Gold nanoparticles (AuNP) exert immunostimulatory and protective effects in shrimp (Litopenaeus vannamei) against Vibrio parahaemolyticus
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Gold nanoparticles (AuNP) stimulate immune responses in mammals but they have not been tested in species of relevance in aquaculture. In this study the immunostimulant and protective potential of orally administered AuNP against V. parahaemolyticus, the causative agent of Acute Hepatopancreatic Necrosis Disease, was determined in shrimp. Synthetized AuNP (18.57 ± 4.37 nm) were moderately dispersed with a negative ζ potential of −10.3 ± 0.208 mV (pH = 7). AuNP were administered (single dose) at 0.2, 2, and 20 μg/g feed in shrimp. Hemolymph samples were withdrawn daily for 6 days. Hemolymph or hemocytes were used to determine total hemocyte counts, immune-related enzymatic activities, and expression of immune-relevant genes. Hepatopancreas was sampled for the analysis of AuNP biodistribution and histological examination. Survival was recorded daily. No mortality or toxicity signs in hepatopancreas were found. AuNP were detected in hepatopancreas. Early (24–48 h) immunostimulation was mainly related to immune gene up-regulation. Upon a challenge with V. parahaemolyticus, survival was higher (80%25) and histopathological damages were lower in shrimp treated with the 2 μg/g dose when compared to the control. Therefore orally administered AuNP are proposed as immunostimulants that protect shrimp against V. parahaemolyticus infection. © 2018 Elsevier Ltd
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Acute hepatopancreatic necrosis disease; AHPND; Crustacean; Diseases; Immune response; Immunostimulants; Metallic nanoparticles catalase; gold nanoparticle; myeloperoxidase; peroxidase; superoxide dismutase; toll like receptor 3; gold; immunological adjuvant; metal nanoparticle; protective agent; animal cell; animal experiment; animal model; animal tissue; Article; bacterial strain; blood cell; cell count; cellular immunity; controlled study; drug distribution; enzyme activity; gene; gene expression; hemolymph; hepatopancreas; histopathology; humoral immunity; immunostimulation; in vivo study; Litopenaeus vannamei; liver necrosis; nonhuman; priority journal; propo gene; single drug dose; upregulation; Vibrio parahaemolyticus; Vibrio parahaemolyticus infection; zeta potential; animal; drug effect; immunology; Penaeidae; physiology; tissue distribution; Vibrio parahaemolyticus; Adjuvants, Immunologic; Animals; Gold; Metal Nanoparticles; Penaeidae; Protective Agents; Tissue Distribution; Vibrio parahaemolyticus
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