dc.creatorCasasnovas, F.
dc.creatorFantini, Emanuel Nicolás
dc.creatorPalazzini, Juan Manuel
dc.creatorGiaj Merlera, Guillermo
dc.creatorChulze, Sofia Noemi
dc.creatorReynoso, Maria Marta
dc.creatorTorres, Adriana Mabel
dc.date.accessioned2017-09-19T18:44:57Z
dc.date.available2017-09-19T18:44:57Z
dc.date.created2017-09-19T18:44:57Z
dc.date.issued2013-03
dc.identifierCasasnovas, F.; Fantini, Emanuel Nicolás; Palazzini, Juan Manuel; Giaj Merlera, Guillermo; Chulze, Sofia Noemi; et al.; Development of amplified fragment length polymorphism (AFLP)-derived specific primer for the detection of Fusarium solani aetiological agent of peanut brown root rot; Wiley; Journal of Applied Microbiology; 114; 6; 3-2013; 1782-1792
dc.identifier1364-5072
dc.identifierhttp://hdl.handle.net/11336/24615
dc.identifierCONICET Digital
dc.identifierCONICET
dc.description.abstractAims: The objective of this work was to design an amplified fragment length polymorphism (AFLP)-derived specific primer for the detection of Fusarium solani aetiological agent of peanut brown root rot (PBRR) in plant material and soil. Methods and Results: Specific primers for the detection of the pathogen were designed based on an amplified region using AFLPs. The banding patterns by AFLPs showed that isolates from diseased roots were clearly distinguishable from others members of the F. solani species complex. Many bands were specific to F. solani PBRR, one of these fragments was selected and sequenced. Sequence obtained was used to develop specific PCR primers for the identification of pathogen in pure culture and in plant material and soil. Primer pair FS1/FS2 amplified a single DNA product of 175 bp. Other fungal isolates occurring in soil, included F. solani non-PBRR, were not detected by these specific primers. The assay was effective for the detection of pathogen from diseased root and infected soils. Conclusions: The designed primers for F. solani causing PBRR can be used in a PCR diagnostic protocol to rapidly and reliably detect and identify this pathogen. Significance and Impact of the Study: These diagnostic PCR primers will aid the detection of F. solani causing PBRR in diseased root and natural infected soils. The method developed could be a helpful tool for epidemiological studies and to avoid the spread of this serious disease in new areas.
dc.languageeng
dc.publisherWiley
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1111/jam.12183
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1111/jam.12183/abstract
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAflp Markers
dc.subjectFusarium Solani Species Complex
dc.subjectPcr-Based Diagnosis
dc.subjectPeanut
dc.subjectRoot Rot
dc.titleDevelopment of amplified fragment length polymorphism (AFLP)-derived specific primer for the detection of Fusarium solani aetiological agent of peanut brown root rot
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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