreatment. The analysis of PCoA based on the weighted UniFrac metrics ( Figure 1B) showed that TRT was not distinctly separated from CON. Principal coordinate 1 and 2 accounted for 75.5 and 16.8% of the total variation, respectively. The ANOSIM analysis revealed a significant difference between CON and TRT (R = 0.125, p = 0.034).
At archaeal genus level, steam explosion pretreatment significantly increased the relative abundance of Methanobrevibacter. While the relative abundance of Methanomassiliicoccus and Methanomicrobium from TRT was lower than that from CON, the decreases were not statistically significant ( Figure 1C). Spearman's rank correlations between the relative abundance of archaeal genera and fermentation parameters were analyzed using the PROC CORR procedure of SAS 9.4 ( Figure 3A). Within the archaeal community, no significant correlations were observed between the relative abundance of archaeal genera and CH 4 production. As the sole producers of CH 4 in rumen, the number of methanogens was considered to be related to CH 4 production (Wallace et al., 2014;Veneman et al., 2015). However, the efficiency of different methanogens was considered to be more important than the number of methanogens in methanogenesis (Shi et al., 2014). Previous studies reported that Methanobrevibacter   had positive correlations with CH 4 production (Zhou et al., 2011;Danielsson et al., 2012;Wallace et al., 2015). Cunha et al. (2017) found that the relative abundance of Methanosphaera had negative correlations with CH 4 production. There are two common methanogenic pathways in rumen: hydrogenotrophic pathway and methylotrophic pathway. Most methanogenic archaea use H 2 and CO 2 as substrates to produce CH 4 , but some species can also metabolize formate, methanol, or acetate for methanogenesis.
Methanobrevibacter is the common hydrogenotrophic archaea, which produces 1 mole of CH 4 for each mole of CO 2 by hydrogenotrophic pathway (Hook et al., 2010), while Methanosphaera requires 4 moles of methanol to produce 3 moles of CH 4 by methylotrophic pathway (Fricke et al., 2006). Methanomassiliicoccus has ability to use methylamine substrates to generate CH 4 by H 2 -dependent methylotrophic pathway (Moissl-Eichinger et al., 2018). Methanogenic archaea commonly acquired substrates from environment, while some species would improve efficiency by building contacts with protozoa, which generated large amounts of H 2 using hydrogenosomes (Embley et al., 2003). In rumen, Methanobrevibacter is recognized as the most common protozoa-associated methanogens, and the contribution of Methanomicrobium to protozoa-associated methanogenic community is different among studies (Belanche et al., 2014). In the present study, the improvement of corn stover in fermentation efficiency may be related to changes in archaeal community structure. Steam explosion mainly reduces cellulose degree of polymerization to enhance the digestibility of lignocellulosic biomass (Yu et al., 2015;Jin et al., 2016). Steam explosion pretreatment also increased the release of soluble nonstructural carbohydrates to improve the fermentation efficiency of corn stover (Zhao et al., 2018;Du et al., 2019). During the incubation in vitro, cellulose, hemicellulose, and soluble nonstructural carbohydrates are hydrolyzed to glucose and other monosaccharides, which are further metabolized to VFAs, CO 2 , and metabolic hydrogen (Beauchemin et al., 2020). The improvement of fermentation efficiency produced more fermentation products, including more metabolic hydrogen. Methanogenesis is the main route to remove metabolic hydrogen in rumen and Methanobrevibacter is an efficient hydrogenotrophic methanogenic archaea through the reduction of CO 2 via H 2 to produce CH 4 (Hook et al., 2010). To keep the fermentation continuing, metabolic hydrogen must be removed to keep the partial pressure H 2 low (Moss et al., 2000). Therefore, steam explosion pretreatment increased the relative abundance of Methanobrevibacter to enhance fermentation efficiency of corn stover.
At bacterial phylum level, steam explosion pretreatment significantly increased the relative abundance of Spirochaetes, Elusimicrobia, and Fibrobacteres ( Figure 2D). In rumen, Spirochetes can ferment xylan, pectin, and arabinogalactan, which are polymers commonly present in plant materials. Hydrolysis products of plant polymers (e.g., d-xylose, ʟ-arabinose, d-galacturonic acid, d-glucuronic acid, and cellobiose) also can be utilized as growth substrates by Spirochetes cultured from rumen fluid. Spirochetes fermented glucose to formate and acetate, some of them also produced succinate or ethanol (Paster and Canale-Parola, 1982). Succinate is not the end product of rumen fermentation and it will be further metabolized to propionate by other rumen species (Scheifinger and Wolin, 1973). Some important species belong to Spirochaetes, such as Treponema bryantii and Treponema saccharophilum, which were engaged primarily in the fermentation of soluble carbohydrates (Stanton and Canale-Parola, 1980). Steam explosion pretreatment destructed the integrity of cover stover and increased the release of sugars (Zhao et al., 2018), which could be served as fermentation substrates