2016
DOI: 10.1016/j.fgb.2016.03.002
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Chasing stress signals – Exposure to extracellular stimuli differentially affects the redox state of cell compartments in the wild type and signaling mutants of Botrytis cinerea

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Cited by 17 publications
(24 citation statements)
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References 74 publications
(113 reference statements)
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“…They used a fungal Δbap1 mutant strain expressing radiometric redox-sensitive green fluorescent protein (roGFP2), to measure the dynamics of the glutathione pool in B. cinerea in vivo and in planta. This sensor was later used to study the temporal changes to redox state in various other mutants (Marschall et al, 2016a). Also, the glutaredoxin-bound GFP (Grx1-roGFP2) vector has been expressed in M. oryzae to understand the antioxidant defense system of the rice blast fungus in planta, with this work concluding that plant oxidative bursts were not sufficient to prevent infection (Samalova et al, 2014).…”
Section: Hyper Redox Sensorsmentioning
confidence: 99%
“…They used a fungal Δbap1 mutant strain expressing radiometric redox-sensitive green fluorescent protein (roGFP2), to measure the dynamics of the glutathione pool in B. cinerea in vivo and in planta. This sensor was later used to study the temporal changes to redox state in various other mutants (Marschall et al, 2016a). Also, the glutaredoxin-bound GFP (Grx1-roGFP2) vector has been expressed in M. oryzae to understand the antioxidant defense system of the rice blast fungus in planta, with this work concluding that plant oxidative bursts were not sufficient to prevent infection (Samalova et al, 2014).…”
Section: Hyper Redox Sensorsmentioning
confidence: 99%
“…Accordingly, the intracellular content of H 2 O 2 decreased when S. scitamineum cells were exposed to H 2 O 2 for 30 minutes, whereas after 180 minutes, H 2 O 2 content entered in a redox homeostasis restoring the initial environment. These results over again supported the earlier statement that an adaptive response is in course such as those seen for other systems (MARSCHALL et al, 2016). In C. albicans, for instance, the antioxidant system activation contributed to acquisition of an adaptive response to H 2 O 2 (JAMIESON et al, 1996;GONZÁLEZ-PÁRRAGA et al, 2003).…”
Section: Discussionsupporting
confidence: 87%
“…C. albicans has developed antioxidant systems, required for adaptation to ROS exposure from the host throughout evolution (Alonso-Monge et al, 2003;Herrero-de-Dios et al, 2010). This is also true for plant pathogens (MARSCHALL et al, 2016;MENTGES;BORMANN, 2015; MARSCHALL; TUDZYNSKI, 2014) and potentially for S. scitamineum, the cell redox state also changes when exposed to stress by means of an adaptative response and signaling to maintain its biotrophic lifestyle.…”
Section: Discussionmentioning
confidence: 98%
“…Z-stacks were displayed as average projections via the CLSM software. Further evaluation was done with the Image J program (v.1.44f; http://rsb.info.nih.gov/ij/ ) as it was shown before [ 33 ].…”
Section: Methodsmentioning
confidence: 99%
“…In fungi, Nox complexes exhibit distinct functions [ 1 , 49 ]. While the NoxA (Nox1) complex is controlling fruiting body formation [ 7 , 28 , 31 ], formation of sclerotia [ 14 , 40 , 42 ] and conidial anastomosis tubes (CATs) [ 38 ], virulence [ 23 , 42 , 53 ] and cellulose degradation [ 5 ], the NoxB (Nox2) complex is responsible for penetration of host tissue [ 12 , 42 ], the production of ROS [ 33 ] and ascospore germination [ 7 , 31 ]. However, the exact composition of the Nox complexes, their site of action as well as the integration in existing signaling pathways are still poorly elucidated.…”
Section: Introductionmentioning
confidence: 99%