2013
DOI: 10.1007/s11032-013-9922-0
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Differentially expressed proteins during an incompatible interaction between common bean and the fungus Pseudocercospora griseola

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Cited by 9 publications
(6 citation statements)
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“…Pathogen/herbivore activity that results in damage to photosynthetic machinery, loss of photosynthetic tissue, and/ or disruption of the vasculature affecting water and sugar transport has been shown to negatively impact photosynthesis (Aldea et al, 2005;Zou et al, 2005;Gutsche et al, 2009;Nabity et al, 2009;Kerchev et al, 2012). In addition, pathogen/herbivore attack has been shown to suppress components of photosynthesis at the levels of gene expression and of protein abundance (Zou et al, 2005;Jung et al, 2007;Denoux et al, 2008;Ishiga et al, 2009;Bilgin et al, 2010;Sugano et al, 2010;Chen et al, 2011b;Gohre et al, 2012;Guo et al, 2012;Borges et al, 2013). The negative impact of defense on photosynthesis has been best demonstrated in response to JA treatment, which results in a reduction of components essential for light harvesting and carbon fixation (Wierstra and Kloppstech, 2000;Chen et al, 2011b;Shan et al, 2011;Guo et al, 2012) as well as a substantial decrease in photosynthetic activities and chlorophyll contents in Arabidopsis (Jung, 2004).…”
Section: Impacts On Photosynthesismentioning
confidence: 99%
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“…Pathogen/herbivore activity that results in damage to photosynthetic machinery, loss of photosynthetic tissue, and/ or disruption of the vasculature affecting water and sugar transport has been shown to negatively impact photosynthesis (Aldea et al, 2005;Zou et al, 2005;Gutsche et al, 2009;Nabity et al, 2009;Kerchev et al, 2012). In addition, pathogen/herbivore attack has been shown to suppress components of photosynthesis at the levels of gene expression and of protein abundance (Zou et al, 2005;Jung et al, 2007;Denoux et al, 2008;Ishiga et al, 2009;Bilgin et al, 2010;Sugano et al, 2010;Chen et al, 2011b;Gohre et al, 2012;Guo et al, 2012;Borges et al, 2013). The negative impact of defense on photosynthesis has been best demonstrated in response to JA treatment, which results in a reduction of components essential for light harvesting and carbon fixation (Wierstra and Kloppstech, 2000;Chen et al, 2011b;Shan et al, 2011;Guo et al, 2012) as well as a substantial decrease in photosynthetic activities and chlorophyll contents in Arabidopsis (Jung, 2004).…”
Section: Impacts On Photosynthesismentioning
confidence: 99%
“…In support of the growth-defense tradeoff theory, diversion of plant resources has been shown to occur at all levels, including machinery involved in transcription, translation, and protein secretion from cells as well as prioritization of carbon and nitrogen towards production of defense compounds. Transcriptomic and proteomic studies have demonstrated transcriptional reprogramming and altered protein profiles upon pathogen/herbivore detection to promote defense at the expense of growth Jung et al, 2007;Denoux et al, 2008;Bilgin et al, 2010;Sugano et al, 2010;Chen et al, 2011b;Gohre et al, 2012;Guo et al, 2012;Borges et al, 2013). Production and secretion of proteins with specific defensive properties, such as PR proteins, place a significant demand on the protein folding and secretory systems, which have also been shown to be required for defense (Wang et al, 2005;Kwon et al, 2008;Pajerowska-Mukhtar et al, 2012).…”
Section: Resource Diversionmentioning
confidence: 99%
“…The current proteomic analysis further indicated that 2-Cys Prx was specifically up-accumulated in the O 3 -exposed fruits that had been inoculated with B. cinerea . 2-Cys Prx is a distinct subgroup within the family of peroxiredoxins (PRXs) that are associated with resistance of plants to both biotic and abiotic stress, while in apple fruits, their downregulation has been linked to A. alternata susceptibility ( Borges et al, 2013 ; Ni et al, 2017 ; Ojeda et al, 2018 ). Given that PRXs are highly conserved antioxidant proteins that scavenge reactive oxygen species (ROS) ( Zhang et al, 2019 ), it can be hypothesized that the increased abundance of 2-Cys Prx in O 3 -treated fruit reduces ROS level in the host and protects apple cells from the pathogen invasion.…”
Section: Discussionmentioning
confidence: 99%
“…The Andean cultivar AND 277, developed by the International Center for Tropical Agriculture, Colombia (CIAT; Arruda et al., 2008), is considered an important source of resistance to multiple diseases such as ANT, ALS, and rust and has been widely used in bean breeding programs in Brazil and Southern Africa (Arruda et al., 2008; Carvalho et al., 1998). Notably, AND 277 possesses a resistance gene cluster at Pv01 containing two strongly linked disease resistance loci Co‐1 4 and Phg‐1 (Gonçalves‐Vidigal et al., 2011), exhibiting a broad‐spectrum resistance to races 9, 23, 64, 65, 67, 73, 75, 81, 83, 87, 89, 97, 117, 119, 339, 343, 449, 453, 1033, 2047, and 3481 of C. lindemuthianum (Alzate‐Marin et al, 2003; Arruda et al., 2008; Lima Castro et al., 2017) and races 7–15, 15–7, 23–23, 31–7, 31–17, 31–31, 31–39, 47–39, 61–31, 61–41, 63–6, 63–7, 63–19, 63–23, 63–31, 63–35, 63–47, and 63–63 of Pseudocercospora griseola (Borges et al., 2013; Caixeta et al., 2005). Still, a low genetic variability is observed in the Andean common bean gene pool relative to the Mesoamerican gene pool; therefore, timely information on resistance genes in cultivars belonging to this group provides an additional variability source reservoir.…”
Section: Introductionmentioning
confidence: 99%