SEPTAL PORES IN THE HETEROBASIDIOMYCETIDAE,PUCCINIA GRAMINIS AND P. RECONDITA

The septal pores in uredial mycelium of Puccinia graminis and P. recondita lack the septal swelling and septal pore cap (dolipore-parenthosome configuration) typically associated with the pores of previously investigated Homobasidiomycetidae and the Tremellales among the Heterobasidiomycetidae. The pores in young hyphae of these two species of Puccinia are characterized by the presence of a cytoplasmic matrix which apparently occludes the pore and acts as a plug, thus preventing the migration of organelles from cell to cell. Large vesicles are typically present at the periphery of the pore matrix and the matrix may be very incompletely bounded by a membrane. Nuclei and other cytoplasmic structures migrate from cell to cell through an opening in the septum lateral to the pore. The available evidence indicates that this peripheral gap in the septum results from a breakdown of a portion of an initially complete septum rather than from incomplete septum formation. In addition to the centripetally formed septa, the hyphae of P. graminis and P. recondita are further compartmentalized by shallow infoldings of the lateral wall and limited unilateral septum formation. There is apparent free passage of cellular material between adjacent compartments.     

FINE STRUCTURE OF ANNELLOPHORES. I. SCOPULARIOPSIS BREVICAULIS AND S. KONINGII

Fine-structure observations of annelloconidium production in filamentous Hyphomycetes are reported for the first time. The difference in conidium morphology between Scopulariopsis brevicaulis and S. koningii was quite distinct. In S. brevicaulis, verrucosities appeared early in conidium ontogeny and formed an integral part of the primary wall layer of mature conidia. In S. koningii, verrucosities were absent. In S. brevicaulis, annellations did not invariably result on conidiophore necks with the production of each conidium in the basipetal sequence, but alternatively could be left on subapical regions of subsequently formed conidia. In S. koningii, annellations were more distinct, and the position of a conidium-delimiting septum was variable. If a septum were formed at a position proximal to previous septa, a portion of the annellophore neck remained attached to the base f the seceding conidium. In both species, a spherical electron-dense body, perhaps analogous to septal pore plugs in vegetative hyphae, plugged the pore between conidia and conidiophores and remained embedded in the base of seceded conidia.     

The central role of septa in the basidiomycete Schizophyllum commune hyphal morphogenesis

The purpose of the present research was to observe in the filamentous basidiomycete Schizophyllum commune, the connection between the nuclear division and polymerization of the contractile actin ring with subsequent formation of septa in living hyphae. The filamentous actin was visualized using Lifeact-mCherry and the nuclei with EGFP tagged histone 2B (H2B). Time-lapse fluorescence microscopy confirmed that in monokaryotic and dikaryotic hyphae, the first signs of the contractile actin ring occur at the site of the nuclear division, in one to two minutes after division. At this stage, the telophase nuclei have moved tens of micrometers from the division site. The actin ring is replaced by the septum in six minutes. The apical cells treated with filamentous actin disrupting drug latrunculin A, had swollen tips but the cells were longer than in control samples due to the absence of the actin rings. The nuclear pairing and association with clamp cell development as well as the clamp cell fusion with the subapical cell was disrupted in latrunculin-treated dikaryotic hyphae, indicating that actin filaments are involved in these processes, also regulated by the A and B mating-type genes. This suggests that the actin cytoskeleton may indirectly be a target for mating-type genes.     

Griseofulvin-induced alterations in site of dividing nuclei and structure of septa in a dikaryon ofSchizophyllum commune

Summary Ultrastructural study of a dikaryon of the basidiomyceteSchizophyllum commune showed that treatment with griseofulvin affected the site of the dividing nuclei and the location and structure of the septa. The microtubules were considered to be the primary target of griseofulvin, since they participate in nuclear division and movement in the hyphae, and their assembly is known to be in other organisms than fungi inhibited by griseofulvin. It is pointed out that dikaryotic hyphae with two nuclei and a clamp connection per cell are more sensitive indicators of the effect of griseofulvin than homokaryotic hyphae, whose structure is less complex.     

