2014
DOI: 10.1139/cjm-2013-0805
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Influence of dietary docosahexaenoic acid supplementation on the overall rumen microbiota of dairy cows and linkages with production parameters

Abstract: The rumen microbiota contributes to greenhouse gas emissions and has an impact on feed efficiency and ruminant product fatty acid composition. Dietary fat supplements have shown promise in reducing enteric methane production and in altering the fatty acid profiles of ruminant-derived products, yet in vivo studies on how these impact the rumen microbiota are limited. In this study, we investigated the rumen bacterial, archaeal, fungal, and ciliate protozoan communities of dairy cows fed diets supplemented with … Show more

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Cited by 11 publications
(8 citation statements)
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“…Total nucleic acid was extracted from freeze dried piglet faecal samples using a proprietary method (South Australian Research and Development Institute, Adelaide, Australia) [19][20][21]. The V3-V4 region of the 16S rRNA gene was sequenced using the illumina MiSeq platform using 300 bp paired end reads (forward primer: CCTAYGGGRBGCASCAG and reverse primer: GGACTACNNGGGTATCTAAT), following a standard protocol by the Australian Genome Research Facility for next generation sequencing (Melbourne, Australia).…”
Section: Dna Extraction and 16s Rrna Amplicon Sequencingmentioning
confidence: 99%
“…Total nucleic acid was extracted from freeze dried piglet faecal samples using a proprietary method (South Australian Research and Development Institute, Adelaide, Australia) [19][20][21]. The V3-V4 region of the 16S rRNA gene was sequenced using the illumina MiSeq platform using 300 bp paired end reads (forward primer: CCTAYGGGRBGCASCAG and reverse primer: GGACTACNNGGGTATCTAAT), following a standard protocol by the Australian Genome Research Facility for next generation sequencing (Melbourne, Australia).…”
Section: Dna Extraction and 16s Rrna Amplicon Sequencingmentioning
confidence: 99%
“…Total nucleic acid was extracted from 10 mL of freeze-dried ruminal fluid using a modification (Torok et al, 2008) of a South Australian Research and Development Institute (SARDI, West Beach, Australia) proprietary method (Stirling et al, 2004), as previously described by Torok et al (2014). Terminal restriction fragment (T-RF) length polymorphism was conducted to investigate the bacterial, archaeal, fungal, and protozoan communities.…”
Section: Rumen Microbial Profilingmentioning
confidence: 99%
“…Terminal restriction fragment (T-RF) length polymorphism was conducted to investigate the bacterial, archaeal, fungal, and protozoan communities. The PCR primers used for bacterial profiling were 27F/907R (Torok et al, 2008), whereas Ar109f/Ar912r were used for Archaea, ITS1-F/ITS4 for fungi, and CS322F/EU929R for protozoa (Torok et al, 2014). For each primer pair, one primer was 5 labeled with 6-carboxyfluorescein (FAM; 27F, Ar109f, ITS1-F, and EU929R) to enable subsequent detection of T-RF.…”
Section: Rumen Microbial Profilingmentioning
confidence: 99%
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“…Although diet has been investigated as a means of altering the adult cow microbiota (16,17) and production (18,19), calf feed has not been as fully assessed. Previous dietary work with dairy calves focused on weight gain, as this is positively associated with increased downstream milk production (20).…”
mentioning
confidence: 99%