{"id":16,"date":"2017-01-15T21:05:44","date_gmt":"2017-01-16T05:05:44","guid":{"rendered":"http:\/\/labs.wsu.edu\/tanaka-lab\/?page_id=16"},"modified":"2025-02-26T13:24:42","modified_gmt":"2025-02-26T21:24:42","slug":"publications","status":"publish","type":"page","link":"https:\/\/labs.wsu.edu\/tanaka-lab\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"
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Home<\/a> | Research <\/a>| Publications<\/span><\/strong>\u00a0<\/strong><\/span>|\u00a0<\/strong>Personnel <\/a>| Opportunities<\/a> |\u00a0<\/strong>Lab News<\/a><\/strong><\/span><\/p>\n

 <\/p>\n

Tanaka Lab – Publications<\/strong><\/h1>\n

 <\/p>\n

2025<\/span><\/strong><\/p>\n

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\"\"<\/a>Jayasinghe SK<\/strong>, Moroz N<\/strong>, Yuan P, Kolomiets MV, Tanaka K<\/strong> (2025) Salicylic Acid Plays a Major Role in Potato Defense Against Powdery Scab Pathogen, Spongospora subterranea<\/em> f. sp. subterranea<\/em>. Molecular Plant-Microbe Interactions <\/em>(in press)
\nhttps:\/\/doi.org\/10.1094\/MPMI-12-24-0154-R<\/a><\/p>\n

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 <\/p>\n

2024<\/span><\/strong><\/p>\n

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\"\"<\/a>Kamal H<\/strong>, Charlton B, Sathuvalli V, Tanaka K<\/strong> (2024) Root infection and minituber yield response to powdery scab in plant growth chamber conditions. PhytoFrontiers<\/em>\u00a04: 781-791
\nhttps:\/\/doi.org\/10.1094\/PHYTOFR-06-24-0067-R<\/a><\/p>\n

 <\/p>\n

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\"\"<\/a>Moroz N<\/strong>, Colvin B<\/strong>, Jayasinghe SK<\/strong>, Gleason C, Tanaka K<\/strong> (2024) Phytocytokine StPep1-secreting bacteria suppress potato powdery scab disease. Phytopathology<\/em> 114: 2055-2063
\nhttps:\/\/doi.org\/10.1094\/PHYTO-01-24-0019-R<\/a><\/p>\n

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\"\"<\/a>Kamal H<\/strong>, Kotapati KV, Tanaka K<\/strong>, Pappu HR (2024) Investigating the roles of coat protein and triple gene block proteins of potato mop-top virus using a heterologous expression system. International Journal of Molecular Sciences<\/em>\u00a025: 6990
\nhttps:\/\/doi.org\/10.3390\/ijms25136990<\/a><\/p>\n

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\"\"<\/a>Sowders JM<\/strong>, Jewell JB<\/strong>, Tanaka K<\/strong> (2024) FERONIA orchestrates P2K1-driven purinergic signaling in plant roots. Plant signaling & Behavior<\/em> 19: e2370706
\nhttps:\/\/doi.org\/10.1080\/15592324.2024.2370706<\/a><\/p>\n

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\"\"<\/a>Sowders JM<\/strong>, Jewell JB<\/strong>, Tanaka K<\/strong> (2024) CPK28 is a modulator of purinergic signaling in plant growth and defense. Plant Journal<\/em> 118: 1086-1101
\nhttps:\/\/doi.org\/10.1111\/tpj.16656 <\/a><\/p>\n

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\"\"<\/a>Kamal H<\/strong>, Lynch-Holm V, Pappu HR, Tanaka K<\/strong> (2023) Starch plays a key role in sporosorus formation by the powdery scab pathogen Spongospora subterranea. Phytopathology<\/em> 114: 568-579
\nhttps:\/\/doi.org\/10.1094\/PHYTO-07-23-0224-R<\/a><\/p>\n

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2023<\/span><\/strong><\/p>\n

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\"\"<\/a>Basu S, Moroz N<\/strong>, Lee BW, Tanaka K<\/strong>, Oeller L, Baerlocher C, Crowder DW (2023) Diversity and traits of multiple biotic stressors elicit differential defense responses in legumes. Agriculture<\/em> 13: 2093
\nhttps:\/\/doi.org\/10.3390\/agriculture13112093<\/a><\/p>\n

