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  4. Six Hours after Infection, the Metabolic Changes Induced by WSSV Neutralize the Host's Oxidative Stress Defenses
 
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Six Hours after Infection, the Metabolic Changes Induced by WSSV Neutralize the Host's Oxidative Stress Defenses

Journal
Scientific Reports
Journal Volume
6
Date Issued
2016
Author(s)
Chen, I-Tung
Lee, Der-Yen
Huang, Yun-Tzu
Kou, Guang-Hsiung
Wang, Han-Ching
GEEN-DONG CHANG  
Lo, Chu-Fang
DOI
10.1038/srep27732
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/452632
https://www2.scopus.com/inward/record.uri?eid=2-s2.0-84973603509&doi=10.1038%2fsrep27732&partnerID=40&md5=9b18ec981693d3e450aa4a80c7f8adec
Abstract
Levels of intracellular ROS (reactive oxygen species) were significantly increased in hemocytes collected from WSSV-infected shrimp within the first 30-120 min after infection. Measurement of the NADPH/NADP(+) and GSH/GSSG ratios revealed that after a significant imbalance toward the oxidized forms at 2 hpi, redox equilibrium was subsequently restored. Meanwhile, high levels of lactic acid production, elevated NADH/NAD(+) ratios, and metabolic changes in the glycolysis pathway show that the Warburg effect was triggered by the virus. The timing of these changes suggests that WSSV uses this metabolic shift into aerobic glycolysis to counteract the high levels of ROS produced in response to viral infection. We further show that if the Warburg effect is inhibited by chemical inhibition of the PI3K-Akt-mTOR signaling pathway, or if the pentose phosphate pathway is chemically inhibited, then in both cases, the production of intracellular ROS is sustained. We conclude that WSSV uses the PI3K-Akt-mTOR-regulated Warburg effect to restore host redox balance and to counter the ROS produced by the host in response to WSSV infection. We also found that pyruvate kinase activity was inhibited by WSSV. This inhibition is likely to increase the availability of the raw materials essential for WSSV gene expression and replication.
SDGs

[SDGs]SDG3

Type
journal article

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