Light and electron microscopy of the interaction between the sunflower rust fungus (Puccinia helianthi) and leaves of the nonhost plant, French bean (Phaseolus vulgaris)

1986 ◽  
Vol 64 (11) ◽  
pp. 2476-2486 ◽  
Author(s):  
Lesley A. Wood ◽  
Michèle C. Heath

Growth of the sunflower rust fungus (Puccinia helianthi Schw.) was compared by light microscopy in sunflower leaves, in untreated French bean leaves, in bean leaves given a preinoculation heat treatment, and on collodion membranes. Results suggested that fungal growth was slightly reduced and the formation of haustorial mother cells was inhibited in untreated bean leaves. Haustorial mother cells, when present, did not form haustoria and adjacent mesophyll cell walls usually were highly refractive. Preinoculation heat treatment reduced the incidence of refractive cell walls and increased that of haustorial mother cells and haustoria. Ultrastructurally, infection hyphae in unheated bean leaves appeared unusually vacuolate and often contained wall appositions where they touched the plant cells. Silicalike deposits were present in and on mesophyll cell walls at most infection sites. In heated plants, necrotic haustoria with small bodies were seen at the few sites that lacked silicalike deposits. At other sites, the fungus appeared to have stopped growing during the formation of the penetration peg or the haustorial neck, and such necks were encrusted with silicalike material. At most sites, penetration pegs were occluded resulting in the unusual situation in which the haustorial mother cell remained seemingly alive in spite of the necrosis of the haustorium.

1991 ◽  
Vol 69 (8) ◽  
pp. 1642-1646 ◽  
Author(s):  
Myriam R. Fernandez ◽  
Michèle C. Heath

Bean leaves inoculated 24 h previously with the bean rust fungus were inoculated with spores of Cochliobolus heterostrophus, Stemphylium sarcinaeforme, Stemphylium botryosum, or Cladosporium fulvum. For all species except C. fulvum, hyphal growth resulting from stomatal penetrations was greater than that in leaves that were not rust-infected but did not continue for more than about 24 h. The incidence of direct penetrations for these three fungi also was increased by prior rust infection, and the incidence of epidermal wall appositions was reduced. Growth of C. fulvum in rust-infected leaves only exceeded that in control leaves when spores were injected into the intercellular spaces of the mesophyll tissue. Rust infection either had little effect on the incidence of cell death, normally induced by all of the tested fungi except C. fulvum, or it enhanced this response in association with greater fungal growth. From this and previous studies, it seems that successful rust infection increases the growth of a wider array of fungi nonparasitic to beans than treatments with growth regulators or intercellular washing fluids from rusted tissue. Its effect is most closely mimicked by preinoculation treatments with heat or protein synthesis inhibitors, but it does not induce indiscriminate susceptibility. Its effect may, in part, be due to the suppression of defenses involving wall modifications. Key words: Uromyces appendiculatus, induced susceptibility, nonhost resistance.


1991 ◽  
Vol 69 (6) ◽  
pp. 1199-1206 ◽  
Author(s):  
C. Y. Chen ◽  
Michele C. Heath

The cytological responses to the monokaryotic primary hyphae of the cowpea rust fungus (Uromyces vignae Barcl.) were observed in vein epidermal cells of a resistant and a susceptible cowpea cultivar. Unlike the previously examined response to haustoria of a nonpathogenic powdery mildew fungus, plant cell walls did not become autofluorescent in response to fungal penetration, and the primary hypha only rarely became encased. Following fungal penetration, the response of invaded cells of the resistant, intact plant could be divided into the following stages: (I) cytoplasmic streaming normal; (II) cytoplasmic streaming slow or stopped, Brownian motion of particles visible in the vacuole, granulated cytoplasm aggregated along the cell walls, some host nuclei disappeared; and (III) protoplast collapsed. Epidermal tissue of the resistant cultivar did not exhibit stages II–III when detached and mounted in water 12 h after inoculation and examined 9 h later. The frequency of stage III increased when the tissue was mounted in CaCl2, Ca(NO3)2, and KNO3, but only in a kinetin solution did it approximate that in attached tissue. Although kinetin inhibited fungal growth in both the resistant and the susceptible cultivar, the hypersensitive response occurred only in the former, suggesting that kinetin affects the hypersensitive response directly rather than through its inhibitory effect on the fungus. Key words: cowpea, Vigna unguiculata, cowpea rust fungus, Uromyces vignae (Barcl.), hypersensitivity.


