Ultrastructural studies on infection of sclerotia of Sclerotinia sclerotiorum by Talaromyces flavus

1989 ◽  
Vol 67 (7) ◽  
pp. 2199-2205 ◽  
Author(s):  
D. L. McLaren ◽  
H. C. Huang ◽  
S. R. Rimmer ◽  
E. G. Kokko

Talaromyces flavus is a destructive hyperparasite capable of infecting sclerotia of Sclerotinia sclerotiorum. Examinations of sclerotia by transmission electron microscopy at 3, 7, and 12 days after inoculation revealed that hyphae of T. flavus penetrated the rind cell walls directly. Etching of the cell walls at the penetration site was evident. This suggests that wall-lysing enzymes may be involved in the process of infection. Hyphae of T. flavus grew both intercellularly and intracellularly throughout the rind, cortical, and medullary tissues. Ramification of the hyperparasite in the sclerotium resulted in destruction and collapse of sclerotial tissues.

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.


1989 ◽  
Vol 67 (2) ◽  
pp. 394-406 ◽  
Author(s):  
Linda M. Kohn ◽  
Douglas J. Grenville

As part of comparative anatomical, histochemical, and ultrastructural studies of stromata in the Sclerotiniaceae, mature stromata produced in vitro by 11 species representing six genera and one form-genus were examined using transmission electron microscopy. Sclerotial-stromatal taxa were Sclerotinia sclerotiorum, S. trifoliorum, S. minor, Sclerotium cepivorum, Botrytis cinerea, B. porri, Monilinia fructicola, and Myriosclerotinia borealis. Substratal-stromatal taxa were Sclerotinia homoeo-carpa, Rutstroemia sydowiana, and Lambertella subrenispora. Three types of rind were observed: a living cellular rind, a dead cellular rind, and a stromatal rind. Sclerotial species were distinguished from stromatal species not only by the rind type, but also by the confluent extracellular matrix around cortical and medullary cell walls. Presence of lacunae in this matrix distinguished Sclerotinia spp. and M. borealis from Botrytis spp. and Monilinia fructicola. Rind, cortical, and medullary cells contained abundant storage vacuoles in most taxa. The distribution and proportion of organelles to storage vacuoles differed among taxa. Plugged septal pores with associated Woronin bodies were similar among the taxa where they were observed. Sclerotia of Sclerotium cepivorum, which has no known teleomorph, are ultrastructurally most like sclerotia of Sclerotinia or Botrytis anamorphs of Botryotinia species. Substratal stromata of S. homoeocarpa showed unusually complex cellular organization. Sclerotial stromata of M. fructicola contained unusual storage vacuoles with heterogeneous contents.


HortScience ◽  
1995 ◽  
Vol 30 (1) ◽  
pp. 102-103 ◽  
Author(s):  
Keryl K. Jacobi ◽  
Don Gowanlock

Mature green `Kensington' mango fruit were submerged in hot water at 46C until the fruit center reached 45C and then held for 30 minutes. The fruit were allowed to ripen for 7 to 10 days after the hot water treatment, and then damaged areas of skin and mesocarp tissue were prepared for observation by scanning and transmission electron microscopy. Heating-related injuries included rupturing the patterned cuticle and exocarp and exposing the underlying cells and hollow cavities (which varied in size and shape) randomly distributed within the mesocarp beneath the skin. Starch deposits still were present in the mesocarp parenchyma cells. The cell walls of damaged mesocarp parenchyma cells were convoluted and thickened in places. The injury suggested disruption of enzymes involved in carbohydrate metabolism.


1985 ◽  
Vol 63 (4) ◽  
pp. 757-761 ◽  
Author(s):  
E. Untiedt ◽  
K. Müller

Lyophyllum palustre (Peck) Singer, a basidiomycete (Tricholomataceae) parasitizing Sphagnum, was examined for points of contact between hyphae and Sphagnum cells with the help of light microscopy, scanning electron microscopy, and transmission electron microscopy. Results indicate that the fungus attacks Sphagnum cells by penetrating cell walls and altering host cell protosplasm. In addition, the formation of additional partitioning cell walls in attacked living Sphagnum cells was observed.


