Abstract
Long before nature was ‘red in tooth and claw’, it was sundered by nano-spears and seeping poisons. Microorganisms were the first predators, and predation has since deeply shaped all major branches of life — from individual traits to collective systems, community dynamics and major evolutionary transitions. Yet, we have only begun to understand how microbial predation influences the genetics, morphology, behaviour, ecology and evolution of microorganisms in natural communities and, in turn, the macroscopic biosphere. With the field advancing rapidly on diverse fronts, integrative conceptual frameworks, questions and research approaches are needed to promote synthetic development of the field. In this Review, we explore the remarkably diverse forms of microbial predation that have evolved so far, considering organismal traits and their molecular foundations alongside the evolutionary ecology of predator–prey interactions in community contexts. Building on a process-based definition, forms of microbial predation are conceptualized along gradients, including gradients of evolutionary adaptedness for predation and of privatization of prey-derived nutrients. Important future research themes include predation origins and early stages of predatory adaptation, effects of diverse forms of predation on community diversity and stability, predator–prey co-evolution in complex communities, and multi-approach development of unicellular predators as biocontrol agents.
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References
Kaplan, M. et al. Bdellovibrio predation cycle characterized at nanometre-scale resolution with cryo-electron tomography. Nat. Microbiol. 8, 1267–1279 (2023).
Zhang, S. et al. A chemical radar allows bacteria to detect and kill predators. Cell 188, 2495–2504.e20 (2025).
Vasse, M., Fiegna, F., Kriesel, B. & Velicer, G. J. Killer prey: ecology reverses bacterial predation. PLoS Biol. 22, e3002454 (2024).
Nair, R. R. et al. Bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences. Nat. Commun. 10, 4301 (2019).
Jain, R. et al. Fatty acid metabolism and the oxidative stress response support bacterial predation. Proc. Natl Acad. Sci. USA 122, e2420875122 (2025).
Hiltunen, T. et al. Dual-stressor selection alters eco-evolutionary dynamics in experimental communities. Nat. Ecol. Evolution 2, 1974–1981 (2018).
Joblot, L. Descriptions et Usages de Plusieurs Nouveaux Microscopes, Tant Simples Que Composez (Collombat, Jacques, 1718).
Baker, H. The Microscope Made Easy 4th edn (Printed for R. and J. Dodsley, and sold by M. Cooper, 1754).
Dujardin, F. Histoire naturelle des zoophytes: Infusoires, comprenant la physiologie et la classification de ces animaux, et la manière de les étudier à l’aide du microscope (Roret, 1841).
D’Hérelle, F. Sur un microbe invisible antagoniste des bacilles dysentériques. Comptes Rendus Académie des Sciences 165, 373–375 (1917).
Rosenberg, E. & Varon, M. in Myxobacteria: Development and Cell Interactions (ed. Rosenberg, E.) 109–125 (Springer, 1984).
Lai, T. F., Ford, R. M. & Huwiler, S. G. Advances in cellular and molecular predatory biology of Bdellovibrio bacteriovorus six decades after discovery. Front. Microbiol. 14, 1168709 (2023).
Pérez, J., Moraleda-Muñoz, A., Marcos-Torres, F. J. & Muñoz-Dorado, J. Bacterial predation: 75 years and counting! Environ. Microbiology 18, 766–779 (2016).
Kumbhar, C., Mudliar, P., Bhatia, L., Kshirsagar, A. & Watve, M. Widespread predatory abilities in the genus Streptomyces. Arch. Microbiol. 196, 235–248 (2014).
Kingsland, S. & Alfred, J. Lotka and the origins of theoretical population ecology. Proc. Natl Acad. Sci. USA 112, 9493–9495 (2015).
Gause, G. F. The Struggle for Existence (The Williams & Wilkins Company, 1934).
Křivan, V. in Encyclopedia of Ecology (eds Jørgensen, S. E. & Fath, B. D.) 2929–2940 (Academic Press, 2008).
Solomon, M. E. The natural control of animal populations. J. Anim. Ecol. 18, 1–35 (1949).
Holling, C. S. Some characteristics of simple types of predation and parasitism. Can. Entomologist 91, 385–398 (1959).
Krebs, C. J. Some historical thoughts on the functional responses of predators to prey density. Front. Ecol. Evol. https://doi.org/10.3389/fevo.2022.1052289 (2022).
Bengtson, S. Origins and early evolution of predation. Paleontol. Soc. Pap. 8, 289–318 (2002).
Taylor, R. J. in Predation (ed. Taylor, R. J.) 1–5 (Springer Netherlands, 1984).
Ispolatov, Y., Doebeli, C. & Doebeli, M. On the evolutionary emergence of predation. J. Theor. Biol. 572, 111578 (2023).
Sanchis Pla, L. & van Gestel, J. Exploring the microbial savanna: predator-prey interactions in the soil. Mol. Syst. Biol. 20, 477–480 (2024).
Hamm, J. N. et al. The parasitic lifestyle of an archaeal symbiont. Nat. Commun. 15, 6449 (2024).
White, J. F. et al. in PGPR Amelioration in Sustainable Agriculture (eds Singh, A. K., Kumar, A. & Singh, P. K.) 167–193 (Woodhead Publishing, 2019).
Hillesland, K. L., Velicer, G. J. & Lenski, R. E. Experimental evolution of a microbial predator’s ability to find prey. Proc. R. Soc. B Biol. Sci. 276, 459–467 (2009).
Parratt, S. R. & Laine, A.-L. The role of hyperparasitism in microbial pathogen ecology and evolution. ISME J. 10, 1815–1822 (2016).
Kiørboe, T. Predation in a microbial world: mechanisms and trade-offs of flagellate foraging. Annu. Rev. Mar. Sci. 16, 361–381 (2024).
Gómez, F. The function of the ocelloid and piston in the dinoflagellate Erythropsidinium (Gymnodiniales, Dinophyceae). J. Phycol. 53, 629–641 (2017).
