Publications


2024

Anna Coll, Tjaša Lukan, Katja Stare, Maja Zagorščak, Tjaša Mahkovec Povalej, Špela Baebler, Salomé Prat, Núria S. Coll, Marc Valls, Marko Petek, Kristina Gruden

The StPti5 ethylene response factor acts as a susceptibility factor by negatively regulating the potato immune response to pathogens

New Phytol. 2024 Aug 11, doi: 10.1111/nph.20004


Kacprzyk J, Burke R, Armengot L, Coppola M, Tattrie SB, Vahldick H, Bassham DC, Bosch M, Brereton NJB, Cacas JL, Coll NS, Gallois P, Kuchitsu K, Nowack MK, Rogers HJ, Van Breusegem F, Gunawardena AHLAN, McCabe PF

Roadmap for the next decade of plant programmed cell death research

New Phytol. 2024 Mar 27. doi: 10.1111/nph.19709


Cao M, Platre MP, Tsai HH, Zhang L, Nobori T, Armengot L, Chen Y, He W, Brent L, Coll NS, Ecker JR, Geldner N, Busch W

Spatial IMA1 regulation restricts root iron acquisition on MAMP perception

Nature. 2024 Jan;625(7996):750-759


Zhang W, Planas-Marquès M, Mazier M, Šimkovicová M, Rocafort M, Mantz M, Huesgen PF, Takken FLW, Stintzi A, Schaller A, Coll NS, Valls M

The tomato P69 subtilase family is involved in resistance to bacterial wilt

Plant J. 2023 Dec 27. doi: 10.1111/tpj.16613


de Pedro-Jové R, Corral J, Rocafort M, Puigvert M, Azam FL, Vandecaveye A, Macho AP, Balsalobre C, Coll NS, Orellano E, Valls M

Gene expression changes throughout the life cycle allow a bacterial plant pathogen to persist in diverse environmental habitats

PLoS Pathog. 2023 Dec 19;19(12):e1011888


2023

Zhang W, Jiménez-Jiménez Á, Capellades M, Rencoret J, Kashyap A, Coll NS

Determination of De Novo Suberin-Lignin Ferulate Deposition in Xylem Tissue Upon Vascular Pathogen Attack

Methods Mol Biol. 2024;2722:117-127. doi: 10.1007/978-1-0716-3477-6_9


Ruiz-Solaní N, Salguero-Linares J, Armengot L, Santos J, Pallarès I, van Midden KP, Phukkan UJ, Koyuncu S, Borràs-Bisa J, Li L, Popa C, Eisele F, Eisele-Bürger AM, Hill SM, Gutiérrez-Beltrán E, Nyström T, Valls M, Llamas E, Vilchez D, Klemenčič M, Ventura S, Coll NS

Arabidopsis metacaspase MC1 localizes in stress granules, clears protein aggregates, and delays senescence

Plant Cell. 2023 Sep 1;35(9):3325-3344. doi: 10.1093/plcell/koad172


Pitsili E, Rodriguez-Trevino R, Ruiz-Solani N, Demir F, Kastanaki E, Dambire C, de Pedro-Jové R, Vercammen D, Salguero-Linares J, Hall H, Mantz M, Schuler M, Tuominen H, Van Breusegem F, Valls M, Munné-Bosch S, Holdsworth MJ, Huesgen PF, Rodriguez-Villalon A, Coll NS

A phloem-localized Arabidopsis metacaspase (AtMC3) improves drought tolerance

New Phytol. 2023 Aug;239(4):1281-1299. doi: 10.1111/nph.19022


Kashyap A, Jiménez-Jiménez Á, Figueras M, Serra O, Valls M, Coll NS

The Tomato Feruloyl Transferase FHT Promoter Is an Accurate Identifier of Early Development and Stress-Induced Suberization

Plants (Basel). 2023 May 5;12(9):1890. doi: 10.3390/plants12091890


Salguero-Linares, J. & Coll, N. S.

Cell death as a defense strategy against pathogens in plants and animals

PLoS Pathog. 2023 Apr 6;19(4):e1011253. doi: 10.1371/journal.ppat.1011253


Maekawa T, Kashkar H, Coll N. S.

