196 Fertilization Rate in Superovulated Criolla Goats Following Artificial Insemination or Natural Mating

2018 ◽  
Vol 30 (1) ◽  
pp. 238
Author(s):  
M. I. Cueto ◽  
J. Fernandez ◽  
M. M. Bruno-Galarraga ◽  
F. Pereyra-Bonnet ◽  
A. Gibbons

The Criolla breed is a local genetic resource, distributed in Patagonia, Argentina, whose primary production is meat. In the Criolla goat, efforts were made to locate productively superior males and to conserve their genetic material. Studies were carried on the feasibility of obtaining superior offspring through the implementation of embryo transfer programs. We assessed the fertilization rate and embryo production following AI with frozen semen or natural mating in Criolla goats subjected to a superovulation program. During the breeding season (May, 41° S), 26 Criolla goats were treated for oestrus with sponges (60 mg of medroxyprogesterone acetate, Progespon®, Syntex, Buenos Aires, Argentina) placed for 13 days. Goat donors were superovulated with a total of 80 mg of porcine (p)FSH (Folltropin V®, Bioniche, Ontario, Canada) every 12 h in 6 decreasing doses (18, 18, 14, 14, 8, and 8 mg) during the last 3 days of progestagen treatment. A dose of 125 μg of cloprostenol (Estrumate®, Schering-Plough, Quebec, Canada) was given in conjunction with the first dose of pFSH. Oestrus detection was performed every 12 h, starting at 24 h after sponge removal. Females were considered to be in oestrus if they passively accepted buck mounting. Goats were randomly assigned to the following treatments: (1) natural mating (NM, n = 12): donors detected in oestrus were individually mated with one proven fertile buck at oestrus and 12 h post-oestrus; does were remove from the male in between (Conventionally accepted treatment); (2) AI (n = 14): donors detected in oestrus were inseminated 12 ± 2 h after the onset of oestrus by laparoscopy with frozen-thawed semen (200 × 106 spermatozoa) from the same fertile buck. Embryo recovery was done by surgical prepubic laparotomy at Day 8 after sponge removal. Superovulation response was estimated by counting the number of corpora lutea (CL). Analysis of variance was used to compare fertilization rate (total number of embryos recovered for each animal, expressed as a proportion of the total number of embryos/oocytes recovered) and embryo production between treatments. Results were expressed as mean ± SEM. Statistical significance was accepted at P < 0.05. A total of 92.3% goats were recorded in oestrus (24/26) between 24 and 48 h after sponge removal (10 and 14 goats for NM and AI, respectively). An average of 16.6 ± 2.0 CL (range: 2–32) was observed in response to superovulation treatment. The recovery rate of embryos/oocytes was 60.0 ± 6.9%. No statistical difference was observed in the fertilization rate (52.1 ± 12.1 and 68.6 ± 12.1% for AI and NM, respectively) or the number of total (6.8 ± 2.0 and 4.8 ± 2.4 for AI and NM, respectively) and transferable embryos (5.6 ± 1.4 and 4.0 ± 1.7 for AI and NM, respectively) between treatments (P > 0.05). In conclusion, fertilization rates did not differ following laparoscopic insemination with frozen semen compared to natural mating in superovulated Criolla goats.

2015 ◽  
Vol 36 (6Supl2) ◽  
pp. 4215
Author(s):  
João Bosco Loiola Filho ◽  
Alane Pains Oliveira do Monte ◽  
Thais Thatiane Dos Santos Souza ◽  
Mayara De Souza Miranda ◽  
Lívia Correia Magalhães ◽  
...  

