Ultrastructural and cytochemical study of colonization of xylem vessel elements of susceptible and resistant Dianthus caryophyllus by Fusarium oxysporum f.sp. dianthi

1999 ◽  
Vol 77 (5) ◽  
pp. 644-663 ◽  
Author(s):  
G.B. Ouellette ◽  
R.P. Baayen ◽  
M. Simard ◽  
D. Rioux
1999 ◽  
Vol 77 (5) ◽  
pp. 644-663 ◽  
Author(s):  
G B Ouellette ◽  
R P Baayen ◽  
M Simard ◽  
D Rioux

The colonization processes of the xylem in the susceptible carnation cv. Early Sam and the resistant cv. Novada were studied ultrastructurally following inoculation with Fusarium oxysporum f.sp. dianthi. Samples from 1 to 3 cm above the incision were collected over 5 weeks and processed following conventional procedures as well as with probes for cellulose, N-acetyl-glucosamine, and pectin. The fungus grew profusely in the vessel lumina of the susceptible cultivar. Some of the colonized vessels were lined with coating material connected to the fungal cell wall and extending into the host cell wall through microfilamentous-like structures. Coatings did not label for pectin or cellulose. The pathogen crossed from one vessel element to another (and at times to parenchyma cells) usually directly through pit membranes; often the invading structures of the fungus appeared to be either only membrane-bound or formed solely of microfilamentous-like entities. The fungus subsequently invaded extensively, generally by means of microhyphae, the vessel intercalary walls from the pit membranes and vessel wall junctures. Microhyphae had thin or imperceptible walls and contained only some of the normal cytoplasmic components. Initially, the invading hyphae dislocated the host cell walls, apparently mechanically more than by lysis; however, more pronounced lysis occurred following general tissue invasion. Host parenchyma cells seemed relatively unaffected, even after the surrounding walls had undergone severe degradation. Colonization of resistant plants was restricted. Degradation of tissues did not occur and microhyphae were not observed. Inoculated vessel elements in the 'Novada' plants contained numerous fungal cells and little occluding material, whereas the surrounding vessels were almost completely occluded. The initially invaded xylem became tangentially compartmentalized by parenchyma cell wall thickenings and by hyperplastic parenchyma. Occasionally, hyperplastic tissues were slightly re-invaded, forming secondary invasion pockets. Vessel-occluding material varied in structure and opacity, not only from vessel to vessel but also within the same vessel, and contained microfilamentous-like structures and other types of fine fibrillar material. Some vessel elements in or near the secondary invasion pockets contained only the finer fibrils that reacted strongly with an antibody specific for pectin. Vessel elements rarely contained tyloses.Key words: cellulose, chitin, Dianthus caryophyllus, Fusarium wilt, gels and gums, host wall degradation, microhyphae, pectin, tyloses.


Plants ◽  
2020 ◽  
Vol 9 (12) ◽  
pp. 1715
Author(s):  
Eleftheria Roumeli ◽  
Leah Ginsberg ◽  
Robin McDonald ◽  
Giada Spigolon ◽  
Rodinde Hendrickx ◽  
...  

Individual plant cells are the building blocks for all plantae and artificially constructed plant biomaterials, like biocomposites. Secondary cell walls (SCWs) are a key component for mediating mechanical strength and stiffness in both living vascular plants and biocomposite materials. In this paper, we study the structure and biomechanics of cultured plant cells during the cellular developmental stages associated with SCW formation. We use a model culture system that induces transdifferentiation of Arabidopsis thaliana cells to xylem vessel elements, upon treatment with dexamethasone (DEX). We group the transdifferentiation process into three distinct stages, based on morphological observations of the cell walls. The first stage includes cells with only a primary cell wall (PCW), the second covers cells that have formed a SCW, and the third stage includes cells with a ruptured tonoplast and partially or fully degraded PCW. We adopt a multi-scale approach to study the mechanical properties of cells in these three stages. We perform large-scale indentations with a micro-compression system in three different osmotic conditions. Atomic force microscopy (AFM) nanoscale indentations in water allow us to isolate the cell wall response. We propose a spring-based model to deconvolve the competing stiffness contributions from turgor pressure, PCW, SCW and cytoplasm in the stiffness of differentiating cells. Prior to triggering differentiation, cells in hypotonic pressure conditions are significantly stiffer than cells in isotonic or hypertonic conditions, highlighting the dominant role of turgor pressure. Plasmolyzed cells with a SCW reach similar levels of stiffness as cells with maximum turgor pressure. The stiffness of the PCW in all of these conditions is lower than the stiffness of the fully-formed SCW. Our results provide the first experimental characterization of the mechanics of SCW formation at single cell level.


