Recent from talks
Nothing was collected or created yet.
Hemileia vastatrix
View on Wikipedia
| Hemileia vastatrix | |
|---|---|
| Symptoms of coffee rust caused by Hemileia vastatrix on foliage | |
| Scientific classification | |
| Kingdom: | Fungi |
| Division: | Basidiomycota |
| Class: | Pucciniomycetes |
| Order: | Pucciniales |
| Family: | Zaghouaniaceae |
| Genus: | Hemileia |
| Species: | H. vastatrix
|
| Binomial name | |
| Hemileia vastatrix | |
| Synonyms | |
|
Wardia vastatrix J.F.Hennen & M.M.Hennen (2003) | |



Hemileia vastatrix is a multicellular basidiomycete fungus of the order Pucciniales (previously also known as Uredinales) that causes coffee leaf rust (CLR), a disease affecting the coffee plant. Coffee serves as the obligate host of coffee rust, that is, the rust must have access to and come into physical contact with coffee (Coffea sp.) in order to survive.
CLR is one of the most economically important diseases of coffee, worldwide.[1] Previous epidemics have destroyed coffee production of entire countries.[2] In more recent history, an epidemic in Central America in 2012 reduced the region's coffee output by 16%.[1]
The primary pathological mechanism of the fungus is a reduction in the plant's ability to derive energy through photosynthesis[3] by covering the leaves with fungus spores and/or causing leaves to drop from the plant.[1] The reduction in photosynthetic ability (plant's metabolism) results in a reduction in quantity and quality of flower and fruit production, which ultimately reduces the beverage quality. [4]
Appearance
[edit]The mycelium with uredinia looks yellow-orange and powdery, and appears on the underside of leaves as points ~0.1 mm in diameter. Young lesions appear as chlorotic or pale yellow spots some millimetres in diameter, the older being a few centimetres in diameter. Hyphae are club-shaped with tips bearing numerous pedicels on which clusters of urediniospores are produced.
Telia are pale yellowish teliospores often produced in uredinia; teliospores more or less spherical to limoniform, 26–40 × 20–30 μm in diameter, wall hyaline to yellowish, smooth, 1 μm thick, thicker at the apex, pedicel hyaline.
Urediniospores are more or less reniform, 26–40 × 18-28 μm, with hyaline to pale yellowish wall, 1–2 μm thick, strongly warted on the convex side, smooth on the straight or concave side, warts frequently longer (3–7 μm) on spore edges.
There have been no known reports of a host capable of supporting an aecial stage of the fungus.[5]
Life cycle
[edit]Hemileia's life cycle begins with the germination of uredospores through germ pores in the spore. It mainly attacks the leaves and is only rarely found on young stems and fruit. Appressoria are produced, which in turn produce vesicles, from which entry into the substomatal cavity is gained. Within 24–48 hours, infection is completed. After successful infection, the leaf blade is colonized and sporulation will occur through the stomata. One lesion produces 4–6 spore crops over a 3–5 month period releasing 300–400,000 spores.
There is currently no known alternate host nor reported cases of infection by basidiospores of H. vastatrix, yet the fungus is able to overcome resistance by plants and scientists do not know exactly how.[5] The predominant hypothesis is that H. vastatrix is heteroecious, completing its life cycle on an alternate host plant which has not yet been found.[5] An alternative hypothesis is that H. vastatrix actually represents an early-diverging autoecious rust, in which the teliospores are non-functional and vestigial, and the sexual life cycle is completed by the urediniospores. Hidden meiosis and sexual reproduction (cryptosexuality)[6] have been found within the generally asexual urediniospores.[7] This finding may explain why new physiological races have arisen so often and so quickly in H. vastatrix.
Control
[edit]Recent studies and research papers have shown that CLR is under-researched compared to pathogens of other cash crops and that there are many factors that can influence the incidence and severity of the disease. Therefore, an integrated approach that includes genetic, chemical, and cultural controls is the best course of action.
Resistant cultivars
[edit]The most effective and durable strategy against CLR is the use of resistant cultivars.[8][9] This has a number of benefits beyond disease control and can include the reduction in use of agrochemicals as control.[8][4] A reduction in chemical application also has positive economic effects for farmers by reducing the cost of production. However, in lieu of deploying new, resistant plant stock, or in the interim between initiation of a renewal program and complete renewal, other methods of control are available.
Professional research and breeding programs such as CIRAD are developing F1 hybrid coffee trees such as Starmaya that have broad genetic resistance to CLR as well as good yield and cup quality, with research showing that F1 hybrids have higher yields and cup quality than conventional Coffea arabica cultivars.[10] Research is also being done on how to democratize the use of F1 hybrids by smallholder coffee farmers who too often can not afford to utilize F1 hybrids.[11] For example, Starmaya is the first F1 hybrid coffee tree that can be propagated in a seed garden rather than the more complicated and expensive process of somatic embryogenesis. [11]
Chemicals
[edit]There are social, environmental, and economic concerns associated with any chemical control of plant diseases and some of these have a more direct and immediate impact than others on a farmer's decision to use chemicals. The use of chemicals must first and foremost make economic sense, and the cost of their use can be as much as 50% of the total cost of production.[8] For smallholder farmers, this can be cost-prohibitive. Copper-based fungicides, such as Bordeaux mixture, have proven to be effective and economical, and work best when applied at inoculum levels below 10%.[3][12]
Typically copper-based mixtures are used as preventative measures and systemic fungicides are used as curative measures.[8]
By reducing disease incidence, chemical control can help mitigate the reduction in fruit quality and quantity that is caused by the disease.[4]
Cultural
[edit]The extended presence of water on the leaves allows H vastatrix to infect the plant more easily and therefore cultural methods can be directed at reducing the time and the amount of water that remains on leaves. Cultural methods such as pruning branches to allow more air circulation and light penetration can help dry the moisture on the leaves. Increasing spacing between rows and preventing weed growth also allows for more air circulation and light penetration.[3]
Plant nutrition
[edit]The correct amount of plant nutrients can also play a role in host resistance.[13] Adequate nutrition allows the plant's natural, biochemical defenses to perform at optimal levels.[13] For example, nitrogen and potassium are two critical, macronutrients that assist a coffee tree to resist infection. Nitrogen is a critical component of chlorophyll, which is central to photosynthesis. Potassium helps to increase the thickness of a leaf's epidermis, which acts as a barrier to pathogen attack. It also aids in recovery of tissues after an attack by H. vastatrix.[13]
Pruning
[edit]Experiments have shown that removal of infected leaves can possibly reduce the final amount of the disease by a significant amount.[3]
Fruit thinning
[edit]Fruit thinning combined with chemical application (cyproconazole and epoxiconazole for example) can increase effective control.[14]
Shade
[edit]There is a complex interaction between shade, meteorological effects such as rainfall or dry periods, and aerial dispersal of rust.[1] Researchers have found that shade may suppress spore dispersal under dry conditions but assist spore dispersal during wet conditions.[1] The researchers acknowledge the need for further research on the topic.
Ecology
[edit]Hemileia vastatrix is an obligate parasite that lives mainly on the plants of genus Coffea but is also capable of invading Arabidopsis thaliana but does not develop haustoria.[15]
The rust needs suitable temperatures to develop (between 16 °C and 28 °C).[16] High altitude plantations are generally colder, so inoculum will not develop as easily as in plantations located in warmer regions. The presence of free water is required for infection to be completed. Loss of moisture after germination starts inhibits the whole infection process.
Sporulation is most influenced by temperature, humidity, and host resistance. The colonization process is not dependent on leaf wetness but is influenced greatly by temperature and by plant resistance. The main effect of temperature is to determine the length of time for the colonization process (incubation period).
Hemileia vastatrix has two fungal parasites, Verticillium haemiliae and Verticillium psalliotae.
The fungus is of East African origin, but is currently endemic to all producing regions.[17]: 171–2 Coffee originates in high altitude regions of Ethiopia, Sudan, and Kenya, and the rust pathogen is believed to have originated in the same mountains. The earliest reports of the disease hail from the 1860s. It was reported first by a British explorer from regions of Kenya around Lake Victoria in 1861, from where it is believed to have spread to Asia and the Americas.
