Diverse responses of wild and cultivated tomato to BABA, oligandrin and Oidium neolycopersici infection

. 2017 Mar 01 ; 119 (5) : 829-840.

Jazyk angličtina Země Anglie, Velká Británie Médium print

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid27660055

BACKGROUND AND AIMS: Current strategies for increased crop protection of susceptible tomato plants against pathogen infections include treatment with synthetic chemicals, application of natural pathogen-derived compounds or transfer of resistance genes from wild tomato species within breeding programmes. In this study, a series of 45 genes potentially involved in defence mechanisms was retrieved from the genome sequence of inbred reference tomato cultivar Solanum lycopersicum 'Heinz 1706'. The aim of the study was to analyse expression of these selected genes in wild and cultivated tomato plants contrasting in resistance to the biotrophic pathogen Oidium neolycopersici , the causative agent of powdery mildew. Plants were treated either solely with potential resistance inducers or by inducers together with the pathogen. METHODS: The resistance against O. neolycopersici infection as well as RT-PCR-based analysis of gene expression in response to the oomycete elicitor oligandrin and chemical agent β-aminobutyric acid (BABA) were investigated in the highly susceptible domesticated inbred genotype Solanum lycopersicum 'Amateur' and resistant wild genotype Solanum habrochaites . KEY RESULTS: Differences in basal expression levels of defensins, germins, β-1,3-glucanases, heveins, chitinases, osmotins and PR1 proteins in non-infected and non-elicited plants were observed between the highly resistant and susceptible genotypes. Moreover, these defence genes showed an extensive up-regulation following O. neolycopersici infection in both genotypes. Application of BABA and elicitin induced expression of multiple defence-related transcripts and, through different mechanisms, enhanced resistance against powdery mildew in the susceptible tomato genotype. CONCLUSIONS: The results indicate that non-specific resistance in the resistant genotype S. habrochaites resulted from high basal levels of transcripts with proven roles in defence processes. In the susceptible genotype S. lycopersicum 'Amateur', oligandrin- and BABA-induced resistance involved different signalling pathways, with BABA-treated leaves displaying direct activation of the ethylene-dependent signalling pathway, in contrast to previously reported jasmonic acid-mediated signalling for elicitins.

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Anand A, Lei ZT, Sumner LW, et al. 2004. Apoplastic extracts from a transgenic wheat line exhibiting lesion-mimic phenotype have multiple pathogenesis-related proteins that are antifungal. Molecular Plant-Microbe Interactions 17: 1306–1317. PubMed

Bengtsson T, Holefors A, Witzell J, Andreasson E, Liljeroth E.. 2014a. Activation of defence responses to

Bengtsson T, Weighill D, Proux-Wera E, et al. 2014b. Proteomics and transcriptomics of the BABA-induced resistance response in potato using a novel functional annotation approach. BMC Genomics 15. PubMed PMC

Benhamou N, Belanger RR, Rey P, Tirilly Y.. 2001. Oligandrin, the elicitin-like protein produced by the mycoparasite

Bonnet P, Bourdon E, Ponchet M, Blein JP, Ricci P.. 1996. Acquired resistance triggered by elicitins in tobacco and other plants. European Journal of Experimental Botany 102: 181–192.

Chang WC, Lee TY, Huang HD, Huang HY, Pan RL.. 2008. PlantPAN: plant promoter analysis navigator, for identifying combinatorial PubMed PMC

Cohen Y. 2002. β-Aminobutyric acid-induced resistance against plant pathogens. Plant Disease 86: 448–457. PubMed

Cohen Y, Niderman T, Mosinger E, Fluhr R.. 1994. Beta-aminobutyric acid induces the accumulation of pathogenesis-related proteins in tomato ( PubMed PMC

Cohen Y, Rubin AE, Kilfin G.. 2010. Mechanisms of induced resistance in lettuce against Bremia lactucae by DL-β-amino-butyric acid (BABA). European Journal of Plant Pathology 126: 553–573.

Cohn JR, Martin GB.. 2005. PubMed

Conrath U. 2009. Priming of induced plant defense responses. Plant Innate Immunity 51: 361–395.