Fungal relationships and structural identity of their ectomycorrhizae

Aproximately 5,000–6,000 fungal species form ectomyorrhizae (ECM), the symbiotic organs with roots of predominantly trees. The contributing fungi are not evenly distributed over the system of fungi. Within Basidiomycota exclusively Hymenomycetes and within Ascomycota exclusively Ascomycetes contribute to the symbiosis. Hymenomycetes play a big part, Ascomycetes a minor role; Zygomycetes only form exceptionally ECM. Responsible for ascomycetous ECM are mostly Pezizales with their hypogeous derivatives, whereas Boletales, Gomphales, Thelephorales, Amanitaceae, Cantharellaceae, Cortinariaceae, Russulaceae, and Tricholomataceae are the most important ectomycorrhizal relationships within Hymenomycetes. ECM, as transmitting organs between soil and roots, are transporting carbohydrates for growth of mycelium and fruitbodies from roots and have to satisfy the tree’s demand for water and nutrients. The latter task particularly influences the structure of ECM as nutrients are patchily distributed in the soil and saprotrophic as well as ectomycorrhizal fungi can act as strong competitors for nutrients. In focusing these requirements, ECM developed variously structured hyphal sheaths around the roots, the so-called mantles, and differently organized mycelium that emanates from the mantle, the so-called extramatrical mycelium. The mantles can be plectenchymatous consisting of loosely woven, differently arranged hyphae or they are densely packed, forming a pseudoparenchyma similar to the epidermis of leaves. The extramatrical mycelium grows either as simple scattered hyphae from the mantle into the soil or it can be united to undifferentiated rhizomorphs with a small reach or to highly organized root-like organs with vessel-like hyphae for efficient water and nutrient transport from distances of decimeters. Cystidia, sterile and variously shaped hyphal ends, possibly appropriate for preventing animal attack, in addition, can cover mantles and rhizomorphs. Although only a limited number of species could be considered, some general conclusions are possible.The genus Tuber forms needle-shaped cystidia and lacks rhizomorphs and clamps. Gomphales ECM are identified by rhizomorphs with ampullate inflations at septa of some hyphae and by oleoacanthocystidia or/and oleoacanthohyphae. Thelephoraceae reveal a great diversity of mantle structures and of extramatrical mycelium, with some additional optional characters, i.e., dark brown color, cystidia, blue granules, amyloid hyphae, or amyloid septa. Bankeraceae are mostly characterized by plectenchymatous mantles with star-like pattern and chlamydospores. Russulaceae possess smooth and hydrophilic ECM. Russula forms plectenchymatous mantles with knob-bearing cystidia, so-called russuloid cystidia, or pseudoparenchymatous mantles without cystidia. Lactarius lacks cystidia and shows laticifers within plectenchymatous or within pseudoparenchymatous mantles. The Boletales families Boletaceae, Gyroporaceae, Melanogastraceae, Paxillaceae, Rhizopogonaceae, Sclerodermataceae, and Suillaceae have the most advanced rhizomorph type, the so-called boletoid rhizomorphs, and reveal generally plectenchymatous mantles, frequently with ring-like patterns. Gomphidiaceae and Albatrellaceae provide cystidia, plectenchymatous mantles, and amyloidy; Gomphidiaceae are generally growing in ECM of Suillaceae and Rhizopogonaceae. Cortinariaceae reveal plectenchymatous mantles and undifferentiated or differentiated rhizomorphs or lack rhizomorphs at all. Cortinarius and Dermocybe are distinct by irregularly shaped, bent to tortuous ECM with many rhizomorphs, some growing over the mycorrhizal tip into the soil. Inocybe lacks rhizomorphs and its emanating hyphae are furnished by many secondary septa and prominent clamps with a hole. Rozites lacks rhizomorphs, too, and reveals a distinctly amyloid gelatinous mantle matrix. Descolea and Descomyces are covered by bolbitioid cystidia. Lastly, the genus Tricholoma forms plectenchymatous mantles and a high diversity of rhizomorphs. Some of the ectomycorrhizal features are used to hypothesize relationships at different taxonomic levels. These conclusions are compared with recently developed molecular hypotheses. Correspondence between the two types of hypotheses are evident, while some conflicts wait for a settlement.     

Nuove segnalazioni di funghi entomogeni

Abstract

New records of entomogenous fungi. — New records of six entomogenous fungi, three Ascomycetes (Cordyceps lloydii Fawcett, C. memorabilis Ces., C. riverae Pacioni) and three Deuteromycetes (Akantomyces aranearum (Petch) Mains, Hirsutella citriformis Speare, Troglobiomyces guignardii (Maheu) Pacioni) are given. The new records allow to expand the known area of distribution of these parasites, to confirm the particular condition for fructification needed by some of them and to give new details for the less common species.     