Dying in self-defence: a comparative overview of immunogenic cell death signalling in animals and plants

Cell Death & Differentiation. 2023 Oct 4. DOI: 10.1038/s41418-022-01060-6


Phukan, U. J., Stael, S., Gonçalves, A., Van Breusegem, F., & Coll, N. S

Detection and Quantification of Protein Aggregates in Plants

Methods in molecular biology. 2023; 2581:221-228. doi:10.1007/978-1-0716-2784-6_15


2022

Salguero-Linares, J., Serrano, I., Ruiz-Solani, N., Salas-Gómez, M., Phukan, U. J., González, V. M., Bernardo-Faura, M., Valls, M., Rengel, D., & Coll, N. S.

Robust transcriptional indicators of immune cell death revealed by spatiotemporal transcriptome analyses

Molecular Plant, 15(6), 1059-1075. 2022 June 06. DOI: 10.1016/j.molp.2022.04.010


Salguero-Linares, J., Lema-Asqui, S., Salas-Gómez, M., Froilán-Soares, A., Coll, N.S.

Detection and Quantification of the Hypersensitive Response Cell Death in Arabidopsis thaliana

Plant Proteases and Plant Cell Death, Methods in Molecular Biology, 2447, 193–204. 2022 May 19. DOI: 10.1007/978-1-0716-2079-3_16


Hikichi Y, Valls M, Genin S.

Editorial: Ralstonia solanacearum-Plant Interactions: Plant Defense Responses, Virulence Mechanisms and Signaling Pathways

Plant Science, 13: 890877. 2022 May 5. DOI: 10.3389/fpls.2022.890877


Kashyap, A., Capellades, M., Zhang, W., Srinivasan, S., Laromaine, A., Serra, O., Figueras, M., Rencoret, J., Gutiérrez, A., Valls, M., & Coll, N. S.

Induced ligno-suberin vascular coating and tyramine-derived hydroxycinnamic acid amides restrict Ralstonia solanacearum colonization in resistant tomato roots

New Phytologist, 234(4), 1411-1429. 2022 February 13. DOI: 10.1111/nph.17982


Niu, Y., Fu, S., Chen, G., Wang, H., Wang, Y., Hu, J., Jin, X., Zhang, M., Lu, M., He, Y., Wang, D., Chen, Y., Zhang, Y., Coll, N. S., Valls, M., Zhao, C., Chen, Q., & Lu, H.

Different epitopes of Ralstonia solanacearum effector RipAW are recognized by two Nicotiana species and trigger immune responses

Molecular Plant Pathology, 23(2), 188–203. 2022 Febrary. DOI: 10.1111/mpp.13153


Yang, L., Wei, Z., Valls, M., & Ding, W.

Metabolic Profiling of Resistant and Susceptible Tobaccos Response Incited by Ralstonia pseudosolanacearum Causing Bacterial Wilt

Frontiers in Plant Science, 12. 2022 January 07. DOI: 10.3389/fpls.2021.780429


2021

Sebastià, P., de Pedro-Jové, R., Daubech, B., Kashyap, A., Coll, N. S., & Valls, M.

The Bacterial Wilt Reservoir Host Solanum dulcamara Shows Resistance to Ralstonia solanacearum Infection

Frontiers in Plant Science , 12. 2021 November 10. DOI: 10.3389/fpls.2021.755708


Ferreira, V., González, M., Pianzzola, M. J., Coll, N. S., Siri, M. I., & Valls, M.

Molecular Detection of Ralstonia solanacearum to Facilitate Breeding for Resistance to Bacterial Wilt in Potato

Methods in Molecular Biology, 375–385. 2021 August 27. DOI: 10.1007/978-1-0716-1609-3_18


Menna, A., Dora, S., Sancho-Andrés, G., Kashyap, A., Meena, M. K., Sklodowski, K., Gasperini, D., Coll, N. S., & Sánchez-Rodríguez, C.

A primary cell wall cellulose-dependent defense mechanism against vascular pathogens revealed by time-resolved dual transcriptomics

BMC Biology, 19(7). 2021 August 17. DOI: 10.1186/s12915-021-01100-6


Yang, L., Guan, D., Valls, M., & Ding, W.

