2021
DOI: 10.1556/446.2020.20018
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In vitro antimicrobial activity of plant active components against Pseudomonas lundensis and Listeria monocytogenes

Abstract: This work aimed to study the antimicrobial activity of eight various components of plant origin on the growth of Pseudomonas lundensis and Listeria monocytogenes. Different in vitro methods were used: agar plate diffusion, micro atmosphere, agar hole diffusion, micro-dilution, and gradient-plate method. In the first agar plate assay, p-cymene and γ-terpinene did not inhibit the growth of the tested bacteria therefore they were not used in further experiments. Both α-pinene and limonene were only partially effe… Show more

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Cited by 5 publications
(2 citation statements)
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“…Cz, Ov EOs and mGR-OLI were all capable of significantly inhibiting the bacterial growth, with Cz EO turning out to be the strongest against S. Typhimurium strains, while Ov the best against E. coli strains. These results confirm the important role played by the EOs vapor phase that had already been highlighted in previous works [81][82][83][84], suggesting the possibility of nebulizing Cz, Ov EOs and mGR-OLI in animals' houses to reduce bacterial contamination as alternative prophylactic natural treatment able to sanitize the environment of intensive farming.…”
Section: Discussionsupporting
confidence: 90%
“…Cz, Ov EOs and mGR-OLI were all capable of significantly inhibiting the bacterial growth, with Cz EO turning out to be the strongest against S. Typhimurium strains, while Ov the best against E. coli strains. These results confirm the important role played by the EOs vapor phase that had already been highlighted in previous works [81][82][83][84], suggesting the possibility of nebulizing Cz, Ov EOs and mGR-OLI in animals' houses to reduce bacterial contamination as alternative prophylactic natural treatment able to sanitize the environment of intensive farming.…”
Section: Discussionsupporting
confidence: 90%
“…Antibacterial activity of the BV extract was assessed by the agar well diffusion method (Hussein et al, 2020) where each isolated microbe was subculture on the recommended specific media for each microorganism at 35-37 °C for 25 h. 100 mg of the BV extract were sterilized by filtration through a membrane filter. 6 mm discs were impregnated with sterile cock borer and 30 µl of BV extract was placed in the wells of agar plates inoculated with microbial culture (after dilution) including standard and then incubated all the plates 37 °C for 16 hours.…”
Section: Antimicrobial Activitymentioning
confidence: 99%