Cited by 138Ruminant Nutrition and Digestive PhysiologyMycotoxins in Agriculture and FoodAnimal Nutrition and Physiology

Bacterial and fungal core microbiomes associated with small grain silages during ensiling and aerobic spoilage

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Duniere, Lysiane, Xu, Shanwei, Long, Jin, Elekwachi, Chijioke, Wang, Yuxi, Turkington, Kelly, Forster, Robert, McAllister, Tim A.·2017·BMC Microbiology

Abstract

BACKGROUND: Describing the microbial populations present in small grain silage and understanding their changes during ensiling is of interest for improving the nutrient value of these important forage crops. Barley, oat and triticale forages as well as an intercropped mixture of the 3 crops were harvested and ensiled in mini silos for a period of 90 days, followed by 14 days of aerobic exposure. Changes in fermentation characteristics and nutritive value were assessed in terminal silages and bacterial and fungal communities during ensiling and aerobic exposure were described using 16S and 18S rDNA sequencing, respectively. RESULTS: All small grain silages exhibited chemical traits that were associated with well ensiled forages, such as low pH value (4.09 ± 0.28) and high levels of lactic acid (59.8 ± 14.59 mg/g DM). The number of microbial core genome operational taxonomic units (OTUs) decreased with time of ensiling. Taxonomic bacterial community profiles were dominated by the Lactobacillales after fermentation, with a notable increase in Bacillales as a result of aerobic exposure. Diversity of the fungal core microbiome was shown to also be reduced during ensiling. Operational taxonomic units assigned to filamentous fungi were found in the core microbiome at ensiling and after aerobic exposure, whereas the Saccharomycetales were the dominate yeast population after 90 days of ensiling and aerobic exposure. Bacterial and fungal orders typically associated with silage spoilage were identified in the core microbiome after aerobic exposure. CONCLUSION: Next Generation Sequencing was successfully used to describe bacterial communities and the first record of fungal communities throughout the process of ensiling and utilization. Adequately describing the microbial ecology of silages could lead to improved ensiling practices and the selection of silage inoculants that act synergistically with the natural forage microbiome.

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References 74 · Cited by 138

Authors
Duniere, L., Xu, S., Long, J., Elekwachi, C., Wang, Y., Turkington, K., Forster, R., & McAllister, T. A.
Affiliations
Agriculture and Agri-Food Canada (CA)
Corresponding author
McAllister, Tim A.
Venue
BMC Microbiology
Published
2017-03-03
Volume
17
Issue
1
Pages
50-50
ISSN
1471-2180 (ISSN-L)
OpenAlex
W2594718762
Cited by
138
References
74
Citations by year
2026: 8 · 2025: 9 · 2024: 12 · 2023: 22 · 2022: 20 · 2021: 21 · 2020: 21 · 2019: 11 · 2018: 11 · 2017: 3
FWCI
21.85
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • BMC Microbiology (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Federal Open Science Repository of Canada / Le Dépôt fédéral de science ouverte du Canada (submittedVersion, cc-by)
  • HAL (submittedVersion, other-oa)
Funders
Barley Cluster of Agriculture and Agri-Food Canada
Topics
  • Life Sciences › Agricultural and Biological Sciences › Agronomy and Crop Science › Ruminant Nutrition and Digestive Physiology
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Mycotoxins in Agriculture and Food
  • Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Nutrition and Physiology
Keywords
silage fermentation, aerobic spoilage, barley, oat, triticale, Lactobacillales, Bacillales, filamentous fungi, Saccharomycetales, silage inoculants, forage quality
MeSH terms
Triticale, Aerobiosis, Bacteria, Hordeum, Base Sequence, Edible Grain, DNA, Bacterial, DNA, Fungal, Ecology, Fermentation, Food Analysis, Fungi, Phylogeny, RNA, Ribosomal, 16S, RNA, Ribosomal, 18S, Silage, Temperature, Avena, Lactic Acid, Biodiversity, High-Throughput Nucleotide Sequencing, Microbiota

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