2009
DOI: 10.1002/jsfa.3717
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In vitro effects of phlorotannins from Ascophyllum nodosum (brown seaweed) on rumen bacterial populations and fermentation

Abstract: BACKGROUND: Use of brown algae (seaweed) in ruminant diets is increasing, but the effects of its phlorotannins (PT) on rumen microbial ecology have not been determined. Mixed forage (50 : 25 : 25 ground barley silage-alfalfa hay-grass hay) was used as substrate in a batch culture ruminal incubation that included PT extracted from Ascophyllum nodosum, with and without polyethylene glycol. Principal ruminal bacteria were quantified using real-time polymerase chain reaction.

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Cited by 72 publications
(58 citation statements)
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“…Primers and annealing temperatures were as described previously for F. succinogenes, P. bryantii, R. flavefaciens, S. ruminantium (Tajima et al, 2001) and R. albus (Wang et al, 1997). Detailed information on PCR cycling conditions, plasmid standards and reference bacterial strains are as described by Wang et al (2009). Universal 16S primer sequences: 16S-F: CTCCTACGGGAGGCAGCAGT and 16S-R: TTACCGCGGCTGCTGGCAC were used to detect total bacteria using amplification conditions: one cycle at 95°C for 3 min, 30 cycles of denaturation at 95°C for 15 s, annealing at 60°C for 30 s, and extension at 72°C for 30 s. A total of 25 μL of PCR mixture containing 150 nM of each 16S primer was used.…”
Section: Methodsmentioning
confidence: 99%
“…Primers and annealing temperatures were as described previously for F. succinogenes, P. bryantii, R. flavefaciens, S. ruminantium (Tajima et al, 2001) and R. albus (Wang et al, 1997). Detailed information on PCR cycling conditions, plasmid standards and reference bacterial strains are as described by Wang et al (2009). Universal 16S primer sequences: 16S-F: CTCCTACGGGAGGCAGCAGT and 16S-R: TTACCGCGGCTGCTGGCAC were used to detect total bacteria using amplification conditions: one cycle at 95°C for 3 min, 30 cycles of denaturation at 95°C for 15 s, annealing at 60°C for 30 s, and extension at 72°C for 30 s. A total of 25 μL of PCR mixture containing 150 nM of each 16S primer was used.…”
Section: Methodsmentioning
confidence: 99%
“…Primers and annealing temperatures have been described previously for F. succinogenes, P. bryantii, R. amylophilus, R. flavefaciens, S. ruminantium and S. bovis , R. albus , total bacterial and methanogen 16S rRNA For PCR, 25 ng of extracted DNA template was added. Detailed information on PCR cycling conditions, plasmid standards and reference bacterial strains has been provided previously . Copies of species‐specific, total bacterial and methanogen 16S rRNA were used to estimate the abundance of microbial populations.…”
Section: Methodsmentioning
confidence: 99%
“…Moreover, they observed that the effect of CT depends on, among others, the molecular weight and chemical structure of tannins. Similarly, addition of phlorotannins to rumen bacterial cultures inhibited growth of Fibrobacter succinogenes, but stimulated growth of Streptococcus bovis and Prevotella bryantii (Wang et al, 2009). The lack of effect of tannins in these studies may be due to inhibitory effects on some bacterial species and stimulatory effects on others.…”
Section: Controlmentioning
confidence: 96%