Knockout of MITOGEN-ACTIVATED PROTEIN KINASE 3 causes barley root resistance against Fusarium graminearum

. 2022 Nov 28 ; 190 (4) : 2847-2867.

Jazyk angličtina Země Spojené státy americké Médium print

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid35993881

Grantová podpora
P20 GM103476 NIGMS NIH HHS - United States

The roles of mitogen-activated protein kinases (MAPKs) in plant-fungal pathogenic interactions are poorly understood in crops. Here, microscopic, phenotypic, proteomic, and biochemical analyses revealed that roots of independent transcription activator-like effector nuclease (TALEN)-based knockout lines of barley (Hordeum vulgare L.) MAPK 3 (HvMPK3 KO) were resistant against Fusarium graminearum infection. When co-cultured with roots of the HvMPK3 KO lines, F. graminearum hyphae were excluded to the extracellular space, the growth pattern of extracellular hyphae was considerably deregulated, mycelia development was less efficient, and number of appressoria-like structures and their penetration potential were substantially reduced. Intracellular penetration of hyphae was preceded by the massive production of reactive oxygen species (ROS) in attacked cells of the wild-type (WT), but ROS production was mitigated in the HvMPK3 KO lines. Suppression of ROS production in these lines coincided with elevated abundance of catalase (CAT) and ascorbate peroxidase (APX). Moreover, differential proteomic analysis revealed downregulation of several defense-related proteins in WT, and the upregulation of pathogenesis-related protein 1 (PR-1) and cysteine proteases in HvMPK3 KO lines. Proteins involved in suberin formation, such as peroxidases, lipid transfer proteins (LTPs), and the GDSL esterase/lipase (containing "GDSL" aminosequence motif) were differentially regulated in HvMPK3 KO lines after F. graminearum inoculation. Consistent with proteomic analysis, microscopic observations showed enhanced suberin accumulation in roots of HvMPK3 KO lines, most likely contributing to the arrested infection by F. graminearum. These results suggest that TALEN-based knockout of HvMPK3 leads to barley root resistance against Fusarium root rot.

Zobrazit více v PubMed

Almagro L, Gómez Ros LV, Belchi-Navarro S, Bru R, Ros Barceló A, Pedreño MA (2009) Class III peroxidases in plant defence reactions. J Exp Bot 60: 377–390 PubMed

Barna B, Fodor J, Harrach BD, Pogány M, Király Z (2012) The Janus face of reactive oxygen species in resistance and susceptibility of plants to necrotrophic and biotrophic pathogens. Plant Physiol Biochem 59: 37–43 PubMed

Bedawy IMA, Dehne HW, Léon J, Naz AA (2018) Mining the global diversity of barley for Fusarium resistance using leaf and spike inoculations. Euphytica 214: 18

Bernards MA, Summerhurst DK, Razem FA (2004) Oxidases, peroxidases and hydrogen peroxide: the suberin connection. Phytochem Rev 3: 113–126

Bigeard J, Colcombet J, Hirt H (2015) Signaling mechanisms in pattern-triggered immunity (PTI). Mol Plant 8: 521–539 PubMed

Boenisch MJ, Schäfer W (2011) Fusarium graminearum forms mycotoxin producing infection structures on wheat. BMC Plant Biol 11: 110. PubMed PMC

Boudaoud A, Burian A, Borowska-Wykret D, Uyttewaal M, Wrzalik R, Kwiatkowska D, Hamant O (2014) Fibriltool, an ImageJ plug-in to quantify fibrillar structures in raw microscopic images. Nat Prot 9: 457–463 PubMed

Camagna M, Takemoto D (2018) Hypersensitive response in plants. eLS. John Wiley & Sons Ltd., Hoboken, NJ, pp 1–7

Camejo D, Guzmán-Cedeño Á, Moreno A (2016) Reactive oxygen species, essential molecules, during plant-pathogen interactions. Plant Physiol Biochem 103: 10–23 PubMed

Cenis JL (1992) Rapid extraction of fungal DNA for PCR amplification. Nucleic Acids Res 20: 2380. PubMed PMC

Chen J, Wang L, Yuan M (2021) Update on the roles of rice MAPK cascades. Int J Mol Sci 22: 1679. PubMed PMC

