The objective was to evaluate growth performance and carcass traits of finishing beef heifers sourced and finished in different regions in the U.S. Heifers [n = 190; initial body weight (BW) 483 ± 0.4 kg and 425 ± 1.9 kg for SD and TX sourced, respectively] were used in a 2 × 2 factorial arrangement of origin state (SD vs. TX) and finishing state (SD vs. TX) was used. Heifers were allotted on d -1 to: 1) sourced from SD and finished in SD (SD-SD), 2) sourced from SD and finished in TX (SD-TX), 3) sourced from TX and finished in SD (TX-SD), and 4) sourced from TX and finished in TX (TX-TX). Heifers were weighed on d -1, 3, 15, 28, 56, 78 (TX-TX and SD-TX) and 90 (SD-SD and TX-SD). On d 0, SD-TX and TX-SD heifers were shipped to their respective finishing locations. The following morning (d 1), SD-TX and TX-SD heifers were individually weighed to determine transit shrink. To monitor transit stress effects, vaginal temperature probes were used on all SD-TX and TX-SD heifers and a portion of SD-SD and TX-TX heifers on d -1 and removed on d 3. Clinical attitude scores (CAS) were recorded on d -1, 0, 1, 2 and 3 for bovine respiratory disease symptoms. Transported heifers had decreased temperatures (P ≤ 0.01) during transit and post-transit and increased (P ≤ 0.01) vaginal temperature during loading and unloading compared to non-transported heifers. On d 0, 1, and 3 there was a shift in the distribution of heifers that had a CAS score greater than 0 for TX-TX, SD-TX and TX-SD. Heifers endured elevated ambient temperatures (temperature humidity index > 75) for 54% and 18% of the feeding period for TX and SD. Growth performance and carcass trait interactions were significant (P < 0.01) except for d -1 BW, percent shrink during transit, average daily gain, dressing percent, ribeye area and liver abscess severity, which did not differ (P > 0.30). A shift in the distribution (P < 0.02) towards a greater proportion of Yield Grade 1 and Select carcasses for was observed for TX versus SD. Overall, heifers transported to higher ambient temperatures had improved overall yield grades, but decreased dry matter intake, quality grades (QG) and limited growth recovery (45 kg lighter) following transit than non-transported heifers. Heifers transported to lower ambient temperatures recovered growth and had improved QG (P < 0.02) at the same thickness of rib fat compared to non-transported heifers but had decreased overall yield and yield grades.
This study was to evaluate the effects of dietary adding of phytosterol (PS) on growth, antioxidant capacity, tissue morphology and gut microbiota of largemouth bass (Micropterus salmoides). A total of 540 largemouth bass (13.75 ± 0.37g) were selected and randomly divided into six groups and fed with diets supplemented with 0, 0.01 %, 0.02 %, 0.03 %, 0.04 % and 0.05 % of PS (ontrol, PS1-PS5) for 56 d. The results showed that the rate of weight gain (WGR) and condition factor (CF) of largemouth bass increased significantly (P < 0.05) with the increasing PS addition levels. In addition, PS significantly increased the activities of superoxide dismutase (SOD) and catalase (CAT) in serum compared to group C (P < 0.05), as well as increased relative expression of pituitary Insulin-like growth factor (igf1ra, igf1rb, and igf2r), hypothalamic growth hormone gh and insulin receptor ir, compared with group C (P < 0.05). Histopathological analysis showed that the addition of 0.04 % PS to the feed resulted in a tighter cellular arrangement and a significant reduction in vacuolisation in the liver of largemouth bass. It also significantly increased intestinal fold width and muscle wall thickness (P < 0.05). Analysis of the intestinal flora showed a significant decrease in the α-diversity of the flora in the PS4 group compared to the C group (P < 0.05). Notably, at the phylum level, the addition of PS to feed significantly reduced the relative abundance of Proteobacteria and Bacteroidota. At the genus level, PS significantly increased the relative abundance of Cetobacterium (P < 0.05). The addition of 0.04 % PS to the feed promotes growth, antioxidant capacity, improved tissue morphology and increased abundances of beneficial gut microbiotas in largemouth bass.
