Cited by 94Plant-Microbe Interactions and ImmunityMicrobial Community Ecology and PhysiologyBacterial Genetics and Biotechnology

Frenemies of the soil: Bacillus and Pseudomonas interspecies interactions

Open access
Lyng, Mark, Kovács, Ákos T.·2023·Trends in Microbiology

Abstract

Bacillus and Pseudomonas ubiquitously occur in natural environments and are two of the most intensively studied bacterial genera in the soil. They are often coisolated from environmental samples, and as a result, several studies have experimentally cocultured bacilli and pseudomonads to obtain emergent properties. Even so, the general interaction between members of these genera is virtually unknown. In the past decade, data on interspecies interactions between natural isolates of Bacillus and Pseudomonas has become more detailed, and now, molecular studies permit mapping of the mechanisms behind their pairwise ecology. This review addresses the current knowledge about microbe-microbe interactions between strains of Bacillus and Pseudomonas and discusses how we can attempt to generalize the interaction on a taxonomic and molecular level.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.tim.2023.02.003

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Bacterial consortia in wastewater treatment plants present a promising approach to mitigating ARG dissemination, particularly when combined with bioaugmentation and nanotechnology.

    “The use of bacterial consortia in wastewater treatment plants presents a promising approach to mitigating ARG dissemination, particularly when combined with advanced bioremediation technologies such as bioaugmentation and nanotechnology [215,321].”

    From Harnessing bacterial consortia for effective bioremediation: targeted removal of heavy metals, hydrocarbons, and persistent pollutants (2025) · cites this paper as [215]

    The References (page not available) cite a study of a microbial consortium treating wastewater effluents for nutrient removal, and “Mutually beneficial coexistence” describes the biotechnological potential of Bacillus–Pseudomonas consortia. Neither passage supports mitigating ARG dissemination or combining consortia with bioaugmentation and nanotechnology. (LLM, conf=0.76)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

No references could be resolved yet.

