AI Article Synopsis

  • The global dairy industry is grappling with heat stress (HS), impacting milk production and cow health, yet the cellular responses of cows to HS remain unclear.
  • The study analyzed liver biopsies from 9 Holstein dairy cows under heat stress, pair-fed, and thermoneutral conditions, revealing significant reductions in dry matter intake and milk yield in heat-stressed cows.
  • Transcriptomic analysis identified 483 differentially expressed genes, showing downregulation of mitochondrial genes and upregulation of heat shock proteins, indicating HS disrupts mitochondrial function and energy production, providing crucial insights for improving dairy cow welfare and productivity.

Article Abstract

Background: The global dairy industry is currently facing the challenge of heat stress (HS). Despite the implementation of various measures to mitigate the negative impact of HS on milk production, the cellular response of dairy cows to HS is still not well understood. Our study aims to analyze transcriptomic dynamics and functional changes in the liver of cows subjected to heat stress (HS). To achieve this, a total of 9 Holstein dairy cows were randomly selected from three environmental conditions - heat stress (HS), pair-fed (PF), and thermoneutral (TN) groups - and liver biopsies were obtained for transcriptome analysis.

Results: Both the dry matter intake (DMI) and milk yield of cows in the HS group exhibited significant reduction compared to the TN group. Through liver transcriptomic analysis, 483 differentially expressed genes (DEGs) were identified among three experimental groups. Especially, we found all the protein coding genes in mitochondria were significantly downregulated under HS and 6 heat shock proteins were significant upregulated after HS exposure, indicating HS may affect mitochondria integrity and jeopardize the metabolic homeostasis in liver. Furthermore, Gene ontology (GO) enrichment of DEGs revealed that the protein folding pathway was upregulated while oxidative phosphorylation was downregulated in the HS group, corresponding to impaired energy production caused by mitochondria dysfunction.

Conclusions: The liver transcriptome analysis generated a comprehensive gene expression regulation network upon HS in lactating dairy cows. Overall, this study provides novel insights into molecular and metabolic changes of cows conditioned under HS. The key genes and pathways identified in this study provided further understanding of transcriptome regulation of HS response and could serve as vital references to mitigate the HS effects on dairy cow health and productivity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10360291PMC
http://dx.doi.org/10.1186/s12864-023-09484-1DOI Listing

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