Hormonal modulation of plant immunity.

By C. Pieterse, Dieuwertje Van der Does, C. Zamioudis, Antonio León-Reyes, Saskia C. M. Van Wees. Annual Review of Cell and Developmental Biology, 2012

2,636 citations recorded by the source corpus.

Subfields: Plant Science

View Paper: https://www.semanticscholar.org/paper/2175433d04e14fc304fd09e413a30fd48b8aacd6

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Citations in the corpus

Trade-Offs in Arbuscular Mycorrhizal Symbiosis: Disease Resistance, Growth Responses and Perspectives for Crop Breeding (2017, positive): “(2012) suggest that host plants initially treat AMF as potential invaders, activating defence programs that are later downregulated to allow colonization [32].”
Signaling mechanisms in pattern-triggered immunity (PTI). (2015, background): “) (Pieterse et al., 2009; RobertSeilaniantz et al., 2011; Naseem and Dandekar, 2012; Pieterse et al., 2012; Thaler et al., 2012; O’Brien and Benkova, 2013; De Bruyne et al., 2014).”
Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. (2013, background): “It has been recently reviewed in detail, with reference to its role in plant immunity (Pieterse et al., 2012).”
Induced systemic resistance by beneficial microbes. (2014, background): “In contrast, evidence is accumulating for a cytosolic function of NPR1 in JA/ET signaling and ISR (111, 122, 140, 143).”
Ecological and phytohormonal aspects of plant volatile emission in response to single and dual infestations with herbivores and phytopathogens (2013, background): “Rapid advances in our knowledge on the underlying mechanisms of plant defences have shown that the interactions under a multiple attack scenario are complex (Pieterse et al. 2012).”
Plant pathogens structure arthropod communities across multiple spatial and temporal scales (2013, background): “Here, one promising direction is to explore the different phytohormonal signalling pathways expressed in response to pathogens and herbivores (Pieterse et al. 2012; Thaler, Humphrey & Whiteman 2012), where several generalizations have recently emerged.”
Endophytic fungi promote plant growth and mitigate the adverse effects of stem rot: an example of Penicillium citrinum and Aspergillus terreus (2015, background): “…SA and JA content, we have determined that resistance to pathogenic infection might be induced (Durrant & Dong 2004; Halim et al. 2006), indicating the enduring and active role of endophytes in resistance to a broad range of pathogens (Halim et al. 2006; Aimé et al. 2008; Pieterse et al. 2012).”
Plant Defense Signaling and Responses Against Necrotrophic Fungal Pathogens (2016, neutral): “Plants defend against biotrophic pathogens like P. syringae through the SA-NPR1-TGA signaling cascade, but the toxin coronatine, produced by P. syringae acts as a strong analog of JA-Ile which binds to its receptor SCF COI1 to suppress the SA-mediated defense (Pieterse and others 2012).”
Plant hormone-mediated regulation of stress responses (2016, background): “Nevertheless, recent findings have proven beyond doubt that besides playing critical roles at individual levels, different plant hormones also crosstalk to facilitate the coordination of an array of genes and their regulators involved in stress remediation [42].”
Asymmetry of plant-mediated interactions between specialist aphids and caterpillars on two milkweeds (2014, background): “Our observation that even closely related congeners have very different SA-JA responses to their specialist herbivores is perhaps consistent with the vulnerability inherent to plants for maintaining such trade-offs, which can be exploited by attackers (Cui et al. 2005; Zarate, Kempema & Walling 2007”
Three‐way interactions between plants, microbes and insects (2013, background): “In the past two decades, molecular biologists have made vast progress in unravelling the complex regulation of the plant’s induced responses to biotic agents (e.g. Pieterse et al. 2012).”
Principles of Plant-Microbe Interactions (2015, background): “In SA signaling, NPR1 is clearly connected to a nuclear function (Fu and Dong 2013), while in JA/ET signaling and ISR evidence is accumulating for a cytosolic function of NPR1 (Spoel et al. 2003; Stein et al. 2008; Pieterse et al. 2012).”