scholarly journals First Report of Potato Cyst Nematode Globodera pallida Infecting Potato (Solanum tuberosum) in Kenya

Plant Disease ◽  
2018 ◽  
Vol 102 (8) ◽  
pp. 1671-1671 ◽  
Author(s):  
H. Mburu ◽  
L. Cortada ◽  
G. Mwangi ◽  
K. Gitau ◽  
A. Kiriga ◽  
...  
1982 ◽  
Vol 99 (2) ◽  
pp. 325-328 ◽  
Author(s):  
M. F. B. Dale ◽  
M. S. Phillips

SUMMARYThe inheritance of resistance to Globodera pallida was studied in seedling progenies derived from Solanum tuberosum ssp. andigena CPC 2802 (H3) and S. vernei and compared with resistance to G. rostochiensis derived from S. tuberosum ssp. andigena CPC 1673(H1). The resistance of CPC 2802 was originally thought to be due to a major gene (H3), but results presented here demonstrate that it and that derived from S. vernei are inherited in a similar manner quite distinct from the major gene inheritance from CPC 1673 (HI). It is concluded that the resistances derived from CPC 2802 and S. vernei are both polygenic in nature. These findings are discussed in relation to breeding policy and screening methods.


Nematology ◽  
2012 ◽  
Vol 14 (7) ◽  
pp. 869-873 ◽  
Author(s):  
Ayano Sasaki-Crawley ◽  
Rosane Curtis ◽  
Michael Birkett ◽  
Apostolos Papadopoulos ◽  
Rod Blackshaw ◽  
...  

This paper demonstrates a simple novel in vitro method using Pluronic F-127 aqueous solution to study the development of the potato cyst nematode, Globodera pallida, in Solanum spp. without any need for sterilisation of either the plants or the nematodes. In this study, this method was successfully applied to comparative studies on the development of G. pallida in Solanum tuberosum (potato) or S. sisymbriifolium (sticky nightshade). The protocol described here could be useful for screening transgenic plants or different plant cultivars/species for their ability to allow development not only of G. pallida but also any other plant-parasitic nematodes.


Nematology ◽  
2017 ◽  
Vol 19 (6) ◽  
pp. 739-747 ◽  
Author(s):  
Patrick M. Norshie ◽  
Ivan G. Grove ◽  
Matthew A. Back

As part of a broader study to evaluate the efficacy of fluensulfone for control of the potato cyst nematode,Globodera pallida, two field experiments in Shropshire (at Woodcote and Howle in 2010 and 2011, respectively) England, were used to monitor the persistence of fluensulfone in potato beds treated with Nimitz 15G®(fluensulfone) at 27 kg ha−1. Fluensulfone dissipated at similar rates in the two fields, with a trend best described by a sigmoidal curve. The time to 50% dissipation (DT50) was 24.3 days at Woodcote, and 23.7 days at Howle. No differences were found between the DT50for fluensulfone and that observed for fosthiazate. The short DT50demonstrated for fluensulfone in this study is a positive attribute as this nematicide may pose a negligible hazard to the environment. However, its persistence at an effective dose may be long enough to be effective over the peak hatch period ofG. pallida.


Plant Disease ◽  
2012 ◽  
Vol 96 (5) ◽  
pp. 773-773 ◽  
Author(s):  
S. Širca ◽  
B. Geric Stare ◽  
P. Strajnar ◽  
G. Urek ◽  
I. Miklic Lautar

The potato cyst nematodes (PCN) Globodera rostochiensis (Woll.) Behrens and G. pallida (Stone) Behrens are considered the most important nematode threat to potato production worldwide, and they are subject to strict quarantine regulations in many countries. The first report of the PCN in Slovenia dates back to 1971, when a single cyst of G. rostochiensis was detected (3). In the last decade, G. rostochiensis was detected several times, mainly in the central and northern parts of the country (2). Interceptions of G. pallida in imported consignments of ware potato were made several times, but had not been detected in soil in Slovenia. Therefore, the country was declared as a protected zone for G. pallida in the European Union by the national authorities in 2003. During the official PCN systematic survey in autumn 2011, the pale potato cyst nematode, G. pallida, was found in a soil sample. Two viable cysts were extracted and the nematode species was identified. The posterior part of the cysts containing eggs and juveniles were used for morphometrical analysis, while the anterior parts were used for DNA extraction and molecular analyses. The ribosomal internal transcribed spacer (ITS) region was amplified using ITS5 and PITSp4 primers and detected in real-time PCR using ABI7500 (Applied Biosystems, Life Technologies, Carlsbad, CA,) (1). Also, the ribosomal DNA region that extends from the 3′ end of the 18S ribosomal subunit and includes all of ITS1, 5.8S, and ITS2, to the 5′ end of the 28S ribosomal subunit, was used to generate a DNA sequence. The sequence obtained was compared with those from several Globodera species, revealing unequivocal similarity to G. pallida. The infested soil sample originated from a ware potato field near Ivancna Gorica, central Slovenia. Subsequently, an additional 69 samples were taken from the surroundings and viable G. pallida cysts were found in another five samples taken from two neighboring fields (one of grassland and the other of clover). Three fields, totaling 1.9 ha, were declared as G. pallida-infested. The eradication of the pest will take place by enforcing strict phytosanitary measures. Ware potatoes originating from areas where the pests occur is considered to be the most probable pathway for the introduction of G. pallida in Slovenia. A ware potato processing facility is situated in very close proximity to the infested fields. The waste waters from potato tuber washing were discharging onto the grassland, never used for potato or other field crop production in which the G. pallida infestation was found. The facility processes imported ware potato from several European and non-European countries. This case demonstrates that ware potato may pose a serious risk for the introduction of such pests, and should be therefore subjected to more intensive phytosanitary inspection. References: (1) J. Bacic et al. Russ. J. Nematol. 16:63, 2008. (2) S. Širca et al. Phytopathol. Mediterr. 49:361, 2010. (3) G. Urek et al. Nematology 5:391, 2003.