Cosio C, Ranocha P, Francoz E, Burlat V, Zheng Y, Perry SE, Ripoll JJ, Yanofsky M, Dunand C (2017) The class III peroxidase PRX17 is a direct target of the MADS-box transcription factor AGAMOUS-LIKE15 (AGL15) and participates in lignified tissue formation. New Phytol 213: 250–263 PubMed

Cui H, Wang Y, Xue L, Chu J, Yan C, Fu J, Chen M, Innes RW, Zhou JM (2010) Pseudomonas syringae effector protein AvrB perturbs Arabidopsis hormone signaling by activating MAP kinase 4. Cell Host Microbe 7: 164–175 PubMed PMC

Cui L, Yang G, Yan J, Pan Y, Nie X (2019) Genome-wide identification, expression profiles and regulatory network of MAPK cascade gene family in barley. BMC Genom 20: 750 PubMed PMC

Desmond OJ, Manners JM, Stephens AE, Maclean DJ, Schenk PM, Gardiner DM, Gardiner DM, Munn AL, Kazan K (2008) The Fusarium mycotoxin deoxynivalenol elicits hydrogen peroxide production, programmed cell death and defence responses in wheat. Mol Plant Pathol 9: 435–445 PubMed PMC

Edqvist J, Blomqvist K, Nieuwland J, Salminen TA (2018) Plant lipid transfer proteins: are we finally closing in on the roles of these enigmatic proteins? J Lipid Res 59: 1374–1382 PubMed PMC

Edstam MM, Blomqvist K, Eklöf A, Wennergren U, Edqvist J (2013) Coexpression patterns indicate that GPI-anchored non-specific lipid transfer proteins are involved in accumulation of cuticular wax, suberin and sporopollenin. Plant Mol Biol 83: 625–649 PubMed

Erayman M, Turktas M, Akdogan G, Gurkok T, Inal B, Ishakoglu E, Ilhan E, Unver T (2015) Transcriptome analysis of wheat inoculated with Fusarium graminearum. Front Plant Sci 6: 867. PubMed PMC

Eschen-Lippold L, Jiang X, Elmore JM, Mackey D, Shan L, Coaker G, Scheel D, Lee J (2016) Bacterial AvrRpt2-Like cysteine proteases block activation of the Arabidopsis mitogen-activated protein kinases, MPK4 and MPK11. Plant Physiol 171: 2223–2238 PubMed PMC

Fåhraeus G (1957) The infection of clover root hairs by nodule bacteria studied by a simp le glass slide technique. J Gen Microbiol 16: 374–381 PubMed

Fry SC (2004) Oxidative coupling of tyrosine and ferulic acid residues: intra- and extra-protoplasmic occurrence, predominance of trimers and larger products, and possible role in inter-polymeric cross-linking. Phytochem Rev 3: 97–111

Hong L, Brown J, Segerson NA, Rose JKC, Roeder AHK (2017) CUTIN SYNTHASE 2 maintains progressively developing cuticular ridges in Arabidopsis sepals. Molec Plant 10: 560–574 PubMed

Johrde A, Schweizer P (2008) A class III peroxidase specifically expressed in pathogen-attacked barley epidermis contributes to basal resistance. Mol Plant Pathol 9: 687–696 PubMed PMC

Kámán-Tóth E, Dankó T, Gullner G, Bozsó Z, Palkovics L, Pogány M (2019) Contribution of cell wall peroxidase- and NADPH oxidase-derived reactive oxygen species to Alternaria brassicicola-induced oxidative burst in Arabidopsis. Mol Plant Pathol 20: 485–499 PubMed PMC

Kishi-Kaboshi M, Okada K, Kurimoto L, Murakami S, Umezawa T, Shibuya N, Yamane H, Miyao A, Takatsuji H, Takahashi A, et al. (2010) A rice fungal MAMP-responsive MAPK cascade regulates metabolic flow to antimicrobial metabolite synthesis. Plant J 63: 599–612 PubMed PMC

Komis G, Illés P, Beck M, Šamaj J (2011) Microtubules and mitogen-activated protein kinase signalling. Curr Opin Plant Biol 14: 650–657 PubMed

Komis G, Šamajová O, Ovečka M, Šamaj J (2018) Cell and developmental biology of plant mitogen-activated protein kinases. Annu Rev Plant Biol 69: 237–265 PubMed

