Xylella fastidiosa

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Xylella fastidiosa
Xylella-fastidiosa-1508x706 c.jpg
Scientific classification
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X. fastidiosa
Binomial name
Xylella fastidiosa
Wells et al., 1987

Xylella fastidiosa is an aerobic, Gram-negative bacterium of the genus Xylella. [1] It is a plant pathogen, that grows in the water transport tissues of plants (xylem vessels) and is transmitted exclusively by xylem sap-feeding insects such as sharpshooters and spittlebugs. [1] [2] [3] [4] Many plant diseases are due to infections of X. fastidiosa, including bacterial leaf scorch, oleander leaf scorch, coffee leaf scorch (CLS), alfalfa dwarf, phony peach disease, and the economically important Pierce's disease of grapes (PD), [5] olive quick decline syndrome (OQDS), [6] [7] and citrus variegated chlorosis (CVC). [8] While the largest outbreaks of X. fastidiosa–related diseases have occurred in the Americas and Europe, this pathogen has also been found in Taiwan, Israel, and a few other countries worldwide. [9] [10]

Xylella fastidiosa can infect an extremely wide range of plants, many of which do not show any symptoms of disease. [11] Disease occurs in plant species that are susceptible due to blockage of water flow in the xylem vessels caused by several factors: bacterial obstruction, overreaction of the plant immune response (tylose formation), and formation of air embolisms. [12] [13] [14] A strain of X. fastidiosa responsible for citrus variegated chlorosis was the first bacterial plant pathogen to have its genome sequenced, in part because of its importance in agriculture. [15] Due to the significant impacts of this pathogen on agricultural crops around the world there is substantial investment in scientific research related to X. fastidiosa and the diseases it causes. [16]

Pathogen anatomy and disease cycle

Xylella fastidiosa is rod-shaped, and at least one subspecies has two types of pili on only one pole; longer, type IV pili are used for locomotion, while shorter, type I pili assist in biofilm formation inside their hosts. As demonstrated using a PD-related strain, the bacterium has a characteristic twitching motion that enables groups of bacteria to travel upstream against heavy flow, such as that found in xylem vessels. [17] It is obligately insect-vector transmitted from xylem-feeding insects directly into xylem, but infected plant material for vegetative propagation (e.g. grafting) can produce mature plants that also have an X. fastidiosa disease. [18] In the wild, infections tend to occur during warmer seasons, when insect vector populations peak. The bacterium is not seed transmitted, but instead is transmitted through "xylem feed-ing, suctorial homopteran insects such as sharpshooter leafhoppers and spittle bugs" [19] and has been historically difficult to culture (fastidious), [20] [21] as its specific epithet, fastidiosa, reflects.

X. fastidiosa can be divided into four subspecies that affect different plants and have separate origins. X. fastidiosa subsp. fastidiosa is the most studied subspecies, as it is the causal agent of PD; it is thought to have originated in southern Central America, and also affects other species of plants. X. f. multiplex affects many trees, including stone-fruit ones such as peaches and plums, and is thought to originate in temperate and southern North America. X. f. pauca is believed to have originated in South America. It is the causal agent of citrus variegated chlorosis (CVC) in Brazil [22] and also affects South American coffee crops, causing coffee leaf scorch. X. f. sandyi is thought to have originated in the southern part of the United States, and is notable for causing oleander leaf scorch. [23]

X. fastidiosa has a two-part lifecycle, which occurs inside an insect vector and inside a susceptible plant. While the bacterium has been found across the globe, only once the bacterium reaches systemic levels do symptoms present themselves. Once established in a new region, X. fastidiosa spread is dependent on the obligate transmission by xylem-sap feeding insect. [24] Within susceptible plant hosts, X. fastidiosa forms a biofilm-like layer within xylem cells and tracheary elements that can completely block the water transport in affected vessels. [25]

Strains

EB92-1 is a nonpathogenic strain of X. f. which is used as a biocontrol of its relatives. [26] (Really it is dramatically less pathogenic. It does colonize grape vines but rarely and less severely.) [26] Zhang et al., 2011 finds very little genomic distance between pathogenic and EB92-1 strains. [26]