Occurence of microtubules and microfilaments,and origin of septa in dikaryotic hyphae ofSchizophyllum commune

Summary In an electron microscopic study on the dikaryotic hyphae ofSchizophyllum commune, microtubules were observed during the nuclear division, and close to the non-dividing nuclei of apical cells and older cells. Microtubules of the spindle were connected with semicircular bodies at nuclear poles. Microfilaments were detected in the distal part of the apical cells. Vesicles similar to those in the tips of the hyphae occured also at the sites of septa formation. The occurrence of microtubules and the structure of semicircular bodies are compared with those in other basidiomycetes. It is suggested that vesicles are involved in the primary growth of the septal cross wall.     

Leucosporidium fellii sp. nov., a basidiomycetous yeast that degrades L(+)-tartaric acid

A new species of basidiomycetous yeast Leucosporidium fellii was isolated from soil in Portugal on a selective L(+)-tartaric acid medium. This yeast is self-sporulating but forms dikaryotic hyphae with clamp connections and is presumably homothallic. It differs from the type strain of Leucosporidium scottii in its life cycle, assimilation pattern and guanine-cytosine content and from the other described Leucosporidium species by additional characteristics.     

Impact of biological (Rotstop) and chemical (urea) treatments on fungal community structure in freshly cut Picea abies stumps

To control the infections by root rot fungi Heterobasidion spp., surfaces of freshly cut Norway spruce stumps are covered either by a biological (Rotstop; spore suspension of competitive saprotrophic fungus Phlebiopsis gigantea), or by a chemical (35% aqueous solution of urea) compound. In Fennoscandia, Rotstop and urea are applied, respectively, on 47,000 ha and on 2000 ha of forestland each year. The aim of this work was to assess the impact of biological and chemical control on biodiversity in communities of non-target fungi in freshly cut (7-week-old) stumps. Isolation of fungi to pure culture was accomplished from 402 wood samples taken from 63 stumps, 21 treated with each of the compounds and 21 untreated. The isolations yielded 368 distinct fungal strains representing 47 species. Stump treatment led to decrease of species richness both in Rotstop-treated (by 15%) and in urea-treated (by 19%) stumps. Nevertheless, the stumps subjected to the biological compound were colonized mainly by the same fungi that occurred naturally in untreated stumps (Sorensen similarity indices; S_S=0.69; S_N=0.68). By contrast, chemical treatment strongly promoted stump colonization by Ascomycetes and Deuteromycetes, led to significant decrease of Zygomycetes, and almost completely eliminated Basidiomycetes (including Heterobasidion spp.). Thus, resemblance to a natural community was low (S_S=0.45; S_N=0.34). Rotstop treatment decreased significantly the extent of stump colonization by Heterobasidion spp., and increased that of P. gigantea. All strains of the latter were genetically identical among themselves and to the Rotstop strain. The mechanisms of biological and chemical control, and biodiversity aspects are discussed.     

Direct microscopic studies of clamp connection formation in growing hyphae of Schizophyllum commune

Summary Photomicroscopic studies of clamp connection formation were collated with microscopic measurements of apical extension and mitosis in rapidly growing dikaryotic hyphae of Schizophyllum commune. Intercalary clamp connection formation was described in sub-terminal regions of the dikaryon. Conventional (i.e., rearward) clamp initiation was compared to forward clamp connection formation. Primary branch emergence was observed from clamp connections in growing hyphae and contrasted to sub-basidial branching in the hymenium of dikaryotic fruit-bodies.     

Sporogenesis in Streptomyces melanochromogenes

The mode of spore differentiation in a strain of Streptomyces melanochromogenes was followed by analysis of ultrathin sections of sporulating aerial hyphae at various stages of sporogenesis. A special accent was laid on the formation of the sporulation septum and its alterations in the course of spore delimitation and separation. Distinct differences in formation and substructure have been observed between the cross walls of vegetative hyphae and the sporulation septa.Cross walls of vegetative hyphae are formed in a way typical for Gram-positive bacteria by a centripetal annular ingrowth of cytoplasmic membrane, on which wall material immediately is deposited. The development of the sporulation septa is characterized by the accumulation of amorphous material in addition to the newly synthesized wall layer inside the invaginating cytoplasmic membrane. This amorphous septal material will later be decomposed presumably by two lytic systems which cause the separation of the spores. The central region of the finished sporulation septum is perforated by microplasmodesmata. Spores are released by a break down of the surface sheath. The complete spores are enveloped by a twolayered cell wall and the spiny surface sheath.     

