An ultrastructural study of the late-blight fungus Phytophthora infestans and its interaction with the foliage of two potato cultivars possessing different levels of general (field) resistance

1983 ◽  
Vol 61 (10) ◽  
pp. 2669-2685 ◽  
Author(s):  
Michael D. Coffey ◽  
Una E. Wilson

In the susceptible reaction of foliage of the cultivar Majestic there was extensive colonization of the host tissue prior to the onset of necrosis. The development of intracellular hyphae was confined to the initially parasitized palisade cells. Thereafter the fungus grew as intercellular hyphae, which penetrated host cells and formed haustoria. Haustorial morphology was highly variable, ranging in type from small spherical to much larger digitlike structures. Haustorial formation was preceded by the laying down of a moderately electron-dense penetration matrix bounded by the host plasmalemma. This material probably constituted the extrahaustorial matrix once haustorial development had taken place. The matrical material stained with silver proteinate reagent, and this reaction was blocked by dimedone, indicating that it was carbohydrate in nature. In the resistant reaction of foliage of the cultivar Shamrock, the epidermal cells rapidly became necrotic. Quantities of exceedingly electron-dense granules appeared in the necrotic host cells. Host organelles were no longer recognizable, but the fungal cytoplasm remained intact. In adjoining host cells, thin cell wall appositions were formed, which had a heterogeneous composition. On occasions when the fungus attempted to invade an underlying mesophyll cell, papillae usually formed in that cell at the site of incipient penetration.

Author(s):  
Celso A. Reis ◽  
Rudolf Tauber ◽  
Véronique Blanchard

AbstractSARS-CoV-2 causes the respiratory syndrome COVID-19 and is responsible for the current pandemic. The S protein of SARS-CoV-2-mediating virus binding to target cells and subsequent viral uptake is extensively glycosylated. Here we focus on how glycosylation of both SARS-CoV-2 and target cells crucially impacts SARS-CoV-2 infection at different levels: (1) virus binding and entry to host cells, with glycosaminoglycans of host cells acting as a necessary co-factor for SARS-CoV-2 infection by interacting with the receptor-binding domain of the SARS-CoV-2 spike glycoprotein, (2) innate and adaptive immune response where glycosylation plays both a protective role and contributes to immune evasion by masking of viral polypeptide epitopes and may add to the cytokine cascade via non-fucosylated IgG, and (3) therapy and vaccination where a monoclonal antibody-neutralizing SARS-CoV-2 was shown to interact also with a distinct glycan epitope on the SARS-CoV-2 spike protein. These evidences highlight the importance of ensuring that glycans are considered when tackling this disease, particularly in the development of vaccines, therapeutic strategies and serological testing.


1981 ◽  
Vol 59 (2) ◽  
pp. 251-263 ◽  
Author(s):  
X. Mourichon ◽  
G. Sallé

An electron microscopic study was performed on haustoria of Phytophthora cactorum (L. et C.) Schroeter developed in tissues of two cultivars of apple fruits: a susceptible variety ('Golden delicious') and a resistant one ('Belle de Boskoop'). Ultrastructure of intercellular hyphae and some aspects of their penetration between contiguous host cells were described. A light dissolution of the host cell walls was observed. Ontogenic investigations indicated that in the susceptible host, the wall of the fungal haustoria was covered with a dense-stained extrahaustorial matrix. Its origin and its polysaccharide nature were demonstrated. On the other hand, the resistant host developed, immediately after the inoculation, a papilla which gave rise, later on, to a sheath enclosing adult haustoria. The role of these callosic structures in the phenomenon of resistance was discussed.


2014 ◽  
Vol 2014 ◽  
pp. 1-12 ◽  
Author(s):  
M. K. Daud ◽  
Lei Mei ◽  
M. T. Variath ◽  
Shafaqat Ali ◽  
Cheng Li ◽  
...  

Chromium (Cr) is present in our environment as a toxic pollutant, which needs to be removed using phytoremediation technology. In present study, two transgenic cotton cultivars (J208, Z905) and their hybrid line (ZD14) were used to explore their Cr uptake and tolerance potential using multiple biomarkers approach. Four different levels of Cr (CK, 10, 50, and 100 μM) were applied. Cr caused a significant reduction in root/shoot length, number of secondary roots, and root fresh and dry biomasses at 100μM. Cr accumulated more in roots and was found higher in hybrid line (ZD14) as compared with its parent lines (J208, Z905) at all Cr stress levels (10, 50, and 100 μM). Cr translocation was less than 1 in all cultivars. Ultrastructural studies at 100 μM Cr showed an increase in number of nuclei and vacuoles and presence of Cr dense granules in dead parts of the cell (vacuoles/cell wall). Malondialdehyde (MDA), hydrogen peroxide (H2O2), total soluble proteins, superoxide dismutase (SOD), peroxidase (POD), ascorbate peroxidase (APX), catalase (CAT), and glutathione reductase (GR) as a whole were upregulated with elevated levels of Cr. Higher Cr uptake by roots, accelerated metabolism, and Cr sequestration in dead parts of the cell indicate that these cotton cultivars can be useful for Cr accumulation and tolerance.


