1997
DOI: 10.1023/b:joec.0000006348.62578.fd
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Antinutritive and Oxidative Components as Mechanisms of Induced Resistance in Cotton to Helicoverpa zea

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Cited by 121 publications
(81 citation statements)
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“…Anionic PODs have been implicated in a variety of leaftoughening responses, such as lignin biosynthesis (Gaspar et al, 1985;Díaz and Merino, 1998), suberization (Espelie et al, 1986;McDougall, 1993), and crosslinking of cell walls and extensin polymers (Ridge and Osborne, 1970;Everdeen et al, 1988;Bostock and Stermer, 1989). Such toughening processes may decrease the nutritional quality of the plant tissue for herbivores (Bi et al, 1997) as well as prevent secondary pathogen infection (Vance et al, 1980;Bostock and Stermer, 1989).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Anionic PODs have been implicated in a variety of leaftoughening responses, such as lignin biosynthesis (Gaspar et al, 1985;Díaz and Merino, 1998), suberization (Espelie et al, 1986;McDougall, 1993), and crosslinking of cell walls and extensin polymers (Ridge and Osborne, 1970;Everdeen et al, 1988;Bostock and Stermer, 1989). Such toughening processes may decrease the nutritional quality of the plant tissue for herbivores (Bi et al, 1997) as well as prevent secondary pathogen infection (Vance et al, 1980;Bostock and Stermer, 1989).…”
Section: Discussionmentioning
confidence: 99%
“…Considering the induction in greenhouse seedlings of isozymes A4.4, A4.1, and A3.9, and previous studies of POD wound responsiveness in other plants (e.g., Felton et al, 1994;Bi and Felton, 1995;Bi et al, 1997), we expected total soluble POD activity to increase in response to wounding and JA treatments. Surprisingly, total POD activity was reduced by JA treatment (Figure 1) and was generally unrelated to the isoform values in any clear way.…”
Section: Discussionmentioning
confidence: 99%
“…In N. attenuata, these herbivore-induced defenses include nicotine and TPI (Steppuhn et al, 2004;Zavala et al, 2004b). Because AZ plants have lost their TPI defense mechanism (Wu et al, 2007b), we analyzed the levels of nicotine as well as two phenolic compounds, chlorogenic acid and rutin, which are putative antiherbivore defenses (Isman and Duffey, 1982;Bi et al, 1997) and may constitute part of N. attenuata's direct defense.…”
Section: Ut and Az Produce Different Levels Of Antiherbivory Secondarmentioning
confidence: 99%
“…Little is known about how CAB and other VOCs, which may also act as indirect defense compounds, are synthesized and regulated in N. attenuata. The synthesis of phenolic compounds in N. attenuata and their possible influence on M. sexta performance also remains to be characterized; some studies have revealed potential antiherbivore functions of phenolic compounds (Isman and Duffey, 1982;Bi et al, 1997). Further biochemical and genetic studies are needed to elucidate the ELPs in biosynthetic genes that may underlie the differential regulation of these compounds.…”
Section: Natural Variation Of Secondary Metabolitesmentioning
confidence: 99%
“…Chewing by free-living insects induces defensive biochemical responses in many tree species (Karban and Baldwin, 1997), including chestnut oak, which responds to gypsy moth (Lymantria dispar L.) attack by increasing production of polyphenols in the leaves (Hunter and Schultz, 1995). Plant defense responses may also include increased activity of oxidative enzymes such as peroxidases (POXs) and polyphenol oxidase (PPO), which activate and polymerize polyphenols and are implicated in biochemical responses to insects and pathogens (Vaughn and Duke, 1984;Appel, 1993;Felton et al, 1994;Bi et al, 1997). The Nutrition Hypothesis predicts that such defensive responses should be suppressed in tissues consumed by galling insects.…”
Section: Introductionmentioning
confidence: 99%