Metabolic Response of Black Tiger Shrimp (<i>Penaeus monodon</i>) to Acute Ammonia Nitrogen Stress

High concentrations of ammonia nitrogen could result in the death of aquatic animals and cause a huge economic loss in the aquaculture industry. However, the metabolic responses to acute ammonia nitrogen stress remain largely unknown in <i>Penaeus monodon</i>. In this study, we first inv...

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Main Authors: Yangyang Ding, Shigui Jiang, Song Jiang, Yundong Li, Qibin Yang, Lishi Yang, Jianhua Huang, Jianzhi Shi, Pengying Li, Hongshan Diao, Falin Zhou
Format: Article
Language:English
Published: MDPI AG 2025-05-01
Series:Biology
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Online Access:https://www.mdpi.com/2079-7737/14/5/501
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author Yangyang Ding
Shigui Jiang
Song Jiang
Yundong Li
Qibin Yang
Lishi Yang
Jianhua Huang
Jianzhi Shi
Pengying Li
Hongshan Diao
Falin Zhou
author_facet Yangyang Ding
Shigui Jiang
Song Jiang
Yundong Li
Qibin Yang
Lishi Yang
Jianhua Huang
Jianzhi Shi
Pengying Li
Hongshan Diao
Falin Zhou
author_sort Yangyang Ding
collection DOAJ
description High concentrations of ammonia nitrogen could result in the death of aquatic animals and cause a huge economic loss in the aquaculture industry. However, the metabolic responses to acute ammonia nitrogen stress remain largely unknown in <i>Penaeus monodon</i>. In this study, we first investigated the histological change in tissues in <i>Penaeus monodon</i> under 96 h acute ammonia nitrogen stress. The result of the paraffin section showed that acute ammonia nitrogen stress induced severe epithelial detachment and lumen dilatation of the hepatopancreas, swollen and hemocyte infiltration of the gills, and mucosa exfoliation and shortened villi of the intestine in <i>Penaeus monodon</i>, suggesting the impairment of the normal physiological function in these tissues. We next examined the change in the metabolic product in the plasma and the enzyme activity in the hepatopancreas after ammonia nitrogen stress. Upon ammonia stress, both the concentration of ammonia and urea nitrogen significantly increased, while there was no significant increase in the concentration of uric acid, which is consistent with the results that the enzyme activity of glutamine synthetase (GS), glutamate dehydrogenase (GDH), and aspartate transaminase (GOT) became significantly elevated and the enzyme activity of adenosine deaminase (ADA) in the purine metabolism pathway significantly decreased after ammonia stress, suggesting that shrimp could convert excessive ammonia to urea for ammonia detoxification through the ammonia–nitrogen metabolism pathways. Interestingly, we also observed a significant increase in superoxide dismutase (SOD) activity, suggesting a potential role of this antioxidant enzyme in the clearance of reactive oxygen species (ROS) induced via ammonia stress. Moreover, we found that acute ammonia nitrogen stress inhibited the enzyme activity of caspase 3 and caspase 8, suggesting an important role of apoptosis in protecting <i>Penaeus monodon</i> against acute ammonia stress. Overall, our findings revealed that <i>Penaeus monodon</i> may employ metabolic and purine pathways and undergo oxidative stress and apoptosis for ammonia detoxification under ammonia nitrogen stress, thus providing new insight into the metabolic response of shrimp to acute ammonia stress.