Sustainable natural bioresources in crop protection: antimicrobial hydroxycoumarins induce membrane depolarization-associated changes in the transcriptome of Ralstonia solanacearum

BPest Management Science, 77(11), 5170–5185. 2021 July 13. DOI: 10.1002/ps.6557


de Pedro-Jové, R., Puigvert, M., Sebastià, P., Macho, A. P., Monteiro, J. S., Coll, N. S., Setúbal, J. C., & Valls, M.

Dynamic expression of Ralstonia solanacearum virulence factors and metabolism-controlling genes during plant infection

BMC Genomics, 22(1). 2021 March 09. DOI: 10.1186/s12864-021-07457-w


Kashyap, A., Planas-Marquès, M., Capellades, M., Valls, M., & Coll, N. S.

Blocking intruders: inducible physico-chemical barriers against plant vascular wilt pathogens

Journal of Experimental Botany, 72(2), 184–198. . 2021 Feb 2. DOI: 10.1093/jxb/eraa444


Daniel J. Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, Mahmoud Abdellatif, Asghar Abdoli, [...], Coll, N. S., [...], Yong Lin, Shigeru Oshima, Yueguang Rong, Judith C. Sluimer, Christina L. Stallings & Chun-Kit Tong.

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Autophagy, 17:1, 1-382. 2021 Febrary 08. DOI: 10.1080/15548627.2020.1797280


Alonso-Díaz, A., Satbhai, S. B., de Pedro-Jové, R., Berry, H. M., Göschl, C., Argueso, C. T., Novak, O., Busch, W., Valls, M., & Coll, N. S.

A genome-wide association study reveals cytokinin as a major component in the root defense responses against Ralstonia solanacearum

Journal of Experimental Botany, 72(7), 2727–2740. 2021 January 21. DOI: 10.1093/jxb/eraa610


Moon, H., Pandey, A., Yoon, H., Choi, S., Jeon, H., Prokchorchik, M., Jung, G., Witek, K., Valls, M., McCann, H. C., Kim, M., Jones, J. D. G., Segonzac, C., & Sohn, K. H.

Identification of RipAZ1 as an avirulence determinant of Ralstonia solanacearum in Solanum americanum

Molecular Plant Pathology, 22(3), 317–333. 2021 January 3. DOI: 10.1111/mpp.13030


de Pedro Jové, R., Sebastià, P., & Valls, M.

Identification of Type III Secretion Inhibitors for Plant Disease Management

Plant Chemical Genomics. Methods in Molecular Biology, 2113, 39–48. 2021 January. DOI: 10.1007/978-1-0716-0954-5_4


2020

Tondo, M. L., de Pedro-Jové, R., Vandecaveye, A., Piskulic, L., Orellano, E. G., & Valls, M.

KatE From the Bacterial Plant Pathogen Ralstonia solanacearum Is a Monofunctional Catalase Controlled by HrpG That Plays a Major Role in Bacterial Survival to Hydrogen Peroxide

Frontiers in Plant Science, 11. 2020 July 31. DOI: 10.3389/fpls.2020.01156


Pitsili, E., Phukan, U. J., & Coll, N. S.

Cell Death in Plant Immunity

Spring Harbor Perspectives in Biology, 12(6): a036483. 2020 Jun 1. DOI: 10.1101/cshperspect.a036483


Planas-Marquès M, Kressin JP, Kashyap A, Panthee DR, Louws FJ, Coll N.S, Valls M..

Four bottlenecks restrict colonization and invasion by the pathogen Ralstonia solanacearum in resistant tomato

Journal of Experimental Botany, 71(6):2157-2171. 2020 Mar 25. DOI: 10.1093/jxb/erz562


Minina, E. A., Staal, J., Alvarez, V. E., Berges, J. A., Berman-Frank, I., Beyaert, R., Bidle, K. D., Bornancin, F., Casanova, M., Cazzulo, J. J., Choi, C. J., Coll, N. S., Dixit, V. M., Dolinar, M., Fasel, N., Funk, C., Gallois, P., Gevaert, K., Gutierrez-Beltran, E., . . . Bozhkov, P. V.

