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Pathogenic properties of a Corynebacterium diphtheriae strain isolated from a case of osteomyelitis
Author(s) -
Renata Stavracakis Peixoto,
Elena Hacker,
Camila Azevedo Antunes,
Dulanthi Weerasekera,
AA Dias,
Carlos Alberto Martins,
Raphael Hirata,
Kátia Regietto dos Santos,
Andreas Burkovski,
Ana Luíza MattosGuaraldi
Publication year - 2016
Publication title -
journal of medical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.91
H-Index - 117
eISSN - 1473-5644
pISSN - 0022-2615
DOI - 10.1099/jmm.0.000362
Subject(s) - microbiology and biotechnology , corynebacterium diphtheriae , biology , strain (injury) , gentamicin protection assay , osteomyelitis , hela , pseudomonas aeruginosa , diphtheria , bacteria , virology , in vitro , immunology , vaccination , cancer , genetics , anatomy , biochemistry , metastasis
Corynebacterium diphtheriae is typically recognized as a colonizer of the upper respiratory tract (respiratory diphtheria) and the skin (cutaneous diphtheria). However, different strains of Corynebacteriumdiphtheriae can also cause invasive infections. In this study, the characterization of a non-toxigenic Corynebacteriumdiphtheriae strain (designated BR-INCA5015) isolated from osteomyelitis in the frontal bone of a patient with adenoid cystic carcinoma was performed. Pathogenic properties of the strain BR-INCA5015 were tested in a Caenorhabditis elegans survival assay showing strong colonization and killing by this strain. Survival rates of 3.8±2.7 %, 33.6±7.3 % and 0 % were observed for strains ATCC 27010T, ATCC 27012 and BR-INCA5015, respectively, at day 7. BR-INCA5015 was able to colonize epithelial cells, showing elevated capacity to adhere to and survive within HeLa cells compared to other Corynebacteriumdiphtheriae isolates. Intracellular survival in macrophages (THP-1 and RAW 264.7) was significantly higher compared to control strains ATCC 27010T (non-toxigenic) and ATCC 27012 (toxigenic). Furthermore, the ability of BR-INCA5015 to induce osteomyelitis was confirmed by in vivo assay using Swiss Webster mice.

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