Please use this identifier to cite or link to this item: http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/3371
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dc.contributor.authorMenike, G.D.N.
dc.contributor.authorRatnayake, R.M.R.N.K
dc.date.accessioned2021-07-08T08:01:05Z
dc.date.accessioned2022-07-07T06:42:16Z-
dc.date.available2021-07-08T08:01:05Z
dc.date.available2022-07-07T06:42:16Z-
dc.date.issued2020
dc.identifier.issn2465-6143
dc.identifier.urihttp://repo.lib.jfn.ac.lk/ujrr/handle/123456789/3371-
dc.description.abstractPostharvest decay in harvested fruits and vegetables causes considerable economic losses. Synthetic chemicals are the primary means to control these losses. With the rising concerns on food security and food safety, chemical applications for the control of postharvest diseases are now being questioned. Biological control has become an effective and promising alternative to overcome and environmentally friendly alternative for those adverse effects caused by synthetic chemicals. Therefore, this study was conducted to explore the potential biological control agents in the mango bio-system mainly targeting the phyllosphere and rhizosphere. Leaves, stem parts, inflorescence, and fruits of mango from different locations in Anuradhapura District and soils from organically maintained orchards and home gardens were used for the isolation of microorganisms to be tested for potential antagonism against Colletotrichum gloeosporioides (Cg) causing anthracnose disease in mango. Potato Dextrose Agar (PDA), Nutrient Agar (NA), King’s B, Yeast Mannitol Agar with Congo Red (YEPD) and Liquid Glucose Medium have been used for the isolations. Identification of the isolates was done observing colony and spore morphologies and bioassays. So far, bacteria (28), fungi (14) and yeasts (08) were found and all the isolates were tested against C. gloeosporioides for the biocontrol efficacy using dual culture technique. Cell suspensions of bacterial isolates and spore suspensions of fungal isolates at a concentration of 106 CFU/mL as a dip application were used for in-vivo experiments. Six treatments including T1 (Cg + yeast iso 02), T2 (Cg+ fungi iso 07), T3 (Cg+fungi iso 12), T4 (Cg+ bacteria iso 03), T5 (Cg+ bacteria iso 05) and T6 (control treatment with sterile distilled water) with three replicates to each treatment were used in in-vivo studies. From the isolates, one yeast, two fungal and two bacterial isolates showed potential antagonism against C. gloeosporioides in-vitro but none of them showed significant control over C. gloeosporioides in in-vivo experiments in variety Karaththakolomban. Percentage inhibition (PI) of the 06 treatments in in-vivo experiment is 2.17 ±0.15a for T1, 2.57 ± 0.40a for T2, 2.55 ± 0.07 a for T3, 2.43 ± 0.12 a for T4, 2.53 ± 0.06 a for T5 and 2.60 ± 0.35 a for T6.en_US
dc.language.isoenen_US
dc.publisherUniversity of Jaffnaen_US
dc.subjectAnthracnoseen_US
dc.subjectBiological controlen_US
dc.subjectColletotrichum gloeosporioidesen_US
dc.subjectMangoen_US
dc.subjectPostharvest decayen_US
dc.titleExploitation of Phyllospheric and Rhizospheric Microorganisms as Biological Control Agents against Colletotrichum gloeosporioides Causing Anthracnose Disease of Mangoen_US
dc.typeArticleen_US
Appears in Collections:ICDA 2020



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