Classification and nomenclature of metacaspases and paracaspases: no more confusion with caspases

Molecular Cell, 77(5), 927–929. 2020 March 05. doi/org/10.1016/j.molcel.2019.12.020


Corral, J., Sebastià, P., Coll, N. S., Barbé, J., Aranda, J., & Valls, M.

Twitching and Swimming Motility Play a Role in Ralstonia solanacearum Pathogenicity

MSphere, 5(2). 2020 March 04. DOI: 10.1128/mSphere.00740-19


2019

Planas-Marquès, M., Kressin, J. P., Kashyap, A., Panthee, D. R., Louws, F. J., Coll, N. S., & Valls, M.

Four bottlenecks restrict colonization and invasion by the pathogen Ralstonia solanacearum in resistant tomato

Journal of Experimental Botany, 71(6), 2157–2171. 2019 December 24. DOI: 10.1093/jxb/erz562


Wang, H., Hu, J., Lu, Y., Zhang, M., Qin, N., Zhang, R., He, Y., Wang, D., Chen, Y., Zhao, C., Coll, N. S., Valls, M., Chen, Q., & Lu, H.

A quick and efficient hydroponic potato infection method for evaluating potato resistance and Ralstonia solanacearum virulence

Plant Methods, 15(1). 2019 Nov 30;15:145. 2019 November 30. DOI: 10.1186/s13007-019-0530-9


Soler, M., Verdaguer, R., Fernández-Piñán, S., Company-Arumí, D., Boher, P., Góngora-Castillo, E., Valls, M., Anticó, E., Molinas, M., Serra, O., & Figueras, M.

Silencing against the conserved NAC domain of the potato StNAC103 reveals new NAC candidates to repress the suberin associated waxes in phellem

Plant Science, 291, 110360. 2019 November 27. DOI: 10.1016/j.plantsci.2019.110360

Zhao, C., Wang, H., Lu, Y., Hu, J., Qu, L., Li, Z., Wang, D., He, Y., Valls, M., Coll, N. S., Chen, Q., & Lu, H.

Deep Sequencing Reveals Early Reprogramming of Arabidopsis Root Transcriptomes Upon Ralstonia solanacearum Infection

Molecular Plant-Microbe Interactions, 32(7), 813–827. 2019 May 28. DOI: 10.1094/mpmi-10-18-0268-r


Salguero-Linares, J., & Coll, N. S.

Plant proteases in the control of the hypersensitive response

Journal of Experimental Botany, 70(7), 2087–2095. 2019 March 15. DOI: 10.1093/jxb/erz030


Alonso-Díaz, A., Floriach-Clark, J., Fuentes, J., Capellades, M., Coll, N. S., & Laromaine, A.

Enhancing Localized Pesticide Action through Plant Foliage by Silver-Cellulose Hybrid Patches

ACS Biomaterials Science & Engineering, 5(2), 413–419. 2019 January 11. DOI: 10.1021/acsbiomaterials.8b01171


2018

Puigvert, M., Solé, M., López‐Garcia, B., Coll, N. S., Beattie, K. D., Davis, R. A., Elofsson, M., & Valls, M.

Type III secretion inhibitors for the management of bacterial plant diseases

Molecular Plant Pathology, 20(1), 20–32. 2018 July 30. DOI: 10.1111/mpp.12736


Avin-Wittenberg, T., Baluška, F., Bozhkov, P. V., Elander, P. H., Fernie, A. R., Galili, G., Hassan, A., Hofius, D., Isono, E., le Bars, R., Masclaux-Daubresse, C., Minina, E. A., Peled-Zehavi, H., Coll, N. S., Sandalio, L. M., Satiat-Jeunemaitre, B., Sirko, A., Testillano, P. S., & Batoko, H.

Autophagy-related approaches for improving nutrient use efficiency and crop yield protection

Journal of Experimental Botany, 69(6), 1335–1353. 2018 March 14. DOI: 10.1093/jxb/ery069


Planas-Marquès, M., Bernardo-Faura, M., Paulus, J., Kaschani, F., Kaiser, M., Valls, M., van der Hoorn, R. A., & Coll, N. S.