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\"\"<\/a>Sowders JM<\/strong>, Jewell JB<\/strong>, Tripathi D<\/strong>, Tanaka K<\/strong> (2023) The intrinsically disordered C-terminus of purinoceptor P2K1 fine-tunes plant responses to extracellular ATP. FEBS Letters <\/em>597: 2059-2071
\nhttps:\/\/doi.org\/10.1002\/1873-3468.14703<\/a><\/p>\n

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\"\"<\/a>Sowders JM<\/strong>, Tanaka K<\/strong> (2023) A histochemical reporter system to study extracellular ATP response in plants. Frontiers in Plant Sciences<\/em> 14: 1183335 https:\/\/doi.org\/10.3389\/fpls.2023.1183335<\/a><\/p>\n

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\"\"<\/a>Tanaka K<\/strong>, Mattupalli C (2023) Nano tools for managing plant diseases. WSU CSANR Blog<\/em>. May 30, 2023
\nhttps:\/\/doi.org\/10.7273\/b3rq-6v30<\/a><\/p>\n

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\"\"<\/a>Tanaka K<\/strong>, Mudgil Y, Tunc-Ozdemir M (2023) Editorial: Abiotic stress and plant immunity \u2013 a challenge in climate change. Frontiers in Plant Sciences<\/em> 14: 1197435
\nhttps:\/\/doi.org\/10.3389\/fpls.2023.1197435<\/a><\/p>\n

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\"\"<\/a>Masudulla K, Tanaka K<\/strong> (2023) Purpureocillium lilacinum for plant growth promotion and biocontrol against root-knot nematodes infecting eggplant. PLoS One<\/em> 18: e0283550
\nhttps:\/\/doi.org\/10.1371\/journal.pone.0283550<\/a><\/p>\n

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\"\"<\/a>Braley LE<\/strong>, Jewell JB<\/strong>, Figueroa J, Humann JL, Main D, Mora-Romero GA<\/strong>, Moroz N<\/strong>, Woodhall JW, White RA III, Tanaka K<\/strong> (2023) Nanopore sequencing with GraphMap for comprehensive pathogen detection in potato field soil. Plant Disease<\/em> 107: 2288-2295
\nhttps:\/\/doi.org\/10.1094\/PDIS-01-23-0052-SR<\/a><\/p>\n

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2022<\/span><\/strong><\/p>\n

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\"\"<\/a>Jewell JB<\/strong>, Berim A, Tripathi D<\/strong>, Gleason C, Olaya C, Pappu HR, Gang DR, Tanaka K<\/strong> (2022) Activation of indolic glucosinolate pathway by extracellular ATP in Arabidopsis. Plant Physiology<\/em> 190: 1574-1578
\nhttps:\/\/doi.org\/10.1093\/plphys\/kiac393<\/a><\/p>\n

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\"\"Tanaka K<\/strong>, DeShields JB<\/strong>, Moroz N<\/strong>, Woodhall JW (2022) Isothermal amplification for potato disease diagnosis: what have we learned from detection of the powdery scab pathogen? Potato Progress<\/em> 22 (4)
\nhttps:\/\/doi.org\/10.7273\/000004646<\/a><\/p>\n

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\"\"<\/a>Wei W, Xu L, Peng H, Zhu W, Tanaka K<\/strong>, Cheng J, Sanguinet KA, Vandemark G, Chen W (2022) A novel fungal extracellular effector inactivates plant polygalacturonase-inhibiting protein. Nature Communications<\/em> 13: 2213
\nhttps:\/\/doi.org\/10.1038\/s41467-022-29788-2<\/a><\/p>\n

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\"\"<\/strong><\/a>Mora-Romero GA<\/strong>, F\u00e9lix-Gast\u00e9lum R, Bomberger RA, Romero-Ur\u00edas C, Tanaka K<\/strong> (2022) Common potato disease symptoms: ambiguity of symptom-based identification of causal pathogens and value of on-site molecular diagnostics. Journal of General Plant Pathology<\/em> 88: 89-104
\nhttps:\/\/doi.org\/10.1007\/s10327-021-01045-2<\/a><\/p>\n

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\"\"<\/strong><\/a>Yuan P, Tanaka K<\/strong>, Poovaiah BW (2022) Calcium\/Calmodulin-mediated defense signaling: what is looming on the horizon for AtSR1\/CAMTA3-mediated signaling in plant immunity. Frontiers in Plant Sciences<\/em> 12: 795353
\nhttps:\/\/doi.org\/10.3389\/fpls.2021.795353<\/a><\/p>\n

