Heat stress is an important cause of poor development and low survival rates in bovine embryos. Experiments were conducted to test the hypothesis that Bos indicus embryos are more resistant to heat stress than are Bos taurus embryos. In experiment 1, Nelore and Jersey embryos from oocyte pick-up-derived oocytes were submitted to heat stress (96 hours post-insemination, 41 °C, 6 hours), developmental ratios were assessed at Day 7 (Day 0 = day of fertilization), and blastocysts were frozen for RNA extraction. Experiment 2 evaluated expression of COX2, CDX2, HSF1, and PLAC8 in previously frozen blastocysts. In experiment 3, Nellore and Angus embryos from oocyte pick-up-derived oocytes were submitted to heat stress (96 hours post-insemination, 41 °C, 12 hours) and transferred to recipients on Day 7. In experiment 4, embryos developed as in experiment 3 were fixed for Terminal deoxynucleotidyl transferase dUTP nick end labeling labeling and total cell counting. In experiment 1, heat stress decreased the percentage of Jersey oocytes that became blastocysts, but had no effect on Nellore embryos (34.6%, 25.0%, 39.5%, and 33.0% for Jersey control, Jersey heat-stressed, Nellore control, and Nellore heat-stressed oocytes, respectively; P < 0.05). In experiment 2, heat stress decreased (P < 0.05) expression of CDX2 and PLAC8, with higher expression of these genes in Nellore embryos than in Jersey embryos. Heat stress also decreased (P < 0.05) expression of COX2 in Jersey embryos, but had no effect on Nellore embryos. Expression of HSF1 was decreased (P < 0.05) by heat stress in both breeds, with a greater effect in Nellore embryos. In experiment 3, heat stress tended (P = 0.1) to decrease the percentage of pregnancies among cows (Day 30 to 35) that received Angus embryos. In experiment 4, heat stress increased (P < 0.05) the percentage of apoptotic blastomeres, but had no breed-specific effects. In addition, Nellore embryos had fewer (P < 0.05) Terminal deoxynucleotidyl transferase dUTP nick end labeling- positive blastomeres than did Angus embryos. We concluded that the detrimental effects of heat stress were dependent upon embryo breed and were more evident in Bos taurus embryos than in Bos indicus embryos.

The present study determined the transcriptome profile in Nelore and Holstein oocytes subjected to heat shock during IVM and the mRNA abundance of selected candidate genes in Nelore and Holstein heat-shocked oocytes and cumulus cells (CC). Holstein and Nelore cows were subjected to in vivo follicle aspiration. Cumulus-oocyte complexes were assigned to control (38.5°C, 22h) or heat shock (41°C for 12h, followed by 38.5°C for 10h) treatment during IVM. Denuded oocytes were subjected to bovine microarray analysis. Transcriptome analysis demonstrated 127, nine and six genes were differentially expressed between breed, temperature and the breed×temperature interaction respectively. Selected differentially expressed genes were evaluated by real-time polymerase chain reaction in oocytes and respective CC. The molecular motor kinesin family member 3A (KIF3A) was upregulated in Holstein oocytes, whereas the pro-apoptotic gene death-associated protein (DAP) and the membrane trafficking gene DENN/MADD domain containing 3 (DENND3) were downregulated in Holstein oocytes. Nelore CC showed increased transcript abundance for tight junction claudin 11 (CLDN11), whereas Holstein CC showed increased transcript abundance for antioxidant metallothionein 1E (MT1E) . Moreover, heat shock downregulated antioxidant MT1E mRNA expression in CC. In conclusion, oocyte transcriptome analysis indicated a strong difference between breeds involving organisation and cell death. In CC, both breed and temperature affected mRNA abundance, involving cellular organisation and oxidative stress.

