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A novel streptococcal integrative conjugative element involved in iron acquisition

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Author(s)

Zoe Heather, Matthew T. G. Holden, Karen F. Steward, Julian Parkhill, Lijiang Song, Gregory L. Challis, Carl Robinson, Nicholas Davis-Poynter, Andrew S. Waller

School/Research organisations

Abstract

In this study, we determined the function of a novel non-ribosomal peptide synthetase (NRPS) system carried by a streptococcal integrative conjugative element (ICE), ICESe2. The NRPS shares similarity with the yersiniabactin system found in the high-pathogenicity island of Yersinia sp. and is the first of its kind to be identified in streptococci. We named the NRPS product 'equibactin' and genes of this locus eqbA-N. ICESe2, although absolutely conserved in Streptococcus equi, the causative agent of equine strangles, was absent from all strains of the closely related opportunistic pathogen Streptococcus zooepidemicus. Binding of EqbA, a DtxR-like regulator, to the eqbB promoter was increased in the presence of cations. Deletion of eqbA resulted in a small-colony phenotype. Further deletion of the irp2 homologue eqbE, or the genes eqbH, eqbI and eqbJ encoding a putative ABC transporter, or addition of the iron chelator nitrilotriacetate, reversed this phenotype, implicating iron toxicity. Quantification of (55)Fe accumulation and sensitivity to streptonigrin suggested that equibactin is secreted by S. equi and that the eqbH, eqbI and eqbJ genes are required for its associated iron import. In agreement with a structure-based model of equibactin synthesis, supplementation of chemically defined media with salicylate was required for equibactin production.

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Details

Original languageEnglish
Pages (from-to)1274-1292
Number of pages19
JournalMolecular Microbiology
Volume70
Issue number5
DOIs
Publication statusPublished - Dec 2008

    Research areas

  • BIOSYNTHETIC GENE-CLUSTER, NONRIBOSOMAL PEPTIDE SYNTHETASES, STREPTOMYCES-COELICOLOR GENOME, HIGH-PATHOGENICITY ISLAND, IN-VITRO RECONSTITUTION, TOXIN REPRESSOR DTXR, ARAC-TYPE REGULATOR, PSEUDOMONAS-AERUGINOSA, MYCOBACTERIUM-TUBERCULOSIS, YERSINIA-PESTIS

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