Rusts are a group of plant pathogenic fungi which both cause aesthetic damage and inhibit healthy plant growth. Individual rust fungi have very limited host ranges, but often alternate between two hosts as part of their life cycle.
Symptoms and SignsEdit
Rusts are primarily foliar diseases, and the most obvious sign is the presence of the fruiting bodies on the leaves, which are brown or orange ("rust colored"). Further symptoms include yellowing and dying leaves, and overall weakness of infected plants.
Rust Fungi in HorticultureEdit
Rusts are fungi of the order Uredinales. Many of these species are plant parasites. Some are superficially similar to the smuts, although their relation to each other is not clear. The taxonomy of Urediniomycota, as a whole, is in a state of flux.
Many of the rusts have two or more hosts (referred to as heteroecious) and up to five spore stages. However they most commonly reproduce via asexual spore production. Their spores are airborne and can travel great distances. They mostly cause foliar infections.
The group received its common name from the fact that some species have a reddish spore stage, which resembles the corrosion process known as rust.
Rust occurs on many species of plant, but in most causes any one species of rust can only infect one species of plant. The following describes the infection process of asexual spores.
When a rust conidia spore lands on a plant surface it needs to attach to it, or it would simply be washed off. First, weak, hydrophobic interactions are formed between the spore and the cutin of the plant cell surface. Then unknown signals cause the production of hydrophobic mucilaginous macromolecules called adhesins. These will stick the spore irreversibly to the plant surface. Once attached, the spore will germinate.
Germ Tube ElongationEdit
Rust fungi penetrate the plant by using the natural opening of the stomata, but first the growing germ tube must locate it. Rust fungi have evolved to more efficiently locate stomata by the use of thigmotropism. The germ tube grows in a random manor until it reaches a ridge between epidermal cells. At this point it will start to grow perpendicular to the ridge, greatly increasing its chances of locating a stomata.
The stomata is the site of appresorium formation, a structure that functions to both firmly anchor the fungus and aid in penetration. In the rust fungi appresorial formation is controlled by a process of thigmodifferentiation. Appresoria are formed when the germ tube detects ridges that match the dimensions of the stomatal lips of its host species.
It has been proposed that this process is mediated by a mechanosensitive calcium ion channel that is located at the germ tube tip. This ion channel would transduce the stretching of the cell membrane caused by changes in leaf topography into ion fluxes that lead to changes in gene expression and appresorium formation.. This theory is supported by experiments that show that applying Ca2+ externally to the germ tube causes differentiation.
From the appresoria an infection peg growns down into the plant and between the mesophyll cells.
Rust fungi are biotrophs, meaning they gain their nutrients from living cells. This requires a specialised entension of the fungi into a living plant cell called a haustoria. This develops from a haustorial mother cell. The plant cell membrane invaginates around the main haustorial body and the space between the two membranes becomes known as the extra-haustorial matrix. An iron and phosphorous rich neck band bridges the plant and fungal membranes and acts as a seal preventing the escape of nutrients into the plant apoplast. The haustoria contains amino acid and hexose sugar transporters and H+-ATPases for the active transport of nutrients from the plant cell.
The rust fungi will then continue to grow and invade the plant until it is ready for sporulation.
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