Symptoms

Significant variation in symptoms is seen between diseases, though some symptoms are expressed across species. On a macroscopic scale, plants infected with a X. fastidiosa-related disease exhibit symptoms of water, zinc, and iron deficiencies, [27] manifesting as leaf scorching and stunting in leaves turning them yellowish-brown, gummy substance around leaves, [27] fruit reduction in size and quality, [27] and overall plant height. As the bacterium progressively colonizes xylem tissues, affected plants often block off their xylem tissue, which can limit the spread of this pathogen; blocking can occur in the form of polysaccharide-rich gels, tyloses, or both. These plant defenses do not seem to hinder the movement of X. fastidiosa. Occlusion of vascular tissue, while a normal plant response to infection, makes symptoms significantly worse; as the bacterium itself also reduces vascular function, a 90% reduction of vascular hydraulic function was seen in susceptible Vitis vinifera . [28] This bacterium rarely completely blocks vascular tissue. There usually is a slight amount of vascular function that keeps the plant alive, but makes its fruit or branches die, making the specific plant economically nonproductive. This can cause a massive drop on supply of quality fruit. [27] Smaller colonies usually occur throughout a high proportion of xylem vessels of a symptomatic plant.[ citation needed ]

X. fastidiosa is a Gram-negative, xylem-limited illness that is spread by insects. It can damage a variety of broadleaved tree species that are commonly grown in the United States. X. fastidiosa can be found in about 600 different plant species.[ citation needed ]

Pierce's disease

Severe PD symptoms include shriveled fruit, leaf scorching, and premature abscission of leaves, with bare petioles remaining on stems. [29]

Citrus variegated chlorosis

This disease is named after the characteristic spotty chlorosis on upper sides of citrus leaves. Fruits of infected plants are small and hard. [8]

Leaf scorches

In coffee, premature abscission of leaves and fruits is of bigger concern than scorching. Some isolates cause Almond leaf scorch, in California that includes CFBP8071 and M23. [30] Coffee Leaf Scorch (CLS) is a disease caused by the causal agent Xylella fastidiosa that is economically significant in Brazil. [31] Citrus variegated chlorosis (CVC), another significant disease in this region caused by a strain of X. fastidiosa has been shown to infect coffee plants with CLS. The disease has also been found in Costa Rica's Central Valley where it is referred to as ‘crespera’ disease by coffee growers. [32] Symptoms of the bacterial infection in coffee plants feature curling leaf margins, chlorosis and irregularly shaped leaves, stunting and reduced plant growth, and branch atrophy. [32] The disease reduced coffee production by up to 30% in plantations across Brazil. [31] X. fastidiosa was discovered in Apulia, Italy in 2013 for the first time as a destructive disease agent of olive trees and likely came from strains present in asymptomatic plant material imported from Costa Rica. [33]

Environment

X. fastidiosa occurs worldwide, though its diseases are most prominent in riparian habitats including the southeastern United States, California, and South America.

Symptoms of X. fastidiosa diseases worsen during hot, dry periods in the summer; lack of water and maximum demand from a full canopy of leaves, combined with symptoms due to disease, stress infected plants to a breaking point. Cold winters can limit the spread of the disease, [21] as it occurs in California, but not in regions with milder winters such as Brazil. Additionally, dry summers seem to delay symptom development of PD in California. [18]

Any conditions that increase vector populations can increase disease incidence, such as seasonal rainfall and forests or tree cover adjacent to crops, which serve as alternate food sources and overwintering locations for leafhoppers. [18]

Alexander Purcell, an expert on X. fastidiosa, hypothesized that plants foreign to X. fastidiosa's area of origin, the neotropical regions, are more susceptible to symptom development. Thus, plants from warmer climates are more resistant to X. fastidiosa disease development, while plants from areas with harsher winters, such as grapes, are more severely affected by this disease. [21]

Host species

X. fastidiosa has a very wide host range; as of 2020, its known host range was 595 plant species, with 343 species confirmed by two different detection methods, in 85 botanical families. [34] Most X. fastidiosa host plants are dicots, but it has also been reported in monocots and ginkgo, a gymnosperm. However, the vast majority of host plants remain asymptomatic, making them reservoirs for infection.[ citation needed ]

Due to the temperate climates of South America and the southeastern and west coast of the United States, X. fastidiosa can be a limiting factor in fruit crop production, particularly for stone fruits in northern Florida and grapes in California. [25] In South America, X. fastidiosa can cause significant losses in the citrus and coffee industries; a third of today's citrus crops in Brazil has CVC symptoms. [29]

X. fastidiosa also colonizes the foreguts of insect vectors, which can be any xylem-feeding insects, often sharpshooters in the Cicadellidae subfamily Cicadellinae. [3] [21] After an insect acquires X. fastidiosa, it has a short latent period around 2 hours, then the bacterium is transmissible for a period of a few months or as long as the insect is alive.[ citation needed ] The bacterium multiplies within its vectors, forming a "bacterial carpet" within the foregut of its host. If the host sheds its foregut during molting, the vector is no longer infected, but can reacquire the pathogen. At present, no evidence shows that the bacterium has any detrimental effect on its insect hosts.

