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

FIG 4.

FIG 4

Dynamics of S. eriocheiris entry into S2 cells. (A) S. eriocheiris was labeled with the green fluorescent dye Alexa 488 (green). CLSM images of the experimental group at 48 h are shown. Scale bar, 10 μm. (B) Absolute real-time PCR was conducted to detect the copy number of S. eriocheiris in S2 cells. The data are means ± the SD for three independent experiments. (C) TEM images of S2 cells infected with S. eriocheiris for 48 h and control cells. Magnifications: left, ×700 (scale bar, 5 μm); right, ×1,200 (scale bar, 2 μm). High-magnification images of inclusion bodies and major intracellular vacuolization are shown. The arrow indicates the location of the inclusion body where the S. eriocheiris gathers. N, nucleus; S, Spiroplasma inclusion bodies; C, vacuolization.