Evidence for reductive genome evolution and lateral acquisition of virulence functions in two Corynebacterium pseudotuberculosis strains.

Background: Corynebacterium pseudotuberculosis, a Gram-positive, facultative intracellular pathogen, is the etiologic agent of the disease known as caseous lymphadenitis (CL). CL mainly affects small ruminants, such as goats and sheep; it also causes infections in humans, though rarely. This species is distributed worldwide, but it has the most serious economic impact in Oceania, Africa and South America. Although C. pseudotuberculosis causes major health and productivity problems for livestock, little is known about the molecular basis of its pathogenicity. Methodology and Findings: We characterized two C. pseudotuberculosis genomes (Cp1002, isolated from goats; and CpC231, isolated from sheep). Analysis of the predicted genomes showed high similarity in genomic architecture, gene content and genetic order. When C. pseudotuberculosis was compared with other Corynebacterium species, it became evident that this pathogenic species has lost numerous genes, resulting in one of the smallest genomes in the genus. Other differences that could be part of the adaptation to pathogenicity include a lower GC content, of about 52%, and a reduced gene repertoire. The C. pseudotuberculosis genome also includes seven putative pathogenicity islands, which contain several classical virulence factors, including genes for fimbrial subunits, adhesion factors, iron uptake and secreted toxins. Additionally, all of the virulence factors in the islands have characteristics that indicate horizontal transfer. Conclusions: These particular genome characteristics of C. pseudotuberculosis, as well as its acquired virulence factors in pathogenicity islands, provide evidence of its lifestyle and of the pathogenicity pathways used by this pathogen in the infection process. All genomes cited in this study are available in the NCBI Genbank database (http://www.ncbi.nlm.nih.gov/ genbank/) under accession numbers CP001809 and CP001829.

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Main Authors: RUIZ, J. C., D'AFONSECA, V., SILVA, A., ALI, A., PINTO, A. C., SANTOS, A. R., ROCHA, A. A. M. C., LOPES, D. O., DORELLA, F. A., PACHECO, L. G. C., COSTA, M. P., TURK, M. Z., SEYFFERT, N., MORAES, P. M. R. O., SOARES, S. C., ALMEIDA, S. S., CASTRO, T. L. P., ABREU, V. A. C., TROST, E., BAUMBACH, J., TAUCH, A., SCHNEIDER, M. P. C., McCULLOCH, J., CERDEIRA, L. T., RAMOS, R. T. J., ZERLOTINI, A., DOMINITINI, A., RESENDE, D. M., COSER, E. M., OLIVEIRA, L. M., PEDROSA, A. L., VIEIRA, C. U., GUIMARÃES, C. T., BARTHOLOMEU, D. C., OLIVEIRA, D. M., SANTOS, F. R., RABELO, É. M., LOBO, F. P., FRANCO, G. R., COSTA, A. F., CASTRO, I. M., DIAS, S. R. C., FERRO, J. A., ORTEGA, J. M., PAIVA, L. V., GOULART, L. R., ALMEIDA, J. F., FERRO, M. I. T., CARNEIRO, N. P., FALCÃO, P. R. K., GRYNBERG, P., TEIXEIRA, S. M. R., BROMMONSCHENKEL, S., OLIVEIRA, S. C., MEYER, R., MOORE, R. J., MIYOSHI, A., OLIVEIRA, G. C., AZEVEDO, V.