Krasylenko Y, Komis G, Hlynska S, Vavrdová T, Ovečka M, Pospíšil T, Šamaj J (2021) GR24, a synthetic strigolactone analog, and light affect the organization of cortical microtubules in Arabidopsis hypocotyl cells. Front Plant Sci 12: 675981. PubMed PMC

Křenek P, Chubar E, Vadovič P, Ohnoutková L, Vlčko T, Bergougnoux V, Cápal P, Ovečka M, Šamaj J (2021) CRISPR/Cas9-induced loss-of-function mutation in the barley mitogen-activated protein kinase 6 gene causes abnormal embryo development leading to severely reduced grain germination and seedling shootless phenotype. Front Plant Sci 12: 670302. PubMed PMC

Křenek P, Niks RE, Vels A, Vyplelová P, Šamaj J (2015) Genome-wide analysis of the barley MAPK gene family and its expression patterns in relation to Puccinia hordei infection. Acta Physiol Plant 37: 1–16

Kristiansen KA, Jensen PE, Møller IM, Schulz A (2009) Monitoring reactive oxygen species formation and localisation in living cells by use of the fluorescent probe CM-H2DCFDA and confocal laser microscopy. Physiol Plant 136: 369–383 PubMed

Kumar J, Schäfer P, Hückelhoven R, Langen G, Baltruschat H, Stein E, Nagarajan S, Kogel KH (2002) Bipolaris sorokiniana, a cereal pathogen of global concern: cytological and molecular approaches towards better control double dagger. Mol Plant Pathol 3: 185–195 PubMed

Lanoue A, Burlat V, Henkes GJ, Koch I, Schurr U, Röse USR (2010) De novo biosynthesis of defense root exudates in response to Fusarium attack in barley. New Phytol 185: 577–588 PubMed

Lee D, Lal NK, Lin ZJD, Ma S, Liu J, Castro B, Toruño T, Dinesh-Kumar SP, Coaker G (2020) Regulation of reactive oxygen species during plant immunity through phosphorylation and ubiquitination of RBOHD. Nat Commun 11: 1838. PubMed PMC

Liu Y, Ren D, Pike S, Pallardy S, Gassmann W, Zhang S (2007) Chloroplast-generated reactive oxygen species are involved in hypersensitive response-like cell death mediated by a mitogen-activated protein kinase cascade. Plant J 51: 941–954 PubMed

Lozovaya VV, Lygin AV, Zernova OV, Li S, Widholm JM, Hartman GL (2006) Lignin degradation by Fusarium solani f. sp. glycines. Plant Dis 90: 77–82 PubMed

Ma L-J,, GeiserDM, , ProctorRH, , RooneyAP, , O'Donnell K,, Trail F,, Gardiner D,, MannersJM, , Kazan K (2013) Fusarium pathogenomics. Ann Rev Microbiol 67: 399–416 PubMed

Mao G, Meng X, Liu Y, Zheng Z, Chen Z, Zhang S (2011) Phosphorylation of a WRKY transcription factor by two pathogen-responsive MAPKs drives phytoalexin biosynthesis in Arabidopsis. Plant Cell 23: 1639–1653 PubMed PMC

Mascher M, Gundlach H, Himmelbach A, Beier S, Twardziok SO, Wicker T, Radchuk V, Dockter C, Hedley PE, Russell J, et al. (2017) A chromosome conformation capture ordered sequence of the barley genome. Nature 544: 427–433 PubMed

Masuda D, Ishida M, Yamaguchi K, Yamaguchi I, Kimura M, Nishiuchi T (2007) Phytotoxic effects of trichothecenes on the growth and morphology of Arabidopsis thaliana. J Exp Bot 58: 1617–1626 PubMed

Meng X, Zhang S (2013) MAPK cascades in plant disease resistance signaling. Annu Rev Phytopathol 51: 245–266 PubMed

Misas-Villamil JC, van der Hoorn RAL, Doehlemann G (2016) Papain-like cysteine proteases as hubs in plant immunity. New Phytol 212: 902–907 PubMed

Mishler-Elmore JW, Zhou Y, Sukul A, Oblak M, Tan L, Faik A, Held MA (2021) Extensins: self-assembly, crosslinking, and the role of peroxidases. Front Plant Sci 12: 664738. PubMed PMC