List of Subspecies fastidiosa Susceptible Plants (recreated from EFSA Panel) [34]
FamilyGenus
Adoxaceae Sambucus
Amaranthaceae Alternanthera, Chenopodium
Anacardiaceae Rhus, Toxicodendron
Apiaceae Conium, Datura, Daucus, Oenanthe
Apocynaceae Nerium, Vinca
Araliaceae Hedera
Asteraceae Ambrosia, Artemisia, Baccharis, Callistephus, Conyza, Franseria, Helianthus, Lactuca, Solidago, Sonchus, Xanthium
Betulaceae Alnus
Boraginaceae Amsinckia
Brassicaceae Brassica
Cannaceae Canna
Caprifoliaceae Lonicera, Symphoricarpos
Convolvulaceae Convolvulus, Ipomoea
Cyperaceae Cyperus
Fabaceae Acacia, Chamaecrista, Cytisus, Genista, Lathyrus, Lupinus, Medicago, Melilotus, Spartium, Trifolium, Vicia
Fagaceae Quercus
Geraniaceae Erodium, Pelargonium
Juglandaceae Juglans
Lamiaceae Callicarpa, Origanum, Melissa, Mentha, Rosmarinus, Salvia
Lauraceae Persea, Umbellularia
Magnoliaceae Magnolia
Malvaceae Malva
Myrtaceae Eucalyptus, Eugenia, Metrosideros
Oleaceae Fraxinus, Syringa
Onagraceae Epilobium, Fuchsia, Clarkia, Oenothera
Pittosporaceae Pittosporum
Platanaceae Platanus
Poaceae Avena, Bromus, Cynodon, Digitaria, Echinochloa, Eragrostis, Eriochola, Festuca, Holcus, Hordeum, Lolium, Paspalum, Pennisetum, Phalaris, Phleum, Poa, Setaria, Sorghum
Polygonaceae Persicaria, Polygonum, Rheum, Rumex
Portulacaceae Montia, Portulaca
Resedaceae Reseda
Rhamnaceae Rhamnus
Rosaceae Cotoneaster, Fragaria, Photinia, Prunus, Rosa, Rubus
Rubiaceae Coffea, Coprosma
Rutaceae Citrus
Salicaceae Populus, Salix
Sapindaceae Acer, Aesculus
Scrophulariaceae Veronica
Simmondsiaceae Simmondsia
Solanaceae Datura, Lycopersicon, Nicotiana, Solanum
Urticaceae Urtica
Verbenaceae Duranta
Vitaceae Ampelopsis, Parthenocissus, Vitis

Oleander

Oleander leaf scorch is a disease of landscape oleanders (Nerium oleander) caused by a X. fastidiosa strain that has become prevalent in California and Arizona, starting in the mid-1990s. This disease is transmitted by a type of leafhopper (insect) called the glassy-winged sharpshooter (Homalodisca coagulata). Oleander is commonly used in decorative landscaping in California, so the plants serve as widely distributed reservoirs for Xylella.[ citation needed ]

Both almond and oleander plants in the Italian region of Apulia have also tested positive for the pathogen. [35]

Grape vines

Pierce's disease (PD) was discovered in 1892 [36] by Newton B. Pierce (1856–1916; California's first professional plant pathologist) on grapes in California near Anaheim, [22] where it was known as "Anaheim disease". [37] The disease is endemic in Northern California, being spread by the blue-green sharpshooter, which attacks only grapevines adjacent to riparian habitats. It became a real threat to California's wine industry when the glassy-winged sharpshooter, native to the Southeast United States, was discovered in the Temecula Valley in California in 1996; it spreads PD much more extensively than other vectors. [38]

Symptoms of infection on grape vines

When a grape vine becomes infected, the bacterium causes a gel to form in the xylem tissue of the vine, preventing water from being drawn through the vine. [39] Leaves on vines with Pierce's disease turn yellow and brown, and eventually drop off the vine. Shoots also die. After one to five years, the vine itself dies. The proximity of vineyards to citrus groves compounds the threat, because citrus is not only a host of sharpshooter eggs, but also is a popular overwintering site for this insect. [40]

Collaborative efforts for solutions

In a unique effort, growers, administrators, policy makers, and researchers are working on a solution for this immense X. fastidiosa threat. No cure has been found, [41] but the understanding of X. fastidiosa and glassy-winged sharpshooter biology has markedly increased since 2000, when the California Department of Food and Agriculture, in collaboration with different universities, such as University of California, Davis; University of California, Berkeley; University of California, Riverside, and University of Houston–Downtown started to focus their research on this pest. The research explores the different aspects of the disease propagation from the vector to the host plant and within the host plant, to the impact of the disease on California's economy. All researchers working on Pierce's disease meet annually in San Diego in mid-December to discuss the progress in their field. All proceedings from this symposium can be found on the Pierce's disease website, [42] developed and managed by the Public Intellectual Property Resource for Agriculture (PIPRA). [43]

