2019
DOI: 10.1371/journal.pone.0216211
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Utilizing the fecal microbiota to understand foal gut transitions from birth to weaning

Abstract: A healthy gastrointestinal (GI) tract with a properly established microbiota is necessary for a foal to develop into a healthy weanling. A foal’s health can be critically impacted by aberrations in the microbiome such as with diarrhea which can cause great morbidity and mortality in foals. In this study, we hypothesized that gut establishment in the foal transitioning from a diet of milk to a diet of grain, forage, and pasture would be detectable through analyses of the fecal microbiotas. Fecal samples from 37… Show more

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Cited by 36 publications
(73 citation statements)
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“…, but colonization is probably restricted by differences in diet and intestinal environment. Similar observations were recently reported by De La Torre et al: the foalmicrobiota was very different from the adults at day 7, and developing towards the adult composition at day 2823 . Their day 7 gut microbiota was similar with our observations at the family level.…”
supporting
confidence: 91%
“…, but colonization is probably restricted by differences in diet and intestinal environment. Similar observations were recently reported by De La Torre et al: the foalmicrobiota was very different from the adults at day 7, and developing towards the adult composition at day 2823 . Their day 7 gut microbiota was similar with our observations at the family level.…”
supporting
confidence: 91%
“…DNA concentration was determined using a NanoDrop UV spectrophotometer (ThermoFisher Scientific). Primers F515 (forward: 5′-GTGCCAGCMGCCGCGGTAA-3′) and R806 (5′-GGACTACHVGGGTWTCTAAT-3′) were used to amplify the V4 domain bacterial 16S rRNA genes, along with a unique barcode on each forward primer for each sample [ 20 22 ]. PCR, product purification, and agarose gel electrophoresis visualization were performed as previously described [ 20 ].…”
Section: Main Textmentioning
confidence: 99%
“…Primers F515 (forward: 5′-GTGCCAGCMGCCGCGGTAA-3′) and R806 (5′-GGACTACHVGGGTWTCTAAT-3′) were used to amplify the V4 domain bacterial 16S rRNA genes, along with a unique barcode on each forward primer for each sample [ 20 22 ]. PCR, product purification, and agarose gel electrophoresis visualization were performed as previously described [ 20 ]. Combined barcoded libraries were submitted to the University of California Davis Genome Center DNA Technologies Core for 250 bp paired-end sequencing using the Illumina MiSeq platform.…”
Section: Main Textmentioning
confidence: 99%
“…Enriched taxa were also analyzed using LEfSe (Linear Discriminant Analysis Effect Size) [38]. DCM and SFM foals were analyzed separately for each of their 6 age groups (Tables 3 and 4).…”
Section: Differences In Community Compositionmentioning
confidence: 99%
“…Enriched taxa by management group and time were identi ed using LEfSe [38]. Statistical analysis and visualization were completed using R [39].…”
Section: Dna Extraction and Sequencingmentioning
confidence: 99%