Profiling of circulating microRNA and pathway analysis in normal- versus over-conditioned dairy cows during the dry period and early lactation.


Journal

Journal of dairy science
ISSN: 1525-3198
Titre abrégé: J Dairy Sci
Pays: United States
ID NLM: 2985126R

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 30 01 2020
accepted: 07 06 2020
pubmed: 24 8 2020
medline: 19 12 2020
entrez: 24 8 2020
Statut: ppublish

Résumé

The objective of this study was to determine the circulating microRNA (miRNA) profile in over-conditioned (HBCS) versus normal-conditioned (NBCS) dairy cows in combination with pathway enrichment analyses during the transition period. Thirty-eight multiparous Holstein cows were selected 15 wk before anticipated calving date based on their current and previous body condition scores (BCS) for forming either a HBCS group (n = 19) or a NBCS group (n = 19). They were fed different diets during late lactation to reach the targeted differences in BCS and backfat thickness until dry-off. A subset of 15 animals per group was selected based on their circulating concentrations of nonesterified fatty acids (on d 14 postpartum) and β-hydroxybutyrate (on d 21 postpartum), representing the greater or the lower extreme values within their BCS group. Blood serum obtained at d -49 and 21 relative to parturition (3 pools with 5 cows per each group and time point) were used to identify miRNA that were differentially expressed (DE) between groups or time points using miRNA sequencing. No DE-miRNA were discovered between NBCS versus HBCS. Comparing pooled samples from d -49 and d 21 resulted in 7 DE-miRNA in the NBCS group, of which 5 miRNA were downregulated and 2 miRNA were overexpressed on d 21 versus -49. The abundance of 5 of these DE-miRNA was validated in all individual samples via quantitative PCR and extended to additional time points (d -7, 3, 84). Group differences were observed for miR-148a, miR-122 as well as miR-455-5p, and most DE-miRNA (miR-148a, miR-122, miR-30a, miR-450b, miR-455-5p) were downregulated directly after calving. Subsequently, the DE-miRNA was used for bioinformatics analysis to identify putative target genes and the most enriched biological pathways. The most significantly enriched pathways of DE-miRNA were associated with cell cycle and insulin signaling as well as glucose and lipid metabolism. Overall, we found little differences in circulating miRNA in HBCS versus NBCS cows around calving.

Identifiants

pubmed: 32828512
pii: S0022-0302(20)30617-2
doi: 10.3168/jds.2020-18283
pii:
doi:

Substances chimiques

Circulating MicroRNA 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

9534-9547

Informations de copyright

Copyright © 2020 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.

Auteurs

Laura A Webb (LA)

Institute of Animal Science, Physiology Unit, University of Bonn, 53115 Bonn, Germany.

Morteza H Ghaffari (MH)

Institute of Animal Science, Physiology Unit, University of Bonn, 53115 Bonn, Germany.

Hassan Sadri (H)

Department of Clinical Science, Faculty of Veterinary Medicine, University of Tabriz, 5166616471 Tabriz, Iran.

Katharina Schuh (K)

Institute of Animal Science, Physiology Unit, University of Bonn, 53115 Bonn, Germany; Department of Life Sciences and Engineering, Animal Nutrition and Hygiene Unit, University of Applied Sciences Bingen, 55411 Bingen am Rhein, Germany.

Valentina Zamarian (V)

Dipartimento di Medicina Veterinaria, Università di Milano, 20133 Milano, Italy.

Christian Koch (C)

Educational and Research Center for Animal Husbandry, Hofgut Neumuehle, 67728 Muenchweiler an der Alsenz, Germany.

Nares Trakooljul (N)

Leibniz-Institute for Farm Animal Biology (FBN), Institute for Genome Biology, 18196 Dummerstorf, Germany.

Klaus Wimmers (K)

Leibniz-Institute for Farm Animal Biology (FBN), Institute for Genome Biology, 18196 Dummerstorf, Germany.

Cristina Lecchi (C)

Dipartimento di Medicina Veterinaria, Università di Milano, 20133 Milano, Italy.

Fabrizio Ceciliani (F)

Dipartimento di Medicina Veterinaria, Università di Milano, 20133 Milano, Italy.

Helga Sauerwein (H)

Institute of Animal Science, Physiology Unit, University of Bonn, 53115 Bonn, Germany. Electronic address: sauerwein@uni-bonn.de.

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