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Infection and Immunity, April 2004, p. 2254-2262, Vol. 72, No. 4
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.4.2254-2262.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Growth Control of Small-Colony Variants by Genetic Regulation of the Hemin Uptake System

Andreas Roggenkamp,* Harald Hoffmann, and Mathias W. Hornef

Max von Pettenkofer Institute for Hygiene and Medical Microbiology, Department of Bacteriology, University Hospital Großhadern, Ludwig-Maximilian University, D-81377 Munich, Germany

Received 8 September 2003/ Returned for modification 18 November 2003/ Accepted 29 December 2003

Small-colony variants (SCVs) are slow-growing variants of human bacterial pathogens. They are associated with chronic persistent infections, and their biochemical identification and antimicrobial treatment are impaired by altered metabolic properties. To contribute to the understanding of SCV-mediated infections, we analyzed a clinical SCV isolate derived from a chronic prosthetic hip infection. A sequence analysis of housekeeping genes identified an Enterobacter hormaechei-like organism. The SCV phenotype, with growth as microcolonies, was caused by a block within the heme biosynthesis pathway through deletion of the hemB locus, as shown by hybridization and complementation experiments. At a low frequency, large-colony variants (LCVs) arose that were dependent on exogenous hemin. To investigate this phenomenon, we cloned and sequenced the 5.8-kb hemin uptake system, denoted ehu. Gene expression analysis indicated regulation of this locus in wild-type bacteria by the global iron regulator Fur. Inactivation of Fur in LCVs caused the derepression of ehu expression and facilitated bacterial growth. Genetic alterations of the fur locus in LCVs were identified as insertions of IS1A elements and point mutations. In contrast, SCVs could utilize exogenous hemin only in the absence of iron. Thus, we provide the first molecular characterization of the growth properties of a clinical SCV isolate, which may help to improve the diagnostic and therapeutic management of patients with chronic persistent infections.

* Corresponding author. Mailing address: Max von Pettenkofer Institute for Hygiene and Medical Microbiology, Department of Bacteriology, University Hospital Großhadern, Ludwig-Maximilian University, Marchioninistr. 15, D-81377 Munich, Germany. Phone: 49-089-2180 78202. Fax: 49-089-2180 78207. E-mail: Andreas.Roggenkamp{at}med.uni-muenchen.de.

Editor: V. J. DiRita

Infection and Immunity, April 2004, p. 2254-2262, Vol. 72, No. 4
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.4.2254-2262.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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