Research works printed but not linked: 104

  1. Magnabosco, 2018, The biomass and biodiversity of the continental subsurface, Nat. Geosci., 11, 707, 10.1038/s41561-018-0221-6 · DOI · Paper page
  2. Chiellini, 2019, Pseudomonas strains isolated from different environmental niches exhibit different antagonistic ability, Ethol. Ecol. Evol., 31, 399, 10.1080/03949370.2019.1621391 · DOI
  3. Yadav, 2015, Diversity and phylogenetic profiling of niche-specific Bacilli from extreme environments of India, Ann. Microbiol., 65, 611, 10.1007/s13213-014-0897-9 · DOI
  4. Compant, 2011, Endophytes of grapevine flowers, berries, and seeds: identification of cultivable bacteria, comparison with other plant parts, and visualization of niches of colonization, Microb. Ecol., 62, 188, 10.1007/s00248-011-9883-y · DOI
  5. Roberts, 2020, Environmental consortium containing Pseudomonas and Bacillus species synergistically degrades polyethylene terephthalate plastic, mSphere, 5, 10.1128/mSphere.01151-20 · DOI
  6. Bodawatta, 2020, Great tit (Parus major) uropygial gland microbiomes and their potential defensive roles, Front. Microbiol., 11, 1735, 10.3389/fmicb.2020.01735 · DOI
  7. Lozano, 2019, Introducing THOR, a model microbiome for genetic dissection of community behavior, mBio, 10, 10.1128/mBio.02846-18 · DOI
  8. Kehe, 2021, Positive interactions are common among culturable bacteria, Sci. Adv., 7, 10.1126/sciadv.abi7159 · DOI
  9. Palmer, 2022, Bacterial species rarely work together, Science, 376, 581, 10.1126/science.abn5093 · DOI
  10. Ludington, 2022, Higher-order microbiome interactions and how to find them, Trends Microbiol., 30, 618, 10.1016/j.tim.2022.03.011 · DOI
  11. Monmeyran, 2021, Four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel, NPJ Biofilms Microbiomes, 7, 64, 10.1038/s41522-021-00233-4 · DOI
  12. Chakraborty, 2016, Deciphering a survival strategy during the interspecific competition between Bacillus cereus MSM-S1 and Pseudomonas sp. MSM-M1, R. Soc. Open Sci., 3, 10.1098/rsos.160438 · DOI
  13. Leinweber, 2017, Cheating fosters species co-existence in well-mixed bacterial communities, ISME J., 11, 1179, 10.1038/ismej.2016.195 · DOI
  14. Burman, 2021, Microbial community interactions are sensitive to small changes in temperature, Front. Microbiol., 12, 10.3389/fmicb.2021.672910 · DOI
  15. Zhou, 2021, Antimicrobial activity screening of rhizosphere soil bacteria from tomato and genome-based analysis of their antimicrobial biosynthetic potential, BMC Genomics, 22, 29, 10.1186/s12864-020-07346-8 · DOI
  16. Boopathi, 2022, Bacillus subtilis BR4 derived stigmatellin Y interferes Pqs-PqsR mediated quorum sensing system of Pseudomonas aeruginosa, J. Basic Microbiol., 62, 801, 10.1002/jobm.202200017 · DOI
  17. Nestor, 2023, Interactions between culturable bacteria are predicted by individual species’ growth, mSystems, 8, 10.1128/msystems.00836-22 · DOI
  18. Boyer, 2009, Dissecting the bacterial type VI secretion system by a genome wide in silico analysis: what can be learned from available microbial genomic resources?, BMC Genomics, 10, 104, 10.1186/1471-2164-10-104 · DOI
  19. Bernal, 2018, Type VI secretion systems in plant-associated bacteria, Environ. Microbiol., 20, 1, 10.1111/1462-2920.13956 · DOI
  20. Molina-Santiago, 2019, The extracellular matrix protects Bacillus subtilis colonies from Pseudomonas invasion and modulates plant co-colonization, Nat. Commun., 10, 1919, 10.1038/s41467-019-09944-x · DOI
  21. Pérez-Lorente, 2023, Sporulation Activated via σW Protects Bacillus from a Tse1 Peptidoglycan Hydrolase Type VI Secretion System Effector, Microbiol Spectr, 11, 10.1128/spectrum.05045-22 · DOI
  22. Molina-Santiago, 2021, Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence, Cell Rep., 36, 10.1016/j.celrep.2021.109449 · DOI
  23. Vick, 2021, Delving into defence: identifying the Pseudomonas protegens Pf-5 gene suite involved in defence against secreted products of fungal, oomycete and bacterial rhizosphere competitors, Microb. Genom., 7
  24. Powers, 2015, Inhibition of cell differentiation in Bacillus subtilis by Pseudomonas protegens, J. Bacteriol., 197, 2129, 10.1128/JB.02535-14 · DOI
  25. Andrić, 2021, Lipopeptide interplay mediates molecular interactions between soil Bacilli and Pseudomonads, Microbiol. Spectr., 9, 10.1128/spectrum.02038-21 · DOI
  26. Nithya, 2010, Bacillus pumilus of Palk Bay origin inhibits quorum-sensing-mediated virulence factors in Gram-negative bacteria, Res. Microbiol., 161, 293, 10.1016/j.resmic.2010.03.002 · DOI
  27. Andrić, 2022, Plant-associated Bacillus mobilizes its secondary metabolites upon perception of the siderophore pyochelin produced by a Pseudomonas competitor, ISME J., 17, 263, 10.1038/s41396-022-01337-1 · DOI
