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The ‘prime-ome’: towards a holistic approach to priming

Balmer, Andrea, Pastor, Victoria, Gamir, Jordi, Flors, Victor, Mauch-Mani, Brigitte·2015·Trends in Plant Science

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Show all 62 references

Research works printed but not linked: 27

  1. Pastor, 2014, Preparing to fight back: generation and storage of defensive compounds during the priming phase in Arabidopsis, Front. Plant Sci., 5, 295, 10.3389/fpls.2014.00295 · doi:10.3389/fpls.2014.00295
  2. Wang, 2015, Response of direct or priming defence against Botrytis cinerea to methyl jasmonate treatment at different concentrations in grape berries, Int. J. Food Microbiol., 194C, 32, 10.1016/j.ijfoodmicro.2014.11.006 · doi:10.1016/j.ijfoodmicro.2014.11.006
  3. Mandal, 2012, Progeny of tobacco mosaic virus-infected Nicotiana tabacum plants exhibit trans-generational changes in metabolic profiles, Biocatal. Agric. Biotechnol., 1, 115, 10.1016/j.bcab.2012.01.004 · doi:10.1016/j.bcab.2012.01.004
  4. Brotman, 2012, Transcript and metabolite analysis of the Trichoderma-induced systemic resistance response to Pseudomonas syringae in Arabidopsis thaliana, Microbiology, 158, 139, 10.1099/mic.0.052621-0 · doi:10.1099/mic.0.052621-0
  5. Coruzzi, 2000, Amino acids, Biochem. Mol. Biol. Plant, 358
  6. Rico, 2010, Agroinfiltration reduces ABA levels and suppresses Pseudomonas syringae-elicited salicylic acid production in Nicotiana tabacum, PLoS ONE, 5, e8977, 10.1371/journal.pone.0008977 · doi:10.1371/journal.pone.0008977
  7. Scalschi, 2013, Hexanoic acid is a resistance inducer that protects tomato plants against Pseudomonas syringae by priming the jasmonic acid and salicylic acid pathways, Mol. Plant Pathol., 14, 342, 10.1111/mpp.12010 · doi:10.1111/mpp.12010
  8. Luzzatto, 2007, Priming of antimicrobial phenolics during induced resistance response towards Pectobacterium carotovorum in the ornamental monocot Calla lily, J. Agric. Food Chem., 55, 10315, 10.1021/jf072037+ · doi:10.1021/jf072037+
  9. Luzzato-Knaan, 2014, Priming of protein expression in the defense response of Zantedeschia aethiopica to Pectobacterium carotovorum, Mol. Plant Pathol., 15, 364, 10.1111/mpp.12100 · doi:10.1111/mpp.12100
  10. Lim, 2013, Proteomics analysis suggests broad functional changes in potato leaves triggered by phosphites and a complex indirect mode of action against Phytophthora infestans, J. Proteomics, 93, 207, 10.1016/j.jprot.2013.03.010 · doi:10.1016/j.jprot.2013.03.010
  11. Arasimowicz-Jelonek, 2013, The proteome response of potato leaves to priming agents and S-nitrosoglutathione, Plant Sci., 198, 83, 10.1016/j.plantsci.2012.10.004 · doi:10.1016/j.plantsci.2012.10.004
  12. Anup, 2015, Proteomic analysis of elicitation of downy mildew disease resistance in pearl millet by seed priming with β-aminobutyric acid and Pseudomonas fluorescens, J. Proteomics, 120, 58, 10.1016/j.jprot.2015.02.013 · doi:10.1016/j.jprot.2015.02.013
  13. Małolepsza, 2005, Spatial and temporal variation of reactive oxygen species and antioxidant enzymes in o-hydroxyethylorutin-treated tomato leaves inoculated with Botrytis cinerea, Plant Pathol., 54, 317, 10.1111/j.1365-3059.2005.01167.x · doi:10.1111/j.1365-3059.2005.01167.x
  14. Chavan, 2013, Temporal modulation of oxidant and antioxidative responses in Brassica carinata during β-aminobutyric acid-induced resistance against Alternaria brassicae, Physiol. Mol. Plant Pathol., 83, 35, 10.1016/j.pmpp.2013.03.002 · doi:10.1016/j.pmpp.2013.03.002
