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. 2011 Jun 16;7(6):e1002088. doi: 10.1371/journal.ppat.1002088

Figure 2. Production of progeny virus in CD36+ EPCs under hypoxia vs. normoxia.

Figure 2

Day 8 CD36+ EPCs were infected with B19V at a low MOI (1,000 gc/cell) under either hypoxia or normoxia. At 72 hrs p.i., infected cells were lysed by repeated freeze-thaw cycles, to release progeny virus. After a brief spin, one third of the lysate from each culture was used to infect fresh day 8 CD36+ EPCs cultured under the same conditions. (A&B) At each passage, infected cells were examined by immunofluorescence to detect staining with an anti-B19V capsid antibody (detection for assembled capsids). (C&D)The production of progeny virus was quantified by qPCR-based assessment of the number of copies of the viral genome (C) and assessed for infectious units by titration of ffu (D).