2012
DOI: 10.1007/s10526-012-9442-6
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Exploring the biocontrol potential of fungal endophytes from an Andean Colombian Paramo ecosystem

Abstract: We studied the diversity and biocontrol potential of 100 fungal endophytes isolated from Espeletia spp., endemic plant species from the Paramo in the Andean mountain range. Our sample was genotypically highly diverse at all ITS similarity levels. The antagonistic properties of these isolates were tested against common crop pathogens in Colombia, including Pectobacterium carotovorum, Ralstonia solanacearum, Pseudomonas syringae, Xanthomonas campestris, Rhizoctonia solani, Botrytis cinerea, Fusarium oxysporum, a… Show more

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Cited by 56 publications
(48 citation statements)
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“…Endophyte DNA was isolated according to previously reported methodologies, with some modifications (12,19). Briefly, the plant tissue was surface sterilized by washing with sterile H 2 O to remove dirt, placed in NAP buffer (124 mM Na 2 HPO 4 ), and vortexed for 1 min to dislodge epiphytes.…”
Section: Methodsmentioning
confidence: 99%
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“…Endophyte DNA was isolated according to previously reported methodologies, with some modifications (12,19). Briefly, the plant tissue was surface sterilized by washing with sterile H 2 O to remove dirt, placed in NAP buffer (124 mM Na 2 HPO 4 ), and vortexed for 1 min to dislodge epiphytes.…”
Section: Methodsmentioning
confidence: 99%
“…Briefly, the plant tissue was surface sterilized by washing with sterile H 2 O to remove dirt, placed in NAP buffer (124 mM Na 2 HPO 4 ), and vortexed for 1 min to dislodge epiphytes. Leaves were then shaved to remove the pubescence on their surface, which facilitates the subsequent sterilization process (12), washed with sterile H 2 O, submerged in 90% ethanol (60 s), 5.25% sodium hypochlorite solution (6 min), and 70% ethanol (30 s), and finally rinsed with sterile distilled H 2 O. Sterilization was checked by taking an imprint of the leaf on malt extract medium (12) and incubating at 25°C. One gram of the previously treated material was cut into 0.1-to 0.5-mm sections, placed in a 1.5-ml Eppendorf tube containing 1 g of sterile 0.1-mm-diameter glass beads and 1 ml TE (10 mM Tris, 10 mM EDTA, pH 8.0), and homogenized in a Mini-BeadBeater (BioSpec Products) for 5 min.…”
Section: Methodsmentioning
confidence: 99%
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“…Trichoderma harzianum strain T22, known to control plant-pathogenic fungus, could make maize roots deeper and more robust with a greater surface area compared with the untreated control (Harman et al 2004). aureobasidium pullulans and Paraconiothyrium sporulosum were not only antagonistic to the tomato pathogen R. solani, but also exhibited tomato growth promotion (Miles et al 2012). Piriformospora indica was found in endophytically colonized roots and could promote the root growth of a number of plant species, including maize, tobacco, and parsley (Varma et al 1999).…”
Section: Discussionmentioning
confidence: 99%