Few resistant Vitis vinifera varieties are known, and Chardonnay and Pinot noir are especially susceptible, but muscadine grapes (V. rotundifolia) have a natural resistance. [41] Pierce's disease is found in the Southeastern United States and Mexico. Also, it was reported by Luis G. Jiménez-Arias in Costa Rica, and Venezuela, [44] and possibly in other parts of Central and South America. In 2010, X. fastidiosa became apparent in Europe, posing a serious, real threat. [45] There are isolated hot spots of the disease near creeks in Napa and Sonoma in Northern California. [41] Work is underway at UC Davis to breed PD resistance from V. rotundifolia into V. vinifera. The first generation was 50% high-quality V. vinifera genes, the next 75%, the third 87% and the fourth 94%. In the spring of 2007, seedlings that are 94% V. vinifera were planted. [46]

A resistant variety, 'Victoria Red', was released for use especially in Coastal Texas. [47]

Nerium oleander infected with X. fastidiosa in Phoenix, Arizona OleanderLeafScorch.jpg
Nerium oleander infected with X. fastidiosa in Phoenix, Arizona

Olive trees

An olive grove infested with X. fastidiosa in Puglia, Italy in 2019 Olivenhain mit Xylella fastidiosa bei Surano LE 190710.jpg
An olive grove infested with X. fastidiosa in Puglia, Italy in 2019

In October 2013, the bacterium was found infecting olive trees in the region of Apulia in southern Italy. [35] The disease caused rapid decline in olive grove yields, and by April 2015, was affecting the whole Province of Lecce and other zones of Apulia, [7] [48] though it had not previously been confirmed in Europe. [49] The subspecies involved in Italy is X. f. pauca, which shows a marked preference for olive trees and warm conditions and is thought to be unlikely to spread to Northern Europe. [50]

The cycle in olives has been called olive quick decline syndrome (in Italian : complesso del disseccamento rapido dell'olivo). [49] [51] The disease causes withering and desiccation of terminal shoots, distributed randomly at first but then expanding to the rest of the canopy [51] resulting in the collapse and death of trees. [51] In affected groves, all plants normally show symptoms. [51] The most severely affected olives are the century-old trees of local cultivars Cellina di Nardò and Ogliarola salentina. [52]

By 2015, the disease had infected up to a million olive trees in Apulia [53] and Xylella fastidiosa had reached Corsica, [54] By October 2015, it had reached Mainland France, near Nice, in Provence-Alpes-Côte d'Azur, affecting the non-native myrtle-leaf milkwort ( Polygala myrtifolia ). This is the subspecies X. fastidiosa subsp. multiplex which is considered to be a different genetic variant of the bacterium to that found in Italy. [55] [56] On 18 August 2016 in Corsica, 279 foci of the infection have been detected, concentrated mostly in the south and the west of the island. [57] In August 2016, the bacterium was detected in Germany in an oleander plant. [58] In January 2017 it was detected in Mallorca and Ibiza. [59]

Notably, in 2016, olive leaf scorch was first detected in X. fastidiosa's native range, in Brazil. [22]

In June 2017, it was detected in the Iberian peninsula, specifically in Guadalest, Alicante. [60] In 2018, it was detected elsewhere in Spain [61] and Portugal, [62] and in Israel in 2019. [63]

Citrus

Xylella infection was detected in South American citrus in the 1980s and subsequently in the USA but had limited spread beyond the America's until the detection in citrus groves in Portugal in 2023. [64]

Genome sequencing

The genome of X. fastidiosa was sequenced by a pool of over 30 research laboratories in the state of São Paulo, Brazil, funded by the São Paulo Research Foundation. [65]