Rust was first reported in the major coffee growing regions of Sri Lanka (then called Ceylon) in 1867. The causal fungus was first fully described by the English mycologist Michael Joseph Berkeley and his collaborator Christopher Edmund Broome after an analysis of specimens of a "coffee leaf disease" collected by George H.K. Thwaites in Ceylon. Berkeley and Broome named the fungus Hemileia vastatrix, "Hemileia" referring to the half smooth characteristic of the spores and "vastatrix" for the devastating nature of the disease.[18]
It is unknown exactly how the rust reached Ceylon from Ethiopia. Over the years that followed, the disease was recorded in India in 1870, Sumatra in 1876, Java in 1878, and the Philippines in 1889. During 1913 it crossed the African continent from Kenya to the Congo, where it was found in 1918, before spreading to West Africa, the Ivory Coast (1954), Liberia (1955), Nigeria (1962–63) and Angola (1966).
Uredospores are disseminated across long distances mainly by wind and can end up thousands of miles from where they were produced. Over short distances, uredospores are disseminated by both wind and rain splash.[19] Other agents, such as animals, mainly insects and contaminated equipment, occasionally have been shown to be involved with dissemination.
Pathogenesis
[edit]Hemileia vastatrix affects the plant by covering part of the leaf surface area or inducing defoliation, both resulting in a reduction in the rate of photosynthesis.[3] Because berry yield is generally linked to the amount of foliage, a reduction in photosynthesis and more importantly, defoliation can affect yield.[3] Continuous colonization of the pathogen depletes the plants resources for surviving until the plant no longer has enough energy to grow or survive.[20]
Coffee plants bred for resistance succeed because of cytological and biochemical resistance mechanisms. Such mechanisms involve transmitting signals to the infection site to stop cell function. The plants' cell degradation response frequently occurs after the formation of the first haustorium and results in rapid hypersensitive cell death. Because Hemileia vastatrix is an obligate parasite, it can no longer survive when surrounded by dead cells. This can be recognized by the presence of browning cells in local regions on a leaf.[21]
Environment
[edit]Temperature and moisture specifically play the largest role in infection rate of the coffee plant. Humidity is not enough to allow infection to occur. There must be a presence of water on the leaf for the urediospores to infect, although dry urediospores can survive up to six weeks without water. Dispersal happens primarily by wind, rain, or a combination of both. Transmission over large distances is likely the result of human intervention by spores clinging to clothes, tools, or equipment. Dispersal by insects is unlikely and therefore insignificant.[22] Spore germination only happens when the temperature is 13–31 °C (55–88 °F), and peaks at 21 °C (70 °F); furthermore. Appressorium formation is highest at 11 °C (52 °F) and has a linear decline in production until 32 °C (90 °F), when there is little to no production.[23] Although temperature and moisture are key factors for infection, dispersal, and colonization, plant resistance is also important in determining whether Hemileia vastatrix will survive.
History
[edit]
The disease coffee leaf rust (CLR) was first described and named by Berkley and Broom in the November 1869 edition of the Gardeners Chronicle.[17]: 171 They used specimens sent from Sri Lanka, where the disease was already causing enormous damage to productivity. Many coffee estates in Sri Lanka were forced to collapse or convert their crops to alternatives not affected by CLR, such as tea.[17]: 171–2 The planters nicknamed the disease "Devastating Emily"[24] and it affected Asian coffee production for over twenty years.[25] By 1890, the coffee industry in Sri Lanka was nearly destroyed, although coffee estates still exist in some areas. Historians suggest that the devastated coffee production in Sri Lanka is one of the reasons why Britons have come to prefer tea, as Sri Lanka switched to tea production as a consequence of the disease.[26]
By the 1920s CLR was widely found across much of Africa and Asia, as well as Indonesia and Fiji. It reached Brazil in 1970 and from there it rapidly spread at a rate enabling it to infect all coffee areas in the country by 1975.[17]: 171–2 From Brazil, the disease spread to most coffee-growing areas in Central and South America by 1981, hitting Costa Rica and Colombia in 1983.
As of 1990, coffee rust has become endemic in all major coffee-producing countries.[17]: 171–2
2012 coffee leaf rust epidemic
[edit]In 2012, there was a major increase in coffee rust across ten Latin American and Caribbean countries. The disease became an epidemic and the resulting crop losses led to a fall in supply, outstripping demand. Coffee prices rose as a result, although other factors such as growing demand for gourmet beans in China, Brazil, and India also contributed.[27][28]
USAID estimates that between 2012 and 2014, CLR caused $1 billion in damage and affected over 2 million people in Latin America.[29]
The reasons for the epidemic remain unclear but an emergency rust summit meeting in Guatemala in April 2013 compiled a long list of shortcomings. These included a lack of resources to control the rust, the dismissal of early warning signs, ineffective fungicide application techniques, lack of training, poor infrastructure and conflicting advice. In a keynote talk at the "Let's Talk Roya" meeting (El Salvador, November 4, 2013), Dr Peter Baker, a senior scientist at CAB International, raised several key points regarding the epidemic including the proportional lack of investment in research and development in such a high value industry and the lack of investment in new varieties in key coffee producing countries such as Colombia.[18]
Typical coffee cultivars maintained by farmers before the epidemic included Caturra, Bourbon, Mundo Novo, and Typica,[29] all of which are susceptible to H. vastatrix. Also before the epidemic of 2012, 82% of farms were certified organic,[29] which limits the agrochemicals farmers can use. However, there are a number of fungicides that can be used in certified organic systems, such as copper-based Bordeaux mix as well as commercial mixtures.[30]
Honduras
[edit]During this period, Honduras experienced a significant epidemic of CLR. 80,000 hectares of coffee farms were infected and The Honduran National Institute of Coffee (IHCAFE) estimates that 30,000 farmers lost over half of their coffee production capacity and a third of those—10,000 farmers—suffered a complete loss of coffee production capacity.[31] Roughly 84% of coffee producers in Honduras are smallholders[31] and are therefore more vulnerable to loss of production than estate farmers.
Further
[edit]Coffee crops in Guatemala have been ruined by coffee rust, and a state of emergency has been declared in February 2013.[32][33]
CLR has been a problem in Mexico.[34][35]
CLR disease is a big problem in coffee plantations in Peru, declared in sanitary emergency by government (Decreto Supremo N° 082-2013-PCM).
In late October 2020, USDA ARS detected rust on Maui. Immediately the Hawaii Department of Agriculture began inspections around the state, not just on Maui itself. They initially found plants they suspect to also be infected in Hilo on the big island, however these plants tested negative to CLR, though it was detected on plants in the Kailua-Kona region of the island.[36][37][38] In January, 2021, additional infections have been found on the islands of Oahu and Lanai, and plant quarantines have gone into effect as of March 2021 for interisland transport of coffee plants or parts between the four islands that CLR has been found on.[39]
Economic impact
[edit]Coffee leaf rust (CLR) has direct and indirect economic impacts on coffee production. Direct impacts include decreased quantity and quality of yield produced by the diseased plant and the cost of inputs meant specifically to control the disease.[40] Indirect impacts include increased costs to combat and control the disease. Methods of combating and controlling the disease include fungicide application and stumping diseased plants and replacing them with resistant breeds. Both methods include significant labor and material costs and in the case of stumping, include a years-long decline in production (coffee seedlings are not fully productive for three to five years after planting).
