Preimplantation Genetic Testing for Aneuploidy (PGT-A) Reveals High Levels of Chromosomal Errors in In Vivo-Derived Pig Embryos, with an Increased Incidence When Produced In Vitro

Author:

Jochems Reina1ORCID,Canedo-Ribeiro Carla2ORCID,Silvestri Giuseppe2ORCID,Derks Martijn F. L.34,Hamland Hanne1,Zak Louisa J.3,Knol Egbert F.3,Handyside Alan H.2,Grindflek Eli1,Griffin Darren K.2ORCID

Affiliation:

1. Norsvin SA, 2317 Hamar, Norway

2. School of Biosciences, University of Kent, Canterbury CT2 7NH, UK

3. Topigs Norsvin Research Center, 6641 SZ Beuningen, The Netherlands

4. Animal Breeding and Genomics, Wageningen University & Research, 6700 AH Wageningen, The Netherlands

Abstract

Preimplantation genetic testing for aneuploidy (PGT-A) is widespread, but controversial, in humans and improves pregnancy and live birth rates in cattle. In pigs, it presents a possible solution to improve in vitro embryo production (IVP), however, the incidence and origin of chromosomal errors remains under-explored. To address this, we used single nucleotide polymorphism (SNP)-based PGT-A algorithms in 101 in vivo-derived (IVD) and 64 IVP porcine embryos. More errors were observed in IVP vs. IVD blastocysts (79.7% vs. 13.6% p < 0.001). In IVD embryos, fewer errors were found at blastocyst stage compared to cleavage (4-cell) stage (13.6% vs. 40%, p = 0.056). One androgenetic and two parthenogenetic embryos were also identified. Triploidy was the most common error in IVD embryos (15.8%), but only observed at cleavage, not blastocyst stage, followed by whole chromosome aneuploidy (9.9%). In IVP blastocysts, 32.8% were parthenogenetic, 25.0% (hypo-)triploid, 12.5% aneuploid, and 9.4% haploid. Parthenogenetic blastocysts arose from just three out of ten sows, suggesting a possible donor effect. The high incidence of chromosomal abnormalities in general, but in IVP embryos in particular, suggests an explanation for the low success of porcine IVP. The approaches described provide a means of monitoring technical improvements and suggest future application of PGT-A might improve embryo transfer success.

Funder

The Research Council of Norway

Biotechnology and Biological Sciences Research Council (BBSRC) LINK awards scheme

Publisher

MDPI AG

Subject

General Medicine

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