Effect of three schemes of ovum pick-up on the follicular dynamics, gene expression, and in-vitro developmental competence of oocytes in Sahiwal cattle.


Journal

Reproduction in domestic animals = Zuchthygiene
ISSN: 1439-0531
Titre abrégé: Reprod Domest Anim
Pays: Germany
ID NLM: 9015668

Informations de publication

Date de publication:
Oct 2022
Historique:
revised: 16 06 2022
received: 13 05 2022
accepted: 28 06 2022
pubmed: 1 7 2022
medline: 12 10 2022
entrez: 30 6 2022
Statut: ppublish

Résumé

This study aimed to compare the effect of three schemes of ovum pick-up (OPU) on follicular dynamics, oocytes recovery, oocytes quality, gene expression, nuclear maturation and in-vitro developmental competence of oocytes in Sahiwal cattle. Considering the follicle population, all the cows were divided equally in a 3 × 3 cross over design, and each cow received one of the three treatments: (a) twice weekly (TW; n = 6), (b) once weekly (OW; n = 6) and (c) bi-weekly OPU (BW; n = 6) in three periods, with the first OPU conducted on 4, 7 and 14 days after second dominant follicle puncture (DFP) in the TW, OW and BW OPU interval groups, respectively. The collected cumulus oocytes complexes (COCs) were graded into A, B, C and D grades depending on the number of layers of cumulus cells and homogeneous nature of cytoplasm. Nuclear maturation was assessed by staining the oocytes with Hoechst 33342. The growth rate (mm/day) of dominant follicle (DF) (F1) (0.49 ± 0.21 vs. 0.71 ± 0.26 vs. 1.30 ± 0.27) and first subordinate follicle (F2) (0.85 ± 0.27 vs. 0.71 ± 0.25 vs. 1.06 ± 0.29) did not differ (p > .05) among all the three groups. The proportion of animals bearing a corpus luteum (CL) in the BW OPU interval group (53.3%) was significantly higher (p < .05) as compared to TW (13.3%) and OW (18.3%) OPU interval groups. The number of medium-sized follicles and oocyte with grade A and B were significantly higher (p < .05) in the TW (1.16 ± 0.21 and 33.88 ± 0.03) OPU interval group as compared to the OW (0.88 ± 0.22 and 21.54 ± 0.03) and BW (0.55 ± 0.21 and 21.89 ± 0.02) OPU interval groups. However, the number of degenerated oocytes in BW (0.85 ± 0.16) OPU interval group was significantly higher (p < .05) as compared to the TW (0.16 ± 0.15) and OW (0.44 ± 0.16) OPU interval groups. Expression level of growth differentiation factor 9 in TW OPU interval group was significantly higher (p < .05) as compared to the OW and BW OPU interval groups. Likewise, expression level of bone morphogenetic protein 15 (BMP15) in the TW and BW OPU interval groups was significantly higher (p < .05) as compared to the OW OPU interval group. The nuclear maturation rate was significantly higher in the TW (63.64 ± 0.07) and BW (59.26 ± 0.08) OPU groups as compared to OW (51.43 ± 0.06) OPU interval group. However, the cleavage rate (59.30 ± 0.06 vs. 44.29 ± 0.06 vs. 56.67 ± 0.06) did not differ (p > .05) among the three groups. Whereas, the blastocyst rate tended to be higher (p = .06) in the TW (29.07 ± 0.05) and BW (28.33 ± 0.04) OPU interval groups as compared to OW (18.57 ± 0.05) OPU interval group. Taken together, it can be concluded that TW OPU interval scheme enhances the medium-sized follicles resulting in good quality oocytes, regulates the oocyte-derived paracrine factors, leading to higher nuclear maturation rates and improved embryonic development in-vitro.

Identifiants

pubmed: 35771838
doi: 10.1111/rda.14198
doi:

Substances chimiques

Bone Morphogenetic Protein 15 0
Growth Differentiation Factor 9 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1230-1243

Subventions

Organisme : Technology Development Fund (Higher Education Commission, Pakistan)
ID : TDF-02-059

Informations de copyright

© 2022 Wiley-VCH GmbH.

