Ectomycorrhizal and ectendomycorrhizal associations of Phialophorafinlandia with Pinusresinosa, Picearubens, and Betulaalleghaniensis

1987 ◽  
Vol 17 (8) ◽  
pp. 976-990 ◽  
Author(s):  
H. E. Wilcox ◽  
C. J. K. Wang
Keyword(s):  
Large Diameter ◽  
Root Surface ◽  
Epidermal Cells ◽  
Cortical Cells ◽  
Hartig Net ◽  
Mycorrhizal Associations ◽  
Intracellular Invasion ◽  
Inner Cortex ◽  
Root Axis ◽  
Distributed Clusters

Mycorrhizal associations formed by Phialophorafinlandia in Pinusresinosa were both ectomycorrhizal and ectendomycorrhizal with randomly distributed clusters of spherical hyphae within cells of the cortex. The ectomycorrhizal condition was common for short distances in the apices of short roots and in smaller diameter long roots, but intracellular invasion from the Hartig net occurred proximal to this zone, resulting in an ectendomycorrhizal structure. In large diameter long-root branches both conditions were found at different positions along the root axis. In addition, sclerotia-like inclusions occurred in the inner cortical cells, often radially opposite to the protoxylem. Mycorrhizal associations in Picearubens and Betulaalleghaniensis were predominantly ectomycorrhizal in all roots; sclerotial bodies could be present in the inner cortex of both hosts. The Hartig net extended to the endodermis in the spruce, but it surrounded only the epidermis in birch. The epidermal cells of birch ectendomycorrhizae elongated radially and obliquely to the root surface, but in spruce the mycorrhizal condition had no effect on radial dimensions of cortical cells.

Structure and ontogeny of Betula alleghaniensis – Pisolithus tinctorius ectomycorrhizae

1990 ◽  
Vol 68 (3) ◽  
pp. 579-593 ◽  
Author(s):  
H. B. Massicotte ◽  
R. L. Peterson ◽  
C. A. Ackerley ◽  
L. H. Melville
Keyword(s):  
Root Hairs ◽  
Root Surface ◽  
Pisolithus Tinctorius ◽  
Initial Contact ◽  
Broad Host Range ◽  
Betula Alleghaniensis ◽  
Cortical Cells ◽  
Structural Modifications ◽  
Hartig Net ◽  
Primary Roots

The ontogeny and ultrastructure of ectomycorrhizae synthesized between Betula alleghaniensis (yellow birch) and Pisolithus tinctorius, a broad host range fungus, were studied to determine the structural modifications in both symbionts during ectomycorrhiza establishment. A number of stages, including initial contact of hyphae with the root surface, early mantle formation, and mature mantle formation, were distinguished. Interactions between hyphae and root hairs were frequent. As a paraepidermal Hartig net developed, root epidermal cells elongated in a radial direction, but wall ingrowths were not formed. Repeated branching of Hartig net hyphae resulted in extensive fine branches and the compartmentalization of hyphal cytoplasm. Nuclei and elongated mitochondria were frequently located in the narrow cytoplasmic compartments, and [Formula: see text] thickenings developed along walls of cortical cells in primary roots.

scholarly journals Seed-transmitted beneficial endophytic Stagonospora sp. can penetrate the walls of the root epidermis, but does not proliferate in the cortex, of Phragmites australis

2006 ◽  
Vol 84 (6) ◽  
pp. 981-988 ◽  
Author(s):  
Kexiang Gao ◽  
Kurt Mendgen
Keyword(s):  
Phragmites Australis ◽  
Endophytic Fungus ◽  
Hyphal Growth ◽  
Root Surface ◽  
Cortical Layer ◽  
Epidermal Cells ◽  
Cortical Cells ◽  
Root Epidermis ◽  
Wall Appositions

