The

reaction was terminated by heating at 95°C for 5 minutes. Prior to analysis, the cDNA was diluted by addition of 180 μl RNase-free water. Quantitative real-time PCR Q-PCR was performed as previously described [72]. Gene-specific oligonucleotide primers (Table 4) were designed using Primer Express 2.0 (Applied Biosystems) and were tested to determine amplification specificity, efficiency and for linearity of the amplification with RNA concentration. A typical 25 μl reaction contained 12.5 μl of SYBR Green Master Mix, 250 nM of each primer, and 5 μl of cDNA sample. Quantification reactions for the target transcripts at each timepoint were performed in triplicate and normalized to concurrently run 16 s rRNA levels from the same sample. Relative quantification of gene expression was determined using the 2-ΔΔCt method of Livak and Schmittgen where ΔΔCt = (Ct,Target – Ct,16 s)Timex – (Ct,Target – Ct,16 s)Control [73]. selleck screening library Table 4 Primers used for quantitative-PCR Primera Sequence 5′ to 3′ QPCR-16s-F TCGTCAGCAAGAAAGCAAGCT QPCR-16s-R GCTGGCGGCAGGCTTAA QPCR-adhC-F CTGCTGAATGTGGCGAATGT QPCR-adhC-R CTGACCATCTGGCATTAAGC QPCR-hxuC-F CGAGGGTTAAGTGATAATCGTGTT Dorsomorphin QPCR-hxuC-R AGCTACTTGGTCCTTTGATTACTTCAATT QPCR-fhuA-F CCGTCGTTTCGGTGATAACAA QPCR-fhuA-R TCGTGATCAATTTCGCTTTCG QPCR-fhuC-F AATTAATCGGCATGGGACGTT QPCR-fhuC-R TTTATCCGCCGCCGTTT a Primer pairs used to assay

for each gene. Primer pair QPCR-fhuA-F and QPCR-fhuA-R are used to assay transcriptional status of r2846.1777. Acknowledgements This work was supported in part by Public Health Service Grant AI29611 from the National Institute of Allergy and Infectious Disease to TLS and by health research contract HR-06-080 from The Oklahoma Center for the Advancement of Science and Technology to DJM. The authors gratefully acknowledge the support of the Children’s Resveratrol Hospital Foundation. The authors thank Dr. Arnold Smith for providing strain R2846 and strain R2866, Drs. Derrick Crook, Derek Hood and Richard Moxon for providing strain 10810 and Dr. Lauren Bakaletz for providing strain 86-028NP. References 1. Turk DC: The pathogenicity

of Haemophilus influenzae . J Med Microbiol 1984, 18:1–16.PubMedCrossRef 2. Panek H, O’Brian MR: A whole genome view of prokaryotic haem biosynthesis. Microbiology 2002, 148:2273–2282.PubMed 3. White DC, Granick S: Hemin biosynthesis in Haemophilus . J Bacteriol 1963, 85:842–850.PubMed 4. Schlor S, Herbert M, Rodenburg M, Blass J, Reidl J: Characterization of ferrochelatase ( hemH ) mutations in Haemophilus influenzae . Infect Immun 2000, 68:3007–3009.PubMedCrossRef 5. Loeb MR: Ferrochelatase activity and protoporphyrin IX utilization in Haemophilus influenzae . J Bacteriol 1995, 177:3613–3615.PubMed 6. Morton DJ, Stull TL: Haemophilus. In Iron Transport in Bacteria. Edited by: Crosa JH, Mey AR, Payne SM. Washington, DC: American Society for Microbiology; 2004:273–292. 7. Genco CA, Dixon DW: Emerging strategies in microbial haem capture.