Références

Aboul-Ela, M. (2000). Superovulation in the buffalo: Constraints and manipulation. Buffalo Journal, 16, 1-20.
Acosta, T., Hayashi, K., Ohtani, M., & Miyamoto, A. (2003). Local changes in blood flow within the preovulatory follicle wall and early corpus luteum in cows. Reproduction-Cambridge, 125, 759-767.
Ali, A., & Hayder, M. (2008). Seasonal variation of reproductive performance, foetal development and progesterone concentrations of sheep in the subtropics. Reproduction in Domestic Animals, 43, 730-734.
Badinga, L., Thatcher, W., Wilcox, C., Morris, G., Entwistle, K., & Wolfenson, D. (1994). Effect of season on follicular dynamics and plasma concentrations of estradiol-17β, progesterone and luteinizing hormone in lactating Holstein cows. Theriogenology, 42, 1263-1274.
Baruselli, P., Batista, E., Vieira, L., Ferreira, R., Guerreiro, B., Bayeux, B., Sales, J., Souza, A., & Gimenes, L. (2018). Factors that interfere with oocyte quality for in vitro production of cattle embryos: Effects of different developmental & reproductive stages. Animal Reproduction, 13, 264-272.
Boni, R., Roelofsen, M. W. M., Pieterse, M. C., Kogut, I., & Kruip, T. A. M. (1997). Follicular dynamics, repeatability and predictability of follicular recruitment in cows submitted to repeated follicular puncture. Theriogenology, 48, 277-289.
Chaubal, S., Molina, J. A., Ohlrichs, C. L., Ferre, L. B., Faber, D. C., Bols, P. E. J., Riesen, J. W., Tian, X., & Yang, X. (2006). Comparison of different transvaginal ovum pick-up protocols to optimise oocyte retrieval and embryo production over a 10-week period in cows. Theriogenology, 65(8), 1631-1648.
Chazotte, B. (2011). Labeling nuclear DNA with Hoechst 33342. Cold Spring Harbor Protocols, 2011, pdb-prot5557.
Di Francesco, S., Novoa, M. V. S., Vecchio, D., Neglia, G., Boccia, L., Campanile, G., Zicarelli, L., & Gasparrini, B. (2012). Ovum pick-up and in vitro embryo production (OPU-IVEP) in Mediterranean Italian buffalo performed in different seasons. Theriogenology, 77, 148-154.
Dorice, A. K., Ferdinand, N., Justin, K., Augustave, K., & Linda, K. K. (2019). Effects of breed, age, body condition score, and nutritional status on follicular population, oocyte yield, and quality in three cameroonian zebus cattle Bos indicus. Advances in Agriculture, 2019, 15. https://doi.org/10.1155/2019/2979740
Ferguson, J. D., Galligan, D. T., & Thomsen, N. (1994). Principal descriptors of body condition score in Holstein cows. Journal of Dairy Science, 77, 2695-2703.
Ferraz, M. L., Sá Filho, M. F. D., Batista, E. O. S., Watanabe, Y. F., Watanabe, M. R., Dayan, A., Joaquim, D. C., Accorsi, M. R., Gimenes, L. U., & Vieira, L. M. (2015). Paradoxical effects of bovine somatotropin treatment on the ovarian follicular population and in vitro embryo production of lactating buffalo donors submitted to ovum pick-up. Animal Reproduction Science, 154, 1-7.
Gibbons, J., Beal, W., Krisher, R., Faber, E., Pearson, R., & Gwazdauskas, F. (1994). Effects of once-versus twice-weekly transvaginal follicular aspiration on bovine oocyte recovery and embryo development. Theriogenology, 42, 405-419.
Glass, E. J., Preston, P. M., Springbett, A., Craigmile, S., Kirvar, E., Wilkie, G., & Brown, C. D. (2005). Bos taurus and Bos indicus (Sahiwal) calves respond differently to infection with Theileria annulata and produce markedly different levels of acute phase proteins. International Journal for Parasitology, 35, 337-347.
Guilbault, L., Rouillier, P., Matton, P., Glencross, R., Beard, A., & Knight, P. (1993). Relationships between the level of atresia and inhibin contents (α subunit and α-β dimer) in morphologically dominant follicles during their growing and regressing phases of development in cattle. Biology of Reproduction, 48, 268-276.
Hendriksen, P., Steenweg, W., Harkema, J., Merton, J., Bevers, M., Vos, P., & Dieleman, S. (2004). Effect of different stages of the follicular wave on in vitro developmental competence of bovine oocytes. Theriogenology, 61, 909-920.
