Ditylenchus dipsaci (stem and bulb nematode)
Index
- Pictures
- Identity
- Taxonomic Tree
- Notes on Taxonomy and Nomenclature
- Description
- Distribution
- Distribution Table
- Risk of Introduction
- Hosts/Species Affected
- Host Plants and Other Plants Affected
- Growth Stages
- Symptoms
- List of Symptoms/Signs
- Biology and Ecology
- Natural enemies
- Means of Movement and Dispersal
- Seedborne Aspects
- Pathway Vectors
- Plant Trade
- Impact
- Diagnosis
- Detection and Inspection
- Similarities to Other Species/Conditions
- Prevention and Control
- References
- Distribution Maps
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Top of pagePreferred Scientific Name
- Ditylenchus dipsaci (Kühn, 1857) Filip'ev, 1936
Preferred Common Name
- stem and bulb nematode
Other Scientific Names
- Anguillula devastatrix Kühn, 1869
- Anguillula dipsaci Kühn, 1857
- Anguillula secalis Nitschke, 1868
- Anguillulina dipsaci (Kühn, 1857) Gervais & Van Beneden, 1859
- Anguillulina dipsaci var. communis Steiner & Scott, 1935
- Ditylenchus allocotus (Steiner, 1934) Filip'ev & Sch. Stek., 1
- Ditylenchus amsinckiae (Steiner & Scott, 1935) Filip'ev & Sch.
- Ditylenchus dipsaci var. tobaensis Schneider, 1937
- Ditylenchus fragariae Kir'yanova, 1951
- Ditylenchus sonchophila Kir'yanova, 1958
- Ditylenchus trifolii Skarbilivich, 1958
- Tylenchus allii Beijerinck, 1883
- Tylenchus devastator
- Tylenchus devastatrix (Kühn) Oerley
- Tylenchus dipsaci (Kühn, 1857) Bastian, 1865
- Tylenchus havensteinii Kühn, 1881
- Tylenchus hyacinthi Prillieux, 1881
- Tylenchus putrefaciens Kühn, 1879
International Common Names
- English: brown ring disease of hyacinth; bulb eelworm; onion bloat; ring disease of bulbs
- Spanish: acebollado del centeno; anguilulosis de la avena; anguilulosis de la cebolla; cebollino del centeno; nematodo de la cebolla; nematodo del tallo
- French: anguillule commune des tiges; anguillule des cereales et des bulbes; nématode des tiges; poireaute avoine; seigle oignonne
Local Common Names
- Denmark: stængelnematod
- Finland: varsiankeroinen
- Germany: ruebenkopf-älchen; stengel-älchen; stock-älchen
- Italy: anguillula delle piante erbacee
- Japan: kuki-sentyubyo; nami-kuki-sentyu
- Netherlands: stengelaaltje
- Norway: stengelnematode
- Sweden: stjälknematod
- Turkey: sogan sak nematodo
EPPO code
- DITYDI (Ditylenchus dipsaci)
Taxonomic Tree
Top of page- Domain: Eukaryota
- Kingdom: Metazoa
- Phylum: Nematoda
- Class: Secernentea
- Order: Tylenchida
- Family: Anguinidae
- Genus: Ditylenchus
- Species: Ditylenchus dipsaci
Notes on Taxonomy and Nomenclature
Top of pageTo conclude, there seem to exist two or more valid species in the D. dipsaci complex, but they have not yet been validly or completely described and differentiated.
Description
Top of pageBody almost straight when killed by heat. Cuticle marked by transverse annuli about 1 µm apart; lateral fields with 4 lines occupying 1/6-1/8 of body width. Phasmid-like structures are present dorsal to the lateral fields (Sturhan and Rahi, 1996). Lip region low, unstriated, slightly flattened, barely set off from the body. Head framework moderately developed, stylet about 10-12 µm long with distinct basal knobs. Procorpus of oesophagus cylindrical, narrowing slightly as it joins the fusiform median bulb. Isthmus narrow, surrounded by nerve ring where it begins to expand into posterior oesophageal glands that end at, or slightly overlap, the intestine; small valve present at oesophago-intestinal junction. Excretory pore opposite the basal bulb. Tail conoid, 4-5 anal-body widths, with a sharply pointed terminus. Vulva distinct, anterior ovary outstretched with oocytes in a single (rarely double) row, sometimes reaching the oesophageal region. Post-vulval sac present, extending about half-way to the anus.
