Gymnosporangium sabinae | |
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Gymnosporangium sabinae on pear leaf, Sivas, Turkey | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Fungi |
Division: | Basidiomycota |
Class: | Pucciniomycetes |
Order: | Pucciniales |
Family: | Gymnosporangiaceae |
Genus: | Gymnosporangium |
Species: | G. sabinae |
Binomial name | |
Gymnosporangium sabinae | |
Synonyms [1] | |
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Gymnosporangium sabinae is a species of rust fungus in the subdivision Pucciniomycotina. Known as pear rust, European pear rust, or pear trellis rust, it is a heteroecious plant pathogen with Juniperus sabina (savin juniper) as the main primary (telial) host and Pyrus communis (common pear) as the main secondary (aecial) host.
Like many rusts, G. sabinae requires two different hosts to complete its life cycle from year to year. Juniper is the winter host and pear is the summer host. Spores (called aeciospores) are produced from the fungal lantern-shaped growths which protrude from the blisters on the underside of the pear leaf which become airborne and infect junipers. This fungus overwinters in swellings or galls on infected twigs and branches of susceptible juniper plants. In the spring after a rain or heavy dew, the galls on the juniper produce tiny dark horn-like growths that become covered with an orange-brown gelatinous mass called telia. The corresponding stage on the pear trees is known as aecia. The telia and aecia release wind borne resting or hibernating spores (called teliospores and aeciospores) capable of infecting susceptible pear leaves and Juniper respectively. Spores produced from the fungus-induced swellings on juniper stems can be infectious up to 6 km. The disease causes a yellow-orange spot that turns bright red on leaves of pear trees. The disease can be particularly damaging on pear, resulting in complete defoliation and crop loss if not treated. The fungus feeds on the living cells of the host plant and is not capable of surviving on dead plant material, and so must either alternate with a different host or produce resting spores to pass the dormant season.
Juniperus sabina (savin juniper) is the main primary (telial) host, but G. sabinae also occurs on Juniperus chinensis and other species in Juniperus sect. Sabinae. The north European Juniperus communis (common juniper) is not a host. The main secondary (aecial) host is Pyrus communis (common pear), but other pear species, such as the ornamental Pyrus calleryana (Bradford pear), are also susceptible. [2] [3]
The native distribution of Gymnosporangium sabinae follows that of Juniperus sabina, a montane shrub with a range extending from southern Europe and the Alps into North Africa and Asia, and Pyrus communis (common pear) with a native range in continental Europe, the Middle East, and western Asia. The fungus has, however, extended its range in Europe as far north as Scandinavia [4] and the British Isles [5] through the frequent use of savin and other junipers as ornamental garden shrubs. Gymnosporangium sabinae has also been reported from North America. [2] Pear rust is a regulated disease in some countries.
Pruning out any infected juniper twigs and branches in winter and early spring can help reduce the spread of G. sabinae. [5] The vulnerable point of the fungus lies in its usual inability once established on a tree to reinfect it. Generally, the fungus must cross over to the opposite tree host. The most direct method of control is to exterminate juniper hosts near pear trees, though spores can travel at least 6 km from one host to another. If there is a chance of infection, spraying pear trees with a fungicide in spring and summer (typically a systemic one that is certified as capable of dealing with rust) may help, although this is often not considered worthwhile.
Gymnosporangium is a genus of heteroecious plant-pathogenic fungi which alternately infect members of the family Cupressaceae, primarily species in the genus Juniperus (junipers), and members of the family Rosaceae in the subfamily Amygdaloideae. The common name cedar-apple rusts has been used for these fungi. According to the Dictionary of the Fungi, there was 57 species in the genus. In 2023, Species Fungorum lists up to 74 species.
A heteroecious parasite is one that requires at least two hosts. The primary host is the host in which the parasite spends its adult life; the other is the secondary host. Both hosts are required for the parasite to complete its life cycle. This can be contrasted with an autoecious parasite which can complete its life cycle on a single host species. Many rust fungi have heteroecious life cycles:
Rusts are fungal plant pathogens of the order Pucciniales causing plant fungal diseases.
Juniperus sabina, the savin juniper or savin, is a species of juniper native to the mountains of central and southern Europe and western and central Asia, from Spain to eastern Siberia, typically growing at altitudes of 1,000–3,300 metres.
Cronartium ribicola is a species of rust fungus in the family Cronartiaceae that causes the disease white pine blister rust. Other names include: Rouille vésiculeuse du pin blanc pin (French), white pine Blasenrost (German), moho ampolla del pino blanco (Spanish).
Teliospore is the thick-walled resting spore of some fungi, from which the basidium arises.
Anders Sandøe Ørsted, also written as Anders Sandoe Oersted or Anders Sandö Örsted was a Danish botanist, mycologist, zoologist and marine biologist. He was the nephew of physicist Hans Christian Ørsted and of politician Anders Sandøe Ørsted.
Gymnosporangium globosum is a fungal plant pathogen that causes cedar-hawthorn rust.
