Small intestinal transcriptome analysis revealed changes of genes involved in nutrition metabolism and immune responses in growth retardation piglets1. (20th June 2019)

• Record Type: Journal Article
• Authors: Qi, Ming; Tan, Bie; Wang, Jing; Li, Jianjun; Liao, Simeng; Yan, Jiameng; Liu, Yanhong; Yin, Yulong
• Is Part Of: Journal of animal science. Volume 97:Number 9(2019)
• Page Start: 3795
• Page End: 3808
• Publication Date: 2019-06-20
• Subjects: immune response -- nutrition metabolism -- postnatal growth retardation -- small intestine -- transcriptomic analysis; Livestock -- Periodicals; Livestock; Electronic journals; Periodicals; 636.005
• DOI: 10.1093/jas/skz205
• Languages: English
• ISSNs: 0021-8812

Abstract

Abstract: Postnatal growth retardation (PGR ) is common in piglets. Abnormal development in small intestine was casually implicated in impaired growth, but the exact mechanism is still implausible. The present study unveiled transcriptome profile of jejunal mucosa, the major site of nutrient absorption, in PGR and healthy piglets using RNA-sequencing (RNA-seq ). The middle segments of jejunum and ileum, and jejunal mucosa were obtained from healthy and PGR piglets at 42 d of age. Total RNA samples extracted from jejunal mucosa of healthy and PGR piglets were submitted for RNA-seq. Lower villus height was observed in both jejunum and ileum from PGR piglets suggesting structural impairment in small intestine ( P < 0.05). RNA-seq libraries were constructed and sequenced, and produced average 4.8 × 10 7 clean reads. Analysis revealed a total of 499 differently expressed genes (DEGs ), of which 320 DEGs were downregulated in PGR piglets as compared to healthy piglets. The functional annotation based on Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) highlighted that most DEGs were involved in nutrient metabolism and immune responses. Our results further indicated decreased gene expression associated with glucose, lipid, protein, mineral, and vitamin metabolic process, detoxication ability, oxidoreductase activity, and mucosal barrier function; as well as the increased insulin resistance and inflammatory response in the jejunal mucosa of PGR piglets. These results characterized the transcriptomic profile of the jejunal mucosa in PGR piglets, and could provide valuable information with respect to better understanding the nutrition metabolism and immune responses in the small intestine of piglets.