Plant Disease ◽  
2020 ◽  
Vol 104 (1) ◽  
pp. 293 ◽  
Author(s):  
I. Niragire ◽  
M. Couvreur ◽  
G. Karssen ◽  
B. Uwumukiza ◽  
W. Bert

Plant Disease ◽  
2020 ◽  
Vol 104 (11) ◽  
pp. 3082
Author(s):  
L. Cortada ◽  
J. Omagwa ◽  
J. Kisitu ◽  
M. Adhiambo ◽  
S. Haukeland ◽  
...  

Plant Disease ◽  
2016 ◽  
Vol 100 (8) ◽  
pp. 1794-1794 ◽  
Author(s):  
T. Narabu ◽  
T. Ohki ◽  
K. Onodera ◽  
T. Fujimoto ◽  
K. Itou ◽  
...  

Nematology ◽  
2004 ◽  
Vol 6 (3) ◽  
pp. 375-387 ◽  
Author(s):  
N. Aileen Ryan ◽  
Peter Jones

AbstractSeventy bacteria, isolated from the rhizosphere of the potato cyst nematode (PCN) host plant, potato, were cultured in the presence and absence of potato root leachate (PRL) and the resultant culture filtrates were analysed for their ability to affect the hatch in vitro of the two PCN species. Of the isolates tested, nine had a significant effect on PCN hatch. Six affected Globodera pallida hatch and three affected G. rostochiensis hatch. Five of the isolates significantly increased hatch only when cultured in the presence of PRL. Three of the isolates decreased PCN hatch significantly in PRL. Only one isolate increased hatch significantly in the absence of PRL. No isolate affected the hatch of both species. Six of the nine isolates that significantly affected PCN hatch had been pre-selected by culturing on PRL. Bacterial isolates from PCN non-hosts (14 from wheat, 17 from sugar beet) were also tested for hatching activity. The principal effect of the hatch-active isolates from the PCN non-host plants was to increase PCN hatch in the presence of PRL. In contrast to the host bacteria results, the isolates from non-host plants affected only G. rostochiensis hatch (three wheat isolates and four sugar beet isolates significantly increased G. rostochiensis hatch); no such isolate affected G. pallida hatch significantly in the presence of PRL. Ten isolates (32%) from non-host plants had the ability to increase significantly the hatch of PCN in the absence of PRL (eight of these affected G. rostochiensis hatch and four affected G. pallida hatch), compared to only one bacterial isolate (1%) from a host plant. The majority of the isolates from non-hosts produced PCN species-specific effects, as with the bacteria isolated from potatoes, although two wheat isolates increased the hatch of both species significantly in the absence of PRL. Of 20 hatch-active bacterial isolates (from all three plants) identified, 70% were Bacillus spp. Other genera identified were Arthrobacter , Acinetobacter and Staphylococcus .


Genes ◽  
2020 ◽  
Vol 11 (12) ◽  
pp. 1429
Author(s):  
Kyriakos Varypatakis ◽  
Pierre-Yves Véronneau ◽  
Peter Thorpe ◽  
Peter J. A. Cock ◽  
Joanne Tze-Yin Lim ◽  
...  

Although the use of natural resistance is the most effective management approach against the potato cyst nematode (PCN) Globodera pallida, the existence of pathotypes with different virulence characteristics constitutes a constraint towards this goal. Two resistance sources, GpaV (from Solanum vernei) and H3 from S. tuberosum ssp. andigena CPC2802 (from the Commonwealth Potato Collection) are widely used in potato breeding programmes in European potato industry. However, the use of resistant cultivars may drive strong selection towards virulence, which allows the increase in frequency of virulent alleles in the population and therefore, the emergence of highly virulent nematode lineages. This study aimed to identify Avirulence (Avr) genes in G. pallida populations selected for virulence on the above resistance sources, and the genomic impact of selection processes on the nematode. The selection drive in the populations was found to be specific to their genetic background. At the genomic level, 11 genes were found that represent candidate Avr genes. Most of the variant calls determining selection were associated with H3-selected populations, while many of them seem to be organised in genomic islands facilitating selection evolution. These phenotypic and genomic findings combined with histological studies performed revealed potential mechanisms underlying selection in G. pallida.


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