The Salicylate-Derived Mycobactin Siderophores of Mycobacterium Tuberculosis Are Essential for Growth in Macrophages

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 97; no. 3; pp. 1252 - 1257
• Main Authors: De Voss, James J., Rutter, Kerry, Schroeder, Benjamin G., Su, Hua, Zhu, YaQi, Barry, Clifton E.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences of the United States of America 01.02.2000; National Acad Sciences; National Academy of Sciences; The National Academy of Sciences
• Subjects: Bacteria; Bacterial Proteins - genetics; Bacterial Proteins - physiology; Biological Sciences; Biosynthesis; Cell growth; Enzymes; Gene Deletion; Humans; Infections; Iron; Iron - metabolism; Macrophages; Macrophages - microbiology; mbtB gene; MbtB protein; Microbiology; Molecules; Mycobacterium tuberculosis; Mycobacterium tuberculosis - growth & development; Mycobacterium tuberculosis - pathogenicity; Mycobacterium tuberculosis - physiology; mycobactin; mycobactins; Oxazoles - metabolism; Peptide Synthases - deficiency; Peptide Synthases - genetics; Peptide Synthases - physiology; Salicylates; salicylic acid; Salicylic Acid - metabolism; Serine - metabolism; Siderophores; Siderophores - metabolism; Tumor Cells, Cultured; Virulence
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.97.3.1252

Mycobacterium tuberculosis is an important pathogen of mammals that relies on 2-hydroxyphenyloxazoline-containing siderophore molecules called mycobactins for the acquisition of iron in the restrictive environment of the mammalian macrophage. These compounds have been proposed to be biosynthesized through the action of a cluster of genes that include both nonribosomal peptide synthase and polyketide synthase components. One of these genes encodes a protein, MbtB, that putatively couples activated salicylic acid with serine or threonine and then cyclizes this precursor to the phenyloxazoline ring system. We have used gene replacement through homologous recombination to delete the mbtB gene and replace this with a hygromycin-resistance cassette in the virulent strain of M. tuberculosis H37Rv. The resulting mutant is restricted for growth in iron-limited media but grows normally in iron-replete media. Analysis of siderophore production by this organism revealed that the biosynthesis of all salicylate-derived siderophores was interrupted. The mutant was found to be impaired for growth in macrophage-like THP-1 cells, suggesting that siderophore production is required for virulence of M. tuberculosis. These results provide conclusive evidence linking this genetic locus to siderophore production.