Leander, B. S. Predatory protists. Curr. Biol. 30, R510–R516 (2020).
de Schaetzen, F. et al. Random encounters and amoeba locomotion drive the predation of Listeria monocytogenes by Acanthamoeba castellanii. Proc. Natl Acad. Sci. USA 119, e2122659119 (2022).
Seymour, J. R., Brumley, D. R., Stocker, R. & Raina, J.-B. Swimming towards each other: the role of chemotaxis in bacterial interactions. Trends Microbiol. 32, 640–649 (2024).
Summers, J. K. & Kreft, J.-U. The role of mathematical modelling in understanding prokaryotic predation. Front. Microbiol. 13, 1037407 (2022).
Hu, M., Ma, Y. & Chua, S. L. Bacterivorous nematodes decipher microbial iron siderophores as prey cue in predator–prey interactions. Proc. Natl Acad. Sci. USA 121, e2314077121 (2024).
Fryer, E. et al. A high-throughput behavioral screening platform for measuring chemotaxis by C. elegans. PLoS Biol. 22, e3002672 (2024).
Li, S., Liu, S. Y., Chan, S. Y. & Chua, S. L. Biofilm matrix cloaks bacterial quorum sensing chemoattractants from predator detection. ISME J. 16, 1388–1396 (2022).
Rashidi, G. & Ostrowski, E. A. Phagocyte chase behaviours: discrimination between Gram-negative and Gram-positive bacteria by amoebae. Biol. Lett. 15, 20180607 (2019).
Schulz-Bohm, K. et al. The prey’s scent – volatile organic compound mediated interactions between soil bacteria and their protist predators. ISME J. 11, 817–820 (2017).
Sathyamoorthy, R. et al. To hunt or to rest: prey depletion induces a novel starvation survival strategy in bacterial predators. ISME J. 15, 109–123 (2021).
Lloyd, D. G. & Whitworth, D. E. The myxobacterium Myxococcus xanthus can sense and respond to the quorum signals secreted by potential prey organisms. Front. Microbiol. 8, 439 (2017).
Thiery, S. & Kaimer, C. The predation strategy of Myxococcus xanthus. Front. Microbiol. 11, 2 (2020).
Song, H. et al. Two-step localization driven by peptidoglycan hydrolase in interbacterial predation. ISME J. 19, wraf208 (2025).
Bulbert, M. & Wignall, A. Luring. Curr. Biol. 26, R1212–R1213 (2016).
Yu, X. et al. Fatal attraction of Caenorhabditis elegans to predatory fungi through 6-methyl-salicylic acid. Nat. Commun. 12, 5462 (2021).
Niu, Q. et al. A Trojan horse mechanism of bacterial pathogenesis against nematodes. Proc. Natl Acad. Sci. USA 107, 16631–16636 (2010).
Shi, W. & Zusman, D. R. Fatal attraction. Nature 366, 414–415 (1993).
Suzuki-Tellier, S., Kiørboe, T. & Simpson, A. G. B. The function of the feeding groove of ‘typical excavate’ flagellates. J. Eukaryot. Microbiol. 71, e13016 (2024).
Rotem, O. et al. Cell-cycle progress in obligate predatory bacteria is dependent upon sequential sensing of prey recognition and prey quality cues. Proc. Natl Acad. Sci. USA 112, E6028–E6037 (2015).
Seef, S. et al. A Tad-like apparatus is required for contact-dependent prey killing in predatory social bacteria. eLife 10, e72409 (2021).
Thiery, S., Turowski, P., Berleman, J. E. & Kaimer, C. The predatory soil bacterium Myxococcus xanthus combines a Tad- and an atypical type 3-like protein secretion system to kill bacterial cells. Cell Rep. 40, 111340 (2022).
Tikhonenkov, D. V. et al. Microbial predators form a new supergroup of eukaryotes. Nature 612, 714–719 (2022).
Tyson, J. et al. Prey killing without invasion by Bdellovibrio bacteriovorus defective for a MIDAS-family adhesin. Nat. Commun. 15, 3078 (2024).
Vigneron, A., Cruaud, P., Lovejoy, C. & Vincent, W. F. Genomic evidence of functional diversity in DPANN archaea, from oxic species to anoxic vampiristic consortia. ISME Commun. 2, 4 (2022).
Santin, Y. G., Sogues, A., Bourigault, Y., Remaut, H. K. & Laloux, G. Lifecycle of a predatory bacterium vampirizing its prey through the cell envelope and S-layer. Nat. Commun. 15, 3590 (2024).
Waite, D. W. et al. Proposal to reclassify the proteobacterial classes Deltaproteobacteria and Oligoflexia, and the phylum Thermodesulfobacteria into four phyla reflecting major functional capabilities. Int. J. Syst. Evolut. Microbiol. 70, 5972–6016 (2020).
Shatzkes, K. et al. Predatory bacteria attenuate Klebsiella pneumoniae burden in rat lungs. mBio 7, e01847-16 (2016).
Moreira, D., Zivanovic, Y., López-Archilla, A. I., Iniesto, M. & López-García, P. Reductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii. Nat. Commun. 12, 2454 (2021).
Yang, H., Hu, Z., Shang, L., Deng, Y. & Tang, Y. Z. A strain of the toxic dinoflagellate Karlodinium veneficum isolated from the East China Sea is an omnivorous phagotroph. Harmful Algae 93, 101775 (2020).
Whitfield, G. B. & Brun, Y. V. The type IVc pilus: just a tad different. Curr. Opin. Microbiol. 79, 102468 (2024).
Herrou, J. et al. Tad pili with adaptable tips mediate contact-dependent killing during bacterial predation. Nat. Commun. 16, 4425 (2025).
Lewin, R. A. Saprospira grandis: a flexibacterium that can catch bacterial prey by “Ixotrophy”. Microb. Ecol. 34, 232–236 (1997).