  28. Feliatra, 2021, The potentials of secondary metabolites from Bacillus cereus SN7 and Vagococcus fluvialis CT21 against fish pathogenic bacteria, Microb. Pathog., 158, 10.1016/j.micpath.2021.105062 · DOI
  29. Vaca, 2020, Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study, J. Antibiot., 73, 798, 10.1038/s41429-020-0333-2 · DOI
  30. Baron, 1981, Antibiotic action of pyocyanin, Antimicrob. Agents Chemother., 20, 814, 10.1128/AAC.20.6.814 · DOI
  31. Fontoura, 2009, Purification and characterization of an antimicrobial peptide produced by Pseudomonas sp. strain 4B, World J. Microbiol. Biotechnol., 25, 205, 10.1007/s11274-008-9882-4 · DOI
  32. Rahman, 2009, Development of a simple and low cost microbioreactor for high-throughput bioprocessing, Biotechnol. Lett., 31, 209, 10.1007/s10529-008-9853-8 · DOI
  33. Ahmad, 2013, Pseudomonas putida strain FStm2 isolated from shark skin: a potential source of bacteriocin, Probiotics Antimicrob. Proteins, 5, 165, 10.1007/s12602-013-9140-4 · DOI
  34. Raaijmakers, 2006, Cyclic lipopeptide production by plant-associated Pseudomonas spp.: diversity, activity, biosynthesis, and regulation, MPMI, 19, 699, 10.1094/MPMI-19-0699 · DOI
  35. Geudens, 2018, Cyclic lipodepsipeptides from Pseudomonas spp. – biological Swiss-army knives, Front. Microbiol., 9, 1867, 10.3389/fmicb.2018.01867 · DOI
  36. Grgurina, 2002, A new syringopeptin produced by bean strains of Pseudomonas syringae pv. syringae, Biochem. Biophys. Acta, 1597, 81
  37. Bassarello, 2004, Tolaasins A–E, five new lipodepsipeptides produced by Pseudomonas tolaasii, J. Nat. Prod., 67, 811, 10.1021/np0303557 · DOI
  38. Rokni-Zadeh, 2012, Genetic and functional characterization of cyclic lipopeptide white-line-inducing principle (WLIP) production by rice rhizosphere isolate Pseudomonas putida RW10S2, Appl. Environ. Microbiol., 78, 4826, 10.1128/AEM.00335-12 · DOI
  39. Kissoyan, 2019, Natural C. elegans microbiota protects against infection via production of a cyclic lipopeptide of the viscosin group, Curr. Biol., 29, 1030, 10.1016/j.cub.2019.01.050 · DOI
  40. Reder-Christ, 2012, Model membrane studies for characterization of different antibiotic activities of lipopeptides from Pseudomonas, Biochim. Biophys. Acta Biomembr., 1818, 566, 10.1016/j.bbamem.2011.08.007 · DOI
  41. Geudens, 2016, Membrane interactions of natural cyclic lipodepsipeptides of the viscosin group, Biochim. Biophys. Acta, 1859, 331, 10.1016/j.bbamem.2016.12.013 · DOI
  42. Kiesewalter, 2021, Genomic and chemical diversity of Bacillus subtilis secondary metabolites against plant pathogenic fungi, mSystems, 6, 10.1128/mSystems.00770-20 · DOI
  43. Grau, 2015, A duo of potassium-responsive histidine kinases govern the multicellular destiny of Bacillus subtilis, mBio, 6, 10.1128/mBio.00581-15 · DOI
  44. Kearns, 2003, Swarming motility in undomesticated Bacillus subtilis, Mol. Microbiol., 49, 581, 10.1046/j.1365-2958.2003.03584.x · DOI
  45. Jautzus, 2022, Complex extracellular biology drives surface competition during colony expansion in Bacillus subtilis, ISME J., 16, 2320, 10.1038/s41396-022-01279-8 · DOI
  46. Niu, 2016, Bacillus cereus AR156 activates PAMP-triggered immunity and induces a systemic acquired resistance through a NPR1-and SA-dependent signaling pathway, Biochem. Biophys. Res. Commun., 469, 120, 10.1016/j.bbrc.2015.11.081 · DOI
  47. Niu, 2011, The plant growth-promoting rhizobacterium Bacillus cereus AR156 induces systemic resistance in Arabidopsis thaliana by simultaneously activating salicylate-and jasmonate/ethylene-dependent signaling pathways, Mol. Plant-Microbe Interact., 24, 533, 10.1094/MPMI-09-10-0213 · DOI
  48. Wang, 2018, Bacillus cereus AR156 activates defense responses to Pseudomonas syringae pv. tomato in Arabidopsis thaliana similarly to flg22, Mol. Plant-Microbe Interact., 31, 311, 10.1094/MPMI-10-17-0240-R · DOI
  49. Khabbaz, 2015, Characterisation of antagonistic Bacillus and Pseudomonas strains for biocontrol potential and suppression of damping-off and root rot diseases, Ann. Appl. Biol., 166, 456, 10.1111/aab.12196 · DOI
  50. Diaz De Rienzo, 2016, Effect of mono and di-rhamnolipids on biofilms pre-formed by Bacillus subtilis BBK006, Curr. Microbiol., 73, 183, 10.1007/s00284-016-1046-4 · DOI
  51. Vasileva-Tonkova, 2011, The effect of rhamnolipid biosurfactant produced by Pseudomonas fluorescens on model bacterial strains and isolates from industrial wastewater, Curr. Microbiol., 62, 427, 10.1007/s00284-010-9725-z · DOI
  52. Dusane, 2010, Rhamnolipid mediated disruption of marine Bacillus pumilus biofilms, Colloids Surf. B Biointerfaces, 81, 242, 10.1016/j.colsurfb.2010.07.013 · DOI
  53. Díaz De Rienzo, 2016, Antibacterial properties of biosurfactants against selected Gram-positive and -negative bacteria, FEMS Microbiol. Lett., 363, 10.1093/femsle/fnv224 · DOI
