Efficiency of rep-PCR fingerprinting as a useful technique for molecular typing of plant pathogenic fungal species: Botryosphaeriaceae species as a case study
Corresponding Author
Jafar Abdollahzadeh
Department of Plant Protection, Faculty of Agriculture, University of Kurdistan, Sanandaj, Iran
Correspondence: Jafar Abdollahzadeh, Department of Plant Protection, Faculty of Agriculture, University of Kurdistan, P. O. Box 416, Sanandaj, Iran.
Tel.: +98 (0) 8733620552;
fax: +98 (0) 8733620553;
e-mail: [email protected]
Search for more papers by this authorSajedeh Zolfaghari
Department of Plant Protection, Faculty of Agriculture, University of Kurdistan, Sanandaj, Iran
Search for more papers by this authorCorresponding Author
Jafar Abdollahzadeh
Department of Plant Protection, Faculty of Agriculture, University of Kurdistan, Sanandaj, Iran
Correspondence: Jafar Abdollahzadeh, Department of Plant Protection, Faculty of Agriculture, University of Kurdistan, P. O. Box 416, Sanandaj, Iran.
Tel.: +98 (0) 8733620552;
fax: +98 (0) 8733620553;
e-mail: [email protected]
Search for more papers by this authorSajedeh Zolfaghari
Department of Plant Protection, Faculty of Agriculture, University of Kurdistan, Sanandaj, Iran
Search for more papers by this authorAbstract
Progress in molecular biology and the advent of rapid and accurate molecular techniques have contributed to precise and rapid detection and differentiation of microbial pathogens. Identification of the Botryosphaeriaceae species based on morphology has been problematic over time. In this study, we used rep-PCR technique as a molecular tool for typing and differentiation of the Botryosphaeriaceae species, well-known and cosmopolitan fungal pathogens on woody plants. Three primer sets BOX, ERIC and REP were used to differentiate 27 species belong to eight genera. The majority of them were examined in terms of typing and differentiation using molecular methods for the first time. All the primer sets were able to generate species-specific DNA fingerprints from all the tested strains, with two exceptions in the genera Diplodia and Spencermartinsia. Despite the deficiency of each primer sets to separate a few species, cluster analysis of combined data sets indicated the ability of rep-PCR technique to separate 26 out of 27 examined species in highly supported clusters corresponded to the species recognized based on DNA sequence data. Our findings revealed the efficiency of rep-PCR for detection and differentiation of the Botryosphaeriaceae species, especially cryptic species with the same ITS sequences and similar morphology.
Supporting Information
Filename | Description |
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fml12624-sup-0001-FigS1.pptxapplication/mspowerpoint, 90.5 KB | Fig. S1. One of the 24 most parsimonious trees obtained from combined ITS and EF1-α sequence data. |
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