Fig. 1From: Validation of the anti-infective potential of a polyherbal ‘Panchvalkal’ preparation, and elucidation of the molecular basis underlining its efficacy against Pseudomonas aeruginosaEffect of Panchvalkal formulation (PF) on various traits of P. aeruginosa, in vitro. a. Effect of PF on growth and QS-regulated pigment production in P. aeruginosa. b. PF enhances susceptibility of P. aeruginosa to lysis in presence of human serum. c. Effect of PF (750 μg/mL) on P. aeruginosa biofilm formation, eradication, and viability. d. P. aeruginosa challenged with PF (500 μg/mL) and antibiotic together. e. P. aeruginosa challenged with PF (750 μg/mL) and antibiotic together. f. P. aeruginosa challenged with antibiotic following pre-treatment with PF. g. Effect of PF on P. aeruginosa growth, pyoverdine unit, and pyocyanin unit remained unaltered after repeated exposure to PF. Bacterial growth was measured as OD764; OD of pyoverdine was measured at 405 nm, and Pyoverdine Unit was calculated as the ratio OD405/OD764 (an indication of pyoverdine production per unit of growth), Pyocyanin Unit was calculated as the ratio OD520/OD764 (an indication of pyocyanin production per unit of growth); ‘Control’ in this figure is the ‘vehicle control’ representing the % change values in comparison to the ‘growth control’ i.e. tube containing only growth medium plus organism, but no DMSO; 0.5% v/v DMSO used as ‘vehicle control’ did not affect biofilm of the bacterium; Crystal violet assay was performed to measure biofilm formation, and biofilm eradication, followed by the measurement of OD at 580 nm; Cell viability in biofilm was estimated through MTT assay, wherein OD was measured at 540 nm; *p < 0.05, **p < 0.01, ***p < 0.001Back to article page