To evaluate the effect of pFSH dose on the in vivo embryo production of Dorper ewes in the semi-arid northeast of Brazil, 40 sheep females were distributed into two groups of 20 animals that received intravaginal CIDR for 14 days, and two days before device removal, they received one of the following treatments: in the FSH200 group, the ewes received 200 mg of pFSH; and in the FSH128 group, the ewes received a total of 128 mg in decreasing doses every 12 h. Beginning 12 h after the conclusion of the treatments, estrus detection was performed every four hours using two Dorper rams of proven fertility. The ewes were mated at estrus onset and 24 hours later. Seven days after intravaginal device removal, the superovulatory response was evaluated, and embryo collection was performed using the laparotomy method. The recovered flushings were subjected to embryo searches under a stereomicroscope and classified according to their qualities. Analyses of variance (ANOVAs) and LSD tests were used to compare the different parameters. The data expressed as percentages were analysed by chi-square test. The ovulation rate was higher in the FSH200 group, which had 16.3 ± 0.3 corpora lutea (CL), than in the FSH128 group, which had 11.3 ± 0.3 CL (P<0.05). However, higher fertilization rate (83.6% vs. 62.4%) and higher transferable (86.0% vs. 71.6%) and freezable (67.9% vs. 40.8%) embryo rates were observed in the FSH 128 group compared with the group that received 200 mg. Furthermore, no significant differences in the remaining parameters were observed between the experimental groups (P>0.05), demonstrating that pFSH dose reduction promoted a greater production of freezable and transferable embryos in Dorper ewes subjected to MOET.


2010 ◽  
Vol 22 (9) ◽  
pp. 40
Author(s):  
K. H. Beilby ◽  
Y. B. Kaurivi ◽  
W. M. C. Maxwell ◽  
G. Evans ◽  
S. P. De Graaf ◽  
...  

Flow cytometric sex-sorting of sperm that has previously been cryopreserved allows sex-sorting technology to be applied more widely. While offspring have been produced following artificial insemination of synchronised ewes with frozen-thawed, sex-sorted and refrozen-thawed (FSF) sperm (1), the fertility of FSF-sperm in superovulated ewes has not been reported. The aim of this study was to determine the effect of cryopreservation prior to sperm sex-sorting and freezing on embryo production in superovulated ewes. Several ejaculates from 2 rams were either frozen-thawed, then sex-sorted and re-frozen (FSF X- and Y-chromosome enriched sperm), or immediately sex-sorted before freezing (SF X- and Y-chromosome enriched sperm). A portion of each ejaculate was also cryopreserved without sex-sorting (control). Thirty-one ewes were superovulated and inseminated (15 ×106 sperm per insemination dose) with either SF X, SF Y, FSF X, FSF Y or control sperm as previously described (2). Embryos were recovered 6 d after insemination and assessed. The superovulatory response (mean number of corpora lutea per ewe: 11.8 ± 1.3) and the embryo recovery rates (72.0 ± 5.9%) did not differ significantly among the groups. The fertilisation rates tended to differ (P=0.068) as a result of sperm treatment (control: 33%; SF: 54%; FSF: 18%) and were unaffected by sperm sex (X: 33%; Y: 37%). Of the embryos that were recovered, those derived from FSF-sperm were predominantly at the blastocyst stage (65%), whereas those derived from SF-sperm were evenly distributed among the blastocyst (30%), morula (38%) and arrested (32%) stages, suggesting that fertilisation lifespan of SF-sperm was greater than that of FSF-sperm. A greater proportion of embryos derived from Y-sperm were at the blastocyst stage compared with embryos derived from X-sperm (53% vs. 26%; P < 0.05). This study is the first to demonstrate that FSF-sperm is capable of fertilising oocytes of superovulated ewes. (1) de Graaf et al (2007) Theriogenology 67: 391–8.(2) de Graaf et al (2007) Theriogenology 67: 550–5.


2015 ◽  
Vol 36 (6Supl2) ◽  
pp. 4215 ◽  
Author(s):  
João Bosco Loiola Filho ◽  
Alane Pains Oliveira do Monte ◽  
Thais Thatiane Dos Santos Souza ◽  
Mayara De Souza Miranda ◽  
Lívia Correia Magalhães ◽  
...  

