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Microbiology 148 (2002), 2191-2201
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Microbiology (2002), 148, 2191-2201.
© 2002 Society for General Microbiology


Research Paper

Swarming-coupled expression of the Proteus mirabilis hpmBA haemolysin operona

Gillian M. Fraser1, Laurent Claret1, Richard Furness1, Srishti Gupta1 and Colin Hughes1

Cambridge University Department of Pathology, Tennis Court Road, Cambridge CB2 1QP, UK1

Author for correspondence: Colin Hughes. Tel: +44 1223 333732. Fax: +44 1223 333327. e-mail: ch{at}mole.bio.cam.ac.uk

The HpmA haemolysin toxin of Proteus mirabilis is encoded by the hpmBA locus and its production is upregulated co-ordinately with the synthesis and assembly of flagella during differentiation into hyperflagellated swarm cells. Primer extension identified a {sigma}70 promoter upstream of hpmB that was upregulated during swarming. Northern blotting indicated that this promoter region was also required for concomitant transcription of the immediately distal hpmA gene, and that the unstable hpmBA transcript generated a stable hpmA mRNA and an unstable hpmB mRNA. Transcriptional luxAB fusions to the DNA regions 5' of the hpmB and hpmA genes confirmed that hpmB {sigma}70 promoter activity increased in swarm cells, and that there was no independent hpmA promoter. Increased transcription of the hpmBA operon in swarm cells was dependent upon a 125 bp sequence 5' of the {sigma}70 promoter -35 hexamer. This sequence spans multiple putative binding sites for the leucine-responsive regulatory protein (Lrp), and band-shift assays with purified Lrp confirmed the presence of at least two such sites. The influence on hpmBA expression of the key swarming positive regulators FlhD2C2 (encoded by the flagellar master operon), Lrp, and the membrane-located upregulator of the master operon, UmoB, was examined. Overexpression of each of these regulators moderately increased hpmBA transcription in wild-type P. mirabilis, and the hpmBA operon was not expressed in any of the flhDC, lrp or umoB mutants. Expression in the mutants was not recovered by cross-complementation, i.e. by overexpression of FlhD2C2, Lrp or UmoB. Expression of the zapA protease virulence gene, which like hpmBA is also upregulated in swarm cells, did not require Lrp, but like flhDC it was upregulated by UmoB. The results indicate intersecting pathways of control linking virulence gene expression and swarm cell differentiation.

Keywords: flagella, LRP, toxin, virulence gene expression

a The GenBank accession number for the sequence determined in this work is AJ250100.




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