TY - JOUR
T1 - Energy metabolism and metabolomics response of Pacific whiteshrimp Litopenaeus vannamei to sulfide toxicity
AU - Li, Tongyu
AU - Li, Erchao
AU - Suo, Tantong
AU - Xu, Zhixin
AU - Jia, Yongyi
AU - Qin, Jianguang
AU - Chen, Liqiao
AU - Gu, Zhimin
PY - 2017/2/1
Y1 - 2017/2/1
N2 - The toxicity and poisoning mechanisms of sulfide were studied in Litopenaeus vannamei from the perspective of energy metabolism and metabolomics. The lethal concentrations of sulfide in L. vannamei (LC50) at 24 h, 48 h, 72 h, and 96 h were determined. Sulfide at a concentration of 0, 1/10 (425.5 μg/L), and 1/5 (851 μg/L) of the LC50 at 96 h was used to test the metabolic responses of L. vannamei for 21 days. The chronic exposure of shrimp to a higher sulfide concentration of 851 μg/L decreased shrimp survival but did not affect weight gain or the hepatopancreas index. The glycogen content in the hepatopancreas and muscle and the activity of hepatopancreas cytochrome C oxidase of the shrimp exposed to all sulfide concentrations were significantly lower, and the serum glucose and lactic acid levels and lactic acid dehydrogenase activity were significantly lower than those in the control. Metabolomics assays showed that shrimp exposed to sulfide had lower amounts of serum pyruvic acid, succinic acid, glycine, alanine, and proline in the 425.5 μg/L group and phosphate, succinic acid, beta-alanine, serine, and l-histidine in the 851 μg/L group than in the control. Chronic sulfide exposure could disturb protein synthesis in shrimp but enhance gluconeogenesis and substrate absorption for ATP synthesis and tricarboxylic acid cycles to provide extra energy to cope with sulfide stress. Chronic sulfide exposure could adversely affect the health status of L. vannamei, as indicated by the high amounts of serum n-ethylmaleamic acid, pyroglutamic acid, aspartic acid and phenylalanine relative to the control. This study indicates that chronic exposure of shrimp to sulfide can decrease health and lower survival through functional changes in gluconeogenesis, protein synthesis and energy metabolism.
AB - The toxicity and poisoning mechanisms of sulfide were studied in Litopenaeus vannamei from the perspective of energy metabolism and metabolomics. The lethal concentrations of sulfide in L. vannamei (LC50) at 24 h, 48 h, 72 h, and 96 h were determined. Sulfide at a concentration of 0, 1/10 (425.5 μg/L), and 1/5 (851 μg/L) of the LC50 at 96 h was used to test the metabolic responses of L. vannamei for 21 days. The chronic exposure of shrimp to a higher sulfide concentration of 851 μg/L decreased shrimp survival but did not affect weight gain or the hepatopancreas index. The glycogen content in the hepatopancreas and muscle and the activity of hepatopancreas cytochrome C oxidase of the shrimp exposed to all sulfide concentrations were significantly lower, and the serum glucose and lactic acid levels and lactic acid dehydrogenase activity were significantly lower than those in the control. Metabolomics assays showed that shrimp exposed to sulfide had lower amounts of serum pyruvic acid, succinic acid, glycine, alanine, and proline in the 425.5 μg/L group and phosphate, succinic acid, beta-alanine, serine, and l-histidine in the 851 μg/L group than in the control. Chronic sulfide exposure could disturb protein synthesis in shrimp but enhance gluconeogenesis and substrate absorption for ATP synthesis and tricarboxylic acid cycles to provide extra energy to cope with sulfide stress. Chronic sulfide exposure could adversely affect the health status of L. vannamei, as indicated by the high amounts of serum n-ethylmaleamic acid, pyroglutamic acid, aspartic acid and phenylalanine relative to the control. This study indicates that chronic exposure of shrimp to sulfide can decrease health and lower survival through functional changes in gluconeogenesis, protein synthesis and energy metabolism.
KW - Chronic toxicity
KW - Cytochrome C oxidase
KW - Growth
KW - Lethal concentration
KW - Metabolite
UR - http://www.scopus.com/inward/record.url?scp=85006272409&partnerID=8YFLogxK
U2 - 10.1016/j.aquatox.2016.12.010
DO - 10.1016/j.aquatox.2016.12.010
M3 - Article
VL - 183
SP - 28
EP - 37
JO - AQUATIC TOXICOLOGY
JF - AQUATIC TOXICOLOGY
SN - 0166-445X
ER -