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Genomic analysis of three African strains of Bacillus anthracis demonstrates that they are part of the clonal expansion of an exclusively pathogenic bacterium
Bacillus anthracis is the causative agent of anthrax and is classified as a ‘Category A’ biological weapon. Six complete genomes of B. anthracis (A0248, Ames, Ames Ancestor, CDC684, H0491, and Sterne) are currently available. In this report, we add three African strain genomes: Sen2Col2, Sen3 and Gm...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265047/ https://www.ncbi.nlm.nih.gov/pubmed/25566394 http://dx.doi.org/10.1002/nmi2.62 |
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author | Rouli, L MBengue, M Robert, C Ndiaye, M La Scola, B Raoult, D |
author_facet | Rouli, L MBengue, M Robert, C Ndiaye, M La Scola, B Raoult, D |
author_sort | Rouli, L |
collection | PubMed |
description | Bacillus anthracis is the causative agent of anthrax and is classified as a ‘Category A’ biological weapon. Six complete genomes of B. anthracis (A0248, Ames, Ames Ancestor, CDC684, H0491, and Sterne) are currently available. In this report, we add three African strain genomes: Sen2Col2, Sen3 and Gmb1. To study the pan-genome of B. anthracis, we used bioinformatics tools, such as Cluster of Orthologous Groups, and performed phylogenetic analysis. We found that the three African strains contained the pX01 and pX02 plasmids, the nonsense mutation in the plcR gene and the four known prophages. These strains are most similar to the CDC684 strain and belong to the A cluster. We estimated that the B. anthracis pan-genome has 2893 core genes (99% of the genome size) and 85 accessory genes. We validated the hypothesis that B. anthracis has a closed pan-genome and found that the three African strains carry the two plasmids associated with bacterial virulence. The pan-genome nature of B. anthracis confirms its lack of exchange (similar to Clostridium tetani) and supports its exclusively pathogenic role, despite its survival in the environment. Moreover, thanks to the study of the core content single nucleotide polymorphisms, we can see that our three African strains diverged very recently from the other B. anthracis strains. |
format | Online Article Text |
id | pubmed-4265047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42650472015-01-06 Genomic analysis of three African strains of Bacillus anthracis demonstrates that they are part of the clonal expansion of an exclusively pathogenic bacterium Rouli, L MBengue, M Robert, C Ndiaye, M La Scola, B Raoult, D New Microbes New Infect Original Article Bacillus anthracis is the causative agent of anthrax and is classified as a ‘Category A’ biological weapon. Six complete genomes of B. anthracis (A0248, Ames, Ames Ancestor, CDC684, H0491, and Sterne) are currently available. In this report, we add three African strain genomes: Sen2Col2, Sen3 and Gmb1. To study the pan-genome of B. anthracis, we used bioinformatics tools, such as Cluster of Orthologous Groups, and performed phylogenetic analysis. We found that the three African strains contained the pX01 and pX02 plasmids, the nonsense mutation in the plcR gene and the four known prophages. These strains are most similar to the CDC684 strain and belong to the A cluster. We estimated that the B. anthracis pan-genome has 2893 core genes (99% of the genome size) and 85 accessory genes. We validated the hypothesis that B. anthracis has a closed pan-genome and found that the three African strains carry the two plasmids associated with bacterial virulence. The pan-genome nature of B. anthracis confirms its lack of exchange (similar to Clostridium tetani) and supports its exclusively pathogenic role, despite its survival in the environment. Moreover, thanks to the study of the core content single nucleotide polymorphisms, we can see that our three African strains diverged very recently from the other B. anthracis strains. BlackWell Publishing Ltd 2014-11 2014-09-28 /pmc/articles/PMC4265047/ /pubmed/25566394 http://dx.doi.org/10.1002/nmi2.62 Text en © 2014 The Authors. New Microbes and New Infections published by John Wiley & Sons Ltd on behalf of the European Society of Clinical Microbiology and Infectious Disease. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Rouli, L MBengue, M Robert, C Ndiaye, M La Scola, B Raoult, D Genomic analysis of three African strains of Bacillus anthracis demonstrates that they are part of the clonal expansion of an exclusively pathogenic bacterium |
title | Genomic analysis of three African strains of Bacillus anthracis
demonstrates that they are part of the clonal expansion of an exclusively pathogenic
bacterium |
title_full | Genomic analysis of three African strains of Bacillus anthracis
demonstrates that they are part of the clonal expansion of an exclusively pathogenic
bacterium |
title_fullStr | Genomic analysis of three African strains of Bacillus anthracis
demonstrates that they are part of the clonal expansion of an exclusively pathogenic
bacterium |
title_full_unstemmed | Genomic analysis of three African strains of Bacillus anthracis
demonstrates that they are part of the clonal expansion of an exclusively pathogenic
bacterium |
title_short | Genomic analysis of three African strains of Bacillus anthracis
demonstrates that they are part of the clonal expansion of an exclusively pathogenic
bacterium |
title_sort | genomic analysis of three african strains of bacillus anthracis
demonstrates that they are part of the clonal expansion of an exclusively pathogenic
bacterium |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265047/ https://www.ncbi.nlm.nih.gov/pubmed/25566394 http://dx.doi.org/10.1002/nmi2.62 |
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