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Journal of Bacteriology, December 2004, p. 8123-8136, Vol. 186, No. 23
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.23.8123-8136.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Regulation of Iron Transport in Streptococcus pneumoniae by RitR, an Orphan Response Regulator

Andrew T. Ulijasz,1 David R. Andes,2 Jeremy D. Glasner,3 and Bernard Weisblum1*

Departments of Pharmacology,1 Medicine, University of Wisconsin Medical School,2 School of Veterinary Medicine, University of Wisconsin College of Agriculture and Life Sciences, Madison, Wisconsin3

Received 5 May 2004/ Accepted 29 July 2004

RitR (formerly RR489) is an orphan two-component signal transduction response regulator in Streptococcus pneumoniae that has been shown to be required for lung pathogenicity. In the present study, by using the rough strain R800, inactivation of the orphan response regulator gene ritR by allele replacement reduced pathogenicity in a cyclophosphamide-treated mouse lung model but not in a thigh model, suggesting a role for RitR in regulation of tissue-specific virulence factors. Analysis of changes in genome-wide transcript mRNA levels associated with the inactivation of ritR compared to wild-type cells was performed by the use of high-density DNA microarrays. Genes with a change in transcript abundance associated with inactivation of ritR included piuB, encoding an Fe permease subunit, and piuA, encoding an Fe carrier-binding protein. In addition, a dpr ortholog, encoding an H2O2 resistance protein that has been shown to reduce synthesis of reactive oxygen intermediates, was activated in the wild-type (ritR+) strain. Microarray experiments suggested that RitR represses Fe uptake in vitro by negatively regulating the Piu hemin-iron transport system. Footprinting experiments confirmed site-specific DNA-binding activity for RitR and identified three binding sites that partly overlap the +1 site for transcription initiation upstream of piuB. Transcripts belonging to other gene categories found to be differentially expressed in our array studies include those associated with (i) H2O2 resistance, (ii) repair of DNA damage, (iii) sugar transport and capsule biosynthesis, and (iv) two-component signal transduction elements. These observations suggest that RitR is an important response regulator whose primary role is to maintain iron homeostasis in S. pneumoniae. The name ritR (repressor of iron transport) for the orphan response regulator gene, rr489, is proposed.

* Corresponding author. Mailing address: Pharmacology Department, University of Wisconsin Medical School, 1300 University Avenue, Madison, WI 53706. Phone: (608) 262-0972. Fax: (608) 262-1257. E-mail: weisblum{at}wisc.edu.

Journal of Bacteriology, December 2004, p. 8123-8136, Vol. 186, No. 23
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.23.8123-8136.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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