scholarly journals Ultrastructure of the early stages of Colletotrichum acutatum infection of strawberry tissues

2005 ◽  
Vol 83 (5) ◽  
pp. 491-500 ◽  
Author(s):  
Francisco T Arroyo ◽  
Javier Moreno ◽  
Gregorio García-Herdugo ◽  
Berta De los Santos ◽  
Carmen Barrau ◽  
...  

The early stages of the infection of attached leaves and petioles of strawberry (Fragaria ×ananassa Duch. 'Camarosa') by Colletotrichum acutatum Simmonds were studied using scanning and transmission electron microscopy. Pre-penetration events of these tissues were similar, but the production of secondary conidia (microcyclic conidiation) was detected only on leaves. At the ultrastructural level, different stages of maturation of appressoria were observed and described. In young appressoria, the cell wall was composed of two layers and the plasma membrane displayed a wavy appearance. In the following stage, the appressorium developed a third electron-transparent layer between the cell wall and the plasma membrane. This new electron-transparent material was especially visible in the region of the appressorium near the cuticle. The plasma membrane of this appressorium showed a smooth appearance. Afterwards, a penetration peg emerged through the pore penetrating the cuticle and reached the epidermal wall where it enlarged to form an intramural infection vesicle. Both structures of infection, the penetration peg and the intramural infection vesicle, produced during the early phases of infection of strawbery tissues by C. acutatum, have not been previously reported and confirm that its invasion strategy is that of a subcuticular intramural pathogen. Once the infection was well established, abundant subcuticular and intramural hyphae were produced on petioles, causing severe degradation of the host cell walls. Occasionally, the cuticle appeared disrupted in those regions where the host walls were very degraded and dilated. Differences between colonization of petioles and leaves were observed.Key words: Colletotrichum acutatum, Fragaria ×ananassa, infection vesicle, invasion strategy, penetration peg.

Holzforschung ◽  
2005 ◽  
Vol 59 (6) ◽  
pp. 675-680 ◽  
Author(s):  
Jonas Brändström ◽  
Jean-Paul Joseleau ◽  
Alain Cochaux ◽  
Nathalie Giraud-Telme ◽  
Katia Ruel

Abstract Transmission electron microscopy was used to investigate the ultrastructure of recycled pulp fibers originating from a household collection plant and intended for the production of packaging paper. Three recovered paper grades and recycling processes, including pulping, screening, cleaning and refining, were assessed with emphasis on surface and internal fibrillation as well as xylan localization. Results showed a large heterogeneity with respect to fiber ultrastructure within and between the grades. Screening and cleaning steps had no detectable effects, but refining clearly increased cell-wall delamination and surface fibrillation. Immunolabeling of xylans showed that they were distributed rather evenly across the cell walls. They were also present on fines. Two different mechanisms for fiber delamination and surface fibrillation were found, one which implies that internal and external fibrillation take place simultaneously across the cell wall, and another which implies successive peeling of layers or sub-layers from the outside towards the inside. It is suggested that recycled fibers of chemical pulp origin undergo the former mechanism and recycled fibers that contain lignin binding the cell wall matrix give rise to the latter peeling mechanism. Because several recycled fibers were severely delaminated and almost fractured, we suggest that to produce a good packaging paper, it is important that recycled pulp should contain a significant proportion of fibers with high intrinsic strength.


1964 ◽  
Vol 20 (2) ◽  
pp. 217-233 ◽  
Author(s):  
G. W. Claus ◽  
L. E. Roth

The morphological features of the cell wall, plasma membrane, protoplasmic constituents, and flagella of Acetobacter suboxydans (ATCC 621) were studied by thin sectioning and negative staining. Thin sections of the cell wall demonstrate an outer membrane and an inner, more homogeneous layer. These observations are consistent with those of isolated, gram-negative cell-wall ghosts and the chemical analyses of gram-negative cell walls. Certain functional attributes of the cell-wall inner layer and the structural comparisons of gram-negative and gram-positive cell walls are considered. The plasma membrane is similar in appearance to the membrane of the cell wall and is occasionally found to be folded into the cytoplasm. Certain features of the protoplasm are described and discussed, including the diffuse states of the chromatinic material that appear to be correlated with the length of the cell and a polar differentiation in the area of expected flagellar attachment. Although the flagella appear hollow in thin sections, negative staining of isolated flagella does not substantiate this finding. Severe physical treatment occasionally produces a localized penetration into the central region of the flagellum, the diameter of which is much smaller then that expected from sections. A possible explanation of this apparent discrepancy is discussed.


