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Infection and Immunity, December 1999, p. 6496-6509, Vol. 67, No. 12
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Characterization of the angR Gene of
Vibrio anguillarum: Essential Role in Virulence
A. M.
Wertheimer,1,
W.
Verweij,1
Q.
Chen,1,
L. M.
Crosa,1
M.
Nagasawa,1
M. E.
Tolmasky,2
L. A.
Actis,3 and
J. H.
Crosa1,*
Department of Molecular Microbiology and
Immunology, Oregon Health Sciences University, Portland, Oregon
97201-30981; Department of Biological
Science, California State University Fullerton, Fullerton, California
92834-68502; and Department of
Microbiology, Miami University, Oxford, Ohio 450563
Received 6 June 1999/Returned for modification 21 July
1999/Accepted 31 August 1999
The ability to utilize the iron bound by high-affinity iron-binding
proteins in the vertebrate host is an important virulence factor for
the marine fish pathogen Vibrio anguillarum. Virulence in
septicemic infections is due to the presence of a highly efficient plasmid-encoded iron transport system. AngR, a 110-kDa protein component of this system, appears to play a role in both regulation of
the expression of the iron transport genes fatDCBA and the production of the siderophore anguibactin. Therefore, study of the
expression of the angR gene and the properties of its
product, the AngR protein, may contribute to the understanding of the
mechanisms of virulence of this pathogen. In this work, we present
genetic and molecular evidence from transposition mutagenesis
experiments and RNA analysis that angR, which maps
immediately downstream of the fatA gene, is part of a
polycistronic transcript that also includes the iron transport genes
fatDCBA and angT, a gene located downstream of
angR which showed domain homology to certain thioesterases involved in nonribosomal peptide synthesis of siderophores and antibiotics. In order to dissect the specific domains of AngR associated with regulation of iron transport gene expression, anguibactin production, and virulence, we also generated a panel of
site-directed angR mutants, as well as deletion
derivatives. Both virulence and anguibactin production were
dramatically affected by each one of the angR
modifications. In contrast to the need for an intact AngR molecule for
anguibactin production and virulence, the regulation of iron transport
gene expression does not require the entire AngR molecule, since
truncation of the carboxy terminus carrying the nonribosomal peptide
synthetase cores, as well as the site-directed mutations, resulted in
derivatives that retained their ability to regulate gene expression
which was only abolished after truncation of amino-terminal sequences
containing helix-turn-helix and leucine zipper motifs and a specialized
heterocyclization and condensation domain found in certain nonribosomal
peptide synthetases. The evidence, while not rigorously eliminating the possibility that a separate regulatory polypeptide exists and is
encoded somewhere within the 5'-end region of the angR
gene, strongly supports the idea that AngR is a bifunctional protein and that it plays an essential role in the virulence mechanisms of
V. anguillarum. We also show in this study that the
angT gene, found downstream of angR, intervenes
in the mechanism of anguibactin production but is not essential for
virulence or iron transport gene expression.
*
Corresponding author. Mailing address: Department of
Molecular Microbiology and Immunology, Oregon Health Sciences
University, 3181 Sam Jackson Park Rd., Portland, OR 97201-3098. Phone:
(503) 494-7583. Fax: (503) 494-6862. E-mail:
crosajor{at}ohsu.edu.

Present address: Abbot Laboratories, Abbot Park, IL 60064-3500.

Present address: Eisai Research Institute, Wilmington, MA
01887.
Infection and Immunity, December 1999, p. 6496-6509, Vol. 67, No. 12
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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