PROTOCOL 06-05.1: Desiccation of plant leaves for molecular detection of Phytophthora spp.

Pathogens ◽  
2021 ◽  
Vol 10 (11) ◽  
pp. 1453
Author(s):  
Dominika G. Siegieda ◽  
Jacek Panek ◽  
Magdalena Frąc

Phytopathogenic microorganisms belonging to the genus Phytophthora have been recognized many times as causal agents of diseases that lower the yield of many plants important for agriculture. Meanwhile, Phytophthora cactorum causes crown rot and leather rot of berry fruits, mainly strawberries. However, widely-applied culture-based methods used for the detection of pathogens are time-consuming and often inaccurate. What is more, molecular techniques require costly equipment. Here we show a rapid and effective detection method for the aforementioned targets, deploying a simple molecular biology technique, Loop-Mediated Isothermal Amplification (LAMP). We optimized assays to amplify the translation elongation factor 1-α (EF1a) gene for two targets: Phytophthora spp. And Phytophthora cactorum. We optimized the LAMP on pure strains of the pathogens, isolated from organic plantations of strawberry, and successfully validated the assay on biological material from the environment including soil samples, rhizosphere, shoots and roots of strawberry, and with SYBR Green. Our results demonstrate that a simple and reliable molecular detection method, that requires only a thermoblock and simple DNA isolation kit, can be successfully applied to detect pathogens that are difficult to separate from the field. We anticipate our findings to be a starting point for developing easier and faster modifications of the isothermal detection methods and which can be applied directly in the plantation, in particular with the use of freeze-dried reagents and chemistry, allowing observation of the results with the naked eye.


2007 ◽  
Vol 8 (1) ◽  
pp. 24 ◽  
Author(s):  
Frances S. Ockels ◽  
Matthew V. DiLeo ◽  
Pierluigi Bonello

Conventionally, plant samples collected in the course of field surveys for Phytophthora spp. (e.g., in the context of the US Forest Service-sponsored national P. ramorum survey of forest environments) are either processed immediately or stored at low temperatures and processed as soon as possible for detection by molecular methods. In order to extend the useful life of the sample, a method involving tissue desiccation was explored for effectively storing Phytophthora-infected plant leaves. In one experiment, rhododendron leaves inoculated with an unknown Phytophthora sp. and desiccated for seven days yielded DNA of sufficient quality for species identification via sequencing of the ITS region. In a second experiment, P. ramorum was successfully detected by PCR in inoculated leaves of California bay laurel, California buckeye, bigleaf maple, rhododendron, and viburnum that were desiccated and stored at room temperature for four months. Therefore, desiccation might be a viable, reliable, and less expensive alternative to storing foliar samples at low temperature. Accepted for publication 11 November 2006. Published 2 March 2007.


Author(s):  
N.C. Lyon ◽  
W. C. Mueller

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.


Sign in / Sign up

Export Citation Format

Share Document