THE SEPTAL PORES OF COPFINUS LAGOPUS IN RELATION TO NUCLEAR MIGRATION

The septal pores of homokaryotic and dikaryotic mycelia of Coprinus lagopus have the complex structure characteristic of certain Basidiomycetes. The edge of the pore is thickened and covered on either side by a dome-shaped, perforated, membranous cap. However, in heterokaryotic mycelia in which nuclear migration was believed to be taking place, in addition to the complex pores, simple pores were also observed as well as various intermediate stages interpreted as steps in the breakdown of complex to simple pores. The simple pores may facilitate nuclear migration.     

Cytoplasmic Continuity Revisited: Closure of Septa of the Filamentous Fungus Schizophyllum commune in Response to Environmental Conditions

Background

Mycelia of higher fungi consist of interconnected hyphae that are compartmentalized by septa. These septa contain large pores that allow streaming of cytoplasm and even organelles. The cytoplasm of such mycelia is therefore considered to be continuous.

Methodology/Principal Findings

Here, we show by laser dissection that septa of Schizophyllum commune can be closed depending on the environmental conditions. The most apical septum of growing hyphae was open when this basidiomycete was grown in minimal medium with glucose as a carbon source. In contrast, the second and the third septum were closed in more than 50% and 90% of the cases, respectively. Interestingly, only 24 and 37% of these septa were closed when hyphae were growing in the absence of glucose. Whether a septum was open or closed also depended on physical conditions of the environment or the presence of toxic agents. The first septum closed when hyphae were exposed to high temperature, to hypertonic conditions, or to the antibiotic nourseothricin. In the case of high temperature, septa opened again when the mycelium was placed back to the normal growth temperature.

Conclusions/Significance

Taken together, it is concluded that the septal pores of S. commune are dynamic structures that open or close depending on the environmental conditions. Our findings imply that the cytoplasm in the mycelium of a higher fungus is not continuous perse.     

Molecular architecture of fungal cell walls. An approach by use of fluorescent markers

Fluorescent probes have been applied to analyze the molecular architecture of fungal cell surfaces. Binding patterns of aniline blue and FITC-labeled wheat germ agglutinin (FITC-WGA) elucidated class-specific properties. Aniline-blue-induced fluorescence was distributed over the entire cell walls from Ascomycetes, but was confined to sporangial walls of Zygomocetes, hyphal tips and a few other sites in Basidiomycetes, while no fluorescence was found with sporangia and rhizoids of Chytridiales. FITC-WGA in Zygomycetes and in Ascomycetes was restricted to few sites (e.g. apex of hyphae), in Basidiomycetes and Chytridiales label was evenly associated with the entire surface of hyphal walls, or sporangia and rhizoids. For Oomycetes, Zygomycetes, Ascomycetes, and Basidiomycetes differences in the molecular architecture between apex and hyphal side walls were discerned, although the chemical nature of these differences is distinct for each class. Species specific differences, due to differences in binding patterns of several lectins are not apparent at fungal cell surfaces. The degree of intraspecies variation was found to be larger than interspecies diversification, suggesting changeableness of the molecular architecture of fungal cell walls. This is in contrast to assertions which we made by working on algae. There species-specific lectin binding patterns have been described.     

STRUCTURE AND DEVELOPMENT OF HYPHAL SEPTA IN ALLOMYCES

Development of hyphal septa (pseudosepta) in Allomyces macrogynus begins with the formation of five or more discontinuous pieces of wall material that project inward from the hyphal wall. Lateral fusion of these projections leaves a central pore in the septum that is later filled in by centripetal deposition of wall material. However, lateral fusion of the projections is not complete; peripheral pores remain in the rim of the mature septum. The position of cytoplasmic microtubules corresponds to the position of actively moving cellular particles and organelles. Allomyces reticulatus and A. arbuscula have similar septa.     

