Introductory Plant Pathology

Class 8

"Higher Fungi"
Ascomycetes and Basidiomycetes

Objectives for Today's Class   Mastery Topics
Reference: Agrios Chapter 11   Plant Diseases caused by Ascomycetes
Plant Diseases caused by Basidiomycetes

CHARACTERISTICS OF PLANT PATHOGENIC FUNGI


Morphology

The thallus, vegetative part, of a filamentous fungus is called a Mycelium (plural mycelia). An individual strand of a mycelium is called a Hypha (plural hyphae). Fungal growth takes place at the apex of a hyphae. Spitzenkorpers are vacuolar bodies formed within the the hyphae and migrate where they fuse with the plasma membrane; in a process likened to reverse pinocytosis. Fusion/addition to the membrane facilitates the growth process. This process has been elegantly demonstrated in a number of fungi using pulse-chase labeling experiments which resulted in hyphae with bands of radioactivity perpendicular to the axis of each hyphae.
The rate of mycelial growth is a characteristic unique to each organism. Typically the lower fungi are faster growers in vitro than are the higher fungi.
The ribosomes of all fungi are 80S characteristic of eukaryotic organisms. All other sub-cellular organelles are typical of eukaryotes including; nuclear membranes, mitochondria, vacuoles, etc. Irrespective of apparent color, fungi do not contain chlorophyll.
The cell wall composition of fungi is a diagnostic that separates them from the oomycetous Chromista. Oomycetous chromistan cell walls are composed of complex carbohydrates but do not contain chitin; while fungi contain chitin and carbohydrate compounds in their cell walls.




Septation formed by cross walls is unique to each group of fungi. The ascomyceteous fungi have cross walls that divide hyphae into cellular units even though in some cases there as a whole in the center of the cross wall. Basidiomyceteous fungi have an elaborate cross wall often containing a dolipore septum. This septum serves both as an impediment to subcellular movement from cell to cell and also as an effective baffle against rapid liquid loss or movement.
The combination of cell wall composition and septation from an extremely strong thallus as evidenced by observations of fungi pushing their way through unbroken concrete slabs.






Systematics

Because this is neither a systematics nor a mycology course and because the systematists are not united to any given schema; the presentation below is a greatly simplified version and is specifically selective to the fungi discussed in this course. It is hoped that the student will be able to learn the differences which separate fungal phytopathogens as well as those characters which unite them. For further information check the mycological references.

In fungi, as well as in plants, naming and systematic relationships are based on sexual reproductive morphological characters (telomorph). This causes difficulty and confusion because sexual reproduction has not been observed for many important phytopathogenic fungi. Because of this and because asexual reproductive morphological characters (conidia, mycelium, chlamydospores, sclerotia) are most often observed in the field; an entire nomenclatural system based on asexual characters (anamorphic) has been developed. This nomenclatural system designated "form-genus" and "form-species" to identify and classify fungi is based primarily on spore ontogeny and shape. Use of the word "form" recognizes that nomenclature and identification are based incomplete characters. Over time, use of the word "form" was largely abandoned and a quasi legitimate standing for the name came into common usage. When sexual reproduction is observed, a new name is based on complete morphological (sexual and asexual)characters is constructed often the specific epithet (species name) remains the same while the new genus name takes precedence. An inordinate competitive rush to rename organisms has lead to incorrect renaming, and subsequent renaming, and has resulted in both confusion and a loss in the needed communication when the transitions are made between one name and another.

As students and professionals, it is important to known both the current name and also the synonyms that have been used in the past. It is useful to know both the telomorph (based on complete characters) and the anamorph (based on asexual characters) names for each pathogen. In common usage, quite often the anamorphic name prevails because of history and causal agent-disease relationships.

A certain amount of scientific hyperbole has occurred. One finds that under some schemes Phyla have been raised to Kingdoms. This is owing to molecular research that places fungi closer to animals than to plants and thus some have chose to erect new kingdoms for protozoa, chromista, and fungi. Currently one can find any number of schemes for fungal systematics. The scheme presented below follows Hawkworth et alR. Simply because it is published as an entire treatment of these organisms, including the now Protists and Chromistans. Dr. Agrios' descriptions are informative, useful, and in general agreement with the Berkeley School.

Another, and much simpler, system is presented by Wessels et al R. It is summarized here to encourage students to evaluate this approach as well. Under this scheme the true fungi are placed in the Phylum Eumycota.



Basidiomycotina


Structures of Fungi courtesy: Dr. Donald C. Erwin ; University of California - Riverside


Generic Life Cycle of a Rust

The cyclic sequence of spore production, i.e. Basidiospore - Spermatia - Aeciospore - Urediospore - Teliospore, is the same for all rust fungi. However, with this proviso; not all rusts have complete cycles as indicated on the image as microcyclic and macrocyclic.

Also notice that each spore has a particular reproductive structure , i.e. basidium for basidiospores, for each spore type. The location of these structures is predictable and diagnostic for disease identification. Typically, some are on the abaxial surfaces while others are on the adaxial surfaces.

Notice the nuclear condition of these spores. Only the basidiospore is 2n; therefore, where does sexual recombination occur?

Point to Ponder: Knowing that rusts must complete their spore cycle in order to be viable as disease causing agents and adding to the equation that some rusts require alternate hosts (some spore stages on one host and the others on another), one is able to devise a plant health management strategy for rust control. As with all diseases, if one can break the life cycle one can "control " the disease. Therefore, what are some of the obvious general management strategies that will be effective against any rust fungus.


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This page is authored and maintained by:

Dr. J.E. Partridge, Department of Plant Pathology, University of Nebraska-Lincoln

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