2002
DOI: 10.1023/a:1015634617334
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Cited by 142 publications
(34 citation statements)
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“…This contrasts with what was reported in other legume, broad bean, NHR to rust, where the successful location of stomata by the inappropriate wheat stripe rust was significantly reduced (Cheng et al, 2012). However, similarly to most rust plant hosts (Niks and Rubiales, 2002), pre-penetration resistance mechanisms, including reduction of urediospore germination and fungal development on the leaf surface, seem to be of marginal importance in M. truncatula against U. striatus , at best, in reducing infection levels.…”
Section: Discussionmentioning
confidence: 97%
See 1 more Smart Citation
“…This contrasts with what was reported in other legume, broad bean, NHR to rust, where the successful location of stomata by the inappropriate wheat stripe rust was significantly reduced (Cheng et al, 2012). However, similarly to most rust plant hosts (Niks and Rubiales, 2002), pre-penetration resistance mechanisms, including reduction of urediospore germination and fungal development on the leaf surface, seem to be of marginal importance in M. truncatula against U. striatus , at best, in reducing infection levels.…”
Section: Discussionmentioning
confidence: 97%
“…It is today widely accepted that resistances genetically more complex, based on multiple loci, have the potential to be more durable. Nevertheless, durability is not only dependent on a complex genetic basis, but also on the resistance mechanisms involved, as some single-gene controlled mechanisms have proven to be more durable than others (Niks and Rubiales, 2002). The single-gene resistance most commonly used in rust resistance breeding is typically due to a post-haustorial defense mechanism, in which the plant cell collapses after the rust fungus started to form a haustorium in the cell resulting in hypersensitivity.…”
Section: Introductionmentioning
confidence: 99%
“…Poor germling adhesion to the leaf surface (Mendgen 1978;Wynn and Staples 1981), deviating micromorphology of the epidermal surface (Wynn and Staples 1981), stomatal guard cell morphology (Wynn 1976), epicuticular leaf wax layer (Vaz Patto and Niks 2001), leaf pubescence (Mmbaga et al 1994) and pH gradient on the epidermis (Wynn 1976;Edwards and Bowling 1986;Niks and Rubiales 2002) have been described in different plant species as influencing the germtube growth orientation and could be contributing to the less oriented germtube growth observed in the majority of the L. cicera accessions when compared with the pea check. This might be relevant reducing the infectability by reducing the number of infection units (appressorium over stoma).…”
Section: Discussionmentioning
confidence: 99%
“…Prehaustorial resistance is one of such mechanisms and prevents the formation of haustoria by the fungus. It is very common in nonhost interactions (Heath 1981), but can also be identified in host interactions, as a major component of partial resistance (Niks and Rubiales 2002;Rubiales and Niks 1995). Screening Lathyrus germplasm for disease resistance may result in the discovery of new resistance genes for pyramidation or non-hypersensitive, potentially more durable defence mechanisms to introduce into resistance breeding programs.…”
Section: Introductionmentioning
confidence: 99%
“…Cell death can occur very fast so no haustorium can be observed, or rather slow, allowing formation of some haustoria and secondary hyphae (Prats et al 2007). HR is frequently described in resistance to powdery mildews (Boyd et al 1995;Niks and Rubiales 2002) and is the main mechanism of resistance in er2 and Er3 lines of pea (Fondevilla et al 2006b).…”
Section: Introductionmentioning
confidence: 99%