  54. Anandan, 2019, Quorum quenching activity of AiiA lactonase KMMI17 from endophytic Bacillus thuringiensis KMCL07 on AHL- mediated pathogenic phenotype in Pseudomonas aeruginosa, Microb. Pathog., 132, 230, 10.1016/j.micpath.2019.05.015 · DOI
  55. Djokic, 2022, Novel quorum quenching YtnP lactonase from Bacillus paralicheniformis reduces Pseudomonas aeruginosa virulence and increases antibiotic efficacy in vivo, Front. Microbiol., 13, 10.3389/fmicb.2022.906312 · DOI
  56. Dong, 2000, AiiA, an enzyme that inactivates the acylhomoserine lactone quorum-sensing signal and attenuates the virulence of Erwinia carotovora, PNAS, 97, 3526, 10.1073/pnas.97.7.3526 · DOI
  57. Noor, 2022, Biodiversity of N-acyl homoserine lactonase (aiiA) gene from Bacillus subtilis, Microb. Pathog., 166, 10.1016/j.micpath.2022.105543 · DOI
  58. Xiong, 2021, Quorum sensing signal autoinducer-2 inhibits sporulation of Bacillus by interacting with 2 RapC and functions across species, bioRxiv
  59. Dong, 2002, Identification of quorum-quenching N-acyl homoserine lactonases from Bacillus species, Appl. Environ. Microbiol., 68, 1754, 10.1128/AEM.68.4.1754-1759.2002 · DOI
  60. Musthafa, 2011, Antipathogenic potential of marine Bacillus sp. SS4 on N-acyl-homoserine- lactone-mediated virulence factors production in Pseudomonas aeruginosa (PAO1), J. Biosci., 36, 55, 10.1007/s12038-011-9011-7 · DOI
  61. Boopathi, 2017, Stigmatellin Y – an anti-biofilm compound from Bacillus subtilis BR4 possibly interferes in PQS–PqsR mediated quorum sensing system in Pseudomonas aeruginosa, Bioorg. Med. Chem. Lett., 27, 2113, 10.1016/j.bmcl.2017.03.074 · DOI
  62. Sayem, 2011, Anti-biofilm activity of an exopolysaccharide from a sponge-associated strain of Bacillus licheniformis, Microb. Cell Factories, 10, 74, 10.1186/1475-2859-10-74 · DOI
  63. Vaikundamoorthy, 2018, Development of thermostable amylase enzyme from Bacillus cereus for potential antibiofilm activity, Bioorg. Chem., 77, 494, 10.1016/j.bioorg.2018.02.014 · DOI
  64. Hamza, 2018, Efficacy of cell free supernatant from Bacillus licheniformis in protecting Artemia salina against Vibrio alginolyticus and Pseudomonas gessardii, Microb. Pathog., 116, 335, 10.1016/j.micpath.2018.02.003 · DOI
  65. Cornforth, 2013, Competition sensing: the social side of bacterial stress responses, Nat. Rev. Microbiol., 11, 285, 10.1038/nrmicro2977 · DOI
  66. Garbeva, 2011, Transcriptional and antagonistic responses of Pseudomonas fluorescens Pf0-1 to phylogenetically different bacterial competitors, ISME J., 5, 973, 10.1038/ismej.2010.196 · DOI
  67. Chevrette, 2022, Microbiome composition modulates secondary metabolism in a multispecies bacterial community, PNAS, 119, 10.1073/pnas.2212930119 · DOI
  68. Boopathi, 2022, Investigation of interspecies crosstalk between probiotic Bacillus subtilis BR4 and Pseudomonas aeruginosa using metabolomics analysis, Microb. Pathog., 166, 10.1016/j.micpath.2022.105542 · DOI
  69. Lapouge, 2008, Gac/Rsm signal transduction pathway of γ-proteobacteria: From RNA recognition to regulation of social behaviour, Mol. Microbiol., 67, 241, 10.1111/j.1365-2958.2007.06042.x · DOI
  70. Cheng, 2013, The Gac regulon of Pseudomonas fluorescens SBW25, Environ. Microbiol. Rep., 5, 608, 10.1111/1758-2229.12061 · DOI
  71. Frangipani, 2014, The Gac/Rsm and cyclic-di-GMP signalling networks coordinately regulate iron uptake in Pseudomonas aeruginosa, Environ. Microbiol., 16, 676, 10.1111/1462-2920.12164 · DOI
  72. Cheng, 2016, Role of the GacS sensor kinase in the regulation of volatile production by plant growth-promoting Pseudomonas fluorescens SBW25, Front. Plant Sci., 7, 1706, 10.3389/fpls.2016.01706 · DOI
  73. Sun, 2022, Bacillus velezensis stimulates resident rhizosphere Pseudomonas stutzeri for plant health through metabolic interactions, ISME J., 16, 774, 10.1038/s41396-021-01125-3 · DOI
  74. Comeau, 2021, Interactions between Bacillus spp., Pseudomonas spp. and Cannabis sativa promote plant growth, Front. Microbiol., 12, 10.3389/fmicb.2021.715758 · DOI
  75. Ansari, 2019, Fluorescent Pseudomonas -FAP2 and Bacillus licheniformis interact positively in biofilm mode enhancing plant growth and photosynthetic attributes, Sci. Rep., 9, 4547, 10.1038/s41598-019-40864-4 · DOI
  76. Simões, 2008, Antagonism between Bacillus cereus and Pseudomonas fluorescens in planktonic systems and in biofilms, Biofouling, 24, 339, 10.1080/08927010802239154 · DOI
  77. Lemos, 2014, The effects of surface type on the removal of Bacillus cereus and Pseudomonas fluorescens single and dual species biofilms, Food Bioprod. Process., 93, 234, 10.1016/j.fbp.2014.08.009 · DOI
  78. Simões, 2011, The effects of glutaraldehyde on the control of single and dual biofilms of Bacillus cereus and Pseudomonas fluorescens, Biofouling, 27, 337, 10.1080/08927014.2011.575935 · DOI
