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. 2012 Nov;26(11):4675–4684. doi: 10.1096/fj.12-212142

Figure 5.

Figure 5.

Characterization of the speA+ M1T1 strains 5636 and 5636ΔspeA-comp (solid symbols and bars) and the isogenic speA knockout mutant 5636ΔspeA (open symbols and bars). A) SpeB activity in cell-free stationary phase supernatants (mean±se). B) Percentage survival during coculture with human neutrophils in vitro (mean±se). C) Relative adherence to the human epithelial HEp-2 cell line in vitro (mean±se). D) Capacity to switch to an invasive SpeB phenotype at the site of local infection was determined during a 3-d subcutaneous passage in C57BL/J6 mice. Each data point represents the percentage of SpeB cfu recovered from a single mouse (n=10/strain). E) Relative virulence of 5636 (9.0×106 cfu/dose), 5636ΔspeA (1.4×107 cfu/dose), and 5636ΔspeA-comp (1.4×107 cfu/dose) was assessed over a 10-d period following subcutaneous infection of humanized plasminogen transgenic AlbPLG1 mice (n=10 mice/strain).