Tushara_capstone

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    Tushara_capstone - Presentation Transcript

    1. Interleukin-17 expression in Crassostrea gigas following Escherichia coli exposure Tushara Williamson (Saint Vitus) Steven Roberts
    2. Proposal / Experiment Question: How do Crassostrea gigas oysters respond to a bacterial stressor? The purpose of this experiment is to compare immune response in C. gigas oysters following exposure to heat-killed E. coli bacteria.
    3. Where we’re going • The role of cytokines • The role of interleukin-17 • E. coli bacteria information • Methods and Materials • Results • Discussion / Implications to the scientific community
    4. What are cytokines? • Protein • Functions in the vertebrate immune system • Acts as a messenger between cells to inhibit or stimulate immune functions • Three types: interleukins, interferons, chemokines
    5. Interleukin-17 • T-cell derived cytokine • Implicated in inflammatory diseases such as arthritis, cystic fibrosis and asthma in mammals • Nothing about interleukin-17 expression in invertebrates • Six types: A-F • IL-17B of interest for this experiment
    6. E. coli • Bacteria commonly found in gastrointestinal tract of endotherms • Ferment lactose into gas and acids • Most strains harmless but some can cause infections of the bladder and fatal diarrhea in humans
    7. Methods and Materials • Interleukin-17B primers designed • PCR and gel electrophoresis of C. gigas and O. Conchaphila gill, mantle and muscle tissue carried out to determine where interleukin-17 is expressed in organism • Oyster exposure to heat-killed E.coli trial • RNA extracted from trial oysters; reverse transcribed into cDNA • Quantitative PCR of control and experimental C. gigas gill cDNA
    8. Interleukin-17 primer design • Primers designed using fragment of gene sequence that appeared to be interleukin-17 based on sequence similarity • Primers designed using Geneious, bioinformatics software for sequence alignment (Biomatters, Ltd.) http://www.geneious.com
    9. PCR and Gel Electrophoresis • Polymerase Chain Reaction (PCR) done to show interleukin-17 expression in C.gigas gill, muscle and mantle with Ostrea conchaphila (Olympia oyster) control • Gel electrophoresis done as an 0.8% agarose mix stained with ethidium bromide
    10. C. gigas exposure trial • Two tanks set up (one experimental, one control) • Four adult C. gigas oysters each tank in seawater • Temperature controlled room (15.5˚ C / 60˚F) • Experimental tank exposed to 6.84 x 1011 heat killed bacteria suspended in 2L seawater for three hours
    11. Pictures
    12. Pictures
    13. Pictures
    14. http://video.google.com/videoplay?docid=6469897211658098497&hl=en
    15. RNA Reverse Transcription • Process where single-stranded RNA is transcribed with reverse transcriptase into cDNA
    16. Quantitative PCR • Modification of traditional PCR method • Used to find quantity of DNA, cDNA or RNA present in a sample • Uses fluorescent markers to find DNA (SYBR green) by monitoring fluorescence emitted after each detection cycle
    17. Results • Initial IL-17 C. gigas cDNA gel electrophoresis (gill, muscle, mantle) • Quantitative PCR results from oyster bacterial experimental and control cDNA
    18. IL-17 gel electrophoresis 1. O. conchaphila gill 2. C. gigas gill 3. O. conchaphila mantle 4. C. gigas mantle 5. O. conchaphila muscle 1 2 3 4 5 6 6. C. gigas muscle
    19. Quantitative PCR results Figure 1. Comparison of control and experimental relative expression levels of interleukin-17b in C. gigas gill samples 300 Relative Expression Level 250 1 - 4 Control 6 - 8 Experimental 200 150 100 50 0 1 2 3 4 5 6 7 8
    20. Quantitative PCR results Figure 1. Control cDNA relative expression levels of C. gigas gill tissue samples 1.7 1.8 Relative Expression Level 1.6 1.4 1.2 1 0.8 0.5 0.6 0.4 0.1 0.2 0 0 1 2 3 4 Sample Number
    21. Quantitative PCR results Figure 1. Experimental cDNA relative expression levels of C. gigas gill tissue samples 1000 926.1 900 Relative Expression Level 800 700 600 500 400 300 183.4 200 39.8 100 0.1 0 1 2 3 4 Sample Number
    22. Quantitative PCR results • On average, relative expression level in experimental treatments was 500 times higher than in control treatments
    23. Implications to the scientific community 1. Gain knowledge on IL-17 in invertebrates; provide inspiration and basis for future research a. Majority of information about IL-17 is about mammals, humans more specifically 2. Use IL-17 expression in C. gigas as an indicator of water quality a. IL-17 expression can imply high levels of E. coli, making surrounding waters unsafe for shellfish harvest, swimming and fishing
    24. Implications to the scientific community 3. Marker assisted selection a. Broodstock in aquaculture can be possibly selected based on expression 4. Can give implications as to the effects of other pathogens that can affect C. gigas such as Vibrio sp.
    25. Future directions • Increase sample size • Look at different exposure times • Look at other genes • Look at other pathogens

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