to produce succinate by Spirochaetes and finally converted to propionate by other rumen species. In the present study, the increased relative abundance of Spirochaetes may be related to the higher proportion of propionate in TRT group. Elusimicrobia is an enigmatic bacterial phylum in the hindgut of insects, as well as in rumen where it occurs as symbionts of various flagellated protists or as freeliving bacteria (Méheust et al., 2019). Cultivation and genomebased studies revealed that some species belong to Elusimicrobia are capable of glucose fermentation (Geissinger et al., 2009;Zheng et al., 2016). In the present study, the increase in the relative abundance of Elusimicrobia may be attributed to the more release of sugars of corn stover resulted from steam explosion pretreatment. Fibrobacteres is a small bacterial phylum which currently comprises sole cultured representative genus, Fibrobacter, and Fibrobacter succinogenes and Fibrobacter intestinalis are the two cultured species, which were considered as major bacterial degraders of lignocellulosic material in rumen (Ransom-Jones et al., 2014). Steam explosion pretreatment broke the bonds between lignin and hemicellulose and cellulose, and damaged the surface structure of corn stover, so that fibrotic microbes had better interaction with lignocellulosic material (Zhao et al., 2018). More digestible lignocellulosic material may result in the increased relative abundance of Fibrobacteres.
At bacterial genus level, steam explosion pretreatment significantly increased the relative abundance of Prevotella, Treponema, Ruminococcus, Oscillibacter, Fibrobacter, and Schwartzia ( Figure 2E). Spearman's rank correlations indicated that the relative abundance of Prevotella, Treponema, and Ruminococcus has significantly positive correlations with propionate proportion (r > 0.55, p < 0.05) (Figure 3B). Prevotella is considered as the most abundant genus in rumen (de Menezes et al., 2011;Jami and Mizrahi, 2012) and one of the main propionate producers (Strobel, 1992). Different Prevotella species produced different fermentation end products, including that Prevotella albensis produced acetate, Prevotella brevis and Prevotella bryantii primarily produced propionate, and P. ruminicola produced propionate and acetate (Emerson and Weimer, 2017). Treponema is typically associated with the fermentation of soluble carbohydrates (Stanton and Canale-Parola, 1980). Treponema belongs to the phylum of Spirochaetes, which may be related to the higher proportion of propionate in the present study, as we talked about above. In addition, positive interactions have been demonstrated between T. bryantii and rumen cellulolytic bacteria (Kudo et al., 1987). Ruminococcus plays crucial roles in the fermentation of dietary polysaccharides in rumen (Leschine, 1995). Some Ruminococcus species are cellulolytic, including Ruminococcus flavefaciens and Ruminococcus albus, both of which were originally isolated from the bovine rumen (La Reau and Suen, 2018). Some Ruminococcus species are non-cellulolytic, including Ruminococcus callidus and Ruminococcus bicirculans. R. callidus can ferment saccharides and its major fermentation products are succinate and acetate, with a less amount of formate, lactate, and pyruvate (La Reau and Suen, 2018). Some of Ruminococcus can ferment polysaccharides to produce succinate, which will be further metabolized to propionate by other rumen species (Scheifinger and Wolin, 1973). At bacterial level, the improvement in fermentation efficiency and the shift in fermentation pattern may be achieved by increasing the relative abundance of cellulolytic bacteria and propionate-related bacteria. However, only filtrates were used for DNA isolation, so only the non-adherent (planktonic) community was analyzed in the present study. This community would be expected to be underrepresented with respect to cellulolytic microbes when comparing the microbial data to fiber digestibility. Therefore, the potential bias associated with under-sampling the particle-associated community inevitably existed in the present study.

CONCLUSION
Steam explosion pretreatment improved the fermentation efficiency and changed the fermentation pattern of corn stover during ruminal fermentation in vitro by shifting archaeal and bacterial community structure. Analysis of archaeal community structure revealed that steam explosion pretreatment significantly increased the relative abundance of Methanobrevibacter, which can effectively remove metabolic hydrogen to keep the fermentation continuing. At bacterial level, steam explosion pretreatment significantly increased the relative abundance of cellulolytic bacteria, including Fibrobacteres, Fibrobacter, and Ruminococcus. Steam explosion pretreatment significantly increased the relative abundance of propionate-related bacteria, including Spirochaetes, Elusimicrobia, Prevotella, Treponema, and Ruminococcus.

DATA AVAILABILITY STATEMENT
The datasets generated for this study can be found in the NCBI Sequence Read Archive/accession number SRP189861.

ETHICS STATEMENT
The experimental procedures were approved by the Chinese Academy of Agricultural Sciences Animal Care and Use Committee (Beijing, China).