Due to the complexity of accurately accounting for losses attributed to CLR, there are few records quantifying yield losses. Estimates of yield loss vary by country and can range anywhere between 15 and 80%. Worldwide loss is estimated at 15%.[17]: 174
Some early data from Ceylon documenting the losses in the late 19th century indicate coffee production was reduced by 75%. As farmers shifted from coffee to other crops not affected by CLR,[40] land used for growing coffee was reduced by 80%, from 68,787 to 14,170 ha.[17]: 174
In addition to the costs mentioned above, additional costs include research and development costs in producing resistant cultivars. These costs are normally borne by the industry, local and national governments and international aid agencies.[17]: 174 [40]
Colombia's National Federation of Coffee Growers (Fedecafe) set up a research lab specifically designed to find ways to stop the disease, as the country is a leading exporter of the Coffea arabica bean that is particularly prone to the disease.[26]
References
[edit]- ^ a b c d e Boudrot, Audrey; Pico, Jimmy; Merle, Isabelle; Granados, Eduardo; Vílchez, Sergio; Tixier, Philippe; Filho, Elías de Melo Virginio; Casanoves, Fernando; Tapia, Ana; Allinne, Clémentine; Rice, Robert A.; Avelino, Jacques (June 2016). "Shade Effects on the Dispersal of Airborne Hemileia vastatrix Uredospores". Phytopathology. 106 (6): 572–580. doi:10.1094/PHYTO-02-15-0058-R. ISSN 0031-949X. PMID 26828230.
- ^ "Coffee Rust Threatens Latin American Crop; 150 Years Ago, It Wiped Out An Empire". NPR.org. Retrieved 2018-10-16.
- ^ a b c d e f Kushalappa AC (2017). Coffee Rust. Milton: CRC Press LLC. ISBN 978-1-351-07922-8. OCLC 1111510163.
- ^ a b c Pereira, Dyanna R; Nadaleti, Denis HS; Rodrigues, Eduardo C; Silva, Ackson D; Malta, Marcelo R; Carvalho, Samuel P; Carvalho, Gladyston R (May 2021). "Genetic and chemical control of coffee rust (Hemileia vastatrix Berk et Br.): impacts on coffee (Coffea arabica L.) quality". Journal of the Science of Food and Agriculture. 101 (7): 2836–2845. Bibcode:2021JSFA..101.2836P. doi:10.1002/jsfa.10914. ISSN 0022-5142. PMID 33135174. S2CID 226234213. Retrieved 2021-05-01.
- ^ a b c Koutouleas A, Jørgen Lyngs Jørgensen H, Jensen B, Lillesø JB, Junge A, Ræbild A (December 2019). "On the hunt for the alternate host of Hemileia vastatrix". Ecology and Evolution. 9 (23): 13619–13631. doi:10.1002/ece3.5755. PMC 6912922. PMID 31871671.
- ^ Carvalho, Carlos Roberto; Fernandes, Ronaldo C.; Carvalho, Guilherme Mendes Almeida; Barreto, Robert W.; Evans, Harry C. (2011-11-15). "Cryptosexuality and the Genetic Diversity Paradox in Coffee Rust, Hemileia vastatrix". PLOS ONE. 6 (11). Kirsten Nielsen (ed.): –26387. Bibcode:2011PLoSO...626387C. doi:10.1371/journal.pone.0026387. ISSN 1932-6203. PMC 3216932. PMID 22102860.
- ^ Carvalho CR, Fernandes RC, Carvalho GM, Barreto RW, Evans HC (2011). "Cryptosexuality and the genetic diversity paradox in coffee rust, Hemileia vastatrix". PLOS ONE. 6 (11) e26387. Bibcode:2011PLoSO...626387C. doi:10.1371/journal.pone.0026387. PMC 3216932. PMID 22102860.
- ^ a b c d Talhinhas, Pedro; Batista, Dora; Diniz, Inês; Vieira, Ana; Silva, Diogo N.; Loureiro, Andreia; Tavares, Sílvia; Pereira, Ana Paula; Azinheira, Helena G.; Guerra-Guimarães, Leonor; Várzea, Vítor; Silva, Maria do Céu (October 2017). "The coffee leaf rust pathogen Hemileia vastatrixone and a half centuries around the tropics: Coffee leaf rust caused by Hemileia vastatrix". Molecular Plant Pathology. 18 (8): 1039–1051. doi:10.1111/mpp.12512. ISSN 1464-6722. PMC 6638270. PMID 27885775.
- ^ Talhinhas, Pedro; Batista, Dora; Diniz, Inês; Vieira, Ana; Silva, Diogo N.; Loureiro, Andreia; Tavares, Sílvia; Pereira, Ana Paula; Azinheira, Helena G.; Guerra-Guimarães, Leonor; Várzea, Vítor; Silva, Maria do Céu (October 2017). "The coffee leaf rust pathogen Hemileia vastatrix: one and a half centuries around the tropics: Coffee leaf rust caused by Hemileia vastatrix". Molecular Plant Pathology. 18 (8): 1039–1051. doi:10.1111/mpp.12512. ISSN 1464-6722. PMC 6638270. PMID 27885775.
- ^ Marie, Lison; Abdallah, Cécile; Campa, Claudine; Courtel, Philippe; Bordeaux, Mélanie; Navarini, Luciano; Lonzarich, Valentina; Bosselmann, Aske Skovmand; Turreira-García, Nerea; Alpizar, Edgardo; Georget, Frédéric (2020-04-20). "G × E interactions on yield and quality in Coffea arabica: new F1 hybrids outperform American cultivars". Euphytica. 216 (5): 78. doi:10.1007/s10681-020-02608-8. ISSN 1573-5060.
- ^ a b Georget, Frédéric; Marie, Lison; Alpizar, Edgardo; Courtel, Philippe; Bordeaux, Mélanie; Hidalgo, Jose Martin; Marraccini, Pierre; Breitler, Jean-christophe; Déchamp, Eveline; Poncon, Clément; Etienne, Hervé; Bertrand, Benoit (2019-10-22). "Starmaya: The First Arabica F1 Coffee Hybrid Produced Using Genetic male-sterility". Frontiers in Plant Science. 10: 1344. doi:10.3389/fpls.2019.01344. ISSN 1664-462X. PMC 6818232. PMID 31695719.
- ^ Zambolim, Laercio; Cecon, Paulo (2011). "Chemical approaches to manage coffee leaf rust in drip irrigated trees". Australasian Plant Pathology. 40 (3): 293–300. doi:10.1007/s13313-011-0046-x. S2CID 21988025.
- ^ a b c Pérez, Cristian D. P.; Pozza, Edson A.; Pozza, Adélia A. A.; de Freitas, Aurivan S.; Silva, Marilia G.; da Silva Gomes Guimarães, Daniel (September 2019). "Impact of nitrogen and potassium on coffee rust". European Journal of Plant Pathology. 155 (1): 219–229. doi:10.1007/s10658-019-01765-4. ISSN 1573-8469. S2CID 182722366. Retrieved 2021-04-09.
- ^ Echeverria-Beirute, Fabian; Murray, Seth C.; Klein, Patricia; Kerth, Chris; Miller, Rhonda; Bertrand, Benoit (2018-05-30). "Rust and Thinning Management Effect on Cup Quality and Plant Performance for Two Cultivars of Coffea arabica L". Journal of Agricultural and Food Chemistry. 66 (21): 5281–5292. doi:10.1021/acs.jafc.7b03180. ISSN 1520-5118. PMID 28899100. Retrieved 2021-04-09.
- ^ Periyannan S, Milne RJ, Figueroa M, Lagudah ES, Dodds PN (July 2017). Zipfel C (ed.). "An overview of genetic rust resistance: From broad to specific mechanisms". PLOS Pathogens. 13 (7) e1006380. doi:10.1371/journal.ppat.1006380. PMC 5509339. PMID 28704545.
- ^ Compendium of coffee diseases and pests. Gaitán, Alvaro León. St. Paul, Minnesota. 2015. ISBN 978-0-89054-472-3. OCLC 1060617649.
{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: others (link) - ^ a b c d e f g h Waller JM, Bigger M, Hillocks RJ (2007). Coffee Pests, Diseases & Their Management. CABI. ISBN 978-1-84593-129-2.
- ^ a b "PlantVillage". Archived from the original on 27 June 2015. Retrieved 30 August 2016.
- ^ McCook, Stuart (July 2006). "Global rust belt: Hemileia vastatrix and the ecological integration of world coffee production since 1850". Journal of Global History. 1 (2): 177–195. doi:10.1017/S174002280600012X. ISSN 1740-0228.
- ^ Soque N (2019-04-22). "How to Monitor For & Prevent Coffee Leaf Rust". Perfect Daily Grind. Retrieved 2019-12-11.
