Dairy cow performance is associated with longitudinal microRNA profiles

Madison MacLeay*, Francesc Xavier Donadeu, Georgios Banos*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Modern high producing dairy cows are still affected by poor fertility and disease, despite improvements achieved through genetic selection programs. Additional biomarkers of health and performance traits in cattle could enhance animal welfare and profitability by allowing farmers to cull animals before problems occur. We performed pilot investigations of plasma microRNA (miRNA) profiles during early life as potential biomarkers associated with future performance in dairy cows. The latter included survival to two years of age, age at first calving, yield of milk, fat and protein, mastitis and lameness traits, conception rate, number of services per conception, and calving interval. Using qPCR, we obtained longitudinal measurements and ratios involving nine miRNAs (miR-126-3p, miR-127, miR-142-5p, miR-154b, miR-27b, miR-30c-5p, miR-34a, miR-363, miR-425-3p) in plasma samples from three age groups: calves (<1 month), heifers (14–23 months), and first lactation cows (29–35 months). Changes in miR-126-3p from calf to first lactation cow were associated with first lactation milk yield and second lactation milk somatic cell count (an udder health indicator). Moreover, the miR-127 to miR-30c-5p ratio in cows was associated with milk fat and protein yield in the first two lactations, whereas miR-142-5p levels and several miRNA ratios involving this miRNA, were associated with second calving interval (a cow fertility trait). Our results identified novel early life biomarkers that warrant further investigation to determine whether they may predict dairy cattle performance.

Original languageEnglish
Article numbere0328765
JournalPLoS ONE
Volume20
Issue number8 August
Early online date1 Aug 2025
DOIs
Publication statusFirst published - 1 Aug 2025

Bibliographical note

Publisher Copyright:
© 2025 MacLeay et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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