Male
Anterior region similar to female. Body almost straight when killed by heat. Tail similar to female with sharply pointed terminus; bursa present, beginning opposite the anterior end of the spicules and extending to three quarters of the tail end. Spicules 23-28 µm long, curved ventrally, expanded anteriorly. Gubernaculum short and simple.
Measurements
After Thorne (1945), from teasel (Dipsacus fullonum). Females: L = 1.0-1.3 mm; a = 36-40; b = 6.5-7.1; c = 14-18; V = 80%. Males: L = 1.0-1.3 mm; a = 37-41; b = 6.5-7.3; c = 12-15; T = 65-72.
After Blake in Hooper (1972), from oats (Avena sativa). 48 females: L = 1.3 mm (S.E. = 0.009); a = 62 (S.E. = 5.6); b = 15 (S.E. = 1.4); c = 14 (S.E. = 2.1); V = 80 (S.E. = 1.5). 23 males: : L = 1.3 mm (S.E. = 0.017); a = 63 (S.E. = 11.3); b = 15 (S.E. = 1.7); c = 14 (S.E. = 2.1); T = 72.
After Goodey (1941), giant race from broad bean (Vicia faba). 22 females: L = 1.73-2.23 (1.97) mm; a = 50-64 (58.2); b = 7-12 (9); c = 15.8-20.0 (17.5); V = 76-84 (82). 23 males: L = 1.51-1.93 (1.77) mm; a = 58-74 (67); b = 6-8 (7); c = 14.6-19.1 (16.9).
Distribution
Top of pageD. dipsaci occurs locally in most temperate areas of the world (Europe and the Mediterranean region, North and South America, northern and southern Africa, Asia and Oceania) but it does not seem able to establish itself in tropical regions except at higher altitudes that have a temperate climate. In most countries regulatory measures such as certification schemes are applied to minimize further spread of D. dipsaci. There are several reports of presence in India in the literature (Hooper, 1972; Maqbool, 1991; Sturhan and Brzeski, 1991; Chakraborti, 2001; Logani et al., 2002), although others refer to its absence (Sethi et al., 1972; Rajan and Lal, 2004); EPPO (2005) notes that its presence is not confirmed by the national plant protection service. For Saskatchewan, Canada, CABI/EPPO (1999) incorrectly cites Hannah and Hawn (1975) as the source; this is not a report of D. dipsaci in this province. However, D. dipsaci has been reported from the weed Cirsium arvense in Saskatchewan (Watson and Shorthouse, 1979). The authors indicate that a host-specific race may have evolved. See also CABI/EPPO (1998, No. 160).
A record of D. dipsaci in Taiwan (CABI/EPPO, 1999; EPPO, 2006) published in previous editions of the Compendium was incorrect and has been removed. D. dipsaci has not been found in Taiwan by Dr Tsai of National Chung Hsing University, who has conducted several years study of nematode fauna in Taiwan sponsored by The Bureau of Animal and Plant Health Inspection and Quarantine (BAPHIQ).
Distribution Table
Top of pageThe distribution in this summary table is based on all the information available. When several references are cited, they may give conflicting information on the status. Further details may be available for individual references in the Distribution Table Details section which can be selected by going to Generate Report.