- ^ Silva MD, Várzea V, Guerra-Guimarães L, Azinheira HG, Fernandez D, Petitot AS, et al. (2006). "Coffee resistance to the main diseases: Leaf rust and coffee berry disease". Brazilian Journal of Plant Physiology. 18: 119–147. doi:10.1590/s1677-04202006000100010.
- ^ Arneson PA (2000). "Coffee rust". The Plant Health Instructor. doi:10.1094/PHI-I-2000-0718-02.
- ^ Bebber DP, Castillo ÁD, Gurr SJ (December 2016). "Modelling coffee leaf rust risk in Colombia with climate reanalysis data". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 371 (1709) 20150458. doi:10.1098/rstb.2015.0458. PMC 5095537. PMID 28080984.
- ^ Watson M (10 May 2008). "Why Sri Lanka Is Everyone's Cup of Tea". Western Mail (Cardiff, Wales).[dead link]
- ^ Steiman S. "Hemileia vastatrix". Coffee Research.org. Retrieved April 25, 2009.
- ^ a b Penarredonda J. "The disease that could change how we drink coffee". Retrieved 2017-12-05.
- ^ Kollewe J (2011-04-21). "Coffee prices expected to rise as a result of poor harvests and growing demand". The Guardian. ISSN 0261-3077. Retrieved 2017-12-05.
- ^ "Coffee Price Increase 2011-2012 – Coffee Prices – Coffee Shortage Due to Emerging Markets". Gourmetcoffeelovers. Archived from the original on 2019-07-14. Retrieved 2017-12-05.
- ^ a b c Valencia V, García-Barrios L, Sterling EJ, West P, Meza-Jiménez A, Naeem S (2018-12-01). "Smallholder response to environmental change: Impacts of coffee leaf rust in a forest frontier in Mexico". Land Use Policy. 79: 463–474. doi:10.1016/j.landusepol.2018.08.020. ISSN 0264-8377. S2CID 158795669.
- ^ Beckerman J, Botany P (April 2008). "Using Organic Fungicides". Disease Management Strategies (BP-69-W): 4.
- ^ a b Ward R, Gonthier D, Nicholls C (2017-06-30). "Ecological resilience to coffee rust: Varietal adaptations of coffee farmers in Copán, Honduras". Agroecology and Sustainable Food Systems: 1–18. doi:10.1080/21683565.2017.1345033. ISSN 2168-3565. S2CID 157836251.
- ^ "Guatemala's coffee rust 'emergency' devastates crops". BBC News. 9 February 2013. Retrieved 30 August 2016.
- ^ Guatemala declares national coffee emergency February 08, 2013 BusinessWeek
- ^ Saliba F (26 March 2013). "Coffee rust plagues farmers in Mexico" – via CBS News.
- ^ Avelino, Jacques; Cristancho, Marco; Georgiou, Selena; Imbach, Pablo; Aguilar, Lorena; Bornemann, Gustavo; Läderach, Peter; Anzueto, Francisco; Hruska, Allan J.; Morales, Carmen (2015-04-01). "The coffee rust crises in Colombia and Central America (2008–2013): impacts, plausible causes and proposed solutions". Food Security. 7 (2): 303–321. doi:10.1007/s12571-015-0446-9. hdl:10568/57487. ISSN 1876-4525.
- ^ Ruminski L (2020-10-30). "Coffee leaf rust hits Hawaii Island". Hawaii Tribune-Herald. Retrieved 2020-11-05.
- ^ "Department of Agriculture News Release: Coffee Leaf Rust Confirmed on Maui and Tentatively Found on Hawaiʻi Island". David Y. Ige Governor's Office. 2020-10-30. Retrieved 2020-11-05.
- ^ "Coffee Leaf Rust Confirmed on Hawaiʻi Island". hdoa.hawaii.gov. Retrieved 2021-05-12.
- ^ "Board of Agriculture Expands Coffee Quarantine to O'ahu and Lana'i". hdoa.hawaii.gov. Retrieved 2021-05-12.
- ^ a b c McCook, Stuart; Vandermeer, John (September 2015). "The Big Rust and the Red Queen: Long-Term Perspectives on Coffee Rust Research". Phytopathology. 105 (9): 1164–1173. doi:10.1094/PHYTO-04-15-0085-RVW. ISSN 0031-949X. PMID 26371395.
External links
[edit]- Hemileia vastatrix description at Plantvillage.com
- Coffee Research Institute: Coffee rust
- University of Nebraska-Lincoln: Coffee rust
- The University of Hawaii page on Hemileia vastatrix [1]
- U.S.Dept.Agriculture page on Coffee Leaf Rust [2]
Hemileia vastatrix
View on GrokipediaTaxonomy
Classification
Hemileia vastatrix belongs to the kingdom Fungi, phylum Basidiomycota, subphylum Pucciniomycotina, class Pucciniomycetes, order Pucciniales, family Zaghouaniaceae, genus Hemileia, and species vastatrix.[8] Phylogenetically, H. vastatrix is placed within the Pucciniomycotina subphylum, representing an early-diverging lineage among rust fungi in the order Pucciniales.[1] It is closely related to other rust genera such as Puccinia but distinguished by molecular analyses that confirm its position in the Zaghouaniaceae family, a classification updated from earlier assignments to families like Pucciniaceae or Chaconiaceae based on multi-locus phylogenetic studies.[9] Taxonomically, H. vastatrix is classified as a hemicyclic rust fungus, characterized by the production of urediniospores, teliospores, and basidiospores, but lacking aeciospores and pycniospores—traits that differentiate it from macrocyclic rusts with complete five-stage cycles.[1]Nomenclature
Hemileia vastatrix was originally described and named by the British mycologists Miles Joseph Berkeley and Christopher Edmund Broome in 1869, based on specimens collected from diseased coffee leaves in Ceylon (present-day Sri Lanka). The description appeared in the Gardeners' Chronicle, marking the first formal recognition of the fungus as the causal agent of coffee leaf rust.[10][11] The genus name Hemileia is derived from Greek roots: hemi- meaning "half" and leia meaning "smooth," alluding to the urediniospores' characteristic partial smoothness, where the ventral side lacks the echinulate (spiny) ornamentation seen on the dorsal side. The specific epithet vastatrix comes from Latin, translating to "destroyer" or "devastator," a term Berkeley selected to underscore the fungus's potential for widespread devastation to coffee crops.[12][13] No major synonyms exist for H. vastatrix in contemporary nomenclature, reflecting its stable taxonomic status since its initial description. Historically, the species was classified within the order Uredinales, the traditional grouping for rust fungi; however, modern phylogenetic revisions have reclassified it under Pucciniales.[10][14]Description
Macroscopic Appearance
The macroscopic appearance of Hemileia vastatrix on infected coffee plants is characterized by distinct fungal structures and host responses visible to the naked eye. Initial signs manifest as small, chlorotic (yellowish) spots, typically 2-3 mm in diameter, on the upper surfaces of leaves, often starting near the leaf margins or veins. These spots correspond to underlying fungal activity and expand over time, sometimes coalescing into larger lesions up to several centimeters across in advanced infections.[15][16] On the lower (abaxial) leaf surfaces, the pathogen produces uredinia, which appear as raised, powdery, orange-yellow pustules measuring approximately 0.3-1 mm in diameter. These structures are densely packed, bouquet-shaped clusters of urediniospores that erupt through the stomata, giving a vibrant, powdery texture that can be easily rubbed off, releasing spores. In moderate to severe infections, numerous uredinia cover the leaf underside, creating a characteristic rusty appearance.[16][1][3] As the disease progresses, chlorotic spots on the upper leaf surface may develop necrotic (brown, dead) centers, leading to leaf yellowing, premature senescence, and eventual defoliation, particularly on lower branches. In rare cases, telia form on the leaf undersides in later stages, appearing as darker, crust-like or pale yellowish patches within or replacing uredinia, though they are infrequently observed and do not produce prominent new structures. Severe epidemics can result in widespread leaf drop, stripping trees and reducing canopy density.[16][13][1]Microscopic Features
The urediniospores of Hemileia vastatrix, the primary asexual propagules responsible for disease spread, are typically reniform to oval in shape, with dimensions ranging from 28–36 μm in length and 18–28 μm in width, averaging approximately 32 × 23 μm. Morphological variations, including size differences, have been observed across geographic regions and host cultivars.[17][18] These spores are hyaline to pale yellowish, featuring a thin wall approximately 1.0 μm thick composed of a double-layered structure, with the outer layer exhibiting echinulate ornamentation—warty protuberances covered by a mucilage-like matrix, particularly pronounced on the convex surface and ventral margins.[18][19][3] They possess multiple germ pores, typically 4 in number and positioned equatorially, enabling the extrusion of germ tubes during germination.[20] Teliospores of H. vastatrix, which represent the sexual stage and are less commonly observed, are two-celled, pedicellate structures borne on teliosporophores emerging through host stomata.[21] These spores are approximately 20–28 μm in diameter, with a smooth surface, thick hyaline walls, and a napiform to spherical shape often featuring a terminal papilla.[22][23] Their pedicel attachment and robust wall contribute to dormancy, allowing in situ germination to produce a promycelium with basidiospores.[22] The vegetative phase of H. vastatrix involves dikaryotic hyphae, each cell containing paired nuclei of opposite mating types, which ramify intercellularly within coffee leaf mesophyll tissues to facilitate colonization.[1] Specialized intracellular haustoria arise from haustorial mother cells, penetrating host mesophyll cells while enclosed by an extrahaustorial membrane derived from the host plasmalemma; these structures, with necks featuring a distinctive ring and bodies containing tubular complexes, enable nutrient absorption essential to the fungus's obligate biotrophic nature.[1][24] Ultrastructural analyses reveal that haustoria exhibit fibrillar elements in the surrounding sheath, aiding in material uptake without immediate host cell death.[24]Life Cycle