1989 ◽  
Vol 67 (3) ◽  
pp. 661-669 ◽  
Author(s):  
Myriam R. Fernandez ◽  
Michèle C. Heath

Germination, penetration, and subsequent growth of four saprophytic and five parasitic fungi nonpathogenic on French bean (Phaseolus vulgaris L. cv. Pinto) were examined on, or in, killed, untreated, and heat-treated or blasticidin S treated leaves in the presence (saprophytes only) or absence of additional nutrients. The saprophytes required either an external supply of nutrients or a diffusate from autoclaved leaves to germinate, and they subsequently did not attempt to penetrate untreated or heat-treated living leaves. In contrast, the parasites germinated well, and penetrated untreated tissue almost exclusively through stomata. For some parasites, preinoculation heat treatment increased the incidence of direct penetration and the degree of fungal growth in the tissue. The saprophytes and nonbiotrophic parasites all penetrated and grew well in leaves that had been killed by autoclaving or freezing. The data suggest that living, intact bean leaves are resistant to the fungal saprophytes tested because these fungi lack pathogenicity factors necessary for germination on, and penetration of, the leaf. Resistance to the parasites, in contrast, appears to reside in heat-sensitive and heat- or blasticidin S insensitive defenses in the leaf that may differ with the fungus.


1985 ◽  
Vol 63 (10) ◽  
pp. 1713-1724 ◽  
Author(s):  
J. Chong ◽  
D. E. Harder ◽  
R. Rohringer

Walls of intercellular hyphae and haustorium mother cells of the stem rust fungus in wheat leaves were studied cytochemically using lectin probes, periodate – thiocarbohydrazide – silver proteinate or periodate–chromate–phosphotungstate staining, and protease treatment. Up to six possible layers in the haustorium mother cell walls and four in the hyphal walls were resolved. Three outer layers of the haustorium mother cell walls were continuous with the three outer layers of the hyphal walls. The two innermost layers of the haustorium mother cell walls were not continuous with the hyphal walls but formed part of the septum. These two layers differed from the other layers of the haustorium mother cell walls in having no affinity to concanavalin A. In both hyphal and haustorium mother cell walls, components with an affinity for concanavalin A were extractable with protease treatment. Wheat-germ lectin binding occurred throughout the fungal walls except in the two outermost layers. Periodate-sensitive glycosubstances were also common, but the amounts varied among layers. Although some of these glycosubstances were confirmed as polysaccharides containing sugars with vicinal hydroxyl groups, much of the glycosubstances present in the walls was sensitive to protease treatment, indicating a possible glycoprotein composition.


1972 ◽  
Vol 128 (2) ◽  
pp. 229-235 ◽  
Author(s):  
D. C. Shaw ◽  
J. R. E. Wells

Phaseolain, a carboxypeptidase from French-bean leaves, and a partially purified peptidase from baker's yeast are inhibited by reaction with di-isopropyl phosphorofluoridate. Radioactive di-isopropyl [32P]phosphorofluoridate was used to show that the site of reaction is a unique serine residue and that the sequence of amino acids adjacent to the reactive serine is Glu-Ser-Tyr. This sequence is different from those of other ‘serine’ enzymes previously reported and, for phaseolain, represents an unequivocal example of a ‘serine’ carboxypeptidase.


2013 ◽  
Vol 24 (23) ◽  
pp. 3697-3709 ◽  
Author(s):  
Lihong Li ◽  
Shawna Miles ◽  
Zephan Melville ◽  
Amalthiya Prasad ◽  
Graham Bradley ◽  
...  

Yeast that naturally exhaust the glucose from their environment differentiate into three distinct cell types distinguishable by flow cytometry. Among these is a quiescent (Q) population, which is so named because of its uniform but readily reversed G1 arrest, its fortified cell walls, heat tolerance, and longevity. Daughter cells predominate in Q-cell populations and are the longest lived. The events that differentiate Q cells from nonquiescent (nonQ) cells are initiated within hours of the diauxic shift, when cells have scavenged all the glucose from the media. These include highly asymmetric cell divisions, which give rise to very small daughter cells. These daughters modify their cell walls by Sed1- and Ecm33-dependent and dithiothreitol-sensitive mechanisms that enhance Q-cell thermotolerance. Ssd1 speeds Q-cell wall assembly and enables mother cells to enter this state. Ssd1 and the related mRNA-binding protein Mpt5 play critical overlapping roles in Q-cell formation and longevity. These proteins deliver mRNAs to P-bodies, and at least one P-body component, Lsm1, also plays a unique role in Q-cell longevity. Cells lacking Lsm1 and Ssd1 or Mpt5 lose viability under these conditions and fail to enter the quiescent state. We conclude that posttranscriptional regulation of mRNAs plays a crucial role in the transition in and out of quiescence.


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