Last updated: 22 Dec 2020Continent/Country/Region | Distribution | Last Reported | Origin | First Reported | Invasive | Reference | Notes |
---|---|---|---|---|---|---|---|
Africa |
|||||||
Algeria | Present | ||||||
Kenya | Present, Few occurrences | ||||||
Morocco | Present, Localized | ||||||
Nigeria | Absent, Unconfirmed presence record(s) | ||||||
Réunion | Present, Few occurrences | ||||||
South Africa | Present, Localized | ||||||
Tunisia | Present, Few occurrences | ||||||
Asia |
|||||||
Armenia | Present | ||||||
Azerbaijan | Present | ||||||
China | Present, Localized | ||||||
-Gansu | Present | ||||||
-Hebei | Present | ||||||
-Henan | Present | ||||||
-Shandong | Present | ||||||
-Sichuan | Present | ||||||
-Xinjiang | Present | ||||||
Georgia | Present | ||||||
India | Absent, Unconfirmed presence record(s) | ||||||
-Uttar Pradesh | Absent, Unconfirmed presence record(s) | ||||||
-West Bengal | Absent, Unconfirmed presence record(s) | ||||||
Iran | Present | ||||||
Iraq | Present | ||||||
Israel | Present, Widespread | ||||||
Japan | Present | ||||||
-Honshu | Present | ||||||
Jordan | Present | ||||||
Kazakhstan | Present | ||||||
Kyrgyzstan | Present | ||||||
Oman | Present, Few occurrences | 1993 | |||||
Pakistan | Present | ||||||
South Korea | Present | ||||||
Syria | Present, Few occurrences | ||||||
Taiwan | Absent, Invalid presence record(s) | ||||||
Turkey | Present, Localized | ||||||
Uzbekistan | Present | ||||||
Yemen | Present, Few occurrences | ||||||
Europe |
|||||||
Albania | Present | ||||||
Austria | Present, Widespread | ||||||
Belarus | Present | ||||||
Belgium | Present | ||||||
Bosnia and Herzegovina | Present | ||||||
Bulgaria | Present, Localized | First reported: 192* | |||||
Croatia | Present, Localized | ||||||
Cyprus | Present | ||||||
Czechia | Present, Widespread | ||||||
Czechoslovakia | Present | ||||||
Denmark | Present, Few occurrences | ||||||
Estonia | Present, Few occurrences | ||||||
Finland | Present, Localized | ||||||
France | Present, Localized | ||||||
Germany | Present, Widespread | ||||||
Greece | Present, Localized | ||||||
Hungary | Present, Localized | ||||||
Iceland | Present, Few occurrences | ||||||
Ireland | Present, Few occurrences | ||||||
Italy | Present | ||||||
-Sicily | Present | ||||||
Latvia | Present | ||||||
Lithuania | Present, Localized | ||||||
Malta | Present, Localized | 1976 | |||||
Moldova | Present | ||||||
Netherlands | Present, Localized | Present, in all parts of the area where host crops are grown. | |||||
North Macedonia | Present | ||||||
Norway | Present, Few occurrences | ||||||
Poland | Present, Localized | ||||||
Portugal | Present, Localized | ||||||
-Azores | Present | ||||||
-Madeira | Absent, Invalid presence record(s) | ||||||
Romania | Present, Localized | ||||||
Russia | Present | ||||||
-Central Russia | Present | ||||||
-Russian Far East | Present | ||||||
-Siberia | Present | ||||||
-Southern Russia | Present | ||||||
-Western Siberia | Present | ||||||
Serbia | Present | ||||||
Serbia and Montenegro | Present | ||||||
Slovakia | Present, Widespread | ||||||
Slovenia | Present, Localized | ||||||
Spain | Present, Localized | ||||||
-Canary Islands | Absent, Invalid presence record(s) | ||||||
Sweden | Present, Widespread | ||||||
Switzerland | Present, Widespread | ||||||
Ukraine | Present, Localized | ||||||
United Kingdom | Present, Widespread | ||||||
-England | Present, Widespread | ||||||
-Scotland | Present, Widespread | ||||||
-Wales | Present | ||||||
North America |
|||||||
Canada | Present, Localized | ||||||
-Alberta | Present | ||||||
-British Columbia | Present | ||||||
-Manitoba | Present | ||||||
-Ontario | Present | ||||||
-Prince Edward Island | Present | ||||||
-Quebec | Present | ||||||
-Saskatchewan | Present, Few occurrences | ||||||
Costa Rica | Present | ||||||
Dominican Republic | Present, Localized | ||||||
Haiti | Present, Localized | ||||||
Mexico | Present, Widespread | ||||||
United States | Present, Widespread |
| |||||
-Alabama | Present | ||||||
-Arizona | Present | ||||||
-California | Present | ||||||
-Colorado | Present | ||||||
-District of Columbia | Present | ||||||
-Florida | Absent, Invalid presence record(s) | ||||||
-Hawaii | Present | ||||||
-Idaho | Present | ||||||
-Illinois | Present | ||||||
-Michigan | Present | ||||||
-Minnesota | Present | ||||||
-Montana | Present | ||||||
-Nevada | Present | ||||||
-New Hampshire | Present | ||||||
-New Mexico | Present, Few occurrences | ||||||
