Collaborative impact of bacterial exometabolites governing root microbiota formation

Hafiz Abdul Kareem, Xinwei Hao, Xihui Shen

Stress Biology ›› 2023, Vol. 3 ›› Issue (1) : 38. DOI: 10.1007/s44154-023-00121-1
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Collaborative impact of bacterial exometabolites governing root microbiota formation

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Abstract

The majority of the root microbiota formation derives from soil-dwelling microorganisms. The limited extent of thorough investigation leads to a dearth of knowledge concerning the intricate mechanisms of microbe-microbe interaction implicated in the establishment of root microbiota. Therefore, the taxonomic signatures in bacterial inhibition profiles were determined by in vitro testing of 39,204 binary interbacterial interactions. However, findings from genetic and metabolomic studies elucidated that co-functioning of the antimicrobial 2,4-d iacetylphloroglucinol (DAPG) and the iron chelator pyoverdine as exometabolites has significantly contributed to the potent inhibitory activities of the highly antagonistic Pseudomonas brassicacearum R401. Microbiota restoration with a core of Arabidopsis thaliana root commensals showed that these exometabolites possess a root niche-specific function in establishing root competence and inducing anticipated changes in root surroundings. Both biosynthetic operons are abundant in roots in natural habitats, indicating that these exometabolites co-functioning is an adaptive feature that helps Pseudomonad dominate the root microbiota.

Keywords

Pseudomonas / Exometabolites / Root microbiota / Operons / Pyoverdine

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Hafiz Abdul Kareem, Xinwei Hao, Xihui Shen. Collaborative impact of bacterial exometabolites governing root microbiota formation. Stress Biology, 2023, 3(1): 38 https://doi.org/10.1007/s44154-023-00121-1

References

[1]
Bai Y, Müller DB, Srinivas G, Garrido-oter R, Potthoff E, Rott M, Dombrowski N, Münch PC, Spaepen S, Remus-emsermann M, Hüttel B, Mchardy AC, Vorholt JA (2015) Functional overlap of the Arabidopsis leaf and root microbiota. Nature 16192. https://doi.org/10.1038/nature16192
[2]
CloughSE, JoussetA, ElphinstoneJG, FrimanVP. Combining in vitro and in vivo screening to identify efficient Pseudomonas biocontrol strains against the phytopathogenic bacterium Ralstonia solanacearum. Microbiologyopen, 2022, 11: 1-18
CrossRef Google scholar
[3]
Crits-ChristophA, DiamondS, ButterfieldCN, ThomasBC, BanfieldJF. Novel soil bacteria possess diverse genes for secondary metabolite biosynthesis. Nature, 2018, 558: 440-444
CrossRef Google scholar
[4]
EilersKG, LauberCL, KnightR, FiererN. Shifts in bacterial community structure associated with inputs of low molecular weight carbon compounds to soil. Soil Biol Biochem, 2010, 42: 896-903
CrossRef Google scholar
[5]
FiraD, DimkićI, BerićT, LozoJ, StankovićS. Biological control of plant pathogens by Bacillus species. J Biotechnol, 2018, 285: 44-55
CrossRef Google scholar
[6]
GetzkeF, HassaniMA, CrüsemannM, MalisicM, ZhangP, IshigakiY, BöhringerN, JiménezA. Cofunctioning of bacterial exometabolites drives root microbiota establishment. PNAS, 2023, 120: 1-12
CrossRef Google scholar
[7]
GuS, WeiZ, ShaoZ, FrimanVP, CaoK, YangT, KramerJ, WangX, LiM, MeiX, XuY, ShenQ, KümmerliR, JoussetA. Competition for iron drives phytopathogen control by natural rhizosphere microbiomes. Nat Microbiol, 2020, 5: 1002-1010
CrossRef Google scholar
[8]
KremerJM, SohrabiR, PaaschBC, RhodesD, ThireaultC, TiedjeJM, HeSY. Peat-based gnotobiotic plant growth systems for Arabidopsis microbiome research. Nat Proto, 2021, 16(5):2450-2470
CrossRef Google scholar
[9]
LamontIL, MartinLW, SimsT, ScottA, WallaceM. Characterization of a gene encoding an acetylase required for pyoverdine synthesis in Pseudomonas aeruginosa. J Bacteriol, 2006, 188: 3149-3152
CrossRef Google scholar
[10]
LundbergDS, LebeisSL, ParedesSH, YourstoneS, GehringJ, MalfattiS, TremblayJ, EngelbrektsonA, KuninV, DelRTG, EdgarRC, EickhorstT, LeyRE, HugenholtzP, TringeSG, DanglJL. Defining the core Arabidopsis thaliana root microbiome. Nature, 2012, 488: 86-90
CrossRef Google scholar
[11]
WippelK, TaoK, NiuY, ZgadzajR, KielN, GuanR, DahmsE, ZhangP, JensenDB, LogemannE, RadutoiuS, Schulze-LefertP, Garrido-OterR. Host preference and invasiveness of commensal bacteria in the Lotus and Arabidopsis root microbiota. Nat Microbiol, 2021, 6: 1150-1162
CrossRef Google scholar
[12]
ZhouTT, LiCY, ChenD, WuK, ShenQR, ShenB. PhlF- mutant of Pseudomonas fluorescens J2 improved 2,4-DAPG biosynthesis and biocontrol efficacy against tomato bacterial wilt. Biol Control, 2014, 78: 1-8
CrossRef Google scholar
Funding
National Natural Science Foundation of China(31725003)

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