Protease Activities Triggered by Ralstonia solanacearum Infection in Susceptible and Tolerant Tomato Lines

Molecular & Cellular Proteomics, 17(6), 1112–1125. 2018 March 09. DOI: 10.1074/mcp.RA117.000052


2017

Ferreira, V., Pianzzola, M. J., Vilaró, F. L., Galván, G. A., Tondo, M. L., Rodriguez, M. V., Orellano, E. G., Valls, M., & Siri, M. I.

Interspecific Potato Breeding Lines Display Differential Colonization Patterns and Induced Defense Responses after Ralstonia solanacearum Infection

Frontiers in Plant Science, 8. 2017 August 28. DOI: 10.3389/fpls.2017.01424


Lu, H., Lema A, S., Planas-Marquès, M., Alonso-Díaz, A., Valls, M., & Coll, N. S.

Type III Secretion–Dependent and –Independent Phenotypes Caused by Ralstonia solanacearum in Arabidopsis Roots

Molecular Plant-Microbe Interactions, 31(1), 175–184. 2017 August 17. DOI: 10.1094/MPMI-05-17-0109-FI


Capela, D., Marchetti, M., Clérissi, C., Perrier, A., Guetta, D., Gris, C., Valls, M., Jauneau, A., Cruveiller, S., Rocha, E. P., & Masson-Boivin, C.

Recruitment of a Lineage-Specific Virulence Regulatory Pathway Promotes Intracellular Infection by a Plant Pathogen Experimentally Evolved into a Legume Symbiont

Molecular Biology and Evolution, 34(10), 2503–2521. 2017 May 23. DOI: 10.1093/molbev/msx165


Hofius, D., Li, L., Hafrén, A., & Coll, N. S.

Autophagy as an emerging arena for plant–pathogen interactions

Current Opinion in Plant Biology, 38, 117–123. 2017 May 22. DOI: 10.1016/j.pbi.2017.04.017


Erill, I., Puigvert, M., Legrand, L., Guarischi-Sousa, R., Vandecasteele, C., Setubal, J. C., Genin, S., Guidot, A., & Valls, M.

Comparative Analysis of Ralstonia solanacearum Methylomes

Frontiers in Plant Science, 8. 2017 April 14. DOI: 10.3389/fpls.2017.00504


Puigvert, M., Guarischi-Sousa, R., Zuluaga, P., Coll, N. S., Macho, A. P., Setubal, J. C., & Valls, M.

Transcriptomes of Ralstonia solanacearum during Root Colonization of Solanum commersonii

Frontiers in Plant Science, 8. 2017 March 20 DOI: 10.3389/fpls.2017.00370


Minina, E. A., Coll, N. S., Tuominen, H., & Bozhkov, P. V.

Metacaspases versus caspases in development and cell fate regulation

Cell Death & Differentiation, 24(8), 1314–1325. 2017 Febrary 24. DOI: 10.1038/cdd.2017.18 24:1314-1325


Lema Asqui, S., Vercammen, D., Serrano, I., Valls, M., Rivas, S., van Breusegem, F., Conlon, F. L., Dangl, J. L., & Coll, N. S.

AtSERPIN1 is an inhibitor of the metacaspase AtMC1-mediated cell death and autocatalytic processing in planta

New Phytologist, 218(3), 1156–1166. 2017 Febrary 03. DOI: 10.1111/nph.14446


Huysmans, M., Lema A, S., Coll, N. S., & Nowack, M. K.

Dying two deaths — programmed cell death regulation in development and disease

Current Opinion in Plant Biology, 35, 37–44. 2017 Febrary. DOI: 10.1016/j.pbi.2016.11.005


2016

Popa, C. M., Tabuchi, M., & Valls, M.

Modification of Bacterial Effector Proteins Inside Eukaryotic Host Cells

Frontiers in Cellular and Infection Microbiology, 6. 2016 July 20. DOI: 10.3389/fcimb.2016.00073


Planas-Marquès, M., Lema A., S., & Coll, N. S.