-New York | Present | ||||||
-North Carolina | Present | ||||||
-Ohio | Present | ||||||
-Oregon | Present | ||||||
-South Dakota | Present | ||||||
-Utah | Present | ||||||
-Virginia | Present | ||||||
-Washington | Present | ||||||
-Wyoming | Present | ||||||
Oceania |
|||||||
Australia | Present, Localized | ||||||
-New South Wales | Present | ||||||
-Queensland | Present | ||||||
-South Australia | Present | ||||||
-Tasmania | Present | ||||||
-Victoria | Present | ||||||
-Western Australia | Present | ||||||
New Zealand | Present, Widespread | ||||||
South America |
|||||||
Argentina | Present | 1929 | |||||
Bolivia | Present | ||||||
Brazil | Present | ||||||
-Minas Gerais | Present | ||||||
-Paraiba | Present | ||||||
-Parana | Present | ||||||
-Rio Grande do Sul | Present | ||||||
-Santa Catarina | Present | ||||||
-Sao Paulo | Present | ||||||
Chile | Present, Widespread | ||||||
Colombia | Present | ||||||
Ecuador | Present, Localized | ||||||
Paraguay | Present, Localized | ||||||
Peru | Present | ||||||
Uruguay | Present, Widespread | ||||||
Venezuela | Present |
Risk of Introduction
Top of pageECONOMIC IMPORTANCE High
DISTRIBUTION Worldwide
SEEDBORNE INCIDENCE Low
SEED TRANSMITTED Yes
SEED TREATMENT Yes
OVERALL RISK High
Notes on phytosanitary risk
At present, the distribution of the different races throughout the region is patchy and some countries apply official control measures to limit spread. Other countries regard the pest as being a quality pest which can be effectively controlled by production and use of healthy planting material. Without control, D. dipsaci may cause complete failure of host crops within the EPPO region. EPPO lists it as an A2 quarantine pest. CPPC, IAPSC and NAPPO also consider it to be of quarantine significance.
The implementation of certification schemes for the production of host plants of D. dipsaci can provide planting material free from the pest. Imports of soil and plants for planting and seeds of host plants from countries where this nematode occurs should be restricted. See Anselme (1975) for international phytosanitary regulations for seeds.
Hosts/Species Affected
Top of pageIn addition to the hosts listed, Gnaphalium spicatum, Oxalis corniculata, Amaranthus deflexus and Eupatorium pauciflorum are reported as wild hosts of D. dipsaci.
Host Plants and Other Plants Affected
Top of pageGrowth Stages
Top of pageSymptoms
Top of pageAllium spp. (onions, garlic, leeks, etc.)
Penetration of onion leaves by D. dipsaci causes leaf deformation and leaf swellings or blister-like areas on the surface. The leaves grow in a disorderly fashion, often hang as if wilted and become chlorotic. Young plants can be killed by high infestations. The inner scales of the bulb are usually more severely attacked than the outer scales. As the season advances the bulbs become soft and when cut open show browning of the scales in concentric circles. Conversely, D. dipsaci on garlic does not induce deformation or swellings, but causes leaf yellowing and death (Netscher and Sikora, 1990).
Lucerne
The crop declines in patches in the field and damage is more serious in humid climates. The whole plant becomes desiccated and presents symptoms of stunting and swelling at the base of the stem with conspicuous shortened internodes. With heavy infestation, plants can be killed.
Tobacco
Invasion by the nematode of the lower part of the stem causes stunting and deformation of the plant followed by 'stem break'.
Faba beans, Vetch, Chickpea, Pea and Lentil
D. dipsaci causes swelling and deformation of stem tissue or lesions which turn reddish-brown then black, depending on cultivar and environmental factors. Newly formed pods take on a dark-brown appearance. The lesions envelop the stem and increase in length, often advancing to the edge of an internode. Leaf and petiole necrosis is also common under heavy infestations, but can be confused with symptoms induced by fungal leaf pathogens. Infected seeds are darker, distorted, smaller in size and may have speckle-like spots on the surface. Heavy infestations often kill the main shoots, stimulating secondary tiller formation. The more severe symptoms are usually induced by the 'giant race' on faba beans (Sikora and Greco, 1990). On faba bean (V. faba), D. dipsaci induces necrosis or swelling of the tissue. Infested stems of lentil and vetch (Vicia spp.) are swollen and show shortened internodes. D. dispaci induces local necrosis on pea and a total necrosis of the stem on vetch (Caubel et al., 1998).