Kinetic studies of septum synthesis,erosion and nuclear migration in a growing B-mutant of Schizophyllum commune

Summary Microscopic measurements of apical growth and primary branch elongation were compared with nuclear movements, septum synthesis and erosion in a growing B-mutant of Schizophyllum commune. Apical growth, mitosis, septum formation, and intercalary cell division were similar to wild-type hyphae. Nuclear replication and new cross-wall formation also occurred in either apical cells bounded by eroding septa or in subterminal cells adjoined by eroded septa. An anucleate subterminal unit of the B-mutant hypha was invaded by a migrant nucleus which subsequently replicated and laid down a new septum in this region. Septum erosion occurred as early as 1 h following synthesis. Cellular granules and filaments were implicated in both septum synthesis and erosion.     

A new species of petalosporus

Summary A new species ofPetalosporus, P. anodosus, is described and illustrated. Two isolates representing this species were isolated from dung in California. The new species differs from the only other species of the genus,P. nodulosus, by the lack of thick-walled peridial hyphae with enlargements at the septa and by the absence of disarticulation of peridial elements. Peridial hyphae inP. anodosus have walls which are somewhat thickened and the cells are often variable in diameter. Conglomerate ascospores usually assume the petaloid arrangement characteristic of the genus.     

Fine structure of sporogenesis and septum formation in Micromonospora globosa Kriss and M. fusca Jensen.

Sporogenesis in two species of Micromonospora M. globosa and M. fusca (Actinomycetes) was quite similar. As in fungi, spore formation began as a blowing-out of a hyphal tip with the subsequent centripetal invagination of the plasma membrane. Septal wall material was deposited in a typical three-layered pattern, i.e., two electron-opaque layers separated by an electron-transparent layer. A second electron-opaque wall layer was later formed within the spore and finally a third, less electron-opaque wall was produced. Spore dihiscence was facilitated by the fragmentation of the first-formed wall surrounding the spore. Sporogenesis in Micromonospora is blastic in nature producing terminal, thick-walled spores. In M. fusca, a sporulation process was observed which closely resembled sporangial formation. The process appeared similar to that described for the genus Actinoplanes. Swollen, multiseptate structures were also present. Also in M. fusca, perforate septa with flared pore margins were observed. These septa were similar in appearance to the dolipore septa of Basidiomycetes although they lack a parenthesome and pore plug. Although an extensive membrane system (mesosome) was associated with the finishing septum, its function in the process of septum formation was not determined.     

Bulleromyces genus novum (Tremellales), a teleomorph for Bullera alba,and the occurrence of mating in Bullera variabilis

Mating is observed in Bullera alba and B. variabilis, resulting in the formation of dikaryotic mycelium with clamps, haustorial branches, and lateral and terminal dikaryotic, clavate, lageniform or subglobose cells. These cells develop in B. alba into tremellaceous phragmobasidia. Karyogamy has been observed in young non-divided basidia. Germination of the phragmobasidia occurred by acropetal chains of yeast cells, ballistospores or hyphae. Septal pores are dolipores with parenthesomes made up of U-shaped vesicles (Tremellales type). For the teleomorph of B. alba a new genus, Bulleromyces, is proposed, with only one species, viz. Bulleromyces albus.     

ULTRASTRUCTURE OF THE METABASIDIUM OF AURICULARIA FUSCOSUCCINEA

Maturation of the metabasidium of Auricularia fuscosuccinea was followed with light microscopy and transmission electron microscopy. The basidium was divided into four compartments by septa which developed centripetally as in hyphae. Each septum formed a septal pore apparatus with imperforate pore caps. A band of electron-dense material was situated in the middle of the septal pore. There was a large increase in the volume of cytoplasm, excluding vacuoles, in each compartment during sterigmal outgrowth. Compartments were evacuated in basipetal sequence and vacuole enlargement began at the base of a compartment only when sterigmal formation was well advanced. The septal pore apparatus was intact until late in maturation of a compartment when septal swellings occluded the pore. The metabasidial wall was differentiated from those of other hymenial and subhymenial cells. The pattern of basidial maturation is compared with that in other phragmobasidiate and holobasidiate fungi. Use of the septal pore apparatus for phylogenetic and taxonomic purposes is discussed, as is the concept of primary and adventitious septa.