{"id":6851,"date":"2025-01-13T17:01:58","date_gmt":"2025-01-13T16:01:58","guid":{"rendered":"https:\/\/www.axiom-genetics.com\/cryopreservation-of-porcine-embryos-strategic-research-for-the-future-of-the-pork-industry\/"},"modified":"2025-11-27T09:41:19","modified_gmt":"2025-11-27T08:41:19","slug":"cryopreservation-of-porcine-embryos-strategic-research-for-the-future-of-the-pork-industry","status":"publish","type":"post","link":"https:\/\/www.axiom-genetics.com\/en\/cryopreservation-of-porcine-embryos-strategic-research-for-the-future-of-the-pork-industry\/","title":{"rendered":"Cryopreservation of porcine embryos: strategic research for the future of the pork industry"},"content":{"rendered":"\n

A pork industry in the throes of change <\/strong><\/p><\/h2>\n\n

For several decades now, the pig farming industry has been facing up to major challenges as it embarks on a process of continuous improvement in terms of animal welfare, food safety, consumer image and environmental impact1<\/sup>.<\/p><\/p>\n\n

As Europe’s 3rd largest pork producer, with 2.1 million tonnes of pork to be produced by 2023, the pork industry remains a buoyant, economic sector2<\/sup>. What’s more, pork still accounts for 38% of meat consumption, making it the most widely consumed meat in the world.<\/p><\/p>\n\n

However, the pork sector is threatened by the constant emergence of new diseases, which can become a cause for concern. It has become necessary for operators in the pork industry to have a protocol in place, enabling the conservation of breeds in the event of epidemic outbreaks, whether in the wild or on production farms.<\/p>\n\n

The Cryopig project: what’s in it for the pig industry?<\/strong><\/p><\/h2>\n\n

The aim of the Cryopig project, launched in 2020 in partnership with VetAgroSup, ISARA Lyon and IFIP, is not only to create new scientific knowledge in the field of pig reproductive biotechnology, but also to propose industrializable solutions to the challenges facing the pig industry today.<\/p>\n\n

The study of this still innovative field is a strategic and long-term development axis for the Axiom Group. One of the reasons for this is to safeguard pig breeds, in order to preserve the heritage and genetic diversity of the herd. In the longer term, it is possible to imagine a new tool for genetic dissemination.<\/p>\n\n

This could alleviate the various problems associated with transporting live animals, by focusing solely on maintaining optimum temperature during embryo transport.<\/p>\n\n

In the longer term, it would be possible to envisage the creation of \u201cresponse\u201d centers to speed up the re-implantation of a breed, or the reconstitution of an entire herd after its disappearance due to a particularly virulent epidemic, as was the case in China with ASF (African Swine Fever) in 2018.<\/p>\n\n

The National Cryobank, a contributor to safeguarding genetic variability<\/strong><\/p><\/h2>\n\n

It was against this backdrop that a cryogenic pig seed bank was set up several years ago within the National Cryobank (Cf.\u00a0<\/em>CRB-Anim). But reconstituting an endangered breed or a specific genetic line requires cryopreserved embryos or oocytes. A cryobank of this kind also makes it possible to manage swine genetic diversity, to make long-term use of these resources, and in particular to safeguard local breeds with low numbers, whose situation remains critical in the face of current health risks.<\/p><\/p>\n\n

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Let’s move on to the scientific aspect of this method, by exploring the research carried out by our teams on the stages of in vitro<\/em>\u00a0pig embryo production.<\/strong><\/p><\/p>\n<\/blockquote>\n\n

Although the first successful\u00a0in vitro\u00a0<\/em>production of pig embryos dates back to 1986, the success rate remains relatively variable. The main challenges encountered in the porcine species are the high incidence of polyspermia*, embryo stalling at the four-cell stage (a stage associated with embryonic genome activation in mammals) and low blastocyst rates3<\/sup>.<\/p><\/p>\n\n

Controlling and transforming the composition of culture media (maturation, fertilization and development) is a key factor in overcoming these obstacles. Post-thaw embryo survival has been shown to be highly dependent on culture systems5<\/sup>. Finally, the proper in vivo<\/em> development of an individual depends on the correct establishment of its first cell lines, since it is these that will enable implantation8<\/sup>\u00a0and fetal development.<\/p><\/p>\n\n

\u00ab\u00a0The scientific objective of this project is to characterize the effects and study the interactions of factors that currently compromise the in vitro<\/em> production of porcine embryos and their cryopreservation, with the ultimate aim of preserving embryos \u00a0\u00bb<\/p><\/p>\n\n

Cryopig, what are the main steps in a protocol designed to increase the number of embryos successfully transferred after cryopreservation? <\/strong><\/p><\/h2>\n\n