Cereals (oats and rye)
D. dispaci causes the production of extra tillers at the base and the plants become swollen to give a typical 'tulip-root' appearance.
Narcissus
Narcissus leaves are distorted and often have characteristic pale swellings called 'spikkels'; infested bulbs usually have brown rings when sliced.
List of Symptoms/Signs
Top of pageSign | Life Stages | Type |
---|---|---|
Leaves / abnormal colours | ||
Leaves / abnormal forms | ||
Leaves / abnormal patterns | ||
Leaves / necrotic areas | ||
Seeds / discolorations | ||
Seeds / lesions on seeds | ||
Stems / discoloration of bark | ||
Stems / stunting or rosetting | ||
Vegetative organs / internal rotting or discoloration | ||
Whole plant / dwarfing | ||
Whole plant / plant dead; dieback |
Biology and Ecology
Top of pageIn onion plants at 15°C, the lifecycle takes approximately 20 days. The duration of the life cycle depends on the temperature and differs among isolates of different origins. Maximum activity and invasive ability is generally between 10 and 20°C. Females lay 200-500 eggs each. Fourth-stage juveniles tend to aggregate on or just below the surface of heavily infested tissue to form clumps of 'eelworm wool' and can survive in dry conditions for several years; they may also become attached to the seeds of host plants such as onions, lucerne, Trifolium pratense, faba beans and Phlox drummondii. In clay soils, D. dipsaci may persist for many years. Cool, moist conditions favour invasion of young plant tissue by this nematode.
For further information on the biology of D. dipsaci, see Seinhorst (1956), Dekker (1969), Hooper and Southey (1978), Sturhan and Brzeski (1991), Griffith et al. (1996, 1997a, b, 1999) and Williams-Woodward and Gray (1999).
Natural enemies
Top of pageNatural enemy | Type | Life stages | Specificity | References | Biological control in | Biological control on |
---|---|---|---|---|---|---|
Dactylella lysipaga | Predator | |||||
Drechmeria coniospora | Pathogen | |||||
Hirsutella rhossiliensis | Pathogen | |||||
Rhizoglyphus echinopus | Predator |
Means of Movement and Dispersal
Top of pageSeedborne Aspects
Top of pageIncidence
D. dipsaci has been shown to be seedborne on about 15 plant species (Neergaard, 1977). A survey of commercial seeds samples in the UK showed its widespread occurrence in economically important crops including 36-45% of seed stocks of broad been, red beet and carrots, 14-17% of shallots and runner beans and >3% of peas, onions and leeks (Green and Sime, 1979). High incidences of seed infection have been reported, e.g. 67% in broad bean seeds (Steiner and Lamprecht, 1983). Goodey (1945) traced invasion of D. dipsaci through the pedicel and placenta of the onion mother plant into the ovary wall and later through the short funiculus from which the nematodes become attached to the seed primarily in the vicinity of the hilum The nematode has also been located below the seed coat of Vicia faba (Neergaard, 1977). The pathogen was found in 1-40% of V. faba seeds in Algeria (Sellami et al., 1998).
The distribution of D. dipsaci between seeds in infested samples of broad bean seed was shown to be skewed so that the nematodes were concentrated on a few seeds (Green, 1979). Numbers of nematodes within individual seeds may vary substantially. In one of two samples of seed of Vicia faba, all stages of D. dipsaci were found. The other sample (50 seeds) was negative. In 20 seeds of the infected sample there were 20,035 larvae (over 8000 on one seed) (Pereira and Santos, 1975).
Effect on Seed Quality
Infected seeds are darker, distorted, smaller in size and may have speckle-like spots on the surface (Sikora and Greco, 1990).
