| Autor: |
Kolonitsiou F; Department of Microbiology, School of Medicine, University of Patras, Patras, Greece., Papadimitriou-Olivgeris M; Division of Infectious Diseases, School of Medicine, University of Patras, Patras, Greece., Spiliopoulou A; Department of Microbiology, School of Medicine, University of Patras, Patras, Greece., Drougka E; Department of Microbiology, School of Medicine, University of Patras, Patras, Greece., Jelastopulu E; Department of Public Health, School of Medicine, University of Patras, Patras, Greece., Anastassiou ED; Department of Microbiology, School of Medicine, University of Patras, Patras, Greece., Spiliopoulou I; Department of Microbiology, School of Medicine, University of Patras, Patras, Greece. |
| Jazyk: |
angličtina |
| Zdroj: |
Frontiers in microbiology [Front Microbiol] 2019 Jan 09; Vol. 9, pp. 3310. Date of Electronic Publication: 2019 Jan 09 (Print Publication: 2018). |
| DOI: |
10.3389/fmicb.2018.03310 |
| Abstrakt: |
Methicillin-resistant Staphylococcus aureus (MRSA) remains an important cause of nosocomial and community-associated infections due to its ability to produce toxins and evade host's immune responses. The aim of the present study was to investigate the association of monocytes immune response in terms of cytokines produced after inoculation with different MRSA clones. Thirty-one clinical MRSA strains were selected on the basis of clonal types, accessory gene regulator (agr) groups and toxin genes carriage. Isolates were identified as S. aureus by Gram stain, catalase, coagulase production and PCR for nuc gene. The presence of mecA , lukS/lukF-PV (Panton-Valentine Leukocidin) and tst (Toxic Shock Syndrome Toxin-1) genes, as well as, the determination of agr groups was performed by PCR. Clonality was investigated by means of multi-locus sequence typing (MLST). Peripheral blood mononuclear cells were stimulated with live bacterial cells for 45 min at a ratio of 1:10. Cells were incubated for 10 h and supernatants were collected. The levels of Tumor Necrosis Factor alpha (TNFa), IL-1b, IL-8, IL-6, IL-12p40, IL-10, interferon-gamma (IFN-γ) and IL-2, were measured by Human Cytokine Multiplex Immunoassay kit. Thirteen strains were tst and 12 lukS/lukF-PV -positive. Seven strains belonged to ST80 and ST225, five to ST30 and ST239, while the remaining seven isolates were grouped together as "other." Strains belonging to ST80 induced statistically lower levels of TNFa, IL-1b, IL-8, IL-6, IL-10, IFN-γ, and IL-2. PVL-positive strains classified into ST80 clone induced statistically lower concentrations of most cytokines as compared to PVL-positive strains belonging to other clones, tst -positive strains and toxin-negative ones. Strains of agr 3 group belonging to ST80 induced statistically lower concentrations of most tested cytokines as compared to agr 3 strains not-belonging to ST80, agr 2 or agr 1. This low induction of immune response by MRSA ST80 cannot be attributed to the presence of neither lukS/lukF-PV nor agr3 . |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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