The plant immune system

Structure and functions of the bacterial microbiota of plants

Bulgarelli, D., Schlaeppi, K., Spaepen, S., van Themaat, E. V. L., & Schulze-Lefert, P. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050312-120106 · Cited by 3,308 · see citing works

Induced systemic resistance by beneficial microbes

Pieterse, C. M. J., Zamioudis, C., Berendsen, R. L., Weller, D. M., Van Wees, S. C. M., & Bakker, P. A. H. M. (2014) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-082712-102340 · Cited by 3,272 · see citing works

Jasmonates: Biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany

Wasternack, C., & Hause, B. (2013) · Annals of Botany · doi:10.1093/aob/mct067 · Cited by 2,629 · see citing works

Salicylic acid, a multifaceted hormone to combat disease

Vlot, A. C., Dempsey, D. A., & Klessig, D. F. (2009) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.050908.135202 · Cited by 2,568 · see citing works

Indole-3-acetic acid in microbial and microorganism-plant signaling

Spaepen, S., Vanderleyden, J., & Remans, R. (2007) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2007.00072.x · Cited by 1,954 · see citing works

RNA virus interference via CRISPR/Cas13a system in plants

Aman, R., Ali, Z., Butt, H., Mahas, A., Aljedaani, F., Khan, M. Z., Ding, S., & Mahfouz, M. (2018) · Genome Biology · doi:10.1186/s13059-017-1381-1 · Cited by 1,497 · see citing works

<i>Xanthomonas</i> AvrBs3 Family-Type III Effectors: Discovery and Function

Boch, J., & Bonas, U. (2010) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-080508-081936 · Cited by 978 · see citing works

Plant-rhizobacteria interactions alleviate abiotic stress conditions

DIMKPA, C., WEINAND, T., & ASCH, F. (2009) · Plant, Cell &amp; Environment · doi:10.1111/j.1365-3040.2009.02028.x · Cited by 963 · see citing works

Microbiota and Host Nutrition across Plant and Animal Kingdoms

Hacquard, S., Garrido-Oter, R., González, A., Spaepen, S., Ackermann, G., Lebeis, S., McHardy, A. C., Dangl, J. L., Knight, R., Ley, R., et al. (2015) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2015.04.009 · Cited by 779 · see citing works

Development of biocontrol products for postharvest diseases of fruit: The importance of elucidating the mechanisms of action of yeast antagonists

Spadaro, D., & Droby, S. (2016) · Trends in Food Science &amp; Technology · doi:10.1016/j.tifs.2015.11.003 · Cited by 732 · see citing works

The spectrum of inflammatory responses

Medzhitov, R. (2021) · Science · doi:10.1126/science.abi5200 · Cited by 718 · see citing works

Pattern recognition receptors and central nervous system repair

Kigerl, K. A., de Rivero Vaccari, J. P., Dietrich, W. D., Popovich, P. G., & Keane, R. W. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.01.001 · Cited by 490 · see citing works

Biocontrol yeasts: mechanisms and applications

Freimoser, F. M., Rueda-Mejia, M. P., Tilocca, B., & Migheli, Q. (2019) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-019-2728-4 · Cited by 462 · see citing works

Homeostasis-altering molecular processes as mechanisms of inflammasome activation

Liston, A., & Masters, S. L. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2016.151 · Cited by 459 · see citing works

Jasmonate signaling in plant interactions with resistance-inducing beneficial microbes

Van der Ent, S., Van Wees, S. C. M., & Pieterse, C. M. J. (2009) · Phytochemistry · doi:10.1016/j.phytochem.2009.06.009 · Cited by 443 · see citing works

NLRs at the intersection of cell death and immunity

Ting, J. P.-Y., Willingham, S. B., & Bergstralh, D. T. (2008) · Nature Reviews Immunology · doi:10.1038/nri2296 · Cited by 371 · see citing works

Systemic inflammation and the brain: novel roles of genetic, molecular, and environmental cues as drivers of neurodegeneration

