2021

  • Aerts, N., Pereira Mendes and Van Wees, S.C.M. (2021). Multiple levels of crosstalk in hormone networks regulating plant defense. Plant Journal 105: 489–504. http://doi.org/10.1111/tpj.15124. 

  • Alfonso, E., Stahl, E., Glauser, G., Bellani, E., Raaymakers, T.M., Van den Ackerveken, G., Zeier, J. and Reymond, P. (2021). Insect eggs trigger systemic acquired resistance against fungal and oomycete pathogens. New Phytologist 232: 2491-2505. https://doi.org/10.1111/nph.17732.

  • Annacondia, M.L., Markovic, D., Reig-Valiente, J.L., Scaltsoyiannes, V., Pieterse, C.M.J., Ninkovic, V., Slotkin, R.K. and Martinez, G. (2021). Aphid feeding induces the relaxation of epigenetic control and the associated regulation of the defense response in Arabidopsis. New Phytologist 230: 1185–1200. http://dx.doi.org/10.1111/nph.17226.

  • Bernal, P., Eberl, L., de Jonge, R., Lepek, V.C. and Malone, J.G. (2021). Understanding plant-microorganism interactions to envision a future of sustainable agriculture. Environmental Microbiology 23: 1809-1811. https://doi.org/10.1111/1462-2920.15479. 

  • Cosme, M., Fernández, I., Declerck, S., Van der Heijden, M.G.A. and Pieterse, C.M.J. (2021). A coumarin exudation pathway mitigates arbuscular mycorrhizal incompatibility in Arabidopsis thaliana. Plant Molecular Biology 106:319-334. http://link.springer.com/article/10.1007/s11103-021-01143-x.

  • Courbier, S., Snoek, B.L., Kajala, K., Li. L., Van Wees, S.C.M. and Pierik, R. (2021). Mechanisms of far-red light-mediated dampening of defense against Botrytis cinerea in tomato leaves. Plant Physiology 187: 1250-1266. https://doi.org/10.1093/plphys/kiab354.

  • De Kesel, J., Conrath, U., Flors, V., Luna, E., Mageroy, M.H., Mauch-Mani, B., Pastor, V., Pozo, M.J., Pieterse, C.M.J., Ton, J. and Kyndt, T. (2021). The induced resistance lexicon: do's and don'ts. Trends in Plant Science 26: 685-691. https://doi.org/10.1016/j.tplants.2021.01.001

  • Ebert, M.K., Rangel, L.I., Spanner, R.E., Taliadoros, D., Wang, X., Friesen, T.L., de Jonge, R., Neubauer, J.D., Secor, G.A., Thomma, B.P.H.J., Stuckenbrock, E.H. and Bolton, M.D. (2021). Identification and characterization of Cercospora beticola necrosis-inducing effector CbNip1. Molecular Plant Pathology 22: 301-316. http://doi.org/10.1111/mpp.13026.

  • Garcia-Ruiz, H., Szurek, B. and Van den Ackerveken, G. (2021). Stop helping pathogens: engineering plant susceptibility genes for durable resistance. Current Opinion in Biotechnology 70: 187-195. https://doi.org/10.1016/j.copbio.2021.05.005.

  • Harting, R., Starke, J., Kusch, H., Pöggeler, S., Maurus, I., Schlüter, R., Landesfeind, M., Bulla, I., Nowrousian, M., de Jonge, R., Stahlhut, G., Hoff, K.J., Asshauer, K., Thürmer, A., Stanke, M., Daniel, R., Morgenstern, B., Thomma, B.P.H.J., Kronstad, J.W., Braus-Stromeyer, S.A. and Braus, G.H. (2021). A 20‐kb lineage‐specific genomic region tames virulence in pathogenic amphidiploid Verticillium longisporum. Molecular Plant Pathology 22: 939-953. https://doi.org/10.1111/mpp.13071.

  • Li, E., de Jonge, R., Liu, C. Jiang, H., Friman, V.-P., Pieterse, C.M.J., Bakker, P.A.H.M. and Jousset A. (2021). Rapid evolution of bacterial mutualism in the plant rhizosphere. Nature Communications 12: 3829. https://doi.org/10.1038/s41467-021-24005-y. 

  • Li, E., Zhang, H., Jiang, H., Pieterse, C.M.J., Jousset, A., Bakker, P.A.H.M., de Jonge, R. 2021. Experimental-evolution-driven identification of Arabidopsis rhizosphere competence genes in Pseudomonas protegens. mBio 12:e00927-21. https://doi.org/10.1128/mBio.00927-21.

  • Li, E., Ryo, M., Kowalchuk, G.A., Bakker, P.A.H.M. and Jousset, A. (2021). Rapid evolution of trait correlation networks during bacterial adaptation to the rhizosphere. Evolution 75: 1218–1229. https://doi-org.proxy.library.uu.nl/10.1111/evo.14202.

