2011
DOI: 10.1186/1471-2164-12-383
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Comparative analysis of two complete Corynebacterium ulcerans genomes and detection of candidate virulence factors

Abstract: BackgroundCorynebacterium ulcerans has been detected as a commensal in domestic and wild animals that may serve as reservoirs for zoonotic infections. During the last decade, the frequency and severity of human infections associated with C. ulcerans appear to be increasing in various countries. As the knowledge of genes contributing to the virulence of this bacterium was very limited, the complete genome sequences of two C. ulcerans strains detected in the metropolitan area of Rio de Janeiro were determined an… Show more

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Cited by 89 publications
(150 citation statements)
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References 80 publications
(125 reference statements)
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“…On the other hand, several proteins encoded by genes in the prophage region of C. diphtheriae 31A are homologous to those identified in prophage CULC22IV, which is present in the genome of the closely related tox-negative strain C. ulcerans BR-AD22. The respective prophage has a size of 41 kb, comprises 53 genes, and has been integrated into a tRNA Thr gene of Corynebacterium ulcerans (79). It has been proposed previously that the diphtheria toxin gene was acquired by corynephage ␤ due to the terminal location of tox in the genome of the prophage and the significantly decreased GϩC content of this gene region (7).…”
Section: Resultsmentioning
confidence: 99%
“…On the other hand, several proteins encoded by genes in the prophage region of C. diphtheriae 31A are homologous to those identified in prophage CULC22IV, which is present in the genome of the closely related tox-negative strain C. ulcerans BR-AD22. The respective prophage has a size of 41 kb, comprises 53 genes, and has been integrated into a tRNA Thr gene of Corynebacterium ulcerans (79). It has been proposed previously that the diphtheria toxin gene was acquired by corynephage ␤ due to the terminal location of tox in the genome of the prophage and the significantly decreased GϩC content of this gene region (7).…”
Section: Resultsmentioning
confidence: 99%
“…The primers used for atpA, dnaA, fusA, odhA, and rpoB are identical with the ones used for C. diphtheriae. The primers used for dnaK and leuA were adapted to C. ulcerans according to the genome of C. ulcerans 809 (19) and are given in Table 1. We were able to amplify all MLST loci, atpA (1,029 bp), dnaA (581 bp), fusA (683 bp), odhA (505 bp), rpoB (845 bp), dnaK (687 bp), and leuA (864 bp), using two different PCR cycling conditions.…”
Section: Allelic Variationmentioning
confidence: 99%
“…We obtained 4 atpA, 6 dnaE, 5 dnaK, 3 fusA, 7 leuA, 4 odhA, and 4 rpoB alleles. Additionally, we extracted the sequences of the MLST loci from the published C. ulcerans genomic sequences of isolates 809 (NC_017317.1) (19), BR-AD22 (NC_015683) (19), 0102 (NC_018101.1) (24), and FRC58 (NZ_AYTI00000000) (25) as well as from 7 isolates sequenced in one of the projects at the NCLoD (D. M. Meinel, G. Margos, R. Konrad, S. Krebs, H. Blum, and A. Sing, unpublished data).…”
Section: Allelic Variationmentioning
confidence: 99%
“…Salient highlights from completed genome projects include the following. (i) Virulence genes associated with the production of neuraminidase and phospholipase D in C. ulcerans and C. pseudotuberculosis were elucidated (48,50). (ii) The lack of mycolates in species may be due to the loss of a condensase gene cluster and mycolate reductase gene (46).…”
mentioning
confidence: 99%