2020
DOI: 10.1007/s00253-020-10684-y
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Effects of dietary rumen–protected Lys levels on rumen fermentation and bacterial community composition in Holstein heifers

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Cited by 21 publications
(21 citation statements)
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“…Concerning the ruminal samples from our heifers, Firmicutes was the most abundant phylum (52% and 57%), followed by Bacteroidetes (41% and 36% for the CON and SUP heifers, respectively). The composition of the rumen bacterial population in this study was similar to that of the known bacterial population of cattle, which is dominated mainly by Firmicutes and Bacteroidetes, regardless of breed and diet [39,40]. In crossbred heifers, Martinez-Fernandez [41] also detected a preeminence of Bacteroidetes and Firmicutes; however, in their study, the abundance of Bacteroidetes was greatest in ruminal environments.…”
Section: Discussionsupporting
confidence: 73%
“…Concerning the ruminal samples from our heifers, Firmicutes was the most abundant phylum (52% and 57%), followed by Bacteroidetes (41% and 36% for the CON and SUP heifers, respectively). The composition of the rumen bacterial population in this study was similar to that of the known bacterial population of cattle, which is dominated mainly by Firmicutes and Bacteroidetes, regardless of breed and diet [39,40]. In crossbred heifers, Martinez-Fernandez [41] also detected a preeminence of Bacteroidetes and Firmicutes; however, in their study, the abundance of Bacteroidetes was greatest in ruminal environments.…”
Section: Discussionsupporting
confidence: 73%
“…The DNA extract was analyzed on a 1% agarose gel, and DNA concentration and purity were determined using a NanoDrop 2000 UV–vis spectrophotometer (Thermo Scientific, Wilmington, DE, USA). The hypervariable region V3-V4 of the bacterial 16S rRNA gene was amplified with primer pairs 338F (5′-ACTCCTACGGGAGGCAGCAG-3’) and 806R (5′–GGACTACHVGGGTWTCTAAT-3′) using an ABI GeneAmp ® 9700 PCR thermocycler (ABI, Foster City, CA, USA) [ 38 ]. The PCR amplification of the 16S rRNA gene was performed according to Kong et al [ 38 ].…”
Section: Methodsmentioning
confidence: 99%
“…The hypervariable region V3-V4 of the bacterial 16S rRNA gene was amplified with primer pairs 338F (5′-ACTCCTACGGGAGGCAGCAG-3’) and 806R (5′–GGACTACHVGGGTWTCTAAT-3′) using an ABI GeneAmp ® 9700 PCR thermocycler (ABI, Foster City, CA, USA) [ 38 ]. The PCR amplification of the 16S rRNA gene was performed according to Kong et al [ 38 ]. The PCR product was extracted from a 2% agarose gel and purified using an AxyPrep DNA Gel Extraction Kit (Axygen Biosciences, Union City, CA, USA) according to the manufacturer’s instructions, and quantified using a Quantus™ Fluorometer (Promega, Madison, WI, USA).…”
Section: Methodsmentioning
confidence: 99%
“…After 7 h, 24 h, 30 h, and 48 h of incubation, the content of each sample was filtered through a nylon bag (80 mm × 150 mm size with 42 μm pores), and then dried at 60 °C for 48 h in a forced-air oven (Wujiang Zhongda Electrical Technology Co., Ltd., Wujiang, Jiangsu, China) to analyze and calculate nutrient degradability. The content of dry matter (DM), neutral detergent fiber (NDF), acid detergent fiber (ADF), and crude protein (CP) in the original sample, and residues at 24 h, 30 h, and 48 h were determined according to the previously described method [ 27 ]. The starch content of residues of TMR and corn silage at 7 h was determined using a commercial starch assay kit (BioVision, Inc., San Francisco Bay Area, the United States of America).…”
Section: Methodsmentioning
confidence: 99%