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. 2020 Mar 18;117(13):7317–7325. doi: 10.1073/pnas.1914830117

Fig. 6.

Fig. 6.

Tsf1 contributes to intestinal immunity. (A and B) Tsf1 expression in wild-type and RelE20 guts after (A) Ecc15 and (B) Pe infection, measured by RT-qPCR (n = 20 guts per group). The mean and SD of three independent experiments are shown. (C) Survival rates of wild-type, RelE20, and Tsf1JP94 flies orally infected with P. entomophila. (D) Survival rates of flies with gut-specific (Myo1A) knockdown of Tsf1 are significantly reduced compared to wild-type flies after Pe oral infection. (E) Increased susceptibility of Tsf1JP94 mutant flies to Pe oral infection is rescued by gut-specific overexpression of the wild-type (UAS-Tsf1WT) but not mutated form of Tsf1 (UAS-Tsf1Fe mutant). (F) Survival rates of wild-type and Tsf1JP94 flies orally infected with wild-type, pchE, and pvdP P. aeruginosa PA14. Survival graphs show one representative experiment out of three independent experiments with similar results with two to three cohorts of 20 flies per treatment. *P ≤ 0.05; **P ≤ 0.01; ***P ≤ 0.001; ****P ≤ 0.0001; ns, nonsignificant, P > 0.05.