Abstract:Wild-type Fusarium sp. #CNCM I-1621 does not contain a NEP1-like gene, explaining why it seemed amenable to transformation with high expression, and its virulence was probably enhanced by not cosuppressing the endogenous gene as occurred with Fusarium oxysporum #CNCM I-1622.
“…As the study of semagenesis in parasitic angiosperms converges with the more robust genetic and physiological model organisms of A. thaliana and N. tabacum , a wealth of new experimental approaches should emerge. The results of these studies may contribute to the emerging robust strategies for controlling parasitic plants 19, 49. Furthermore, with more than 50 years of evidence implicating derivatives of plant cell‐wall phenolics in plant growth, development and the oxidative burst response,6, 50 semagenesis may now extend the activity of these compounds to a common language in rhizosphere ecology.…”
Section: Discussionmentioning
confidence: 90%
“…The results of these studies may contribute to the emerging robust strategies for controlling parasitic plants. 19,49 Furthermore, with more than 50 years of evidence implicating derivatives of plant cell-wall phenolics in plant growth, development and the oxidative burst response, 6,50 semagenesis may now extend the activity of these compounds to a common language in rhizosphere ecology. Translating such a language would enrich our understanding of host recognition and parasitic commitment, provide unique insights and strategies for regulating plant growth and development and open new approaches for managing soil ecology.…”
Semagenesis enriches our understanding of the mechanisms available for small-molecule underground information exchange among plants. Critical differences in this process, as used by parasitic plants, are beginning to emerge and point towards new strategies for managing parasitic angiosperms in agricultural settings.
“…As the study of semagenesis in parasitic angiosperms converges with the more robust genetic and physiological model organisms of A. thaliana and N. tabacum , a wealth of new experimental approaches should emerge. The results of these studies may contribute to the emerging robust strategies for controlling parasitic plants 19, 49. Furthermore, with more than 50 years of evidence implicating derivatives of plant cell‐wall phenolics in plant growth, development and the oxidative burst response,6, 50 semagenesis may now extend the activity of these compounds to a common language in rhizosphere ecology.…”
Section: Discussionmentioning
confidence: 90%
“…The results of these studies may contribute to the emerging robust strategies for controlling parasitic plants. 19,49 Furthermore, with more than 50 years of evidence implicating derivatives of plant cell-wall phenolics in plant growth, development and the oxidative burst response, 6,50 semagenesis may now extend the activity of these compounds to a common language in rhizosphere ecology. Translating such a language would enrich our understanding of host recognition and parasitic commitment, provide unique insights and strategies for regulating plant growth and development and open new approaches for managing soil ecology.…”
Semagenesis enriches our understanding of the mechanisms available for small-molecule underground information exchange among plants. Critical differences in this process, as used by parasitic plants, are beginning to emerge and point towards new strategies for managing parasitic angiosperms in agricultural settings.
“…using this approach, but not enough to try field testing (e.g. Meir et al 2009), and it has not been tried with Striga, due to regulatory constraints. There has even been a suggestion to transgenically insert genes into Striga that when disseminated in a population via pollen would render the females sterile (Rector 2009).…”
“…Herbicide resistance would integrate well and augment the biocontrol strategies being developed for Striga 51 and for Orobanche ,52 as it is envisaged that the biocontrol agents, too, would be disseminated on the crop seed. If the biocontrol fungi are not resistant to the target‐site herbicide used, the pathogens will either have to be transformed to resistance or mutagenised and selected for herbicide resistance.…”
Section: Integrating Target‐site Resistance With Other Technologiesmentioning
It is necessary to control root parasitic weeds before or as they attach to the crop. This can only be easily achieved chemically with herbicides that are systemic, or with herbicides that are active in soil. Long-term control can only be attained if the crops do not metabolise the herbicide, i.e. have target-site resistance. Such target-site resistances have allowed foliar applications of herbicides inhibiting enol-pyruvylshikimate phosphate synthase (EPSPS) (glyphosate), acetolactate synthase (ALS) (e.g. chlorsulfuron, imazapyr) and dihydropteroate synthase (asulam) for Orobanche control in experimental conditions with various crops. Large-scale use of imazapyr as a seed dressing of imidazolinone-resistant maize has been commercialised for Striga control. Crops with two target-site resistances will be more resilient to the evolution of resistance in the parasite, if well managed.
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