2005
DOI: 10.1016/j.pmpp.2005.12.001
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Inducers of resistance reduce common bunt infection in wheat seedlings while differentially regulating defence-gene expression

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Cited by 59 publications
(51 citation statements)
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References 62 publications
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“…The reduction in disease cannot be attributed to the toxic effect of the inducers on the fungus because no conidial or spore germination inhibition has been occurred after inducers treatment ( Jakab et al 2001). Furthermore the protection effect is caused by triggering defence response, as reported for other plant-pathogen interaction (Lu et al 2006, Cohen 2001. Our results are in agreement with Thabit (2008) who found that BABA, BTH, IAA, and SA reduced wheat leaf rust infection through the enhanced of pathogenesis related protein, including peroxidase and phenolic compounds.…”
Section: Discussionsupporting
confidence: 92%
“…The reduction in disease cannot be attributed to the toxic effect of the inducers on the fungus because no conidial or spore germination inhibition has been occurred after inducers treatment ( Jakab et al 2001). Furthermore the protection effect is caused by triggering defence response, as reported for other plant-pathogen interaction (Lu et al 2006, Cohen 2001. Our results are in agreement with Thabit (2008) who found that BABA, BTH, IAA, and SA reduced wheat leaf rust infection through the enhanced of pathogenesis related protein, including peroxidase and phenolic compounds.…”
Section: Discussionsupporting
confidence: 92%
“…Induced defense responses are regulated by a network of inter-connecting signal transduction pathways, in which the hormonal signals SA, MeJA, and Eth play a major role. Application of SA, MeJA, and Eth can coordinately activate transcripts of different defense-related proteins (Lu et al, 2006). MeJA treatment increased expression of VTC1 and VTC2 transcripts and enhanced AsA accumulation in Arabidopsis (Sasaki-Sekimoto et al, 2005).…”
Section: Responses Of Vpvtc To Pm Pathogen and Defense Signaling Molementioning
confidence: 99%
“…The relative intensities of the RT-PCR products were obtained using the histogram function in GIMP 2.6 and then normalized to the expression of Actin. Gene-specific primers used for monitoring PR1 expression were PR1-F (5-CGCAGAACTCGCCGCAGGAC-3) and PR1-R (5-GCAGA CGACACGAGCACAGC-3), for AOS (GenBank accession number: AY196004.1) were AOS-F (5-ACGTCGACAAGGTC GAGAAG-3) and AOS-R (5-GGGCAAGATTGCGAAAAGT A-3), for the JA-inducible putative lipase encoding TaBs117A2 (Lu et al 2005) were LIPASE-F (5-CACAAAAATATCGACC CACCAC-3) and LIPASE-R (5-ACTGGGTATTCGTCTGTC AGC-3), and for Actin were Actin8-F (5-ATGAAGATTAAGG TCGTGGCA-3) and Actin8-R (5-TCCGAGTTTGAAGAGGC TAC-3). Sequences of primers used for monitoring NahG and Tubulin expression are detailed above.…”
Section: Rna Isolation and Analysismentioning
confidence: 99%