A synthetic microbial community derived from healthy apple rhizosphere alleviates apple replant disease

Mengli Yang , Yiqi Liu , Yan Xia , Ming Li , Chuanmi Huang , Feifan Hou , Shupei Hu , Xiaoyan Zhu , Miaomiao Wang , Jiangli Shi , Ran Wan , Kunxi Zhang , Pengbo Hao , Yujie Zhao , Yu Liu , Yawen Shen , Liu Cong , Zhonghai Han , Jiancan Feng , Jian Jiao , Xianbo Zheng

Horticulture Research ›› 2025, Vol. 12 ›› Issue (11) : 217

PDF (3029KB)
Horticulture Research ›› 2025, Vol. 12 ›› Issue (11) :217 DOI: 10.1093/hr/uhaf217
Article
research-article
A synthetic microbial community derived from healthy apple rhizosphere alleviates apple replant disease
Author information +
History +
PDF (3029KB)

Abstract

Apple replant disease (ARD) poses a major threat to global orchard productivity, yet its biological causes remain poorly understood. Although microbial dysbiosis in replant soils has been recognized as a major contributing factor, the specific pathogenic agents involved and the efficacy of synthetic microbial communities in mitigating ARD remain unclear. In this study, we integrated physiological, transcriptomic, metabolomic, and microbiome analyses to investigate the effects of replant soils on the growth of Malus domestica rootstock M26. Absolute quantification amplicon sequencing of 16S rRNA and ITS regions revealed a marked decline in rhizospheric microbial diversity in replant soils compared to fallow controls, accompanied by an enrichment of fungal genera such as Fusarium, Aspergillus, and Acremonium. Pathogenicity assays and seedling colonization experiments verified strong pathogenicity for five isolates—Acremonium sp., Aspergillus niger, Fusarium solani, Macrophomina phaseolina, and Aspergillus stellatus—implicating them as potential causal agents of ARD. High-throughput culturing and confrontation assays were used to isolate and screen candidate microbial antagonists. A synthetic microbiota (SynMs) composed of 12 bacterial strains and Trichoderma sp. was developed. Inoculation with SynMs significantly inproved plant height by 133% (P < 0.05) and total root length by 186% (P < 0.01), and effectively suppressed pathogen proliferation of the five pathogenic isolates in replant soils. Collectively, these findings identify key fungal pathogens underlying ARD and propose a sustainable microbiota-based strategy for its effective mitigation, offering both mechanistic insights and practical solutions for microbiome-informed orchard management.

Cite this article

Download citation ▾
Mengli Yang, Yiqi Liu, Yan Xia, Ming Li, Chuanmi Huang, Feifan Hou, Shupei Hu, Xiaoyan Zhu, Miaomiao Wang, Jiangli Shi, Ran Wan, Kunxi Zhang, Pengbo Hao, Yujie Zhao, Yu Liu, Yawen Shen, Liu Cong, Zhonghai Han, Jiancan Feng, Jian Jiao, Xianbo Zheng. A synthetic microbial community derived from healthy apple rhizosphere alleviates apple replant disease. Horticulture Research, 2025, 12(11): 217 DOI:10.1093/hr/uhaf217

登录浏览全文

4963

注册一个新账户 忘记密码

Acknowledgements

This work was supported by a project grant from the Key Research and Development and Promotion Projects of Henan Province (242102111114); the Modern Agricultural Industry Technology Systems Project of Henan Province (HARS-22-09-G3).

Author contributions

All authors read and approved the final manuscript. J.J. and X.Z. conceived and designed the experiments. M.Y. and Y.L. performed the experiments, formal analysis and visualization. Y.X., M.L., C.H., F.H., S.H., and X.Z. helped the data curation and validation. M.Y. wrote the manuscript. M.W., J.S., R.W., K.Z., P.H., Y.Z., Y.L., Y.S., L.C., Z.H., and J.F. interpreted the data and revised the manuscript.

Data availability

All data needed to support the conclusions in this paper are present in the paper and/or Supplementary data.

Conflict of interest statement

The authors declare no conflicts of interest.

Supplementary data

Supplementary data is available at Horticulture Research online.

