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1.
Dev Comp Immunol ; 100: 103421, 2019 11.
Article in English | MEDLINE | ID: mdl-31254562

ABSTRACT

White spot syndrome virus (WSSV) is one of the most virulent and widespread pathogens that infect almost all marine crustaceans and therefore cause huge economic losses in aquaculture. The Bcl2 protein plays a key role in the mitochondrial apoptosis pathway, which is a crucial immune response in invertebrates. However, the role of Bcl2 in apoptosis and immunoregulation in mud crab, Scylla paramamosain, is poorly understood. Here, the Bcl2 homolog (SpBcl2) in S. paramamosain was cloned and its role in WSSV infection explored. The expression of SpBcl2 increased at both the transcriptional level and post-transcriptional level after WSSV infection, while the hemocytes apoptosis decreased significantly. Furthermore, there was increase in the level of cytochrome c coupled with an upregulation in the expression of SpBcl2. These results indicated that SpBcl2 suppressed apoptosis by preventing the release of cytochrome c from mitochondria, thereby promoting WSSV replication in mud crab. The findings here therefore provide novel insight into the immune response of mud crabs to WSSV infection.


Subject(s)
Arthropod Proteins/metabolism , Brachyura/immunology , Immunity, Innate , Proto-Oncogene Proteins c-bcl-2/metabolism , White spot syndrome virus 1/immunology , Animals , Apoptosis/immunology , Aquaculture , Arthropod Proteins/immunology , Brachyura/virology , Cytochromes c/immunology , Cytochromes c/metabolism , Disease Resistance/immunology , Gene Expression Profiling , Hemocytes/cytology , Hemocytes/immunology , Hemocytes/pathology , Mitochondria/immunology , Mitochondria/metabolism , Phylogeny , Proto-Oncogene Proteins c-bcl-2/immunology , Up-Regulation/immunology
2.
Dev Comp Immunol ; 67: 361-376, 2017 02.
Article in English | MEDLINE | ID: mdl-27581742

ABSTRACT

Tumor necrosis factor receptor-associated factor 6 (TRAF6) is a key cytoplasm signal adaptor that mediates signals activated by tumor necrosis factor receptor (TNFR) superfamily and the Interleukin-1 receptor/Toll-like receptor (IL-1/TLR) superfamily. The full-length 2492 bp TRAF6 (Sp-TRAF6) from Scylla paramamosain contains 1800 bp of open reading frame (ORF) encoding 598 amino acids, including an N-terminal RING-type zinc finger, two TRAF-type zinc fingers and a conserved C-terminal meprin and TRAF homology (MATH) domain. Multiple alignment analysis shows that the putative amino acid sequence of Sp-TRAf6 has highest identity of 88% with Pt-TRAF6 from Portunus trituberculatus, while the similarity of Sp-TRAF6 with other crustacean sequences was 54-55%. RT-PCR analysis indicated that Sp-TRAF6 transcripts were predominantly expressed in the hepatopancreas and stomach, whereas it was barely detected in the heart and hemocytes in our study. Moreover, Sp-TRAF6 transcripts were significantly up-regulated after Vibrio parahemolyticus and LPS challenges. RNA interference assay was carried out used by siRNA to investigate the genes expression patterns regulated by Sp-TRAF6. The qRT-PCR results showed that silencing Sp-TRAF6 gene could inhibit SpALF1, SpALF2, SpALF5 and SpALF6 expression in hemocytes, while inhibit SpALF1, SpALF3, SpALF4, SpALF5 and SpALF6 expression in hepatopancreas. Taken together, the acute-phase response to immune challenges and the inhibition of SpALFs gene expression indicate that Sp-TRAF6 plays an important role in host defense against pathogen invasions via regulation of ALF gene expression in S. paramamosain.


Subject(s)
Arthropod Proteins/metabolism , Brachyura/immunology , Hepatopancreas/metabolism , TNF Receptor-Associated Factor 6/metabolism , Vibrio Infections/immunology , Vibrio parahaemolyticus/immunology , Animals , Arthropod Proteins/genetics , Cells, Cultured , Cloning, Molecular , Gene Expression Regulation , Immunity, Innate , Lipopolysaccharides/immunology , Phylogeny , RNA, Small Interfering/genetics , Sequence Alignment , Signal Transduction , TNF Receptor-Associated Factor 6/genetics , Toll-Like Receptors/metabolism , Transcriptome
3.
Fish Shellfish Immunol ; 41(2): 156-62, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25193866

ABSTRACT

In a previous study, bacterial communities of the intestine in three populations of crabs (wild crabs, pond-raised healthy crabs and diseased crabs) were probed by culture-independent methods. In this study, we examined the intestinal communities of the crabs by bacterial cultivation with a variety of media. A total of 135 bacterial strains were isolated from three populations of mud crabs. The strains were screened for antagonistic activity against Vibrio parahaemolyticus using an agar spot assay. Antagonistic strains were then identified by 16S rRNA gene sequence analysis. Three strains (Bacillus subtilis DCU, Bacillus pumilus BP, Bacillus cereus HL7) with the strongest antagonistic activity were further evaluated for their probiotic characteristics. The results showed that two (BP and DCU) of them were able to survive low pH and high bile concentrations, showed good adherence characteristics and a broad spectrum of antibiotic resistance. The probiotic effects were then tested by feeding juvenile mud crabs (Scylla paramamosain) with foods supplemented with 10(5) CFU/g of BP or DCU for 30 days before being subjected to an immersion challenge with V. parahaemolyticus for 48 h. The treated crabs showed significantly higher expression levels of immune related genes (CAT, proPO and SOD) and activities of respiratory burst than that in controlled groups. Crabs treated with BP and DCU supplemented diets exhibited survival rates of 76.67% and 78.33%, respectively, whereas survival rate was 54.88% in crabs not treated with the probiotics. The data showed that indigenous mud-associated microbiota, such as DCU and BP, have potential application in controlling pathogenic Vibriosis in mud crab aquaculture.


Subject(s)
Bacillus/metabolism , Brachyura/immunology , Brachyura/microbiology , Gastrointestinal Tract/microbiology , Microbiota , Probiotics/metabolism , Vibrio parahaemolyticus/immunology , Analysis of Variance , Animals , Bacillus/immunology , Bile , Culture Media/chemistry , DNA Primers/genetics , Genotype , Hydrogen-Ion Concentration , Hydrophobic and Hydrophilic Interactions , Respiratory Burst/physiology
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