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The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages

BACKGROUND: Bacillus anthracis is considered to be a recently emerged clone within the Bacillus cereus sensu lato group. The B. anthracis genome sequence contains four putative lambdoid prophages. We undertook this study in order to understand whether the four prophages are unique to B. anthracis an...

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Autores principales: Sozhamannan, Shanmuga, Chute, Michael D, McAfee, Farrell D, Fouts, Derrick E, Akmal, Arya, Galloway, Darrell R, Mateczun, Alfred, Baillie, Leslie W, Read, Timothy D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1475869/
https://www.ncbi.nlm.nih.gov/pubmed/16600039
http://dx.doi.org/10.1186/1471-2180-6-34
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author Sozhamannan, Shanmuga
Chute, Michael D
McAfee, Farrell D
Fouts, Derrick E
Akmal, Arya
Galloway, Darrell R
Mateczun, Alfred
Baillie, Leslie W
Read, Timothy D
author_facet Sozhamannan, Shanmuga
Chute, Michael D
McAfee, Farrell D
Fouts, Derrick E
Akmal, Arya
Galloway, Darrell R
Mateczun, Alfred
Baillie, Leslie W
Read, Timothy D
author_sort Sozhamannan, Shanmuga
collection PubMed
description BACKGROUND: Bacillus anthracis is considered to be a recently emerged clone within the Bacillus cereus sensu lato group. The B. anthracis genome sequence contains four putative lambdoid prophages. We undertook this study in order to understand whether the four prophages are unique to B. anthracis and whether they produce active phages. RESULTS: More than 300 geographically and temporally divergent isolates of B. anthracis and its near neighbors were screened by PCR for the presence of specific DNA sequences from each prophage region. Every isolate of B. anthracis screened by PCR was found to produce all four phage-specific amplicons whereas none of the non-B. anthracis isolates, produced more than one phage-specific amplicon. Excision of prophages could be detected by a PCR based assay for attP sites on extra-chromosomal phage circles and for attB sites on phage-excised chromosomes. SYBR-green real-time PCR assays indicated that prophage excision occurs at very low frequencies (2 × 10(-5 )- 8 × 10(-8)/cell). Induction with mitomycin C increased the frequency of excision of one of the prophages by approximately 250 fold. All four prophages appear to be defective since, mitomycin C induced culture did not release any viable phage particle or lyse the cells or reveal any phage particle under electron microscopic examination. CONCLUSION: The retention of all four putative prophage regions across all tested strains of B. anthracis is further evidence of the very recent emergence of this lineage and the prophage regions may be useful for differentiating the B. anthracis chromosome from that of its neighbors. All four prophages can excise at low frequencies, but are apparently defective in phage production.
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spelling pubmed-14758692006-06-10 The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages Sozhamannan, Shanmuga Chute, Michael D McAfee, Farrell D Fouts, Derrick E Akmal, Arya Galloway, Darrell R Mateczun, Alfred Baillie, Leslie W Read, Timothy D BMC Microbiol Research Article BACKGROUND: Bacillus anthracis is considered to be a recently emerged clone within the Bacillus cereus sensu lato group. The B. anthracis genome sequence contains four putative lambdoid prophages. We undertook this study in order to understand whether the four prophages are unique to B. anthracis and whether they produce active phages. RESULTS: More than 300 geographically and temporally divergent isolates of B. anthracis and its near neighbors were screened by PCR for the presence of specific DNA sequences from each prophage region. Every isolate of B. anthracis screened by PCR was found to produce all four phage-specific amplicons whereas none of the non-B. anthracis isolates, produced more than one phage-specific amplicon. Excision of prophages could be detected by a PCR based assay for attP sites on extra-chromosomal phage circles and for attB sites on phage-excised chromosomes. SYBR-green real-time PCR assays indicated that prophage excision occurs at very low frequencies (2 × 10(-5 )- 8 × 10(-8)/cell). Induction with mitomycin C increased the frequency of excision of one of the prophages by approximately 250 fold. All four prophages appear to be defective since, mitomycin C induced culture did not release any viable phage particle or lyse the cells or reveal any phage particle under electron microscopic examination. CONCLUSION: The retention of all four putative prophage regions across all tested strains of B. anthracis is further evidence of the very recent emergence of this lineage and the prophage regions may be useful for differentiating the B. anthracis chromosome from that of its neighbors. All four prophages can excise at low frequencies, but are apparently defective in phage production. BioMed Central 2006-04-06 /pmc/articles/PMC1475869/ /pubmed/16600039 http://dx.doi.org/10.1186/1471-2180-6-34 Text en Copyright © 2006 Sozhamannan et al; licensee BioMed Central Ltd.
spellingShingle Research Article
Sozhamannan, Shanmuga
Chute, Michael D
McAfee, Farrell D
Fouts, Derrick E
Akmal, Arya
Galloway, Darrell R
Mateczun, Alfred
Baillie, Leslie W
Read, Timothy D
The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages
title The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages
title_full The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages
title_fullStr The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages
title_full_unstemmed The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages
title_short The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages
title_sort bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1475869/
https://www.ncbi.nlm.nih.gov/pubmed/16600039
http://dx.doi.org/10.1186/1471-2180-6-34
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