Comparison of Biofilm Formation between Major Clonal Lineages of Methicillin Resistant Staphylococcus aureusReportar como inadecuado




Comparison of Biofilm Formation between Major Clonal Lineages of Methicillin Resistant Staphylococcus aureus - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

Objectives

Epidemic methicillin-resistant S. aureus MRSA clones cause infections in both hospital and community settings. As a biofilm phenotype further facilitates evasion of the host immune system and antibiotics, we compared the biofilm-forming capacities of various MRSA clones.

Methods

Seventy-six MRSA classified into 13 clones USA300, EMRSA-15, Hungarian-Brazilian etc., and isolated from infections or from carriers were studied for biofilm formation under static and dynamic conditions. Static biofilms in microtitre plates were quantified colorimetrically. Dynamic biofilms Bioflux 200, Fluxion, USA were studied by confocal laser-scanning and time-lapse microscopy, and the total volume occupied by live-dead bacteria quantified by Volocity 5.4.1 Improvision, UK.

Results

MRSA harbouring SCCmec IV produced significantly more biomass under static conditions than SCCmec I–III P = 0.003, and those harbouring SCCmec II significantly less than those harbouring SCCmec I or III P<0.001. In the dynamic model, SCCmec I–III harbouring MRSA were significantly better biofilm formers than SCCmec IV P = 0.036. Only 16 strains successfully formed biofilms under both conditions, of which 13 harboured SCCmec IV and included all tested USA300 strains n = 3. However, USA300 demonstrated remarkably lower percentages of cell-occupied space 6.6% compared to the other clones EMRSA-15 = 19.0% under dynamic conditions. Time-lapse microscopy of dynamic biofilms demonstrated that USA300 formed long viscoelastic tethers that stretched far from the point of attachment, while EMRSA-15 consisted of micro-colonies attached densely to the surface.

Conclusions

MRSA harbouring SCCmec types IV and I–III demonstrate distinct biofilm forming capacities, possibly owing to their adaptation to the community and hospital settings, respectively. USA300 demonstrated abundant biofilm formation under both conditions, which probably confers a competitive advantage, contributing to its remarkable success as a pathogen.



Autor: Evelyn Vanhommerig , Pieter Moons , Daniel Pirici, Christine Lammens, Jean-Pierre Hernalsteens, Henri De Greve, Samir Kumar-Singh

Fuente: http://plos.srce.hr/



DESCARGAR PDF




Documentos relacionados