See also

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References

  1. 1 2 Rapicavoli, Jeannette; Ingel, Brian; Blanco-Ulate, Barbara; Cantu, Dario; Roper, Caroline (April 2018). "Xylella fastidiosa : an examination of a re-emerging plant pathogen: Xylella fastidiosa". Molecular Plant Pathology. 19 (4): 786–800. doi:10.1111/mpp.12585. PMC   6637975 . PMID   28742234.
  2. Krugner, Rodrigo; Sisterson, Mark S; Backus, Elaine A; Burbank, Lindsey P; Redak, Richard A (May 2019). "Sharpshooters: a review of what moves Xylella fastidiosa". Austral Entomology. 58 (2): 248–267. doi: 10.1111/aen.12397 . ISSN   2052-174X. S2CID   182504242.
  3. 1 2 Redak, Richard A.; Purcell, Alexander H.; Lopes, João R.S.; Blua, Matthew J.; Mizell III, Russell F.; Andersen, Peter C. (3 December 2003). "The biology of xylem fluid–feeding insect vectors of Xylella fastidiosa and their relation to disease epidemiology". Annual Review of Entomology. 49 (1): 243–270. doi:10.1146/annurev.ento.49.061802.123403. ISSN   0066-4170. PMID   14651464.
  4. Cornara, Daniele; Saponari, Maria; Zeilinger, Adam R.; de Stradis, Angelo; Boscia, Donato; Loconsole, Giuliana; Bosco, Domenico; Martelli, Giovanni P.; Almeida, Rodrigo P. P.; Porcelli, Francesco (2017-03-01). "Spittlebugs as vectors of Xylella fastidiosa in olive orchards in Italy". Journal of Pest Science. 90 (2): 521–530. doi:10.1007/s10340-016-0793-0. ISSN   1612-4766. PMC   5320020 . PMID   28275326.
  5. "Pierce's Disease". UC IPM. Retrieved 2022-12-04.
  6. Martelli, G. P.; Boscia, D.; Porcelli, F.; Saponari, M. (2016-02-01). "The olive quick decline syndrome in south-east Italy: a threatening phytosanitary emergency". European Journal of Plant Pathology. 144 (2): 235–243. Bibcode:2016EJPP..144..235M. doi:10.1007/s10658-015-0784-7. ISSN   1573-8469. S2CID   254475576.
  7. 1 2 "Minimizing the Spread of Disease in Italy's Famous Olive Trees". Our Environment at Berkeley. University of California, Berkeley, Department of Environmental Science, Policy, and Management (ESPM). 9 February 2015. Retrieved 5 May 2015.
  8. 1 2 Coletta-Filho, Helvecio Della; Castillo, Andreina I.; Laranjeira, Francisco Ferraz; de Andrade, Eduardo Chumbinho; Silva, Natalia Teixeira; de Souza, Alessandra Alves; Bossi, Mariana Esteves; Almeida, Rodrigo P. P.; Lopes, João R. S. (2020-06-01). "Citrus Variegated Chlorosis: an Overview of 30 Years of Research and Disease Management". Tropical Plant Pathology. 45 (3): 175–191. doi:10.1007/s40858-020-00358-5. ISSN   1983-2052. S2CID   218652922.
  9. Su, Chiou-Chu; Chang, Chung Jan; Chang, Che-Ming; Shih, Hsien-Tzung; Tzeng, Kuo-Ching; Jan, Fuh-Jyh; Kao, Chin-Wen; Deng, Wen-Ling (June 2013). "Pierce's Disease of Grapevines in Taiwan: Isolation, Cultivation and Pathogenicity of Xylella fastidiosa". Journal of Phytopathology. 161 (6): 389–396. doi:10.1111/jph.12075.
  10. Zecharia, Noa; Krasnov, Helena; Vanunu, Miri; Siri, Andreina Castillo; Haberman, Ami; Dror, Orit; Vakal, Lera; Almeida, Rodrigo P. P.; Blank, Lior; Shtienberg, Dani; Bahar, Ofir (November 2022). "Xylella fastidiosa Outbreak in Israel: Population Genetics, Host Range, and Temporal and Spatial Distribution Analysis". Phytopathology. 112 (11): 2296–2309. doi:10.1094/PHYTO-03-22-0105-R. ISSN   0031-949X. PMID   35778787. S2CID   250218193.
  11. "Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2021". www.efsa.europa.eu. 12 January 2022. Retrieved 2022-12-04.
  12. Petit, Giai; Bleve, Gianluca; Gallo, Antonia; Mita, Giovanni; Montanaro, Giuseppe; Nuzzo, Vitale; Zambonini, Dario; Pitacco, Andrea (2021). "Susceptibility to Xylella fastidiosa and functional xylem anatomy in Olea europaea: revisiting a tale of plant–pathogen interaction". AoB Plants. 13 (4): plab027. doi:10.1093/aobpla/plab027. PMC   8300559 . PMID   34316336.
