2022
DOI: 10.1101/2022.10.28.514180
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High air humidity dampens salicylic acid pathway and plant resistance via targeting of NPR1

Abstract: The occurrence of plant disease is determined by interactions among host, pathogen and climate conditions. Air humidity has long been recognized to profoundly influence diseases in the phyllosphere, and high air humidity (e.g., after rain falls) is known as a prerequisite for numerous disease outbreaks in the field. However, the molecular basis of how high humidity interferes with plant resistance mechanisms to favor disease remained elusive. Here we show that high humidity is associated with an immune-comprom… Show more

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Cited by 2 publications
(2 citation statements)
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“…In the current study, more SA-defence pathway genes (except PR2-i) were upregulated in response to both mock and Psa 3 inoculation in 'Hortgem Tahi' than in 'Zesy002 or 'Hayward', thus reflecting on possible diverse genetics associated with tolerance and resistance response to Psa in each of the polyploid cultivars [54,55]. Conversely, studies in Arabidopsis showed that the SA pathway (including PR1, PR2 and PR5) was inhibited under high humidity and this was considered a significant determinant of enhanced susceptibility to Pst DC3000 [56].…”
Section: Discussionmentioning
confidence: 99%
“…In the current study, more SA-defence pathway genes (except PR2-i) were upregulated in response to both mock and Psa 3 inoculation in 'Hortgem Tahi' than in 'Zesy002 or 'Hayward', thus reflecting on possible diverse genetics associated with tolerance and resistance response to Psa in each of the polyploid cultivars [54,55]. Conversely, studies in Arabidopsis showed that the SA pathway (including PR1, PR2 and PR5) was inhibited under high humidity and this was considered a significant determinant of enhanced susceptibility to Pst DC3000 [56].…”
Section: Discussionmentioning
confidence: 99%
“…Pathogen-infected leaves at 23°C or 28°C were harvested at 1 day after infection. Pip extraction and quantification were performed based on previous reports with slight modifications (Yao et al, 2023). Approximately 100 mg leaf tissue was frozen and ground in liquid nitrogen, and Pip was extracted at 4℃ for 1h in 600 µL ice-cold extraction buffer (80% methanol in water, 0.1 g/L butylated hydroxytoluene).…”
Section: Pip Metabolite Extraction and Quantificationmentioning
confidence: 99%