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      Mycobacterial Esx-3 is required for mycobactin-mediated iron acquisition.

      Proceedings of the National Academy of Sciences of the United States of America
      Animals, Bacterial Proteins, genetics, metabolism, Genome, Bacterial, Iron, pharmacology, Macrophages, drug effects, microbiology, Mice, Mutation, Mycobacterium, growth & development, Mycobacterium Infections, Oxazoles, chemistry, Protein Binding, Secretory Pathway, Siderophores, biosynthesis, Transcription, Genetic, Up-Regulation

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          Abstract

          The Esx secretion pathway is conserved across Gram-positive bacteria. Esx-1, the best-characterized system, is required for virulence of Mycobacterium tuberculosis, although its precise function during infection remains unclear. Esx-3, a paralogous system present in all mycobacterial species, is required for growth in vitro. Here, we demonstrate that mycobacteria lacking Esx-3 are defective in acquiring iron. To compete for the limited iron available in the host and the environment, these organisms use mycobactin, high-affinity iron-binding molecules. In the absence of Esx-3, mycobacteria synthesize mycobactin but are unable to use the bound iron and are impaired severely for growth during macrophage infection. Mycobacteria thus require a specialized secretion system for acquiring iron from siderophores.

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