dc.contributor.author |
Meinecke, Colton D.
|
|
dc.contributor.author |
De Vos, Lieschen
|
|
dc.contributor.author |
Yilmaz, Neriman
|
|
dc.contributor.author |
Steenkamp, Emma Theodora
|
|
dc.contributor.author |
Wingfield, Michael J.
|
|
dc.contributor.author |
Wingfield, Brenda D.
|
|
dc.contributor.author |
Villari, Caterina
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|
dc.date.accessioned |
2024-09-12T12:02:45Z |
|
dc.date.available |
2024-09-12T12:02:45Z |
|
dc.date.issued |
2023-10 |
|
dc.description.abstract |
The pine pitch canker pathogen Fusarium circinatum is endemic in the southeastern United States and Central America and represents an invasive threat globally. This ecologically adaptable fungus readily infects all parts of its pine hosts, leading to widespread mortality of nursery seedlings and decline in the health and productivity of forest stands. Because trees infected by F. circinatum can remain asymptomatic for long periods of time, accurate and rapid tools are needed for real-time diagnostics and surveillance at ports, in nurseries, and in plantations. To meet this need and to limit the spread and impact of the pathogen, we developed a molecular test using loop-mediated isothermal amplification (LAMP), a technology that allows for the rapid detection of pathogen DNA on portable, field-capable devices. LAMP primers were designed and validated to amplify a gene region unique to F. circinatum. Using a globally representative collection of F. circinatum isolates and other closely related species, we have demonstrated that the assay can be used to identify F. circinatum across its genetic diversity and that it is sensitive to as few as 10 cells from purified DNA extracts. The assay can also be used with a simple, pipette-free DNA extraction method and is compatible with testing symptomatic pine tissues in the field. This assay has the potential to facilitate diagnostic and surveillance efforts both in the laboratory and in the field and, thus, to reduce the spread and impact of pitch canker worldwide. |
en_US |
dc.description.department |
Biochemistry, Genetics and Microbiology (BGM) |
en_US |
dc.description.department |
Forestry and Agricultural Biotechnology Institute (FABI) |
en_US |
dc.description.librarian |
am2024 |
en_US |
dc.description.sdg |
SDG-15:Life on land |
en_US |
dc.description.sponsorship |
The USDA NIFA AFRI CARE program, the D.B. Warnell School of Forestry and Natural Resources, University of Georgia, and the Forestry and Agricultural Biotechnology Institute, University of Pretoria. |
en_US |
dc.description.uri |
https://apsjournals.apsnet.org/loi/pdis |
en_US |
dc.identifier.citation |
Meinecke, C.d., De Vos, L., Yilmaz, N. et al. 2023, 'A LAMP assay for rapid detection of the pitch canker pathogen Fusarium circinatum', Plant Disease, vol. 107, pp. 2916-2923. https://DOI.org/10.1094/PDIS-04-22-0972-SR. |
en_US |
dc.identifier.issn |
0191-2917 (print) |
|
dc.identifier.issn |
1943-7692 (online) |
|
dc.identifier.other |
10.1094/PDIS-04-22-0972-SR |
|
dc.identifier.uri |
http://hdl.handle.net/2263/98163 |
|
dc.language.iso |
en |
en_US |
dc.publisher |
American Phytopathological Society |
en_US |
dc.rights |
© 2023 The American Phytopathological Society |
en_US |
dc.subject |
Crude DNA |
en_US |
dc.subject |
Forest health and protection |
en_US |
dc.subject |
Pinus |
en_US |
dc.subject |
Rapid detection |
en_US |
dc.subject |
Deoxyribonucleic acid (DNA) |
en_US |
dc.subject |
SDG-15: Life on land |
en_US |
dc.subject |
Loop-mediated isothermal amplification (LAMP) |
en_US |
dc.title |
A LAMP assay for rapid detection of the pitch canker pathogen Fusarium circinatum |
en_US |
dc.type |
Article |
en_US |