Spore Stages
Hemileia vastatrix exhibits a hemicyclic life cycle, characterized by the absence of pycnial and aecial stages typical in macrocyclic rust fungi, relying primarily on an urediniosporic cycle supplemented by a potential sexual phase via teliospores.[21] This reduced cycle allows the pathogen to complete its reproduction solely on the coffee host, Coffea species, without requiring an alternate host for the missing stages.[1] The hemicyclic nature streamlines dispersal and infection, with urediniospores serving as the dominant propagule for epidemic development.[3] Urediniospores are the primary asexual, dikaryotic spores produced in uredinia, which are subepidermal, bouquet-shaped structures forming on the abaxial surfaces of infected coffee leaves.[1] These reniform spores measure 28–36 × 18–28 µm, with a hyaline, warted wall, and germinate rapidly—within 5 hours at 21–29°C in the presence of free water—through germ pores to initiate new infections.[1] As the main source of inoculum, urediniospores are dispersed primarily by wind, enabling long-distance spread, and a single lesion can produce up to 300,000 spores over 3–5 months, sustaining repeated cycles under favorable conditions.[3] Teliospores represent the sexual phase and are rarely observed in nature, forming in telia under cooler, drier conditions, and are two-celled, thick-walled, dikaryotic structures measuring 20–28 µm in diameter with a smooth, hyaline wall.[21] Upon maturation, karyogamy occurs within the teliospore, followed by meiosis during germination, which produces a promycelium (basidium) bearing four haploid basidiospores.[1] These basidiospores are rarely observed in nature and have not been shown to infect coffee, suggesting a vestigial role or potential for an undetected alternate host; teliospores primarily function in overwintering and long-term survival.[21] Unlike typical macrocyclic rusts, no confirmed heteroecious cycle exists for H. vastatrix, with the pathogen maintaining an autoecious lifestyle on coffee.[25]Infection Process
The infection process of Hemileia vastatrix begins with the germination of urediniospores, which requires free water on the leaf surface and occurs optimally at temperatures around 24°C, typically within 3-6 hours under high humidity conditions (20-25°C).[1] Germination proceeds through one or two germ pores, accompanied by heightened metabolic activity involving increased mitochondria and endoplasmic reticulum, leading to the formation of a germ tube that grows toward the nearest stoma.[26] Within 12-17 hours after inoculation, the germ tube differentiates into an appressorium positioned directly over the stoma, where it adheres to the leaf surface via esterase enzymes, preparing for entry without enzymatic degradation of the cuticle.[27] Penetration occurs passively through the open stoma, relying on turgor pressure rather than mechanical force or hydrolytic enzymes, with the penetration hypha extending into the substomatal chamber to form a substomatal vesicle within 24-48 hours.[1] This vesicle serves as the initial infection site, producing haustorial mother cells that penetrate adjacent subsidiary cells. From there, primary hyphae emerge and grow intercellularly through the mesophyll tissue, invading the spongy and palisade parenchyma layers without direct cell wall penetration.[28] Colonization involves the formation of haustoria from haustorial mother cells, which invaginate host mesophyll cell walls to establish nutrient-absorbing connections, becoming visible around 48 hours after inoculation and proliferating extensively by 20 days.[1] This biotrophic phase features intercellular hyphal expansion, allowing the fungus to remain subclinical during an incubation period of approximately 15-25 days, during which initial growth occurs without visible symptoms or sporulation.[29] The latent period, from infection to the onset of sporulation, spans about 20-30 days, culminating in the production of urediniosori through the stomata.[30]Ecology and Distribution
Host Plants
Hemileia vastatrix primarily infects species within the genus Coffea of the Rubiaceae family, with Coffea arabica (Arabica coffee) being the most susceptible host, leading to severe yield losses in commercial plantations. Coffea canephora (Robusta coffee) serves as another key host but exhibits greater resistance due to specific genetic factors, such as the SH6-SH9 genes, which have been utilized in breeding programs to enhance tolerance in hybrid varieties. Although the Coffea genus encompasses over 100 species, extensive testing has shown that H. vastatrix predominantly affects cultivated C. arabica, with limited impact on most wild congeners.[1] The host range of H. vastatrix is restricted to the Rubiaceae family and primarily the Coffea genus, with no confirmed natural infections on wild non-coffee plants outside of experimental conditions. While other Rubiaceae genera like Gardenia have been reported as potential hosts in some surveys, these remain unverified in field settings and do not represent significant reservoirs for the pathogen. This specificity underscores the pathogen's obligate biotrophic lifestyle, tightly linked to coffee physiology.[1][3] Genetic variation in H. vastatrix manifests through over 50 physiological races, such as those designated C1, C2, and C3, which exhibit host specialization by overcoming specific resistance genes in Coffea species. These races, identified via differential host interactions, highlight the pathogen's adaptability within its narrow host spectrum, with certain lineages capable of infecting both C. arabica and C. canephora. Ongoing genomic analyses reveal clonal reproduction dominating these lineages, facilitating persistence on primary hosts.[1][2] Searches for alternate hosts continue, with hypotheses focusing on Rubiaceae relatives like Psychotria mahonii and Rosaceae species such as Rubus apetalus, based on co-occurrence modeling and phylogenetic proximity. However, experimental inoculations and field observations have not confirmed these as viable hosts, suggesting H. vastatrix lacks a confirmed sexual stage or alternate host essential for completing its life cycle beyond Coffea.[21]Geographic Range
Hemileia vastatrix is native to East Africa, with origins traced to regions including Ethiopia, Kenya, and the Great Lakes area.[31] The fungus was first documented outside its native range in Sri Lanka in 1869, marking the beginning of its global dissemination, and by the early 20th century, it had established in major coffee-growing areas across Africa and Asia.[32] Its introduction to the Americas began with Brazil in 1970, followed by rapid spread to other South American countries such as Colombia, Peru, and Venezuela, and into Central America during the 1980s.[3] In Oceania, the pathogen reached Papua New Guinea in 1965 and subsequently spread to other Pacific coffee regions.[3] Today, H. vastatrix is endemic to virtually all coffee-producing regions worldwide, including Africa, Asia, the Americas, and Oceania, with the notable exception of Hawaii until its recent incursion.[33] The fungus invaded Hawaii in 2021, with the outbreak on Maui linked to the MLG10 lineage originating from Central American populations, representing the first confirmed establishment in the islands.[32] In 2024, new physiological races of H. vastatrix were identified in Peruvian coffee fields, highlighting ongoing genetic diversification and potential shifts in local distributions.[5] Dispersal of H. vastatrix occurs through multiple mechanisms, with long-distance spread primarily driven by wind currents carrying urediniospores across continents.[3] Short-distance transmission within fields is facilitated by rain splash, which dislodges spores from infected leaves onto nearby healthy plants.[34] Human-mediated dispersal has played a critical role in historical introductions, often via the transport of infected seedlings or plant material through international trade.[1]Pathogenesis
Disease Symptoms
