FIGURE SUMMARY
Title

Modulation of the Tissue Expression Pattern of Zebrafish CRP-Like Molecules Suggests a Relevant Antiviral Role in Fish Skin

Authors
Bello-Perez, M., Adamek, M., Coll, J., Figueras, A., Novoa, B., Falco, A.
Source
Full text @ Biology (Basel)

Gene expression analysis of crp1–7 in tissues of healthy zebrafish. The expression of crp1–7 was determined by RT-qPCR by using specific primers for each isoform (Table S1). ef1a mRNA was used as the endogenous control to normalize data, which are represented as the mean relative expression level × 103 ± SD of four different individuals. Statistical differences (p < 0.05, one-way ANOVA) between tissues are represented by: a (different from up to 1–2 tissues), b (different from up to 3–4 tissues), and c (different from up to 5–6 tissues). Data in bar graphs are summarized in a final double gradient colormap (descending blue gradient for values from 0 to 1 and ascending red gradient from values from 1 to ≥750).

Expression modulation of crp1–7 in zebrafish tissues in response to spring viremia of carp virus (SVCV) infection. The transcription levels of crp1–7 and SVCV n in tissues from SVCV-infected zebrafish at 2 and 5 dpi (black and white bars, respectively) were quantified by RT-qPCR. ef1a mRNA was used as the endogenous control in all cases. crp1–7 transcription levels were also normalized to the values obtained from the corresponding samples in non-infected fish. Data are represented as the mean fold changes ± SD for crps and as the mean relative expression level ± SD for SVCV n (four different individuals in all cases). Significant differences were determined by two-way ANOVA and Sidak’s multiple comparison test. Statistical differences between the 2- and 5-dpi groups are represented by keys together with a, b, and c letters on top. Statistical differences between the 2- or 5-dpi groups and the non-infected group are represented by a, b, and c letters just on top of the corresponding bars. a, p ≤ 0.05; b, p ≤ 0.01; c, p ≤ 0.001.

Gene expression analysis of crp1–7 in tissues of healthy zebrafish. The expression of crp1–7 was determined by RT-qPCR by using specific primers for each isoform (Table S1). ef1a mRNA was used as the endogenous control to normalize data, which are represented as the mean relative expression level × 103 ± SD of four different individuals. Statistical differences (p < 0.05, one-way ANOVA) between tissues are represented by: a (different from up to 1–2 tissues), b (different from up to 3–4 tissues), and c (different from up to 5–6 tissues). Data in bar graphs are summarized in a final double gradient colormap (descending blue gradient for values from 0 to 1 and ascending red gradient from values from 1 to ≥750).

Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Biology (Basel)