Jin, J.-I., Ghanem, N., Kim, S.-S., Choi, B.-H., Ha, A.-N., Lee, K.-L., Sun, D.-W., Lim, H.-T., Lee, J.-G., & Kong, I.-K. (2016). Interaction of donor age, parity and repeated recovery of cumulus-oocyte complexes by ovum pick-up on in vitro embryo production and viability after transfer. Livestock Science, 188, 43-47.
Kastrop, P., Bevers, M., Destree, O., & Kruip, T. A. (1990). Analysis of protein synthesis in morphologically classified bovine follicular oocytes before and after maturation in vitro. Molecular Reproduction and Development, 26, 222-226.
Khan, M. J., Abbas, A., Naeem, M., Ayaz, M. M., & Akhter, S. (2013). Current issues and future prospects of dairy sector in Pakistan. Science, Technology and Development, 32, 126-139.
Khan, M., Khan, M., & Waheed, A. (2018). Morphological measurements and their heritabilities for Sahiwal cattle in Pakistan. JAPS, Journal of Animal and Plant Sciences, 28, 431-440.
Konrad, J., Clérico, G., Garrido, M. J., Taminelli, G., Yuponi, M., Yuponi, R., Crudeli, G., & Sansinena, M. (2017). Ovum pick-up interval in buffalo (Bubalus bubalis) managed under wetland conditions in Argentina: Effect on follicular population, oocyte recovery, and in vitro embryo development. Animal Reproduction Science, 183, 39-45.
Kruip, T. A., Pieterse, M., Van Beneden, T. H., Vos, P., Wurth, Y., & Taverne, M. (1990). Increased success rate of IVM and IVF in the bovine after sonographic guided transvaginal collections of the oocytes. Theriogenology, 33, 269.
Li, Y., Li, R.-Q., Ou, S.-B., Zhang, N.-F., Ren, L., Wei, L.-N., Zhang, Q.-X., & Yang, D.-Z. (2014). Increased GDF9 and BMP15 mRNA levels in cumulus granulosa cells correlate with oocyte maturation, fertilization, and embryo quality in humans. Reproductive Biology and Endocrinology, 12, 1-9.
Livak, K. J., & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods, 25, 402-408.
Lonergan, P., Monaghan, P., Rizos, D., Boland, M., & Gordon, I. (1994). Effect of follicle size on bovine oocyte quality and developmental competence following maturation, fertilization, and culture in vitro. Molecular Reproduction and Development, 37, 48-53.
Lopes, A., Martinussen, T., Greve, T., & Callesen, H. (2006). Effect of days post-partum, breed and ovum pick-up scheme on bovine oocyte recovery and embryo development. Reproduction in Domestic Animals, 41, 196-203.
Lozano, J., Abecia, J., Forcada, F., Zarazaga, L., & Alfaro, B. (1998). Effect of undernutrition on the distribution of progesterone in the uterus of ewes during the luteal phase of the estrous cycle. Theriogenology, 49, 539-546.
Lucy, M. (2001). Reproductive loss in high-producing dairy cattle: Where will it end? Journal of Dairy Science, 84, 1277-1293.
Merton, J., De Roos, A., Mullaart, E., De Ruigh, L., Kaal, L., Vos, P., & Dieleman, S. (2003). Factors affecting oocyte quality and quantity in commercial application of embryo technologies in the cattle breeding industry. Theriogenology, 59, 651-674.
Montjean, D., Entezami, F., Lichtblau, I., Belloc, S., Gurgan, T., & Menezo, Y. (2012). Carnitine content in the follicular fluid and expression of the enzymes involved in beta oxidation in oocytes and cumulus cells. Journal of Assisted Reproduction and Genetics, 29, 1221-1225.
Nawaz, M., Saleem, M., Ullah, F., Shabbir Khan, G., Zahoor, I., Ahmad, N., & Riaz, A. (2022). Exogenous progesterone-dependent modulation in the follicular dynamics of Bos indicus cattle undergoing repeated ovum pick-up sessions. Reproduction in Domestic Animals, 57, 55-63.
Nawaz, M., Saleem, M., Yaseen, M., Sagheer, M., Zahoor, I., Ahmad, N., & Riaz, A. (2021). Ovarian stimulation through FSH improves follicular harvesting and blastocyst yield in Bos indicus cattle.
Neglia, G., Gasparrini, B., Vecchio, D., Boccia, L., Varricchio, E., Di Palo, R., Zicarelli, L., & Campanile, G. (2011). Long term effect of ovum pick-up in buffalo species. Animal Reproduction Science, 123, 180-186.
