Role of Soil Microbiome in Suppressing Soil-Borne Pathogens
Main Article Content
Abstract
The soil microbiome constitutes a vast and complex community of bacteria, fungi, archaea, protists, and viruses that play pivotal roles in maintaining soil health and agricultural productivity. Among its numerous ecological functions, the suppression of soil-borne plant pathogens stands out as one of the most agriculturally significant. Soil-borne pathogens, including Fusarium, Pythium, Rhizoctonia and Phytophthora species, are responsible for enormous economic losses in global agriculture annually. The inherent capacity of certain soils to suppress these pathogens—termed disease-suppressive soils—has been linked directly to the richness, diversity, and functional activity of the resident microbial communities. This review comprehensively examines the mechanisms through which the soil microbiome suppresses soil-borne pathogens, including antibiosis, competition for nutrients and space, induced systemic resistance, mycoparasitism and volatile compound production. It further explores the ecological and agronomic factors that shape microbial community structure and suppressive capacity, including soil pH, organic matter content, crop rotation, and the application of biological control agents. Understanding the intricate interactions within the rhizosphere and bulk soil microbiome offers transformative opportunities for the development of sustainable, microbiome-mediated disease management strategies, reducing dependence on chemical fungicides while maintaining high crop yields. Despite these advances, a critical knowledge gap persists in translating mechanistic insights into consistent, field-applicable biocontrol outcomes, particularly under variable soil conditions and diverse agricultural systems. Future research should prioritize the development of predictive microbiome-based models, the standardization of synthetic community formulations, and the integration of multi-omics approaches to unlock the full suppressive potential of soil microbial ecosystems for next-generation, sustainable crop protection.
Article Details
Copyright (c) 2026 Bhullar M.

This work is licensed under a Creative Commons Attribution 4.0 International License.
Fierer N. Embracing the unknown: disentangling the complexities of the soil microbiome. Nat Rev Microbiol. 2017;15(10):579-590. Available from: https://dx.doi.org/10.1038/nrmicro.2017.87
Berendsen RL, Pieterse CMJ, Bakker PAHM. The rhizosphere microbiome and plant health. Trends Plant Sci. 2012;17(8):478-486. Available from: https://dx.doi.org/10.1016/j.tplants.2012.04.001
Lamichhane JR, Venturi V. Synergisms between microbial pathogens in plant disease complexes: a growing trend. Front Plant Sci. 2015;6:385. Available from: https://dx.doi.org/10.3389/fpls.2015.00385
Köhl J, Kolnaar R, Ravensberg WJ. Mode of action of microbial biological control agents against plant diseases: relevance beyond efficacy. Front Plant Sci. 2019;10:845. Available from: https://dx.doi.org/10.3389/fpls.2019.00845
Weller DM, Raaijmakers JM, Gardener BBM, Thomashow LS. Microbial populations responsible for specific soil suppressiveness to plant pathogens. Annu Rev Phytopathol. 2002;40:309-348. Available from: https://dx.doi.org/10.1146/annurev.phyto.40.030402.110010