2019 ◽  
Vol 48 (2) ◽  
pp. 5-14
Author(s):  
Santiago Monroy-Mena ◽  
Aura L. Chacon-Parra ◽  
Julieth P. Farfan-Angarita ◽  
Sixta T. Martinez-Peralta ◽  
Harold D. Ardila-Barrantes

En el presente trabajo se seleccionaron y validaron genes de referencia para estudios transcripcionales en el modelo clavel - Fusarium oxysporum f. sp. dianthi. Para ello, se seleccionaron genes asociados a procesos básicos celulares que han sido usados como genes de referencia en otros modelos planta-patógeno y se determinó el efecto de la inoculación del patógeno sobre su expresión. Se realizó un diseño de cebadores para los diferentes genes candidatos con el fin de verificar tanto su presencia en el genoma de claveles cultivados en Colombia, como su transcripción constitutiva en los diferentes tejidos por medio de la técnica de transcripción reversa y posterior reacción en cadena de la polimerasa (RT-PCR por sus siglas en ingles). Posteriormente, se evaluaron los niveles transcripcionales de los genes candidatos usando RT-qPCR en tallos y raíces de dos variedades con diferentes niveles de resistencia a la enfermedad, que fueron inoculados con este patógeno. La validación estadística realizada, usando ANOVA y los programas GeNorm y Normfinder, determinó que los genes codificantes para una histona H3 y el ARNr18S no presentan variación en sus niveles de expresión por efecto de la inoculación, permitiendo su uso como genes de referencia en estudios transcripcionales en esta interacción planta-patógeno.


2001 ◽  
Vol 56 (7) ◽  
pp. 717-721 ◽  
Author(s):  
Paolo Curir ◽  
Marcello Dolci ◽  
Virginia Lanzotti ◽  
Orazio Taglialatela-Scafati

1985 ◽  
Vol 63 (3) ◽  
pp. 638-646 ◽  
Author(s):  
R. Harling ◽  
G. S. Taylor

An anatomical study of infection by Fusarium oxysporum Schlecht. f.sp. dianthi (Prill, et Del.) Snyd. and Hans, in the stems of a resistant carnation (Dianthus caryophyllus L.) cultivar, and a susceptible cultivar, was carried out to determine host structural responses to infection which might be important in resistance to the fungus. Histological examination of stems at 2–24 days following inoculation revealed certain features of infection which were common to both the resistant and the susceptible cultivars. These were colonization of the xylem vessels and surrounding tissues, hyperplasia, hypertrophy and altered cytoplasmic activity of the xylem parenchyma, blockage of vessels with gels, and swelling of the vessel pit membranes between pit pairs. Gel formation was associated with paratracheal parenchyma cells. However, the extent and timing of some of these features were different between the two cultivars. The susceptible cultivar showed extensive colonization and destruction of xylem vessels and surrounding tissues, limited hyperplasia, and limited vascular gelation which was also slow to occur. In contrast, the resistant cultivar had less colonization and destruction of xylem, extensive areas of hyperplastic xylem parenchyma which sometimes surrounded groups of infected vessels, and rapid and extensive gelation of the xylem vessels in advance of fungal colonization. The rapid gelation response, together with the hyperplasia, were considered to be responsible for the physical containment of the fungus in the resistant cultivar and are therefore an important part of the defence mechanism in this host against the pathogen.


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