Rapid Detection of Fusarium oxysporum Using Insulated Isothermal PCR and a Rapid, Simple DNA Preparation Protocol
Open Access
- 31 October 2022
- journal article
- research article
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 23 (21) , 13253
Abstract
We developed an insulated isothermal PCR (iiPCR) method for the efficient and rapid detection of Fusarium oxysporum (Fo), which is a fungus that infects various hosts and causes severe crop losses. The Fo iiPCR method was sensitive enough to detect up to 100 copies of standard DNA template and 10 fg of Fo genomic DNA. In addition, it could directly detect 1 pg of mycelium and 10 spores of Fo without DNA extraction. Our study compared the performance of Fo iiPCR to that of three published in planta molecular detection methods—conventional PCR, SYBR green-based real-time PCR, and hydrolysis probe-based real-time PCR—in field detection of Fo. All diseased field samples yielded positive detection results with high reproducibility when subjected to an Fo iiPCR test combined with a rapid DNA extraction protocol compared to Fo iiPCR with an automated magnetic bead-based DNA extraction protocol. Intraday and interday assays were performed to ensure the stability of this new rapid detection method. The results of detection of Fo in diseased banana pseudostem samples demonstrated that this new rapid detection method was suitable for field diagnosis of Fusarium wilt and had high F1 scores for detection (the harmonic mean of precision and recall of detection) for all asymptomatic and symptomatic Fo-infected banana samples. In addition, banana samples at four growth stages (seedling, vegetative, flowering and fruiting, and harvesting) with mild symptoms also showed positive detection results. These results indicate that this new rapid detection method is a potentially efficient procedure for on-site detection of Fo.Keywords
Funding Information
- Council of Agriculture (104AS-10.10.1-BQ-B1(8))
- Ministry of Science and Technology, Taiwan, R.O.C. (105-2311-B-020-001, 107-2311-B-020-001, 108-2313-B-020-009, 110-2637-B-020-001, 111-2637-B-020-004)
- National Pingtung University of Science and Technology, Taiwan
This publication has 46 references indexed in Scilit:
- Development of a loop-mediated isothermal amplification assay for rapid and sensitive detection of Fusarium oxysporum f. sp. cubense race 4European Journal of Plant Pathology, 2012
- Development of TaqMan Probe-Based Insulated Isothermal PCR (iiPCR) for Sensitive and Specific On-Site Pathogen DetectionPLOS ONE, 2012
- Detection of white spot syndrome virus by polymerase chain reaction performed under insulated isothermal conditionsJournal of Virological Methods, 2012
- A thermally baffled device for highly stabilized convective PCRBiotechnology Journal, 2012
- Development of the molecular methods for rapid detection and differentiation of Fusarium oxysporum and F. oxysporum f. sp. niveum in TaiwanNew Biotechnology, 2010
- Development of a molecular marker for specific detection of Fusarium oxysporum f. sp. cubense race 4European Journal of Plant Pathology, 2008
- Monoclonal antibodies for the detection of Puccinia striiformis urediniosporesMycological Research, 2007
- Fusarium Wilt of Banana Is Caused by Several Pathogens Referred to as Fusarium oxysporum f. sp. cubensePhytopathology®, 2006
- Molecular detection ofFusarium oxysporumf. sp.niveumandMycosphaerella melonisin infected plant tissues and soilFEMS Microbiology Letters, 2005
- Genetic Diversity of Human Pathogenic Members of the Fusarium oxysporum Complex Inferred from Multilocus DNA Sequence Data and Amplified Fragment Length Polymorphism Analyses: Evidence for the Recent Dispersion of a Geographically Widespread Clonal Lineage and Nosocomial OriginJournal of Clinical Microbiology, 2004