Pig production is an agricultural sector of great economic and social relevance to Brazil and global markets. Feed efficiency traits directly influence the sustainability of pig production due to the economic impact of feed costs on the production system and the environmental footprint of the industry. Therefore, breeding for improved feed efficiency has been a target of worldwide pig breeding programs. Genome-wide association studies (GWAS) enable the assessment of the genetic background of complex traits, which contributes to a better understanding of the biological mechanisms regulating their phenotypic expression. In this context, the primary objective of this study was to identify and validate genomic regions and candidate genes associated with feed conversion ratio (FCR) and residual feed intake (RFI) in pigs based on a comprehensive systematic review and meta-analysis of GWAS. The METAL software was used to implement the meta-analysis and the Bonferroni multiple testing correction considering a significance threshold of 0.05. The significant single nucleotide polymorphisms (SNPs) in the meta-analysis were used to identify candidate genes, followed by a functional genomic enrichment analysis. The systematic review identified 13 studies, of which 7 evaluated FCR, 3 evaluated RFI, and 3 studies investigated both traits, with 160 and 96 SNPs identified for FCR and RFI, respectively. After the meta-analysis, 145 markers were significantly associated with FCR and 90 with RFI. The gene annotation process resulted in 105 and 114 genes for FCR and RFI, respectively. The enrichment analysis for FCR resulted in 16 significant gene ontology (GO) terms, while six terms were identified for RFI. The main GO terms were actin cytoskeleton (GO_BP:0030036), membrane (GO_CC:0016020), integral components of the peroxisomal membrane (GO_CC:0005779), and carbohydrate binding (GO_MF:0030246). The main candidate genes identified were MED18, PHACTR4, ABCC2, TRHDE, FRS2, FAR2 and FIS1 for FCR, and ADGRL2, ASGR1, ASGR2, and MAN2B1 for RFI. These findings contribute to a better understanding of the genetic mechanisms associated with feed efficiency traits in pigs, providing a foundation for future improvements in pig breeding programs.
Background: Enterotoxigenic F4 E. coli (F4-ETEC) pose an economic threat to the swine industry through reduced growth, increased mortality and morbidity, and increased costs associated with treatment. Prevention and treatment of F4-ETEC often relies on antimicrobials; however, due to the threat of antimicrobial resistance, antimicrobial use is being minimized, and hence alternative control methods are needed. This study investigated the effects of postbiotics in the form of Lactobacillus acidophilus fermentation products (LFP) and Saccharomyces cerevisiae fermentation products (SFP), on pigs challenged with an F4 ETEC strain. Eighty pigs were selected based on a pre-screening F4-ETEC susceptibility test. The animals were divided into five treatments each with four replicate pens. Pigs were assigned to five different diets: a control diet (CON); CON diet with 3,000 ppm ZnO (ZnO); CON diet with 2,000 ppm LFP (LFP); CON diet with 2,000 ppm SFP (SFP); CON diet with both 2,000 ppm LFP and 2,000 ppm SFP (LAS). Pigs were inoculated per os with F4-ETEC twice, on day 0 and day1 of the experiment.
Results: No significant differences in fecal consistency scores or fecal F4-ETEC concentration in pigs supplemented with LFP and/or SFP were detected. An increased diversity and abundance of Lactobacillaceae in the fecal microbiome of pigs supplemented with LFP were detected, as well as an increased final liveweight of pigs supplemented with LFP and/or SFP.
Conclusion: This study demonstrated that the fecal microbiome is modified in F4-ETEC-challenged pigs supplemented with the combination of LFP and SFP, with these modifications previously associated with increased growth performance and health status in young pigs. Pigs receiving this combination of postbiotics also demonstrated an increased final liveweight, indicating that management of ETEC-associated performance loss may not require the complete removal of ETEC from a production system.