Mueller AN, Ziemann S, Treitschke S, Aßmann D, Doehlemann G (2013) Compatibility in the ustilago maydis–maize interaction requires inhibition of host cysteine proteases by the fungal effector Pit2. PLoS Pathol 9: e1003177 PubMed PMC

O’Brien JA, Daudi A, Finch P, Butt VS, Whitelegge JP, Souda P, Ausubel FM, Bolwell GP (2012) A peroxidase-dependent apoplastic oxidative burst in cultured Arabidopsis cells functions in MAMP-elicited defense. Plant Physiol 158: 2013–2027 PubMed PMC

Passardi F, Cosio C, Penel C, Dunand C (2005) Peroxidases have more functions than a Swiss army knife. Plant Cell Rep 24: 255–265 PubMed

Passardi F, Penel C, Dunand C (2004) Performing the paradoxical: how plant peroxidases modify the cell wall. Trends Plant Sci 9: 534–540 PubMed

Pitzschke A, Datta S, Persak H (2014) Salt stress in Arabidopsis: lipid transfer protein AZI1 and its control by mitogen-activated protein klinase MPK3. Mol Plant 7: 722–738 PubMed PMC

Qi J, Wang J, Gong Z, Zhou JM (2017) Apoplastic ROS signaling in plant immunity. Curr Opin Plant Biol 38: 92–100 PubMed

Qiu JL, Fiil BK, Petersen K, Nielsen HB, Botanga CJ, Thorgrimsen S, Palma K, Suarez-Rodriguez MC, Sandbech-Clausen S, Lichota J, et al. (2008) Arabidopsis MAP kinase 4 regulates gene expression through transcription factor release in the nucleus. EMBO J 27: 2214–2221 PubMed PMC

Qiu H, Zhao X, Fang W, Wu H, Abubakar YS, Lu G, Wang Z, Zheng W (2019) Spatiotemporal nature of Fusarium graminearum-wheat coleoptile interactions. Phytopathol Res 1: 26

Ralph J, Bunzel M, Marita JM, Hatfield RD, Lu F, Kim H, Schatz PF, Grabber JH, Steinhart H (2004) Peroxidase-dependent cross-linking reactions of p-hydroxycinnamates in plant cell walls. Phytochem Rev 3: 79–96

Ren D, Yang H, Zhang S (2002) Cell death mediated by MAPK is associated with hydrogen peroxide production in Arabidopsis. J Biol Chem 277: 559–565 PubMed

Rózewicz M, Wyzinska M, Grabinski J (2021) The most important fungal diseases of cereals - problems and possible solutions. Agronomy 11: 714

Rudd JJ, Keon J, Hammond-Kosack KE (2008) The wheat mitogen-activated protein kinases TaMPK3 and TaMPK6 are differentially regulated at multiple levels during compatible disease interactions with Mycosphaerella graminicola. Plant Physiol 147: 802–815 PubMed PMC

Sasaki K, Iwai T, Hiraga S, Kuroda K, Seo S, Mitsuhara I, Miyasaka A, Iwano M, Ito H, Matsui H, et al. (2004) Ten rice peroxidases redundantly respond to multiple stresses including infection with rice blast fungus. Plant Cell Physiol 45: 1442–1452 PubMed

Shetty NP, Mehrabi R, Lütken H, Haldrup A, Kema GHJ, Collinge DB, Jørgensen HJL (2007) Role of hydrogen peroxide during the interaction between the hemibiotrophic fungal pathogen Septoria tritici and wheat. New Phytol 174: 637–647 PubMed

Schumacher J (2012) Tools for Botrytis cinerea: new expression vectors make the gray mold fungus more accessible to cell biology approaches. Fungal Genet Biol 49: 483–497 PubMed

Sewelam N, Kazan K, Schenk PM (2016) Global plant stress signaling: Reactive oxygen species at the cross-road. Front Plant Sci 7: 187. PubMed PMC

Sexauer M, Shen D, Schön M, Andersen TG, Markmann K (2021) Visualizing polymeric components that define distinct root barriers across plant lineages. Development 148: dev199820 doi:10.1242/dev.199820 PubMed PMC

