Animal Reproduction Research in Assisted Reproductive Technologies
Animal Reproduction Research in Assisted Reproductive Technologies
Animal Reproduction Research in Assisted Reproductive Technologies
In Vitro Fertilization
As an alternative to collecting embryos from donor animals, methods have been
developed recently to produce embryos in vitro (in the laboratory). The methods are also
called in vitroembryo production or IVP. Immature oocytes (female eggs) can be obtained
from ovaries of infertile or aged females, or from regular embryo donors (described
above). Ovum (egg) pick up is a nonsurgical technique that uses ultrasound and a guided
needle to aspirate immature oocytes from the ovaries. Once the immature oocytes have
been removed from the ovary, they are matured, fertilized, and cultured in vitro for up to
seven days until they develop to a stage that is suitable for transfer or freezing. NIFA has
supported a number of basic research projects to understand the physiological
mechanisms associated with production of embryos in vitro.
The ability to sex semen has a large potential for commercialization; thus, much of the
research to develop and refine sperm sexing technology has been conducted in the
private sector. XY, Inc., a small company in Ft. Collins, CO, has been the leader in
developing sperm sexing technology in cattle, horses, and pigs. Researchers at
the USDA Agricultural Research Servicehave also played a major role in developing
sperm sexing technology for poultry and swine.
NIFA has supported basic and applied studies on male reproductive physiology that have
laid the groundwork for many of the advances made by private industry. In addition, NIFA
has supported basic research to develop novel methods to determine the sex of bovine
embryos:
Sex determination of bovine embryos by noninvasive immuno-PCR (NRI grant 98-
35208-6598).
Non-invasive bovine embryo sexing via sperm-mediated transgenesis.
The technique involves culturing somatic cells from an appropriate tissue (fibroblasts)
from the animal to be cloned. Nuclei from the cultured somatic cells are then microinjected
into an enucleated oocyte obtained from another individual of the same or a closely
related species. Through a process that is not yet understood, the nucleus from the
somatic cell is reprogrammed to a pattern of gene expression suitable for directing normal
development of the embryo. After further culture and development in vitro, the embryos
are transferred to a recipient female and ultimately result in the birth of live offspring. The
success rate for propagating animals by nuclear transfer is often less than 10 percent and
depends on many factors, including the species, source of the recipient ova, cell type of
the donor nuclei, treatment of donor cells prior to nuclear transfer, the techniques used
for nuclear transfer, etc. NIFA has supported research projects to obtain a better
understanding of the basic cellular mechanisms associated with nuclear reprogramming.