Stagonospora sp. (4/99-1) is a beneficial endophytic fungus frequently transmitted by seeds of Phragmites australis [Cav.] Trin. ex Steudel. Here we show that this fungus also penetrates the root epidermis. At first, hyphae were attracted by the root and proliferated on the root surface, preferably over the anticlinal walls. Penetration occurred directly by undifferentiated hyphae or was facilitated by hyphopodia. Hyphal growth within the root was restricted to the walls of epidermal cells and the walls of the cells of the outermost cortical layer. Deeper growth by the fungus elicited wall appositions and ingress into the cytoplasm of cortical cells was blocked by papillae. In the rare cases, the fungus managed to penetrate into cortical cells, these reacted with necrosis. Immunological studies suggested that fungal material reached the host plasmalemma and may have been taken up by endocytotic events. Our observations explain the endophytic lifestyle of hyphae close to the epidermis and the restricted development within the cortex.

Structure and ontogeny of Alnus crispa – Alpova diplophloeus ectomycorrhizae

1986 ◽  
Vol 64 (1) ◽  
pp. 177-192 ◽  
Author(s):  
H. B. Massicotte ◽  
R. L. Peterson ◽  
C. A. Ackerley ◽  
Y. Piché
Keyword(s):  
Structural Changes ◽  
Hyphal Growth ◽  
Root Surface ◽  
Epidermal Cells ◽  
Transfer Cells ◽  
Wall Ingrowths ◽  
Alnus Crispa ◽  
Hartig Net ◽  
Fungal Hyphae ◽  
Branching System

Alnus crispa (Ait.) Pursh seedlings were grown in plastic pouches and inoculated with Frankia to induce nodules and subsequently with Alpova diplophloeus (Zeller & Dodge) Trappe & Smith to form ectomycorrhizae. The earliest events in ectomycorrhiza formation involved contact of the root surface by hyphae, hyphal proliferation to form a thin mantle, and further hyphal growth to form a thick mantle. Structural changes in the host, the mycosymbiont, and the fungus–epidermis interface were described at various stages in the ontogeny of ectomycorrhizae. Fungal hyphae in contact with epidermal cells in the regions of intercellular penetration and paraepidermal Hartig net developed numerous rough endoplastic reticulum cisternae. In more proximal regions of the mycorrhiza, these gradually became fewer in number and smooth. A complicated labyrinthine wall branching system also developed in the fungus in these regions. Concurrently, epidermal cells formed wall ingrowths in regions adjacent to Hartig net hyphae. There was a gradient in the formation of these epidermal transfer cells as the mycorrhiza developed, and an additional deposition of secondary cell wall over the wall ingrowths occurred as transfer cells senesced. Nonmycorrhizal control roots did not develop epidermal wall ingrowths. Electron-dense material, which was also autofluorescent, was deposited in the outer tangential walls of the exodermis contiguous to the paraepidermal Hartig net.

In vitro mycorrhization of Casuarina and Allocasuarina species by Pisolithus isolates

1990 ◽  
Vol 68 (12) ◽  
pp. 2537-2542 ◽  
Author(s):  
Daniel Thoen ◽  
Bassirou Sougoufara ◽  
Yvon Dommergues
Keyword(s):  
Epidermal Cells ◽  
Casuarina Equisetifolia ◽  
Cortical Cells ◽  
Fungal Isolates ◽  
Hartig Net ◽  
Casuarina Cunninghamiana

Five Casuarina species and five Allocasuarina species were inoculated in vitro with three isolates of Pisolithus sp. (Ors.X004 and Ors.7870 from Senegal, PR86 from Australia) to test their ability to form ectomycorrhizas. The mycorrhiza-forming ability varied between fungal isolates. The greatest differences occurred between Casuarina and Allocasuarina species. On Casuarina species, Pisolithus isolates formed only a fungal sheath. However, Ors.X004 induced well-developed ectomycorrhizas on Casuarina equisetifolia, whereas PR86 failed to form any fungal sheath on Casuarina cunninghamiana. On Allocasuarina species, Pisolithus isolates formed generally well-developed ectomycorrhizas. In addition, isolates Ors.7870 and PR86 invaded the cortical cells of Allocasuarina luehmannii and Allocasuarina decaisneana, respectively, thus forming ectendomycorrhizas. Epidermal cells of both Casuarina and Allocasuarina mycorrhizas showed tannin deposits. In fully developed ectomycorrhizas, the epidermal cells were radially elongated and the Hartig net never developed beyond the epidermal cells. In general, the ability to form ectomycorrhizas was more common with the genus Allocasuarina than the genus Casuarina.Key words: Casuarina, Allocasuarina, Pisolithus, ectomycorrhizas.