  15. Li, 2011, Transcriptome analysis of H2O2-treated wheat seedlings reveals a H2O2-responsive fatty acid desaturase gene participating in powdery mildew resistance, PLoS ONE, 6, e28810, 10.1371/journal.pone.0028810 · doi:10.1371/journal.pone.0028810
  16. Gamir, 2012, Identification of indole-3-carboxylic acid as mediator of priming against Plectosphaerella cucumerina, Plant Physiol. Biochem., 61, 169, 10.1016/j.plaphy.2012.10.004 · doi:10.1016/j.plaphy.2012.10.004
  17. Gamir, 2014, Targeting novel chemical and constitutive primed metabolites against Plectosphaerella cucumerina, Plant J., 2, 227, 10.1111/tpj.12465 · doi:10.1111/tpj.12465
  18. Chung, 2011, Specificity of induced resistance in tomato against specialist lepidopteran and coleopteran species, J. Chem. Ecol., 37, 378, 10.1007/s10886-011-9937-0 · doi:10.1007/s10886-011-9937-0
  19. Arimura, 2009, Chemical and molecular ecology of herbivore-induced plant volatiles: proximate factors and their ultimate functions, Plant Cell Physiol., 50, 911, 10.1093/pcp/pcp030 · doi:10.1093/pcp/pcp030
  20. Zhong, 2014, DL-β-Aminobutyric acid-induced resistance in soybean against Aphis glycines Matsumura (Hemiptera: Aphididae), PLoS ONE, 9, e85142, 10.1371/journal.pone.0085142 · doi:10.1371/journal.pone.0085142
  21. Ye, 2013, Priming of jasmonate-mediated antiherbivore defense responses in rice by silicon, Proc. Natl. Acad. Sci. U.S.A., 110, 3631, 10.1073/pnas.1305848110 · doi:10.1073/pnas.1305848110
  22. Sato, 2013, Metabolomic profiling of the response of susceptible and resistant soybean strains to foxglove aphid Aulacorthum solani Kaltenbach, J. Chromatogr. B: Analyt. Technol. Biomed. Life Sci., 925, 95, 10.1016/j.jchromb.2013.02.036 · doi:10.1016/j.jchromb.2013.02.036
  23. Kim, 2012, Insect eggs can enhance wound response in plants: a study system of tomato Solanum lycopersicum L. and Helicoverpa zea Boddie, PLoS ONE, 7, e37420, 10.1371/journal.pone.0037420 · doi:10.1371/journal.pone.0037420
  24. Groux, 2014, Role of methyl salicylate on oviposition deterrence in Arabidopsis thaliana, J. Chem. Ecol., 40, 754, 10.1007/s10886-014-0470-9 · doi:10.1007/s10886-014-0470-9
  25. Pérez-Hedo, 2014, Prospects for predatory mirid bugs as biocontrol agents of aphids in sweet peppers, J. Pest Sci., 88, 65, 10.1007/s10340-014-0587-1 · doi:10.1007/s10340-014-0587-1
  26. Boubakri, 2013, Methionine elicits H2O2 generation and defense gene expression in grapevine and reduces Plasmopara viticola infection, J. Plant Physiol., 170, 1561, 10.1016/j.jplph.2013.06.008 · doi:10.1016/j.jplph.2013.06.008
  27. Sang, 2014, Priming-mediated systemic resistance in cucumber induced by Pseudomonas azotoformans GC-B19 and Paenibacillus elgii MM-B22 against Colletotrichum orbiculare, Phytopathology, 104, 834, 10.1094/PHYTO-11-13-0305-R · doi:10.1094/phyto-11-13-0305-r

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Metadata

Authors
Balmer, A., Pastor, V., Gamir, J., Flors, V., & Mauch-Mani, B.
Venue
Trends in Plant Science
Publisher
Elsevier BV
Published
2015-07
Volume
20
Issue
7
Pages
443-452
ISSN
1360-1385 (ISSN-L)
OpenAlex
W2088579419
Cited by
313
References
62
FWCI
3.23
Type
journal article
Language
en
Open access
closed
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)

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Balmer, A., Pastor, V., Gamir, J., Flors, V., & Mauch-Mani, B. (2015). The ‘prime-ome’: towards a holistic approach to priming. Trends in Plant Science. https://doi.org/10.1016/j.tplants.2015.04.002

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