References

[1]

Turrini A, Agnolucci M, Palla M. et al. Species diversity and community composition of native arbuscular mycorrhizal fungi in apple roots are affected by site and orchard management. Appl Soil Ecol. 2017; 116:42-54

[2]

Yin C, Xiang L, Wang G. et al. How to plant apple trees to reduce replant disease in apple orchard: a study on the phenolic acid of the replanted apple orchard. PLoS One. 2016; 11:1-17

[3]

Manici LM, Kelderer M, Caputo F. et al. Involvement of Dactylonec-tria and Ilyonectria spp. in tree decline affecting multi-generation apple orchards. Plant Soil. 2018; 425:217-30

[4]

Grunewaldt-Stöckera G, Mahnkoppb F, Popp C. Diagnosis of apple replant disease (ARD): microscopic evidence of early symptoms in fine roots of different apple rootstock genotypes. Sci Hortic. 2019; 243:583-94

[5]

Winkelmann T, Smalla K, Amelung W. et al. Apple replant disease: causes and mitigation strategies. Curr Issues Mol Biol. 2019; 30:89-106

[6]

Yim B, Baumann A, Grunewaldt-Stöcker G. et al. Rhizosphere microbial communities associated to rose replant disease: links to plant growth and root metabolites. Hortic Res. 2020; 7:1-16

[7]

Annmarie-Deetja R, Jannika S, Katharina C. et al. Split-root approach reveals localized root responses towards apple replant disease (ARD) in terms of ARD biomarker gene expression and content of phenolic compounds. Sci Hortic. 2021; 286:110117

[8]

Simon M, Lehndorff E, Wrede A. et al. In-field heterogeneity of apple replant disease: relations to abiotic soil properties. Sci Hortic. 2020; 259:108809

[9]

Cavael U, Lentzsch P, Schwärzel H. et al. Assessment of agro-ecological apple replant disease (ARD) management strategies: organic fertilisation and inoculation with mycorrhizal fungi and bacteria. Agronomy. 2021; 11:272

[10]

Kanfra X, Liu B, Beerhues L. et al. Free-living nematodes together with associated microbes play an essential role in apple replant disease. Front Plant Sci. 2018; 9:1-13

[11]

Sun J, Zhang Q, Li X. et al. Apple replant risorder of Pingyitiancha rootstock is rlosely associated with rhizosphere fungal commu-nity development. J Phytopathol. 2017; 165:162-73

[12]

Duan Y, Jiang W, Zhang R. et al. Discovery of Fusarium proliferatum f. sp. malus domestica causing apple replant disease in China. Plant Dis. 2022; 106:2958-66

[13]

Tilston E, Deakin G, Bennett J. et al. Candidate causal organisms for apple replant disease in the United Kingdom. Phytobiomes J. 2018; 2:261-74

[14]

Moein S, Mazzola M, Ntushelo N. et al. Apple nursery trees and irrigation water as potential external inoculum sources of apple replant disease in South Africa. Eur J Plant Pathol. 2019; 153: 1131-47

[15]

Nyoni M, Mazzola M, Wessels JPB. et al. The efficacy of semiselective chemicals and chloropicrin/1, 3-dichloropropene-containing fumigants in managing apple replant disease in South Africa. Plant Dis. 2019; 103:1363-73

[16]

Yim B, Hanschen F, Wrede A. et al. Effects of using Bras-sica juncea and Raphanus sativus in comparison to disinfec-tion using Basamid on apple plant growth and soil micro-bial communities at three field sites. Plant Soil. 2016; 406: 389-408

[17]

Du P, He H, Zhou L. et al. Different biodegradation potential and the impacted soil functions of epoxiconazole in two soils. J Hazard Mater. 2022; 422:126787

[18]

Wang Y, Ma Z, Wang X. et al. Effects of biochar on the growth of apple seedlings, soil enzyme activities and fungal commu-nities in replant disease soil. Sci Hortic (Amsterdam). 2019; 256: 108641

[19]

Duan Y, Chen R, Zhang R. et al. Isolation and identification of Bacillus vallismortis HSB-2 and its biocontrol potential against apple replant disease. Biol Control. 2022; 170:104921

[20]

Li Z, Bai X, Jiao S. et al. A simplified synthetic community rescues Astragalus mongholicus from root rot disease by activating plant-induced systemic resistance. Microbiome. 2021; 9:1-20

[21]

Zhou X, Wang J, Liu F. et al. Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease. Nat Com-mun. 2022; 13:1-17

[22]

Goers L, Freemont P, Polizzi KM. Co-culture systems and tech-nologies: taking synthetic biology to the next level. JRSoc Interface. 2014; 11:20140065

[23]

Roell GW, Zha J, Carr RR. et al. Engineering microbial consortia by division of labor. Microb Cell Factories. 2019; 18:1-11

[24]

Wen T, Yuan J, He X. et al. Enrichment of beneficial cucumber rhizosphere microbes mediated by organic acid secretion. Hortic Res. 2020; 7:154

[25]

Fitzpatrick CR, Salas-González I, Conway JM. et al. The plant microbiome: from ecology to reductionism and beyond. Ann Rev Microbiol. 2020; 74:81-100

[26]

