A non‐RD1 gene cluster is required for Snm secretion in Mycobacterium tuberculosis
- 19 August 2005
- journal article
- Published by Wiley in Molecular Microbiology
- Vol. 57 (6) , 1653-1663
- https://doi.org/10.1111/j.1365-2958.2005.04800.x
Abstract
The Snm secretion system is a crucial virulence determinant of Mycobacterium tuberculosis. Genes encoding all known components of this alternative secretion pathway are clustered at the same genetic locus, known as RD1. Here, we show that a mutant M. tuberculosis strain containing a transposon insertion in the Rv3615c gene, which is situated outside the RD1 locus, results in loss of Snm secretion. Complementation analysis revealed that both Rv3615c and the downstream gene Rv3614c are required for Snm secretion. Thus, we have renamed the two genes snm9 and snm10 respectively. The snm9::Tn mutant phenocopies bona fide snm mutants, exhibiting attenuation in mice, macrophage growth defects and failure to suppress cytokine induction. Furthermore, yeast two-hybrid analysis revealed a physical interaction between Snm10 and Snm7 (Rv3882c), suggesting that Snm10 may function in complex with other Snm proteins during secretion. Thus, snm9 and snm10 are the first genes located outside the RD1 locus identified as critical components of Snm secretion. These data indicate that Snm secretion consists of an elaborate network of interactions that likely arose from multiple duplication events during the evolution of M. tuberculosis.Keywords
This publication has 29 references indexed in Scilit:
- A Protein Secretion Pathway Critical for Mycobacterium tuberculosis Virulence Is Conserved and Functional in Mycobacterium smegmatisJournal of Bacteriology, 2005
- Tuberculous Granuloma Formation Is Enhanced by a Mycobacterium Virulence DeterminantPLoS Biology, 2004
- CFP10 discriminates between nonacetylated and acetylated ESAT‐6 of Mycobacterium tuberculosis by differential interactionProteomics, 2004
- Use of Recombinant ESAT-6:CFP-10 Fusion Protein for Differentiation of Infections of Cattle by Mycobacterium bovis and by M. avium subsp. avium and M. avium subsp. paratuberculosisClinical and Vaccine Immunology, 2004
- Individual RD1‐region genes are required for export of ESAT‐6/CFP‐10 and for virulence of Mycobacterium tuberculosisMolecular Microbiology, 2004
- Deletion of RD1 fromMycobacterium tuberculosisMimics Bacille Calmette‐Guérin AttenuationThe Journal of Infectious Diseases, 2003
- ideR , an Essential Gene in Mycobacterium tuberculosis : Role of IdeR in Iron-Dependent Gene Expression, Iron Metabolism, and Oxidative Stress ResponseInfection and Immunity, 2002
- Conclusive Evidence That the Major T-cell Antigens of theMycobacterium tuberculosis Complex ESAT-6 and CFP-10 Form a Tight, 1:1 Complex and Characterization of the Structural Properties of ESAT-6, CFP-10, and the ESAT-6·CFP-10 ComplexJournal of Biological Chemistry, 2002
- Protein secretion and the pathogenesis of bacterial infectionsGenes & Development, 2001
- Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequenceNature, 1998