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. 2019 Oct 18;87(11):e00233-19. doi: 10.1128/IAI.00233-19

FIG 7.

FIG 7

S. eriocheiris invasion of S2 cells was independent of caveolin-mediated endocytosis. (A) Cells treated with different concentrations of MβCD (25, 50, and 100 μM). (a) Cell viability was assessed by using CCK-8 after S. eriocheiris infection. Only DMSO was used as a positive control. Cells added to DMSO were infected with S. eriocheiris as a negative control. (b) The copy numbers of S. eriocheiris were obtained by real-time PCR. Cells added to DMSO were infected with S. eriocheiris as a negative control. (B) Cells treated with different concentrations of nystatin (5, 10, and 15 μM). (a) Cell viability was assessed by using CCK-8 after S. eriocheiris infection. Only DMSO was used as a positive control. Cells added to DMSO were infected with S. eriocheiris as a negative control. (b) The copy numbers of S. eriocheiris were obtained by real-time PCR. Cells added to DMSO were infected with S. eriocheiris as a negative control. Different letters indicate significant differences (P < 0.05). The data are means ± the SD of three independent experiments.