Research Letter
High-resolution melting analysis allowed fast and accurate closed-tube genotyping of Fusarium oxysporum formae speciales complex
Article first published online: 3 JUL 2012
DOI: 10.1111/j.1574-6968.2012.02610.x
© 2012 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved
Additional Information
How to Cite
Ganopoulos, I., Madesis, P., Zambounis, A. and Tsaftaris, A. (2012), High-resolution melting analysis allowed fast and accurate closed-tube genotyping of Fusarium oxysporum formae speciales complex. FEMS Microbiology Letters, 334: 16–21. doi: 10.1111/j.1574-6968.2012.02610.x
Publication History
- Issue published online: 1 AUG 2012
- Article first published online: 3 JUL 2012
- Accepted manuscript online: 7 JUN 2012 03:31AM EST
- Manuscript Accepted: 31 MAY 2012
- Manuscript Revised: 22 MAY 2012
- Manuscript Received: 24 FEB 2012
Keywords:
- genotyping;
- HRM;
- Fusarium oxysporum;
- formae speciales complex;
- internal transcribed spacer
Abstract
The fungus Fusarium oxysporum is a highly complex species composed by many strains put together into groups called formae speciales. As it is difficult and laborious to discriminate Fusarium formae specials via biochemical or phenotypic methods, it is very important to develop novel, rapid, and simple to perform identification methods. Herein, real-time PCR assay [using universal internal transcribed spacer (ITS) primers] coupled with high-resolution melting (HRM) analysis was developed for identifying and distinguishing F. oxysporum formae speciales complex. The melting curve analysis of these amplicons specifically classified all isolates into seven F. oxysporum formae speciales and generated seven HRM curve profiles. The smallest DNA sequence difference recognized in this study was one nucleotide. The results presented show that HRM curve analysis of Fusarium ITS sequences is a simple, quick, and reproducible method that allows both the identification of seven F. oxysporum formae speciales and at the same time their screening for variants. Our genotyping assay uses the combined information of simultaneously acquired HRM data from an unlabeled probe and the full-length amplicon. Finally, the completion of both reaction and analysis in a closed tube saves time by eliminating the separate steps and reduces the risk of contamination.

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