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\"\"<\/strong><\/a>Marcec MJ<\/strong>, Tanaka K<\/strong> (2022) Crosstalk between calcium and ROS signaling during flg22-triggered immune response in Arabidopsis leaves. Plants<\/em> 11: 14
\nhttps:\/\/doi.org\/10.3390\/plants11010014<\/a><\/p>\n

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2021<\/span><\/strong><\/p>\n

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\"\"<\/strong><\/a>Yuan P, Tanaka K<\/strong>, Poovaiah BW (2021) Calmodulin-binding transcription activator AtSR1\/CAMTA3 fine-tunes plant immune response by transcriptional regulation of the salicylate receptor NPR1. Plant, Cell & Environment<\/em> 44: 3140-3154
\nhttps:\/\/doi.org\/10.1111\/pce.14123<\/a><\/p>\n

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\"\"<\/a>Tanaka K<\/strong>, Heil M (2021) Damage-associated molecular patterns (DAMPs) in plant innate immunity: applying the danger model and evolutionary perspectives. Annual Review of Phytopathology<\/em> 59: 53-75
\nhttps:\/\/doi.org\/10.1146\/annurev-phyto-082718-100146<\/a><\/p>\n

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\"\"<\/b><\/a>Combest MM, Moroz N<\/strong>, Tanaka K<\/strong>, Rogan CJ, Anderson JC, Thura L, Rakotondrafara AM, Goyer A (2021) StPIP1, a PAMP-induced peptide in potato, elicits plant defenses and is associated with disease symptom severity in a compatible interaction with potato virus Y. Journal of Experimental Botany<\/em> 72: 4472-4488
\nhttps:\/\/doi.org\/10.1093\/jxb\/erab078<\/a><\/p>\n

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2020<\/span><\/strong><\/p>\n

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\"\"<\/b><\/a>Yuan P, Jewell JB<\/strong>, Behera S, Tanaka K<\/strong>, Poovaiah BW (2020) Distinct molecular pattern-induced calcium signatures lead to different downstream transcriptional regulations via AtSR1\/CAMTA3. International Journal of Molecular Sciences<\/em> 21: 8163
\nhttps:\/\/doi.org\/10.3390\/ijms21218163<\/a><\/p>\n

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\"\"<\/a>Kumar S<\/b>, Tripathi D<\/b>, Okubara PA, Tanaka K<\/b> (2020) Purinoceptor P2K1\/DORN1 enhances plant resistance against a soilborne fungal pathogen, Rhizoctonia solani<\/em>. Frontiers in Plant Science<\/em> 11: 572920
\nhttps:\/\/doi.org\/10.3389\/fpls.2020.572920<\/a>
\n<\/b><\/p>\n

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\"\"<\/a>Moroz N<\/b>, Tanaka K<\/b> (2020) FlgII-28 is a major flagellin-derived defense elicitor for potato. Molecular Plant-Microbe Interactions\u00a0<\/i>33: 247-255
\nhttps:\/\/doi.org\/10.1094\/MPMI-06-19-0164-R\u00a0<\/a><\/i><\/p>\n

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 <\/p>\n

2019<\/span><\/strong><\/p>\n

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\"\"<\/a>DeShields JB<\/b>, Moroz N<\/b>, Braley LE<\/b>, Mora-Romero GA<\/b>, Tanaka K<\/b> (2019) Recombinase polymerase amplification (RPA) for the rapid isothermal detection of Spongospora subterranea<\/em> f. sp. subterranea<\/em> and potato mop-top virus. American Journal of Potato Research <\/em>96: 617-624
\nhttps:\/\/doi.org\/10.1007\/s12230-019-09750-7<\/a><\/p>\n

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\"\"<\/a>Jewell, JB<\/strong>, Tanaka K<\/strong> (2019) Transcriptomic perspective on extracellular ATP signaling: a few curious trifles. Plant Signaling & Behavior <\/em>14: e1659079
\nhttps:\/\/doi.org\/10.1080\/15592324.2019.1659079<\/a><\/p>\n

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\"\"<\/a>Marcec MJ<\/strong>, Gilroy S, Poovaiah BW, Tanaka K<\/strong> (2019) Mutual interplay of Ca2+<\/sup> and ROS signaling in plant immune response. Plant Science<\/em> 283: 343-354
\nhttps:\/\/doi.org\/10.1016\/j.plantsci.2019.03.004<\/a><\/p>\n

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\"\"<\/a>Ramachandran SR<\/strong>, Kumar S<\/strong>, Tanaka K<\/strong> (2019) Quantification of extracellular ATP in plant suspension cell cultures. Methods in Molecular Biology <\/em>1991: 43-54
\nhttps:\/\/doi.org\/10.1007\/978-1-4939-9458-8_5<\/a><\/p>\n