Fibroblast growth factor (FGF10) acts at the cumulus oocyte complex, increasing the expression of cumulus cell expansion-related genes and oocyte competency genes. We tested the hypothesis that addition of FGF10 to the maturation medium improves oocyte maturation, decreases the percentage of apoptotic oocytes and increases development to the blastocyst stage while increasing the relative abundance of developmentally important genes (COX2, CDX2 and PLAC8). In all experiments, oocytes were matured for 22 h in TCM-199 supplemented with 0, 2.5, 10 or 50 ng/ml FGF10. In Experiment 1, after maturation, oocytes were stained with Hoechst to evaluate meiosis progression (metaphase I, intermediary phases and extrusion of the first polar body) and submitted to the TUNEL assay to evaluate apoptosis. In Experiment 2, oocytes were fertilized and cultured to the blastocyst stage. Blastocysts were frozen for analysis of COX2, CDX2 and PLAC8 relative abundance. In Experiment 1, 2.5 ng/ml FGF10 increased (p < 0.05) the percentage of oocytes with extrusion of the first polar body (35%) compared to 0, 10 and 50 ng/ml FGF10 (21, 14 and 12%, respectively) and FGF10 decreased the percentage of oocytes that were TUNEL positive in all doses studied. In Experiment 2, there was no difference in the percentage of oocytes becoming blastocysts between treatments and control. Real-time RT-PCR showed a tendency of 50 ng/ml FGF10 to increase the relative abundance of COX2 and PLAC8 and of 10 ng/ml FGF10 to increase CDX2. In conclusion, the addition of FGF10 to the oocyte maturation medium improves oocyte maturation in vitro, decreases the percentage of apoptotic oocytes and tends to increase the relative abundance of developmentally important genes.

Members of the IGF family are key intra-ovarian regulators of follicle growth, selection, and atresia. Growth differentiation factor 9 (GDF9) induces follicular somatic cells to undergo mitosis and differentiation during follicular development. Cattle from Bos indicus breeds are slower to reach sexual maturity and have longer calving intervals when compared with Bos taurus breeds (Luna-Nevarez et al. 2011). On the other hand, indicine cattle have greater number of ovarian follicles recruited per oestrous cycle when compared with taurine breeds (Alvarez et al. 2000). Our objective was to evaluate the expression of IGF1, IGFR1, IGF2, and GDF9 genes in follicles dissected from Nelore and Angus heifers with high (HFC) and low (LFC) follicle counts. Eighteen Nelore heifers and 22 Angus heifers (≈24 months old) were kept on Brachiaria brizantha grass and fed with a mix of grains with minerals and water ad libitum. Oestrous cycle was synchronized with 2 doses of PGF2α 11 days apart. Heifers were scanned with an ultrasound device (US; Mindray Vet DPS 2200, São Paulo, Brazil) with a 7.5-MHz probe 1 day after ovulation for 3 consecutive oestrous cycles. Animals were slaughtered ≈24 h after ovulation of the third cycle; 3 follicles from 2 to 4 mm in diameter were dissected from the ovary contralateral to the CL. Total RNA was extracted using the RNeasy Microarray Tissue Mini Kit (Qiagen, Valencia, CA, USA). Gene expression was evaluated using oligo-dT reverse transcription, Sybr Green Master Mix and Step One Plus (AB, Foster City, CA, USA) Real-Time PCR Detection System. Samples were analysed in duplicates and CT values were normalized to the housekeeping gene PPIA using the ΔCT method. Results were analysed using the PROC MIXED procedure of SAS with follicle as the repeated measure and cow as the subject. Individual differences were analysed using contrast (SAS 9.2). The effects of group (LFC × HFC), breed, and follicle diameter on mNRA abundance were tested. Follicle LSmean was higher (P < 0.05) in Nelore heifers (32 ± 3.1; LFC = 18; HFC = 52) when compared with Angus heifers (20 ± 2.6; LFC = 10; HFC = 27). Follicle diameter did not differ between breeds or groups. Expression of IGF1 and GDF9 was not different between follicles from Nelore and Angus heifers or between groups. Expression of IGFR1 was higher in follicles from Angus heifers (fold change 1.74; P < 0.04) when compared with follicles derived from Nelore heifers but not different between HFC and LFC groups within each breed. Expression of IGF2 mRNA was also higher (fold change 1.70; P < 0.04) in Angus heifers but not different between HFC and LFC groups within each breed. In conclusion, the higher expression of IGFR1 and IGF2 in Angus early antral follicles might be involved in important reproductive traits commonly observed in Bos taurus breeds. However, expression of IGF1, IGFR1, IGF2, and GDF9 in the follicle are not involved in the mechanisms determining different number of follicle recruited through the oestrous cycle in the same breed. This research and scholarship for Loureiro, Ereno, Favoureto, and Pupulim was from FAPESP.