4.7 Article

The forkhead box O transcription factor regulates lipase and anti-microbial peptide expressions to promote lipid catabolism and improve innate immunity in the Eriocheir sinensis with hepatopancreatic necrosis disease

Journal

FISH & SHELLFISH IMMUNOLOGY
Volume 124, Issue -, Pages 107-117

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2022.03.047

Keywords

Hepatopancreatic necrosis disease; Forkhead box O transcription Factor; Lipase; Antimicrobial peptide; Eriocheir sinensis

Funding

  1. Jiangsu Provincial Depart-ment of Science and Technology [BE2019393]
  2. National Natural Science Foundation of China [31902397]
  3. Natural Science Foundation of Jiangsu Province [BK20190698]
  4. Start-up Fund of Research of Nanjing Normal University [184080H202B220]

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In this study, a FOXO gene (EsFOXO) from E. sinensis was cloned and its involvement in the immune and metabolic regulation of crabs with hepatopancreatic necrosis disease (HPND) was investigated. The expression of EsFOXO was significantly upregulated in the intestine of crabs with HPND compared to normal crabs. RNA interference analysis showed that EsFOXO positively regulates the expression of pancreatic lipases, anti-lipopolysaccharide factors, and crustins. Our study suggests that crabs with HPND adopt strategies of increased antimicrobial peptide synthesis and upregulated expression of enzymes involved in lipid catabolism to survive under starvation.
Eriocheir sinensis is a crustacean with great economic value, but the occurrence of hepatopancreatic necrosis disease (HPND) severely restricts the development of crab aquaculture. Study on the survival mechanism of crabs with HPND is beneficial to provide new strategies for disease prevention and control. The Forkhead box O (FOXO) transcription factor family is involved in various key biological processes of organisms. In this study, a FOXO gene (named as EsFOXO) from E. sinensis was cloned. The full-length cDNA of EsFOXO is 2592 bp containing a 2133 bp open reading frame that encodes 710 amino acids. EsFOXO was widely distributed in multiple immune tissues. Further study found that the expression of EsFOXO in the intestine of crabs with HPND was significantly upregulated compared with that in the normal crabs. However, whether EsFOXO is involved in the immune and metabolic regulation of crabs remains unknown. RNA interference analysis showed that EsFOXO participates in the positive regulation of the expression of two pancreatic lipases, three anti-lipopolysaccharide factors, and three crustins. Results from our research suggest that two strategies are adopted by crabs with HPND for survival under starvation: on the one hand, the synthesis of antimicrobial peptides is increased to improve the innate immunity; on the other hand, the expression of enzymes correlated with lipid catabolism is up-regulated that mobilizes the fat in the crab, going through catabolism. Our study provides more evidence for an in-depth understanding of the survival mechanism of crabs with HPND.

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