1995 ◽  
Vol 73 (10) ◽  
pp. 1604-1610 ◽  
Author(s):  
C. Hoffert ◽  
S. Gharibian ◽  
C. Breuil ◽  
D. L. Brown

Polyclonal antibodies were raised against proteinase K and were used to immunolocalize the major extracellular proteinase of the sap-staining fungus Ophiostoma piceae (Münch) H. and P. Sydow. Immunodot blotting showed that the IgG antibodies recognized both enzymes but reacted more strongly with proteinase K than with the O. piceae proteinase. Immunogold labelling and transmission electron microscopy revealed that the O. piceae proteinase was localized in the cell walls of O. piceae grown either in liquid media or wood. Key words: Ophiostoma piceae, proteinase, immunogold labelling, transmission electron microscopy, antibody, proteinase K.


IAWA Journal ◽  
2018 ◽  
Vol 39 (1) ◽  
pp. 37-42
Author(s):  
Adya P. Singh ◽  
Andrew H.H. Wong ◽  
Yoon Soo Kim ◽  
Seung Gon Wi

Naturally durable heartwoods, where available, continue to be used as support structures in environments considered hazardous, particularly in ground contact. However, durability of heartwoods against wood decay microorganisms varies. Therefore, it is important to evaluate heartwood products for their in-service performance in order to maximise benefits derived from this valuable natural resource of limited supply. In the work presented, wood pieces from a kempas (Koompassia malaccensis) utility pole that had been placed in service in an acidic soil in Malaysia, and in time had softened at the ground-line position, were examined by light and transmission electron microscopy to evaluate the cause of deterioration.Light microscopy (LM) provided evidence of extensive attack on fibre cell walls by cavity-producing soft rot fungi. Transmission electron microscopy (TEM) revealed in greater detail the distribution and micromorphologies of cavities as well as their relationships to the fine structure of fibre cell walls, which consisted of a highly electron dense middle lamella, a moderately dense S1 layer and a multilamellar S2 layer with variable densities, reflecting differences in lignin concentration. The resistance of the moderately dense S1 layer to soft rot was a feature of particular interest and is the main focus of the work presented. The resistance appeared to be correlated with high lignification of the outermost region of the S2 wall, interfacing with the S1 layer, an unusual cell wall feature not previously described for normal wood.


Weed Science ◽  
1982 ◽  
Vol 30 (3) ◽  
pp. 243-248 ◽  
Author(s):  
James L. Jordan ◽  
David W. Staniforth ◽  
Catalina M. Jordan

Pennsylvania smartweed (Polygonum pensylvanicum L.) achenes were harvested from plants growing either free from competition or in competition with corn (Zea mays L. ‘Pioneer 3780′) plants. Seeds were dormant when harvested. After 15 weeks of prechilling, 4 and 35% of the seeds germinated from plants with and without corn competition, respectively; after 30 weeks of prechilling, more than 92% of all seeds germinated. Scanning electron microscopy revealed that the carpel walls of achenes from plants with corn competition were porous with many channels. Carpel walls of achenes from plants without corn competition were without pores and channels. Transmission electron microscopy showed more lipid bodies in the embryo epidermal cells of seeds from plants with corn competition. Cell walls of embryos from non-prechilled seeds from plants with corn competition contained lipoidosomes that traversed cell walls. Lipoidosomes did not occur in cells of prechilled seeds.


Parasitology ◽  
2019 ◽  
Vol 146 (6) ◽  
pp. 740-745
Author(s):  
J. P. Dubey

AbstractFour species of Cystoisospora, C. canis, C. ohioensis, C. neorivolta and C. burrowsi are described from feces of dogs. Of these, the oocysts of C. canis are the largest and easily distinguished from the remaining three species. Oocysts of C. ohioensis, C. neorivolta and C. burrowsi are difficult to distinguish because of overlap in their sizes. However, based on endogenous developmental stages, C. ohioensis is distinct from C. neorivolta and C. burrowsi because its endogenous stages are confined to surface epithelium of intestine whereas endogenous stages of C. neorivolta and C. burrowsi are predominantly in the lamina propria. There are uncertainties regarding the endogenous stages of C. neorivolta and C. burrowsi and there is no way now to determine whether C. burrowsi and C. neorivolta are different parasites; therefore, these are referred as C. ohioensis-like organisms. Additionally, mode of division of asexual stages of coccidia of dogs is largely unknown and ultrastructural studies are lacking. In the present study, development of asexual and sexual stages of a C. ohioensis-like organism in a naturally infected dog is described by light microscopy and by transmission electron microscopy. Merozoites divided by endodyogeny/merogony. Meronts were crescent/merozoite-shaped and contained a maximum of eight nuclei. A distinctive feature of merozoites was the presence of many PAS-positive amylopectin granules that were absent or rare in immature microgamonts making it possible to distinguish them.


Sign in / Sign up

Export Citation Format

Share Document