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Published on: June 23, 2013
Overexpression of Pasteurella multocida OmpA induces transcriptional changes and its possible implications for the
Xiaohong Yang1, Qiaoyu Fu1, Wencan Zhang1
1Hainan Key Lab of Tropical Animal Reproduction, Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Lab of Haikou, School of Animal Science and Technology, Hainan University, Haikou, Hainan, China.
Abstract:
Pasteurella multocida (P. multocida) is a highly infectious, zoonotic pathogen. Outer membrane protein A (OmpA) is an important virulence component of the outer membrane of P. multocida. OmpA mediates bacterial biofilm formation, eukaryotic cell infection, and immunomodulation. It is unclear how OmpA affects the host immune response. We estimated the role of OmpA in the pathogenesis of P. multocida by investigating the effect of OmpA on the immune cell transcriptome. Changes in the transcriptome of rat alveolar macrophages (NR8383) upon overexpression of P. multocida OmpA were demonstrated. A model cell line for stable transcription of OmpA was constructed by infecting NR8383 cells with OmpA-expressing lentivirus. RNA was extracted from cells and sequenced on an Illumina HiSeq platform. Key gene analysis of genes in the RNA-seq dataset were performed using various bioinformatics methods, such as gene ontology enrichment analysis, Kyoto Encyclopedia of Genes and Genomes enrichment analysis, Gene Set Enrichment Analysis, and Protein-Protein Interaction Analysis. Our findings revealed 1340 differentially expressed genes. Immune-related pathways that were significantly altered in rat alveolar macrophages under the effect of OmpA included focal adhesion, extracellular matrix and vascular endothelial growth factor signaling pathways, antigen processing and presentation, nucleotide oligomerization domain-like receptor and Toll-like receptor signaling pathways, and cytokine-cytokine receptor interaction. The key genes screened were Vegfa, Igf2r, Fabp5, P2rx1, C5ar1, Nedd4l, Gas6, Cxcl1, Pf4, Pdgfb, Thbs1, Col7a1, Vwf, Ccl9, and Arg1. Data of associated pathways and altered gene expression indicated that OmpA might cause the conversion of rat alveolar macrophages to M2-like. The related pathways and key genes can serve as a reference for OmpA of P. multitocida and host interaction mechanism studies.
Insights
Pasteurella multocida outer membrane protein A (OmpA) alters immune cell gene expression, potentially shifting macrophages to an M2-like state. This study identifies key pathways and genes involved in P. multocida pathogenesis.
Area of Science:
- Microbiology and Immunology
- Pathogen-Host Interactions
- Genomics and Transcriptomics
Background:
- Pasteurella multocida (P. multocida) is a significant zoonotic pathogen.
- Outer membrane protein A (OmpA) is a key virulence factor in P. multocida, implicated in biofilm formation, cell infection, and immunomodulation.
- The precise impact of OmpA on host immune responses remains incompletely understood.
Purpose of the Study:
- To elucidate the role of P. multocida OmpA in pathogenesis by examining its effect on the immune cell transcriptome.
- To investigate how OmpA influences the gene expression profile of rat alveolar macrophages (NR8383).
Main Methods:
- Established a stable OmpA-overexpressing cell line (NR8383) using lentiviral transduction.
- Performed RNA sequencing (Illumina HiSeq) on OmpA-expressing NR8383 cells.
- Utilized bioinformatics analyses, including GO, KEGG, GSEA, and PPI, to analyze differentially expressed genes and pathways.
Main Results:
- Identified 1340 differentially expressed genes in response to OmpA overexpression.
- Significantly altered immune-related pathways included focal adhesion, ECM-receptor interaction, VEGF signaling, antigen processing, NOD-like and Toll-like receptor signaling, and cytokine-cytokine receptor interaction.
- Key identified genes include Vegfa, Igf2r, Fabp5, P2rx1, C5ar1, Nedd4l, Gas6, Cxcl1, Pf4, Pdgfb, Thbs1, Col7a1, Vwf, Ccl9, and Arg1.
Conclusions:
- OmpA expression in rat alveolar macrophages leads to significant transcriptomic alterations.
- The observed pathway and gene expression changes suggest OmpA may induce a phenotypic shift in macrophages towards an M2-like state.
- The identified pathways and genes provide a foundation for further research into P. multocida OmpA-host interaction mechanisms.
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