  13. Ingel, Brian; Reyes, Clarissa; Massonnet, Mélanie; Boudreau, Bailey; Sun, Yuling; Sun, Qiang; McElrone, Andrew J.; Cantu, Dario; Roper, M. Caroline (February 2021). "Xylella fastidiosa causes transcriptional shifts that precede tylose formation and starch depletion in xylem". Molecular Plant Pathology. 22 (2): 175–188. doi:10.1111/mpp.13016. ISSN   1464-6722. PMC   7814960 . PMID   33216451.
  14. Roper, M. Caroline; Greve, L. Carl; Labavitch, John M.; Kirkpatrick, Bruce C. (2007-11-15). "Detection and Visualization of an Exopolysaccharide Produced by Xylella fastidiosa In Vitro and In Planta". Applied and Environmental Microbiology. 73 (22): 7252–7258. Bibcode:2007ApEnM..73.7252R. doi:10.1128/AEM.00895-07. ISSN   0099-2240. PMC   2168192 . PMID   17827325.
  15. Simpson, A. J. G.; Reinach, F. C.; Arruda, P.; Abreu, F. A.; Acencio, M.; Alvarenga, R.; Alves, L. M. C.; Araya, J. E.; Baia, G. S.; Baptista, C. S.; Barros, M. H.; Bonaccorsi, E. D.; Bordin, S.; Bové, J. M.; Briones, M. R. S. (July 2000). "The genome sequence of the plant pathogen Xylella fastidiosa". Nature. 406 (6792): 151–157. doi: 10.1038/35018003 . ISSN   1476-4687. PMID   10910347. S2CID   17344899.
  16. Lindow, Steven (2019-02-01). "Money Matters: Fueling Rapid Recent Insight Into Xylella fastidiosa—An Important and Expanding Global Pathogen". Phytopathology. 109 (2): 210–212. doi: 10.1094/PHYTO-09-18-0325-PER . ISSN   0031-949X. PMID   30644806. S2CID   58611726.
  17. Meng, Yizhi; Li, Yaxin; Galvani, Cheryl D.; Hao, Guixia; Turner, James N.; Burr, Thomas J.; Hoch, H. C. (2005-08-15). "Upstream Migration of Xylella fastidiosa via Pilus-Driven Twitching Motility". Journal of Bacteriology. 187 (16): 5560–5567. doi:10.1128/jb.187.16.5560-5567.2005. ISSN   0021-9193. PMC   1196070 . PMID   16077100.
  18. 1 2 3 Mizell, Russell F.; Andersen; Tipping (January 2003). "Xylella Fastidiosa Diseases and Their Leafhopper Vectors" (PDF). University of Florida IFAS Extension. Archived from the original (PDF) on February 25, 2021. Retrieved November 30, 2017.
  19. Hill, B. L.; Purcell, A. H. (1997). "Populations of Xylella fastidiosa in Plants Required for Transmission by an Efficient Vector". Phytopathology. 87 (12): 1197–1201. doi: 10.1094/phyto.1997.87.12.1197 . PMID   18945018.
  20. Coletta-Filho, Helvécio Della; Carvalho, Sérgio Alves; Silva, Luis Fernando Carvalho; Machado, Marcos Antonio (2014-07-01). "Seven years of negative detection results confirm that Xylella fastidiosa, the causal agent of CVC, is not transmitted from seeds to seedlings". European Journal of Plant Pathology. 139 (3): 593–596. Bibcode:2014EJPP..139..593C. doi:10.1007/s10658-014-0415-8. ISSN   0929-1873. S2CID   15561623.
  21. 1 2 3 4 Purcell, Alexander (2013-08-04). "Paradigms: Examples from the Bacterium Xylella fastidiosa". Annual Review of Phytopathology. 51 (1): 339–356. doi:10.1146/annurev-phyto-082712-102325. ISSN   0066-4286. PMID   23682911.
  22. 1 2 3 Sicard, Anne; Zeilinger, Adam R.; Vanhove, Mathieu; Schartel, Tyler E.; Beal, Dylan J.; Daugherty, Matthew P.; Almeida, Rodrigo P.P. (2018-08-25). "Xylella fastidiosa: Insights into an Emerging Plant Pathogen" (PDF). Annual Review of Phytopathology . 56 (1). Annual Reviews: 181–202. doi:10.1146/annurev-phyto-080417-045849. ISSN   0066-4286. PMID   29889627. S2CID   48353386.(AS ORCID: 0000-0002-0575-195X).
  23. "Xylella fastidiosa (Pierce's disease of grapevines)". www.cabi.org. Retrieved 2017-11-06.
  24. https://www.cabdirect.org/cabdirect/abstract/20203319742.{{cite web}}: Missing or empty |title= (help)
  25. 1 2 Chatterjee, Subhadeep; Almeida, Rodrigo P. P.; Lindow, Steven (2008-08-04). "Living in two Worlds: The Plant and Insect Lifestyles of Xylella fastidiosa". Annual Review of Phytopathology. 46 (1): 243–271. doi:10.1146/annurev.phyto.45.062806.094342. ISSN   0066-4286. PMID   18422428.
  26. 1 2 3
  27. 1 2 3 4 Almedia, Rodrigo (2013). "Xylella Fastidiosa".{{cite web}}: Missing or empty |url= (help)
