과제정보
This research was supported by grants from the Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, and Forestry (120080-05-1-HD030), funded by the Ministry of Agriculture, Food and Rural Affairs, Republic of Korea. JB was supported by a research fellowship from the Brain Korea 21 Four Program.
참고문헌
- Abbink, T. E. M., Peart, J. R., Mos, T. N. M., Baulcombe, D. C., Bol, J. F. and Linthorst, H. J. M. 2002. Silencing of a gene encoding a protein component of the oxygen-evolving complex of photosystem II enhances virus replication in plants. Virology 295:307-319. https://doi.org/10.1006/viro.2002.1332
- Ahlquist, P. 2002. RNA-dependent RNA polymerases, viruses, and RNA silencing. Science 296:1270-1273. https://doi.org/10.1126/science.1069132
- Ahlquist, P., Noueiry, A. O., Lee, W.-M., Kushner, D. B. and Dye, B. T. 2003. Host factors in positive-strand RNA virus genome replication. J. Virol. 77:8181-8186. https://doi.org/10.1128/JVI.77.15.8181-8186.2003
- Alazem, M., He, M.-H., Moffett, P. and Lin, N.-S. 2017. Abscisic acid induces resistance against bamboo mosaic virus through Argonaute 2 and 3. Plant Physiol. 174:339-355. https://doi.org/10.1104/pp.16.00015
- Alazem, M., Kim, K.-H. and Lin, N.-S. 2019. Effects of abscisic acid and salicylic acid on gene expression in the antiviral RNA silencing pathway in Arabidopsis. Int. J. Mol. Sci. 20:2538.
- Alazem, M. and Lin, N.-S. 2015. Roles of plant hormones in the regulation of host-virus interactions. Mol. Plant Pathol.16:529-540. https://doi.org/10.1111/mpp.12204
- Alazem, M., Tseng, K.-C., Chang, W.-C., Seo, J.-K. and Kim, K.- H. 2018. Elements involved in the Rsv3-mediated extreme resistance against an avirulent strain of soybean mosaic virus. Viruses 10:581.
- Allan, A. C., Lapidot, M., Culver, J. N. and Fluhr, R. 2001. An early tobacco mosaic virus-induced oxidative burst in tobacco indicates extracellular perception of the virus coat protein. Plant Physiol. 126:97-108. https://doi.org/10.1104/pp.126.1.97
- Asada, K. 2006. Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiol. 141:391-396. https://doi.org/10.1104/pp.106.082040
- Balasubramaniam, M., Kim, B.-S., Hutchens-Williams, H. M. and Loesch-Fries, L. S. 2014. The photosystem II oxygenevolving complex protein PsbP interacts with the coat protein of alfalfa mosaic virus and inhibits virus replication. Mol. Plant-Microbe Interact. 27:1107-1118. https://doi.org/10.1094/MPMI-02-14-0035-R
- Bhat, S., Folimonova, S. Y., Cole, A. B., Ballard, K. D., Lei, Z., Watson, B. S., Sumner, L. W. and Nelson R. S. 2013. Influence of host chloroplast proteins on tobacco mosaic virus accumulation and intercellular movement. Plant Physiol. 161:134-147. https://doi.org/10.1104/pp.112.207860
- Bhattacharyya, D. and Chakraborty, S. 2018. Chloroplast: the Trojan horse in plant-virus interaction. Mol. Plant Pathol. 19:504-518. https://doi.org/10.1111/mpp.12533
- Boatwright, J. L. and Pajerowska-Mukhtar, K. 2013. Salicylic acid: an old hormone up to new tricks. Mol. Plant Pathol. 14:623-634. https://doi.org/10.1111/mpp.12035
- Bobik, K. and Burch-Smith, T. M. 2015. Chloroplast signaling within, between and beyond cells. Front. Plant Sci. 6:781.
- Budziszewska, M. and Obrepalska-Steplowska, A. 2018. The role of the chloroplast in the replication of positive-sense singlestranded plant RNA viruses. Front. Plant Sci. 9:1776.
