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15 results for “Globodera”

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zenodo40/100

Fig. 2 in Current Distribution Of Golden Potato Cyst Nematode, Globodera Rostochiensis (Tylenchida, Heteroderidae), In Ukraine

Fig. 2. Occurrence of Golden potato cyst nematode, Globodera rostochiensis, on the territory of Ukraine: A — Volynska; B — Rivnenska; C — Zhytomyrska; D — Kyivska; E — Сhernihivska; F — Sumska; G — Lvivska; H — Ternopilska; I — Khmelnytska; J — Cherkaska; K — Poltavska; L — Kharkivska; M — Luhanska; N — Zakarpatska; O — Ivano-Frankivska; P — Chernivetska; Q — Vinnytska; R — Kirovogradska; S — Dnipropetrovska; T — Donetska; U — Odeska; V— Mylolaivska; W — Khersonska; X — Zaporizka; Y — AR Krym.

opencc-by-4.0Dec 2021View details →
zenodo40/100

Fig. 1 in Current Distribution Of Golden Potato Cyst Nematode, Globodera Rostochiensis (Tylenchida, Heteroderidae), In Ukraine

Fig. 1. Study area of monitoring survey of G. rostochiensisin soils of private farm plots (own data, 2017–2018) 1. Chernihiv Region: а — Horodniansky District; b — Chernihivsky District; c — Mensky District; d — Koryukivsky District; e — Novhorod-Siversky District. 2. Kyiv Region: а — Borodiansky District.

opencc-by-4.0Dec 2021View details →
zenodo40/100

Figure 2 in Biology, pathotype, and virulence of Globodera rostochiensis populations from Kenya

Figure 2: Figure showing the mean number of different developmental stages of Globodera rostochiensis, of 'HAR1' and 'Ecosse' populations in resistant cv. 'Laura' and susceptible cv. 'Désirée' in the glasshouse in the second experiment.

opencc-by-4.0Dec 2020View details →
zenodo40/100

Figure 1 in Biology, pathotype, and virulence of Globodera rostochiensis populations from Kenya

Figure 1: Figure showing the mean number of different developmental stages of Globodera rostochiensis, 'HAR1' and 'Ecosse' populations in resistant cv. 'Laura' and susceptible cv. 'Désirée' in the glasshouse during the first experiment.

opencc-by-4.0Dec 2020View details →
zenodo40/100

Figure 4 in Biology, pathotype, and virulence of Globodera rostochiensis populations from Kenya

Figure 4: Percentage hatch of Globodera rostochiensis 'HAR1' population in PRD for three successive generations of cysts without diapause. Vertical bars are mean percentage ± standard error (n = 4).

opencc-by-4.0Dec 2020View details →
zenodo40/100

Figure 3 in Biology, pathotype, and virulence of Globodera rostochiensis populations from Kenya

Figure 3: Mean reproduction factor (±SE) of six populations of Globodera rostochiensis from Kenya on the susceptible cultivar 'Désirée' for three successive generations without diapause. Vertical bars show the standard error of the mean (n = 6). Means within a population with the same small letter are not significantly different (p> 0.05).

opencc-by-4.0Dec 2020View details →
zenodo40/100

Figure 2 in First report of morphological and molecular characterization of Moroccan populations of Globodera pallida

Figure 2: Photomicrographs of morphological characterization of cyst, egg, and second-stage juvenile. A, B: Cyst of GlOBOdeRa pallida, C: Vulva (v), anus (a), and cuticular ridges (r) of cyst, D, E: Stylet knob shape of J2, F: Juvenile tail.

opencc-by-4.0Dec 2020View details →
zenodo40/100

Figure 3 in First report of morphological and molecular characterization of Moroccan populations of Globodera pallida

Figure 3: Amplified PCR products from GlOBOdeRa Spp. digested by three enzymes AluI, MboI, and RsaI. A: Amplified PCR products, B: AluI, C: RsaI, D: MboI, MW: molecular weight markers (1 kb), NC: negative control, PC: undigested DNA, S1-S2: Eastern region samples, S3-S4: Western region samples (Gharb), S5-S6: Doukkala region samples.

opencc-by-4.0Dec 2020View details →
zenodo36/100

Figure 1 in First report of morphological and molecular characterization of Moroccan populations of Globodera pallida

Figure 1: Sampled areas and regions infested with GlOBOdeRa pallida in Morocco.

opencc-by-4.0Dec 2020View details →
dryad32/100

VCF file of multiple single-cyst-derived Ro1 and Ro2 lines of New York fields on Globodera rostochiensis genome

<p>The potato cyst nematode, <em>Globodera rostochiensis</em>, is a regulated pest posing a serious threat to potato production worldwide. Although the endemic pathotype (Ro1) of <em>G. rostochiensis</em> has been confined to New York State for several decades as a result of quarantine regulations and management with resistant potato cultivars, a virulent pathotype, Ro2, has emerged, for which control measures are scarce. The ability to detect Ro2 early in fields is necessary to sustain the success of <em>G. rostochiensis</em> quarantine in the US. Here, we report the comparative analysis of whole-genome sequences of multiple single-cyst-derived Ro1 and Ro2 lines, propagated from original field populations. The identified discriminant variants are good targets for developing molecular diagnostic tools for differentiating <em>G. rostochiensis</em> pathotypes in NY.</p>

opencc-zeroOct 2020View details →
dryad32/100

VCF file of multiple single-cyst-derived Ro1 and Ro2 lines of New York fields on Globodera rostochiensis genome

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publicOct 2020View details →
dryad28/100

Data from: The genome of the yellow potato cyst nematode Globodera rostochiensis reveals insights into the basis of parasitism and virulence

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publicMay 2017View details →
dryad28/100

Data from: Exploring the causes of small effective population sizes in cyst nematodes using artificial Globodera pallida populations

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publicDec 2018View details →
dryad24/100

Data from: Adaptation to resistant hosts increases fitness on susceptible hosts in the plant parasitic nematode Globodera pallida

Trade-offs between virulence (defined as the ability to infect a resistant host) and life-history traits are of particular interest in plant pathogens for durable management of plant resistances. Adaptation to plant resistances (i.e., virulence acquisition) is indeed expected to be associated with a fitness cost on susceptible hosts. Here, we investigated whether life-history traits involved in the fitness of the potato cyst nematode Globodera pallida are affected in a virulent lineage compared to an avirulent one. Both lineages were obtained from the same natural population through experimental evolution on resistant and susceptible hosts, respectively. Unexpectedly, we found that virulent lineages were more fit than avirulent lineages on susceptible hosts: they produced bigger cysts, containing more larvae and hatching faster. We thus discuss possible reasons explaining why virulence did not spread into natural G. pallida populations.

opencc-zeroDec 2015View details →
dryad24/100

Data from: Adaptation to resistant hosts increases fitness on susceptible hosts in the plant parasitic nematode Globodera pallida

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publicFeb 2017View details →

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