Mendes R, Kruijt M, de Bruijn I, Dekkers E, van der Voort M, Schneider JHM, Piceno YM, DeSantis TZ, Andersen GL, Bakker PAHM, Raaijmakers JM. Deciphering the rhizosphere microbiome for disease-suppressive bacteria. Science. 2011;332(6033):1097-1100. Available from: https://dx.doi.org/10.1126/science.1203980
Raaijmakers JM, Mazzola M. Soil immune responses. Science. 2016;352(6292):1392-1393. Available from: https://dx.doi.org/10.1126/science.aaf3252
Torsvik V, Ovreas L. Microbial diversity and function in soil: from genes to ecosystems. Curr Opin Microbiol. 2002;5(3):240-245. Available from: https://dx.doi.org/10.1016/S1369-5274(02)00324-7
Tedersoo L, Bahram M, Polme S, Koljalg U, Yorou NS, Wijesundera R, Abarenkov K. Global diversity and geography of soil fungi. Science. 2014;346(6213):1256688. Available from: https://dx.doi.org/10.1126/science.1256688
Williamson KE, Fuhrmann JJ, Wommack KE, Radosevich M. Viruses in soil ecosystems: an unknown quantity within an unexplored territory. Annu Rev Virol. 2017;4:201-219. Available from: https://dx.doi.org/10.1146/annurev-virology-101416-041639
Mendes R, Garbeva P, Raaijmakers JM. The rhizosphere microbiome: significance of plant beneficial, plant pathogenic, and human pathogenic microorganisms. FEMS Microbiol Rev. 2013;37(5):634-663. Available from: https://dx.doi.org/10.1111/1574-6976.12028
Rudrappa T, Czymmek KJ, Pare PW, Bais HP. Root-secreted malic acid recruits beneficial soil bacteria. Plant Physiol. 2008;148(3):1547-1556. Available from: https://dx.doi.org/10.1104/pp.108.127613
Haas D, Keel C. Regulation of antibiotic production in root-colonizing Pseudomonas spp. and relevance for biological control of plant disease. Annu Rev Phytopathol. 2003;41:117-153. Available from: https://dx.doi.org/10.1146/annurev.phyto.41.052002.095656
Weller DM, Van Pelt JA, Mavrodi DV, Pieterse CMJ, Bakker PAHM, Van Loon LC. Induced systemic resistance (ISR) in Arabidopsis against Pseudomonas syringae pv. tomato by 2,4-diacetylphloroglucinol (DAPG)-producing Pseudomonas fluorescens. Phytopathology. 2007;94:S108.
Ongena M, Jacques P. Bacillus lipopeptides: versatile weapons for plant disease biocontrol. Trends Microbiol. 2008;16(3):115-125. Available from: https://dx.doi.org/10.1016/j.tim.2007.12.009
Kinkel LL, Bakker MG, Schlatter DC. A coevolutionary framework for managing disease-suppressive soils. Annu Rev Phytopathol. 2011;49:47-67. Available from: https://dx.doi.org/10.1146/annurev-phyto-072910-095232
O’Sullivan DJ, O’Gara F. Traits of fluorescent Pseudomonas spp. involved in suppression of plant root pathogens. Microbiol Rev. 1992;56(4):662-676. Available from: https://dx.doi.org/10.1128/mr.56.4.662-676.1992
Raaijmakers JM, Paulitz TC, Steinberg C, Alabouvette C, Moenne-Loccoz Y. The rhizosphere: a playground and battlefield for soilborne pathogens and beneficial microorganisms. Plant Soil. 2009;321(1-2):341-361. Available from: https://dx.doi.org/10.1007/s11104-008-9568-6
Bonanomi G, Antignani V, Capodilupo M, Scala F. Identifying the characteristics of organic soil amendments that suppress soil-borne plant diseases. Soil Biol Biochem. 2010;42(2):136-144. Available from: https://dx.doi.org/10.1016/j.soilbio.2009.10.012
Lugtenberg B, Kamilova F. Plant-growth-promoting rhizobacteria. Annu Rev Microbiol. 2009;63:541-556. Available from: https://dx.doi.org/10.1146/annurev.micro.62.081307.162918
