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Effects of the sulfated polysaccharides dextran sulfate and heparin on shrimp immunity and infection by white spot syndrome virus and Vibrio parahaemolyticus
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Metadata
Document Title
Effects of the sulfated polysaccharides dextran sulfate and heparin on shrimp immunity and infection by white spot syndrome virus and Vibrio parahaemolyticus
Author
Amphan S.
Name from Authors Collection
Scopus Author ID
6508068998
Affiliations
Program in Biotechnology, Faculty of Science, Chulalongkorn University, Phyathai Rd., Patumwan, Bangkok, 10330, Thailand; Center of Excellence in Structural and Computational Biology, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Phyathai Rd., Patumwan, Bangkok, 10330, Thailand; Center of Excellence for Molecular Biology and Genomics of Shrimp, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Phyathai Rd., Patumwan, Bangkok, 10330, Thailand; National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Pathum Thani, 12120, Thailand; Department of Biochemistry, Cell and Systems Biology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, United Kingdom
Type
Article
Source Title
Aquaculture Reports
ISSN
23525134
Year
2025
Volume
42
Open Access
All Open Access; Gold Open Access; Green Open Access
Publisher
Elsevier B.V.
DOI
10.1016/j.aqrep.2025.102735
Abstract
White spot syndrome virus (WSSV) and Vibrio parahaemolyticus are major pathogens of the economically important shrimp, Litopenaeus vannamei, causing white spot syndrome and hepatopancreatic necrosis disease (AHPND), respectively. In animals, sulfated glycosaminoglycans, particularly heparan sulfate, are key regulators controlling cell communication and infectivity of pathogens. We have tested the hypothesis that dextran sulfate and heparin would afford some protection against white spot syndrome and AHPND. Injection of dextran sulfate (1 % w/v), and heparin (0.3 % w/v) were not toxic, and encouragingly, co-injection of these with WSSV provided some delay in mortality to the shrimp. We then used shrimp feed supplemented with 1 % (w/w) dextran sulfate and 0.1 % (w/w) heparin for 14 days prior to infection by cohabitation with WSSV-infected shrimp or addition of V. parahaemolyticus to tank water. In the absence of pathogen, these feeds altered the shrimp immune response: enhancing PO activity and the expression of Lvpo1, Lvpo2, Lvlyso2, Lvpen3, Lvalf1, and Lvalf2, though no effect on the shrimp microbiome was observed. These activities of dextran sulfate and heparin differed, likely due to their different patterns of sulfated sugars. In the infection challenge, these feeds delayed mortality of the shrimp in WSSV infection, but not with V. parahaemolyticus. The data demonstrate that sulfated polysaccharides can modulate shrimp immunity and prolong the survival of WSSV-infected shrimp. Given there are many natural sulfated polysaccharides of diverse structure, there may be more effective and cheaper food supplements which would go some way to resolving WSSV infections in aquaculture. © 2025 The Authors
Keyword
Dextran sulfate | Heparin | Shrimp | Vibrio parahaemolyticus | White spot syndrome virus (WSSV)
License
CC BY
Rights
Authors
Publication Source
Scopus