Related Experiment Video
Updated: Mar 9, 2026

The Use of Mouse Splenocytes to Assess Pathogen-associated Molecular Pattern Influence on Clock Gene Expression
Published on: July 24, 2018
Molecular characterization of a p38 mitogen-activated protein kinase gene from Scylla paramamosain and its expression
Zehui Yu1, Yi Geng1, Anming Huang1
1College of Veterinary Medicine, Sichuan Agricultural University, Wenjiang, Sichuan 625014, PR China.
Abstract:
A novel p38 MAPK gene from S. paramamosain was cloned and characterized by rapid amplification of cDNA ends (RACE) technology. S. paramamosain p38 (Sp-p38) MAPK gene consists of an open reading frame of 1095bp encoding a 365-amino-acid protein, which showed close phylogenetic relationship to Litopenaeus vannamei p38 MAPK. The tissue distribution patterns showed that Sp-p38 MAPK was widely expressed in all examined tissues, with the highest expression in hemocytes and intestines. The expression levels of Sp-p38 MAPK in hemocytes was up-regulated post-stimulation, which reached the peak at 6h and 12h after bacteria (S. aureus and V. harveyi) and WSSV infection, respectively. In conclusion, our data contributed to define the biological characteristics of Sp-p38 MAPK and further demonstrated the critical role of Sp-p38 MAPK in vivo during the viral and bacterial infection.
Insights
A novel p38 MAPK gene was identified in S. paramamosain, showing wide tissue expression and increased levels upon bacterial and viral infection, highlighting its immune role.
Area of Science:
- * Molecular Biology
- * Immunology
- * Crustacean Research
Background:
- * The p38 MAPK signaling pathway is crucial for cellular responses to stress and pathogens.
- * Understanding immune gene function in shrimp is vital for aquaculture and disease management.
Purpose of the Study:
- * To clone and characterize a novel p38 MAPK gene from the shrimp S. paramamosain.
- * To investigate the tissue distribution and expression patterns of the Sp-p38 MAPK gene.
- * To elucidate the role of Sp-p38 MAPK in immune responses against bacterial and viral infections.
Main Methods:
- * Rapid amplification of cDNA ends (RACE) technology for gene cloning.
- * Phylogenetic analysis to determine evolutionary relationships.
- * Quantitative expression analysis in various tissues and post-infection.
Main Results:
- * A novel p38 MAPK gene (Sp-p38) was successfully cloned and characterized.
- * Sp-p38 MAPK exhibited broad tissue distribution, with highest expression in hemocytes and intestines.
- * Expression levels significantly increased following bacterial (S. aureus, V. harveyi) and WSSV infections.
Conclusions:
- * The Sp-p38 MAPK gene plays a significant role in the immune defense of S. paramamosain.
- * This study provides foundational data on Sp-p38 MAPK's biological characteristics and in vivo function.
- * Findings contribute to understanding shrimp immunity against common pathogens.
More Related Videos
10:27Determining Genetic Expression Profiles in C. elegans Using Microarray and Real-time PCR
Published on: July 30, 2011
09:25Implementation of a Permeable Membrane Insert-based Infection System to Study the Effects of Secreted Bacterial Toxins on Mammalian Host Cells
Published on: August 19, 2016