Organization and regulation of the neurotoxin genes in Clostridium botulinum and Clostridium tetani

被引:34
作者
Raffestin, S
Marvaud, JC
Cerrato, R
Dupuy, B
Popoff, MR
机构
[1] Inst Pasteur, Unite Bacteries Anaerobies & Toxines, F-75724 Paris 15, France
[2] Inst Pasteur, Unite Genet Mol Bacterienne, F-75724 Paris 15, France
关键词
Clostridium botulinum; Clostridium tetani; neurotoxin; genetics; toxinogenesis;
D O I
10.1016/j.anaerobe.2004.01.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Botulinum and tetanus neurotoxins are structurally and functionally related 150 kDa proteins that are potent inhibitors of neuroexocytosis. Botulinum neurotoxin associates with non-toxic proteins to form complexes of various sizes. The botulinum neurotoxin and non-toxic protein genes are clustered in a DNA segment called the botulinum locus. This locus is probably located on a mobile or degenerate mobile element, which accounts for the various genomic localizations (chromosome, plasmid, phage) in different Clostridium botulinum types. The botulinum neurotoxin and non-toxic protein genes are organized in two polycistronic operons (ntnh-bont and ha operons) transcribed in opposite orientations. The gene that separates the two operons of the botulinum locus in C. botulinum A encodes a 21 kDa protein BotR/A, which is a positive regulator of the expression of the botulinum locus genes. Similarly, in Clostridium tetani, the gene located immediately upstream of the tetanus toxin gene, encodes a positive regulatory protein, TetR. BotR and TetR are possibly alternative sigma factors related to TxeR and UviA, which regulate C. difficile toxin and C. perfrigens bacteriocin production. respectively. TxeR and UviA define a new sub-group of the sigma(70) family of RNA polymerase initiation factors. In addition. the C. botulinum genome contains predicted two-component system genes, some of which are possibly involved in regulation of toxinogenesis. (C) 2004 Elsevier Ltd. All rights reserved.
引用
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页码:93 / 100
页数:8
相关论文
共 53 条
[1]  
[Anonymous], AVIAN BOTULISM
[2]   Molecular characterization of the clusters of genes encoding the botulinum neurotoxin complex in Clostridium botulinum (Clostridium argentinense) type G and nonproteolytic Clostridium botulinum type B [J].
Bhandari, M ;
Campbell, KD ;
Collins, MD ;
East, AK .
CURRENT MICROBIOLOGY, 1997, 35 (04) :207-214
[3]   CHARACTERIZATION AND TRANSFERABILITY OF CLOSTRIDIUM-PERFRINGENS PLASMIDS [J].
BREFORT, G ;
MAGOT, M ;
IONESCO, H ;
SEBALD, M .
PLASMID, 1977, 1 (01) :52-66
[4]   The genome sequence of Clostridium tetani, the causative agent of tetanus disease [J].
Brüggemann, H ;
Bäumer, S ;
Fricke, WF ;
Wiezer, A ;
Liesegang, H ;
Decker, I ;
Herzberg, C ;
Martínez-Arias, R ;
Merkl, R ;
Henne, A ;
Gottschalk, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :1316-1321
[5]   Neurotoxin gene clusters in Clostridium botulinum type A strains:: Sequence comparison and evolutionary implications [J].
Dineen, SS ;
Bradshaw, M ;
Johnson, EA .
CURRENT MICROBIOLOGY, 2003, 46 (05) :345-352
[6]   Regulated transcription of Clostridium difficile toxin genes [J].
Dupuy, B ;
Sonenshein, AL .
MOLECULAR MICROBIOLOGY, 1998, 27 (01) :107-120
[7]  
DZIEJMAN M, 1995, 2 COMPONENT SIGNAL T, P305
[8]   Organization and phylogenetic interrelationships of genes encoding components of the botulinum toxin complex in proteolytic Clostridium botulinum types A, B, and F: Evidence of chimeric sequences in the gene encoding the nontoxic nonhemagglutinin component [J].
East, AK ;
Bhandari, M ;
Stacey, JM ;
Campbell, KD ;
Collins, MD .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1996, 46 (04) :1105-1112
[9]   BACTERIOPHAGE AND TOXIGENICITY OF CLOSTRIDIUM BOTULINUM TYPE-C [J].
EKLUND, MW ;
POYSKY, FT ;
REED, SM ;
SMITH, CA .
SCIENCE, 1971, 172 (3982) :480-&
[10]   INTERCONVERSION OF TYPE-C AND D STRAINS OF CLOSTRIDIUM-BOTULINUM BY SPECIFIC BACTERIOPHAGES [J].
EKLUND, MW ;
POYSKY, FT .
APPLIED MICROBIOLOGY, 1974, 27 (01) :251-258