Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2114
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dc.contributor.authorJanakiev, Tamaraen_US
dc.contributor.authorDimkić, Ivicaen_US
dc.contributor.authorUnković, Nikolaen_US
dc.contributor.authorLjaljević-Grbić, Milicaen_US
dc.contributor.authorOpsenica, Dejanen_US
dc.contributor.authorGašić, Urošen_US
dc.contributor.authorStanković, Slavišaen_US
dc.contributor.authorBerić, Tanjaen_US
dc.date.accessioned2019-10-22T09:56:17Z-
dc.date.available2019-10-22T09:56:17Z-
dc.date.issued2019-10-01-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/2114-
dc.description.abstractEuropean plum (Prunus domestica L.) is a significant commercial crop in Serbia in terms of total fruit production, and is traditionally processed into slivovitz brandy. The brown rot disease caused by Monilinia laxa drastically reduces plum yield almost every year. Fungal communities associated with leaves and fruits of four local Serbian plum cultivars (Požegača, Ranka, Čačanska Lepotica and Čačanska Rodna) were investigated in two phenological stages during early (May) and late (July) fruit maturation. Alpha diversity indices showed that fungal communities were heterogeneous and Beta diversity indicated that autochthonous fungal communities depended upon seasonal changes and the cultivars themselves. The phylum Ascomycota was the most abundant in all samples, with relative abundance (RA) between 46% in the Požegača cultivar (May) and 89% in the Lepotica cultivar (July). The most abundant genus for all plum cultivars in May was Aureobasidium, with RA from 19.27 to 33.69%, followed by Cryptococcus, with 4.8 to 48.80%. In July, besides Cryptococcus, different genera (Metschnikowia, Fusarium, and Hanseniaspora) were dominant on particular cultivars. Among all cultivable fungi, molecular identification of eleven M. laxa isolates from four plum cultivars was performed simultaneously. Bacterial isolates from the plum phyllosphere were tested for their potential antifungal activity against indigenous M. laxa isolates. The most potent antagonist P4/16_1, which significantly reduced mycelial growth of M. laxa, was identified as Pseudomonas synxantha. Further characterization of P4/16_1 revealed the production of volatile organic compounds and phenazine-1-carboxylic acid (PCA). Crude benzene extract of PCA exhibited 57–63% mycelial growth inhibition of M. laxa. LC/MS analysis of the crude extract confirmed the presence of phenazine derivatives amongst other compounds. Scanning electron microscopy revealed morpho-physiological changes in the hyphae of M. laxa isolates caused by the cell culture and the P. synxantha P4/16_1 crude benzene extract. This is the first report of antagonistic activity of P. synxantha against M. laxa induced by diffusible and volatile antifungal compounds, and it appears to be a promising candidate for further investigation for potential use as a biocontrol agent against brown rot-causing fungi.en_US
dc.language.isoenen_US
dc.relation.ispartofFrontiers in Microbiologyen_US
dc.subjectNGSen_US
dc.subjectFungal diversityen_US
dc.subjectPlum cultivarsen_US
dc.subjectBiocontrolen_US
dc.subjectMonilinia laxaen_US
dc.subjectPseudomonas synxantha.en_US
dc.titlePhyllosphere fungal communities of plum and antifungal activity of indigenous phenazine-producing Pseudomonas synxantha against Monilinia laxaen_US
dc.typeArticleen_US
dc.identifier.doi10.3389/fmicb.2019.02287-
dc.description.rankM21en_US
dc.description.impact=4.259en_US
dc.description.startpage2287en_US
dc.description.volume10en_US
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.deptChair of Algology, Mycology and Lichenology-
crisitem.author.deptChair of Algology, Mycology and Lichenology-
crisitem.author.deptChair of Microbiology-
crisitem.author.deptChair of Microbiology-
crisitem.author.orcid0000-0003-3933-9610-
crisitem.author.orcid0000-0002-0425-5938-
crisitem.author.orcid0000-0001-8872-2099-
crisitem.author.orcid0000-0003-0541-7713-
crisitem.author.orcid0000-0003-0527-8741-
crisitem.author.orcid0000-0002-4860-2225-
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