Other Authors: JERÔNIMO C. RUIZ, Research Center René Rachou/Oswaldo Cruz Foundation; VÍVIAN D'AFONSECA, UFMG; ARTUR SILVA, UFPA; AMJAD ALI, UFMG; ANNE C. PINTO, UFMG; ANDERSON R. SANTOS, UFMG; ARYANNE A. M. C. ROCHA, UFMG; DÉBORA O. LOPES, UFSJ; FERNANDA A. DORELLA, UFMG; LUIS G. C. PACHECO, UFMG, UFBA; MARCÍLIA P. COSTA, UECE; MERITXELL Z. TURK, UFMG; NÚBIA SEYFFERT, UFMG; PABLO M. R. O. MORAES, UFMG; SIOMAR C. SOARES, UFMG; SINTIA S. ALMEIDA, UFMG; THIAGO L. P. CASTRO, UFMG; VINICIUS A. C. ABREU, UFMG; EVA TROST, University of Bielefeld; JAN BAUMBACH, Max-Planck-Institut fur Informatik; ANDREAS TAUCH, University of Bielefeld; MARIA PAULA C. SCHNEIDER, UFPA; JOHN MCCULLOCH, UFPA; LOUISE T. CERDEIRA, UFPA; ROMMEL T. J. RAMOS, UFPA; ADHEMAR ZERLOTINI, Research Center René Rachou/Oswaldo Cruz Foundation; ANDERSON DOMINITINI, Research Center René Rachou/Oswaldo Cruz Foundation; DANIELA M. RESENDE, Research Center René Rachou/Oswaldo Cruz Foundation, UFOP; ELISÂNGELA M. COSER, Research Center René Rachou/Oswaldo Cruz Foundation; LUCIANA M. OLIVEIRA, UFOP; ANDRÉ L. PEDROSA, UFOP, UFTM; CARLOS U. VIEIRA, UFU; CLÁUDIA TEIXEIRA GUIMARÃES, CNPMS; DANIELA C. BARTHOLOMEU, UFMG; DIANA M. OLIVEIRA, UECE; FABRÍCIO R. SANTOS, UFMG; ÉLIDA MARA RABELO, UFMG; FRANCISCO P. LOBO, UFMG; GLÓRIA R. FRANCO, UFMG; ANA FLÁVIA COSTA, UFMG; IESO M. CASTRO, UFOP; SÍLVIA REGINA COSTA DIAS, UFMG; JESUS A. FERRO, Unesp; JOSÉ MIGUEL ORTEGA, UFMG; LUCIANO V. PAIVA, UFV; LUIZ R. GOULART, UFU; JULIANA FRANCO ALMEIDA, UFU; MARIA INÊS T. FERRO, Unesp; NEWTON PORTILHO CARNEIRO, CNPMS; PAULA REGINA KUSER FALCÃO, CNPTIA; PRISCILA GRYNBERG, UFMG; SANTUZA M. R. TEIXEIRA, UFMG; SÉRGIO BROMMONSCHENKEL, UFV; SÉRGIO C. OLIVEIRA, UFMG; ROBERTO MEYER, UFBA; ROBERT J. MOORE, CSIRO Livestock Industries; ANDERSON MIYOSHI, UFMG; GUILHERME C. OLIVEIRA, Oswaldo Cruz Foundation; VASCO AZEVEDO, UFMG.
Format: Artigo de periódico biblioteca
Language:English
eng
Published: 2012-02-08
Subjects:Genoma de C pseudotuberculosis, Análise de genoma, Ilhas de patogenicidade, Corynebacterium Pseudotuberculosis, Caseous lymphadenitis, Pathogenicity,
Online Access:http://www.alice.cnptia.embrapa.br/alice/handle/doc/914696
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Summary:Background: Corynebacterium pseudotuberculosis, a Gram-positive, facultative intracellular pathogen, is the etiologic agent of the disease known as caseous lymphadenitis (CL). CL mainly affects small ruminants, such as goats and sheep; it also causes infections in humans, though rarely. This species is distributed worldwide, but it has the most serious economic impact in Oceania, Africa and South America. Although C. pseudotuberculosis causes major health and productivity problems for livestock, little is known about the molecular basis of its pathogenicity. Methodology and Findings: We characterized two C. pseudotuberculosis genomes (Cp1002, isolated from goats; and CpC231, isolated from sheep). Analysis of the predicted genomes showed high similarity in genomic architecture, gene content and genetic order. When C. pseudotuberculosis was compared with other Corynebacterium species, it became evident that this pathogenic species has lost numerous genes, resulting in one of the smallest genomes in the genus. Other differences that could be part of the adaptation to pathogenicity include a lower GC content, of about 52%, and a reduced gene repertoire. The C. pseudotuberculosis genome also includes seven putative pathogenicity islands, which contain several classical virulence factors, including genes for fimbrial subunits, adhesion factors, iron uptake and secreted toxins. Additionally, all of the virulence factors in the islands have characteristics that indicate horizontal transfer. Conclusions: These particular genome characteristics of C. pseudotuberculosis, as well as its acquired virulence factors in pathogenicity islands, provide evidence of its lifestyle and of the pathogenicity pathways used by this pathogen in the infection process. All genomes cited in this study are available in the NCBI Genbank database (http://www.ncbi.nlm.nih.gov/ genbank/) under accession numbers CP001809 and CP001829.