Dana MD, Pintor-Toro JA, Cubero B.. 2006. Transgenic tobacco plants overexpressing chitinases of fungal origin show enhanced resistance to biotic and abiotic stress agents. Plant Physiology 142: 722–730. PubMed PMC

Exposito-Rodriguez M, Borges AA, Borges-Perez A, Perez JA.. 2008. Selection of internal control genes for quantitative real-time RT-PCR studies during tomato development process. BMC Plant Biology 8. PubMed PMC

Foolad MR. 2007. Genome mapping and molecular breeding of tomato. International Journal of Plant Genomics 2007: 1–52. PubMed PMC

Glazebrook J. 2005. Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annual Review of Phytopathology 43: 205–227. PubMed

Iqbal N, Trivellini A, Masood A, Ferrante A, Khan NA.. 2013. Current understanding on ethylene signalling in plants: the influence of nutrient availability. Plant Physiology and Biochemistry 73: 128–138. PubMed

Jakab G, Cottier V, Toquin V, et al. 2001. β-Aminobutyric acid-induced resistance in plants. European Journal of Experimental Botany 107: 29–37.

Jupe J, Stam R, Howden AJM, et al. 2013. PubMed PMC

Kamoun S, Young M, Glascock CB, Tyler BM.. 1993. Extracellular protein elicitors from

Kawamura Y, Hase S, Takenaka S, et al. 2009. INF1 elicitin activates jasmonic acid- and ethylene-mediated signalling pathways and induces resistance to bacterial wilt disease in tomato. Journal of Phytopathology 157: 287–297.

Kim YS, Choi D, Lee MM, Lee SH, Kim WT.. 1998. Biotic and abiotic stress-related expression of 1-aminocyclopropane-1-carboxylate oxidase gene family in PubMed

Koressaar T, Remm M.. 2007. Enhancements and modifications of primer design program Primer3. Bioinformatics 23: 1289–1291. PubMed

Lebeda A, Reinink K.. 1994. Histological characterization of resistance in

Lebeda A, Mieslerová B, Petřivalský M, et al. 2014. Resistance mechanisms of wild tomato germplasm to infection of

Lherminier J, Benhamou N, Larrue J, et al. 2003. Cytological characterization of elicitin-induced protection in tobacco plants infected by PubMed

Li GJ, Meng XZ, Wang RG, Mao GH, Han L, Liu YD, Zhang SQ.. 2012. Dual-level regulation of ACC synthase activity by MPK3/MPK6 cascade and its downstream WRKY transcription factor during ethylene induction in PubMed PMC

Lin T, Zhu GT, Zhang JH, et al. 2014. Genomic analyses provide insights into the history of tomato breeding. Nature Genetics 46: 1220–1226. PubMed

Lincoln JE, Campbell AD, Oetiker J, et al. 1993. Le-Acs4, a fruit ripening and wound-induced 1-aminocyclopropane-1-carboxylate synthase gene of tomato ( PubMed

Liu D, Raghothama KG, Hasegawa PM, Bressan RA.. 1994. Osmotin overexpression in potato delays development of disease symptoms. Proceedings of the National Academy of Sciences of the USA 91: 1888–1892. PubMed PMC

Lopez-Kleine L, Pinzon A, Chaves D, Restrepo S, Riano-Pachon DM.. 2013. Chromosome 10 in the tomato plant carries clusters of genes responsible for field resistance/defence to PubMed

Luna E, van Hulten M, Zhang Y, et al. 2014. Plant perception of beta-aminobutyric acid is mediated by an aspartyl-tRNA synthetase. Nature Chemical Biology 10: 450–456. PubMed PMC

Malá J, Machová P, Cvrčková H, et al. 2009. Micropropagation of wild service tree (

Menda N, Strickler SR, Edwards JD, et al. 2014. Analysis of wild-species introgressions in tomato inbreds uncovers ancestral origins. BMC Plant Biology 14. PubMed PMC

Mieslerová B, Lebeda A, Chetelat RT.. 2000. Variation in response of wild

Nicot N, Hausman JF, Hoffmann L, Evers D.. 2005. Housekeeping gene selection for real-time RT-PCR normalization in potato during biotic and abiotic stress. Journal of Experimental Botany 56: 2907–2914. PubMed

Oka Y, Cohen Y.. 2001. Induced resistance to cyst and root-knot nematodes in cereals by dl-beta-amino-N-butyric acid. European Journal of Plant Pathology 107: 219–227.