Mark GL, Dow JM, Kiely PD, Higgins H, Haynes J, Baysse C, Abbas A, Foley T, Franks A, Morrissey J, O’Gara F. Transcriptome profiling of bacterial responses to root exudates identifies genes involved in microbe-plant interactions. Proc Natl Acad Sci U S A. 2005;102(48):17454-17459. Available from: https://dx.doi.org/10.1073/pnas.0506407102
Van Loon LC, Bakker PAHM, Pieterse CMJ. Systemic resistance induced by rhizosphere bacteria. Annu Rev Phytopathol. 1998;36:453-483. Available from: https://dx.doi.org/10.1146/annurev.phyto.36.1.453
Pieterse CMJ, Zamioudis C, Berendsen RL, Weller DM, Van Wees SCM, Bakker PAHM. Induced systemic resistance by beneficial microbes. Annu Rev Phytopathol. 2014;52:347-375. Available from: https://dx.doi.org/10.1146/annurev-phyto-082712-102340
Pozo MJ, Azcon-Aguilar C. Unraveling mycorrhiza-induced resistance. Curr Opin Plant Biol. 2007;10(4):393-398. Available from: https://dx.doi.org/10.1016/j.pbi.2007.05.004
Mukherjee PK, Horwitz BA, Kenerley CM. Secondary metabolism in Trichoderma—a genomic perspective. Microbiology. 2012;158(1):35-45. Available from: https://dx.doi.org/10.1099/mic.0.053801-0
Benhamou N, Kloepper JW, Tuzun S. Induction of resistance against Fusarium wilt of tomato by combination of chitosan with an endophytic bacterial strain: ultrastructure and cytochemistry of the host response. Planta. 2012;204(2):153-168.
Ryu CM, Farag MA, Hu CH, Reddy MS, Kloepper JW, Paré PW. Bacterial volatiles induce systemic resistance in Arabidopsis. Plant Physiol. 2004;134(3):1017-1026. Available from: https://dx.doi.org/10.1104/pp.103.026583
Vinale F, Sivasithamparam K, Ghisalberti EL, Marra R, Woo SL, Lorito M. Trichoderma–plant–pathogen interactions. Soil Biol Biochem. 2008;40(1):1-10. Available from: https://dx.doi.org/10.1016/j.soilbio.2007.07.002
Qian X, Chen L, Guo X, He D, Shi X, Zhang D. Alterations of microbial community structure and functional genes in the rhizosphere of Bt-transgenic rice. Plant Soil. 2012;372(1-2):553-565. Available from: https://dx.doi.org/10.1007/s11104-013-1758-3
Rousk J, Bääth E, Brookes PC, Lauber CL, Lozupone C, Caporaso JG, Knight R, Fierer N. Soil bacterial and fungal communities across a pH gradient in an arable soil. ISME J. 2010;4(10):1340-1351. Available from: https://dx.doi.org/10.1038/ismej.2010.58
Schlatter D, Kinkel L, Thomashow L, Weller D, Paulitz T. Disease suppressive soils: new insights from the soil microbiome. Phytopathology. 2017;107(11):1284-1297. Available from: https://dx.doi.org/10.1094/PHYTO-03-17-0111-RVW
Mazzola M, Manici LM. Apple replant disease: role of microbial ecology in cause and control. Annu Rev Phytopathol. 2012;50:45-65. Available from: https://dx.doi.org/10.1146/annurev-phyto-081211-173005
Sturz AV, Christie BR. Beneficial microbial allelopathies in the root zone: the management of soil quality and plant disease with rhizobacteria. Soil Tillage Res. 2003;72(2):107-123. Available from: https://dx.doi.org/10.1016/S0167-1987(03)00082-5
Compant S, Samad A, Faist H, Sessitsch A. A review on the plant microbiome: ecology, functions, and emerging trends in microbial application. J Adv Res. 2019;19:29-37. Available from: https://dx.doi.org/10.1016/j.jare.2019.03.004
Haichar FEZ, Santaella C, Heulin T, Achouak W. Root exudates mediated interactions belowground. Soil Biol Biochem. 2014;77:69-80. Available from: https://dx.doi.org/10.1016/j.soilbio.2014.06.017
Bakker PAHM, Pieterse CMJ, de Jonge R, Berendsen RL. The soil-borne legacy. Cell. 2018;172(6):1178-1180. Available from: https://dx.doi.org/10.1016/j.cell.2018.02.024