Author(s):  
Lukasz Wejnerowski ◽  
Slawek Cerbin ◽  
Maria K. Wojciechowicz ◽  
Marcin K. Dziuba

<p>Recent studies have shown that the filamentous cyanobacterium <em>Aphanizomenon gracile</em> Lemmermann, strain SAG 31.79, consists of two types of filaments that differ in thickness. These two types are known to vary in resistance to <em>Daphnia</em> <em>magna</em> grazing: thin filaments (&lt;2.5 µm) are more vulnerable to grazing than the thick ones (&gt;2.5 µm). In this study, we investigated whether the difference in the vulnerability to grazing of thin and thick filaments is a result of different thickness of their cell walls, a filament stiffness determinant. We expected thick filaments to have thicker cell walls than the thin ones. Additionally, we analysed whether cell wall thickness correlates with filament thickness regardless of the filament type. A morphometric analysis of cell walls was performed using transmission electron micrographs of ultra-thin sections of the batch-cultured cyanobacterial material.  Our study revealed that the thin type of filaments had thinner cell walls than the thick filaments. Moreover, cell wall thickness was positively correlated with filament thickness. TEM (transmission electron microscopy) observations also revealed that the thin type of filaments was often at different stages of autocatalytic cell destruction, which was mainly manifested in the increase in cell vacuolization and degradation of the cytoplasm content. Based on our findings, we assume that previously reported higher resistance of thick filaments to <em>Daphnia</em> grazing results from greater stiffness and excellent physiological conditions of thick filaments. </p>


Holzforschung ◽  
1999 ◽  
Vol 53 (2) ◽  
pp. 111-117 ◽  
Author(s):  
A.O. Rapp ◽  
H. Bestgen ◽  
W. Adam ◽  
R.-D. Peek

Summary A literature survey was performed to find progress in techniques for monitoring penetration of synthetic resins in wood cell walls. Electron energy loss spectroscopy (EELS) in combination with transmission electron microscopy (TEM) was successfully applied for the high resolution examination of the distribution of a partly methylated hydroxymethyl melamine resin in Norway spruce (Picea abies Karst.) earlywood cell walls. The nitrogen of the resin was found as clearly detectable signals in all layers of the lignified cell wall, thus allowing the quantification of resin which had penetrated into the different layers. Possible principles of decay protection of wood which has been upgraded with low concentrated aqueous solutions of modified hydroxymethyl melamine resins with medium to low hydroxymethyl/melamine ratios are discussed.


Silica deposition is described for two protistan flagellates, Synura petersenii (Chrysophyceae, algae) and Stephanoeca diplocostata (Choanoflagellida, Protozoa). Both taxa produce silica units intracellularly and subsequently assemble them outside the protoplast to form a ‘cell wall’. In Synura the cell wall consists of a scale case to which scales are added throughout the cell cycle. In Stephanoeca individual siliceous, costal strips are accumulated outside the protoplast and assembled into a lorica once sufficient strips have been produced. In both taxa silica is laid down within silica deposition vesicles (s.d.vs) of uncertain origin. Microtubules are involved in the orientation and support of s.d.vs during early stages of silica unit biogenesis. Detailed comparisons of silica deposition are made between Synura and Stephanoeca and between these and other silica-depositing protistans.


1987 ◽  
Vol 65 (12) ◽  
pp. 2483-2489 ◽  
Author(s):  
H. C. Huang ◽  
E. G. Kokko

Transmission electron microscopy revealed that hyphae of the hyperparasite Coniothyrium minitans invade sclerotia of Sclerotinia sclerotiorum, resulting in the destruction and disintegration of the sclerotium tissues. The dark-pigmented rind tissue is more resistant to invasion by the hyperparasite than the unpigmented cortical and medullary tissues. Evidence from cell wall etching at the penetration site suggests that chemical activity is required for hyphae of C. minitans to penetrate the thick, melanized rind walls. The medullary tissue infected by C. minitans shows signs of plasmolysis, aggregation, and vacuolization of cytoplasm and dissolution of the cell walls. While most of the hyphal cells of C. minitans in the infected sclerotium tissue are normal, some younger hyphal cells in the rind tissue were lysed and devoid of normal contents.