1990 ◽  
Vol 68 (2) ◽  
pp. 381-390 ◽  
Author(s):  
C. Coulomb ◽  
P. J. Coulomb ◽  
I. Saimmaime ◽  
Y. Lizzi ◽  
C. Polian

Elicitation of a sensitive sweet pepper (Capsicum annuum) cultivar roots by immersion in the culture medium of Trichoderma album induces resistance in leaves infected by Phytophthora capsici. In infected tissues, host cells are intact and develop wall formations that look like typical wall appositions, but differ from them by the presence of a substance of cytoplasmic origin, which is phagocytized and degraded, conferring a lytic function and unusual dynamics to these structures. The involvement of the endoplasmic reticulum and peroxysomes in eventual detoxification processes is discussed. The resistance induced by this elicitor seems to be programmed by the establishment of a reactive physiological state, which produces the defense response.


1997 ◽  
Vol 75 (9) ◽  
pp. 1509-1517 ◽  
Author(s):  
K. Enkerli ◽  
C. W. Mims ◽  
M. G. Hahn

Immunolabeling and transmission electron microscopic techniques were used to investigate the chemical nature of wall appositions in roots of susceptible and resistant soybean plants inoculated with Phytophthora sojae race 2. The extrahaustorial matrix associated with the haustorium of Phytophthora sojae also was examined. Antibodies against (1 → 3)-β-glucan, a terminal α-fucosyl-containing epitope present in xyloglucan and rhamnogalacturonan I, and an arabinosylated (1 → 6)-β-galactan epitope present in arabinogalactan proteins were used. (1 → 3)-β-Glucan (callose), xyloglucan, and arabinogalactan proteins were found to be localized in all wall appositions regardless of how long after inoculation the appositions developed or whether plants were susceptible or resistant to Phytophthora sojae. (1 → 3)-β-Glucan also was found in fungal walls and at host cell plasmodesmata. None of the four antibodies labeled the extrahaustorial matrix. The antibody against arabinogalactan protein recognized the host plasma membrane, but not the invaginated host plasma membrane associated with the extrahaustorial matrix. This result indicates that the properties or the composition of the host plasma membrane may change locally once it becomes an extrahaustorial membrane. Key words: Phytophthora sojae, Glycine max, callose, immunolabeling, wall appositions, papillae.


1987 ◽  
Vol 65 (8) ◽  
pp. 1586-1598 ◽  
Author(s):  
L. Shain ◽  
U. Järlfors

The infection process in four clones of eastern cottonwood susceptible or resistant to leaf rust caused by Melampsora medusae was studied by light and electron microscopy. Infection was initiated by stomatal rather than direct entry. Typical dikaryotic haustoria were observed in all clones within 1 day of inoculation. Some healthy-appearing haustoria were observed in susceptible clones throughout the duration of the study, which was terminated during the initiation of uredial production. Incompatibility was expressed differently in the two resistant clones. In clone St 75, most haustoria and invaded host cells that were observed appeared necrotic within 2 days of inoculation. Cell wall appositions appeared during this time in cells adjoining necrotic host cells. Some infected cells disintegrated within 4 days of inoculation. Affected host cells of clone St 92, on the other hand, plasmolyzed during the first 2 to 3 days after inoculation. Necrotic host cells were not observed in this clone until the 4th day after inoculation. Hyphal ramification and host plasmolysis were extensive at 6 days after inoculation.


2015 ◽  
Vol 38 (5) ◽  
Author(s):  
S. V. Pawar ◽  
G. D. Deshpande ◽  
Utpal Dey

A study was conducted at Badnapur in the district of Jalna on the behavior of two hundred and forty-eight pigeonpea germplasm lines representing different levels of resistance to pigeonpea wilt disease. Out of 248 germplasm lines Resistant (R), Moderately Resistant (MR), Moderately Susceptible (MS), Susceptible (S), Highly Susceptible (HS) and Very Highly Susceptible (VHS) reaction was given by 2, 8, 10, 25, 131 and 72 entries, respectively. Germplasm lines GL<sub>4</sub> (7088) and GL<sub>90</sub> (ICP-8863) expressed significantly highest resistance over the rest of germplasm lines tested. All the intraplot sickness checks at all sites from SCS<sub>1</sub> to SCS<sub>50</sub> responded with significantly highest wilt (%) and were at par indicating uniform inoculum load throughout the sick plot. In testing stability of resistance in donor lines, it was revealed that 9 donors responded with significantly least wilt (%) having consistent Resistant “R” reaction thereby indicating their stability as resistance donors.