  28. Sun, Qiang; Sun, Yuliang; Walker, M. Andrew; Labavitch, John M. (2013-03-01). "Vascular Occlusions in Grapevines with Pierce's Disease Make Disease Symptom Development Worse". Plant Physiology. 161 (3): 1529–1541. doi:10.1104/pp.112.208157. ISSN   0032-0889. PMC   3585614 . PMID   23292789.
  29. 1 2 Hopkins, D. L.; Purcell, A. H. (2002-10-01). "Xylella fastidiosa: Cause of Pierce's Disease of Grapevine and Other Emergent Diseases". Plant Disease. 86 (10): 1056–1066. doi: 10.1094/pdis.2002.86.10.1056 . ISSN   0191-2917. PMID   30818496.
  30. 1 2 Li, W.-B.; Pria, W. D.; Teixeira, D. C.; Miranda, V. S.; Ayres, A. J.; Franco, C. F.; Costa, M. G.; He, C.-X.; Costa, P. I.; Hartung, J. S. (2001-05-01). "Coffee Leaf Scorch Caused by a Strain of Xylella fastidiosa from Citrus". Plant Disease. 85 (5): 501–505. doi:10.1094/PDIS.2001.85.5.501. ISSN   0191-2917. PMID   30823125.
  31. 1 2 Montero-Astúa, Mauricio; Chacón-Díaz, Carlos; Aguilar, Estela; Rodríguez, Carlos Mario; Garita, Laura; Villalobos, William; Moreira, Lisela; Hartung, John S.; Rivera, Carmen (October 2008). "Isolation and molecular characterization of Xylella fastidiosa from coffee plants in Costa Rica". The Journal of Microbiology. 46 (5): 482–490. doi:10.1007/s12275-008-0072-8. ISSN   1225-8873. PMID   18974947. S2CID   40097733.
  32. Sicard, Anne; Saponari, Maria; Vanhove, Mathieu; Castillo, Andreina I.; Giampetruzzi, Annalisa; Loconsole, Giuliana; Saldarelli, Pasquale; Boscia, Donato; Neema, Claire; Almeida, Rodrigo P. P. (2021). "Introduction and adaptation of an emerging pathogen to olive trees in Italy". Microbial Genomics. 7 (12): 000735. doi: 10.1099/mgen.0.000735 . ISSN   2057-5858. PMC   8767334 . PMID   34904938.
  33. 1 2 European Food Safety Authority (2020). "Scientific report on the update of the Xylella spp. host plant database – systematic literature search up to 30 June 2019". EFSA Journal. 18 (4): 61. doi: 10.2903/j.efsa.2020.6114 . ISSN   1831-4732. PMC   7448098 . PMID   32874307.
  34. 1 2 Kinver, Mark (9 January 2015). "'Major consequences' if olive disease spreads across EU". BBC News . Retrieved 1 March 2015.
  35. Pierce, Newton Barris (1892). The California Vine Disease: A Preliminary Report of Investigations. Bulletins. Government Printing Office, Washington, DC US: United States Department of Agriculture, Division of Vegetable Pathology. ISBN   978-1331970958. OCLC   4512989. ISBN   1331970954.
  36. Pinney, Thomas (1989). A History of Wine in America from the Beginnings to Prohibition . University of California Press. pp.  27. ISBN   978-0520062245.
  37. Haviland, David R; Stone-Smith, Beth; Gonzalez, Minerva (2021-01-01). "Control of Pierce's Disease Through Areawide Management of Glassy-Winged Sharpshooter (Hemiptera: Cicadellidae) and Roguing of Infected Grapevines". Journal of Integrated Pest Management. 12 (1). doi: 10.1093/jipm/pmab008 . ISSN   2155-7470.
  38. Meyer, Brittnay (2018). "Pierce's Disease on grapes". Texas Plant Disease Diagnostic Lab. Retrieved 2023-05-05.
  39. Pollard, Herschel N.; Kaloostian, George H. (1961-08-01). "Overwintering Habits of Homalodisca coagulata, the Principal Natural Vector of Phony Peach Disease Virus". Journal of Economic Entomology. 54 (4): 810–811. doi:10.1093/jee/54.4.810. ISSN   1938-291X.
  40. 1 2 3 winepros.com.au. Oxford Companion to Wine. "Pierce's disease". Archived from the original on 2008-08-08. Retrieved 2008-05-07.
  41. PIPRA Pierce's Disease website. "Pierce's disease".
  42. "Public Intellectual Property Resource for Agriculture (PIPRA)". Archived from the original on 5 March 2016.
  43. Jiménez A., L.G. (July–September 1985). "Evidencia inmunológica del mal de pierce de la vid en Venezuela". Turrialba. 35 (3): 243–247.
  44. Janse, J.D.; Obradovic, A. (2010). "Xylella Fastidiosa: ITS Biology, Diagnosis, Control and Risks". Journal of Plant Pathology. 92: S35–S48. ISSN   1125-4653. JSTOR   41998754.
