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. Author manuscript; available in PMC: 2010 Nov 1.
Published in final edited form as: Int J Med Microbiol. 2009 May 17;299(7):479–488. doi: 10.1016/j.ijmm.2009.03.004

Fig. 1.

Fig. 1

A) Growth of the H. influenzae nontypeable strain 86-028NP and the hbpA insertion mutant strain HI2092 in hdBHI supplemented with heme as the sole heme source. Wild-type strain 86-028NP at 2 μg ml−1 heme (solid circles), at 1 μg ml−1 (solid triangles), and at 500 ng ml−1 (solid squares). The hbpA insertion mutant strain HI12092 at 2 μg ml−1 heme (open circles), at 1 μg ml−1 (open triangles), and at 500 ng ml−1 (open squares). B) Growth of the H. influenzae nontypeable strain 86-028NP and the hbpA insertion mutant strain HI2092 in hdBHI supplemented with hemoglobin, hemoglobin–haptoglobin, or heme–human serum albumin complexes as the sole heme source. Wild-type strain 86-028NP in heme–albumin 200 ng ml−1 heme equivalent (solid circles), in hemoglobin 10 μg ml−1 (solid squares), and in hemoglobin–haptoglobin 10 μg ml−1 hemoglobin equivalent (solid triangles). The hbpA insertion mutant strain HI2092 in heme–albumin 200 ng ml−1 heme equivalent (open circles), in hemoglobin 10 μg ml−1 (open squares), and in hemoglobin–haptoglobin 10 μg ml−1 hemoglobin equivalent (open triangles). Results are mean ± SD for quintuplicate results from representative experiments. The Kruskal-Wallis test was used to compare growth of 86-028NP and HI2092 in all heme sources at all heme concentrations p<0.0001.