Double-dose β-glucan treatment in WSSV-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ROS production
In our research efforts to reduce the impact of white spot syndrome virus (WSSV) disease outbreaks in shrimp aquaculture, we studied the effect of β-glucan administration to activate the prophenoloxidase (proPO) enzymatic cascade prior to WSSV challenge. Injection of a single dose of β-glucan (5μg/g...
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th-mahidol.331452018-11-09T09:59:34Z Double-dose β-glucan treatment in WSSV-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ROS production Siripong Thitamadee Jiraporn Srisala Suparat Taengchaiyaphum Kallaya Sritunyalucksana Mahidol University Thailand National Center for Genetic Engineering and Biotechnology Agricultural and Biological Sciences Environmental Science Medicine In our research efforts to reduce the impact of white spot syndrome virus (WSSV) disease outbreaks in shrimp aquaculture, we studied the effect of β-glucan administration to activate the prophenoloxidase (proPO) enzymatic cascade prior to WSSV challenge. Injection of a single dose of β-glucan (5μg/g) prior to WSSV challenge resulted in activation of the proPO system and reduced shrimp mortality (25-50%) when compared to controls (100%). By contrast, no significant reduction was observed using yellow head virus (YHV) in a similar protocol. We subsequently hypothesized that administration of a second dose of β-glucan after WSSV challenge might reduce shrimp mortality further. Surprisingly, the opposite occurred, and mortality of the WSSV-infected shrimp increased to 100% after the second β-glucan dose. Both immunofluorescence and RT-PCR assays revealed low WSSV levels in hemocytes of shrimp collected after the second dose of β-glucan administration, suggesting that the cause of increased mortality was unlikely to be increased WSSV replication. We found from measured phenoloxidase acitivity (PO) and H<inf>2</inf>O<inf>2</inf> production that the higher mortality may have resulted from a combination of WSSV infection plus over-production of reactive oxygen species (ROS) stimulated by two doses of β-glucan. Thus, caution may be prudent in continuous or prolonged activation of the shrimp immune system by β-glucan administration lest it exacerbate shrimp mortality in the event of WSSV infection. © 2014 Elsevier Ltd. 2018-11-09T01:47:57Z 2018-11-09T01:47:57Z 2014-01-01 Article Fish and Shellfish Immunology. Vol.40, No.2 (2014), 478-484 10.1016/j.fsi.2014.07.033 10959947 10504648 2-s2.0-84908343871 https://repository.li.mahidol.ac.th/handle/123456789/33145 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84908343871&origin=inward |
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Agricultural and Biological Sciences Environmental Science Medicine Siripong Thitamadee Jiraporn Srisala Suparat Taengchaiyaphum Kallaya Sritunyalucksana Double-dose β-glucan treatment in WSSV-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ROS production |
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In our research efforts to reduce the impact of white spot syndrome virus (WSSV) disease outbreaks in shrimp aquaculture, we studied the effect of β-glucan administration to activate the prophenoloxidase (proPO) enzymatic cascade prior to WSSV challenge. Injection of a single dose of β-glucan (5μg/g) prior to WSSV challenge resulted in activation of the proPO system and reduced shrimp mortality (25-50%) when compared to controls (100%). By contrast, no significant reduction was observed using yellow head virus (YHV) in a similar protocol. We subsequently hypothesized that administration of a second dose of β-glucan after WSSV challenge might reduce shrimp mortality further. Surprisingly, the opposite occurred, and mortality of the WSSV-infected shrimp increased to 100% after the second β-glucan dose. Both immunofluorescence and RT-PCR assays revealed low WSSV levels in hemocytes of shrimp collected after the second dose of β-glucan administration, suggesting that the cause of increased mortality was unlikely to be increased WSSV replication. We found from measured phenoloxidase acitivity (PO) and H<inf>2</inf>O<inf>2</inf> production that the higher mortality may have resulted from a combination of WSSV infection plus over-production of reactive oxygen species (ROS) stimulated by two doses of β-glucan. Thus, caution may be prudent in continuous or prolonged activation of the shrimp immune system by β-glucan administration lest it exacerbate shrimp mortality in the event of WSSV infection. © 2014 Elsevier Ltd. |
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Mahidol University |
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Mahidol University Siripong Thitamadee Jiraporn Srisala Suparat Taengchaiyaphum Kallaya Sritunyalucksana |
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Siripong Thitamadee Jiraporn Srisala Suparat Taengchaiyaphum Kallaya Sritunyalucksana |
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Siripong Thitamadee |
title |
Double-dose β-glucan treatment in WSSV-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ROS production |
title_short |
Double-dose β-glucan treatment in WSSV-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ROS production |
title_full |
Double-dose β-glucan treatment in WSSV-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ROS production |
title_fullStr |
Double-dose β-glucan treatment in WSSV-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ROS production |
title_full_unstemmed |
Double-dose β-glucan treatment in WSSV-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ROS production |
title_sort |
double-dose β-glucan treatment in wssv-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ros production |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/33145 |
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1763493793777057792 |