Detection and Quantification of Protein Aggregates in Plants

Methods in Molecular Biology, 195–203. 2016 July 16. DOI: 10.1007/978-1-4939-3759-2_15


Popa, C., Li, L., Gil, S., Tatjer, L., Hashii, K., Tabuchi, M., Coll, N. S., Ariño, J., & Valls, M.

The effector AWR5 from the plant pathogen Ralstonia solanacearum is an inhibitor of the TOR signalling pathway

Scientific Reports, 6(1). 2016 June 03. DOI: 10.1038/srep27058


Popa, C., Coll, N. S., Valls, M., & Sessa, G.

Yeast as a Heterologous Model System to Uncover Type III Effector Function

PLOS Pathogens, 12(2), e1005360. 2016 Febrary 25. DOI: 10.1371/journal.ppat.1005360


Fujiwara, S., Kawazoe, T., Ohnishi, K., Kitagawa, T., Popa, C., Valls, M., Genin, S., Nakamura, K., Kuramitsu, Y., Tanaka, N., & Tabuchi, M.

RipAY, a Plant Pathogen Effector Protein, Exhibits Robust γ-Glutamyl Cyclotransferase Activity When Stimulated by Eukaryotic Thioredoxins

Journal of Biological Chemistry, 291(13), 6813–6830. 2016 January 28 DOI: 10.1074/jbc.m115.678953


Daniel J Klionsky, Kotb Abdelmohsen, Akihisa Abe, Md Joynal Abedin, Hagai Abeliovich, [...], Coll, N. S, [...],Christos E Zois, Teresa Zoladek, Wei-Xing Zong, Antonio Zorzano & Susu M Zughaier.

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Autophagy, 12:1, 1-222. 2016 January 21. DOI: 10.1080/15548627.2015.1100356


Guarischi-Sousa, R., Puigvert, M., Coll, N. S., Siri, M. I., Pianzzola, M. J., Valls, M., & Setubal, J. C.

Complete genome sequence of the potato pathogen Ralstonia solanacearum UY031

Standards in Genomic Sciences, 11(1). 2016 January 15. DOI: 10.1186/s40793-016-0131-4


2015

Salvesen, G. S., Hempel, A., & Coll, N. S.

Protease signaling in animal and plant-regulated cell death

The FEBS Journal, 283(14), 2577–2598. 2015 December 09. DOI: 10.1111/febs.13616


Olvera-Carrillo, Y., van Bel, M., van Hautegem, T., Fendrych, M., van Durme, M., Huysmans, M., ŠImášková, M., Buscaill, P., Rivas, S., Coll, N. S., Maere, S., Coppens, F., & Nowack, M. K.

A conserved core of PCD indicator genes discriminates developmentally and environmentally induced programmed cell death in plants

Plant Physiology, pp.00769.2015. 2015 December. DOI: 10.1104/pp.15.00769


Zuluaga, A., Coll, N. S., & Valls, M.

Quantification of Ralstonia solanacearum Colonization of Potato Germplasm Using Luminescence

BIO-PROTOCOL, 5(9). 2015 May 5. DOI: 10.21769/bioprotoc.1461


Zuluaga, A. P., Solé, M., Lu, H., Góngora-Castillo, E., Vaillancourt, B., Coll, N. S., Buell, C. R., & Valls, M.

Transcriptome responses to Ralstonia solanacearum infection in the roots of the wild potato Solanum commersonii

BMC Genomics, 16(1). 2015 March 26. DOI: 10.1186/s12864-015-1460-1


Stael, S., Kmiecik, P., Willems, P., van der Kelen, K., Coll, N. S., Teige, M., & van Breusegem, F.

Plant innate immunity - sunny side up?

Trends in Plant Science, 20(1), 3–11. 2015 January. DOI: 10.1016/j.tplants.2014.10.002


2014

Stael, S., Nowack, M. K., van Breusegem, F., Valls, M., & Coll, N. S.