Characterization of the interaction between the dark septate fungus Phialocephala fortinii and Asparagus officinalis roots

2001 ◽  
Vol 47 (8) ◽  
pp. 741-753 ◽  
Author(s):  
T Yu ◽  
A Nassuth ◽  
R L Peterson
Keyword(s):  
Root Hairs ◽  
Root Surface ◽  
Epidermal Cells ◽  
Asparagus Officinalis ◽  
Structural Basis ◽  
Root Penetration ◽  
Root Tips ◽  
Cortical Cells ◽  
Phialocephala Fortinii

Phialocephala fortinii Wang & Wilcox is a member of root-inhabiting fungi known collectively as dark septate endophytes (DSE). Although very common and distributed worldwide, few studies have documented their interaction with roots on a structural basis. The objective of this study was to determine the early colonization events and formation of microsclerotia of P. fortinii in roots of Asparagus officinalis L., a species known to have DSE. A loose network of hyphae accumulated at the root surface, and coils formed around root hairs and external to epidermal cells overlying short cells of the dimorphic, suberized exodermis. Root penetration occurred via swollen, appressorium-like structures into epidermal cells where coiling of hyphae occurred along the periphery of the cells. Hyphae penetrated from the epidermis into short exodermal cells and from these into cortical cells. Hyphae colonized the cortex up to the endodermis and sometimes entered the vascular cylinder. Some root tips were colonized as well. Microsclerotia in epidermal and exodermal short cells accumulated glycogen, protein, and polyphosphate. Energy-dispersive X-ray spectroscopy on distinct bodies visible in microsclerotial hyphae revealed high levels of phosphorus.Key words: Mycelium radicis atrovirens, Phialocephala fortinii, microsclerotia, DSE.

Structure and development of Pinus banksiana – Wilcoxina ectendomycorrhizae

1991 ◽  
Vol 69 (10) ◽  
pp. 2135-2148 ◽  
Author(s):  
Pamela F. Scales ◽  
R. L. Peterson
Keyword(s):  
Electron Microscopy ◽  
Pinus Banksiana ◽  
Cortical Cell ◽  
Root Surface ◽  
Cell Plasma Membrane ◽  
Cortical Cells ◽  
Hartig Net ◽  
Transmission Electron ◽  
Cell Plasma ◽  
Wilcoxina Mikolae

Seedlings of Pinus banksiana were grown in growth pouches and inoculated with Wilcoxina mikolae var. mikolae, Wilcoxina mikolae var. tetraspora, and Wilcoxina rehmii. Ectendomycorrhizae formed between P. banksiana and W. mikolae var. mikolae developed rapidly following inoculation. The mantle was of variable width, and a large amount of mucigel was evident on the root surface. Intracellular penetration of the cortical cells by hyphae occurred one to two cells distal to Hartig net formation. Both light and transmission electron microscopy revealed labyrinthic growth of Hartig net hyphae that were densely cytoplasmic during early penetration stages but became vacuolate as the association aged. Intracellular colonization of the cortex was extensive, with the hyphae highly branched and surrounded by an interfacial matrix and cortical cell plasma membrane. The external morphology and anatomy of ectendomycorrhizae formed between W. mikolae var. tetraspora and W. rehmii and P. banksiana were similar to those described for W. mikolae var. mikolae. Key words: ectendomycorrhizae, Wilcoxina, Pinus banksiana, intracellular, Hartig net, E-strain.

Phylogenetic relationships among Halymenia (Halymeniaceae, Rhodophyta) species on the Brazilian coast with description of Halymenia cearensis sp. nov.