2005 ◽  
Vol 95 (5) ◽  
pp. 528-532 ◽  
Author(s):  
Aloysius Ebelechukwu Ibeagha ◽  
Ralph Hückelhoven ◽  
Patrick Schäfer ◽  
Devendra Pal Singh ◽  
Karl-Heinz Kogel

We investigated the interaction of several differentially resistant wheatwith the hemibiotrophic phytopathogenic fungus Bipolaris sorokiniana (teleomorph Cochliobolus sativus). Wheat genotypes Yangmai, M 3 (W7976), Shanghai 4, and Chirya 7 showed higher levels of resistancewith cv. Sonalika, used as a susceptible control. In amicroscopic inspection, we found that fungal penetration intoepidermal layer failed mostly through a cell wall-associated defense. In cases where the fungus successfully overcame epidermal, its spread within the mesophyll tissue (necrotrophic phase) wasin the more resistant genotypes. Epidermal cell wall-associated, spreading as well as the extent of electrolyte leakage of infected, correlated well with field resistance. We propose that cellular hostsuch as formation of cell wall appositions as well as the degreeearly mesophyll spreading of fungal hyphae are indicative of thepotential of the respective host genotype and, therefore, could befor the characterization of new spot blotch resistance traits in cereals.


1978 ◽  
Vol 56 (17) ◽  
pp. 2097-2108 ◽  
Author(s):  
Verna J. Higgins ◽  
G. L. Lazarovits

As part of a continuing study of non-host resistance, red clover leaves inoculated with the clover pathogen Stemphylium sarcinaeforme, or the closely related alfalfa pathogen S. botryosum, were examined by light and electron microscopy to compare the events occurring in the initial stages of infection. Stemphylium botryosum penetrated leaves primarily via the stomata with resultant death of the guard cells and with varying effects on adjacent epidermal cells. Appressoria were frequently formed, and although they rarely resulted in successful penetrations, the contacted epidermal cells were often markedly affected as judged by toluidine blue staining. Growth of hyphae was intercellular but very limited in its extent. At some infection sites, one to several mesophyll cells underwent extensive plasmolysis and cytoplasmic disruption. Less severely affected mesophyll cells contained large lipid bodies, abundant rough endoplasmic reticulum, and Golgi vesicles and had wall appositions at points of contact with necrotic cells or with hyphae. Stemphylium sarcinaeforme generally penetrated between or directly through the epidermal cells, causing death of the contacted cells. Hyphae grew intercellularly or intracellularly in the palisade tissue and hyphal elongation was considerably more rapid than that of S. botryosum. Palisade cells adjacent to, or containing, the hyphae underwent several different types of cytoplasmic deterioration. Mesophyll cells surrounding these areas showed the same features as comparable cells in tissue infected by S. botryosum. In tissue infected by either fungus, the exterior of host cell walls was coated with a layer of extracellular material.


2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Congshan Yang ◽  
Chenrong Wang ◽  
Jing Liu ◽  
Qun Liu

Abstract Background Neospora caninum is an obligate intracellular parasite that invades host cells and replicates within the parasitophorous vacuole (PV), which resists fusion with host cell lysosomal compartments. To modify the PV, the parasite secretes an array of proteins, including dense granule proteins (GRAs). The vital role of GRAs in the Neospora life cycle cannot be overestimated. Despite this important role, only a subset of these proteins have been identified, and most of their functions have not been elucidated. Our previous study demonstrated that NcGRA17 is specifically targeted to the delimiting membrane of the parasitophorous vacuole membrane (PVM). In this study, we utilize proximity-dependent biotin identification (BioID) to identify novel components of the dense granules. Methods NcGRA17 was BirA* epitope-tagged in the Nc1 strain utilizing the CRISPR/Cas9 system to create a fusion of NcGRA17 with the biotin ligase BirA*. The biotinylated proteins were affinity-purified for mass spectrometric analysis, and the candidate GRA proteins from BioID data set were identified by gene tagging. To verify the biological role of novel identified GRA proteins, we constructed the NcGRA23 and NcGRA11 (a–e) knockout strains using the CRISPR/Cas9 system and analyzed the phenotypes of these mutants. Results Using NcGRA17-BirA* fusion protein as bait, we have identified some known GRAs and verified localization of 11 novel GRA proteins by gene endogenous tagging or overexpression in the Nc1 strain. We proceeded to functionally characterize NcGRA23 and NcGRA11 (a–e) by gene knockout. The lack of NcGRA23 or NcGRA11 (a–e) did not affect the parasite propagation in vitro and virulence in vivo. Conclusions In summary, our findings reveal that BioID is effective in discovering novel constituents of N. caninum dense granules. The exact biological functions of the novel GRA proteins are yet unknown, but this could be explored in future studies. Graphical abstract


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