The initial symptoms of Hemileia vastatrix infection on coffee leaves typically appear 7 to 14 days after spore germination, manifesting as small, irregular chlorotic or pale yellow spots measuring 2-4 mm in diameter on the upper leaf surfaces, often concentrated near the leaf edges or veins.[35][1] These spots result from the host plant's response to fungal penetration and haustoria formation in the mesophyll tissues, without initial necrosis or browning.[1] As the infection progresses over 2-3 weeks, the chlorotic spots enlarge to 5-10 mm, developing into necrotic lesions with yellow halos on the upper surface, while the undersides produce clusters of orange-yellow powdery uredinia containing urediniospores.[35][36] Affected leaves exhibit overall yellowing, followed by premature senescence and drop, particularly in humid conditions that favor spore dispersal.[1][36] Severe infections lead to systemic effects, including widespread defoliation that weakens plant vigor, causes branch dieback, and reduces branching and vegetative growth.[35][36] This defoliation impairs photosynthesis, resulting in yield losses of 20-90% in subsequent seasons, depending on epidemic severity and lack of control measures.[37] The disease is distinguishable from other coffee leaf spots, such as brown leaf spot caused by Cercospora coffeicola, by the characteristic orange powdery uredinia on the leaf undersides, whereas C. coffeicola produces dark brown, shot-hole lesions without such spores.[36][38]Pathogenic Mechanisms
Hemileia vastatrix is an obligate biotrophic fungus that depends entirely on living host cells of coffee plants for its nutrition and survival, unable to complete its life cycle on dead or artificial media.[1] This lifestyle is facilitated by the formation of haustoria, specialized intracellular structures that penetrate mesophyll cells without killing them, establishing a nutrient-absorbing interface surrounded by an extrahaustorial membrane.[1] Through these haustoria, the pathogen extracts sugars, amino acids, and other essential nutrients from the host, modifying the plant's metabolic processes to favor fungal growth while preserving host cell viability during the infection period.[39] The haustoria also serve as sites for the secretion of effector proteins that manipulate host physiology to suppress defense responses.[39] At the physiological level, H. vastatrix infection disrupts coffee plant photosynthesis by degrading chlorophyll content, leading to chlorotic areas that reduce the leaf's photosynthetic capacity by 32–40% in susceptible varieties during advanced infection stages.[40] This degradation, coupled with damage to photosystem II efficiency (evidenced by reduced Fv/Fm ratios to 0.74–0.77), impairs energy production and carbon assimilation.[41] Additionally, the pathogen induces stomatal closure in infected leaves, limiting CO₂ uptake and further exacerbating photosynthetic inhibition as a consequence of altered host signaling and resource diversion to defense.[42] Molecularly, H. vastatrix employs effector proteins, such as HvEC-016, to suppress plant immune responses by interfering with pathogen-associated molecular pattern-triggered immunity and promoting fungal colonization in compatible interactions.[43] These effectors follow a gene-for-gene model, where avirulence effectors are recognized by host resistance (R) genes like SH1, triggering effector-triggered immunity in resistant genotypes, but evading detection in susceptible hosts lacking matching R-genes.[43] Virulence is enhanced by the pathogen's over 55 physiological races, each defined by specific virulence genes (v1–v9) that overcome corresponding R-genes (SH1–SH9) in Coffea arabica, such as race XXXVI defeating SH3-derived resistance introgressed from C. liberica.[39] In contrast, some coffee varieties exhibit polygenic horizontal resistance, involving multiple quantitative trait loci that provide partial, durable protection against multiple races without hypersensitive cell death.[44]Environmental Factors
Climatic Requirements
Hemileia vastatrix, the causal agent of coffee leaf rust, exhibits specific temperature optima for key life cycle stages, including spore germination, infection, and sporulation. Urediniospore germination occurs optimally between 19–23°C, with maximum rates around 22°C, though broader viability extends from 16–28°C; processes are inhibited below 15°C or above 30°C.[45][46] Germ tube growth and appressorium formation, essential precursors to infection, peak at slightly lower temperatures of 19–22°C for growth and 13–16°C for appressoria, with infection favored by a diurnal decline from approximately 23°C to 17°C.[45] Sporulation reaches its maximum at around 22°C, though some studies indicate higher rates near 28°C under field conditions.[46][47] High humidity and leaf wetness are critical for H. vastatrix spore germination and infection, requiring relative humidity above 90%—ideally exceeding 95%—for 6–12 hours to initiate processes.[48][49] Free moisture on leaf surfaces, typically from dew, rain, or fog, is essential for urediniospore germination, which begins after 2–3 hours and completes within 8–24 hours under optimal conditions; continuous wetness of 24–48 hours supports full infection.[50][3] Rain splash facilitates short-distance dispersal of spores, enhancing local epidemic buildup during moist periods.[49] Altitude influences H. vastatrix prevalence, with ideal conditions between 600–1600 m above sea level, where cooler temperatures and higher humidity align with coffee cultivation zones; disease severity declines at higher elevations due to lower temperatures inhibiting development.[51] Dry periods significantly limit epidemics by reducing moisture availability, suppressing germination and sporulation.[52] Seasonally, disease peaks during wet periods when humidity and rainfall promote infection cycles, while dry seasons curtail spread.[53] The fungus survives unfavorable periods primarily as mycelium within living coffee plants or as urediniospores on infected tissues and debris. Teliospores, though rare, have been observed in some regions under cool, dry conditions and may aid survival.[22][54]Influence of Climate Change
Climate change is exacerbating the threat posed by Hemileia vastatrix to coffee production through shifts in temperature and precipitation patterns that favor the pathogen's spread and intensity. Warmer temperatures, projected to rise by 2–2.5°C globally by mid-century according to IPCC assessments, are enabling the fungus to infect coffee plants at higher altitudes, where cooler conditions previously limited its range.[55] Altered rainfall regimes, including more frequent droughts followed by heavy rains, heighten epidemic risks in previously dry regions by stressing host plants and creating optimal wet conditions for spore dispersal.[56] A notable recent example is the 2012 coffee leaf rust epidemic in Central America, which caused harvest reductions of up to 50% across the region, displacing over two million workers and linked to drought-induced host stress combined with warmer nighttime temperatures that accelerated fungal development.[55] In vulnerable areas like East Africa, similar dynamics could amplify yield losses by 30–50%, as rising minimum temperatures during critical growing seasons—projected to increase by 0.63–1.23°C under moderate emissions scenarios—enhance rust prevalence in highland coffee zones.[57] Modeling studies using CMIP6 climate scenarios predict range expansions for H. vastatrix in Latin American countries like Brazil and Colombia, with increased suitability in mid-altitude regions under +2°C warming by 2050, while long-term projections (2081–2100) show mixed outcomes including reduced highly favorable areas in core production zones like Minas Gerais due to excessive heat.[58] In Asia and parts of East Africa, models forecast broader distribution into former highland refuges, diminishing safe elevations for arabica coffee cultivation as the pathogen tracks warming trends.[56] These shifts underscore a contraction of rust-free highlands, potentially displacing traditional coffee farming.[59] Adaptation faces challenges from accelerated pathogen evolution under climate variability, as H. vastatrix demonstrates high evolutionary potential, with new physiological races emerging rapidly to overcome host resistances amid fluctuating conditions.[60] Interactions between environmental stress and the pathogen further complicate responses, as drought-weakened coffee plants exhibit heightened susceptibility, shortening the rust's latent period and amplifying infection rates in tandem with elevated temperatures.[61]History
Discovery and Early Spread
