4.7 Article

The argininosuccinate synthetase can differentially regulate nitric oxide synthase in yellow catfish Pelteobagrus fulvidraco

Journal

FISH & SHELLFISH IMMUNOLOGY
Volume 127, Issue -, Pages 991-1000

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2022.07.044

Keywords

Ammonia; Argininosuccinate synthetase; Urea synthesis; Nitric oxide synthase; Pelteobagrus fulvidraco

Funding

  1. National Natural Science Foundation of China [32072948]
  2. Guizhou Province Science and Technology Projects [ZK2022-145]
  3. Natural Science Research Fund (Specialpost) of Guizhou University [2021-26]
  4. Fundamental Research Funds for the Provincial Universities of Zhejiang [SJLY2020009]
  5. Natural Science Foundation of Ningbo City [202003N412]
  6. Key Research and Development Program of Lishui City [2019ZDYS13]

Ask authors/readers for more resources

Fish are at high risk of ammonia exposure in aquaculture systems, which can lead to increased susceptibility to diseases. The study investigated the role of argininosuccinate synthetase (ASS) in regulating urea synthesis and nitric oxide synthesis in fish. The results showed a correlation between ASS expression and disease outbreak. The targeted regulation of ASS improved immune response in fish under ammonia stress.
Fish are at high risk of exposure to ammonia in aquaculture systems. When ammonia stress occurs, fish are more prone to disease outbreaks, but the mechanism is not very clear. The argininosuccinate synthetase (ASS) plays an important role in the regulation of urea synthesis and nitric oxide synthesis. We speculated that there must be some relationship between ASS expression and disease outbreak. In this study, ASS was cloned from the yellow catfish. The full-length cDNAs of ASS was 1558 bp, with open reading frames of 1236 bp. The mRNA expression of ASS gene was the highest in liver, kidney and brain. This study consists of two parts: 1) For ammonia challenge in vivo, yellow catfish (15.00 +/- 1.50 g) were divided into control group, low ammonia group (1/10 96 h LC50), and high ammonia group (1/2 96 h LC50). The experiment continued for 192 h. The results showed that ammonia stress elevated serum ammonia content, and inhibited urea synthesis enzymes activities but up-regulated the expression levels of related genes except ARG, and induced arginine accumulation and nitric oxide synthase (nNOS and iNOS) different expression, and decreased resistance to Aeromonas hydrophage; 2) For ammonia challenge in vitro, the primary culture of liver cell was divided into four groups: control group, BPP group (Bj-BPP-10c was added as ASS activator), Amm group (96 h LC50), and Amm + BPP group. The experiment continued for 96 h. The results showed that the Bj-BPP-10c can inhibit nNOS activity and improve cell survival rate, and enhance iNOS activity and immune response (lysozyme, complement, respiratory burst, and phagocytic index) by activate ASS when ammonia stress occurred. Our results indicated that targeted regulation of ASS can improve iNOS activity, and enhance the immune response of yellow catfish under ammonia stress.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available