Gymnosporangium juniperi-virginianae is a plant pathogen that causes cedar-apple rust. In virtually any location where apples or crabapples (Malus) and Eastern red cedar coexist, cedar apple rust can be a destructive or disfiguring disease on both the apples and cedars. Apples, crabapples, and eastern red cedar are the most common hosts for this disease. Similar diseases can be found on Quince and hawthorn and many species of juniper can substitute for the eastern red cedars.
Puccinia schedonnardii is a basidiomycete fungus that affects cotton. More commonly known as a “rust,” this pathogen typically affects cotton leaves, which can decrease the quality of the boll at time of harvest. As large percentages of cotton in the United States are resistant to various rust varieties, there is little economic importance to this disease. In places where rust is prevalent, however, growers could see up to a 50% reduction in yield due to rust infection.
Puccinia coronata is a plant pathogen and causal agent of oat and barley crown rust. The pathogen occurs worldwide, infecting both wild and cultivated oats. Crown rust poses a threat to barley production, because the first infections in barley occur early in the season from local inoculum. Crown rusts have evolved many different physiological races within different species in response to host resistance. Each pathogenic race can attack a specific line of plants within the species typical host. For example, there are over 290 races of P. coronata. Crops with resistant phenotypes are often released, but within a few years virulent races have arisen and P. coronata can infect them.
Puccinia helianthi is a macrocyclic and autoecious fungal plant pathogen that causes rust on sunflower. It is also known as "common rust" and "red rust" of sunflower.
Uromyces viciae-fabae var. viciae-fabae is a plant pathogen commonly known as faba-bean rust. The rust is distinguished by the typical rust-like marks on the stem and leaves, causing defoliation and loss of photosynthetic surface along with reduction in yield. The disease is fungal and is autoecious meaning it has one plant host. The rust of faba beans is macrocyclic, or contains 5 spores during its life cycle.
Telium, plural telia, are structures produced by rust fungi as part of the reproductive cycle. They are typically yellow or orange drying to brown or black and are exclusively a mechanism for the release of teliospores which are released by wind or water to infect the alternate host in the rust life-cycle. The telial stage provides an overwintering strategy in the life cycle of a parasitic heteroecious fungus by producing teliospores; this occurs on cedar trees. A primary aecial stage is spent parasitizing a separate host plant which is a precursor in the life cycle of heteroecious fungi. Teliospores are released from the telia in the spring. The spores can spread many kilometers through the air, however most are spread near the host plant.
Gymnosporangium clavariiforme is a species of rust fungus which alternately infects Juniperus and hawthorns.
Phomopsisblight of juniper is a foliar disease discovered in 1917 caused by the fungal pathogen Phomopsis juniperovora. The fungus infects new growth of juniper trees or shrubs, i.e. the seedlings or young shoots of mature trees. Infection begins with the germination of asexual conidia, borne from pycnidia, on susceptible tissue, the mycelia gradually move inwards down the branch, and into the main stem. Management strategies mainly include removing and destroying diseased tissue and limiting the presence of moisture on plants. Junipers become resistant to infection as they mature and the young yellow shoots turn dark green. Preventive strategies include planting only resistant varieties and spraying new growth with fungicide until plants have matured.
Pine-pine gall rust, also known as western gall rust, is a fungal disease of pine trees. It is caused by Endocronartium harknessii, an autoecious, endocyclic, rust fungus that grows in the vascular cambium of the host. The disease is found on pine trees with two or three needles, such as ponderosa pine, jack pine and scots pine. It is very similar to pine-oak gall rust, but its second host is another Pinus species. The fungal infection results in gall formation on branches or trunks of infected hosts. Gall formation is typically not detrimental to old trees, but has been known to kill younger, less stable saplings. Galls can vary from small growths on branch extremities to grapefruit-sized galls on trunks.
Spruce broom rust or yellow witches' broom rust is a fungal plant disease caused by the basidiomycete fungus known as Chrysomyxa arctostaphyli. It occurs exclusively in North America, with the most concentrated outbreaks occurring in northern Arizona and southern Colorado on blue and Engelmann spruce, as well as in Alaska on black and white spruce. This disease alternates its life cycle between two hosts, with the spruce serving as the primary host and bearberry serving as the secondary or alternate host. The name for the disease comes from the distinctive “witches broom”, commonly yellow in color, which forms on the spruce after young needles have been infected. Management must be carried out through physical or mechanical methods, such as the pruning of brooms or the removal of the secondary host from the area, because no chemical control measures have yet been determined to be economically effective. Generally, spruce broom rust is seen as a mostly cosmetic issue, and it is very rarely the direct cause of tree death; however, research has shown a reduction in overall productivity and health of infected trees, making it an important issue for logging and timber companies.
Phakopsora euvitis is a rust fungus that causes disease of grape leaves. This rust fungus has been seen in regions including: Eastern Asia, Southern Asia, Southwestern Brazil, the Americas, and northern Australia. It is widely distributed in eastern and southern Asia but was first discovered on grapevines in Darwin, Australia in 2001 and was identified as Asian grapevine leaf rust by July 2007.
Cronartium quercuum, also known as pine-oak gall rust is a fungal disease of pine and oak trees. Similar to pine-pine gall rust, this disease is found on pine trees but its second host is an oak tree rather than another pine.