Comparison of static immersion and intravenous injection systems for exposure of zebrafish embryos to the natural pathogen Edwardsiella tarda
| Autor: | Annemarie H. Meijer, Herman P. Spaink, Anita Ordas, Joost J. van Soest, Guido V. Bloemberg, Oliver W. Stockhammer |
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| Rok vydání: | 2011 |
| Předmět: |
lcsh:Immunologic diseases. Allergy
animal structures Embryo Nonmammalian Immunology Interleukin-1beta Virulence Microbiology Immune system Gene expression Immersion Cytochrome P-450 CYP1A1 Escherichia coli Animals Pseudomonas Infections Pathogen Zebrafish Edwardsiella tarda Escherichia coli Infections Hydro-Lyases Regulator gene Innate immune system biology Gene Expression Profiling Enterobacteriaceae Infections Zebrafish Proteins biology.organism_classification Microarray Analysis Gene Expression Regulation Matrix Metalloproteinase 9 embryonic structures Injections Intravenous Pseudomonas aeruginosa lcsh:RC581-607 Research Article |
| Zdroj: | BMC Immunology BMC Immunology, Vol 12, Iss 1, p 58 (2011) |
| ISSN: | 1471-2172 |
| Popis: | Background The zebrafish embryo is an important in vivo model to study the host innate immune response towards microbial infection. In most zebrafish infectious disease models, infection is achieved by micro-injection of bacteria into the embryo. Alternatively, Edwardsiella tarda, a natural fish pathogen, has been used to treat embryos by static immersion. In this study we used transcriptome profiling and quantitative RT-PCR to analyze the immune response induced by E. tarda immersion and injection. Results Mortality rates after static immersion of embryos in E. tarda suspension varied between 25-75%, while intravenous injection of bacteria resulted in 100% mortality. Quantitative RT-PCR analysis on the level of single embryos showed that expression of the proinflammatory marker genes il1b and mmp9 was induced only in some embryos that were exposed to E. tarda in the immersion system, whereas intravenous injection of E. tarda led to il1b and mmp9 induction in all embryos. In addition, microarray expression profiles of embryos subjected to immersion or injection showed little overlap. E. tarda-injected embryos displayed strong induction of inflammatory and defense genes and of regulatory genes of the immune response. E. tarda-immersed embryos showed transient induction of the cytochrome P450 gene cyp1a. This gene was also induced after immersion in Escherichia coli and Pseudomonas aeruginosa suspensions, but, in contrast, was not induced upon intravenous E. tarda injection. One of the rare common responses in the immersion and injection systems was induction of irg1l, a homolog of a murine immunoresponsive gene of unknown function. Conclusions Based on the differences in mortality rates between experiments and gene expression profiles of individual embryos we conclude that zebrafish embryos cannot be reproducibly infected by exposure to E. tarda in the immersion system. Induction of il1b and mmp9 was consistently observed in embryos that had been systemically infected by intravenous injection, while the early transcriptional induction of cyp1a and irg1l in the immersion system may reflect an epithelial or other tissue response towards cell membrane or other molecules that are shed or released by bacteria. Our microarray expression data provide a useful reference for future analysis of signal transduction pathways underlying the systemic innate immune response versus those underlying responses to external bacteria and secreted virulence factors and toxins. |
| Databáze: | OpenAIRE |
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