The Death of Plant Cells: From Proteases to Field Applications

Cell Death & Differentiation, 21(12), 160. 2014 December 10. DOI: 10.1038/cdd.2014.160


Coll, N. S., Smidler, A., Puigvert, M., Popa, C., Valls, M., & Dangl, J. L.

The plant metacaspase AtMC1 in pathogen-triggered programmed cell death and aging: Functional linkage with autophagy

Cell Death & Differentiation, 21(9), 1399–1408. 2014 March 02. DOI: 10.1038/cdd.2014.50


Cruz, A. P. Z., Ferreira, V., Pianzzola, M. J., Siri, M. I., Coll, N. S., & Valls, M.

A novel, sensitive method to evaluate potato germplasm for bacterial wilt resistance using a luminescent Ralstonia solanacearum reporter strain

Molecular Plant-Microbe Interactions, 27(3), 277–285. 2014 Febrary 04. DOI: 10.1094/mpmi-10-13-0303-fi


2013

Zuluaga, A. P., Puigvert, M., & Valls, M.

Novel plant inputs influencing Ralstonia solanacearum during infection

Frontiers in Microbiology, 4. 2013 November 20. DOI: 10.3389/fmicb.2013.00349


Peeters, N., Guidot, A., Vailleau, F., & Valls, M.

Ralstonia solanacearum, a widespread bacterial plant pathogen in the post-genomic era

Molecular Plant Pathology, 14(7), 651–662. 2013 May 30. DOI: 10.1111/mpp.12038


Coll, N. S., & Valls, M.

Current knowledge on the Ralstonia solanacearum type III secretion system

Microbial Biotechnology, 6(6), 614–620. 2013 April 26. DOI: 10.1111/1751-7915.12056


2012

Monteiro, F., Genin, S., van Dijk, I., & Valls, M.

A luminescent reporter evidences active expression of Ralstonia solanacearum type III secretion system genes throughout plant infection

Microbiology, 158(8), 2107–2116. 2012 August 01 DOI: 10.1099/mic.0.058610-0


Solé, M., Popa, C., Mith, O., Sohn, K. H., Jones, J. D. G., Deslandes, L., & Valls, M.

The awr gene family encodes a novel class of Ralstonia solanacearum type III effectors displaying virulence and avirulence activities

Molecular Plant-Microbe Interactions, 25(7), 941–953. 2012 June 05. DOI: 10.1094/mpmi-12-11-0321


Monteiro, F., Solé, M., van Dijk, I., & Valls, M.

A chromosomal insertion toolbox for promoter probing, mutant complementation and pathogenicity studies in Ralstonia solanacearum

Molecular Plant-Microbe Interactions, 25(4), 557–568. 2012 March 12. DOI: 10.1094/mpmi-07-11-0201


2011

Coll, N. S., Epple, P., & Dangl, J. L.

Programmed cell death in the plant immune system

Cell Death & Differentiation, 18(8), 1247–1256. 2011 April 08. DOI: 10.1038/cdd.2011.3718


2010

Plener, L., Manfredi, P., Valls, M., & Genin, S.

PrhG, a transcriptional regulator responding to growth conditions, is involved in the control of the type III secretion system regulon in Ralstonia solanacearum

Journal of Bacteriology, 192(4), 1011–1019. 2010 December 20. DOI: 10.1128/jb.01189-09


Coll, N. S., Vercammen, D., Smidler, A., Clover, C., van Breusegem, F., Dangl, J. L., & Epple, P.

Arabidopsis type I metacaspases control cell death

Science, 330(6009), 1393–1397. 2010 November 18. DOI: 10.1126/science.1194980


Lumbreras, V., Vilela, B., Irar, S., Solé, M., Capellades, M., Valls, M., Coca, M., & Pagès, M.

MAPK phosphatase MKP2 mediates disease responses in Arabidopsis and functionally interacts with MPK3 and MPK6

THE PLANT JOURNAL 63, 2010 September 16. DOI: 10.1111/j.1365-313x.2010.04297.x


Muñoz, A., Valls, M., & de Lorenzo, V.

Extreme DNA bending: molecular basis of the regulatory breadth of IHF

Bacterial Chromatin, 365–393. 2010. DOI: 10.1007/978-90-481-3473-1_16