The purpose of this study was to evaluate the effects of butyrate infusion on
rumen epithelial transcriptome. Next-generation sequencing (NGS) and
bioinformatics are used to accelerate our understanding of regulation in rumen
epithelial transcriptome of cattle in the dry period induced by butyrate
infusion at the level of the whole transcriptome. Butyrate, as an essential
element of nutrients, is a histone deacetylase (HDAC) inhibitor that can alter
histone acetylation and methylation, and plays a prominent role in regulating
genomic activities influencing rumen nutrition utilization and function. Ruminal
infusion of butyrate was following 0-hour sampling (baseline controls) and
continued for 168 hours at a rate of 5.0 L/day of a 2.5 M solution as a
continuous infusion. Following the 168-hour infusion, the infusion was stopped,
and cows were maintained on the basal lactation ration for an additional
168 hours for sampling. Rumen epithelial samples were serially collected via
biopsy through rumen fistulae at 0-, 24-, 72-, and 168-hour (D1, D3, D7) and
168-hour post-infusion (D14). In comparison with pre-infusion at 0 hours, a
total of 3513 genes were identified to be impacted in the rumen epithelium by
butyrate infusion at least once at different sampling time points at a stringent
cutoff of false discovery rate (FDR) < 0.01. The maximal effect of butyrate
was observed at day 7. Among these impacted genes, 117 genes were responsive
consistently from day 1 to day 14, and another 42 genes were lasting through day
7. Temporal effects induced by butyrate infusion indicate that the
transcriptomic alterations are very dynamic. Gene ontology (GO) enrichment
analysis revealed that in the early stage of rumen butyrate infusion (on day 1
and day 3 of butyrate infusion), the transcriptomic effects in the rumen
epithelium were involved with mitotic cell cycle process, cell cycle process,
and regulation of cell cycle. Bioinformatic analysis of cellular functions,
canonical pathways, and upstream regulator of impacted genes underlie the
potential mechanisms of butyrate-induced gene expression regulation in rumen
epithelium. The introduction of transcriptomic and bioinformatic technologies to
study nutrigenomics in the farm animal presented a new prospect to study
multiple levels of biological information to better apprehend the whole animal
response to nutrition, physiological state, and their interactions. The
nutrigenomics approach may eventually lead to more precise management of
utilization of feed resources in a more effective approach.