<p>To evaluate the effect of pFSH dose on the <em>in vivo </em>embryo production of Dorper ewes in the semi-arid northeast of Brazil, 40 sheep females were distributed into two groups of 20 animals that received intravaginal CIDR for 14 days, and two days before device removal, they received one of the following treatments: in the FSH200 group, the ewes received 200 mg of pFSH; and in the FSH128 group, the ewes received a total of 128 mg in decreasing doses every 12 h. Beginning 12 h after the conclusion of the treatments, estrus detection was performed every four hours using two Dorper rams of proven fertility. The ewes were mated at estrus onset and 24 hours later. Seven days after intravaginal device removal, the superovulatory response was evaluated, and embryo collection was performed using the laparotomy method. The recovered flushings were subjected to embryo searches under a stereomicroscope and classified according to their qualities. Analyses of variance (ANOVAs) and LSD tests were used to compare the different parameters. The data expressed as percentages were analysed by chi-square test. The ovulation rate was higher in the FSH200 group, which had 16.3 ± 0.3 corpora lutea (CL), than in the FSH128 group, which had 11.3 ± 0.3 CL (P&lt;0.05). However, higher fertilization rate (83.6% vs. 62.4%) and higher transferable (86.0% vs. 71.6%) and freezable (67.9% vs. 40.8%) embryo rates were observed in the FSH 128 group compared with the group that received 200 mg. Furthermore, no significant differences in the remaining parameters were observed between the experimental groups (P&gt;0.05), demonstrating that pFSH dose reduction promoted a greater production of freezable and transferable embryos in Dorper ewes subjected to MOET.</p>


2010 ◽  
Vol 9 (2) ◽  
pp. 1
Author(s):  
O. I. Azawi, and M. K. M. A. Al-Mola

The present study was undertaken to investigate the contribution of laparoscopic insemination to the improvement of fertilization and embryo recovery. The experiment was conducted in the breeding season. Twelve nonpregnant and cycling Awassi ewes of 3-4 years of age were randomly allocated in equal number (n = 6) to two groups. Each ewe was treated with progesterone impregnated intravaginal sponge for 12 days. All ewes were superovulated with eCG (equine chorionic gonadotropin) 1200 IU once by intramuscular injection 48 h prior to sponge removal. Ewes of group 1 were mated naturally at least two times with Awassi rams of proven fertility. Ewes of group 2 had intrauterine insemination and were conducted 44-46 h after sponge removal, under laparoscopic visualization of uterine horns, depositing 1 ml of semen in the distal portion of each uterine horn. Ovarian response was assessed by determining the number of corpora lutea by laparoscopy on day 6 after mating. Embryo recovery was performed by semi-laparoscopic and by flushing of both uterine horns. Results of the present study revealed a high number of unfertilized ova (P<0.05) was observed in ewes when naturally inseminated than ewes inseminated intrauterine using the laparoscopic technique. The higher rate of embryo recovery (P<0.05) was achieved when ewes inseminated via intrauterine (4.66 ± 0.66) than ewes naturally mated (2.16 ± 0.74). The fertilization rate in ewes inseminated intrauterine using laparoscopic techniques and naturally mated were 79.93% and 40.07%, respectively. Fertilization failure in ewes inseminated intrauterine using laparoscopic techniques and naturally mated were 7.37% and 49.35%, respectively. It could be concluded that the use of eCG to induce superovulation in Awassi ewes combined with laparoscopic intrauterine insemination can increase the fertilization rate.


2013 ◽  
Vol 25 (1) ◽  
pp. 268
Author(s):  
M. Kaymaz ◽  
A. R. Agaoglu ◽  
K. Karakas ◽  
I. Pir Yagci ◽  
O. Korkmaz Agaoglu ◽  
...  

