Globodera ellingtonae

 

Contents

 

Rev 04/12/2022

  Classification Hosts
Morphology and Anatomy Life Cycle
Return to Globodera Menu Economic Importance Damage
Distribution Management
Return to Heteroderidae Menu Feeding  References
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Classification:

      Tylenchida
       Tylenchina
        Tylenchoidea
         Heteroderidae
          Punctoderinae
                  
        Globodera ellingtonae Handoo, Carta, Skantar & Chitwood 2012
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Morphology and Anatomy:

 

Females:

  • Stylet length 20-22.5 mm,
  • Head with one annule and labial disc.
  • Cuticle with heavy punctations.
  • Body globose, spherical, with a short neck and no terminal cone.

G. ellingtonae females. Photo from Handoo et al. (2012) 

All eggs retained in body (no egg-mass).

 

 

Males:

  • Vermiform; body twisted into a C or S shape. 
  • Stylet length of 21-25 �m
  • Spicule length 30-37 �m with a pointed thorn-like tip. 
  • Tail short, hemispherical.

 

Second-stage juveniles:

  • Stylet 19-22.5 �m long, basal knobs rounded.
  • Tail 39-55 mm with hyaline tail terminus 20-32.5 mm, tapering uniformly but abruptly constricted near the posterior third of the hyaline portion, finely rounded to pointed terminus.

Molecular Diagnosis:

  • Internal transcribed spacer (ITS) sequences of G. ellingtonae n. sp. are distinct from G. pallida, G. rostochiensis, G. tabacum and G. mexicana.
  • Bayesian and Maximum Parsimony analysis of cloned ITS rRNA gene sequences indicated three clades, with intraspecific variability as high as 2.8%.
  • In silico analysis revealed ITS restriction fragment length polymorphisms for enzymes Bsh1236I, Hinf I, and Rsa I that overlap patterns for other Globodera species.
  • Appears to be closer to G. rostochiensis than to G. pallida (Zasada et al., 2013).
Cysts:
Spherical to sub-spherical, dark to light brown and circumfenestrate.
Cyst wall pattern is ridge-like with heavy punctations.
Cyst passes through a golen color stage as it matures, similar to G. rostochiensis.


 
Circumfenestrate vulval cone of G. ellingtonae.  Photo from Handoo et al. (2012) 

Ref. Handoo et al. (2012)

Reported median body size for this species (Length mm; width micrometers; weight micrograms) - Click:

 

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Distribution:

  Recorded from one potato field in Oregon, one in Idaho and also a field of unknown crop history in Idaho (Handoo et al., 2012; Zasada et al., 2013a). Also reported from Argentina and Chile (Zasada et al., 2019).

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Economic Importance:

 

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Feeding:

Sedentary semi-endoparasite of roots

Feeding site and feeding patterns typical of genus Globodera.

Nurse cell system is a multinucleate syncytium.

Hatches in response to root diffustaes of tomato and potato.

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Hosts:

Potato and tomato.

For an extensive host range list for this species, click

 

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Life Cycle:

Ecophysiological Parameters:

For Ecophysiological Parameters for this species, click If species level data are not available, click for genus level parameters

 
On potato, eggs hatched after planting and the first adult females were observed between 387 and 449 DD6.  The second generation egg hatch occurred between 927 and 1073 DD6.  In soil, 76-96% of eggs hatched or otherwise disappeared from cysts, within 63 days after planting in the presence of potato,  but only 55-73% of the eggs hatched in the same period under bare soil (Phiilips et al. 2017).

Nematode goes into diapause between host crops; 75 % egg hatch in response to root diffusates of potato and tomato within 3 days; also eggs hatch readily in water.

Egg hatch stimulants for G. rostochiensis and G. pallida (sodium metavanadate, sodium orthovanadate, sodium thiocyanate) also stimulate egg hatch of G. ellingtonae.

Egg hatch was suppressed when cysts were exposed to host root diffusate and then transferred to root diffusates of arugula (Eruca satva, sudangrass (Sorghum bicolor ssp. drummondii, or vetch (Vicia sativa) (Zasada et al., 2013b).
 
   
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Damage:

In field and microplot studies, the effect of G. ellingtonae on yield of potato was inconsistent across years and experimental venues. In different trials there was a significant yield reduction of cultivars Russet Burbank and Ranger Russet. The nematode reproduced to various degrees, however, on all varieties tested in different individual experiments (Zasada et al., 2019)

 

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Management:

  Host Plant Resistance, Non-hosts and Crop Rotation alternatives:

Potato varieties resistant to G. rostochiensis pathotype Ro1 are resistant to G. ellingtonae (Zasada et al., 2013a). Resistance to G. rostochiensis pathotypes Ro1 and Ro2 is conferred by the H1 gene. Current evidence suggeste that the H1 gene may also confer resistance to G. ellingtonae because many cultivars resistant to G. rostochiensis are also resistant to G. ellingtonae (Whitworth et al., 2018).

For plants reported to have some level of resistance to this species, click
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References:

Handoo, Z.A., Carta, L.K, Skantar, A.M., Chitwood, D.J. 2012. Description of Globodera ellingtonae n. sp. (Nematoda: Heteroderidae) from Oregon. J. Nematology 44:40-57.

Phillips, W.S., Kitner, M., Zasada, I.A. 2017. Developmental Dynamics of Globodera ellingtonae in Field-Grown Potato. Plant Disease 101:1182-1187.

Whitworth, J.L., R.G. Novy, I.A. Zasada, X. Wang, L-M. Dandurand, and J. C. Kuhl 2018. Resistance of Potato Breeding Clones and Cultivars to Three Species of Potato Cyst Nematode. Plant Disease 102:2120-2128.

Zasada, I., Ingham, R.E., Phillips, W. 2013a. Current state of knowledge of Globodera ellingtonae: a new cyst nematode species.  ONTA Absrtacts, La Serena, Chile.

Zasada, I., Ingham, R.E., Baker, H., Phillips, W. 2019. Impact of Globodera ellingtonae on yield of potato (Solanum tuberosum). J. Nematology 51:DOI: 10.21307/jofnem-2019-073.

Zasada, I., Navarre, R.A., Peetz, A., Wade, N., Ingham, R.E. 2013b.  Host status of different potato (Solabnum tuberosum) varieties and hatching in root diffusate of Globodera ellingtonae. SON Abstracts, Knoxville.

 

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Copyright © 1999 by Howard Ferris.
Revised: April 12, 2022.