Hemileia vastatrix, the causal agent of coffee leaf rust, was first reported in 1861 on wild Coffea species near Lake Victoria in the Kenya region of East Africa by a British explorer.[3] The pathogen likely originated in this area, where it existed asymptomatically on native coffee plants before the expansion of cultivated arabica coffee (Coffea arabica).[1] In cultivated plantations, the disease was first observed in 1867 in Ceylon (modern-day Sri Lanka), where infected plants had been imported from East Africa.[62] The fungus was formally described in 1869 by Miles Joseph Berkeley and Christopher Edmund Broome as Hemileia vastatrix, named for the half-smooth (hemileia) appearance of its urediniospores and its devastating (vastatrix) impact on coffee.[1] The initial epidemic in Ceylon began in 1869 and rapidly intensified over the following decade, leading to severe defoliation and significant yield losses by the late 1870s.[63] This outbreak destroyed vast tracts of arabica plantations, prompting many growers to abandon coffee cultivation entirely in favor of tea.[49] From Ceylon, the pathogen spread to southern India in 1870 via infected seedlings and trade networks, causing similar widespread damage to emerging coffee estates.[64] By 1879, it had reached Java (modern-day Indonesia), where it devastated highland arabica farms, further illustrating the pathogen's rapid dissemination through colonial planting materials.[65] Throughout the late 19th and early 20th centuries, H. vastatrix moved along colonial trade routes, infecting coffee regions in Sumatra (1876), the Philippines (1889), and across Africa, where it transitioned from unmanaged native hosts to commercial plantations.[65] Early eradication efforts, such as those in Pacific islands like Papua New Guinea during the early 1900s, repeatedly failed due to reinfection from wind-dispersed urediniospores and inadequate quarantine measures.[66] By the 1920s, the fungus was firmly established across major Asian and African coffee-growing areas, with initial responses including ineffective quarantines and a gradual shift toward more rust-tolerant robusta coffee (Coffea canephora) in regions like Java and Indonesia.[67]Major Epidemics
The introduction of Hemileia vastatrix to the Americas marked a significant escalation in its global impact, beginning with its detection in Bahia, Brazil, in January 1970, where it was likely introduced from Africa through infected coffee seedlings transported via international trade routes.[3][13] This initial incursion rapidly expanded within Brazil, prompting widespread quarantine measures, though the pathogen's airborne urediniospores facilitated further dissemination.[68] By 1983, the fungus reached Central America, first confirmed in Costa Rica after crossing from Panama, and quickly spread northward, affecting Mexico by the late 1980s through wind dispersal and human-mediated transport of planting material.[1][69] These early outbreaks in the Western Hemisphere led to substantial yield reductions, with Brazil experiencing up to 30% losses in affected regions shortly after arrival.[68] One of the most severe modern epidemics occurred in 2012–2013 across Central America, Colombia, and Peru, triggered by the emergence of a more aggressive physiological race of H. vastatrix that overcame partial resistance in common cultivars, compounded by drought-stressed plants that reduced plant vigor and increased susceptibility.[70][71] The outbreak devastated over 50% of coffee-growing areas in the region, resulting in harvest losses of 20–50% and economic damages exceeding $1 billion, alongside the loss of more than 1 million jobs, primarily among smallholder farmers in Guatemala, Honduras, and Nicaragua.[70][72] This event highlighted the pathogen's ability to exploit environmental stressors, with prolonged dry conditions in 2011–2012 weakening host defenses and promoting rapid spore dispersal.[70] More recent outbreaks underscore the pathogen's continued expansion and adaptation. In Hawaii, the first recorded U.S. incidence occurred in October 2020 on the Big Island, with subsequent spread to Maui by 2021, attributed to the multilocus genotype (MLG) 10 lineage originating from Central American populations via likely windborne or human-assisted dispersal.[32][69] In Peru, surveys in 2024 identified two novel races of H. vastatrix—with virulence profiles v2,4,5,7,8 (or v2,4,5,7,8,9) and v1,2,4,5,7,8 (or v1,2,4,5,7,8,9)—alongside five known races, rendering widely planted Catimor varieties highly susceptible and necessitating updated resistance screening.[73] In East Africa, ongoing epidemics in countries like Kenya and Ethiopia have intensified since the 2010s, linked to climate variability such as rising temperatures and altered rainfall patterns that extend the pathogen's favorable conditions for infection and sporulation.[74][75] Major epidemics of H. vastatrix exhibit recurrent patterns, occurring approximately every 10–20 years in affected regions, primarily driven by the evolution of new physiological races that circumvent host resistance derived from genes like SH1–SH9.[76] This cyclical nature is evident in the progression from the 1980s Central American incursions to the 2012 crisis and subsequent events, where mutation and selection pressure on diverse H. vastatrix populations enable breakthroughs against previously resistant cultivars.[1] Such dynamics emphasize the pathogen's high evolutionary potential, with over 50 races documented globally, perpetuating vulnerability in monoculture systems.[76]Control Measures
Cultural Practices
Cultural practices play a crucial role in suppressing Hemileia vastatrix, the causal agent of coffee leaf rust, by modifying the plant microenvironment and reducing disease-favorable conditions without relying on chemical interventions. These methods focus on maintaining plant health, minimizing inoculum sources, and optimizing growth conditions to enhance natural resistance and limit pathogen spread.[77] Pruning and sanitation are foundational techniques for managing coffee leaf rust. Regular pruning involves removing infected branches and leaves to eliminate sources of urediniospores, the primary inoculum, while opening the canopy to improve airflow and reduce humidity within the plant structure. This practice not only destroys potential infection sites but also enhances light penetration, which discourages fungal development. Sanitation further entails collecting and destroying fallen debris, such as infected leaves, through methods like burning (where permitted), composting in covered piles for at least six weeks, or solarization under direct sunlight for a similar period to kill viable spores, which can persist for up to six weeks without a host. Effective implementation of these measures can significantly lower disease incidence, particularly when combined with desuckering to limit new susceptible growth.[78][77] Balanced nutrition through appropriate fertilization supports plant vigor and indirectly suppresses rust development. A well-managed NPK regimen, emphasizing adequate potassium levels, strengthens cell walls and enhances physiological resistance to H. vastatrix infection; for instance, higher potassium concentrations (up to 8 mmol L⁻¹ in nutrient solutions) have been shown to reduce rust intensity in controlled settings. Conversely, excess nitrogen should be avoided, as it promotes succulent, tender growth that increases susceptibility to the pathogen by facilitating spore germination and penetration. Proper nutrient application post-pruning aids regrowth and overall resilience without exacerbating disease pressure.[79][80][77] Shade management and plant spacing are essential for creating less hospitable microclimates for rust. Intercropping coffee with shade trees, such as Erythrina poeppigiana, reduces ambient humidity and temperature extremes (optimal for rust at 22–25°C and high relative humidity), thereby limiting spore dispersal and infection rates compared to unshaded systems. Wider spacing, typically around 2 × 2 m between plants, promotes better ventilation and drier foliage, decreasing leaf wetness duration—a key factor in urediniospore germination, which requires at least six hours of moisture. Periodic pruning of shade trees maintains optimal cover without excessive shading that could trap humidity.[77][81] Additional practices include fruit thinning to alleviate plant stress from heavy loads, which otherwise heightens rust vulnerability by diverting resources from defense mechanisms. Timely harvesting ensures fruits are removed promptly, preventing over-maturity that weakens plants, while irrigation should be managed to minimize prolonged leaf wetness, such as through drip systems that avoid overhead wetting. These integrated approaches foster sustainable suppression of H. vastatrix by bolstering plant health and disrupting the pathogen's lifecycle.[77]Chemical and Biological Controls
