Phage regulatory circuits and virulence gene expression

被引:164
作者
Waldor, MK
Friedman, DI [1 ]
机构
[1] Tufts Univ, Sch Med, Dept Microbiol, Boston, MA 02111 USA
[2] Howard Hughes Med Inst, Boston, MA 02111 USA
[3] Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1016/j.mib.2005.06.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In many pathogenic bacteria, genes that encode virulence factors are located in the genomes of prophages. Clearly bacteriophages are important vectors for disseminating virulence genes, but, in addition, do phage regulatory circuits contribute to expression of these genes? Phages of the lambda family that have genes encoding Shiga toxin are found in certain pathogenic Escherichia coli (known as Shiga toxin producing E coli) and the filamentous phage CTX phi, that carries genes encoding cholera toxin (CTX), is found in Vibrio cholerae. Both the lambda and CTX phi phages have repressor systems that maintain their respective prophages in a quiescent state, and in both types of prophages this repressed state is abolished when the host cell SOS response is activated. In the lambda type of prophages, only binding of the phage-encoded repressor is involved in repression and this repressor ultimately controls Shiga toxin production and/or release. In the CTX phi prophage, binding of LexA, the bacterial regulator of SOS, in addition to binding of the repressor is involved in repression; the repressor has only limited control over CTX production and has no influence on its release.
引用
收藏
页码:459 / 465
页数:7
相关论文
共 56 条
[31]   Characterizing spontaneous induction of Stx encoding phages using a selectable reporter system [J].
Livny, J ;
Friedman, DI .
MOLECULAR MICROBIOLOGY, 2004, 51 (06) :1691-1704
[32]   Enteropathogenic and enterohaemorrhagic Escherichia coli deliver a novel effector called Cif, which blocks cell cycle G2/M transition [J].
Marchès, O ;
Ledger, TN ;
Boury, M ;
Ohara, M ;
Tu, XL ;
Goffaux, F ;
Mainil, J ;
Rosenshine, I ;
Sugai, M ;
De Rycke, J ;
Oswald, E .
MOLECULAR MICROBIOLOGY, 2003, 50 (05) :1553-1567
[33]   Characterization of XerC- and XerD-dependent CTX phage integration in Vibrio cholerae [J].
McLeod, SM ;
Waldor, MK .
MOLECULAR MICROBIOLOGY, 2004, 54 (04) :935-947
[34]   Evidence for a rolling-circle mechanism of phage DNA synthesis from both replicative and integrated forms of CTXφ [J].
Moyer, KE ;
Kimsey, HH ;
Waldor, MK .
MOLECULAR MICROBIOLOGY, 2001, 41 (02) :311-323
[35]   Identification of a novel Citrobacter rodentium type III secreted protein, EspI, and roles of this and other secreted proteins in infection [J].
Mundy, R ;
Petrovska, L ;
Smollett, K ;
Simpson, N ;
Wilson, RK ;
Yu, J ;
Tu, XL ;
Rosenshine, I ;
Clare, S ;
Dougan, G ;
Frankel, G .
INFECTION AND IMMUNITY, 2004, 72 (04) :2288-2302
[36]   Shiga toxin 2-converting bacteriophages associated with clonal variability in Escherichia coli O157:H7 strains of human origin isolated from a single outbreak [J].
Muniesa, M ;
de Simon, N ;
Prats, G ;
Ferrer, D ;
Pañella, H ;
Jofre, J .
INFECTION AND IMMUNITY, 2003, 71 (08) :4554-4562
[37]   Functional and genetic analysis of regulatory regions of coliphage H-19B: location of shiga-like toxin and lysis genes suggest a role for phage functions in toxin release [J].
Neely, MN ;
Friedman, DI .
MOLECULAR MICROBIOLOGY, 1998, 28 (06) :1255-1267
[38]   Sequence of Shiga toxin 2 phage 933W from Escherichia coli O157:H7:: Shiga toxin as a phage late-gene product [J].
Plunkett, G ;
Rose, DJ ;
Durfee, TJ ;
Blattner, FR .
JOURNAL OF BACTERIOLOGY, 1999, 181 (06) :1767-1778
[39]  
Ptashne M., 2004, A genetic switch, V3rd edition
[40]   LexA cleavage is required for CTX prophage induction [J].
Quinones, M ;
Kimsey, HH ;
Waldor, MK .
MOLECULAR CELL, 2005, 17 (02) :291-300