Lien, Y.-W. et al. Mechanism of bacterial predation via ixotrophy. Science 386, eadp0614 (2024).
Sallal, A. K. Lysis of cyanobacteria with Flexibacter spp isolated from domestic sewage. Microbios 77, 57–67 (1994).
Zwarycz, A. S., Page, T., Nikolova, G., Radford, E. J. & Whitworth, D. E. Predatory strategies of Myxococcus xanthus: prey susceptibility to OMVs and moonlighting enzymes. Microorganisms 11, 874 (2023).
Bell, T. et al. Protists have divergent effects on bacterial diversity along a productivity gradient. Biol. Lett. 6, 639–642 (2010).
Stewart, B. et al. The genetic architecture underlying prey-dependent performance in a microbial predator. Nat. Commun. 13, 319 (2022).
Shreenidhi, P. M., Brock, D. A., McCabe, R. I., Strassmann, J. E. & Queller, D. C. Costs of being a diet generalist for the protist predator Dictyostelium discoideum. Proc. Natl Acad. Sci. USA 121, e2313203121 (2024).
Morgan, A. D., MacLean, R. C., Hillesland, K. L. & Velicer, G. J. Comparative analysis of Myxococcus predation on soil bacteria. Appl. Environ. Microbiol. 76, 6920–6927 (2010).
Kikuchi, D. W. et al. The evolution and ecology of multiple antipredator defences. J. Evolut. Biol. 36, 975–991 (2023).
Yang, C.-T. et al. Natural diversity in the predatory behavior facilitates the establishment of a robust model strain for nematode-trapping fungi. Proc. Natl Acad. Sci. USA 117, 6762–6770 (2020).
Pion, M. et al. Bacterial farming by the fungus Morchella crassipes. Proc. R. Soc. B Biol. Sci. 280, 20132242 (2013).
Barron, G. L. in Biodiversity of Fungi (eds Mueller, G. M. et al.) 435–450 (Academic Press, 2004).
Németh, M. Z. et al. Green fluorescent protein transformation sheds more light on a widespread mycoparasitic interaction. Phytopathology 109, 1404–1416 (2019).
Booth, S. C., Smith, W. P. J. & Foster, K. R. The evolution of short- and long-range weapons for bacterial competition. Nat. Ecol. Evolution 7, 2080–2091 (2023).
Peterson, S. B., Bertolli, S. K. & Mougous, J. D. The central role of interbacterial antagonism in bacterial life. Curr. Biol. 30, R1203–R1214 (2020).
Rozen, D. E., Philippe, N., Arjan de Visser, J., Lenski, R. E. & Schneider, D. Death and cannibalism in a seasonal environment facilitate bacterial coexistence. Ecol. Lett. 12, 34–44 (2009).
Stubbusch, A. K. M. et al. Antagonism as a foraging strategy in microbial communities. Science 388, 1214–1217 (2025).
Kumbhar, C. & Watve, M. Why antibiotics: a comparative evaluation of different hypotheses for the natural role of antibiotics and an evolutionary synthesis. Nat. Sci. https://doi.org/10.4236/ns.2013.54A005 (2013).
Cossey, S. M., Yu, Y.-T. N., Cossu, L. & Velicer, G. J. Kin discrimination and outer membrane exchange in Myxococcus xanthus: experimental analysis of a natural population. PLoS ONE 14, e0224817 (2019).
Elgar, M. A. & Crespi, B. J. Cannibalism: Ecology and Evolution among Diverse Taxa (Oxford University Press, 1992).
Rombouts, S. et al. Multi-scale dynamic imaging reveals that cooperative motility behaviors promote efficient predation in bacteria. Nat. Commun. 14, 5588 (2023).
Cairns, J., Moerman, F., Fronhofer, E. A., Altermatt, F. & Hiltunen, T. Evolution in interacting species alters predator life-history traits, behaviour and morphology in experimental microbial communities. Proc. R. Soc. B Biol. Sci. 287, 20200652 (2020).
La Fortezza, M., Rendueles, O., Keller, H. & Velicer, G. J. Hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria. Commun. Biol. 5, 77 (2022).
Duncan, M. C. et al. High-throughput analysis of gene function in the bacterial predator Bdellovibrio bacteriovorus. mBio https://doi.org/10.1128/mBio.01040-19 (2019).
van Gestel, J. et al. Bacillus subtilis in defense mode: switch-like adaptations to protistan predation. Proc. Natl Acad. Sci. USA 122, e2518989122 (2025).
Lai, T. F., Jankov, D., Grossmann, J., Roschitzki, B. & Huwiler, S. G. Quantitative proteome of bacterial periplasmic predation by Bdellovibrio bacteriovorus reveals a prey-lytic protease. Commun. Biol. 8, 1491 (2025).
Caulton, S. G. et al. Bdellovibrio bacteriovorus uses chimeric fibre proteins to recognize and invade a broad range of bacterial hosts. Nat. Microbiol. 9, 214–227 (2024).
Remy, O. et al. Distinct dynamics and proximity networks of hub proteins at the prey-invading cell pole in a predatory bacterium. J. Bacteriol. 206, e00014-24 (2024).
Kawecki, T. J. et al. Experimental evolution. Trends Ecol. Evol. 27, 547–560 (2012).
Bremer, N., Tria, F. D. K., Skejo, J., Garg, S. G. & Martin, W. F. Ancestral state reconstructions trace mitochondria but not phagocytosis to the last eukaryotic common ancestor. Genome Biol. Evol. 14, evac079 (2022).
Davidov, Y. & Jurkevitch, E. Diversity and evolution of Bdellovibrio-and-like organisms (BALOs), reclassification of Bacteriovorax starrii as Peredibacter starrii gen. nov., comb. nov., and description of the Bacteriovorax–Peredibacter clade as Bacteriovoracaceae fam. nov. Int. J. Syst. Evolut. Microbiol. 54, 1439–1452 (2004).
