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Double-dose ß-glucan treatment in WSSV-challenged shrimp reduces viral replication but causes mortality possibly due to excessive ROS production.
Thitamadee, Siripong; Srisala, Jiraporn; Taengchaiyaphum, Suparat; Sritunyalucksana, Kallaya.
Afiliación
  • Thitamadee S; Center of Excellence for Shrimp Molecular Biology and Biotechnology, Faculty of Science, Mahidol University, RamaVI Rd., Bangkok 10400, Thailand; Department of Biotechnology, Faculty of Science, Mahidol University, RamaVI Rd., Bangkok 10400, Thailand.
  • Srisala J; Shrimp-virus interaction laboratory (ASVI), National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Rama VI Rd., Bangkok 10400, Thailand.
  • Taengchaiyaphum S; Center of Excellence for Shrimp Molecular Biology and Biotechnology, Faculty of Science, Mahidol University, RamaVI Rd., Bangkok 10400, Thailand.
  • Sritunyalucksana K; Center of Excellence for Shrimp Molecular Biology and Biotechnology, Faculty of Science, Mahidol University, RamaVI Rd., Bangkok 10400, Thailand; Department of Biotechnology, Faculty of Science, Mahidol University, RamaVI Rd., Bangkok 10400, Thailand; Shrimp-virus interaction laboratory (ASVI), Nati
Fish Shellfish Immunol ; 40(2): 478-84, 2014 Oct.
Article en En | MEDLINE | ID: mdl-25107695
ABSTRACT
In our research efforts to reduce the impact of white spot syndrome virus (WSSV) disease outbreaks in shrimp aquaculture, we studied the effect of ß-glucan administration to activate the prophenoloxidase (proPO) enzymatic cascade prior to WSSV challenge. Injection of a single dose of ß-glucan (5 µg/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 ß-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 ß-glucan dose. Both immunofluorescence and RT-PCR assays revealed low WSSV levels in hemocytes of shrimp collected after the second dose of ß-glucan administration, suggesting that the cause of increased mortality was unlikely to be increased WSSV replication. We found from measured phenoloxidase acitivity (PO) and H2O2 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 ß-glucan. Thus, caution may be prudent in continuous or prolonged activation of the shrimp immune system by ß-glucan administration lest it exacerbate shrimp mortality in the event of WSSV infection.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Replicación Viral / Penaeidae / Virus del Síndrome de la Mancha Blanca 1 / Beta-Glucanos Tipo de estudio: Etiology_studies Límite: Animals Idioma: En Revista: Fish Shellfish Immunol Asunto de la revista: BIOLOGIA / MEDICINA VETERINARIA Año: 2014 Tipo del documento: Article País de afiliación: Tailandia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Replicación Viral / Penaeidae / Virus del Síndrome de la Mancha Blanca 1 / Beta-Glucanos Tipo de estudio: Etiology_studies Límite: Animals Idioma: En Revista: Fish Shellfish Immunol Asunto de la revista: BIOLOGIA / MEDICINA VETERINARIA Año: 2014 Tipo del documento: Article País de afiliación: Tailandia