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Fig. 1 Synergistic antibacterial efficacy of combination treatment with tobramycin and quorum-
sensing inhibitors against Pseudomonas aeruginosa in an intraperitoneal foreign-body infection
mouse model. Clearance of implants pre-colonized with wild-type P. aeruginosa inserted in the
peritoneal cavity of BALB/c mice treated with either placebo ( open circles ), QSI ( filled triangles ),
tobramycin (TOB) ( open triangles ), or a combination of TOB and QSI (QSI + TOB) ( filled
squares ). Squares , triangles, and circles represent cfu/implant in individual mice and horizontal
bars represent the medians. The QSIs depicted are furanone C-30 ( a ), Ajoene ( b + d ), and
Horseradish extract ( c + e ). Adopted from Christensen et al. ( 2012 )
infection model. Significant clearance was found with all tested QSIs (C-30,
Ajoene, and horseradish juice), and the authors stressed the point that the best
application of this treatment was on early initiation (Christensen et al. 2012 ) (see
Fig. 1 ). The authors speculated that the effect seen was due to a reduction in
extracellular DNA (eDNA). eDNA has been shown to reduce the effect of
aminoglycoside via cation chelation (Mulcahy et al. 2008 ; Chiang et al. 2013 ),
and the release of eDNA has been shown to be controlled by QS (Allesen-Holm
et al. 2006 ). Further, QS controlled virulence factors (e.g., rhamnolipid) are known
to lyse immune cells which leads to release of the host DNA (Jensen et al. 2007 ;
Alhede et al. 2009 ). The presence of eDNA from both bacteria and host seems to be
suppressed by QSIs and could thus explain the higher susceptibility to tobramycin.
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