Phytotaxa ◽  
2016 ◽  
Vol 280 (3) ◽  
pp. 241 ◽  
Author(s):  
CAROLINA ANGÉLICA ARAÚJO DE AZEVEDO ◽  
VALÉRIA CASSANO ◽  
MARIANA CABRAL OLIVEIRA
Keyword(s):  
Species Diversity ◽  
Phylogenetic Relationships ◽  
Brazilian Coast ◽  
Molecular Tools ◽  
Ecological Data ◽  
Cortical Cells ◽  
Broad Base ◽  
Molecular Studies ◽  
Marine Flora ◽  
Inner Cortex

Phylogenetic relationships and species diversity within the genus Halymenia along the Brazilian coast were investigated through molecular and morphological analyses. Molecular studies included UPA, COI-5P and rbcL markers. A total of five Halymenia species were found: Halymenia cearensis sp. nov., H. ignifera, H. pinnatifida, H. silviae and H. cf. mirabilis. Halymenia cearensis was molecularly distinct from all other Halymenia species included in this study and is morphologically characterized by: cleft, lobate, oblong or obovate blades with broad base; apex irregular in shape; surface with bullations, rugosities, spiny and globular papillae irregularly distributed; abundant and conspicuous ganglionic cells throughout; blades up to 800 µm thick at base; outer cortical cells ellipsoidal or ovoid in shape, higher than broad; and inner cortex cells 4–25 µm in width. Our phylogeny demonstrated that entities attributed to H. floridana and H. elongata occurring in Brazil correspond to two distinct genera, which was also supported by morphological and ecological data. The use of molecular tools was crucial to provide a better understanding of the diversity of Brazilian marine flora.

Refining the Life Cycle of Plasmodiophora brassicae

2020 ◽  
Vol 110 (10) ◽  
pp. 1704-1712 ◽  
Author(s):  
Lijiang Liu ◽  
Li Qin ◽  
Zhuqing Zhou ◽  
Wilhelmina G. H. M. Hendriks ◽  
Shengyi Liu ◽  
...  
Keyword(s):  
Life Cycle ◽  
Plasmodiophora Brassicae ◽  
Secondary Infection ◽  
Life Stage ◽  
Infection Process ◽  
Epidermal Cells ◽  
Sexual Life ◽  
Cortical Cells ◽  
Susceptible Host ◽  
Clubroot Disease

As a soilborne protist pathogen, Plasmodiophora brassicae causes the devastating clubroot disease on Brassicaceae crops worldwide. Due to its intracellular obligate biotrophic nature, the life cycle of P. brassicae is still not fully understood. Here, we used fluorescent probe-based confocal microscopy and transmission electron microscopy (TEM) to investigate the infection process of P. brassicae on the susceptible host Arabidopsis under controlled conditions. We found that P. brassicae can initiate the primary infection in both root hairs and epidermal cells, producing the uninucleate primary plasmodium at 1 day postinoculation (dpi). After that, the developed multinucleate primary plasmodium underwent condensing and cytoplasm cleavage into uninucleate zoosporangia from 1 to 4 dpi. This was subsequently followed by the formation of multinucleate zoosporangia and the production of secondary zoospores within zoosporangium. Importantly, the secondary zoospores performed a conjugation in the root epidermal cells after their release. TEM revealed extensive uninucleate secondary plasmodium in cortical cells at 8 dpi, indicating the establishment of the secondary infection. The P. brassicae subsequently developed into binucleate, quadrinucleate, and multinucleate secondary plasmodia from 10 to 15 dpi, during which the clubroot symptoms appeared. The uninucleate resting spores were first observed in the cortical cells at 24 dpi, marking the completion of a life cycle. We also provided evidence that the secondary infection of P. brassicae may represent the diploid sexual life stage. From these findings, we propose a refined life cycle of P. brassicae which will contribute to understanding of the complicated infection biology of P. brassicae.