Pathogen Transmission
Seed
Seed transmission of D. dipsaci to the planted crop is well established. Seinhorst and Koert (1971) found a strong correlation between the number of nematodes/g of seed and percentage of infected onion bulbs. Aerial photography of three fields of lucerne in the UK were used to monitor the spread of a seedborne infestation of D. dipsaci. Results from the use of an image analyser suggested that infestation develops by the generation of additional colonies from the original foci and by the progressive expansion of the area damaged by an established colony (Atkinson and Sykes, 1981). Planting certified nematode-free seeds is recognized as an important control practice for this disease. In Germany, a tolerance level of five nematodes/300 seeds is used to establish the risk of transmission of the pathogen to seedlings (Knuth, 1993).
Other sources
Nematode-infested soil is an important inoculum source of D. dipsaci. The number of nematodes/500g of soil were well correlated with the number/50 g of harvested onion seeds (Seinhorst and Koert, 1971). A tolerance threshold of 2-3 nematodes/250 cm³ soil is used in Germany to indicate risk of plant infection (Knuth, 1993). D. dipsaci-infested weeds are also recognized as a potentially important inoculum source of this nematode (Gentzsch, 1973).
Seed Treatment
Chemical
Treatment of seeds with nematicides or insecticides to control seed transmission of the pathogen has had mixed success (Schiffers et al., 1984; Whitehead and Tite, 1987; Adamova and Rotrekl, 1991; Hooper, 1991). Treatment of infected garlic cloves with abamectin resulted in a 56% yield increase and eliminated all nematodes in 93% of bulbs produced (Becker, 1999) but bulbs subjected to a combination of this chemical and hot-water treatment were somewhat damaged (Jaehn and Kimoto, 1996). In the UK, the best results against the stem nematode in Narcissus were obtained when formaldehyde or peracetic acid (at 1.0 and 1.5%) were used in combination with thiabendazole (Hanks and Linfield, 1999).
Ciesla et al. (2010) suggest that methyl iodide could be used as a fumigant to eradicate D. dipsaci from alfalfa seeds. Man?asová et al. (2012) propose the use of hydrogen cyanide gas to remove D. dipsaci from seed material.
Physical
Hot-water treatments with different temperature-time combinations, depending on type and state of seed material, can be an efficient means of controlling D. dipsaci (Gratwick and Southey, 1972). Commercial cleaning of the seed has proven to be effective in removing the nematodes along with associated plant debris (Wood and Close, 1974; Neergaard, 1977).
Seed Health Tests
Sieve test (Augustin and Sikora, 1989b)
- A sample of a minimum of 300 seeds should be examined.
- The seed is submerged for 24 h in 500-1000 ml of water, insuring sufficient oxygen for the nematode mobility and survival. An extraction temperature of 10°C is the optimum for nematode extraction and simultaneously reducing turbidity of the solution.
- The nematodes in the solution are concentrated by decantation through a 25 µm sieve and are then counted.
- Microscopic examination at 1000 times magnification is necessary for correct identification of the nematode species.
Pathway Vectors
Top of pageVector | Notes | Long Distance | Local | References |
---|---|---|---|---|
Clothing, footwear and possessions | Carrying bulbs, tubers, etc | Yes | ||
Containers and packaging - wood | Carrying bulbs, tubers, etc | Yes | ||
Soil, sand and gravel | Yes |
Plant Trade
Top of pagePlant parts liable to carry the pest in trade/transport | Pest stages | Borne internally | Borne externally | Visibility of pest or symptoms |
---|---|---|---|---|
Bulbs/Tubers/Corms/Rhizomes | Yes | |||
Flowers/Inflorescences/Cones/Calyx | adults; cysts; eggs; juveniles | Yes | ||
Fruits (inc. pods) | adults; cysts; eggs; juveniles | Yes | ||
Leaves | adults; cysts; eggs; juveniles | Yes | ||
Seedlings/Micropropagated plants | adults; cysts; eggs; juveniles | Yes | ||
Stems (above ground)/Shoots/Trunks/Branches | adults; cysts; eggs; juveniles | Yes | ||
True seeds (inc. grain) | adults; cysts; eggs; juveniles | Yes |
Plant parts not known to carry the pest in trade/transport |
---|
Bark |
Growing medium accompanying plants |
Roots |
Wood |
Impact
Top of pageD. dispaci is sometimes associated with other pathogens. For example, it transmits Corynebacterium insidiosum to lucerne plants (Hawn, 1963). Experimental infection of onions with D. dipsaci and Peronospora schleidenii together was 36.5% greater than with nematodes alone (Yakimenko and Efremenko, 1973).