Milner, D. S. et al. Ras GTPase-like protein MglA, a controller of bacterial social-motility in myxobacteria, has evolved to control bacterial predation by Bdellovibrio. PLoS Genet. 10, e1004253 (2014).
Chu, H., Gao, G.-F., Ma, Y., Fan, K. & Delgado-Baquerizo, M. Soil microbial biogeography in a changing world: recent advances and future perspectives. mSystems https://doi.org/10.1128/msystems.00803-19 (2020).
Hillesland, K. L., Lenski, R. E. & Velicer, G. J. Ecological variables affecting predatory success in Myxococcus xanthus. Microb. Ecol. 53, 571–578 (2007).
Im, H. et al. Viscosity has dichotomous effects on Bdellovibrio bacteriovorus HD100 predation. Environ. Microbiol. 21, 4675–4684 (2019).
Cerini, F., O’Brien, D., Wolfe, E., Besson, M. & Clements, C. F. Phenotypic response to different predator strategies can be mediated by temperature. Ecol. Evol. 13, e10474 (2023).
Fussmann, K. E., Schwarzmüller, F., Brose, U., Jousset, A. & Rall, B. C. Ecological stability in response to warming. Nat. Clim. Change 4, 206–210 (2014).
Glücksman, E., Bell, T., Griffiths, R. I. & Bass, D. Closely related protist strains have different grazing impacts on natural bacterial communities. Environ. Microbiol. 12, 3105–3113 (2010).
Burian, A. et al. Predation increases multiple components of microbial diversity in activated sludge communities. ISME J. 16, 1086–1094 (2022).
Johnke, J. et al. A generalist protist predator enables coexistence in multitrophic predator-prey systems containing a phage and the bacterial predator Bdellovibrio. Front. Ecol. Evol. https://doi.org/10.3389/fevo.2017.00124 (2017).
Liu, C. et al. Protist predation promotes antimicrobial resistance spread through antagonistic microbiome interactions. ISME J. 18, wrae169 (2024).
Saleem, M., Fetzer, I., Dormann, C. F., Harms, H. & Chatzinotas, A. Predator richness increases the effect of prey diversity on prey yield. Nat. Commun. 3, 1305 (2012).
Geisen, S., Hu, S., dela Cruz, T. E. E. & Ciska Veen, G. F. Protists as catalyzers of microbial litter breakdown and carbon cycling at different temperature regimes. ISME J. 15, 618–621 (2021).
Abrams, P. A. The evolution of predator-prey interactions: theory and evidence. Annu. Rev. Ecol. Evol. Syst. 31, 79–105 (2000).
Laplane, L. et al. Why science needs philosophy. Proc. Natl Acad. Sci. USA 116, 3948–3952 (2019).
Beauchamp, G. Social Predation: How Group Living Benefits Predators and Prey (Elsevier, 2013).
Wucher, B. R., Elsayed, M., Adelman, J. S., Kadouri, D. E. & Nadell, C. D. Bacterial predation transforms the landscape and community assembly of biofilms. Curr. Biol. 31, 2643–2651.e3 (2021).
Wucher, B. R., Winans, J. B., Elsayed, M., Kadouri, D. E. & Nadell, C. D. Breakdown of clonal cooperative architecture in multispecies biofilms and the spatial ecology of predation. Proc. Natl Acad. Sci. USA 120, e2212650120 (2023).
Dahl, J. L., Ulrich, C. H. & Kroft, T. L. Role of phase variation in the resistance of Myxococcus xanthus fruiting bodies to Caenorhabditis elegans predation. J. Bacteriol. 193, 5081–5089 (2011).
Velicer, G. J. & Vos, M. Sociobiology of the myxobacteria. Annu. Rev. Microbiology 63, 599–623 (2009).
Krause, J. & Ruxton, G. D. Living in Groups (Oxford University Press, 2002).
Berleman, J. E. et al. FrzS regulates social motility in Myxococcus xanthus by controlling exopolysaccharide production. PLoS ONE 6, e23920 (2011).
Rodriguez, A. M. & Spormann, A. M. Genetic and molecular analysis of cglB, a gene essential for single-cell gliding in Myxococcus xanthus. J. Bacteriol. 181, 4381–4390 (1999).
Rosenberg, E., Keller, K. H. & Dworkin, M. Cell density-dependent growth of Myxococcus xanthus on casein. J. Bacteriol. 129, 770–777 (1977).
Seccareccia, I., Kost, C. & Nett, M. Quantitative analysis of Lysobacter predation. Appl. Environ. Microbiol. 81, 7098–7105 (2015).
Hirakata, Y. et al. Identification and cultivation of anaerobic bacterial scavengers of dead cells. ISME J. 17, 2279–2289 (2023).
Wright, B. M., Stredulinsky, E. H., Ellis, G. M. & Ford, J. K. B. Kin-directed food sharing promotes lifetime natal philopatry of both sexes in a population of fish-eating killer whales, Orcinus orca. Anim. Behav. 115, 81–95 (2016).
Middelburg, J. J. Stable isotopes dissect aquatic food webs from the top to the bottom. Biogeosciences 11, 2357–2371 (2014).
Jürgens, K. & Matz, C. Predation as a shaping force for the phenotypic and genotypic composition of planktonic bacteria. Antonie Van Leeuwenhoek 81, 413–434 (2002).
Gross, C. P. et al. The biogeography of community assembly: latitude and predation drive variation in community trait distribution in a guild of epifaunal crustaceans. Proc. R. Soc. B Biol. Sci. 289, 20211762 (2022).
Hoque, M. M., Espinoza-Vergara, G. & McDougald, D. Protozoan predation as a driver of diversity and virulence in bacterial biofilms. FEMS Microbiol. Rev. 47, fuad040 (2023).
