To win the battle: the chloroplast is a key battleground in plant-pathogen interactions

Lu Rui , Zhujiang Cong , Xinghuang Zhou , Qing Yang , Zhanchun Wang , Wei Wang

Horticulture Research ›› 2026, Vol. 13 ›› Issue (2) : 294

PDF (1285KB)
Horticulture Research ›› 2026, Vol. 13 ›› Issue (2) :294 DOI: 10.1093/hr/uhaf294
Mini Review
research-article
To win the battle: the chloroplast is a key battleground in plant-pathogen interactions
Author information +
History +
PDF (1285KB)

Abstract

The interaction between plants and pathogens represents a complex evolutionary arms race. Plants employ a sophisticated innate immune system to combat pathogen invasion. However, pathogens inhibit plant immunity by secreting effectors into the host cell. The chloroplast is an indispensable organelle for photosynthesis and metabolism in plants. Notably, increasing evidence has recently revealed the pivotal role of chloroplasts in plant immunity, including reactive oxygen species production, phytohormone biosynthesis, and signal transduction. Accordingly, chloroplasts have emerged as key targets for pathogen effectors. In this review, we summarize the role of chloroplasts in plant immunity and update the identification of pathogen effectors that enhance pathogenicity by targeting chloroplasts. We also discuss the diverse mechanisms by which pathogen effectors hijack chloroplasts to manipulate plant immunity, shedding light on the functional complexity and importance of chloroplasts in plant-pathogen interactions.

Cite this article

Download citation ▾
Lu Rui, Zhujiang Cong, Xinghuang Zhou, Qing Yang, Zhanchun Wang, Wei Wang. To win the battle: the chloroplast is a key battleground in plant-pathogen interactions. Horticulture Research, 2026, 13(2): 294 DOI:10.1093/hr/uhaf294

登录浏览全文

4963

注册一个新账户 忘记密码

Acknowledgements

This work was supported by grants from the National Natural Science Foundation of China (32370302), the Natural Science Foundation of Fujian Province, China (2024J09022), and the Open Fund of Fujian Provincial Key Laboratory of Eco-Industrial Green Technology (WYKF-EIGT2022-6).

Authors contributions

L.R., Z.W., and W.W. conceptualized the manuscript, L.R., Z.C., X.Z., and Q.Y. collected the reference and wrote the manuscript, L.R., Z.C., X.Z., Z.W., and W.W. reviewed, revised, and edited the manuscript, L.R. and W.W. received funding acquisition.

Data availability

The data presented in this study are available in the article.

Conflicts of interest statement

The authors declare no conflict of interest.

References

[1]

Jones JDG, Staskawicz BJ, Dangl JL. The plant immune sys-tem: from discovery to deployment. Cell. 2024; 187:2095-116

[2]

Wu G, Wang W. Recent advances in understanding the role of two mitogen-activated protein kinase cascades in plant immunity. J Exp Bot. 2024; 75:2256-65

[3]

Rui L, Yang SQ, Zhou XH. et al. The important role of chloro-plasts in plant immunity. Plant Commun. 2025; 6:101420

[4]

Liu M, Zhang S, Hu J. et al. Phosphorylation-guarded light-harvesting complex II contributes to broad-spectrum blast resistance in rice. Proc Natl Acad Sci USA. 2019; 116:17572-7

[5]

Murmu J, Wilton M, Allard G. et al. Arabidopsis GOLDEN2-LIKE (GLK) transcription factors activate jasmonic acid (JA)-dependent disease susceptibility to the biotrophic pathogen Hyaloperonospora arabidopsidis, as well as JA-independent plant immunity against the necrotrophic pathogen Botrytis cinerea. Mol Plant Pathol. 2014; 15:174-84

[6]

Gurlebeck D, Jahn S, Gurlebeck N. et al. Visualization of novel virulence activities of the Xanthomonas type III effectors AvrBs1, AvrBs3 and AvrBs4. Mol Plant Pathol. 2009; 10:175-88

[7]