- Burgyan, J., Rubino, L. and Russo, M. 1996. The 5'-terminal region of a tombusvirus genome determines the origin of multivesicular bodies. J. Gen. Virol. 77:1967-1974. https://doi.org/10.1099/0022-1317-77-8-1967
- Bwalya, J., Alazem, M. and Kim, K.-H. 2022. Photosynthesisrelated genes induce resistance against soybean mosaic virus: evidence for involvement of the RNA silencing pathway. Mol. Plant Pathol. 23:543-560. https://doi.org/10.1111/mpp.13177
- Calil, I. P. and Fontes, E. P. B. 2017. Plant immunity against viruses: antiviral immune receptors in focus. Ann. Bot. 119:711-723. https://doi.org/10.1093/aob/mcw200
- Caplan, J. L., Mamillapalli, P., Burch-Smith, T. M., Czymmek, K. and Dinesh-Kumar, S. P. 2008. Chloroplastic protein NRIP1 mediates innate immune receptor recognition of a viral effector. Cell 132:449-462. https://doi.org/10.1016/j.cell.2007.12.031
- Cheng, D.-J., Xu, X.-J., Yan, Z.-Y., Tettey, C. K., Fang, L., Yang, G.-L., Geng. C., Tian Y.-P. and Li, X.-D. 2021. The chloroplast ribosomal protein large subunit 1 interacts with viral polymerase and promotes virus infection. Plant Physiol. 187:174-186. https://doi.org/10.1093/plphys/kiab249
- Cheng, S.-F., Huang, Y.-P., Chen, L.-H., Hsu, Y.-H. and Tsai, C.-H. 2013. Chloroplast phosphoglycerate kinase is involved in the targeting of bamboo mosaic virus to chloroplasts in Nicotiana benthamiana plants. Plant Physiol. 163:1598-1608. https://doi.org/10.1104/pp.113.229666
- Cheng, Y.-Q., Liu, Z.-M., Xu, J., Zhou, T., Wang, M., Chen, Y.-T., Li, H.-F. and Fan, Z.-F. 2008. HC-Pro protein of sugar cane mosaic virus interacts specifically with maize ferredoxin-5 in vitro and in planta. J. Gen. Virol. 89:2046-2054. https://doi.org/10.1099/vir.0.2008/001271-0
- Cowan, G. H., Roberts, A. G., Chapman, S. N., Ziegler, A., Savenkov, E. I. and Torrance, L. 2012. The potato mop-top virus TGB2 protein and viral RNA associate with chloroplasts and viral infection induces inclusions in the plastids. Front. Plant Sci. 3:290.
- De Graaff, M., Coscoy, L. and Jaspars, E. M. J. 1993. Localization and biochemical characterization of alfalfa mosaic virus replication complexes. Virology 194:878-881. https://doi.org/10.1006/viro.1993.1335
- den Boon, J. A., Diaz, A. and Ahlquist, P. 2010. Cytoplasmic viral replication complexes. Cell Host Microbe 8:77-85. https://doi.org/10.1016/j.chom.2010.06.010
- Diez, J., Ishikawa, M., Kaido, M. and Ahlquist, P. 2000. Identification and characterization of a host protein required for efficient template selection in viral RNA replication. Proc. Natl. Acad. Sci. U. S. A. 97:3913-3918. https://doi.org/10.1073/pnas.080072997
- Dreher, T. W. 1999. Functions of the 3'-untranslated regions of positive strand RNA viral genomes. Annu. Rev. Phytopathol. 37:151-174. https://doi.org/10.1146/annurev.phyto.37.1.151
- Dreher, T. W. and Miller, W. A. 2006. Translational control in positive strand RNA plant viruses. Virology 344:185-197. https://doi.org/10.1016/j.virol.2005.09.031
- Gadh, I. P. S. and Hari, V. 1986. Association of tobacco etch virus related RNA with chloroplasts in extracts of infected plants. Virology 150:304-307. https://doi.org/10.1016/0042-6822(86)90292-8
- Ganusova, E. E., Rice, J. H., Carlew, T. S., Patel, A., Perrodin-Njoku, E., Hewezi, T. and Burch-Smith, T. M. 2017. Altered expression of a chloroplast protein affects the outcome of virus and nematode infection. Mol. Plant-Microbe Interact. 30:478-488. https://doi.org/10.1094/MPMI-02-17-0031-R
