ABSTRACT
The frequency of heat waves and hot days are increasing due to climate change, which leads to an increase in the occurrence of heat stress in dairy cattle. Previous studies have shown that dairy cattle identified as high immune responders have a reduced incidence of disease and improved vaccine response compared to average and low responders. Additionally, it has been observed that when cells from immune phenotyped cattle are exposed to in-vitro heat challenge, high immune responders exhibit increased heat tolerance compared to average and low immune responders. Therefore, the objective of this study was to evaluate physiological parameters and the function of blood mononuclear cells of immune phenotyped dairy cattle exposed to in-vivo heat challenge. A total of 24 immune phenotyped lactating dairy cattle (8 high, 8 average and 8 low) were housed in the tie-stall area of the barn and exposed to an in-vivo heat challenge for 4 h on 2 subsequent days, where the temperature was set at 29 â. Blood samples were taken both pre- and post-challenge each day and manual respiration rates and rectal temperatures were recorded pre challenge and every 30 min during the challenge. Temperature and humidity measurements were taken in correspondence with all respiration rate and rectal temperature measurements to calculate the temperature humidity index pre heat challenge and at 30-minute intervals during the heat challenge. Blood mononuclear cells were isolated from blood collected pre and post challenge and the concentration of heat shock protein 70 and cell proliferation were assessed. Results showed that average and low responders had significantly greater respiration rates compared to high responders at a temperature humidity index of 77 and above. No significant difference was observed between phenotypes for rectal temperature. High responders had a higher heat shock protein 70 concentration and greater cell proliferation after in-vivo heat challenges compared to average and low responders. These results paralleled those found during in-vitro heat challenge adding further credence to the concept that high responders may be more resilient to heat stress compared average and low responders.
Subject(s)
Cattle Diseases , Heat Stress Disorders , Animals , Cattle , Female , Heat Stress Disorders/veterinary , Heat-Shock Response , Hot Temperature , Humidity , Lactation , Leukocytes, MononuclearABSTRACT
Heat stress negatively affects health and production in cows. Examining the cellular response to heat stress could reveal underlying protective molecular mechanisms associated with superior resilience and ultimately enable selection for more resilient cattle. This type of investigation is increasingly important as future predictions for the patterns of heat waves point to increases in frequency, severity, and duration. Cows identified as high immune responders based on High Immune Response technology (HIR) have lower disease occurrence compared to their average and low immune responder herd-mates. In this study, our goal was to identify epigenetic differences between high and low immune responder cows in response to heat stress. We examined genome-wide DNA methylation of blood mononuclear cells (BMCs) isolated from high and low cows, before and after in vitro heat stress. We identified differential methylation of promoter regions associated with a variety of biological processes including immune function, stress response, apoptosis, and cell signalling. The specific differentially methylated promoter regions differed between samples from high and low cows, and results revealed pathways associated with cellular protection during heat stress.
Subject(s)
DNA Methylation , Dairying , Monocytes/metabolism , Phenotype , Animals , Cattle , Climate Change , Female , Gene Regulatory Networks , Heat-Shock Response/genetics , Immunophenotyping , Promoter Regions, GeneticABSTRACT
Fertility plays a key role in the success of calf production, but there is evidence that reproductive efficiency in beef cattle has decreased during the past half-century worldwide. Therefore, identifying animals with superior fertility could significantly impact cow-calf production efficiency. The objective of this research was to identify candidate regions affecting bull fertility in beef cattle and positional candidate genes annotated within these regions. A GWAS using a weighted single-step genomic BLUP approach was performed on 265 crossbred beef bulls to identify markers associated with scrotal circumference (SC) and sperm motility (SM). Eight windows containing 32 positional candidate genes and five windows containing 28 positional candidate genes explained more than 1% of the genetic variance for SC and SM, respectively. These windows were selected to perform gene annotation, QTL enrichment, and functional analyses. Functional candidate gene prioritization analysis revealed 14 prioritized candidate genes for SC of which MAP3K1 and VIP were previously found to play roles in male fertility. A different set of 14 prioritized genes were identified for SM and five were previously identified as regulators of male fertility (SOD2, TCP1, PACRG, SPEF2, PRLR). Significant enrichment results were identified for fertility and body conformation QTLs within the candidate windows. Gene ontology enrichment analysis including biological processes, molecular functions, and cellular components revealed significant GO terms associated with male fertility. The identification of these regions contributes to a better understanding of fertility associated traits and facilitates the discovery of positional candidate genes for future investigation of causal mutations and their implications.
Subject(s)
Fertility/genetics , Genome-Wide Association Study/veterinary , Quantitative Trait Loci , Scrotum/physiology , Sperm Motility/genetics , Animals , Cattle , Cell Cycle Proteins/genetics , Chaperonin Containing TCP-1/genetics , Gene Frequency , Male , Receptors, Prolactin/genetics , Superoxide Dismutase/geneticsABSTRACT
In mammals, birds, snakes and many lizards and fish, sex is determined genetically (either male XY heterogamy or female ZW heterogamy), whereas in alligators, and in many reptiles and turtles, the temperature at which eggs are incubated determines sex. Evidently, different sex-determining systems (and sex chromosome pairs) have evolved independently in different vertebrate lineages. Homology shared by Xs and Ys (and Zs and Ws) within species demonstrates that differentiated sex chromosomes were once homologous, and that the sex-specific non-recombining Y (or W) was progressively degraded. Consequently, genes are left in single copy in the heterogametic sex, which results in an imbalance of the dosage of genes on the sex chromosomes between the sexes, and also relative to the autosomes. Dosage compensation has evolved in diverse species to compensate for these dose differences, with the stringency of compensation apparently differing greatly between lineages, perhaps reflecting the concentration of genes on the original autosome pair that required dosage compensation. We discuss the organization and evolution of amniote sex chromosomes, and hypothesize that dosage insensitivity might predispose an autosome to evolving function as a sex chromosome.