Differences in the colonization of Pinus banksiana roots by sib-monokaryotic and dikaryotic strains of ectomycorrhizal Laccaria bicolor

1989 ◽  
Vol 67 (6) ◽  
pp. 1717-1726 ◽  
Author(s):  
Ken K. Y. Wong ◽  
Yves Piché ◽  
Diane Montpetit ◽  
Bradley R. Kropp
Keyword(s):  
Pinus Banksiana ◽  
Intraspecific Variability ◽  
Root Cell ◽  
Laccaria Bicolor ◽  
Cortical Cells ◽  
Aseptic Culture ◽  
Hartig Net ◽  
Cell Layers ◽  
The Mean ◽  
Root Surfaces

First-order laterals of Pinus banksiana seedlings were inoculated with variant strains of ectomycorrhizal Laccaria bicolor in an aseptic culture system. Macroscopic observations of 10 fungal strains indicated that 6 are mycorrhizal and 4 are apparently nonmycorrhizal. Furthermore, light microscopic examinations revealed significant intraspecific variation in mycorrhizal structures. The mean mantle thickness, mean mantle density, and mean Hartig net penetration of the six mycorrhizal strains ranged from 2.5 to 13.4 hyphae, 278 to 411 hyphae/mm and 2 to 2.8 root cell layers, respectively. Three of these strains formed fewer macroscopically observable mycorrhizae and developed significantly thinner mantles but their Hartig nets usually separated cortical cells more extensively. Three of the four apparently nonmycorrhizal strains showed infrequent and poor Hartig net development (mean penetration of 0.3 to 0.8 root cell layer), poor surface colonization, and no mantle development. These three strains were better able to colonize long roots. Only one strain could be considered truly nonmycorrhizal because it only colonized root surfaces poorly and never showed mantle or Hartig net formation. The observed intraspecific variability raises questions concerning the determinants of mycorrhiza development and structure.

scholarly journals Effect of Temperature on and Histopathology of the Interaction Between Meloidogyne incognita and Thielaviopsis basicola on Cotton

1999 ◽  
Vol 89 (8) ◽  
pp. 613-617 ◽  
Author(s):  
N. R. Walker ◽  
T. L. Kirkpatrick ◽  
C. S. Rothrock
Keyword(s):  
Meloidogyne Incognita ◽  
Vascular Tissue ◽  
Root Surface ◽  
Effect Of Temperature ◽  
Infested Soil ◽  
Thielaviopsis Basicola ◽  
Root Knot Nematode ◽  
Cortical Cells ◽  
Node Ratio ◽  
Cotton Seeds

Controlled environments were used to study the relationship between the root-knot nematode (Meloidogyne incognita) and Thielaviopsis basicola on cotton. Temperature treatments were continuous 20, 24, and 28°C or two cyclic linear regimes with ranges of 14 to 32 or 18 to 28°C over 24 h. Cotton seeds were planted in fumigated soil infested with T. basicola, M. incognita, or both. After 42 days, pathogen effects on plant growth and pathogen development were evaluated. Histology was conducted on roots collected 14, 28, and 42 days after planting in the continuous 24°C treatment. Reductions in plant height-to-node ratio and total fresh weight were observed for soils infested with both pathogens compared with the control or with soils infested with either pathogen, except for M. incognita-infested soil at 28°C. T. basicola reduced root galling and reproduction of the nematode at all temperatures. Vascular discoloration caused by T. basicola was greater in the presence of M. incognita compared with that by T. basicola alone. At 2 and 4 weeks, histological studies showed that plants grown in all T. basicola-infested soils contained chlamydospore chains on the root surface and in cortical cells. The fungus was not observed inside the vascular cylinder. Roots from 4-week-old plants from soils infested with T. basicola and M. incognita showed fungal sporulation in vascular tissue and localized necrosis of vascular tissue adjacent to the nematodes. At 6 weeks, plants grown in soil infested with T. basicola alone exhibited no remaining cortical tissue and no evidence of vascular colonization by the fungus. Six-week-old plants grown in T. basicola + M. incognita-infested soils exhibited extensive vascular necrosis and sporulation within vascular tissue. These studies suggest that coinfection expands the temperature ranges at which the pathogens are able to cause plant damage. Further, M. incognita greatly increases the access of T. basicola to vascular tissue.

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