Friman, V.-P., Hiltunen, T., Laakso, J. & Kaitala, V. Availability of prey resources drives evolution of predator–prey interaction. Proc. R. Soc. B Biol. Sci. 275, 1625–1633 (2008).
Gallet, R. et al. Predation and disturbance interact to shape prey species diversity. Am. Naturalist 170, 143–154 (2007).
Nair, R. R. & Velicer, G. J. Predatory bacteria select for sustained prey diversity. Microorganisms 9, 2079 (2021).
Matthey, N. et al. Neighbor predation linked to natural competence fosters the transfer of large genomic regions in Vibrio cholerae. eLife 8, e48212 (2019).
Wielgoss, S., Wolfensberger, R., Sun, L., Fiegna, F. & Velicer, G. J. Social genes are selection hotspots in kin groups of a soil microbe. Science 363, 1342–1345 (2019).
Gallet, R., Tully, T. & Evans, M. E. K. Ecological conditions affect evolutionary trajectory in a predator-prey system. Evolution 63, 641–651 (2009).
Mayrhofer, N., Velicer, G. J., Schaal, K. A. & Vasse, M. Behavioral interactions between bacterivorous nematodes and predatory bacteria in a synthetic community. Microorganisms 9, 1362 (2021).
Vasse, M., Torres-Barceló, C. & Hochberg, M. E. Phage selection for bacterial cheats leads to population decline. Proc. R. Soc. B Biol. Sci. 282, 20152207 (2015).
Amaro, F. & Martín-González, A. Microbial warfare in the wild — the impact of protists on the evolution and virulence of bacterial pathogens. Int. Microbiol. 24, 559–571 (2021).
Friman, V.-P., Lindstedt, C., Hiltunen, T., Laakso, J. & Mappes, J. Predation on multiple trophic levels shapes the evolution of pathogen virulence. PLoS ONE 4, e6761 (2009).
Werner, E. E. & Peacor, S. D. A review of trait-mediated indirect interactions in ecological communities. Ecology 84, 1083–1100 (2003).
Yang, J. W. et al. Trade-offs between competitive ability and resistance to top-down control in marine microbes. mSystems 8, e01017-22 (2023).
Crooks, K. R. & Soulé, M. E. Mesopredator release and avifaunal extinctions in a fragmented system. Nature 400, 563–566 (1999).
Örmälä-Odegrip, A.-M. et al. Protist predation can select for bacteria with lowered susceptibility to infection by lytic phages. BMC Evolut. Biol. 15, 81 (2015).
Banerji, A. & Morin, P. J. Trait-mediated apparent competition in an intraguild predator–prey system. Oikos 123, 567–574 (2014).
Allesina, S., Alonso, D. & Pascual, M. A general model for food web structure. Science 320, 658–661 (2008).
Diehl, S. & Feissel, M. Intraguild prey suffer from enrichment of their resources: a microcosm experiment with ciliates. Ecology 82, 2977–2983 (2001).
Pichler, M., Boreux, V., Klein, A.-M., Schleuning, M. & Hartig, F. Machine learning algorithms to infer trait-matching and predict species interactions in ecological networks. Methods Ecol. Evol. 11, 281–293 (2020).
Barel, J. M., Petchey, O. L., Ghaffouli, A. & Jassey, V. E. J. Uncovering microbial food webs using machine learning. Soil. Biol. Biochem. 186, 109174 (2023).
García-Callejas, D., Molowny-Horas, R. & Araújo, M. B. Multiple interactions networks: towards more realistic descriptions of the web of life. Oikos 127, 5–22 (2018).
Stukel, M. R., Décima, M., Fender, C. K., Gutierrez-Rodriguez, A. & Selph, K. E. Gelatinous filter feeders increase ecosystem efficiency. Commun. Biol. 7, 1039 (2024).
Bethany, J., Johnson, S. L. & Garcia-Pichel, F. High impact of bacterial predation on cyanobacteria in soil biocrusts. Nat. Commun. 13, 4835 (2022).
Terborgh, J. W. Toward a trophic theory of species diversity. Proc. Natl Acad. Sci. USA 112, 11415–11422 (2015).
Gauzens, B., Legendre, S., Lazzaro, X. & Lacroix, G. Intermediate predation pressure leads to maximal complexity in food webs. Oikos 125, 595–603 (2016).
Loreau, M. & Hector, A. Partitioning selection and complementarity in biodiversity experiments. Nature 412, 72–76 (2001).
Thébault, E. & Loreau, M. The relationship between biodiversity and ecosystem functioning in food webs. Ecol. Res. 21, 17–25 (2006).
Kéfi, S. et al. Advancing our understanding of ecological stability. Ecol. Lett. 22, 1349–1356 (2019).
Yachi, S. & Loreau, M. Biodiversity and ecosystem productivity in a fluctuating environment: the insurance hypothesis. Proc. Natl Acad. Sci. USA 96, 1463–1468 (1999).
Ross, S. R. P.-J. & Sasaki, T. Limited theoretical and empirical evidence that response diversity determines the resilience of ecosystems to environmental change. Ecol. Res. 39, 115–130 (2024).
Rosenzweig, M. L. Paradox of enrichment: destabilization of exploitation ecosystems in ecological time. Science 171, 385–387 (1971).
Lemmen, K. D. & Pennekamp, F. Food web context modifies predator foraging and weakens trophic interaction strength. Ecol. Lett. 27, e14475 (2024).
Martins, S. J. et al. Predators of soil bacteria in plant and human health. Phytobiomes J. 6, 184–200 (2022).
Pérez, J., Contreras-Moreno, F. J., Marcos-Torres, F. J., Moraleda-Muñoz, A. & Muñoz-Dorado, J. The antibiotic crisis: how bacterial predators can help. Comput. Struct. Biotechnol. J. 18, 2547–2555 (2020).
Zhang, L., Guo, L., Cui, Z. & Ju, F. Exploiting predatory bacteria as biocontrol agents across ecosystems. Trends Microbiol. 32, 398–409 (2024).