Weed Science ◽  
1991 ◽  
Vol 39 (1) ◽  
pp. 6-12 ◽  
Author(s):  
Bernal E. Valverde ◽  
Arnold P. Appleby ◽  
Steven R. Radosevich ◽  
Alfred Soeldner

Primary root cells from five dinitroaniline-resistant (R) and three susceptible (S) goosegrass biotypes from North Carolina and South Carolina were observed by transmission electron microscopy to determine whether resistance was associated with changes in cell wall formation. Cell wall malformations were found in some cells from two of the R-biotypes and in one of the S-biotypes. Malformations consisted of partially deposited cell walls and the inclusion of cell wall material in the cytoplasm. Some of the affected cells also had abnormal, lobed nuclei and malformed mitochondria. There seems to be little or no correlation between dinitroaniline resistance and cell wall malformations.


2012 ◽  
Vol 72 (1) ◽  
pp. 71-77 ◽  
Author(s):  
G. Wolff ◽  
GC Pereira ◽  
EM Castro ◽  
J Louzada ◽  
FF Coelho

This study shows, in a multiple-level approach, the responses of Salvinia auriculata to Cd pollution in aquatic ecosystems. S. auriculata ramets were cultivated in nutrient solution and subjected to five treatments with Cd for ten days. At the end of the experiment, the number of new ramets and the dry biomass were determined. For ultrastructural observations, the leaves of S. auriculata were analyzed using a scanning electron microscope and transmission electron microscope. At the end of the experiment, the plants exposed to Cd showed damage in the leaves including necrosis and chlorosis, stomate deformations and damaged trichomes. We observed a decrease in the number of new ramets and dry biomass of S. auriculata following the increase in Cd concentration in the solution. At the ultrastructural level, leaves exposed to Cd presented chloroplast deformations and deterioration in the cell wall. All the symptoms of toxicity were directly proportionate to the concentration of Cd in the solution. The results suggests that S. auriculata shows good potential for use as a bioindicator and it can be used in the biomonitoring of aquatic ecosystems contaminated by Cd.


2003 ◽  
Vol 81 (11) ◽  
pp. 1083-1090 ◽  
Author(s):  
M KM Wong ◽  
E BG Jones ◽  
M A Abdel-Wahab ◽  
D WT Au ◽  
L LP Vrijmoed

Conidiogenesis and conidial appendage ontogeny of the coelomycete Bartalinia robillardoides Tassi was studied at the light microscope, scanning electron microscope, and transmission electron microscope levels. Conidiogenesis in B. robillardoides is holoblastic. Appendage ontogeny begins as a cellular outgrowth of the apical and the basal cells of the young conidium, the former developing prior to the basal appendage. Conidia detach from the conidiogenous cells schizolytically. Mature conidial cell walls comprise two layers: an outer electron-dense layer, 30–38 nm, and an inner less electron-dense layer, 100–125 nm. The apical appendages arise from an outgrowth of the apical cell, which then branches to form the appendages. The single basal appendage arises from the junction between the basal cell of the conidium and the conidiogenous cell prior to conidial detachment from the conidiogenous cell, as an outgrowth of the conidial cell wall. Conidial appendage ontogeny is compared with those of other coelomycetes.Key words: Annellidic, appendage ontogeny, coelomycetes, holoblastic.


2014 ◽  
Vol 104 (9) ◽  
pp. 977-984 ◽  
Author(s):  
Hao-Xun Chang ◽  
Lou Ann Miller ◽  
Glen L. Hartman

Appressoria of some plant-pathogenic fungi accumulate turgor pressure that produces a mechanical force enabling the direct penetration of hyphae through the epidermis. Melanin functions as an impermeable barrier to osmolytes, which allows appressoria to accumulate high turgor pressure. Deficiency of melanin in appressoria reduces turgor pressure and compromises the infection process. In Phakopsora pachyrhizi, the soybean rust pathogen, the appressoria are hyaline. Our objective was to ensure the absence of a melanin layer specifically between the appressorial cell wall and plasma membrane, as well as to determine the turgor pressure of P. pachyrhizi appressoria. We demonstrated that two melanin biosynthesis inhibitors neither reduced turgor pressure nor compromised the infection process. Transmission electron microscopy also showed the absence of a melanin layer between the appressorial cell wall and plasma membrane. In addition, the turgor pressure of P. pachyrhizi appressoria was 5 to 6 MPa, based on extracellular osmolytes used to simulate different osmotic pressures. This is the first report showing that turgor pressure accumulation of P. pachyrhizi appressoria was independent of melanin.


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