Soler M, Serra O, Molinas M, Huguet G, Fluch S, Figueras M (2007) A genomic approach to suberin biosynthesis and cork differentiation. Plant Physiol 144: 419–431 PubMed PMC

Sorokan AV, Kuluev BR, Burkhanova G, Maksimov IV (2014) RNA silencing of the anionic peroxidase gene impairs potato plant resistance to Phytophthora infestans (Mont.) de Bary. Mol Biol 48: 709–717 PubMed

Takáč T, Křenek P, Komis G, Vadovič P, Ovečka M, Ohnoutková L, Pechan T, Kašpárek P, Tichá T, Basheer J, et al. (2021) TALEN-based HvMPK3 knock-Out attenuates proteome and root hair phenotypic responses to flg22 in barley. Front Plant Sci 12: 666229. PubMed PMC

Takáč T, Šamajová O, Luptovčiak I, Pechan T, Šamaj J (2017) Feedback microtubule control and microtubule-actin cross-talk in Arabidopsis revealed by integrative proteomic and cell biology analysis of KATANIN 1 mutants. Molec Cel Proteomics 16: 1591–1609 PubMed PMC

Takáč T, Šamajová O, Vadovič P, Pechan T, Košútová P, Ovečka M, Husičková A, Komis G, Šamaj J (2014) Proteomic and biochemical analyses show a functional network of proteins involved in antioxidant defense of the Arabidopsis anp2anp3 double mutant. J Proteome Res 13: 5347–5361 PubMed PMC

Takáč T, Vadovič P, Pechan T, Luptovčiak I, Šamajová O, Šamaj J (2016) Comparative proteomic study of Arabidopsis mutants mpk4 and mpk6. Sci Rep 6: 28306. PubMed PMC

Talbot NJ (2019) Appressoria. Curr Biol 29: R144–R146 PubMed

Trail F (2009) For blighted waves of grain: Fusarium graminearum in the postgenomics era. Plant Physiol 149: 103–110 PubMed PMC

Tsuda K,, Katagiri F (2010) Comparing signaling mechanisms engaged in pattern-triggered and effector-triggered immunity. Curr Opin Plant Biol 13: 459–465 PubMed

Ursache R, Andersen TG, Marhavy P, Geldner N (2018) A protocol for combining fluorescent proteins with histological stains for diverse cell wall components. Plant J 93: 399–412 PubMed

Walter S, Nicholson P, Doohan FM (2010) Action and reaction of host and pathogen during Fusarium head blight disease. New Phytol 185: 54–66 PubMed

Wang Q, Buxa SV, Furch A, Friedt W, Gottwald S (2015) Insights into Triticum aestivum seedling root rot caused by Fusarium graminearum. Mol Plant Microbe Interact 28: 1288–1303 PubMed

Wang Q, Shao B, Shaikh FI, Friedt W, Gottwald S (2018) Wheat resistances to fusarium root rot and head blight are both associated with deoxynivalenol- and jasmonate-related gene expression. Phytopathology 108: 602–616 PubMed

Wojtasik W, Kulma A, Dymińska L, Hanuza J, Czemplik M, Szopa J (2016) Evaluation of the significance of cell wall polymers in flax infected with a pathogenic strain of Fusarium oxysporum. BMC Plant Biol 16: 75. PubMed PMC

Xie K, Chen J, Wang Q, Yang Y (2014) Direct phosphorylation and activation of a mitogen-activated proteinkinase by a calcium-dependent protein kinase in rice. Plant Cell 26: 3077. PubMed PMC

Xiong L, Yang Y (2003) Disease resistance and abiotic stress tolerance in rice are inversely modulated by an abscisic acid–inducible mitogen-activated protein kinase. Plant Cell 15: 745–759 PubMed PMC

Zhang WJ, Pedersen C, Kwaaitaal M, Gregersen PL, Mørch SM, Hanisch S, Kristensen A, Fuglsang AT, Collinge DB, Thordal-Christensen H (2012) Interaction of barley powdery mildew effector candidate CSEP0055 with the defence protein PR17c. Mol Plant Pathol 13: 1110–1119 PubMed PMC

Zipfel C (2009) Early molecular events in PAMP-triggered immunity. Curr Opin Plant Biol 12: 414–420 PubMed

Zipfel C (2014) Plant pattern-recognition receptors. Trends Immunol 35: 345–351 PubMed

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...