The Angora, Kilis, Honamli, Hair, and Norduz are native goat breeds in Turkey and are currently in danger of extinction. This study aimed to assess the efficacy of the repeated administration of a superovulatory (SOV) protocol for in vivo embryo production in these breeds. A total of 14 Angora, 15 Kilis, 10 Honamli, 10 Hair, and 9 Norduz goats were used in this work. The synchronization procedure was started on Day 5 after visible oestrus by using controlled internal drug release dispensers (CIDR®) for 11 days. Administration of FSH (Folltropin®) began on Day 9 (twice daily) and continued for 3 days (total dose: 200 mg; 50 mg × 2.30 mg × 2.20 mg × 2). A dose of prostaglandin F2α (1.6 mg; Dalmazin®) was injected together with first FSH injection. Gonadotropin-releasing hormone (Receptal®: 100 µg) was injected 6 h before mating. All goats in oestrus were naturally mated twice a day for 3 days. Ovarian examination (number of corpora lutea) and embryo recovery were performed by laparotomy on Day 6 after CIDR® withdrawal. Each uterine horn was flushed, and the embryos were recovered and counted. To avoid intra-abdominal adhesions, a 2.5% heparin solution was used during flushing. The SOV procedure was repeated once per year during the breeding season (2009 to 2011). Fertilization and recovery rates were calculated. Differences in the SOV response and embryo yields were evaluated by Friedman’s test. In Hair goats, the number of corpora lutea decreased significantly (P < 0.05) during the third SOV cycle (12.7 ± 6.2, 14.0 ± 9.1, and 6.8 ± 5.6, respectively, for cycles 1, 2, and 3), whereas no effect of the cycle was observed in the remainder of breeds. The number of expanded blastocysts increased considerably during the third cycle in Angora (0, 0.2 ± 0.8, and 1.4 ± 2.9, respectively, for cycles 1, 2, and 3), Kilis (0.2 ± 0.4, 0.3 ± 1.3, and 4.2 ± 5.0), and Honamli (0, 1.3 ± 1.7, and 3.6 ± 4.5) goats, whereas a significant decrease was observed in Norduz goats (2.4 ± 5.0, 1.8 ± 2.0, and 0.1 ± 0.3; P < 0.05). The mean numbers of unfertilized oocytes were found to be significantly increased in Angora (0.4 ± 1.6, 0, and 2.1 ± 4.1, respectively, for cycles 1, 2, and 3), Kilis (0, 1.3 ± 3.9, and 3.1 ± 5.2), and Honamli (0, 4.9 ± 5.2, and 4.5 ± 7.8) goats (P < 0.05). As a result, fertilization rates (%) showed a decrease in Angora (50, 100, 24.5, respectively, for cycles 1, 2, and 3) and Honamli (100, 42.5, and 56.3) goats (P < 0.05), whereas recovery rates showed no difference among the different breeds. The methodology presented in this study was found to be an efficient technique for superovulation of the Angora, Kilis, and Honamli goats. Because Hair and Norduz are relatively small breeds, the dosage of FSH might have had a negative effect on the superovulation and embryo yield. Additionally, the use of intra-abdominal washing solutions for preventing adhesions as observed in previous works (data not shown) is believed to have a positive effect on achieving high levels of efficiency in in vivo embryo production.


2011 ◽  
Vol 10 (2) ◽  
pp. 36
Author(s):  
O. I. Azawi

The development of an efficient and practical method for transcervical collection of embryos in Awassi ewes to the improvement of embryo recovery was investigated. Twenty-four non-pregnant Awassi ewes of 3-4 years of age were randomly allocated into two groups (n = 12). Each ewe was treated with a progesterone impregnated intra-vaginal sponge for 12 days. The following superovulation treatment was used: ewes received 1200 IU of eCG once as an intramuscular injection 48 h prior to sponge withdrawal. Ovarian response was assessed by determining the number of corpora lutea by laparoscopy at day 6 after mating. Ewes of group 1 (n = 12) their embryos were recovered using the semi-laparoscopic technique. Ewes of group 2 (n = 12) their embryos were recovered using the transcervical technique. All ewes of this group on the evening of day 5 post inseminations, received an i.m. injection of estradiol 17β 2 mg, 12h later, i.v. injection of 10 IU of oxytocin. A bovine teat dilator introduced into the cervical canal and gradually dilated in order to dilate and open the cervical canal with a help of screw provided with the instrument. Results of the present study showed that there was no significant difference in the number of recovered embryos in superovulated ewes when animals treated with estradiol and oxytocin with transcervical technique and semi-laparoscopic technique. It was possible to pass the catheter through the cervix with the aid of bovine teat dilator enhanced by estradiol and oxytocin treatment. In conclusion, the technique for transcervical collection of the embryo from ewes, as described in the present study, may give new encouragement to embryo transfer programs in this species.


