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Infection and Immunity, September 2005, p. 5706-5719, Vol. 73, No. 9
0019-9567/05/$08.00+0     doi:10.1128/IAI.73.9.5706-5719.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Characterization of Vibrio cholerae RyhB: the RyhB Regulon and Role of ryhB in Biofilm Formation

Alexandra R. Mey,2 Stephanie A. Craig,1 and Shelley M. Payne1,2*

Institute for Cellular and Molecular Biology,1 Section of Molecular Genetics and Microbiology, The University of Texas at Austin, Austin, Texas 78712-10952

Received 13 March 2005/ Returned for modification 27 April 2005/ Accepted 10 May 2005

Vibrio cholerae encodes a small RNA with homology to Escherichia coli RyhB. Like E. coli ryhB, V. cholerae ryhB is negatively regulated by iron and Fur and is required for repression of genes encoding the superoxide dismutase SodB and multiple tricarboxylic acid cycle enzymes. However, V. cholerae RyhB is considerably longer (>200 nucleotides) than the E. coli RNA (90 nucleotides), and it regulates the expression of a variety of genes that are not known to be regulated by RyhB in E. coli, including genes involved in motility, chemotaxis, and biofilm formation. A mutant with a deletion in ryhB had reduced chemotactic motility in low-iron medium and was unable to form wild-type biofilms. The defect in biofilm formation was suppressed by growing the mutant in the presence of excess iron or succinate. The wild-type strain showed reduced biofilm formation in iron-deficient medium, further supporting a role for iron in normal biofilm formation. The ryhB mutant was not defective for colonization in a mouse model and appeared to be at a slight advantage when competing with the wild-type parental strain. Other genes whose expression was influenced by RyhB included those encoding the outer membrane porins OmpT and OmpU, several iron transport systems, and proteins containing heme or iron-sulfur clusters. These data indicate that V. cholerae RyhB has diverse functions, ranging from iron homeostasis to the regulation of biofilm formation.


* Corresponding author. Mailing address: The University of Texas, Section of Molecular Genetics and Microbiology, Austin, TX 78712-1095. Phone: (512) 471-9258. Fax: (512) 471-7088. E-mail: payne{at}mail.utexas.edu.

Editor: F. C. Fang


Infection and Immunity, September 2005, p. 5706-5719, Vol. 73, No. 9
0019-9567/05/$08.00+0     doi:10.1128/IAI.73.9.5706-5719.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




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