Cowan GH, Roberts AG, Chapman SN. et al. The potato mop-top virus TGB2 protein and viral RNA associate with chloro-plasts and viral infection induces inclusions in the plastids.Front. Plant Sci. 2012; 3:290

[8]

Mei Y, Hu T, Wang Y. et al. Two viral proteins translated from one open reading frame target different layers of plant defense. Plant Commun. 2024; 5:100788

[9]

Cai H, Zhao B, Liang K. et al. The Arabidopsis chloroplast protein HHL1 regulates AvrRpt2-triggered immunity via light-dependent. J Integr Plant Biol. 2025; 67:2151-66

[10]

Mu B, Teng Z, Tang R. et al. An effector of Erysiphe necator translocates to chloroplasts and plasma membrane to suppress host immunity in grapevine. Hortic Res. 2023;10:uhad163

[11]

Li J, Yang L, Ding S. et al. Plant PR1 rescues condensation of the plastid iron-sulfur protein by a fungal effector. Nat Plants. 2024; 10:1775-89

[12]

Xu Q, Tang C, Wang X. et al. An effector protein of the wheat stripe rust fungus targets chloroplasts and suppresses chloro-plast function. Nat Commun. 2019; 10:5571

[13]

Wang X, Zhai T, Zhang X. et al. Two stripe rust effectors impair wheat resistance by suppressing import of host Fe-S protein into chloroplasts. Plant Physiol. 2021; 187:2530-43

[14]

Liu R, Chen T, Yin X. et al. A Plasmopara viticola RXLR effector targets a chloroplast protein PsbP to inhibit ROS production in grapevine. Plant J. 2021; 106:1557-70

[15]

Rodriguez-Herva JJ, Gonzalez-Melendi P, Cuartas-Lanza R. et al. A bacterial cysteine protease effector protein inter-feres with photosynthesis to suppress plant innate immune responses. Cell Microbiol. 2012; 14:669-81

[16]

Jin M, Hu S, Wu Q. et al. An effector protein of Fusarium graminearum targets chloroplasts and suppresses cyclic pho-tosynthetic electron flow. Plant Physiol. 2024; 196:2422-36

[17]

Xu M, Sun X, Wu X. et al. Chloroplast protein StFC-II was manip-ulatedbya Phytophthora effector to enhance host susceptibil-ity. Hortic Res. 2024;11:uhae149

[18]

Zhu X, Guo L, Zhu R. et al. Phytophthora sojae effector PsAvh113 associates with the soybean transcription factor GmDPB to inhibit catalase-mediated immunity. Plant Biotech-nol J. 2023; 21:1393-407

[19]

Jiao Z, Tian Y, Cao Y. et al. A novel pathogenicity determinant hijacks maize catalase 1 to enhance viral multiplication and infection. New Phytol. 2021; 230:1126-41

[20]

Yang T, Qiu L, Huang W. et al. Chilli veinal mottle virus HCPro interacts with catalase to facilitate virus infection in Nicotiana tabacum. J Exp Bot. 2020; 71:5656-68

[21]

Cao Y, Zhang Q, Liu Y. et al. The RXLR effector PpE18 of Phytophthora parasitica is a virulence factor and suppresses peroxisome membrane-associated ascorbate peroxidase NbAPX3-1-mediated plant immunity. New Phytol. 2024; 243: 1472-89

[22]

Zhang J, Liu C, Wang Y. et al. Glycine-serine-rich effector Pst-GSRE4 in Puccinia striiformis f. sp. tritici inhibits the activity of copper zinc superoxide dismutase to modulate immunity in wheat. PLoS Pathog. 2022; 18:e1010702

[23]

Du J, Wang Q, Shi H. et al. A prophage-encoded effector from “Candidatus Liberibacter asiaticus” targets ASCORBATE PEROXIDASE6 in citrus to facilitate bacterial infection. Mol Plant Pathol. 2023; 24:302-16

[24]

Gao M, He Y, Yin X. et al. Ca2+ sensor-mediated ROS scav-enging suppresses rice immunity and is exploited by a fungal effector. Cell. 2021; 184:5391-5404.e17

[25]