Chemical control of Hemileia vastatrix, the causal agent of coffee leaf rust, primarily relies on protective and systemic fungicides applied during the rainy season to suppress spore germination and infection. Protective fungicides, such as copper-based formulations including Bordeaux mixture (copper sulfate combined with lime) and copper oxychloride, form a barrier on leaf surfaces to prevent urediniospore attachment and penetration.[66][1] These are typically applied 4-6 times per season, with timing aligned to pre-rain periods for optimal coverage before infection events.[82] Systemic fungicides, absorbed by plant tissues for internal protection, include triazoles like propiconazole and epoxiconazole, as well as strobilurins such as azoxystrobin and pyraclostrobin.[83][84] These provide curative action by inhibiting fungal respiration or sterol biosynthesis, offering longer residual protection compared to contact fungicides.[85] Biological controls offer eco-friendly alternatives or supplements to synthetic fungicides, targeting H. vastatrix through antagonism or induced plant defenses. Antagonistic fungi such as Lecanicillium lecanii act as mycoparasites, directly infecting urediniospores and reducing spore viability in vitro, while Trichoderma spp. produce lytic enzymes like chitinases and glucanases to degrade fungal cell walls and induce systemic resistance in coffee plants.[86] Bacteria like Bacillus subtilis inhibit pathogen growth by secreting antifungal compounds such as lipopeptides and enzymes, alongside triggering induced systemic resistance via jasmonic acid pathways.[87] Essential oils, particularly from cinnamon (Cinnamomum verum), serve as natural alternatives; their active components like trans-cinnamaldehyde disrupt spore membranes and germination, decreasing disease severity in susceptible varieties.[86] These agents are applied foliarly, often in formulations compatible with organic systems. Integrated management combines chemical and biological approaches to enhance efficacy while minimizing environmental impact and resistance development. Fungicide rotation, alternating modes of action (e.g., multi-site copper with single-site triazoles or strobilurins), is essential to prevent H. vastatrix resistance, as overuse of any class can lead to reduced sensitivity.[85] Post-2020 regulatory shifts, including EU restrictions on copper use and concerns over triazole residues, have promoted eco-friendly transitions toward biological agents and reduced synthetic applications in coffee production.[89] When integrated, these methods—such as alternating copper sprays with B. subtilis or essential oils—reduce rust incidence in field trials, though challenges persist in organic systems due to variable environmental conditions and shorter protection durations.[86][8]Resistant Cultivars
Resistance to Hemileia vastatrix in coffee is primarily achieved through genetic mechanisms, categorized as vertical or horizontal. Vertical resistance is conferred by major dominant genes, known as SH genes (SH1 through SH9), which provide race-specific immunity but can be overcome by evolving pathogen races.[1] These genes originate from various Coffea species: SH1, SH2, SH4, and SH5 from C. arabica; SH3 from C. liberica; and SH6 through SH9 from C. canephora (robusta).[1] In contrast, horizontal resistance is polygenic and partial, offering more durable protection against multiple races by reducing disease severity rather than providing complete immunity.[1] Key resistant cultivars have been developed by introgressing robusta-derived genes into arabica backgrounds. Híbrido de Timor (HDT), a natural arabica-robusta hybrid discovered in Timor in the 1920s, carries multiple SH genes (including SH5–SH9) and serves as a foundational source for rust resistance.[1] Derivatives like Catimor, a cross between Caturra and HDT 832/1, incorporate SH4 and exhibit strong resistance, though it often shows yield vigor at the expense of cup quality.[1] Similarly, Sarchimor, derived from Villa Sarchi and HDT 832/2, provides robust resistance suitable for high-altitude regions.[1] More recent releases, such as IPR107 from Brazil's IAPAR program, demonstrate high resistance (scores below 2 on diagrammatic scales) across multiple environments and incorporate pyramided SH genes for broader durability.[90] Breeding efforts focus on introgressing robusta resistance into elite arabica lines to counter over 50 known physiological races of H. vastatrix.[1] Programs initiated in the 1960s at institutions like Portugal's CIFC used HDT to transfer SH genes, followed by backcrossing to recover arabica traits.[1] Marker-assisted selection (MAS) has accelerated progress by targeting linked markers (e.g., AFLP and SCAR) to SH loci, enabling gene pyramiding for resistance against diverse races.[1] Ongoing efforts include development of F1 hybrids, which combine resistance with higher yields and improved quality without robusta introgression.[91] This approach is essential, as single-gene resistances like SH4 in Catimor have been breached by new races in regions like Latin America.[2] Deployment of resistant cultivars varies regionally, with adoption reaching 87% of coffee area in Colombia as of 2025 through government-supported renovation programs.[92] In Latin America overall, resistant varieties are increasingly adopted, limited by challenges such as inferior sensory profiles due to robusta introgression in some hybrids. These issues necessitate ongoing selection for balanced agronomic and quality traits in breeding pipelines.[90]Economic Impact
Yield Losses
Hemileia vastatrix, the causal agent of coffee leaf rust (CLR), induces significant yield reductions in Coffea arabica through premature defoliation and impaired photosynthesis, with typical annual losses averaging 15-20% globally.[3] In severe epidemics, yield declines can reach 70-90%, as extensive leaf damage disrupts nutrient allocation and weakens the plant, often halving the subsequent season's crop due to reduced vegetative growth.[3][15] These per-epidemic losses are exacerbated by the pathogen's polyetic nature, where initial infections compound over multiple seasons, leading to cumulative declines in productivity.[1] Latent infections during the asymptomatic incubation period (typically 20-40 days) further contribute to yield impacts by silently draining plant resources, resulting in smaller bean sizes and lower quality even before visible symptoms appear.[1] Repeated infection cycles amplify this effect, as weakened plants produce fewer and inferior berries, perpetuating reduced yields year after year without intervention. Globally, these losses translate to an estimated 1-2 billion USD annually in arabica coffee production, underscoring CLR's role as a primary constraint on coffee output.[1][5] Yield losses are quantified using disease severity indices, such as the standard 1-5 scale assessing the percentage of leaf area affected (e.g., 1 for <1% coverage, 5 for >50%).[93] Historical data from the 2012 Central American epidemic illustrate this, with regional production dropping by approximately 20-30% overall, and up to 40% in heavily affected areas like Honduras due to widespread defoliation.[94][95]Global Consequences
The 2012 coffee leaf rust epidemic caused by Hemileia vastatrix severely disrupted livelihoods across Central America, leading to an estimated 374,000 job losses in the 2012/13 season as reduced harvests eliminated the need for harvesting labor.[96] Smallholder farmers, who dominate the region's coffee production, were disproportionately affected, with incomes falling by 50–60% over the 2010–2014 period due to crop devastation and compounded vulnerabilities like aging trees and low prior prices.[97] Broader impacts included over 1.7 million coffee workers losing employment, forcing many smallholders to abandon coffee farming entirely or migrate to urban areas in search of alternative work.[98] Market dynamics were profoundly altered by the epidemic, as sharp declines in arabica production—Central America's primary variety—triggered supply shortages and price volatility.[96] Arabica coffee prices surged in response to the reduced output from affected regions, exacerbating global market fluctuations and prompting buyers to source more from unaffected areas.[99] This volatility accelerated a shift toward robusta production in some regions, as robusta beans exhibit greater resistance to H. vastatrix and serve as a more stable alternative for blending and instant coffee markets.[56] Over the longer term, Hemileia vastatrix has inflicted substantial cumulative economic losses on the global coffee industry, with annual damages estimated at $1–2 billion due to recurrent outbreaks and control costs.[100] The 2012-2013 epidemic resulted in approximately $500 million to $1 billion in economic losses across Central America, including direct production declines and recovery costs, highlighting the pathogen's ongoing threat to producer economies.[96][101] In major producing countries like Ethiopia, where coffee accounts for 30–35% of export earnings, rust epidemics pose risks to food security by undermining rural incomes and national revenue streams that support broader agricultural and social programs. As of 2024, Ethiopia's coffee exports reached $1.7 billion despite ongoing rust pressures.[102][103] In response, international aid and industry initiatives have aimed to mitigate these consequences, including USAID-funded programs for coffee farm renovation and varietal replacement in Central America to restore productivity and livelihoods.[104] The sector has also shifted toward sustainable certification schemes, such as those promoted by organizations like Sustainable Harvest, which integrate rust management into eco-friendly practices to enhance farmer resilience and market access.[105]References
- https://www.ctahr.[hawaii](/page/Hawaii).edu/oc/freepubs/pdf/PD-118.pdf