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 (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.
Rust occurs on many species of plant, but in most cases any one species of rust can only infect one species of plant. This can make rust useful in biological control. The following describes the infection process of asexual spores. A picture summarizing the process can be found in the gallery below.
When a rust conidium 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.
Rust fungi penetrate the plant by using the natural opening of the stoma, 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 manner 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 stoma.
The stoma 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 appresorium an infection peg grows 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 fungus into a living plant cell called a haustorium. 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 phosphorus rich neck band bridges the plant and fungal membranes and acts as a seal preventing the escape of nutrients into the plant apoplast. The haustorium contains amino acid and hexose sugar transporters and H+-ATPases for the active transport of nutrients from the plant cell.
The rust fungus will then continue to grow and invade the plant until it is ready for sporulation.