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Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum

BACKGROUND: Proteolytic Clostridium botulinum is the causative agent of botulism, a severe neuroparalytic illness. Given the severity of botulism, surprisingly little is known of the population structure, biology, phylogeny or evolution of C. botulinum. The recent determination of the genome sequenc...

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Autores principales: Carter, Andrew T, Paul, Catherine J, Mason, David R, Twine, Susan M, Alston, Mark J, Logan, Susan M, Austin, John W, Peck, Michael W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2674064/
https://www.ncbi.nlm.nih.gov/pubmed/19298644
http://dx.doi.org/10.1186/1471-2164-10-115
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author Carter, Andrew T
Paul, Catherine J
Mason, David R
Twine, Susan M
Alston, Mark J
Logan, Susan M
Austin, John W
Peck, Michael W
author_facet Carter, Andrew T
Paul, Catherine J
Mason, David R
Twine, Susan M
Alston, Mark J
Logan, Susan M
Austin, John W
Peck, Michael W
author_sort Carter, Andrew T
collection PubMed
description BACKGROUND: Proteolytic Clostridium botulinum is the causative agent of botulism, a severe neuroparalytic illness. Given the severity of botulism, surprisingly little is known of the population structure, biology, phylogeny or evolution of C. botulinum. The recent determination of the genome sequence of C. botulinum has allowed comparative genomic indexing using a DNA microarray. RESULTS: Whole genome microarray analysis revealed that 63% of the coding sequences (CDSs) present in reference strain ATCC 3502 were common to all 61 widely-representative strains of proteolytic C. botulinum and the closely related C. sporogenes tested. This indicates a relatively stable genome. There was, however, evidence for recombination and genetic exchange, in particular within the neurotoxin gene and cluster (including transfer of neurotoxin genes to C. sporogenes), and the flagellar glycosylation island (FGI). These two loci appear to have evolved independently from each other, and from the remainder of the genetic complement. A number of strains were atypical; for example, while 10 out of 14 strains that formed type A1 toxin gave almost identical profiles in whole genome, neurotoxin cluster and FGI analyses, the other four strains showed divergent properties. Furthermore, a new neurotoxin sub-type (A5) has been discovered in strains from heroin-associated wound botulism cases. For the first time, differences in glycosylation profiles of the flagella could be linked to differences in the gene content of the FGI. CONCLUSION: Proteolytic C. botulinum has a stable genome backbone containing specific regions of genetic heterogeneity. These include the neurotoxin gene cluster and the FGI, each having evolved independently of each other and the remainder of the genetic complement. Analysis of these genetic components provides a high degree of discrimination of strains of proteolytic C. botulinum, and is suitable for clinical and forensic investigations of botulism outbreaks.
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spelling pubmed-26740642009-04-28 Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum Carter, Andrew T Paul, Catherine J Mason, David R Twine, Susan M Alston, Mark J Logan, Susan M Austin, John W Peck, Michael W BMC Genomics Research Article BACKGROUND: Proteolytic Clostridium botulinum is the causative agent of botulism, a severe neuroparalytic illness. Given the severity of botulism, surprisingly little is known of the population structure, biology, phylogeny or evolution of C. botulinum. The recent determination of the genome sequence of C. botulinum has allowed comparative genomic indexing using a DNA microarray. RESULTS: Whole genome microarray analysis revealed that 63% of the coding sequences (CDSs) present in reference strain ATCC 3502 were common to all 61 widely-representative strains of proteolytic C. botulinum and the closely related C. sporogenes tested. This indicates a relatively stable genome. There was, however, evidence for recombination and genetic exchange, in particular within the neurotoxin gene and cluster (including transfer of neurotoxin genes to C. sporogenes), and the flagellar glycosylation island (FGI). These two loci appear to have evolved independently from each other, and from the remainder of the genetic complement. A number of strains were atypical; for example, while 10 out of 14 strains that formed type A1 toxin gave almost identical profiles in whole genome, neurotoxin cluster and FGI analyses, the other four strains showed divergent properties. Furthermore, a new neurotoxin sub-type (A5) has been discovered in strains from heroin-associated wound botulism cases. For the first time, differences in glycosylation profiles of the flagella could be linked to differences in the gene content of the FGI. CONCLUSION: Proteolytic C. botulinum has a stable genome backbone containing specific regions of genetic heterogeneity. These include the neurotoxin gene cluster and the FGI, each having evolved independently of each other and the remainder of the genetic complement. Analysis of these genetic components provides a high degree of discrimination of strains of proteolytic C. botulinum, and is suitable for clinical and forensic investigations of botulism outbreaks. BioMed Central 2009-03-19 /pmc/articles/PMC2674064/ /pubmed/19298644 http://dx.doi.org/10.1186/1471-2164-10-115 Text en Copyright © 2009 Carter et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Carter, Andrew T
Paul, Catherine J
Mason, David R
Twine, Susan M
Alston, Mark J
Logan, Susan M
Austin, John W
Peck, Michael W
Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum
title Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum
title_full Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum
title_fullStr Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum
title_full_unstemmed Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum
title_short Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum
title_sort independent evolution of neurotoxin and flagellar genetic loci in proteolytic clostridium botulinum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2674064/
https://www.ncbi.nlm.nih.gov/pubmed/19298644
http://dx.doi.org/10.1186/1471-2164-10-115
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