Plant responses to insect herbivory: the emerging molecular analysis.

By André Kessler, Ian T. Baldwin. Annual Review of Plant Biology, 2002

1,540 citations recorded by the source corpus.

Subfields: Insect Science, Plant Science

View Paper: https://www.semanticscholar.org/paper/ab934d7417eb0cc8acf0d29b306cd9ac7d8067cd

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Insect Science

1. Martin Heil
2. M. Maffei
3. G. Howe
4. M. Dicke
5. C. Pieterse
6. Ian T. Baldwin
7. Matthias Erb
8. Ming-shun Chen

In Plant Science

1. Martin Heil
2. C. Pieterse
3. M. Dicke
4. M. Maffei
5. G. Howe
6. Ian T. Baldwin
7. L. C. van Loon
8. L. Walling

Citations in the corpus

• New approaches for studying and exploiting an old protuberance, the plant trichome. (2004, background): “…exploit trichomes for commercial and agronomic purposes. ã 2004 Annals of Botany Company Keywords: Plant secretion, simple trichomes, glandular trichomes, secreted phytochemicals, arabidopsis, tobacco, gene library, pest resistance, molecular farming, trichome differentiation, trichome functions.”
• Jasmonates and Related Compounds in Plant-Insect Interactions (2004, background): “Interestingly, despite the availability of a large number of mutants and transgenic plants, their potential for elucidating the mechanisms of herbivore resistance elicitation is only recently being realized (Berger 2002; Kessler and Baldwin 2002 ).”
• Sites of synthesis, biochemistry and functional role of plant volatiles (2010, background): “Direct defenses include any plant traits that by themselves affect the susceptibility of host plants to insect attacks (Kessler and Baldwin, 2002), whereas indirect defenses include plant traits that by themselves do not affect the susceptibility of host plants, but can serve as attractants to…”
• Systemic acquired resistance and induced systemic resistance in conventional agriculture (2004, background): “, 1999; Genoud and Méfits the overall fitness of the plant relative to constitutive defense mechanisms (Coley et al., 1985; Hatcher and traux, 1999; Kessler and Baldwin, 2002; McDowell and Dangl, 2000; Walling, 2000).”
• Involvement of Jasmonic Acid and Derivatives in Plant Response to Pathogen and Insects and in Fruit Ripening (2004, background): “JAs are well characterized with respect to their role in regulating defense responses against herbivore attack and infection by some pathogens (Kessler and Baldwin 2002; Turner and others 2002; Wasternack and Hause 2002; Weber 2002).”
• Comparative metabolomics and transcriptomics of plant response to Tomato yellow leaf curl virus infection in resistant and susceptible tomato cultivars (2014, background): “Generally, defense responses to herbivorous insects are mediated by the phytohormones JA and ET (Thomma et al. 2001; Kessler and Baldwin 2002; Glazebrook 2005).”
• The molecular bases of plant resistance and defense responses to aphid feeding: current status (2007, background): “The intricate interactions between aphids and plants comprise an excellent model system with which to study the coadaptations of plants and herbivorous arthropods described in previous reviews of Stotz et al. (1999), Kessler & Baldwin (2002), and Kaloshian (2004).”
• Upregulation of ginsenoside and gene expression related to triterpene biosynthesis in ginseng hairy root cultures elicited by methyl jasmonate (2009, positive): “Methyl jasmonate is a plant-specific signaling molecule which mediates and steers a diverse set of physiological and developmental processes, including root growth, pollen production, and plant resistance against insect and pathogenic attack (Creelman and Mullet 1997; Kessler and Baldwin 2002 ).”
• Role of phytohormones in insect-specific plant reactions (2012, background): “Research aimed at identifying herbivore-derived elicitors has therefore relied on the application of insect oral secretions to wound sites created by mild wounding regimens that do not elicit a strong defense response in the absence of oral secretion [35, 36, 48–50].”
• The Tomato Homolog of CORONATINE-INSENSITIVE1 Is Required for the Maternal Control of Seed Maturation, Jasmonate-Signaled Defense Responses, and Glandular Trichome Development Online version contains Web-only data. Article, publication date, and citation information can be found at www.plantcell.org (2004, background): “These signaling compounds, collectively referred to as JAs, are ubiquitous in the plant kingdom and are well characterized with respect to their role in regulating defense responses against herbivore attack and infection by some pathogens (Kessler and Baldwin, 2002; Turner et al., 2002; Wasternack a”
• The multiple faces of indirect defences and their agents of natural selection (2011, background): “For example, in wild tobacco Nicotiana attenuata, the major herbivore, tomato hornworm (Manduca quinquemaculata) has significant negative effects on plant fitness (Kessler & Baldwin 2002a, 2004).”
• Inducible direct plant defense against insect herbivores: A review (2008, background): “Tel: 785 532 4719; fax: 785 532 6232; email: mchen@ksu.edu defenses consist of three steps: surveillance, signal transduction, and the production of defensive chemicals (Dangl & McDowell, 2006; Ferry et al., 2004; Kessler & Baldwin, 2002; Walling, 2000).”
• Signaling responses in plants to heavy metal stress (2007, background): “The data are illustrated in Table 2. Such an effect has been known for the action of signaling molecules like jasmonates, salicylic acid, ethylene and abscisic acid (Finkelstein et al. 2002; Kessler and Baldwin 2002; Neill et al. 2002; Turner et al. 2002; Wang et al. 2002; Eckardt 2003; Farmer 200”