  • Montes-Osuna, N., Cabanas, C.G.L., Valverde-Corredor, A., Berendsen, R.L., Prieto, P. and Mercado-Blanco, J. (2021). Assessing the involvement of selected phenotypes of Pseudomonas simiae PICF7 in olive root colonization and biological control of Verticillium dahliae. Plants-Basel 10: 412. https://doi.org/10.3390/plants10020412.

  • Nambara, E. and Van Wees, S.C.M. (2021). Plant hormone functions and interactions in biological systems. Plant Journal 105: 287-289. http://doi: 10.1111/tpj.15151.

  • Pereira Mendes, M., Hickman, R., Van Verk, M.C., Nieuwendijk, N., Reinstädler, A., Panstruga, R., Pieterse, C.M.J. and Van Wees, S.C.M. (2021). A family of pathogen-induced cysteine-rich transmembrane proteins is involved in plant disease resistance. Planta 253: 102. http://doi.org/10.1007/s00425-021-03606-3.

  • Pieterse, C.M.J., Berendsen, R.L., de Jonge, R., Stringlis, I.A., Van Dijken, A.J.H., Van Pelt, J.A., Van Wees, S.C.M., Yu, K., Zamioudis, C., Bakker, P.A.H.M. (2021). Pseudomonas simiae WCS417: star track of a model beneficial rhizobacterium. Plant & Soil 461: 245–263. https://doi.org/10.1007/s11104-020-04786-9.

  • Rangel, L.I., Hamilton, O., de Jonge, R., Bolton, M.D. (2021). Fungal social influencers: secondary metabolites as platform for shaping the plant-associated community. Plant Journal 108: 632-645. https://doi.org/10.1111/tpj.15490.

  • Song, Y., Pieterse, C.M.J., Bakker, P.A.H.M. and Berendsen, R.L. (2021). Collection of sterile root exudates from foliar pathogen-inoculated plants. In: The Plant Microbiome: Methods and Protocols. Methods in Molecular Biology 2232: 305-317. https://doi.org/10.1007/978-1-0716-1040-4_23.

  • Stassen, M.J.J., Hsu, S.-H., Pieterse, C.M.J. and Stringlis, I.A. (2021). Coumarin communication along the microbiome-root-shoot axis. Trends in Plant Science 26: 169-183. https://doi.org/10.1016/j.tplants.2020.09.008.

  • Stringlis, I.A. and Pieterse, C.M.J. (2021). Evolutionary "Hide-and-Seek" between bacterial flagellin and the plant immune system. Cell Host & Microbe 29: 548-550. https://doi.org/10.1016/j.chom.2021.03.010.

  • Stringlis, I.A., Teixeira, P.J.P.L., Berendsen, R.L., Pieterse, C.M.J. and Zamioudis, C. (2021). Beneficial microbiota interacting with the plant immune system. Frontiers in Plant Science 12: 698902. https://doi.org/10.3389/fpls.2021.698902.

  • Trapet, P.L., Verbon, E.H., Bosma, R.R., Voorendag, K., Van Pelt, J.A. and Pieterse, C.M.J. (2021). Mechanisms underlying iron deficiency-induced resistance against pathogens with different lifestyles. Journal of Experimental Botany 72: 2231-2241. https://doi-org.proxy.library.uu.nl/10.1093/jxb/eraa535.

  • Van der Woude, L., Piotrowski, M., Klaasse, G., Paulus, J., Krahn, D., Ninck, S., Kaschani, F., Kaiser, M., Novák, O., Ljung, K., Bulder, S., Van Verk, M., Snoek, B., Fiers, M., Martin, N., Van der Hoorn, R., Robert, S., Smeekens, S. and  Van Zanten, M. (2021). The chemical compound ‘Heatin’ stimulates hypocotyl elongation and interferes with the Arabidopsis NIT1-subfamily of nitrilases. Plant Journal 106: 1523-1540. https://doi.org/10.1111/tpj.15250.  

  • Vismans, G., Spooren, J., Pieterse, C.M.J., Bakker, P.A.H.M. and Berendsen, R.L. (2021). Soil-borne legacies of disease in Arabidopsis thaliana. In: The Plant Microbiome: Methods and Protocols. Methods in Molecular Biology 2232: 209-218. https://doi.org/10.1007/978-1-0716-1040-4_17.

  • Yu, K., Stringlis, I.A., Van Bentum, S., De Jonge, R., Snoek, B.L., Pieterse, C.M.J., Bakker, P.A.H.M. and Berendsen, R.L. (2021). Role of root-secreted coumarins in Arabidopsis-mutualist communication. Microorganisms 9: 575. https://doi.org/10.3390/microorganisms9030575. 

  • Zhang, X., Wang, D., Elberse, J., Qi, L., Shi, W., Peng, Y.-L., Schuurink, R.C., Van den Ackerveken, G. and Liu, J. (2021). Structure-guided analysis of Arabidopsis JASMONATE-INDUCED OXYGENASE (JOX) 2 reveals key residues for recognition of jasmonic acid substrate by plant JOXs. Molecular Plant 14: 820-828. http://doi.org/10.1016/j.molp.2021.01.017.