The thesis project is organized as a \u201ccascade\u201d, with the knowledge acquired at each of the different stages of in vitro<\/em> production (maturation, fertilization, development) and cryopreservation of porcine embryos enabling us to move on to the next.<\/p><\/p>\n\n

\"\"<\/figure>\n\n

Step 1: What factors affect the development of in vitro<\/em>-produced embryos?<\/strong><\/p><\/h3>\n\n

Current literature shows that there is currently no universal protocol for in vitro<\/em> production in pigs, mainly due to the absence of chemically defined media, the use of natural products and the uncertain role of numerous additives in these media3<\/sup>. As a result, in vitro<\/em> embryo production rates are relatively low in the vast majority of experiments. At the same time, embryo stage and quality remain largely undetermined.<\/p><\/p>\n\n

The aim of this first stage is therefore to identify all the factors likely to impact on the development of these embryos, right up to the desired embryonic stage. One of the avenues envisaged is the adaptation of culture media. In this way, the embryo could benefit from different additives at different stages of its development, through the use of sequential media. Instead of using a single medium for the whole of its in vitro<\/em> development, the composition of the media could be varied over time to better mimic the needs of the embryo in vivo<\/em>, according to its stage of development.<\/p><\/p>\n\n

Since the embryo does not require the same inputs throughout its development, adding or removing certain molecules at key stages could have a beneficial effect on blastocyst formation*.<\/p><\/p>\n\n

\"\"<\/figure>\n\n

Step 2: What are the optimal conditions for cryopreserving in vitro<\/em> embryos?<\/strong><\/p><\/h3>\n\n

Cryopreservation protocols are based on the use of solutions that protect the embryo from the harmful effects of the physical phenomena of freezing, the nature and concentration of which vary considerably according to the systems studied.<\/p>\n\n

Incubation times in these solutions, as well as adapted cooling and reheating methods (slow freezing, vitrification) can also have an impact on embryo survival.<\/p>\n\n

The aim of this step is to identify the effects of each of these parameters on the survival of embryos produced in vitro<\/em> (morulas or blastocysts), as well as their interactions, in order to establish a cryopreservation protocol adapted to porcine embryos. To this end, the toxicity of cryoprotective solutions will be assessed on embryos produced in vitro<\/em>, without the application of cooling and reheating steps. This step will enable us to draw up a list of solutions with no (or negligible) adverse impact on the maintenance of the embryo after cooling and before rewarming.<\/p><\/p>\n\n

Step 3: The impact of the various factors studied above on the transfer conditions for embryos produced in vitro and then cryopreserved.<\/strong><\/p><\/h3>\n\n

Having identified the optimum conditions for cryopreservation of in vitro<\/em>-produced porcine embryos, the aim of the third stage is to identify the markers characteristic of the embryos’ development potential and therefore of their quality.<\/p><\/p>\n\n

The expression of pluripotency genes (such as\u00a0Oct4<\/em>,\u00a0Nanog<\/em>,\u00a0Sox2<\/em>,\u00a0Cdx2<\/em>)4<\/sup>\u00a0will be assessed in order to observe the establishment of the first embryonic layers (inner cell mass and trophectoderm) required for the in vivo<\/em> development of a new individual8<\/sup>. The expression of these genes is crucial for the establishment of the organism’s organizational plan, which is essential in the early stages of gestation.<\/p><\/p>\n\n

The particular anatomy of the sow’s genital tract has made it difficult to develop simple, non-invasive, or at least minimal, transfer procedures. Over the last decade, new procedures have been developed which allow non-surgical embryo transfers while effectively preserving the embryos. The absence of surgery and the preservation of embryos at this stage are essential to meet societal expectations linked to animal welfare6<\/sup>. Thus, the cryopreservation protocols that deliver the best results will be selected for the production and cryopreservation of porcine embryos.<\/p><\/p>\n\n

As part of the Cryopig project, the transfer method envisaged will be a non-surgical one, with a deep intra-uterine deposition site6<\/sup>. Gestation follow-up will be carried out to confirm embryo implantation and development. For pregnant sows at term, farrowing survival rates will be calculated, and longitudinal monitoring (weekly ultrasound examinations, hormonal profiles) over the 115 days of gestation will confirm that no abortions have occurred.<\/p><\/p>\n\n

Conclusion<\/strong><\/p><\/h2>\n\n

Overall, the development of this technology and the creation of effective protocols at every stage opens up a host of possibilities, and the development of a new genetic dissemination tool that will revolutionize transport and the pig industry as a whole. <\/p>\n\n

Editor(s)<\/strong><\/p><\/h2>\n\n