1988 ◽  
Vol 22 (1) ◽  
pp. 5-15 ◽  
Author(s):  
B. Fischer ◽  
G. Meuser-Odenkirchen

Routinely employed reproductive techniques such as gonadotropin treatment (0·3 mg follicle-stimulating hormone (FSH) subcutaneously twice daily for three consecutive days) followed by natural mating or artificial insemination as well as induction of ovulation by human chorionic gonadotropin (hCG) (75 i.u. hCG intravenously) were analysed in the rabbit after 2 years of consecutive experiments. 85% of gonadotropin-treated animals mated spontaneously. All 222 FSH-primed donor rabbits and 59 hCG-injected non-primed controls ovulated. The average number of ovulations per female was 30 (FSH and hCG) and 7·4 (hCG only). The fertilization rate was 88%, and 22·7 embryos were recovered per FSH-treated donor rabbit. With increasing time after mating the embryo recovery rate decreased (day 1 post coitum (p.c.), 36 embryos per rabbit; day 3 p.c., 26 embryos per rabbit; day 5 p.c., 16 embryos per rabbit) and a higher percentage of females had no embryos recovered. Embryo recovery was poor in donors with ovulation numbers greater than 40. Artificial insemination of non-receptive females yielded smaller numbers of embryos compared with natural mating. Differences in fertility between the seasons of the year was revealed to be small. We conclude that gonadotropin treatment is efficient in increasing the number of embryos. Management of laboratory rabbits (dating, mating and expected number of embryos) is more predictable, and experiments can be performed successfully in all seasons of the year. However, the incidence of embryonic mortality seems to be increased when gonadotropin treatment is applied.


2020 ◽  
Vol 60 (4) ◽  
pp. 497 ◽  
Author(s):  
Pedro Henrique Nicolau Pinto ◽  
Mario Felipe Alvarez Balaro ◽  
Helena Fabiana Reis de Almeida Saraiva ◽  
Viviane Lopes Brair ◽  
Vivian Angélico Pereira Alfradique ◽  
...  

Context In vivo embryo production, also called multiple ovulation and embryo transfer, can accelerate genetic gain, and thus improve animal production. However, there are issues limiting a wider use of this biotechnology in sheep livestock. Aims This study aimed to determine (1) whether a previous response to superovulation (SOV) can be used as a criterion to select ewes for in vivo embryo production, (2) whether the intensity of the SOV response (number of corpora lutea, CL) can affect the embryo recovery rate, and (3) whether the number of CL quantified by colour Doppler ultrasonography can be used to calculate the recovery rate. Methods Twenty-five Santa Inês ewes underwent SOV three times (SOV1, SOV2 and SOV3), with 200 mg FSH and natural mating. The number of CL after each SOV was determined by laparoscopy and by colour Doppler ultrasonography. Key results The number of CL significantly decreased (P &lt; 0.05) after SOV1 (7.5 ± 4.8) to 3.0 ± 5.0 at SOV 2 and 2.2 ± 3.5 at SOV3. Strong correlations were observed between SOV2 and SOV3 in terms of numbers of CL (r = 0.86, r2 = 0.74; P &lt; 0.0001) and viable embryos (r = 0.79, r2 = 0.63; P &lt; 00001). However, no correlations were observed between SOV1 and SOV2 or between SOV1 and SOV3. Recovery rate did not differ with the intensity of the SOV response (≤6, 7–10, &gt;10 CL) or between the methods used to quantify CL. Conclusions Ewes did not show the same pattern of response when submitted to successive FSH-based SOV. The intensity of the SOV response did not affect the recovery rate, and the number of CL estimated by colour Doppler ultrasonography can be used to calculate the recovery rate. Implications Selecting sheep embryo donors by a previous SOV response is not always feasible. The recovery rate is homogeneous and it is not affected by the intensity of the SOV response. A nonsurgical technique can be used to assess the recovery rate, improving animal welfare in MOET programs.


2020 ◽  
Vol 32 (2) ◽  
pp. 159
Author(s):  
J. Berdugo ◽  
A. Tarazona-Morales ◽  
J. Echeverry-Zuluaga ◽  
W. Cardona Maya ◽  
A. López-Herrera ◽  
...  