- Garcia-Marcos, A., Pacheco, R., Manzano, A., Aguilar, E. and Tenllado, F. 2013. Oxylipin biosynthesis genes positively regulate programmed cell death during compatible infections with the synergistic pair potato virus X-potato virus Y and tomato spotted wilt virus. Virol. J. 87:5769-5783. https://doi.org/10.1128/JVI.03573-12
- Hafren, A., Hofius, D., Ronnholm, G., Sonnewald, U. and Makinen, K. 2010. HSP70 and its cochaperone CPIP promote potyvirus infection in Nicotiana benthamiana by regulating viral coat protein functions. Plant Cell 22:523-535. https://doi.org/10.1105/tpc.109.072413
- Hakmaoui, A., Perez-Bueno, M. L., Garcia-Fontana, B., Camejo, D., Jimenez, A., Sevilla, F. and Baron, M. 2012. Analysis of the antioxidant response of Nicotiana benthamiana to infection with two strains of pepper mild mottle virus. J. Exp. Bot. 63:5487-5496. https://doi.org/10.1093/jxb/ers212
- Hatta, T., Bullivant, S. and Matthews, R. E. 1973. Fine structure of vesicles induced in chloroplasts of Chinese cabbage leaves by infection with turnip yellow mosaic virus. J. Gen. Virol. 20:37-50. https://doi.org/10.1099/0022-1317-20-1-37
- Hilaire, J., Tindale, S., Jones, G., Pingarron-Cardenas, G., Bacnik, K., Ojo, M. and Frewer, L. J. 2022. Risk perception associated with an emerging agri-food risk in Europe: plant viruses in agriculture. Agric. Food Secur. 11:21.
- Hyodo, K. and Okuno, T. 2016. Pathogenesis mediated by proviral host factors involved in translation and replication of plant positive-strand RNA viruses. Curr. Opin. Virol. 17:11-18. https://doi.org/10.1016/j.coviro.2015.11.004
- Jakubiec, A., Notaise, J., Tournier, V., Hericourt, F., Block, M. A., Drugeon, G., van Aelst, L. and Jupin, I. 2004. Assembly of turnip yellow mosaic virus replication complexes: interaction between the proteinase and polymerase domains of the replication proteins. J. Virol. 78:7945-7957. https://doi.org/10.1128/JVI.78.15.7945-7957.2004
- Jang, C., Seo, E.-Y., Nam, J., Bae, H., Gim, Y. G., Kim, H. G., Cho, I. S., Lee, Z.-W., Bauchan, G. R., Hammond, J. and Lim, H.-S. 2013. Insights into alternanthera mosaic virus TGB3 functions: interactions with Nicotiana benthamiana PsbO correlate with chloroplast vesiculation and veinal necrosis caused by TGB3 over-expression. Front. Plant Sci. 4:5.
- Jimenez, I., Lopez, L., Alamillo, J. M., Valli, A. and Garcia, J. A. 2006. Identification of a plum pox virus CI-interacting protein from chloroplast that has a negative effect in virus infection. Mol. Plant-Microbe Interact. 19:350-358. https://doi.org/10.1094/MPMI-19-0350
- Jin, X., Jiang, Z., Zhang, K., Wang, P., Cao, X., Yue, N., Wang, X., Zhang, X., Li, Y., Li, D. Kang, B.-H. and Zhang, Y. 2017. Three-dimensional analysis of chloroplast structures associated with virus infection. Plant Physiol. 176:282-294. https://doi.org/10.1104/pp.17.00871
- Jin, Y., Ma, D., Dong, J., Li, D., Deng, C., Jin, J. and Wang, T. 2007. The HC-pro protein of potato virus Y interacts with NtMinD of tobacco. Mol. Plant-Microbe Interact. 20:1505-1511. https://doi.org/10.1094/MPMI-20-12-1505
- Jones, R. A. C. and Naidu, R. A. 2019. Global dimensions of plant virus diseases: current status and future perspectives. Annu. Rev. Virol. 6:387-409. https://doi.org/10.1146/annurev-virology-092818-015606
- Jungfleisch, J., Chowdhury, A., Alves-Rodrigues, I., Tharun, S. and Diez, J. 2015. The Lsm1-7-Pat1 complex promotes viral RNA translation and replication by differential mechanisms. RNA 21:1469-1479. https://doi.org/10.1261/rna.052209.115
- Kaido, M., Abe, K., Mine, A., Hyodo, K., Taniguchi, T., Taniguchi, H., Mise, K. and Okuno, T. 2014. GAPDH: a recruits a plant virus movement protein to cortical virus replication complexes to facilitate viral cell-to-cell movement. PLoS Pathog. 10:e1004505.
