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In the simulation experiment, we fixed r P = 2, d I = 0.1 and the maximal infection efficiency at 0.4.
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Results suggest a metabolic-state-dependent virus infection efficiency, which has not been shown previously.
The infection efficiency was determined by fluorescence intensity of GFP.
However, distinctive difference in infection efficiency was observed in some cloned immortalised cells, with HeV having higher infection efficiency.
Maximal infection occurred at moi = 5 and did not increase at moi>5 (data not shown).
Retroviral infections with GFP were included to assess infection efficiency, and to monitor transgene silencing [16].
HIV infection efficiency was characterized two days after infection using a luciferase-transducing HIV vector.
Infection efficiency in eRMS cells.
Infection efficiency was analyzed by flow cytometry.
A dose-dependent infection efficiency was observed.
A stable infection efficiency of approximately 100% was attained.
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