  79. Gomes, 2021, The effects of chemical and mechanical stresses on Bacillus cereus and Pseudomonas fluorescens single-and dual-species biofilm removal, Microorganisms, 9, 1174, 10.3390/microorganisms9061174 · DOI
  80. Kim, 2022, Detection of Bacillus cereus and Pseudomonas fluorescens in dual-species biofilm via real-time PCR and eradication using grapefruit seed extract, LWT Food Scie. Technol., 165
  81. Ghazy, 2021, Siderophore production by Bacillus subtilis MF497446 and Pseudomonas koreensis MG209738 and their efficacy in controlling Cephalosporium maydis in maize plant, Arch. Microbiol., 203, 1195, 10.1007/s00203-020-02113-5 · DOI
  82. Kalantari, 2018, Improvement of bean yield and Fusarium root rot biocontrol using mixtures of Bacillus, Pseudomonas and Rhizobium, Trop. Plant Pathol., 43, 499, 10.1007/s40858-018-0252-y · DOI
  83. Salaheddin, 2010, Management of bacterial blight of cotton using a mixture of Pseudomonas fluorescens and Bacillus subtilis, Plant Protect. Sci., 46, 41, 10.17221/20/2009-PPS · DOI
  84. Bautista-Cruz, 2019, Phosphate-solubilizing bacteria improve Agave angustifolia Haw. growth under field conditions, J. Sci. Food Agric., 99, 6601, 10.1002/jsfa.9946 · DOI
  85. Kumar, 2016, Synergistic effect of Pseudomonas putida and Bacillus amyloliquefaciens ameliorates drought stress in chickpea (Cicer arietinum L.), Plant Signal. Behav., 11, 10.1080/15592324.2015.1071004 · DOI
  86. Aravinthan, 2016, Synergistic growth of Bacillus and Pseudomonas and its degradation potential on pretreated polypropylene, Prep. Biochem. Biotechnol., 46, 109, 10.1080/10826068.2014.985836 · DOI
  87. Gómez-Guzmán, 2017, Evaluation of nutrients removal (NO3-N, NH3-N and PO4-P) with Chlorella vulgaris, Pseudomonas putida, Bacillus cereus and a consortium of these microorganisms in the treatment of wastewater effluents, Water Sci. Technol., 76, 49, 10.2166/wst.2017.175 · DOI
  88. Bernhardt, 2020, The evolution of competitive ability for essential resources, Philos. Trans. R. Soc. B Biol. Sci., 375, 10.1098/rstb.2019.0247 · DOI
  89. Baliarda, 2021, Dynamic interspecies interactions and robustness in a four-species model biofilm, Microbiologyopen, 10, 10.1002/mbo3.1254 · DOI
  90. Zeriouh, 2014, Surfactin triggers biofilm formation of Bacillus subtilis in melon phylloplane and contributes to the biocontrol activity, Environ. Microbiol., 16, 2196, 10.1111/1462-2920.12271 · DOI
  91. Cuellar-Gaviria, 2021, Role of Bacillus tequilensis EA-CB0015 cells and lipopeptides in the biological control of black Sigatoka disease, Biol. Control, 155, 10.1016/j.biocontrol.2020.104523 · DOI
  92. Lozano-Andrade, 2022, Establishment of a transparent soil system to study Bacillus subtilis chemical ecology, bioRxiv
  93. Rojas-Ruiz, 2015, Analysis of Bacillus thuringiensis population dynamics and its interaction with Pseudomonas fluorescens in soil, Jundishapur J. Microbiol., 8, 10.5812/jjm.27953 · DOI
  94. Durairaj, 2017, Potential for plant biocontrol activity of isolated Pseudomonas aeruginosa and Bacillus stratosphericus strains against bacterial pathogens acting through both induced plant resistance and direct antagonism, FEMS Microbiol. Lett., 364, 10.1093/femsle/fnx225 · DOI
  95. Bais, 2004, Biocontrol of Bacillus subtilis against infection of Arabidopsis roots by Pseudomonas syringae is facilitated by biofilm formation and surfactin production, Plant Physiol., 134, 307, 10.1104/pp.103.028712 · DOI
  96. Vidal-Quist, 2013, Bacillus thuringiensis colonises plant roots in a phylogeny-dependent manner, FEMS Microbiol. Ecol., 86, 474, 10.1111/1574-6941.12175 · DOI
  97. Foster, 2012, Competition, not cooperation, dominates interactions among culturable microbial species, Curr. Biol., 22, 1845, 10.1016/j.cub.2012.08.005 · DOI
  98. Romero, 2011, Antibiotics as signal molecules, Chem. Rev., 111, 5492, 10.1021/cr2000509 · DOI
  99. Straight, 2006, Interactions between Streptomyces coelicolor and Bacillus subtilis: role of surfactants in raising aerial structures, J. Bacteriol., 188, 4918, 10.1128/JB.00162-06 · DOI
  100. Vaz Jauri, 2013, Subinhibitory antibiotic concentrations mediate nutrient use and competition among soil Streptomyces, PLoS One, 8, 10.1371/journal.pone.0081064 · DOI
  101. Ferreiro, 2021, Distinctive features of the Gac-Rsm pathway in plant-associated Pseudomonas, Environ. Microbiol., 23, 5670, 10.1111/1462-2920.15558 · DOI
  102. Kaspar, 2019, Bioactive secondary metabolites from Bacillus subtilis: a comprehensive review, J. Nat. Prod., 82, 2038, 10.1021/acs.jnatprod.9b00110 · DOI
  103. Sansinenea, 2011, Secondary metabolites of soil Bacillus spp, Biotechnol. Lett., 33, 1523, 10.1007/s10529-011-0617-5 · DOI
  104. Gross, 2009, Genomics of secondary metabolite production by Pseudomonas spp, Nat. Prod. Rep., 26, 1408, 10.1039/b817075b · DOI