Oldach KH, Becker D, Lorz H.. 2001. Heterologous expression of genes mediating enhanced fungal resistance in transgenic wheat. Molecular Plant-Microbe Interactions 14: 832–838. PubMed

Picard K, Ponchet M, Blein JP, Rey P, Tirilly Y, Benhamou N.. 2000. Oligandrin. A proteinaceous molecule produced by the mycoparasite PubMed PMC

Piękna-Grochala J, Kępczyńska E.. 2013. Induction of resistance against pathogens by beta-aminobutyric acid. Acta Physiologiae Plantarum 35: 1735–1748.

Piterková J, Petřivalský M, Luhová L, Mieslerová B, Sedlářová M, Lebeda A.. 2009. Local and systemic production of nitric oxide in tomato responses to powdery mildew infection. Molecular Plant Pathology 10: 501–513. PubMed PMC

Piterková J, Hofman J, Mieslerová B, et al. 2011. Dual role of nitric oxide in

Sels J, Mathys J, De Coninck BM, Cammue BP, De Bolle MF.. 2008. Plant pathogenesis-related (PR) proteins: a focus on PR peptides. PubMed

Shi HY, Zhang YX.. 2014. Expression and regulation of pear 1-aminocyclopropane-1-carboxylic acid synthase gene (PpACS1a) during fruit ripening, under salicylic acid and indole-3-acetic acid treatment, and in diseased fruit. Molecular Biology Reports 41: 4147–4154. PubMed

Siegrist J, Orober M, Buchenauer H.. 2000. β-Aminobutyric acid-mediated enhancement of resistance in tobacco to tobacco mosaic virus depends on the accumulation of salicylic acid. Physiological and Molecular Plant Pathology 56: 95–106.

Sim SC, Robbins MD, Van Deynze A, Michel AP, Francis DM.. 2011. Population structure and genetic differentiation associated with breeding history and selection in tomato ( PubMed PMC

Skottke KR, Yoon GM, Kieber JJ, DeLong A.. 2011. Protein phosphatase 2A controls ethylene biosynthesis by differentially regulating the turnover of ACC synthase isoforms. PLoS Genetics 7: e1001370. PubMed PMC

Spoel SH, Dong X.. 2012. How do plants achieve immunity? Defence without specialized immune cells. Nature Reviews Immunology 12: 89–100. PubMed

Tománková K, Luhová L, Petřivalský M, Peč P, Lebeda A.. 2006. Biochemical aspects of reactive oxygen species formation in the interaction between

Ton J, Jakab G, Toquin V, et al. 2005. Dissecting the beta-aminobutyric acid-induced priming phenomenon in arabidopsis. The Plant Cell 17: 987–999. PubMed PMC

van Loon LC, Geraats BPJ, Linthorst HJM.. 2006. Ethylene as a modulator of disease resistance in plants. Trends in Plant Science 11: 184–191. PubMed

Vleeshouwers VGA, Oliver RP.. 2014. Effectors as tools in disease resistance breeding against biotrophic, hemibiotrophic, and necrotrophic plant pathogens PubMed

Worrall D, Holroyd GH, Moore JP, et al. 2012. Treating seeds with activators of plant defence generates long-lasting priming of resistance to pests and pathogens. New Phytologist 193: 770–778. PubMed

Wu CC, Singh P, Chen MC, Zimmerli L.. 2010. l-Glutamine inhibits beta-aminobutyric acid-induced stress resistance and priming in PubMed PMC

Yim WJ, Kim KY, Lee YW, Sundaram SP, Lee Y, Sa TM.. 2014. Real time expression of ACC oxidase and PR-protein genes mediated by PubMed

Zhu BL, Chen THH, Li PH.. 1996. Analysis of late-blight disease resistance and freezing tolerance in transgenic potato plants expressing sense and antisense genes for an osmotin-like protein. Planta 198: 70–77. PubMed

Zimmerli L, Metraux JP, Mauch-Mani B.. 2001. β-Aminobutyric acid-induced protection of PubMed PMC

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