2022
DOI: 10.1016/j.micres.2022.126980
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Antibacterial efficacies and time-kill kinetics of indigenous Ghanaian spice extracts against Listeria monocytogenes and some other food-borne pathogenic bacteria

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Cited by 21 publications
(6 citation statements)
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“…This assay measures the rate of killing, which could be a more useful parameter for projecting the course of the treatment over time ( Doern, 2014 ). Although time-kill kinetics studies are used to determine bactericidal impact, it is a useful tool to provide data in terms of time or concentration-dependent antibacterial activity ( Xedzro et al, 2022 ). The findings of this study are consistent with those published previously, in which the checkerboard approach revealed a synergistic impact whereas the time-kill kinetics method demonstrated additive results.…”
Section: Discussionmentioning
confidence: 99%
“…This assay measures the rate of killing, which could be a more useful parameter for projecting the course of the treatment over time ( Doern, 2014 ). Although time-kill kinetics studies are used to determine bactericidal impact, it is a useful tool to provide data in terms of time or concentration-dependent antibacterial activity ( Xedzro et al, 2022 ). The findings of this study are consistent with those published previously, in which the checkerboard approach revealed a synergistic impact whereas the time-kill kinetics method demonstrated additive results.…”
Section: Discussionmentioning
confidence: 99%
“…The bactericidal and bacteriostatic effects of IPBC on V. parahaemolyticus and S . aureus were investigated as previously described 28 . Overnight cultures of V. parahaemolyticus or S .…”
Section: Methodsmentioning
confidence: 99%
“…Different bacteria strains, i.e., V. parahaemolyticus, E. coli, S. aureus, and S. iniae were cultured in NB medium (8 g/L) at 37 • C for 24 h in a shaking incubator (New Brunswick, NY, USA). Bacteria cultures at the logarithmic growth phase, measured in terms of optical density at 600 nm (OD600), were used to determine the antibacterial activity of the peptides as previously described [17]. Briefly, 10 3 CFU/mL of the bacteria were individually incubated with different concentrations of the peptides (i.e., 500-7.8 µg/mL) for 2 h at 37 • C. Next, 20 µL of the samples were spread onto NB agar plates before incubating at 37 • C for 24 h. Bacteria colonies were counted, and the minimum inhibitory concentration (MIC) was determined, defined as the peptide concentration that inhibited 80% of bacterial growth.…”
Section: Peptide Synthesis and Antibacterial Activity Determinationmentioning
confidence: 99%