Lewis, J. A. & Morran, L. T. Advantages of laboratory natural selection in the applied sciences. J. Evolut. Biol. 35, 5–22 (2022).
Herencias, C., Salgado, S. & Prieto, A. in The Ecology of Predation at the Microscale 173–194 (Springer, 2020).
Shen, X. et al. Lysobacter enzymogenes antagonizes soilborne bacteria using the type IV secretion system. Environ. Microbiol. 23, 4673–4688 (2021).
Ye, X. et al. A predatory myxobacterium controls cucumber Fusarium wilt by regulating the soil microbial community. Microbiome 8, 49 (2020).
Han, J. et al. From predator to protector: Myxococcus fulvus WCH05 emerges as a potent biocontrol agent for fire blight. Front. Microbiol. 15, 1378288 (2024).
Sason, G. et al. Encapsulated predatory bacteria efficiently protect potato tubers from soft rot disease. Plant. Dis. https://doi.org/10.1094/PDIS-02-24-0487-RE (2024).
Eisner, S. A., Fiegna, F., McDonald, B. A. & Velicer, G. J. Bacterial predation of a fungal wheat pathogen: prelude to experimental evolution of enhanced biocontrol agents. Plant. Pathol. 72, 1059–1068 (2023).
Guo, S. et al. Predatory protists reduce bacteria wilt disease incidence in tomato plants. Nat. Commun. 15, 829 (2024).
Dong, H. et al. Myxococcus xanthus R31 suppresses tomato bacterial wilt by inhibiting the pathogen Ralstonia solanacearum with secreted proteins. Front. Microbiol. 12, 801091 (2022).
Hobley, L. et al. Dual predation by bacteriophage and Bdellovibrio bacteriovorus can eradicate Escherichia coli prey in situations where single predation cannot. J. Bacteriol. https://doi.org/10.1128/jb.00629-19 (2020).
Jones, E. M., Marken, J. P. & Silver, P. A. Synthetic microbiology in sustainability applications. Nat. Rev. Microbiol 22, 345–359 (2024).
Erdos, Z. et al. Manipulating multi-level selection in a fungal entomopathogen reveals social conflicts and a method for improving biocontrol traits. PLoS Pathog. 20, e1011775 (2024).
Ngiam, L., Weynberg, K. & Guo, J. Evolutionary and co-evolutionary phage training approaches enhance bacterial suppression and delay the emergence of phage resistance. ISME Commun. 4, ycae082 (2024).
Glonti, T. & Pirnay, J.-P. In vitro techniques and measurements of phage characteristics that are important for phage therapy success. Viruses 14, 1490 (2022).
Hogle, S. L., Ruusulehto, L., Cairns, J., Hultman, J. & Hiltunen, T. Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function. ISME J. 17, 514–524 (2023).
de la Cruz Barron, M. et al. Shifts from cooperative to individual-based predation defense determine microbial predator-prey dynamics. ISME J. 17, 775–785 (2023).
Friman, V.-P., Jousset, A. & Buckling, A. Rapid prey evolution can alter the structure of predator–prey communities. J. Evol. Biol. 27, 374–380 (2014).
Friman, V.-P., Dupont, A., Bass, D., Murrell, D. J. & Bell, T. Relative importance of evolutionary dynamics depends on the composition of microbial predator-prey community. ISME J. 10, 1352–1362 (2016).
Hiltunen, T. & Becks, L. Consumer co-evolution as an important component of the eco-evolutionary feedback. Nat. Commun. 5, 5226 (2014).
Hiltunen, T., Ayan, G. B. & Becks, L. Environmental fluctuations restrict eco-evolutionary dynamics in predator–prey system. Proc. R. Soc. B Biol. Sci. 282, 20150013 (2015).
Krupovic, M., Prangishvili, D., Hendrix, R. W. & Bamford, D. H. Genomics of bacterial and archaeal viruses: dynamics within the prokaryotic virosphere. Microbiol. Mol. Biol. Rev. https://doi.org/10.1128/mmbr.00011-11 (2011).
Gonzalez-Serrano, R. et al. Alteromonas myovirus V22 represents a new genus of marine bacteriophages requiring a tail fiber chaperone for host recognition. mSystems https://doi.org/10.1128/msystems.00217-20 (2020).
Lin, Y.-R. & Lin, C.-S. Genome-wide characterization of Vibrio phage ϕpp2 with unique arrangements of the mob-like genes. BMC Genomics 13, 224 (2012).
Hamm, J. N. et al. Unexpected host dependency of antarctic nanohaloarchaeota. Proc. Natl Acad. Sci. USA 116, 14661–14670 (2019).
Evans, K. J., Lambert, C. & Sockett, R. E. Predation by Bdellovibrio bacteriovorus HD100 requires type IV pili. J. Bacteriol. 189, 4850–4859 (2007).
Enos, B. G., Anthony, M. K., DeGiorgis, J. A. & Williams, L. E. Prey range and genome evolution of Halobacteriovorax marinus predatory bacteria from an estuary. mSphere https://doi.org/10.1128/msphere.00508-17 (2018).
Pasternak, Z. et al. In and out: an analysis of epibiotic vs periplasmic bacterial predators. ISME J. 8, 625–635 (2014).
Davidov, Y., Huchon, D., Koval, S. F. & Jurkevitch, E. A new alpha-proteobacterial clade of Bdellovibrio-like predators: implications for the mitochondrial endosymbiotic theory. Env. Microbiol. 8, 2179–2188 (2006).
Mavromatis, K. et al. Permanent draft genome sequence of the gliding predator Saprospira grandis strain Sa g1 (= HR1). Stand. Genomic Sci. 6, 210–219 (2012).
Taylor, T. B., Silby, M. W. & Jackson, R. W. Pseudomonas fluorescens. Trends Microbiol. 33, 250–251 (2025).
