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1.
Fish Shellfish Immunol ; 99: 27-34, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32001352

RESUMO

Hepcidin links iron metabolism with innate immunity during the inhibition of bacterial infection. Our previous studies had shown that recombinant hepcidin can significantly reduce the mortality rate of Ctenopharyngodon idella infected with Flavobacterium columnare under laboratory conditions. Here, we studied the preventive and therapeutic effects of feed supplemented with different doses of recombinant hepcidin on F. columnare-challenged C. idella reared in a cage culture environment. The results showed that in the prevention groups, 30 and 90 mg/kg of added purified and unpurified hepcidin respectively resulted in a higher survival rate in the early post-infection period, while 60 mg/kg of purified hepcidin significantly improved the survival rate in the therapy group (all compared to the control group). In the hepatopancreas, the expression of hepcidin and ferritin was significantly up-regulated, and the levels of ferroportin and serum iron were significantly decreased, especially in the therapy group. In addition, the expression of iron-related genes in spleen and intestine exhibited a similar trend to that in hepatopancreas. Meanwhile, immune genes were up-regulated to varying degrees, and the therapy group exhibited a significantly improved expression of pro-inflammatory cytokines and specific immunity. In summary, our study shows that different doses of recombinant hepcidin had protective effects against bacterial infection by regulating the iron distribution and immune gene expression, which provides a strong foundation for the application of recombinant hepcidin in aquaculture.


Assuntos
Carpas/imunologia , Suplementos Nutricionais , Infecções por Flavobacteriaceae/veterinária , Hepcidinas/administração & dosagem , Imunidade Inata , Ração Animal , Animais , Aquicultura/métodos , Carpas/microbiologia , Doenças dos Peixes/microbiologia , Doenças dos Peixes/prevenção & controle , Proteínas de Peixes/administração & dosagem , Proteínas de Peixes/imunologia , Infecções por Flavobacteriaceae/prevenção & controle , Flavobacterium , Hepcidinas/genética , Ferro/sangue , Proteínas Recombinantes/administração & dosagem , Proteínas Recombinantes/imunologia
2.
Dev Comp Immunol ; 60: 218-27, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26972738

RESUMO

CpG oligodeoxynucleotides (ODNs) show strong immune stimulatory activity in vertebrate, however, they possess specific sequence feature among species. In this study, we screened out an optimal CpG ODN sequence for grass carp (Ctenopharyngodon idella), 1670A 5'-TCGAACGTTTTAACGTTTTAACGTT-3', from six published sequences and three sequences designed by authors based on grass carp head kidney mononuclear cells and CIK (C. idella kidney) cells proliferation. VP4 mRNA expression was strongly inhibited by CpG ODN 1670A in CIK cells with GCRV infection, showing its strong antiviral activity. The mechanism via toll-like receptor 9 (TLR9)-mediated signaling pathway was measured by real-time quantitative RT-PCR, and TLR21 did not play a role in the immune response to CpG ODN. The late up-regulation of CiRIG-I mRNA expression indicated that RIG-I-like receptors (RLRs) signaling pathway participated in the immune response to CpG ODN which is the first report on the interaction between CpG and RLRs. We also found that the efficient CpG ODN can activates interferon system. Infected with GCRV, type I interferon expression was reduced and type II interferon was induced by the efficient CpG ODN in CIK cells, especially IFNγ2, suggesting that IFNγ2 played an important role in response to the efficient CpG ODN. These results provide a theoretical basis and new development trend for further research on CpG and the application of CpG vaccine adjuvant in grass carp disease control.


Assuntos
Adjuvantes Imunológicos/farmacologia , Carpas/imunologia , Doenças dos Peixes/tratamento farmacológico , Oligodesoxirribonucleotídeos/farmacologia , Infecções por Reoviridae/veterinária , Reoviridae/imunologia , Animais , Antivirais/farmacologia , Carpas/virologia , Proliferação de Células , Avaliação Pré-Clínica de Medicamentos , Doenças dos Peixes/imunologia , Doenças dos Peixes/virologia , Proteínas de Peixes/genética , Proteínas de Peixes/metabolismo , Pesqueiros , Expressão Gênica , Rim Cefálico/efeitos dos fármacos , Rim Cefálico/imunologia , Reoviridae/efeitos dos fármacos , Infecções por Reoviridae/tratamento farmacológico , Infecções por Reoviridae/imunologia , Infecções por Reoviridae/virologia , Transdução de Sinais , Receptores Toll-Like/genética , Receptores Toll-Like/metabolismo
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