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Development of amplified fragment length polymorphism ( AFLP )‐derived specific primer for the detection of F usarium solani aetiological agent of peanut brown root rot
Author(s) -
Casasnovas F.,
Fantini E.N.,
Palazzini J.M.,
GiajMerlera G.,
Chulze S.N.,
Reynoso M.M.,
Torres A.M.
Publication year - 2013
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/jam.12183
Subject(s) - amplified fragment length polymorphism , biology , fusarium solani , polymerase chain reaction , primer (cosmetics) , pathogen , root rot , genetics , microbiology and biotechnology , botany , gene , genetic diversity , population , chemistry , demography , organic chemistry , sociology
Aims The objective of this work was to design an amplified fragment length polymorphism ( AFLP )‐derived specific primer for the detection of F usarium 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 AFLP s. The banding patterns by AFLP s 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 FS 1/ FS 2 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.