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\"\"<\/a>Jewell JB<\/strong>, Sowders JM<\/strong>, He R, Willis MA, Gang DR, Tanaka K<\/strong> (2019)\u00a0Extracellular ATP shapes a defense-related transcriptome both independently and along with other defense signaling pathways.\u00a0Plant Physiology<\/em> 179: 1144-1158
\nhttps:\/\/doi.org\/10.1104\/pp.18.01301<\/a><\/p>\n

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2018<\/span><\/strong><\/p>\n

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\"\"<\/a>Hadwiger LA, Tanaka K<\/strong> (2018) DNA damage and chromatin conformation changes confer nonhost resistance: a hypothesis based on effects of anti-cancer agents on plant defense responses. Frontiers in Plant Science<\/em> 9: 1056
\nhttps:\/\/doi.org\/10.3389\/fpls.2018.01056<\/a><\/p>\n

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\"\"<\/a>Yuan P, Tanaka K<\/strong>, Du L, Poovaiah BW (2018) Calcium signaling in plant autoimmunity: a guard model for AtSR1\/CAMTA3-mediated immune response. Molecular Plant <\/em>11: 637-639
\n<\/em>https:\/\/doi.org\/10.1016\/j.molp.2018.02.014<\/a><\/p>\n

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\"\"<\/a>DeShields JB<\/strong>, Bomberger RA, Woodhall JW, Wheeler DL, Moroz N<\/strong>, Johnson DA, Tanaka K<\/strong> (2018) On-site molecular detection of soil-borne phytopathogens using a portable real-time PCR system. Journal of\u00a0Visualized Experiments <\/em>e56891
\nhttps:\/\/doi.org\/10.3791\/56891<\/a><\/p>\n

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\"\"<\/a>Tripathi D<\/strong>, Tanaka K<\/strong> (2018) A crosstalk between extracellular ATP and JA signaling pathways. Plant Signaling & Behavior<\/em> 13: e1432229
\nhttps:\/\/doi.org\/10.1080\/15592324.2018.1432229<\/a>
\n<\/strong><\/p>\n

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\"\"<\/a>Tripathi D<\/strong>, Zhang T, Koo AJ, Stacey G, Tanaka K<\/strong> (2018) Extracellular ATP acts on jasmonate signaling to reinforce plant defense. Plant Physiology<\/em> 176: 511-523
\nhttps:\/\/doi.org\/10.1104\/pp.17.01477<\/a><\/p>\n

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2017<\/span><\/strong><\/p>\n

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\"\"<\/a>Moroz N<\/strong>, Huffaker A, Tanaka K<\/strong> (2017) Extracellular alkalinization assay for detection of early defense response. Current Protocols in Plant Biology <\/em>2: 210-220
\nhttps:\/\/doi.org\/10.1002\/cppb.20057<\/a><\/p>\n

 <\/p>\n

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\"\"<\/a>Yuan P, Jauregui E, Du L, Tanaka K<\/strong>, Poovaiah BW (2017) Calcium signatures and signaling events orchestrate plant-microbe interactions. Current Opinion in Plant Biology<\/em> 38: 173-183
\nhttps:\/\/doi.org\/10.1016\/j.pbi.2017.06.003<\/a><\/p>\n

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\"\"<\/a>Hadwiger LA, Tanaka K<\/strong> (2017) A Simple and rapid assay for measuring phytoalexin pisatin, an indicator of plant defense response in Pea (Pisum sativum<\/em> L.). Bio-protocol <\/em>7: e2362
\nhttps:\/\/doi.org\/10.21769\/BioProtoc.2362<\/a><\/p>\n

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\"\"<\/a>Hadwiger LA, Tanaka K<\/strong> (2017) Nonhost resistance: DNA damage is associated with SA signaling for induction of PR genes and contributes to the growth suppression of a pea pathogen on pea endocarp tissue. Frontiers in Plant Science<\/em> 8: 446
\nhttps:\/\/doi.org\/10.3389\/fpls.2017.00446<\/a><\/p>\n

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\"\"<\/a>Tanaka K<\/strong>, Hadwiger LA (2017) Nonhost resistance: reactive oxygen species (ROS) signal causes DNA damage prior to the induction of PR genes and disease resistance in pea tissue. Physiological and Molecular Plant Pathology<\/em> 98: 18-24
\nhttps:\/\/doi.org\/10.1016\/j.pmpp.2017.01.007<\/a><\/p>\n