Sturhan and Brzeski (1991) indicate that in heavy infestations, crop losses of 60-80% are not unusual. In Italy up to 60% of onion seedlings died before reaching the transplantation stage. On garlic, losses of 50% were recorded from Italy and more than 90% from France and Poland.
Diagnosis
Top of pageThe development and use of a PCR method for detecting D. dipsaci in Fabaceae seeds is detailed in Kerkoud et al. (2007), and is expanded upon (with computer-assisted characterisation of ribosomal DNA) in Marek et al. (2010). A further PCR protocol is given in Kierzek et al. (2010).
A diagnostic protocol for Ditylenchus dipsaci is described in EPPO (2008).
Detection and Inspection
Top of page
D. dipsaci can be isolated from samples of suspected seed material (according to symptoms) by dissection in water at 20 times magnification. A sample of a minimum of 300 seeds should be examined. The seed is submerged for 24 hours in 500-1000 ml of water, insuring sufficient oxygen for the nematode mobility and survival. An extraction temperature of 10°C is the optimum for nematode extraction and simultaneously reducing turbidity of the solution. The nematodes in the solution are concentrated by decantation through a 25 µm sieve and are then counted (Augustin and Sikora, 1989b). Microscopic examination at 1000 times magnification is necessary for correct identification of the nematode species.
Studies have been made for species identification based on DNA probes (Palmer et al., 1991), monoclonal antibodies (Palmer et al., 1992) and restriction fragment length polymorphisms (Wendt et al., 1994). These molecular methods are very promising, but not yet used routinely. Electrophoretic techniques (Bossis et al., 1998; Tenente and Evans, 1998) and random amplified polymorphic DNA (Esquibet et al., 1998) can be used to identify populations of D. dispaci.
The species morphologically indistinguishable from D. dipsaci cannot be identified by host differentials because of the within-race variations and because some of the races freely interbreed, giving hybrids with host characteristics intermediate between those of their parents (Sturhan and Brzeski, 1991). D. dipsaci can be distinguished from D. destructor by observation of the spiculum shape (Karssen and Willemsen, 2010).
Similarities to Other Species/Conditions
Top of pagePrevention and Control
Top of pageDue to the variable regulations around (de)registration of pesticides, your national list of registered pesticides or relevant authority should be consulted to determine which products are legally allowed for use in your country when considering chemical control. Pesticides should always be used in a lawful manner, consistent with the product's label.
Cultural Control
Control by crop rotation is limited by the polyphagous habit of some races of D. dipsaci and by persistence of the nematode in clay soils but a 3-4 year rotation to lettuce eliminated the nematode in New York State (Lorbeer et al., 1997). Chemical treatments of the soil are not an economic proposition for large areas. However, it may sometimes be worth treating small patches, after lifting and destroying the affected plants (bulbs) together with a margin of surrounding healthy ones, to eradicate a slight infestation before it spreads. Systemic nematicides may be effective to some extent in controlling D. dipsaci in some ornamental crops. The use of tolerant or resistant cultivars can also reduce the damage. Nematophagous fungi such as Verticillium balanoides may be suitable for development as biological control agents for D. dipsaci (Hay and Bateson, 1997).
Soil solarization has been tried in Israel (Siti et al., 1981) and Italy (Greco et al., 1985; Greco and Brandonisio, 1990). Excellent results were seen in the Israel trials.
Sanitation
Certified nematode-free seeds and planting material are most essential to prevent crop damage by D. dipsaci. Hot-water treatments with different temperature-time combinations, depending on type and state of seed material, are operational and efficient to control D. dipsaci (Gratwick and Southey, 1972). Hot-water treatment of narcissus bulbs infected with stem nematodes consist either of storage for 1-2 weeks at 25-30°C, followed by soaking in water for 24 h and hot-water treatment at 45°C for 4 h, or storage for 1-2 weeks at 25-30°C, followed by hot-water treatment at 47°C for 4 h. Routine hot-water treatment for the control of other pests and diseases should be carried out at 43.5°C for 3 h to control any slight, possibly unnoticed nematode infection (Windrich, 1973).
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