Elicitors, effectors, and R genes: the new paradigm and a lifetime supply of questions.

By A. Bent, David Mackey. Annual Review of Phytopathology, 2007

818 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/fce29a242de17eafb1ba4c4aa6b2018177523fd5

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Citations in the corpus

Fungal effector proteins. (2009, background): “Many reviews on bacterial, fungal, and oomycete Avr genes and their cognate R genes in plants have appeared in recent years (8, 24, 47, 67, 68).”
Current Approaches for Enhanced Expression of Secondary Metabolites as Bioactive Compounds in Plants for Agronomic and Human Health Purposes – a Review (2013, background): “One way to generate resistance in plants to stress conditions is the use of elicitors, because their application on plant surface activates multiple signaling pathways of intracellular defense [Bent & Mackey, 2007].”
Of PAMPs and Effectors: The Blurred PTI-ETI Dichotomy[OA] (2011, background): “As a consequence, the molecules that were historically termed elicitors or avirulence factors have more recently been renamed PAMPs and effectors, respectively (Chisholm et al., 2006; Jones and Dangl, 2006; Bent and Mackey, 2007).”
The inflammasomes: guardians of the body. (2009, background): “The vast repertoire of NLRs in plants is believed to be the result of a complex host-pathogen race that promoted the evolution of specific NLR genes that genetically interact with specific avirulence genes from distinct pathogens (47).”
Pattern-recognition receptors in plant innate immunity. (2008, background): “For aspects related to PTI signalling, PTI suppression by effectors and ETI, readers are directed to excellent recent reviews [1 ,2 ,3–7].”
Antibiotic resistance plasmids in wastewater treatment plants and their possible dissemination into the environment (2010, background): “The exogenous are isolated from pathogens or culture medium, while endogenous tissue are isolated from same plant (Ozeretskovskaya and Vasyukova, 2002; Zhao et al., 2005; Bent and Mackey, 2007).”
Growth-defense tradeoffs in plants: a balancing act to optimize fitness. (2014, neutral): “…a much stronger immune response, effectortriggered immunity (ETI), which often results in a type of programmed cell death response known as the hypersensitive response (HR) in pathogen-infected tissue (Chisholm et al., 2006; Jones and Dangl, 2006; Bent and Mackey, 2007; Caplan et al., 2008).”
Primary metabolism and plant defense--fuel for the fire. (2009, background): “…plant defense have shown that rates of photosynthesis are reduced locally after treatment with virulent or avirulent pathogens (Berger et al. 2004; Berger et al. 2007a; Bonfig et al. 2006; Chou et al. 2000; Doehlemann et al. 2008; Horst et al. 2008; Manter et al. 2007; Scharte et al. 2005;…”
Costs and benefits of induced resistance to herbivores and pathogens in plants (2010, background): “an inducibility of resistance that is dependent upon R-Avr gene matching will necessarily vary within and among populations [32, 33].”
Endophytic fungi as biocontrol agents: elucidating mechanisms in disease suppression (2018, background): “…often small cysteine-rich proteins, are secreted during both pathogenic and endophytic colonisation processes to promote compatibility with the host plant, by modulating defence responses and physiology (Bent and Mackey 2007; Rafiqi et al. 2013; Hacquard et al. 2016; Nogueira-Lopez et al. 2018).”