Impact of Sow Transition Diet and Genetic Line on Sow Reproduction Under Heat Stress Conditions

The objective was to evaluate a sow transition diet and genetic line for farrowing duration and sow lactation characteristics. One batch of second parity sows (n = 78) were farrowed at the NCDA Tidewater Research Station in July. Sows consisted of two genetic lines, one selected since 2012 for young age at puberty and the other selected for old age at puberty. From day 109 of gestation until day 3 of lactation, sows were fed either 2.73 kg of a corn-soy lactation diet (3322 Kcal ME/kg, 0.99% SID lysine) once per day or 1.36 kg twice per day of a transition diet (3489 Kcal/kg, 0.71 SID lysine). The transition diet contained 45% wheat middlings, 8% added soybean oil, 3000 FTU/kg of phytase and 500 ppm zinc sulfate. Continuous traits and categorical traits were analyzed in SAS using linear models and chi-square tests, respectively. Results showed sows fed the transition diet farrowed numerically faster (P = 0.18) than those receiving the lactation diet (3:04 vs. 3:47). Transition diet fed sows tended (P = 0.10) to have a shorter wean-to-estrus interval than sows fed the lactation diet (5.27 vs. 5.69 days). Sows from the young puberty genetic line tended (P = 0.07) to have a greater average daily feed intake during lactation when compared to old puberty line females (4.92 vs. 4.71 kg). Young puberty sows also had a greater (P = 0.03) percentage of females exhibiting estrus by day 7 after weaning when compared to the old puberty genetic line (80 vs. 57%). No differences (P = 0.39 to 0.87) were detected between diets or genetic lines for stillborn piglet percentage, average piglet birth weight, average piglet weaning weight or litter size at weaning. Results suggest young puberty sows are more likely to return to estrus under the conditions of this study.

Childhood obesity and multiple sclerosis: A Mendelian randomization study

Background: Higher childhood body mass index (BMI) has been associated with an increased risk of multiple sclerosis (MS). Objective: To evaluate whether childhood BMI has a causal influence on MS, and whether this putative effect is independent from early adult obesity and pubertal timing. Methods: We performed Mendelian randomization (MR) using summary genetic data on 14,802 MS cases and 26,703 controls. Large-scale genome-wide association studies provided estimates for BMI in childhood ( n = 47,541) and adulthood ( n = 322,154). In multivariable MR, we examined the direct effects of each timepoint and further adjusted for age at puberty. Findings were replicated using the UK Biobank ( n = 453,169). Results: Higher genetically predicted childhood BMI was associated with increased odds of MS (odds ratio (OR) = 1.26/SD BMI increase, 95% confidence interval (CI): 1.07–1.50). However, there was little evidence of a direct effect after adjusting for adult BMI (OR = 1.03, 95% CI: 0.70–1.53). Conversely, the effect of adult BMI persisted independent of childhood BMI (OR = 1.43; 95% CI: 1.01–2.03). The addition of age at puberty did not alter the findings. UK Biobank analyses showed consistent results. Sensitivity analyses provided no evidence of pleiotropy. Conclusion: Genetic evidence supports an association between childhood obesity and MS susceptibility, mediated by persistence of obesity into early adulthood but independent of pubertal timing.

Fine mapping genetic variants associated with age at puberty and sow fertility using SowPro90 genotyping array

Sow fertility traits, such as litter size and the number of lifetime parities produced (reproductive longevity), are economically important. Selection for these traits is difficult because they are lowly heritable and expressed late in life. Age at puberty (AP) is an early indicator of reproductive longevity. Here, we utilized a custom Affymetrix single-nucleotide polymorphisms (SNPs) array (SowPro90) enriched with positional candidate genetic variants for AP and a haplotype-based genome-wide association study to fine map the genetic sources associated with AP and other fertility traits in research (University of Nebraska-Lincoln [UNL]) and commercial sow populations. Five major quantitative trait loci (QTL) located on four Sus scrofa chromosomes (SSC2, SSC7, SSC14, and SSC18) were discovered for AP in the UNL population. Negative correlations (r = −0.96 to −0.10; P < 0.0001) were observed at each QTL between genomic estimated breeding values for AP and reproductive longevity measured as lifetime number of parities (LTNP). Some of the SNPs discovered in the major QTL regions for AP were located in candidate genes with fertility-associated gene ontologies (e.g., P2RX3, NR2F2, OAS1, and PTPN11). These SNPs showed significant (P < 0.05) or suggestive (P < 0.15) associations with AP, reproductive longevity, and litter size traits in the UNL population and litter size traits in the commercial sows. For example, in the UNL population, when the number of favorable alleles of an SNP located in the 3′ untranslated region of PTPN11 (SSC14) increased, AP decreased (P < 0.0001), while LTNP increased (P < 0.10). Additionally, a suggestive difference in the observed NR2F2 isoforms usage was hypothesized to be the source of the QTL for puberty onset mapped on SSC7. It will be beneficial to further characterize these candidate SNPs and genes to understand their impact on protein sequence and function, gene expression, splicing process, and how these changes affect the phenotypic variation of fertility traits.