ISSN: 0973-7510

E-ISSN: 3277-3282

Priti Sonavane1 , Prameela Devi2, Raju J3, Deebakamin2 and K. Jayalakshmi3
1IIHR-Central Horticultural Experiment Station, Chettalli, Kodagu-571248, India.
2Division of Plant Pathology, Indian Agricultural Research Institute, New Delhi-110012, India.
3Department of Plant Pathology, University of Agricultural and Horticultural Sciences, Shivamogga, Karnataka 577225, India.
© The Author(s). 2015
J. Pure Appl. Microbiol., 2015, 9 (4): 3277-3282.
Received: 03/08/2015 | Accepted: 06/10/2015 | Published: 31/12/2015
Abstract

Bipolaris spp are the pathogens causing number of diseases in graminaceous crops. Taxonomic delimitation and precise species identification is difficult within this genus because it displays close resemblance with genus Drechslera and Exserohilum in morphological features. DNA barcoding is a novel technology of DNA sequences of standardized genetic markers for the simple and accurate identification of eukaryotic organisms. Here, we attempted to identify a barcode gene using 24 isolates belonging to five species of Bipolaris using five markers i.e. ITS, tef-1, ²-tubulin, LSU and SSU. ITS region was found as the best marker for species discrimination with highest PCR success rate for amplification and sequencing, with more clearly defined Barcode gap and with high probability of correct identification (PCI).

Keywords

Bipolaris, PCR success rate, Barcode gap and PCI .

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