2015
DOI: 10.1371/journal.ppat.1004918
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Characterization of Arabidopsis Transcriptional Responses to Different Aphid Species Reveals Genes that Contribute to Host Susceptibility and Non-host Resistance

Abstract: Aphids are economically important pests that display exceptional variation in host range. The determinants of diverse aphid host ranges are not well understood, but it is likely that molecular interactions are involved. With significant progress being made towards understanding host responses upon aphid attack, the mechanisms underlying non-host resistance remain to be elucidated. Here, we investigated and compared Arabidopsis thaliana host and non-host responses to aphids at the transcriptional level using th… Show more

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Cited by 52 publications
(70 citation statements)
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“…30% more leaf tissue on the cell wall peroxidase-deficient anti-sense transgenic line asFBP1.1 (Bindschedler et al, 2006; Daudi et al 2012), which suggests that cell wall peroxidases are a major source of ROS during herbivore attack as they are during pathogen attack. Although the NADPH oxidases also produce ROS during herbivore and pathogen attack, and contribute to plant defense against aphids (Jaouannet et al, 2015; Miller et al, 2009; Torres et al, 2002, 2005), and caterpillars (Wu et al, 2013), S. flava larvae consumed equal amounts of leaf tissue on the rbohD and rbohF mutants vs. WT plants (Figure 3C). In these latter mutants, any reduction in ROS-mediated resistance to S. flava might be offset by the enhanced propensity for initiating PCD as is the case in the pmr4-1 mutant.…”
Section: Resultsmentioning
confidence: 99%
“…30% more leaf tissue on the cell wall peroxidase-deficient anti-sense transgenic line asFBP1.1 (Bindschedler et al, 2006; Daudi et al 2012), which suggests that cell wall peroxidases are a major source of ROS during herbivore attack as they are during pathogen attack. Although the NADPH oxidases also produce ROS during herbivore and pathogen attack, and contribute to plant defense against aphids (Jaouannet et al, 2015; Miller et al, 2009; Torres et al, 2002, 2005), and caterpillars (Wu et al, 2013), S. flava larvae consumed equal amounts of leaf tissue on the rbohD and rbohF mutants vs. WT plants (Figure 3C). In these latter mutants, any reduction in ROS-mediated resistance to S. flava might be offset by the enhanced propensity for initiating PCD as is the case in the pmr4-1 mutant.…”
Section: Resultsmentioning
confidence: 99%
“…On the route to the phloem, the stylets navigate between epidermal and mesophyll cells, occasionally penetrating these cells during a process known as the pathway feeding phase (Tjallingii, 1985;Tjallingii and Esch, 1993). The ability of an aphid to feed successfully on a plant appears to be partly determined during these penetrations, as the pathway phase still occurs with aphid species unable to establish long-term feeding (Chen et al, 1997;Sauge et al, 1998;Jaouannet et al, 2015;Nam and Hardie, 2012). Furthermore, as with microbial pathogens, aphids are detected through a BAK1-dependent mechanism, although the PRRs involved have remained elusive, with FLAGELLIN-SENSITIVE2 (FLS2), EF-TU RECEPTOR (EFR), CHITIN ELICITOR RECEPTOR KINASE1 (CERK1), PEP1 RECEPTOR1 (PEPR1), and PEPR2 not appearing to play a role (Prince et al, 2014;Chaudhary et al, 2014).…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, insects and mites secrete proteins in their saliva which modulate, and even suppress, the plant defense response (Kant et al, 2015; Villarroel et al, 2016). In the saliva, proteins from arthropod-associated microorganisms, i.e., endosymbiont bacteria and viruses, are also responsible for plant defense elicitation (Chaudhary et al, 2014; Jaouannet et al, 2015). Similarly, plant viruses encode suppressors to efficiently overcome the RNA silencing (Li and Ding, 2006).…”
Section: Introductionmentioning
confidence: 99%