The development of markers for reproductive function has been a goal for the embryo production industry and reproductive biology as a method to improve success and increase the ability to explain reproductive phenomena. Cattle and buffalo are bovines that show different reproductive parameters raised in the same conditions. The aim of this work was to compare the results of the invitro production of cows (Bos indicus) and buffalo (Bubalus bubalis) from animals kept under the same conditions of feeding and handling. This study was conducted in an Argentinian commercial herd of buffalo and cattle located in the province of Corrientes (−27.742859 latitude, −57.773611 longitude) during the breeding season of 2018 (March-May). Twenty animals of each species were used. Anti-Mullerian hormone (AMH) levels of each animal were determined using ELISA. Standardized protocols were used for oocyte aspiration, maturation, fertilisation, and culture of the embryos, and frozen semen of a single proven bull was used in each species. The numbers of follicles, oocytes, and embryos were recorded and analysed individually and grouped by species (Table 1). The normality of the data was evaluated with the D’Agostino and Shapiro-Wilk tests and the comparisons between species using the Mann-Whitney and ANOVA tests, and correlation analysis was performed using the Spearman test. Values are shown as median and range. A P-value &lt;0.05 was considered statistically significant. The AMH levels of the cows were 688.5 pgmL−1 (45.3-2394) and the buffalo were 73.8 pgmL−1 (14.8-262.5); P&lt;0.001. Significant differences were found in the number of recovered oocytes of 9 (0-23) for cows vs. 4.5 (1-11) for buffalo (P&gt;0.05). There were no significant differences in the number of follicles and the quality of the oocytes. Significant differences were found in the number of oocytes cleaved of 4 (0-17) vs. 0.5 (0-4) and blastocysts per animal of 1.5 (0-15) vs. 0.1 (0-2) for cows and buffalo, respectively. The number of blastocysts in relation to the number of oocytes cleaved did not show statistical significance. In spite of the difference in the AMH levels and the embryo production parameters, which were lower in buffalo, no correlation was found between AMH and the parameters studied in both species. The results obtained here are confirmed by others in the literature. Levels of AMH as a marker for embryo production are not useful in cattle and buffalo and do not explain the differences observed, certainly AMH is a marker for quantity as the preserver of the ovarian reserve. Table 1.Comparison of individual values of AMH levels, oocyte quality, and embryo production between cattle and buffalo Parameter Median (range) P-value Cattle Buffalo AMH (pgmL−1) 688.5 (45.3-2394) 73.8 (14.8-262.5) &lt;0.001 Follicles Follicles RO 3 (0-9) 4 (0-6) Follicles LO 5 (0-10) 4 (1-8) Total follicles 7 (2-18) 7 (2-12) Oocyte quality GI 2 (1-3) 1.5 (1-3) 0.22 GII 2 (1-9) 2 (1-6) 0.67 GIII 2.5 (0-18) 2 (1-4) 0.91 GIV 1 (1-5) 2 (1-4) 0.10 Total oocytes 9 (0-23) 4.5 (1-11) 0.02 Total viable 5.5 (0-21) 5 (0-11) 0.36 Cleavage 4 (0-17) 0.5 (0-4) 0.01 Blastocyst 1.5 (0-15) 0.1 (0-2) 0.02


Animals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 216
Author(s):  
Hernan Baldassarre

The potential of laparoscopic ovum pick-up (LOPU) followed by in vitro embryo production (IVEP) as a tool for accelerated genetic programs in ruminants is reviewed in this article. In sheep and goats, the LOPU-IVEP platform offers the possibility of producing more offspring from elite females, as the procedure is minimally invasive and can be repeated more times and more frequently in the same animals compared with conventional surgical embryo recovery. On average, ~10 and ~14 viable oocytes are recovered by LOPU from sheep and goats, respectively, which results in 3–5 transferable embryos and >50% pregnancy rate after transfer. LOPU-IVEP has also been applied to prepubertal ruminants of 2–6 months of age, including bovine and buffalo calves. In dairy cattle, the technology has gained momentum in the past few years stemming from the development of genetic marker selection that has allowed predicting the production phenotype of dairy females from shortly after birth. In Holstein calves, we obtained an average of ~22 viable oocytes and ~20% transferable blastocyst rate, followed by >50% pregnancy rate after transfer, declaring the platform ready for commercial application. The present and future of this technology are discussed with a focus on improvements and research needed.


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