Amano, S. et al. Promomycin, a polyether promoting antibiotic production in Streptomyces spp. J. Antibiotics 63, 486–491 (2010).
Hess, S. & Suthaus, A. The vampyrellid amoebae (Vampyrellida, Rhizaria). Protist 173, 125854 (2022).
Yamaguchi, A., Yubuki, N. & Leander, B. S. Morphostasis in a novel eukaryote illuminates the evolutionary transition from phagotrophy to phototrophy: description of Rapaza viridis n. gen. et sp. (Euglenozoa, Euglenida). BMC Evol. Biol. 12, 29 (2012).
Kim, M., Choi, D. H. & Park, M. G. Cyanobiont genetic diversity and host specificity of cyanobiont-bearing dinoflagellate Ornithocercus in temperate coastal waters. Sci. Rep. 11, 9458 (2021).
Hess, S., Sausen, N. & Melkonian, M. Shedding light on vampires: the phylogeny of vampyrellid amoebae revisited. PLoS ONE 7, e31165 (2012).
Pion, M. et al. Gains of bacterial flagellar motility in a fungal world. Appl. Environ. Microbiol. 79, 6862–6867 (2013).
Lee, C.-H. et al. A carnivorous mushroom paralyzes and kills nematodes via a volatile ketone. Sci. Adv. 9, eade4809 (2023).
Peixoto, R. et al. Microbial solutions must be deployed against climate catastrophe. Commun. Biol. 7, 1466 (2024).
Thompson, A. W., Sweeney, C. P. & Sutherland, K. R. Selective and differential feeding on marine prokaryotes by mucous mesh feeders. Environ. Microbiol. 25, 880–893 (2023).
Soest, R. W. M. V. et al. Global diversity of sponges (Porifera). PLoS ONE 7, e35105 (2012).
Vecchi, M. et al. The toughest animals of the earth versus global warming: effects of long-term experimental warming on tardigrade community structure of a temperate deciduous forest. Ecol. Evol. 11, 9856–9863 (2021).
White, J. F., Kingsley, K. L., Verma, S. K. & Kowalski, K. P. Rhizophagy cycle: an oxidative process in plants for nutrient extraction from symbiotic microbes. Microorganisms 6, 95 (2018).
Cohen, Y. et al. Community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems. Nat. Commun. 12, 5481 (2021).
Brousseau, P.-M., Gravel, D. & Handa, I. T. Trait matching and phylogeny as predictors of predator–prey interactions involving ground beetles. Funct. Ecol. 32, 192–202 (2018).
Nguyen, T. B.-A. et al. Protistan predation selects for antibiotic resistance in soil bacterial communities. ISME J. 17, 2182–2189 (2023).
Ham, D. T. et al. A generalizable Cas9/sgRNA prediction model using machine transfer learning with small high-quality datasets. Nat. Commun. 14, 5514 (2023).
Zhang, L. & Lueders, T. Micropredator niche differentiation between bulk soil and rhizosphere of an agricultural soil depends on bacterial prey. FEMS Microbiol. Ecol. 93, fix103 (2017).
McMullen II, J. G. & Lennon, J. T. Mark-recapture of microorganisms. Environ. Microbiol. 25, 150–157 (2023).
Lima, S. L. Nonlethal effects in the ecology of predator-prey interactions. BioScience 48, 25–34 (1998).
Furey, N. B., Armstrong, J. B., Beauchamp, D. A. & Hinch, S. G. Migratory coupling between predators and prey. Nat. Ecol. Evol. 2, 1846–1853 (2018).
Grupstra, C. G. B., Lemoine, N. P., Cook, C. & Correa, A. M. S. Thank you for biting: dispersal of beneficial microbiota through ‘antagonistic’ interactions. Trends Microbiol. 30, 930–939 (2022).
Livingston, G. et al. Predators regulate prey species sorting and spatial distribution in microbial landscapes. J. Anim. Ecol. 86, 501–510 (2017).
Abrams, P. A. Food web functional responses. Front. Ecol. Evol. https://doi.org/10.3389/fevo.2022.984384 (2022).
Matz, C. & Kjelleberg, S. Off the hook — how bacteria survive protozoan grazing. Trends Microbiol. 13, 302–307 (2005).
Manning, A. J. & Kuehn, M. J. Contribution of bacterial outer membrane vesicles to innate bacterial defense. BMC Microbiol. 11, 258 (2011).
March, C. et al. Role of bacterial surface structures on the interaction of Klebsiella pneumoniae with phagocytes. PLoS ONE 8, e56847 (2013).
Ledvina, H. E. et al. Functional amyloid proteins confer defense against predatory bacteria. Nature 644, 197–204 (2025).
Matz, C. et al. Biofilm formation and phenotypic variation enhance predation-driven persistence of Vibrio cholerae. Proc. Natl Acad. Sci. USA 102, 16819–16824 (2005).
Zanditenas, E. et al. Digestive exophagy of biofilms by intestinal amoeba and its impact on stress tolerance and cytotoxicity. npj Biofilms Microb. 9, 77 (2023).
Blom, J. F., Zimmermann, Y. S., Ammann, T. & Pernthaler, J. Scent of danger: floc formation by a freshwater bacterium is induced by supernatants from a predator-prey coculture. Appl. Environ. Microbiol. 76, 6156–6163 (2010).
Corno, G. & Jürgens, K. Direct and indirect effects of protist predation on population size structure of a bacterial strain with high phenotypic plasticity. Appl. Environ. Microbiol. 72, 78–86 (2006).
Herron, M. D. et al. De novo origins of multicellularity in response to predation. Sci. Rep. 9, 2328 (2019).
Tikhonenkov, D. V. et al. Insights into the origin of metazoan multicellularity from predatory unicellular relatives of animals. BMC Biol. 18, 39 (2020).