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\"\"<\/a>Moroz N<\/strong>, Fritch KR<\/strong>, Marcec MJ<\/strong>, Tripathi D<\/strong>, Smertenko A, Tanaka K<\/strong> (2017) Extracellular alkalinization as a defense response in potato cells. Frontiers in Plant Science<\/em> 8: 32
\nhttps:\/\/doi.org\/10.3389\/fpls.2017.00032<\/a><\/p>\n

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\"\"<\/a>Ramachandran SR, Yin C, Kud J,\u00a0Tanaka K<\/strong>, Mahoney AK, Xiao F, Hulbert SH (2017) Effectors from wheat rust fungi suppress multiple plant defense responses. Phytopathology<\/em> 107: 75-83
\nhttps:\/\/doi.org\/10.1094\/PHYTO-02-16-0083-R<\/a><\/p>\n

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2014 \u2013 2016<\/strong><\/span><\/p>\n

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\"\"<\/a>Nguyen CT, Tanaka K<\/strong>, Cao Y, Cho S-H, Xu D, Stacey G (2016) Computational Analysis of the ligand Binding Site of the Extracellular ATP Receptor, DORN1. PLoS One<\/em> 11: e0161894
\nhttps:\/\/doi.org\/10.1371\/journal.pone.0161894<\/a><\/p>\n

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\"\"<\/a>Hadwiger LA, Tanaka K<\/strong>\u00a0(2015) EDTA a novel inducer of pisatin, a phytoalexin indicator of the non-host resistance in peas. Molecules<\/em> 20: 24-34
\nhttps:\/\/doi.org\/10.3390\/molecules20010024<\/a><\/p>\n

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\"\"<\/a>Tanaka K<\/strong>, Choi J, Cao Y, Stacey G (2014) Extracellular ATP acts as a damage associated molecular pattern (DAMP) signal in plants. Frontiers in Plant Science<\/em> 5: 466
\nhttps:\/\/doi.org\/10.3389\/fpls.2014.00446<\/a><\/p>\n

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 <\/p>\n<\/p><\/div>\n<\/section>\n

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Tanaka lab –<\/span>\u00a0<\/em>Home<\/span> <\/a>| Research <\/a><\/span>| Publications<\/span> <\/a>| Personnel<\/span> <\/a>| Opportunities<\/span><\/a>\u00a0|\u00a0Lab News
\n<\/span><\/a>Department of Plant Pathology<\/a> | Washington State University<\/a> | PO Box 646430, Pullman, WA 99164-6430<\/span><\/p>\n<\/p><\/div>\n<\/section>\n","protected":false},"excerpt":{"rendered":"

Home<\/a> | Research <\/a>| Publications<\/strong>\u00a0<\/strong>|\u00a0<\/strong>Personnel <\/a>| Opportunities<\/a> |\u00a0<\/strong>Lab News<\/a><\/strong><\/p>\n

 <\/p>\n

Tanaka Lab – Publications<\/strong><\/p>\n

 <\/p>\n

2025<\/strong><\/p>\n

\"\"<\/a>Jayasinghe SK<\/strong>, Moroz N<\/strong>, Yuan P, Kolomiets MV, Tanaka K<\/strong> (2025) Salicylic Acid Plays a Major Role in Potato Defense Against Powdery Scab Pathogen, Spongospora subterranea<\/em> f. sp. subterranea<\/em>. Molecular Plant-Microbe Interactions <\/em>(in press)
https:\/\/doi.org\/10.1094\/MPMI-12-24-0154-R<\/a><\/p>\n

 <\/p>\n

2024<\/strong><\/p>\n

\"\"<\/a>Kamal … » More …<\/span><\/a><\/strong><\/p>\n","protected":false},"author":2755,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"template-builder.php","meta":[],"wsuwp_university_location":[],"wsuwp_university_org":[],"_links":{"self":[{"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/pages\/16"}],"collection":[{"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/users\/2755"}],"replies":[{"embeddable":true,"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/comments?post=16"}],"version-history":[{"count":55,"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/pages\/16\/revisions"}],"predecessor-version":[{"id":3428,"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/pages\/16\/revisions\/3428"}],"wp:attachment":[{"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/media?parent=16"}],"wp:term":[{"taxonomy":"wsuwp_university_location","embeddable":true,"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/wsuwp_university_location?post=16"},{"taxonomy":"wsuwp_university_org","embeddable":true,"href":"https:\/\/labs.wsu.edu\/tanaka-lab\/wp-json\/wp\/v2\/wsuwp_university_org?post=16"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}