scholarly journals Investigating the physiological responses of Pacific white shrimp Litopenaeus vannamei to acute cold-stress

PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e7381 ◽  
Author(s):  
Zhenlu Wang ◽  
Yuexin Qu ◽  
Xiaolei Zhuo ◽  
Junyi Li ◽  
Jixing Zou ◽  
...  

Background Litopenaeus vannamei is one of the most important aquaculture shrimps in the world and low temperatures present a serious challenge to its survival, growth, and distribution. Methods To investigate their physiological responses during acute cold-stress, L. vannamei were treated under acute cooling conditions from 28 to 13 °C with a cooling rate of 2.5 °C/2 h and were maintained at 13 °C for 12 h. Plasma metabolite concentrations, histological changes, and relative gene expression related to the unfolded protein response (UPR) pathway and apoptosis in the hepatopancreas and the hemocytes of L. vannamei were investigated. Results The results revealed that the concentrations of triglycerides, total cholesterol, and total protein in plasma reached their peaks at 23 °C, and then decreased to their minimum values at 13 °C for 12 h. The activity of alkaline phosphatase in the plasma decreased to its lowest level while the activity of alanine aminotransferase increased to its highest level at 13 °C for 12 h. The hepatic tubules became necrotic and the basement membranes were ruptured at 13 °C for 12 h. The gene expression related to UPR and apoptosis in the hepatopancreas and hemocytes was significantly altered by the decrease in the temperature. Discussion The results revealed that acute cold-stress caused histological damage in the hepatopancreas of L. vannamei, reducing its immunity. The three UPR pathways were involved in the process of acute cold-stress and the response of activating transcription factor 6 to UPR may be faster and more directthan the IRE1 and PERK pathways.

Aquaculture ◽  
2008 ◽  
Vol 275 (1-4) ◽  
pp. 356-360 ◽  
Author(s):  
Jun Zhou ◽  
Wei-Na Wang ◽  
Guang-Zhi Ma ◽  
An-Li Wang ◽  
Wen-Yin He ◽  
...  

2015 ◽  
Vol 44 (1) ◽  
pp. 265-271 ◽  
Author(s):  
Chih-Chiu Yang ◽  
Chung-Lun Lu ◽  
Sherwin Chen ◽  
Wen-Liang Liao ◽  
Shiu-nan Chen

2017 ◽  
Vol 37 (2) ◽  
pp. 196-204 ◽  
Author(s):  
C Ren ◽  
X Li ◽  
X Li ◽  
Y Xie ◽  
H Fu ◽  
...  

RNA interference (RNAi) is a powerful tool to silence or minimize gene expression, and palate culture in vitro is an important technique for study of the palate development. Our previous study demonstrated that the gene expression of glucose-regulated protein-78 (Grp78) was downregulation in the all-trans retinoic acid-induced mouse models of cleft palate (CP) during embryogenesis. To find the role of Grp78, the small interfering RNA (siRNA) of this gene carried by fluorescent vector was injected with a microinjector, through which about 30 pmol siRNA was injected into the Institute of Cancer Research (ICR) mouse palate explants. After 6, 12, 24, 48, and 72 h, these palate explants were removed from culture to observe their fluorescent and Alcian blue-staining phenotypes, and the expression of the unfolded protein response (UPR) key members (Grp78, Inositol-responsive enzyme 1, protein kinase RNA-like endoplasmic reticulum kinase, activating transcription factor-6 and X-box binding protein-1) was measured. After cultured for 72 h, the partially or completely fused bilateral palates were observed in the control siRNA group, while CPs were found in the Grp78 siRNA group. In the Grp78 siRNA group, the relatively mRNA abundance of the key genes belonged to UPR at each time point was lower than that of the control siRNA group, and their protein expression also displayed the same change. By the system of RNAi strategies with mouse palate culture, we found the siRNA of Grp78 disturbed the fusion of mouse palate cultured in vitro.


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