Matz, C. et al. Impact of violacein-producing bacteria on survival and feeding of bacterivorous nanoflagellates. Appl. Environ. Microbiol. 70, 1593–1599 (2004).
Zaroubi, L. et al. The ubiquitous soil terpene geosmin acts as a warning chemical. Appl. Environ. Microbiol. 88, e00093-22 (2022).
Brown, E. R., Moore, S. G., Gaul, D. A. & Kubanek, J. Predator cues target signaling pathways in toxic algal metabolome. Limnol. Oceanogr. 67, 1227–1237 (2022).
Fiegna, F., Pande, S., Peitz, H. & Velicer, G. J. Widespread density dependence of bacterial growth under acid stress. iScience 26, 106952 (2023).
Wang, X. et al. Bacteria can mobilize nematode-trapping fungi to kill nematodes. Nat. Commun. 5, 5776 (2014).
Richter, I. et al. Toxin-producing endosymbionts shield pathogenic fungus against micropredators. mBio 13, e01440–22 (2022).
Klobutcher, L. A., Ragkousi, K. & Setlow, P. The Bacillus subtilis spore coat provides “eat resistance” during phagocytic predation by the protozoan Tetrahymena thermophila. Proc. Natl Acad. Sci. USA 103, 165–170 (2006).
Müller, S. et al. Bacillaene and sporulation protect Bacillus subtilis from predation by Myxococcus xanthus. Appl. Env. Microbiol. 80, 5603–5610 (2014).
Espinoza-Vergara, G. et al. Vibrio cholerae residing in food vacuoles expelled by protozoa are more infectious in vivo. Nat. Microbiol. 4, 2466–2474 (2019).
Dunn, J. D. et al. Eat prey, live: Dictyostelium discoideum as a model for cell-autonomous defenses. Front. Immunol. 8, 1906 (2017).
Calbet, A. The Wonders of Marine Plankton (Springer Nature, 2024).
Freshwater and other micro-organisms from Germany. Pling https://www.plingfactory.de/Science/Atlas/KennkartenProtista/01e-protista/e-Ciliata/e-source/Holophrya%20teres-Euchlanis.html (2016).
Rotifer Fauna of Germany and Neighbouring Countries: Polyarthra vulgaris CARLIN, 1943; (Synchaetidae, Ploima, Monogononta, Rotifera, Syndermata, Gnathifera, Spiralia, Protostomia, Bilateria, Metazoa, Opisthokonta, Eukaryota). Pling https://www.plingfactory.de/Science/Atlas/KennkartenTiere/Rotifers/01RotEng/source/Polyarthra%20vulgaris.html (2014).
Acknowledgements
The authors thank N. Mayrhofer for extensive assistance with literature research and S. Huwiler, E. Jurkevitch and L. Kroos for helpful comments on the manuscript. They acknowledge the authors of the many excellent publications relevant to this Review from which they learned much but regretfully did not cite due to space restrictions.
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Glossary
- Accidental predation
-
Predation mediated by traits that were not previously selected due to predatory benefits.
- Adapted predation
-
Predation mediated by traits previously selected due to predation benefits. Adapted predation spans various degrees of adaptedness.
- Apparent competition
-
Interspecies interaction caused by sharing a predator rather than competition for resources.
- Endobiotic handling
-
Attachment to and invasion of prey before eating them from the inside.
- Engulfment
-
Swallowing of prey.
- Epibiotic handling
-
Contact-dependent handling, during which the predator remains outside of the prey cell.
- Functional response
-
Relationship between the number of predation events and the density of prey.
- Handling
-
The combined process of killing, decomposing and consuming prey after initial contact.
- Interference competition
-
Directly harming other organisms for a fitness gain.
- Ixotrophy
-
Use of sticky cell surfaces or appendages to capture prey.
- Kin-level predation
-
Predation in which nutrients from prey are consumed by scavenging offspring of predators or other close kin of predators. Kinship in this context might be defined in terms of allelic similarity at genetic elements contributing to the generation of public prey-derived nutrients — elements that might be many in number and diverse in function in any given predator.
- Microbial loop
-
Cycling of organic matter derived from high-trophic-level organisms through microorganisms and then back into higher trophic levels of the food web through predation.
- Non-consumptive effects
-
Modifications of prey behaviour and/or physiology in response to predators when potential prey are not killed.
- Non-portal-epibiotic handling
-
Contact-dependent killing and/or lysis not involving a portal.
- Portal
-
An opening in a prey-cell wall created during sustained predator–prey contact through which a predator cell and/or molecules from either the predator or prey can pass.
- Portal-epibiotic handling
-
Formation of a sustained portal between predator and prey through which killing and/or lytic factors may be delivered into the prey and prey nutrients are taken up into the predator.
- Predation
-
The combined killing and consumption of one organism by another. The definition of predation adopted here encompasses lethal parasitism as a sub-category of predation.
- Prey preference
-
Predator behaviour that increases the probability of consuming some prey types relative to others when both are available as potential prey.
- Prey quality
-
The potential nutritive value of a given prey to a given predator (may depend on ecological context), with all predation-related traits of the two parties considered.
- Prey range
-
The set of microorganisms a given predator can consume as prey.
- Prey-kinesis
-
Increased speed of predator movement in response to prey cues.
- Prey-taxis
-
Directional movement of individual predators in response to prey cues.
- Private–public handling gradient
-
The range of degrees to which diverse modes of handling prey result in prey nutrients becoming available to organisms other than the predator.
- Searching (or foraging)
-
Predator behaviour that increases the likelihood of encountering prey.
- Telebiotic handling
-
Release of diffusible compounds that kill (and potentially lyse) prey remotely; this term is proposed here for consistency with other handling terms.
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Vasse, M., Velicer, G.J. Predation in microbial communities: gradients of nutritive killing. Nat Rev Microbiol (2026). https://doi.org/10.1038/s41579-026-01299-7
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DOI: https://doi.org/10.1038/s41579-026-01299-7


