Figure 4From: Comparison of static immersion and intravenous injection systems for exposure of zebrafish embryos to the natural pathogen Edwardsiella tardaMarker gene expression in immersion tests after fractionation of E. tarda suspension. The E. tarda suspension as used for the immersion experiments in Figure 1-3 was separated into two fractions by centrifugation. Embryos were immersed at 25 hpf for 5 h in the wash fluid obtained after centrifugation, or in the resuspended bacterial pellet (washed bacteria), or in clean egg water as a control. Subsequently, embryos were washed and transferred to fresh egg water. RNA was isolated from pools of 20 embryos at 5 and 24 h after the start of exposure (hpe) and the expression levels of cyp1a (a), irg1l (b), mmp9 (c), and il1b (d) were quantified by qPCR. A representative example of two independent experiments is shown. Relative induction levels are shown with the lowest expression level set at 1.Back to article page