Lozano-Torres JL, Wilbers RH, Warmerdam S. et al. Apoplas-tic venom allergen-like proteins of cyst nematodes modulate the activation of basal plant innate immunity by cell surface receptors. PLoS Pathog. 2014; 10:e1004569

[26]

Xu W, Meng Y, Wise RP. Mla- and Rom1-mediated control of microRNA398 and chloroplast copper/zinc superoxide dismutase regulates cell death in response to the barley powdery mildew fungus. New Phytol. 2014; 201: 1396-412

[27]

Ishiga Y, Ishiga T, Wangdi T. et al. NTRC and chloroplast-generated reactive oxygen species regulate Pseudomonas syringae pv. tomato disease development in tomato and Arabidopsis. Mol Plant-Microbe Interact. 2012; 25: 294-306

[28]

Wang X, Jiang Z, Yue N. et al. Barley stripe mosaic virus γ b protein disrupts chloroplast antioxidant defenses to optimize viral replication. EMBO J. 2021; 40:e107660

[29]

Garcia-Molina A, Altmann M, Alkofer A. et al. LSU network hubs integrate abiotic and biotic stress responses via inter-action with the superoxide dismutase FSD2. J Exp Bot. 2017; 68:1185-97

[30]

Fu Q, Chen T, Wang Y. et al. Plasmopara viticola effector PvCRN20 represses the import of VvDEG5 into chloroplasts to suppress immunity in grapevine. New Phytol. 2024; 243: 2311-31

[31]

Li X, Liu Y, He Q. et al. A candidate secreted effector protein of rubber tree powdery mildew fungus contributes to infec-tion by regulating plant ABA biosynthesis. Front Microbiol. 2020; 11:591387

[32]

Jelenska J, van Hal JA, Greenberg JT. Pseudomonas syringae hijacks plant stress chaperone machinery for virulence. Proc Natl Acad Sci USA. 2010; 107:13177-82

[33]

Sarris PF, Duxbury Z, Huh SU. et al. A plant immune receptor detects pathogen effectors that target WRKY transcription fac-tors. Cell. 2015; 161:1089-100

[34]

Li G, Froehlich JE, Elowsky C. et al. Distinct Pseudomonas type-III effectors use a cleavable transit peptide to target chloroplasts. Plant J. 2013; 77:310-21

[35]

Cao B, Wang J, Ma J. et al. Large-scale screening and function analysis of Rhizoctonia solani effectors targeting rice chloro-plasts. J Agric Food Chem. 2024; 72:24336-46

[36]

Gong X, Su Q, Lin D. et al. The rice OsV4 encoding a novel pentatricopeptide repeat protein is required for chloroplast development during the early leaf stage under cold stress. J Integr Plant Biol. 2014; 56:400-10

[37]

Gao C, Xu H, Huang J. et al. Pathogen manipulation of chloro-plast function triggers a light-dependent immune recogni-tion. Proc Natl Acad Sci USA. 2020; 117:9613-20

[38]

Chang J, Mapuranga J, Wang X. et al. A thaumatin-like effector protein suppresses the rust resistance of wheat and promotes the pathogenicity of Puccinia triticina by targeting TaRCA. New Phytol. 2024; 244:1947-60

[39]

Song L, Yang T, Wang X. et al. Magnaporthe oryzae effector AvrPik-D targets rice rubisco small subunit OsRBCS 4 to sup-press immunity. Plants (Basel). 2024; 13:1214

[40]

Qi Y, Wu J, Yang Z. et al. Chloroplast elongation factors break the growth-immunity trade-off by simultaneously promoting yield and defence. Nat Plants. 2024; 10:1576-91

[41]

Liu T, Song T, Zhang X. et al. Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis. Nat Commun. 2014; 5:4686

[42]

Shen N, Lu C, Wen Y. et al. The Magnaporthe oryzae effec-tor MoCHT1 targets and stabilizes rice OsLLB to suppress jasmonic acid synthesis and enhance infection. J Genet Genomics. 2025; 52:1387-1400.

