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Evidence for Reductive Genome Evolution and Lateral Acquisition of Virulence Functions in Two Corynebacterium pseudotuberculosis Strains


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Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)

NIH (National Institutes of Health) - Fogarty

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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.

Fundação Oswaldo Cruz, Res Ctr Rene Rachou, Ctr Excellence Bioinformat, Natl Inst Sci & Technol, Belo Horizonte, MG, Brazil

Universidade Federal de Minas Gerais (UFMG), Dept Gen Biol, Belo Horizonte, MG, Brazil

Fed Univ Para, Dept Genet, BR-66059 Belem, Para, Brazil

Univ Fed Sao Joao del Rei, Hlth Sci Ctr, Divinopilis, MG, Brazil

Univ Estadual Ceara, Dept Vet Med, Fortaleza, Ceara, Brazil

Univ Bielefeld, Dept Genet, CeBiTech, Bielefeld, Nordrhein Westf, Germany

Max Planck Inst Informat, Dept Comp Sci, Saarbrucken, Saarlan, Germany

Univ Fed Ouro Preto, Dept Pharmaceut Sci, Ouro Preto, MG, Brazil

Univ Fed Ouro Preto, Dept Phis, Ouro Preto, MG, Brazil

Univ Fed Triangulo Mineiro, Dept Biol Sci, Uberaba, MG, Brazil

Universidade Federal de Uberlândia (UFU), Dept Biochem & Genet, BR-38400 Uberlandia, MG, Brazil

Brazilian Agr Res Corp Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA), Sete Lagoas, MG, Brazil

Universidade Federal de Minas Gerais (UFMG), Dept Biochem & Immunol, Belo Horizonte, MG, Brazil

Universidade Federal de Minas Gerais (UFMG), Dept Parasitol, Belo Horizonte, MG, Brazil

Univ Fed Ouro Preto, Dept Pharm, Ouro Preto, MG, Brazil

State Univ São Paulo, Dept Technol, Jaboticabal, SP, Brazil

Universidade Federal de Lavras (UFLA), Dept Chem, Lavras, MG, Brazil

Brazilian Agr Res Corp Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA), Campinas, SP, Brazil

Universidade Federal de Viçosa (UFV), Dept Plant Pathol, Vicosa, MG, Brazil

Universidade Federal da Bahia (UFBA), Dept Biointeract Sci, Salvador, BA, Brazil

CSIRO Livestock Ind, Clayton, Vic, Australia

State Univ São Paulo, Dept Technol, Jaboticabal, SP, Brazil

FAPEMIG: CBB-1181/0

FAPEMIG: REDE-186/08

NIH - Fogarty: TW007012

Document Type Journal article
Language English
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