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Cellulase localization in hyphae of Achlya ambisexualis.

Cellulase (EC 3.2.1.4; beta-1, 4-glucan glucanohydrolase) was localized at the ultrastructural level and found to occur in dictyosomes and vesicles, around the periphery of unidentified storage bodies, between the plasmalemma and the cell wall, and on the outer surface of the cell wall in the male strain (E87) of Achlya ambisexualis after treatment with the sex hormone antheridiol.

Cell Wall↗

Of yeasts and hyphae: a hematologist's approach to antifungal therapy.

Improvements in anticancer treatments, the ability to modify myelosuppression profiles, greater duration and intensity of immunosuppression, and the variety of available antimicrobial therapies have influenced the spectrum of pathogens associated with invasive fungal infection complicating treatment of hematological malignancies and hematopoietic stem cell transplantation. The approaches to the management of these infections encompass strategies of prevention for all those at risk, preemptive therapy based upon surrogates of infection before the onset of clinical disease, empirical therapy for patients with clinical evidence of early disease, and directed or targeted therapy for infected patients with established disease. Chemoprophylaxis is effective if applied to the highest risk patients over the duration of the risk. Preemptive strategies, while promising, have yet to be validated and linked to reliably predictive non-microbiological diagnostic techniques. Empirical antifungal therapy, as it is currently applied, now seems questionable. Patients with probable or proven invasive fungal infection still have suboptimal outcomes despite the availability of promising anti-fungal agents. Strategies examining the concept of dose-intensity and combination regimens require careful study and cannot yet be regarded as an acceptable standard of practice.

Antifungal Agents↗

Radial F-actin arrays precede new hypha formation in Saprolegnia: implications for establishing polar growth and regulating tip morphogenesis.

The roles of cortical F-actin in initiating and regulating polarized cell expansion in the form of hyphal tip morphogenesis were investigated by analyzing long term effects of F-actin disruption by latrunculin B in the oomycete Saprolegnia ferax, and detecting localized changes in the cortical F-actin organization preceding hyphal formation. Tubular hyphal morphology was dependent on proper F-actin organization, since latrunculin induced dose-dependent actin disruption and corresponding changes in hyphal morphology and wall deposition. With long incubation times (1 to 3 hours), abundant subapical expansion occurred, the polar form of which was increasingly lost with increasing actin disruption, culminating in diffuse subapical expansion. These extreme effects were accompanied by disorganized cytoplasm, and novel reorganization of microtubules, characterized by star-burst asters. Upon removing latrunculin, hyperbranching produced abundant polar branches with normal F-actin organization throughout the colony. The results are consistent with F-actin regulating polar vesicle delivery and controlling vesicle fusion at the plasma membrane, and suggest that F-actin participates in establishing polar growth. To test this idea further, we utilized the hyperbranching growth form of Saprolegnia. Early during the recovery time, prior to multiple branch formation, radial arrays of filamentous F-actin were observed in regions with no detectable surface protrusion. Their locations were consistent with those of the numerous branches that formed with longer recovery times. Similar radial arrays preceded germ tube formation in asexual spores. The arrays were important for initiating polar growth since the spores lost their ability to polarize when the F-actin was disrupted with latrunculin, and increased isometrically in size rather than producing germ tubes. Therefore, F-actin participates in initiating tip formation in addition to its previously demonstrated participation in maintenance of hyphal tip growth. The cortical location and radial organization of the arrays suggest that they recruit and stabilize membrane-bound and cytosolic factors required to build a new tip.

Actins↗

[Microorganism in the hyphae of mycorrhiza-forming fungus].

A microorganism with the cell wall and cytoplasmic membrane was found when the endotrophic mycorrhiza of pea was studied by electron microscopy. The wall of the microorganism was in a close contact with the cytoplasm of the fungus. No changes were found in the ultrastructure of the fungus and microorganism caused by their interaction.

Bacteria↗

Ultrastructure of the hyphae and conidia of Arthrinium aureum.

Electron microscopic observations of structures in Arthrinium aureum, which have not previously been described, are presented and discussed. Considerable attention is given to cytoplasmic inclusions, especially nuclei, mitochondria and Woronin bodies.

Cell Nucleus↗

Mitochondrial behaviour during the yeast-hypha transition of Candida albicans.

Yeast cells of Candida albicans were brought to germ tube formation and hyphal growth in liquid synthetic medium. The behaviour of mitochondria and mitochondrial nucleoids (mt-nucleoids) during morphological conversion was examined by fluorescence staining with 2-(4-dimethylaminostyryl)-1-methylpyridinium iodide (DASPMI) and 4',6-diamidino-2-phenylindole (DAPI). Parent yeast cells possessed one or very few branched giant mitochondria which were stained intensely with DASPMI. When a germ tube emerged from the parent cell, one end of a giant mitochondrion extended into the germ tube and developed into the elongated form. In mycelia, apical hyphal cells contained giant mitochondria, whereas older hyphal compartments near the parent cells were vacuolated and possessed small, peripherally located mitochondria. The vacuolated hyphal compartments resynthesized cytoplasm before producing branches and contained giant mitochondria. The cytological model for germ tube formation and hyphal growth proposed by Gow and Gooday (1984) is discussed.

Candida albicans↗