  45. PD/GWSS Board bulletin Archived 2015-05-18 at the Wayback Machine , California Department of Food & Agriculture , Spring 2007 (p. 2)
  46. Moore, James N.; Clark, John R.; Kamas, James; Stein, Larry; Tarkington, Friench; Tarkington, Martha (2011-05-01). "'Victoria Red' Grape". HortScience. 46 (5): 817–820. doi: 10.21273/HORTSCI.46.5.817 . ISSN   0018-5345.
  47. Spagnolo, Chiara (2015-04-29). "Xylella, allarme nuovi focolai, per la Ue interessata tutta la Puglia" [Xylella, new outbreak alarm, for the EU all of Puglia affected]. La Repubblica (in Italian). Retrieved 8 May 2015.
  48. 1 2 "First report of Xylella fastidiosa in the EPPO region". European and Mediterranean Plant Protection Organization (EPPO). Retrieved 1 March 2015.
  49. "Xylella fastidiosa". Plant Health Portal. Department for Environment, Food and Rural Affairs. Retrieved 24 June 2017.
  50. 1 2 3 4 Butler, Julie (29 March 2014). "Expert Says Eradication of New Olive Tree Disease in Europe Unlikely". Olive Oil Times. Retrieved 1 March 2015.
  51. Saponari, M.; Giampetruzzi, A.; Loconsole, G.; Boscia, D.; Saldarelli, P. (2019). "Xylella fastidiosa in Olive in Apulia: Where We Stand". Phytopathology. 109 (2). American Phytopathological Society: 175–186. doi: 10.1094/PHYTO-08-18-0319-FI . hdl: 11586/226511 . PMID   30376439.
  52. Squires, Nick (27 February 2015). "Italy warns deadly olive tree bacteria could spread across Europe". The Telegraph. Retrieved 1 March 2015.
  53. "Olive oil dries up". The Economist. 31 July 2015. Retrieved 2015-07-31.
  54. "Xylella fastidiosa". Plants. European Commission. 2016-10-17. Retrieved 24 June 2017.
  55. "Un premier cas de la bactérie tueuse de végétaux découvert à Nice" [A first case of the plant killer bacterium discovered in Nice]. Nice Matin (in French). 9 October 2015. Retrieved 2015-10-09.
  56. "Xylella : carte et liste des communes en zones délimitées en Corse au 18 août 2016". Direction régionale de l'alimentation, de l'agriculture et de la forêt de Corse (in French). Archived from the original on 23 August 2016. Retrieved 23 August 2016.
  57. Schröder, Elke. "Pflanzen-Killerbakterium: Teile von Zeulenroda-Triebes zur Sperrzone erklärt" [Plant killer bacteria: Parts of Zeulenroda rails declared a restrict zone]. Antenne Thueringen (in German). Archived from the original on August 27, 2016. Retrieved 23 August 2016.
  58. Elcacho, Joaquim. "La plaga vegetal más peligrosa de Europa invade las Baleares" [Europe's most dangerous plant pest invades the Balearic Islands]. La Vanguardia (in Spanish). Retrieved 24 January 2017.
  59. "Tala preventiva de árboles ante el primer caso de 'Xylella fastidiosa' en la península" [Preventive tree lysing in the first case of Xylella fastidiosa on the peninsula]. La Vanguardia (in Spanish). Retrieved 4 July 2017.
  60. "Detectada en Madrid la presencia de una bacteria que obligó a arrancar un millón de olivos en Italia". 20 Minutos (in Spanish). Retrieved 12 April 2018.
  61. "Xylella fastidiosa (XYLEFA) [Portugal]| EPPO Global Database". gd.eppo.int. Retrieved 2020-08-03.
  62. "Xylella fastidiosa (XYLEFA) [Israel]| EPPO Global Database". gd.eppo.int. Retrieved 2020-08-03.
  63. NTC, À Punt (2023-01-11). "Portugal detecta la 'Xylella fastidiosa' en cítrics per primera vegada en la UE" [Portugal detects 'Xylella fastidiosa' in citrus fruits for the first time in the EU]. À Punt (in Catalan). Retrieved 2023-01-20.
  64. Simpson, A. J. G.; Reinach, F. C.; Arruda, P.; Abreu, F. A.; Acencio, M.; Alvarenga, R.; Alves, L. M. C.; Araya, J. E.; Baia, G. S.; Baptista, C. S.; Barros, M. H.; Bonaccorsi, E. D.; Bordin, S.; Bové, J. M.; Briones, M. R. S. (2000). "The genome sequence of the plant pathogen Xylella fastidiosa". Nature. 406 (6792): 151–157. Bibcode:2000Natur.406..151S. doi: 10.1038/35018003 . ISSN   1476-4687. PMID   10910347.

Further reading