Liu H, Li J, Carvalhais L. et al. Evidence for the plant recruitment of beneficial microbes to suppress soil-borne pathogens. New Phytol. 2021; 229:2873-85

[27]

Meng J, Zan F, Liu Z. et al. Genomics analysis reveals the potential biocontrol mechanism of Pseudomonas aeruginosa QY43 against Fusarium pseudograminearum. J Fungi. 2024; 10:298

[28]

Kaur S, Egidi E, Qiu Z. et al. Synthetic community improves crop performance and alters rhizosphere microbial communities. J Sustain Agric Environ. 2022; 1:118-31

[29]

Schmitz L, Yan Z, Schneijderberg M. et al. Synthetic bacterial community derived from a desert rhizosphere confers salt stress resilience to tomato in the presence of a soil microbiome. ISME J. 2022; 16:1907-20

[30]

Wang H, Tang W, Mao Y. et al. Isolation of Trichoderma virens 6PS-2 and its effects on Fusarium proliferatum f. sp. Malus domestica MR5 related to apple replant disease in China. Hortic Plant J. 2024; 10:1291-308

[31]

Macabuhay A, Arsova B, Walker R. et al. Modulators or facilita-tors? Roles of lipids in plant root-microbe interactions. Trends Plant Sci. 2022; 27:180-90

[32]

Jiang W, Chen R, Zhao L. et al. Chemical fumigants control apple replant disease: microbial community structure-mediated inhibition of Fusarium and degradation of phenolic acids. J Hazard Mater. 2022; 440:129786

[33]

Wu L, Yang B, Li M. et al. Modification of rhizosphere bacte-rial community structure and functional potentials to control pseudostellaria heterophylla replant disease. Plant Dis. 2020; 104: 25-34

[34]

Li W, Chen P, Wang Y. et al. Characterization of the microbial community response to replant diseases in peach orchards. J Integr Agric. 2023; 22:1082-92

[35]

Su L, Li H, Wang J. et al. Composition, function and succession of bacterial communities in the tomato rhizosphere during continuous cropping. Biol Fertil Soils. 2023; 59:723-32

[36]

Balbín-Suárez A, Jacquiod S, Rohr AD. et al. Root exposure to apple replant disease soil triggers local defense response and rhizoplane microbiome dysbiosis. FEMS Microbiol Ecol. 2021; 97: 1-14

[37]

He X, Yin B, Zhang J. et al. Exogenous melatonin alleviates apple replant disease by regulating rhizosphere soil microbial community structure and nitrogen metabolism. Sci Total Environ. 2023; 884:163830

[38]

Mickan BS, Abbott LK, Solaiman ZM. et al. Soil disturbance and water stress interact to influence arbuscular mycorrhizal fungi, rhizosphere bacteria and potential for N and C cycling in an agricultural soil. Biol Fertil Soils. 2019; 55:53-66

[39]

Ali A, Elrys AS, Liu L. et al. Cover plants-mediated suppres-sion of Fusarium wilt and root-knot incidence of cucumber is associated with the changes of rhizosphere fungal micro-biome structure-under plastic shed system of North China. Front Microbiol. 2022; 13:1-17

[40]

Zhang J, Zhu W, Goodwin P. et al. Response of Fusarium pseu-dograminearum to biocontrol agent Bacillus velezensis YB-185 by phenotypic and transcriptome analysis. J Fungi. 2022; 8: 763

[41]

Du N, Yang Q, Xue L. et al. Paenibacillus polymyxa NSY50 improves defense against Fusarium oxysporum by increasing photosyn-thetic efficiency, sucrose metabolism, and antioxidant capacity in cucumber. J Plant Growth Regul. 2023; 42:2246-57

[42]

Gao J, Zhang M, Liang J. et al. Isolation and identification of Rhizopus arrhizus causing postharvest bulb rot in Lilium davidii var. unicolor and its biocontrol using the endophytic bacterium Bacillus siamensis B55. Agric Commun. 2024; 2:100025

[43]

Xu H, Wei X, Cheng X. Fungal diversity dominates the response of multifunctionality to the conversion of pure plantations into two-aged mixed plantations. Sci Total Environ. 2023; 866: 161384

[44]

Wu H, Li C, Chakraborti P. et al. First report of watermelon charcoal rot (Macrophomina phaseolina) in China. Plant Dis. 2022; 106:1521

[45]

Singh N, Klingenberg J, Poudel-Ward B. First report of charcoal rotcausedbyMacrophomina phaseolina on stevia (Stevia rebaudi-ana) in Arizona. Plant Dis. 2023; 107:2863

[46]

Zhou X, Zhang J, Muhammad K. et al. Interspecific plant interac-tion via root exudates structures the disease suppressiveness of rhizosphere microbiomes. Mol Plant. 2023; 16:849-64

