Zhao Yuqi, Nie Ximei, Han Zhengxiao, Liu Peng, Xu Hao, Huang Xin, Ren Qian
Jiangsu Province Engineering Research Center for Aquatic Animals Breeding and Green Efficient Aquacultural Technology, College of Marine Science and Engineering, Nanjing Normal University, Nanjing, Jiangsu Province, 210023, China.
Nanjing Forestry University, Nanjing, Jiangsu Province, 210037, China.
Fish Shellfish Immunol. 2022 May;124:107-117. doi: 10.1016/j.fsi.2022.03.047. Epub 2022 Apr 2.
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.
中华绒螯蟹是一种具有很高经济价值的甲壳类动物,但肝胰腺坏死病(HPND)的发生严重制约了河蟹养殖业的发展。研究患HPND河蟹的生存机制有助于为疾病防控提供新策略。叉头框O(FOXO)转录因子家族参与生物体的各种关键生物学过程。在本研究中,克隆了中华绒螯蟹的一个FOXO基因(命名为EsFOXO)。EsFOXO的全长cDNA为2592 bp,包含一个2133 bp的开放阅读框,编码710个氨基酸。EsFOXO广泛分布于多种免疫组织中。进一步研究发现,与正常河蟹相比,患HPND河蟹肠道中EsFOXO的表达显著上调。然而,EsFOXO是否参与河蟹的免疫和代谢调节仍不清楚。RNA干扰分析表明,EsFOXO参与了两种胰脂肪酶、三种抗脂多糖因子和三种抗茵肽的表达的正调控。我们的研究结果表明,患HPND的河蟹在饥饿状态下采取两种生存策略:一方面,增加抗菌肽的合成以提高先天免疫力;另一方面,上调与脂质分解代谢相关酶的表达,动员河蟹体内的脂肪进行分解代谢。我们的研究为深入了解患HPND河蟹的生存机制提供了更多证据。