[43]

Shang S, Liang X, Liu G. et al. A fungal effector suppresses plant immunity by manipulating DAHPS-mediated metabolic flux in chloroplasts. New Phytol. 2024; 244:1552-69

[44]

Miao Y, Wu L, Xue Q. et al. Ralstonia solanacearum type III effector RipAA targets chloroplastic AtpB to modulate an incompatible interaction on Nicotiana benthamiana. Front Microbiol. 2023; 14:1179824

[45]

Seo EY, Nam J, Kim HS. et al. Selective interaction between chloroplast beta-ATPase and TGB1L88 retards severe symp-toms caused by Alternanthera mosaic virus infection. Plant Pathol J. 2014; 30:58-67

[46]

Zhang R, Wu Y, Qu X. et al. The RING-finger ubiquitin E3 ligase TaPIR1 targets TaHRP1 for degradation to suppress chloro-plast function. Nat Commun. 2024; 15:6905

[47]

Caplan JL, Kumar AS, Park E. et al. Chloroplast stromules function during innate immunity. Dev Cell. 2015; 34: 45-57

[48]

Savage Z, Duggan C, Toufexi A. et al. Chloroplasts alter their morphology and accumulate at the pathogen inter-face during infection by Phytophthora infestans. Plant J. 2021; 107:1771-87

[49]

Letanneur C, Brisson A, Bisaillon M. et al. Host-specific and homologous pairs of Melampsora larici-populina effectors unveil novel Nicotiana benthamiana stromule induction fac-tors. Mol Plant-Microbe Interact. 2024; 37:277-89

[50]

Schultink A, Qi T, Lee A. et al. Roq1 mediates recognition of the Xanthomonas and Pseudomonas effector proteins XopQ and HopQ1. Plant J. 2017; 92:787-95

[51]

Meier ND, Seward K, Caplan JL. et al. Calponin homology domain containing kinesin, KIS1, regulates chloroplast stro-mule formation and immunity. Sci Adv. 2023; 9:17

[52]

Erickson JL, Adlung N, Lampe C. et al. The Xanthomonas effector XopL uncovers the role of microtubules in stromule extension and dynamics in Nicotiana benthamiana. Plant J. 2018; 93:856-70

[53]

Pecrix Y, Buendia L, Penouilh-Suzette C. et al. Sunflower resistance to multiple downy mildew pathotypes revealed by recognition of conserved effectors of the oomycete Plas-mopara halstedii. Plant J. 2019; 97:730-48

[54]

Ding X, Jimenez-Gongora T, Krenz B. et al. Chloroplast clus-tering around the nucleus is a general response to pathogen perception in Nicotiana benthamiana. Mol Plant Pathol. 2019; 20:1298-306

[55]

Chen Y, Zhao J, Wang J. et al. RepA protein of citrus chlorotic dwarf-associated virus impairs perinuclear chloroplast clus-tering induced by lemon chloroplast malate dehydrogenase.Mol. Plant Pathol. 2025; 26:e70133

[56]

Hanson MR, Conklin PL. Stromules, functional extensions of plastids within the plant cell. Curr Opin Plant Biol. 2020; 58:25-32

[57]

Prautsch J, Erickson JL, Özyürek S. et al. Effector XopQ-induced stromule formation in Nicotiana benthamiana depends on ETI signaling components ADR1 and NRG1. Plant Physiol. 2023; 191:161-76

[58]

Zhai Y, Yuan Q, Qiu S. et al. Turnip mosaic virus impairs perin-uclear chloroplast clustering to facilitate viral infection. Plant Cell Environ. 2021; 44:3681-99

[59]

Han K, Zheng H, Yan D. et al. Pepper mild mottle virus coat pro-tein interacts with pepper chloroplast outer envelope mem-brane protein OMP24 to inhibit antiviral immunity in plants. Hortic Res. 2023;10:uhad046

[60]

Barton KA, Wozny MR, Mathur N. et al. Chloroplast behaviour and interactions with other organelles in Arabidopsis thaliana pavement cells. J Cell Sci. 2018;131:jcs202275

PDF (1285KB)

369

Accesses

0

Citation

Detail

Sections
Recommended

/