Petyim, S., Båge, R., Hallap, T., Bergqvist, A.-S., Rodrı́guez-Martı́nez, H., & Larsson, B. (2003). Two different schemes of twice-weekly ovum pick-up in dairy heifers: Effect on oocyte recovery and ovarian function. Theriogenology, 60, 175-188.
Rabiee, A., Lean, I., Gooden, J., & Miller, B. (1999). Relationships among metabolites influencing ovarian function in the dairy cow. Journal of Dairy Science, 82, 39-44.
Ratto, M., Peralta, O., Mogollon, G., Strobel, P., & Correa, J. (2011). Transvaginal ultrasound-guided cumulus oocyte complexes aspiration and in vitro embryo production in suckled beef and lactating dairy cattle on pasture-based management conditions. Animal Reproduction Science, 129, 1-6.
Reynolds, L. P., Grazul-Bilska, A. T., & Redmer, D. A. (2000). Angiogenesis in the corpus luteum. Endocrine, 12, 1-9.
Saad, M., Sarwar, Z., Saleem, M., Arshad, U., Shahzad, M., Mushtaq, M. H., Husnain, A., Riaz, A., & Ahmad, N. (2019). Effect of plasma progesterone on oocyte recovery, oocyte quality, and early in-vitro developmental competence of embryos in Bos indicus dairy cows. Animal Reproduction Science, 202, 80-86.
Sagheer, M., Ullah, F., Arshad, U., Saleem, M., Nawaz, M., Sarwar, Z., Saad, M., Riaz, A., Ul Haque, M. N., & Basheer, A. (2020). Effect of photoperiodicity and methods of follicular wave emergence on follicle turn-over, recovery and quality of oocytes, and early in-vitro developmental competence of embryos using ovum pick-up in Nili-Ravi buffaloes: Preliminary evidence. Theriogenology, 157, 508-516.
Saleem, M., Yousuf, M. R., Ghafoor, A., & Riaz, A. (2022). Influence of endometritis on the follicular dynamics, recovery, quality, gene expression, nuclear maturation, and in-vitro developmental competence of oocytes in Sahiwal cattle. Reproduction in Domestic Animals, 1-12. https://doi.org/10.1111/rda.14138
Sartorelli, E. S., Carvalho, L. M., Bergfelt, D., Ginther, O., & Barros, C. M. (2005). Morphological characterization of follicle deviation in Nelore (Bos indicus) heifers and cows. Theriogenology, 63, 2382-2394.
Sartori, R., Spies, C., & Wiltbank, M. C. (2017). Effects of dry matter and energy intake on quality of oocytes and embryos in ruminants. Reproduction, Fertility, and Development, 29, 58-65.
Sarwar, Z., Saad, M., Saleem, M., Husnain, A., Riaz, A., & Ahmad, N. (2020). Effect of follicle size on oocytes recovery rate, quality, and in-vitro developmental competence in Bos indicus cows. Animal Reproduction, 17, e20200011.
Shah, S. I., Bashir, E. L., & Bantel, R. (1994). Animal husbandry. National Book Foundation.
Sudiman, J., Ritter, L. J., Feil, D., Wang, X., Chan, K., Mottershead, D. G., Robertson, D., Thompson, J., & Gilchrist, R. B. (2014). Effects of differing oocyte-secreted factors during mouse in vitro maturation on subsequent embryo and fetal development. Journal of Assisted Reproduction and Genetics, 31, 295-306.
Viana, J., Palhao, M., Siqueira, L., Fonseca, J. F. D., & Camargo, L. D. A. (2010). Ovarian follicular dynamics, follicle deviation, and oocyte yield in Gyr breed (Bos indicus) cows undergoing repeated ovum pick-up. Theriogenology, 73, 966-972.
Walsh, S., Williams, E., & Evans, A. (2011). A review of the causes of poor fertility in high milk producing dairy cows. Animal Reproduction Science, 123, 127-138.
Zhao, S.-Y., Qiao, J., Chen, Y.-J., Liu, P., Li, J., & Yan, J. (2010). Expression of growth differentiation factor-9 and bone morphogenetic protein-15 in oocytes and cumulus granulosa cells of patients with polycystic ovary syndrome. Fertility and Sterility, 94, 261-267.

Auteurs

Muhammad Saleem (M)

Department of Theriogenology, Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore, Pakistan.

Muhammad Rizwan Yousuf (MR)

Department of Theriogenology, Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore, Pakistan.

Aamir Ghafoor (A)

Department of Microbiology, Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore, Pakistan.

Amjad Riaz (A)

Department of Theriogenology, Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore, Pakistan.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH