Comparison of mammalian cell entry operons of mycobacteria: in silico analysis and expression profiling

被引:50
作者
Kumar, A
Chandolia, A
Chaudhry, U
Brahmachari, V
Bose, M [1 ]
机构
[1] Univ Delhi, Vallabh Bhai Patel Chest Inst, Dept Microbiol, Delhi 110007, India
[2] Univ Delhi, Dr BR Ambedkar Ctr Biomed Res, Delhi 110007, India
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2005年 / 43卷 / 02期
关键词
nice operons; mycobacteria; in silico analysis; domains; expression;
D O I
10.1016/j.femsim.2004.08.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mammalian cell entry (mce) operons, implicated in the entry of mycobacteria into host cells, are present in pathogenic and saprophytic species. It is likely that the genes in these operons have functions other than those required for entry into host cells. Using in silico analysis we have identified domains within the mce operons that might justify their occurrence in saprophytic species like Mycobacterium smegmatis. Our analysis identified in addition to the mce domain, the presence of the Tt2B and Ttg2C domains, typical of proteins involved in transport. We have also analysed and compared the expression profile between mce operons of Mycobacterium tuberculosis, Mycobacterium bovis and M. smegmatis under different growth conditions. In case of M. smegmatis, each operon presented domain truncation for at least one gene. We observe differential expression among the operons in M. smegmatis growing under different culture conditions. Bacilli growing in nutritionally rich medium with aeration, only the mce4 operon was expressed while during stationary phase of a standing culture, all four mce operons were expressed. In M. bovis, in addition to the absence of the mce3 operon, several protein domains encoded by the other operons were truncated. We detected expression of the mce2 operon in the exponential and stationary growth phase, while the mce1 operon was only expressed in the stationary growth phase. Differential expression of mce operons and their redundancy in the genome of the majority members of mycobacteria are discussed in view of our results. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Microbiological Societies.
引用
收藏
页码:185 / 195
页数:11
相关论文
共 21 条
[1]   CLONING OF AN MYCOBACTERIUM-TUBERCULOSIS DNA FRAGMENT ASSOCIATED WITH ENTRY AND SURVIVAL INSIDE CELLS [J].
ARRUDA, S ;
BOMFIM, G ;
KNIGHTS, R ;
HUIMABYRON, T ;
RILEY, LW .
SCIENCE, 1993, 261 (5127) :1454-1457
[2]   Mycobacterial infections in domestic and wild animals due to Mycobacterium marinum, M-fortuitum, M-chelonae, M-porcinum, M-farcinogenes, M-smegmatis, M-scrofulaceum. M-xenopi, M-kansasii, M-simiae and M-genavense [J].
Bercovier, H ;
Vincent, V .
REVUE SCIENTIFIQUE ET TECHNIQUE-OFFICE INTERNATIONAL DES EPIZOOTIES, 2001, 20 (01) :265-290
[3]  
CATHERINE PA, 1997, CLIN INFECT DIS, V24, P982
[4]   Recombinant Mycobacterium tuberculosis protein associated with mammalian cell entry [J].
Chitale, S ;
Ehrt, S ;
Kawamura, I ;
Fujimura, T ;
Shimono, N ;
Anand, N ;
Lu, SW ;
Cohen-Gould, L ;
Riley, LW .
CELLULAR MICROBIOLOGY, 2001, 3 (04) :247-254
[5]   Massive gene decay in the leprosy bacillus [J].
Cole, ST ;
Eiglmeier, K ;
Parkhill, J ;
James, KD ;
Thomson, NR ;
Wheeler, PR ;
Honoré, N ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Mungall, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, RM ;
Devlin, K ;
Duthoy, S ;
Feltwell, T ;
Fraser, A ;
Hamlin, N ;
Holroyd, S ;
Hornsby, T ;
Jagels, K ;
Lacroix, C ;
Maclean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Quail, MA ;
Rajandream, MA ;
Rutherford, KM ;
Rutter, S ;
Seeger, K ;
Simon, S ;
Simmonds, M ;
Skelton, J ;
Squares, R ;
Squares, S ;
Stevens, K ;
Taylor, K ;
Whitehead, S ;
Woodward, JR ;
Barrell, BG .
NATURE, 2001, 409 (6823) :1007-1011
[6]   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-+
[7]   CONSTRUCTION OF PHYLOGENETIC TREES [J].
FITCH, WM ;
MARGOLIASH, E .
SCIENCE, 1967, 155 (3760) :279-+
[8]   Disruption of the mycobacterial cell entry gene of Mycobacterium bovis BCG results in a mutant that exhibits a reduced invasiveness for epithelial cells [J].
Flesselles, B ;
Anand, NN ;
Remani, J ;
Loosmore, SM ;
Klein, MH .
FEMS MICROBIOLOGY LETTERS, 1999, 177 (02) :237-242
[9]   HOW CLOSE IS CLOSE - 16S RIBOSOMAL-RNA SEQUENCE IDENTITY MAY NOT BE SUFFICIENT TO GUARANTEE SPECIES IDENTITY [J].
FOX, GE ;
WISOTZKEY, JD ;
JURTSHUK, P .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1992, 42 (01) :166-170
[10]   Effects of growth conditions on expression of mycobacterial murA and tyrS genes and contributions of their transcripts to precursor rRNA synthesis [J].
Gonzalez-Y-Merchand, JA ;
Colston, MJ ;
Cox, RA .
JOURNAL OF BACTERIOLOGY, 1999, 181 (15) :4617-4627