Literature DB >> 16701501

Insights in metabolism and toxin production from the complete genome sequence of Clostridium tetani.

Holger Brüggemann1, Gerhard Gottschalk.   

Abstract

The decryption of prokaryotic genome sequences progresses rapidly and provides the scientific community with an enormous amount of information. Clostridial genome sequencing projects have been finished only recently, starting with the genome of the solvent-producing Clostridium acetobutylicum in 2001. A lot of attention has been devoted to the genomes of pathogenic clostridia. In 2002, the genome sequence of C. perfringens, the causative agent of gas gangrene, has been released. Currently in the finishing stage and prior to publication are the genomes of the foodborne botulism-causing C. botulinum and of C. difficile, the causative agent of a wide spectrum of clinical manifestations such as antibiotic-associated diarrhea. Our team sequenced the genome of neuropathogenic C. tetani, a Gram-positive spore-forming bacterium predominantly found in the soil. In deep wound infections it occasionally causes spastic paralysis in humans and vertebrate animals, known as tetanus disease, by the secretion of potent neurotoxin, designated tetanus toxin. The toxin blocks the release of neurotransmitters from presynaptic membranes of interneurons of the spinal cord and the brainstem, thus preventing muscle relaxation. Fortunately, this disease is successfully controlled through immunization with tetanus toxoid, a formaldehyde-treated tetanus toxin, but nevertheless, an estimated 400,000 cases still occur each year, mainly of neonatal tetanus. The World Health Organization has stated that neonatal tetanus is the second leading cause of death from vaccine preventable diseases among children worldwide. This minireview focuses on an analysis of the genome sequence of C. tetani E88, a vaccine production strain, which is a toxigenic non-sporulating variant of strain Massachusetts. The genome consists of a 2,799,250 bp chromosome encoding 2618 open reading frames. The tetanus toxin is encoded on a 74,082 kb plasmid, containing 61 genes. Additional virulence-related factors as well as an insight into the metabolic strategy of C. tetani with regard to its pathogenic phenotype will be presented. The information from other clostridial genomes by means of comparative analysis will also be explored.

Entities:  

Year:  2004        PMID: 16701501     DOI: 10.1016/j.anaerobe.2003.08.001

Source DB:  PubMed          Journal:  Anaerobe        ISSN: 1075-9964            Impact factor:   3.331


  13 in total

Review 1.  Biochemistry, evolution and physiological function of the Rnf complex, a novel ion-motive electron transport complex in prokaryotes.

Authors:  Eva Biegel; Silke Schmidt; José M González; Volker Müller
Journal:  Cell Mol Life Sci       Date:  2010-11-12       Impact factor: 9.261

2.  Molecular analysis of an extrachromosomal element containing the C2 toxin gene discovered in Clostridium botulinum type C.

Authors:  Yoshihiko Sakaguchi; Tetsuya Hayashi; Yumiko Yamamoto; Keisuke Nakayama; Kai Zhang; Shaobo Ma; Hideyuki Arimitsu; Keiji Oguma
Journal:  J Bacteriol       Date:  2009-03-06       Impact factor: 3.490

3.  Crystallization and preliminary X-ray characterization of the catalytic domain of collagenase G from Clostridium histolyticum.

Authors:  Ulrich Eckhard; Dorota Nüss; Paulina Ducka; Esther Schönauer; Hans Brandstetter
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2008-04-24

4.  Transcriptional program of early sporulation and stationary-phase events in Clostridium acetobutylicum.

Authors:  Keith V Alsaker; Eleftherios T Papoutsakis
Journal:  J Bacteriol       Date:  2005-10       Impact factor: 3.490

Review 5.  Regulatory Networks Controlling Neurotoxin Synthesis in Clostridium botulinum and Clostridium tetani.

Authors:  Michel R Popoff; Holger Brüggemann
Journal:  Toxins (Basel)       Date:  2022-05-24       Impact factor: 5.075

6.  Proteomic protease specificity profiling of clostridial collagenases reveals their intrinsic nature as dedicated degraders of collagen.

Authors:  Ulrich Eckhard; Pitter F Huesgen; Hans Brandstetter; Christopher M Overall
Journal:  J Proteomics       Date:  2013-10-11       Impact factor: 4.044

7.  A Flexible Binding Site Architecture Provides New Insights into CcpA Global Regulation in Gram-Positive Bacteria.

Authors:  Yunpeng Yang; Lu Zhang; He Huang; Chen Yang; Sheng Yang; Yang Gu; Weihong Jiang
Journal:  mBio       Date:  2017-01-24       Impact factor: 7.867

8.  A universal strategy for high-yield production of soluble and functional clostridial collagenases in E. coli.

Authors:  Paulina Ducka; Ulrich Eckhard; Esther Schönauer; Stefan Kofler; Gerhard Gottschalk; Hans Brandstetter; Dorota Nüss
Journal:  Appl Microbiol Biotechnol       Date:  2009-03-31       Impact factor: 4.813

9.  Analysis of the neurotoxin complex genes in Clostridium botulinum A1-A4 and B1 strains: BoNT/A3, /Ba4 and /B1 clusters are located within plasmids.

Authors:  Theresa J Smith; Karen K Hill; Brian T Foley; John C Detter; A Christine Munk; David C Bruce; Norman A Doggett; Leonard A Smith; James D Marks; Gary Xie; Thomas S Brettin
Journal:  PLoS One       Date:  2007-12-05       Impact factor: 3.240

10.  Structural basis for activity regulation and substrate preference of clostridial collagenases G, H, and T.

Authors:  Ulrich Eckhard; Esther Schönauer; Hans Brandstetter
Journal:  J Biol Chem       Date:  2013-05-23       Impact factor: 5.157

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