A non-RD1 gene cluster is required for Snm secretion in Mycobacterium tuberculosis

被引:154
作者
MacGurn, JA [1 ]
Raghavan, S [1 ]
Stanley, SA [1 ]
Cox, JS [1 ]
机构
[1] Univ Calif San Francisco, Dept Immunol & Microbiol, San Francisco, CA 94143 USA
关键词
D O I
10.1111/j.1365-2958.2005.04800.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1653 / 1663
页数:11
相关论文
共 29 条
[1]   Comparative genomics of BCG vaccines by whole-genome DNA microarray [J].
Behr, MA ;
Wilson, MA ;
Gill, WP ;
Salamon, H ;
Schoolnik, GK ;
Rane, S ;
Small, PM .
SCIENCE, 1999, 284 (5419) :1520-1523
[2]   EsxA and EsxB are secreted by an ESAT-6-like system that is required for the pathogenesis of Staphylococcus aureus infections [J].
Burts, ML ;
Williams, WA ;
DeBord, K ;
Missiakas, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (04) :1169-1174
[3]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[4]   A protein secretion pathway critical for Mycobacterium tuberculosis virulence is conserved and functional in Mycobacterium smegmatis [J].
Converse, SE ;
Cox, JS .
JOURNAL OF BACTERIOLOGY, 2005, 187 (04) :1238-1245
[5]   Complex lipid determine tissue specific replication of Mycobacterium tuberculosis in mice [J].
Cox, JS ;
Chen, B ;
McNeil, M ;
Jacobs, WR .
NATURE, 1999, 402 (6757) :79-83
[6]   Global burden of tuberculosis - Estimated incidence, prevalence, and mortality by country [J].
Dye, C ;
Scheele, S ;
Dolin, P ;
Pathania, V ;
Raviglione, RC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (07) :677-686
[7]   Microarray analysis of the Mycobacterium tuberculosis transcriptional response to the acidic conditions found in phagosomes [J].
Fisher, MA ;
Plikaytis, BB ;
Shinnick, TM .
JOURNAL OF BACTERIOLOGY, 2002, 184 (14) :4025-4032
[8]   The RD1 virulence locus of Mycobacterium tuberculosis regulates DNA transfer in Mycobacterium smegmatis [J].
Flint, JL ;
Kowalski, JC ;
Karnati, PK ;
Derbyshire, KM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (34) :12598-12603
[9]   A mycobacterial virulence gene cluster extending RD1 is required for cytolysis, bacterial spreading and ESAT-6 secretion [J].
Gao, LY ;
Guo, S ;
McLaughlin, B ;
Morisaki, H ;
Engel, JN ;
Brown, EJ .
MOLECULAR MICROBIOLOGY, 2004, 53 (06) :1677-1693
[10]   FUSION OF ESCHERICHIA-COLI-LACZ TO THE CYTOCHROME-C GENE OF SACCHAROMYCES-CEREVISIAE [J].
GUARENTE, L ;
PTASHNE, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (04) :2199-2203