[47]

Li T, Zhang J, Shen C. et al. 1-Aminocyclopropane-1-carboxylate: a novel and strong chemoattractant for the plant beneficial rhi-zobacterium Pseudomonas putida UW4. Mol Plant-Microbe Interact. 2019; 32:750-9

[48]

Vorholt JA, Vogel C, Carlström CI. et al. Establishing causality: opportunities of synthetic communities for plant microbiome research. Cell Host Microbe. 2017; 22:142-55

[49]

Li H, Zhang Y, Wang T. et al. Responses of soil denitrifying bacterial communities carrying nirS, nirK, and nosZ genes to revegetation of moving sand dunes. Ecol Indic. 2019; 107: 105541

[50]

Tao C, Wang Z, Liu S. et al. Additive fungal interactions drive biocontrol of Fusarium wilt disease. New Phytol. 2023; 238: 1198-214

[51]

Trivedi P, Leach J, Tringe S. et al. Plant-microbiome interactions: from community assembly to plant health. Nat Rev Microbiol. 2020; 18:607-21

[52]

Qiu K, Xie Y, Xu D. et al. Ecosystem functions including soil organic carbon, total nitrogen and available potassium are cru-cial for vegetation recovery. Sci Rep. 2018; 8:1-11

[53]

Bai T, Dong Z, Zheng X. et al. Auxin and its interaction with ethylene control adventitious root formation and development in apple rootstock. Front Plant Sci. 2020; 11:1-14

[54]

Chen G, Wang L, Fabrice MR. et al. Physiological and nutritional responses of pear seedlings to nitrate concentrations. Front Plant Sci. 2018; 9:1-11

[55]

Kanehisa M, Araki M, Goto S. et al. KEGG for linking genomes to life and the environment. Nucleic Acids Res. 2008;36: D480-4

[56]

Ashburner M, Ball CA, Blake JA. et al. Gene ontology: tool for the unification of biology. Nat Genet. 2000; 25:25-9

[57]

Liao Y, Smyth GK, Shi W. Feature counts: an efficient general purpose program for assigning sequence reads to genomic fea-tures. Bioinformatics. 2014; 30:923-30

[58]

Smets W, Leff JW, Bradford MA. et al. A method for simultane-ous measurement of soil bacterial abundances and community composition via 16S rRNA gene sequencing. Soil Biol Biochem. 2016; 96:145-51

[59]

Bolyen E, Rideout JR, Dillon MR. et al. Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2. Nat Biotechnol. 2019; 37:852-7

[60]

Callahan B, McMurdie P, Rosen M. et al. DADA2: high-resolution sample inference from Illumina amplicon data. Nat Methods. 2016; 13:581-3

[61]

Edgar RC. UPARSE: highly accurate OTU sequences from micro-bial amplicon reads. Nat Methods. 2013; 10:996-8

[62]

Song Z, Sun Y, Liu P. et al. Invasion of Spartina alterniflora on Zostera japonica enhances the abundances of bacteria by absolute quantification sequencing analysis. Ecol Evol. 2022; 12: 1-13

[63]

Hamady M, Lozupone C, Knight R. Fast UniFrac: facilitating high-throughput phylogenetic analyses of microbial communities including analysis of pyrosequencing and PhyloChip data. ISME J. 2010; 4:17-27

[64]

Wen T, Xie P, Yang S. et al. ggClusterNet: an R package for microbiome network analysis and modularity-based multiple network layouts. iMeta. 2022; 1:1-7

[65]

Bastian M, Heymann S, Jacomy M. Gephi: an open source soft-ware for exploring and manipulating networks. Proc Int AAAI Conf Web Soc Media. 2009; 3:361-2

[66]

Louca S, Parfrey LW, Doebeli M. Decoupling function and taxonomy in the global ocean microbiome. Science. 2016; 353: 1272-7

[67]

Nguyen NH, Song Z, Bates ST. et al. FUNGuild: an open annota-tion tool for parsing fungal community datasets by ecological guild. Fungal Ecol. 2016; 20:241-8

[68]

Parks DH, Tyson GW, Hugenholtz P. et al. STAMP: statistical analysis of taxonomic and functional profiles. Bioinformatics. 2014; 30:3123-4

[69]

Zhang X, Zhang J, He X. et al. Comparison of fungal genera isolated from cucumber plants and rhizosphere soil by using various cultural media. J. Fungi. 2023; 9:934

[70]

Zhang J, Liu YX, Guo X. et al. High-throughput cultivation and identification of bacteria from the plant root microbiota. Nat Protoc. 2021; 16:988-1012

PDF (3029KB)

325

Accesses

0

Citation

Detail

Sections
Recommended

/