Oak wilt is a devastating exotic disease, killing some trees rapidly in a single season. Oak wilt is an important disease in
urban areas where trees are highly valued. The disease reduces
property values because of the loss of trees and is economically costly to the
property owner since they or the local government must pay for
tree removal. Additionally, preventing the spread of the disease to
healthy trees is costly and requires vigilance. Oak wilt is also an important disease in a forest setting, as entire
forest stands can die within a few years. There is a narrow window to
salvage diseased trees for
hardwood lumber and often the disease is not discovered within that logging window. The
ecological impacts to forests is also a concern. The disease is currently restricted to North America, but is potentially a serious threat to oaks worldwide. All
Quercus spp. appear susceptible to the disease, with 33 oak species confirmed to be susceptible; including three species of
Castanea, one species of
Castanopsis, one species of
Lithocarpus, and some oaks native to Europe (
Q. petraea,
Q. pubescens, &
Q. robur). Generally, red oaks (
subsection Lobatae) display more severe symptoms with rapid and frequent
mortality (particularly
Q. velutina,
Q. rubra,
Q. ellipsoidalis &
Q. coccinea). White oaks (
subsection Quercus) develop symptoms more slowly, rarely die, and can recover from the pathogen with damage limited to a few branches (particularly
Q. alba, &
Q. macrocarpa).
Live oaks (
Q. fusiformis &
Q. virginiana) display intermediate symptoms compared to red or white oaks. However, live oaks are semi-evergreen, can propagate vegetatively by root
suckering, and cohabitate with other live oaks in dense
stands enabling interconnected root systems. These traits are favorable for local spread of the disease in an
oak-grassland savanna.
History Oak wilt is one of
three devastating North American vascular
wilt diseases that appeared in the early 20th century. The other two vascular wilts are
chestnut blight (1900–1950) and
Dutch elm disease (1928–1980). Each of these diseases have depopulated their respective host tree populations.
Chestnut trees were the dominant
overstory tree species before chestnut blight and
elms were an iconic
landscape tree that bordered streets before Dutch elm disease. Oak wilt and the newly emerging
emerald ash borer have the potential to devastate other important North American tree species with large geographical and cultural significance. Range expansion of oak wilt to the Western United States (or to other
continents) is a major concern. The asexual stage of oak wilt was first described in 1942 in Wisconsin. Soon thereafter the disease was reported throughout the
Upper Midwest and
Central forests. The early
20th Century coincided with oak regeneration after significant logging in the
Mid-Atlantic and
Great Lakes region.
Deforestation and fire suppression in this region altered the ecology to favor
oak–hickory forests, instead of coniferous forests and
grasslands. Subsequently, the host for the disease became more prevalent and promoted oak wilt infections. Moving timber during the late 19th Century and early 20th Century, in the
period of railroad expansion, coincides with the discovery of the oak wilt disease in the United States. The origin of the disease is unknown, but probably emerged from Mexico, Central America, or South America. Mexico is the global center of oak diversity, supporting it as the
endemic range of oak wilt. Any
biocontrol or
disease resistance for this pathogen will likely come from Mexico. The disease currently affects much of the eastern and central US, from northern New York to
Central Texas. It is particularly common in the
Midwest where conditions are usually favorable for spore production and beetle activity during spring and early summer. Oak wilt is a major problem in
Illinois,
Iowa,
Michigan,
Minnesota,
Texas, and
Wisconsin.
Disease cycle The fungus overwinters on dead tissue from diseased trees. Symptoms first appear in spring and summer. Highly susceptible species typically die within one year (often within six weeks) after symptoms appear. Symptoms begin in the tops of trees and can be difficult to notice. The disease progresses inward and downward from the
tree top. Leaves become
chlorotic beginning at the
leaf tip and
leaf edges. An abrupt demarcation of chlorotic
veins and green tissue is often a distinguishing characteristic in live oak infections. The foliage may droop, curl lengthwise, wilt, and begin to
fall. Leaves drop from the tree in the middle of summer, however less susceptible trees may retain leaves longer and resemble seasonal
autumn foliage. Highly susceptible species will exhibit rapid
crown dieback, while less susceptible species may only lose a few scattered branches. Live oaks may survive several years with progressive dieback, but often die within six months. Following
defoliation, fungal
fruiting bodies develop from
mycelium under the
bark of the tree. The mats grow to 10 – 20 cm in size, elliptical in shape, and grey in color with white margins that darken with age. These mats are not found on live oaks and rarely on white oaks. Trees capable of producing mats are called potential spore-producing trees (PSPT). Brown streaks in the
sapwood is also observed in the oak wilt disease. However, this symptom is not always associated with the disease. The oak wilt fungus can spread from diseased trees to healthy trees in several ways. The disease can spread long distances (overland) by
airborne spores in open
wounds caused by
wind damage,
pruning, or other mechanical damage. Alternatively, under ideal conditions (temperature, moisture content, wood pH) spore mats form under the bark of the dead tree. Spore mats develop in the spring or fall for 2–3 weeks. The center of spore mats produce chains of barrel shaped spores, called endoconidia.
Conidia are asexual spores dispersed by air, rain, and insects. If compatible mating types are present, these mats will also produce sexual spores called ascospores in fruiting structures called
perithecia.
Ascospores are spread by water and insects. These spore mats (or pressure pads) increase in size, eventually breaking through the bark and releasing a fruity odor that attracts wildlife, including
sap beetles,
bark beetles, other insects, birds and animals, such as squirrels. Insect
vectors transmit the disease in spring to early summer in the Mid-West and late Winter in Texas. Insect transmission is the primary way new
infection foci originate. The fungus can spread short distances through naturally occurring
root grafts. Root
grafts form when two or more underground roots merge from adjacent trees. Typically,
roots from the same, or similar species, can form root grafts as their
cambia are pressed together and combine. Fungal spores in the
xylem travel to nearby trees through these root grafts and can rapidly kill many trees simultaneously. This transmission method accounts for the vast majority of infections and is particularly devastating as groups of trees are killed. The disease can extend 10 – 20m per year (40m per year in Texas) from the
infection foci to surrounding trees. Diseased trees can continue to harbor and transmit the disease for several years through the root network. The disease results from fungal spores clogging
xylem vessels and preventing water and nutrient flow.
Mycelia growth between and through
vessels end up blocking
xylem pits in the vessel endwalls.
Tylose protrusion and the accumulation of 'gums' will further obstruct vessels. Tylose is an outgrowth of
parenchyma cells created as a plant defense against pathogens, water deficiency, wounding, and
heartwood formation. Tylose formation signals senescence of adjacent parenchyma cells and secretion of
secondary metabolites (called gums), which may include phenolics. The interruption of the xylem vessels precedes tylose formation. Tylose and secreted gums act as a barrier to slow the colonization of the pathogen and play an important part in
plant defenses. However, the action to
compartmentalize the oak wilt fungus ultimately obstructs all water conductance, leading to death. The fungus can survive in the xylem for multiple years, if the tree is not killed. == Management ==