First cloned Bactrian camel (Camelus bactrianus) calf produced by interspecies somatic cell nuclear transfer: A step towards preserving the critically endangered wild Bactrian camels.

Studies were conducted to explore the possibility of employing dromedary camel (Camelus dromedarius) oocytes as recipient cytoplasts for the development of interspecies somatic cell nuclear transfer (iSCNT) embryos using skin fibroblast cells of an adult Bactrian camel (Camelus bactrianus) and Llama (Llama glama) as donor nuclei. Also, the embryos reconstructed with Bactrian cells were transferred into the uterus of synchronized dromedary camel recipients to explore the possibility of using them as surrogate mothers. Serum-starved skin fibroblast cells were injected into the perivitelline space of enucleated mature oocytes, collected from super-stimulated dromedary camels, and fused using an Eppendorf electroporator. After activation with 5μM ionomycin and 6-dimethylaminopurine, they were cultured at 38.5°C in an atmosphere of 5% CO2, 5% O2, and 90% N2 in air. In experiment 1, Day 7 blastocysts were stained with Hoechst to count their cell numbers, while in experiment 2, they were transferred to synchronized dromedary recipients. A lower number (P < 0.05) of blastocysts were obtained from reconstructs utilizing fibroblast cells from Llama when compared with those reconstructed with dromedary and Bactrian fibroblast cells. However, no difference was observed in their cell numbers. In experiment 2, a higher (P < 0.05) proportion of blastocysts were obtained from the cleaved embryos reconstructed with Bactrian fibroblast cells when compared to those reconstructed with dromedary cells. Twenty-six Day 7 blastocysts reconstructed with Bactrian cells were transferred to 23 synchronized dromedary recipients with 5 pregnancies established on Day 30, however, only one of the pregnancies developed to term and a healthy calf weighing 33 kgs was born after completing 392 days of gestation. Unfortunately, the calf died on day 7 due to acute septicemia. In conclusion, the present study reports, for the first time, birth of a cloned Bactrian calf by iSCNT using dromedary camel as a source for oocytes as well as a surrogate for carrying the pregnancy to term

Development of the iSCNT embryos after their reconstruction using dromedary oocytes as recipient cytoplast and Bactrian, Lama and dromedary fibroblast cells as nuclear donors.

<p>Development of the iSCNT embryos after their reconstruction using dromedary oocytes as recipient cytoplast and Bactrian, Lama and dromedary fibroblast cells as nuclear donors.</p

The cloned Bactrian camel calf produced by interspecies somatic cell nuclear transfer to a dromedary camel surrogate mother on 2^nd day of his birth.

<p>The cloned Bactrian camel calf produced by interspecies somatic cell nuclear transfer to a dromedary camel surrogate mother on 2^nd day of his birth.</p

Microsatellite analysis of the Bactrian cloned calf, donor cells, donor animal and surrogate mother.

<p>Microsatellite analysis of the Bactrian cloned calf, donor cells, donor animal and surrogate mother.</p

Development of the iSCNT embryos after their reconstruction using dromedary oocytes as recipient cytoplast and Bactrian and dromedary fibroblast cells as nuclear donors.

<p>Development of the iSCNT embryos after their reconstruction using dromedary oocytes as recipient cytoplast and Bactrian and dromedary fibroblast cells as nuclear donors.</p