Associations of cord metabolome and biochemical parameters with the neonatal deaths of cloned pigs. Issue 12 (12th September 2021)

• Record Type: Journal Article
• Authors: Ao, Zheng; Wu, Zhimin; Zhao, Huaxing; Wu, Zhenfang; Li, Zicong
• Is Part Of: Reproduction in domestic animals. Volume 56:Issue 12(2021)
• Page Start: 1519
• Page End: 1528
• Publication Date: 2021-09-12
• Subjects: biochemical parameters -- cloned pigs -- metabolomics -- neonatal loss -- umbilical cord; Animal breeding -- Periodicals; Veterinary pathology -- Periodicals; Livestock -- Breeding -- Periodicals; 636.082
• DOI: 10.1111/rda.14014
• Languages: English
• ISSNs: 0936-6768

Abstract

Abstract: Neonatal cloned pigs generated via somatic cell nuclear transfer (SCNT) have high incidences of malformation and mortality. The mechanisms underlying the massive loss of cloned pig neonates remain unclear. We compared the cord serum metabolic profiles and biochemical indexes of SCNT‐derived piglets that died within 4 days (SCNT‐DW4), SCNT‐derived piglets that survived over 4 days (SCNT‐SO4) and artificial insemination (AI)‐generated piglets that survived over 4 days (AI‐SO4) to investigate the associations of serum metabolomics and biochemical indexes in umbilical cord (UC) sera at delivery with the neonatal loss of cloned pigs. Results showed that compared with SCNT‐SO4 and AI‐SO4 piglets, SCNT‐DW4 piglets had lower birth weight, placental indexes, placental vascularization scores, UC scores, vitality scores, serum glucose and levels but higher creatinine, urea nitrogen and uric acid levels in cord sera. Metabolomics analysis revealed alterations in lipid, glucose and purine metabolism in the cord sera of SCNT‐DW4 piglets. These results indicated that the disturbance of the cord serum metabolome might be associated with the low birth weight and malformations of cloned neonates. These effects were likely the consequences of the impaired placental morphology and function of SCNT‐derived piglets. This study provides helpful information regarding the potential mechanisms responsible for the neonatal death of cloned pigs and also offers an important basis for the design of effective strategies to improve the survival rate of these animals.