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Fig. 3 tfec function counteracts enhanced microbicidal capacity of cxcr3.2 mutants (A?D) We inhibited Tfec function with the DN-tfec construct (A and B) or overexpressed the gene with the CMV:tfec construct (C and D) in WT embryos (AB/TL) and subsequently infected them with M. marinum mCherry (representative examples are shown). Larvae injected with DN-tfec had a lower bacterial burden than did PBS injected controls at 4 days post-infection (dpi) (A and B), while CMV:tfec injected larvae had a higher bacterial burden (C and D). (E and F) M. marinum ?ERP-infected WT larvae (AB/TL) previously injected with DN-tfec developed fewer (E) and smaller (F) bacterial clusters than did PBS controls and phenocopied cxcr3.2 mutants in their capacity to clear bacteria. (G and H) CMV:tfec-injected cxcr3.2 mutants (cxcr3.2?/?) infected with M. marinum ?ERP lost their enhanced microbicidal capacity and had more (G) and larger (H) bacterial clusters than did WT controls (cxcr3.2+/+). Overall bacterial burden data were analyzed using a two-tailed t test (A?D). Total bacterial clusters per fish were analyzed using a Mann-Whitney test and combined data of three independent replicates of 20?30 larvae (E and G). A Kolmogorov-Smirnov test was used to analyze the distribution of bacterial cluster sizes (F and H). All data are shown as mean ± SEM (?p ? 0.05, ??p ? 0.01, ???p ? 0.001 ????p ? 0.0001; ns, not significant [p > 0.05]).