2017•Unpublished venueRequires access

In Vitro Antifungal Activities of Three Aromatic Plant Extracts Against Fusarium Oxysporum Schlechtend. Fr. F. Sp. Lycopersici (Sacc.) Causal Organism of Fusarium Wilt In Tomato

Akinlolu O. Ohunakin, Omofunmilola O Bolanle

Open publisher page 8 citations

Abstract

In vitro assay of aqueous extracts of Allium sativum, Zingiber officinale and Dysphania ambrosioides were evaluated against Fusarium oxysporum. Five concentrations of cold and hot water aqueous extracts were obtained by infusing 4, 8, 12, 16, and 20 g of powder in 20 ml of sterile distilled water for 24 hours to obtain 20, 40, 60, 80 and 100% concentration, the hot water extracts were obtained using similar procedure with each flask placed in a water bath at 90°C for 90 mins. Food poisoned technique was employed for investigating the fungi toxicity of the plants essential oils (EO) against Fusarium oxysporum growth. An aliquot of 0.1 of the EO was dissolved in 0.9 ml of Tween-20 and mixed with 15 ml of Potato Dextrose Agar medium to achieve 20, 40, and 60% concentration, while the undiluted oil was recorded as 100%. The plates were inoculated with a 6mm assay disc cut from 7 day old culture fungus; observations were recorded on 7th day of incubation. Results indicate a reduction in F. oxysporum growth in the culture media, with hyphae becoming visible 48-50h after inoculation. A. sativum at 100% gave the highest inhibitory effect (71.24%) on mycelial growth, and compete favourably with Carbendazim (80.38%). The hot water extraction revealed better antifungal effects (45.86%) on F. oxysporium than cold water extract (33.80%). A. sativum showed the highest inhibition of 71.24% and 66.92% at 80% and 100% respectively, after Carbendazim (80.38%) at 0.5 mg/ml which is the standard. However, all extracts recorded the lowest mycelia growth at 20% concentration level.

About this research paper

What this paper is about

In vitro assay of aqueous extracts of Allium sativum, Zingiber officinale and Dysphania ambrosioides were evaluated against Fusarium oxysporum. Five concentrations of cold and hot water aqueous extracts were obtained by infusing 4, 8, 12, 16, and 20 g of powder in 20 ml of sterile distilled water for 24 hours to obtain 20, 40, 60, 80 and 100% concentration, the hot water extracts were obtained using similar procedure with each flask placed in a water bath at 90°C for 90 mins. Food poisoned technique was employed for investigating the fungi toxicity of the plants essential oils (EO) against Fusarium oxysporum growth. An aliquot of 0.1 of the EO was dissolved in 0.9 ml of Tween-20 and mixed with 15 ml of Potato Dextrose Agar medium to achieve 20, 40, and 60% concentration, while the undiluted oil was recorded as 100%. The plates were inoculated with a 6mm assay disc cut from 7 day old culture fungus; observations were recorded on 7th day of incubation. Results indicate a reduction in F. oxysporum growth in the culture media, with hyphae becoming visible 48-50h after inoculation. A. sativum at 100% gave the highest inhibitory effect (71.24%) on mycelial growth, and compete favourably with Carbendazim (80.38%). The hot water extraction revealed better antifungal effects (45.86%) on F. oxysporium than cold water extract (33.80%). A. sativum showed the highest inhibition of 71.24% and 66.92% at 80% and 100% respectively, after Carbendazim (80.38%) at 0.5 mg/ml which is the standard. However, all extracts recorded the lowest mycelia growth at 20% concentration level.

Why it matters

OpenAlex reports 8 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

In vitro assay of aqueous extracts of Allium sativum, Zingiber officinale and Dysphania ambrosioides were evaluated against Fusarium oxysporum. Five concentrations of cold and hot water aqueous extracts were obtained by infusing 4, 8, 12, 16, and 20 g of powder in 20 ml of sterile distilled water for 24 hours to obtain 20, 40, 60, 80 and 100% concentration, the hot water extracts were obtained using similar procedure with each flask placed in a water bath at 90°C for 90 mins. Food poisoned technique was employed for investigating the fungi toxicity of the plants essential oils (EO) against Fusarium oxysporum growth. An aliquot of 0.1 of the EO was dissolved in 0.9 ml of Tween-20 and mixed with 15 ml of Potato Dextrose Agar medium to achieve 20, 40, and 60% concentration, while the undiluted oil was recorded as 100%. The plates were inoculated with a 6mm assay disc cut from 7 day old culture fungus; observations were recorded on 7th day of incubation. Results indicate a reduction in F. oxysporum growth in the culture media, with hyphae becoming visible 48-50h after inoculation. A. sativum at 100% gave the highest inhibitory effect (71.24%) on mycelial growth, and compete favourably with Carbendazim (80.38%). The hot water extraction revealed better antifungal effects (45.86%) on F. oxysporium than cold water extract (33.80%). A. sativum showed the highest inhibition of 71.24% and 66.92% at 80% and 100% respectively, after Carbendazim (80.38%) at 0.5 mg/ml which is the standard. However, all extracts recorded the lowest mycelia growth at 20% concentration level.

Key concepts: Fusarium oxysporum, Carbendazim, Mycelium, Distilled water, Horticulture, Inoculation, Biology, Fusarium

Related papers

Back to paper searchBrowse research topicsOriginal source
In Vitro Antifungal Activities of Three Aromatic Plant Extracts Against Fusarium Oxysporum Schlechtend. Fr. F. Sp. Lycopersici (Sacc.) Causal Organism of Fusarium Wilt In Tomato — Research Paper | ScholarLens