Authors
Lyng, M., & Kovács, Á. T.
Affiliations
  • Technical University of Denmark (DK)
  • Leiden University (NL)
Corresponding author
Kovács, Ákos T.
Venue
Trends in Microbiology
Publisher
Elsevier BV
Published
2023-08
Volume
31
Issue
8
Pages
845-857
ISSN
0966-842X (ISSN-L)
OpenAlex
W4323073585
Cited by
94
References
0
Citations by year
2026: 27 · 2025: 40 · 2024: 23 · 2023: 4
FWCI
2.13
Type
journal article
Language
en
Open access
Locations
  • Trends in Microbiology (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Leiden Repository (Leiden University) (submittedVersion, cc-by)
  • Technical University of Denmark, DTU Orbit (Technical University of Denmark, DTU) (submittedVersion, cc-by)
Funders
  • National Research Foundation
  • Danmarks Grundforskningsfond (DNRF137)
  • Novo Nordisk (NNF19SA0059360)
  • Novo Nordisk Fonden (#NNF19SA0059360)
Topics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
  • Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Keywords
Bacillus, Pseudomonas, interspecies interactions, soil bacteria, microbial ecology, bacterial coexistence, soil microbiota
MeSH terms
Bacillus, Bacteria, Pseudomonas, Soil, Soil Microbiology

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review