Selokar Naresh L, Singh Manoj K, Tripathi Gaurav, Patel Kartikey, Verma Ranjeet, Singh Priyanka, Aswal Ajay, Chauhan Manmohan Singh
Embryo Biotechnology Lab, Animal Biotechnology Division (ABTD), ICAR- National Dairy Research Institute, Karnal, 132001, Haryana, India.
Uttarakhand Livestock Development Board, Dehradun, 248001, India.
Sci Rep. 2025 Jul 24;15(1):26957. doi: 10.1038/s41598-025-10225-5.
Somatic cell nuclear transfer (SCNT) allows the multiplication of elite livestock and conservation of endangered species. However, restrictions on cow slaughter limit the access to oocytes for SCNT applications in Indian cattle breeds. To overcome this limitation, we utilized transvaginal ovum pick-up (OPU) method to collect oocytes, which were then used for the production of cloned embryos via the handmade cloning (HMC) technique. A total of 98 Sahiwal oocytes were collected, leading to the successful reconstruction of 24 SCNT Gir embryos. Out of these, five developed into blastocysts, which were transferred into five recipient cows. Two pregnancies were confirmed, but one was lost due to hydro-allantois condition. The other pregnancy continued to term, and a healthy Gir female calf weighing 32 kg was born. Microsatellite DNA analysis confirmed the genetic identity of the cloned calf to its donor. Postnatally, the calf was monitored for serum cytokine parameters, telomere length, and reproductive potentials. Cytokine profiling revealed variations between the cloned calf and naturally conceived counterparts; however, the born cloned calf did not exhibit any pathological conditions and has high telomere length compared to age-matched counterparts, and surviving well. Furthermore, to assess cloned cow utility in reproductive biotechnologies, we produced blastocyst stage embryos (35%) through OPU-IVF method and established one pregnancy from five transfers (20%). In conclusion, this study reports the first successful SCNT of Indian cattle breed and demonstrates the feasibility of the cloned cow for the production of OPU-IVF embryos.
体细胞核移植(SCNT)可实现优良家畜的繁殖以及濒危物种的保护。然而,对奶牛屠宰的限制使得在印度牛品种的SCNT应用中获取卵母细胞受到限制。为克服这一限制,我们采用经阴道采卵(OPU)方法收集卵母细胞,然后通过手工克隆(HMC)技术用于生产克隆胚胎。共收集了98枚萨希瓦尔卵母细胞,成功构建了24枚SCNT吉尔胚胎。其中,5枚发育成囊胚,并移植到5头受体母牛体内。确认了2次妊娠,但其中1次因羊水过多情况而流产。另一次妊娠持续至足月,一头体重32千克的健康吉尔雌性犊牛出生。微卫星DNA分析证实了克隆犊牛与其供体的遗传同一性。产后,对犊牛的血清细胞因子参数、端粒长度和繁殖潜力进行了监测。细胞因子分析显示克隆犊牛与自然受孕的犊牛之间存在差异;然而,出生的克隆犊牛未表现出任何病理状况,与年龄匹配的犊牛相比端粒长度较长,且存活良好。此外,为评估克隆母牛在生殖生物技术中的效用,我们通过OPU-IVF方法生产了囊胚期胚胎(35%),并在5次移植中成功建立了1次妊娠(20%)。总之,本研究报道了首例印度牛品种的成功SCNT,并证明了克隆母牛用于生产OPU-IVF胚胎的可行性。