4.3 Article

Effects of dietary crude protein and tannic acid on rumen fermentation, rumen microbiota and nutrient digestion in beef cattle

Journal

ARCHIVES OF ANIMAL NUTRITION
Volume 73, Issue 1, Pages 30-43

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/1745039X.2018.1545502

Keywords

Beef cattle; crude protein; digestibility; rumen bacteria; rumen fermentation; tannic acid

Funding

  1. National Natural Science Foundation of China [31572428]

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The objectives of the trial were to study the effects of dietary crude protein (CP) and tannic acid (TA) on rumen fermentation, microbiota and nutrient digestion in beef cattle. Eight growing beef cattle (live weight 350 +/- 25 kg) were allocated in a 2x2 crossover design using two levels of dietary CP [111g/kg dry matter (DM) and 136g/kg DM] and two levels of TA (0 and 16.9g/kg DM) as experimental treatments. Each experimental period lasted 19 d, consisting of 14-d adaptation and 5-d sampling. The impacts of dietary CP and TA on ruminal microbiota were analysed using high-throughput sequencing of 16S rRNA gene. Results indicated that no interactions between dietary CP and TA were found on rumen fermentation and nutrient digestibility. Increasing dietary CP level from 111 to 136g/kg DM increased the ruminal concentrations of ammonia nitrogen (NH3-N) (p <0.01) and improved the CP digestibility (p <0.001). Adding TA at 16.9g/kg DM inhibited rumen fermentation and decreased the digestibility of dietary CP (p <0.001), DM (p <0.05) and organic matter (p <0.01). Increasing the dietary CP level or adding TA did not affect the relative abundances of the major bacteria Firmicutes and Proteobacteria at the phylum level and Prevotella_1 and Christensenellaceae_R-7_group at the genus level, even though adding TA increased the Shannon index of the ruminal bacterial community. TA was partly hydrolysed to pyrogallol, gallic acid and resorcinol in rumen fluid and the inhibitory effects of TA on rumen fermentation and nutrient digestibility could have been resulted from the TA metabolites including pyrogallol, gallic acid and resorcinol as well as the protein-binding effect.

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