Publications by authors named "B R J Castillo-Corea"

Article Synopsis
  • Shrimp aquaculture faces significant challenges from infectious diseases like acute hepatopancreatic necrosis disease (AHPND) and white spot disease (WSD), making it crucial to understand the molecular mechanisms behind these diseases for better management.
  • A new gene called arrestin domain containing-3 (LvARRDC3) was identified as playing a significant role in the development of AHPND and WSD, influencing viral gene expression and pathogen interactions.
  • Manipulating LvARRDC3's expression through RNA silencing or overexpression showed a direct impact on the severity of infections, suggesting its potential as a target for disease control and a biomarker for improving shrimp breeding practices.
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In WSSV pathogenesis, the molecular mechanisms and the key host factors that regulate the viral replication and morphogenesis remain unclear. However, like most viruses, WSSV is known to induce metabolic reprogramming in several metabolic pathways including the host glutamine metabolism, and several recent reports have suggested that the sirtuins SIRT3, SIRT4, and SIRT5, which belong to a family of NAD-dependent deacetylases, play an important role in this regulation. Here we focus on characterizing LvSIRT4 from Litopenaeus vannamei and investigate its role in regulating glutamine dehydrogenase (GDH), an important enzyme that promotes glutaminolysis and viral replication.

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The cost of the purification process hinders the extensive use of cytosine phosphate guanosine-oligodeoxynucleotides (CpG-ODNs) for shrimp culture. Therefore, this study used a shuttle vector plasmid to carry 60 copies of CpG-ODN 1668 (pAD43-25_60CpG), which can replicate in Escherichia coli and Bacillus subtilis strain RIK1285. The first experiment used a reverse gavage procedure to deliver a substance (PBS [CK], pAD43-25 [P0], and pAD43-25_60CpG [P60], respectively) directly into the anterior midgut of Penaeus vannamei and transcriptome sequence analysis with a reference genome was performed to examine the expression of well-known immune-related genes.

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