Sankowski, R., Mader, S., & Valdés-Ferrer, S. I. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00028 · Cited by 351 · see citing works

Monoterpenes Support Systemic Acquired Resistance within and between Plants

Riedlmeier, M., Ghirardo, A., Wenig, M., Knappe, C., Koch, K., Georgii, E., Dey, S., Parker, J. E., Schnitzler, J.-P., & Vlot, A. C. (2017) · The Plant Cell · doi:10.1105/tpc.16.00898 · Cited by 323 · see citing works

The influence of evolutionary history on human health and disease

Benton, M. L., Abraham, A., LaBella, A. L., Abbot, P., Rokas, A., & Capra, J. A. (2021) · Nature Reviews Genetics · doi:10.1038/s41576-020-00305-9 · Cited by 291 · see citing works

Specific ER quality control components required for biogenesis of the plant innate immune receptor EFR

Li, J., Zhao-Hui, C., Batoux, M., Nekrasov, V., Roux, M., Chinchilla, D., Zipfel, C., & Jones, J. D. G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905532106 · Cited by 273 · see citing works

NALP Inflammasomes: a central role in innate immunity

Martinon, F., Gaide, O., Pétrilli, V., Mayor, A., & Tschopp, J. (2007) · Seminars in Immunopathology · doi:10.1007/s00281-007-0079-y · Cited by 218 · see citing works

Indole-3-acetaldehyde dehydrogenase-dependent auxin synthesis contributes to virulence of Pseudomonas syringae strain DC3000

McClerklin, S. A., Lee, S. G., Harper, C. P., Nwumeh, R., Jez, J. M., & Kunkel, B. N. (2018) · PLOS Pathogens · doi:10.1371/journal.ppat.1006811 · Cited by 182 · see citing works

Plant–arthropod interactions: who is the winner?

Stahl, E., Hilfiker, O., & Reymond, P. (2018) · The Plant Journal · doi:10.1111/tpj.13773 · Cited by 164 · see citing works

On the move: induced resistance in monocots

Balmer, D., Planchamp, C., & Mauch-Mani, B. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ers248 · Cited by 77 · see citing works

Brassinosteroid action in flowering plants: A Darwinian perspective

Kutschera, U., & Wang, Z.-Y. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers065 · Cited by 77 · see citing works

Differential effectiveness of Serratia plymuthica IC1270-induced systemic resistance against hemibiotrophic and necrotrophic leaf pathogens in rice

De Vleesschauwer, D., Chernin, L., & Höfte, M. M. (2009) · BMC Plant Biology · doi:10.1186/1471-2229-9-9 · Cited by 77 · see citing works

Diverse mechanisms for inflammasome sensing of cytosolic bacteria and bacterial virulence

Zhao, Y., & Shao, F. (2016) · Current Opinion in Microbiology · doi:10.1016/j.mib.2015.10.003 · Cited by 73 · see citing works

The role of nitric oxide-induced atill6 in growth and disease resistance in arabidopsis thaliana

Khan, M., Al Azawi, T. N. I., Pande, A., Mun, B.-G., Lee, D.-S., Hussain, A., Lee, B.-H., & Yun, B.-W. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.685156 · Cited by 61 · see citing works

FORCA, a promoter element that responds to crosstalk between defense and light signaling

Evrard, A., Ndatimana, T., & Eulgem, T. (2009) · BMC Plant Biology · doi:10.1186/1471-2229-9-2 · Cited by 28 · see citing works

Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses

Charbonneau, M.-E., Passalacqua, K. D., Hagen, S. E., Showalter, H. D., Wobus, C. E., & O’Riordan, M. X. D. (2019) · Scientific Reports · doi:10.1038/s41598-019-46526-9 · Cited by 24 · see citing works

Exploring fern pathosystems and immune receptors to bridge gaps in plant immunity

Castel, B., Baker, M., Keller, J., Martinez, Y., Bonhomme, M., Delaux, P.-M., & Jacquet, C. (2025) · BMC Biology · doi:10.1186/s12915-025-02413-6 · Cited by 4 · see citing works