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spelling doaj-art-865b85f56e6f4e9b892c6bd88e0e80f72025-08-20T01:56:20ZengMDPI AGBiology2079-77372025-05-0114550110.3390/biology14050501Metabolic Response of Black Tiger Shrimp (<i>Penaeus monodon</i>) to Acute Ammonia Nitrogen StressYangyang Ding0Shigui Jiang1Song Jiang2Yundong Li3Qibin Yang4Lishi Yang5Jianhua Huang6Jianzhi Shi7Pengying Li8Hongshan Diao9Falin Zhou10Key Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaShenzhen Base of South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shenzhen 518121, ChinaKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, ChinaHigh concentrations of ammonia nitrogen could result in the death of aquatic animals and cause a huge economic loss in the aquaculture industry. However, the metabolic responses to acute ammonia nitrogen stress remain largely unknown in <i>Penaeus monodon</i>. In this study, we first investigated the histological change in tissues in <i>Penaeus monodon</i> under 96 h acute ammonia nitrogen stress. The result of the paraffin section showed that acute ammonia nitrogen stress induced severe epithelial detachment and lumen dilatation of the hepatopancreas, swollen and hemocyte infiltration of the gills, and mucosa exfoliation and shortened villi of the intestine in <i>Penaeus monodon</i>, suggesting the impairment of the normal physiological function in these tissues. We next examined the change in the metabolic product in the plasma and the enzyme activity in the hepatopancreas after ammonia nitrogen stress. Upon ammonia stress, both the concentration of ammonia and urea nitrogen significantly increased, while there was no significant increase in the concentration of uric acid, which is consistent with the results that the enzyme activity of glutamine synthetase (GS), glutamate dehydrogenase (GDH), and aspartate transaminase (GOT) became significantly elevated and the enzyme activity of adenosine deaminase (ADA) in the purine metabolism pathway significantly decreased after ammonia stress, suggesting that shrimp could convert excessive ammonia to urea for ammonia detoxification through the ammonia–nitrogen metabolism pathways. Interestingly, we also observed a significant increase in superoxide dismutase (SOD) activity, suggesting a potential role of this antioxidant enzyme in the clearance of reactive oxygen species (ROS) induced via ammonia stress. Moreover, we found that acute ammonia nitrogen stress inhibited the enzyme activity of caspase 3 and caspase 8, suggesting an important role of apoptosis in protecting <i>Penaeus monodon</i> against acute ammonia stress. Overall, our findings revealed that <i>Penaeus monodon</i> may employ metabolic and purine pathways and undergo oxidative stress and apoptosis for ammonia detoxification under ammonia nitrogen stress, thus providing new insight into the metabolic response of shrimp to acute ammonia stress.https://www.mdpi.com/2079-7737/14/5/501black tiger shrimp (<i>Penaeus monodon</i>)ammonia nitrogen stressmetabolic responseantioxidant enzymescaspase
spellingShingle Yangyang Ding
Shigui Jiang
Song Jiang
Yundong Li
Qibin Yang
Lishi Yang
Jianhua Huang
Jianzhi Shi
Pengying Li
Hongshan Diao
Falin Zhou
Metabolic Response of Black Tiger Shrimp (<i>Penaeus monodon</i>) to Acute Ammonia Nitrogen Stress
Biology
black tiger shrimp (<i>Penaeus monodon</i>)
ammonia nitrogen stress
metabolic response
antioxidant enzymes
caspase
title Metabolic Response of Black Tiger Shrimp (<i>Penaeus monodon</i>) to Acute Ammonia Nitrogen Stress
title_full Metabolic Response of Black Tiger Shrimp (<i>Penaeus monodon</i>) to Acute Ammonia Nitrogen Stress
title_fullStr Metabolic Response of Black Tiger Shrimp (<i>Penaeus monodon</i>) to Acute Ammonia Nitrogen Stress
title_full_unstemmed Metabolic Response of Black Tiger Shrimp (<i>Penaeus monodon</i>) to Acute Ammonia Nitrogen Stress
title_short Metabolic Response of Black Tiger Shrimp (<i>Penaeus monodon</i>) to Acute Ammonia Nitrogen Stress
title_sort metabolic response of black tiger shrimp i penaeus monodon i to acute ammonia nitrogen stress
topic black tiger shrimp (<i>Penaeus monodon</i>)
ammonia nitrogen stress
metabolic response
antioxidant enzymes
caspase
url https://www.mdpi.com/2079-7737/14/5/501
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