Real-Time Quantitative and Ion-Metal Indicator LAMP-Based Assays for Rapid Detection of Sclerotinia sclerotiorum

• Published in: Plant disease Vol. 104; no. 5; p. 1514
• Main Authors: Grabicoski, Edilaine Mauricia Gelinski, Jaccoud-Filho, David de Souza, Lee, David, Henneberg, Luciane, Pileggi, Marcos
• Format: Journal Article
• Language: English
• Published: United States 01.05.2020
• Subjects: Ascomycota; DNA Primers; Metals; Nucleic Acid Amplification Techniques; Polymerase Chain Reaction; calcein; visual detection; diagnostic; field detection; molecular test; white mold
• ISSN: 0191-2917
• DOI: 10.1094/PDIS-07-19-1455-RE

is one of the most devastating and cosmopolitan plant pathogens. Rapid detection of can provide growers an advantage in knowing what control measures should be taken to minimize crop damage and financial losses caused by it. Loop-mediated isothermal amplification (LAMP) is a fast, sensitive, and specific nucleic acid amplification method that does not require a thermal cycler. This study aimed to develop a LAMP-based assay for the specific detection of (Ss-LAMP). A real-time quantitative LAMP reaction (Ss-qLAMP) and a calcein ion indicator-based LAMP reaction (Ss-cLAMP) were designed, optimized, and tested on fungi, plant, and soil samples. The Ss-LAMP reactions were very specific and sensitive. Applying the artificially inoculated soil samples with DNA purified by five protocols in the Ss-qLAMP reaction, it was possible to detect and quantify the pathogen DNA, regardless of the extraction protocol. Naturally infected soybean tissues had the pathogen detected by Ss-cLAMP directly in the reaction tube with no DNA extraction requirement. The assays should be applicable for many types of samples, such as soil, spore traps, and plant tissues from several crops, with no requirement for DNA extraction. The Ss-LAMP reactions took less than 1 h to complete, and they can be made directly in the field with real-time quantitative results (Ss-qLAMP) or qualitative naked-eye visual results (Ss-cLAMP). Results were obtained with 10 pg of DNA or 10 ng of crude mycelium, suggesting a detection limit close to a single DNA copy. Ss-LAMP reactions will allow rapid and accurate diagnosis of and assist in pathogen management and control.