- Kitajima, E. W. and Costa, A. S. 1973. Aggregates of chloroplasts in local lesions induced in Chenopodium quinoa Wild. by turnip mosaic virus. J. Gen. Virol. 20:413-416. https://doi.org/10.1099/0022-1317-20-3-413
- Koonin, E. V. and Dolja, V. V. 1993. Evolution and taxonomy of positive-strand RNA viruses: implications of comparative analysis of amino acid sequences. Crit. Rev. Biochem. Mol. Biol. 28:375-430. https://doi.org/10.3109/10409239309078440
- Kozuleva, M., Klenina, I., Proskuryakov, I., Kirilyuk, I. and Ivanov, B. 2011. Production of superoxide in chloroplast thylakoid membranes: ESR study with cyclic hydroxylamines of different lipophilicity. FEBS Lett. 585:1067-1071. https://doi.org/10.1016/j.febslet.2011.03.004
- Lehto, K., Tikkanen, M., Hiriart, J.-B., Paakkarinen, V. and Aro, E.-M. 2003. Depletion of the photosystem II core complex in mature tobacco leaves infected by the flavum strain of tobacco mosaic virus. Mol. Plant-Microbe Interact. 16:1135-1144. https://doi.org/10.1094/MPMI.2003.16.12.1135
- Li, Y., Cui, H., Cui, X. and Wang, A. 2016. The altered photosynthetic machinery during compatible virus infection. Curr. Opin. Virol. 17:19-24. https://doi.org/10.1016/j.coviro.2015.11.002
- Li, Z., Pogany, J., Panavas, T., Xu, K., Esposito, A. M., Kinzy, T. G. and Nagy P. D. 2009. Translation elongation factor 1A is a component of the tombusvirus replicase complex and affects the stability of the p33 replication co-factor. Virology 385:245-260. https://doi.org/10.1016/j.virol.2008.11.041
- Lin, L., Luo, Z., Yan, F., Lu, Y., Zheng, H. and Chen, J. 2011. Interaction between potyvirus P3 and ribulose-1,5-bisphosphate carboxylase/oxygenase (RubisCO) of host plants. Virus Genes 43:90-92. https://doi.org/10.1007/s11262-011-0596-6
- Martin, M. T., Cervera, M. T., Garcia, J. A. and Bonay, P. 1995. Properties of the active plum pox potyvirus RNA polymerase complex in defined glycerol gradient fractions. Virus Res. 37:127-137. https://doi.org/10.1016/0168-1702(95)00028-O
- Mayhew, D. E. and Ford, R. E. 1974. Detection of ribonucleaseresistant RNA in chloroplasts of corn leaf tissue infected with maize dwarf mosaic virus. Virology 57:503-509. https://doi.org/10.1016/0042-6822(74)90189-5
- Medina-Puche, L., Tan, H., Dogra, V., Wu, M., Rosas-Diaz, T., Wang, L., Ding, X., Zhang, D., Fu, X., Kim, C. and LozanoDuran, R. 2020. A defense pathway linking plasma membrane and chloroplasts and co-opted by pathogens. Cell 182:1109-1124. https://doi.org/10.1016/j.cell.2020.07.020
- Moriceau, L., Jomat, L., Bressanelli, S., Alcaide-Loridan, C. and Jupin, I. 2017. Identification and molecular characterization of the chloroplast targeting domain of turnip yellow mosaic virus replication proteins. Front. Plant Sci. 8:2138.
- Muhlenbock, P., Szechynska-Hebda, M., Plaszczyca, M., Baudo, M., Mateo, A., Mullineaux, P. M., Parker, J. E., Karpinska, B. and Karpinski, S. 2008. Chloroplast signaling and LESION SIMULATING DISEASE1 regulate crosstalk between light acclimation and immunity in Arabidopsis. Plant Cell 20:2339-2356. https://doi.org/10.1105/tpc.108.059618
- Nagy, P. D., Barajas, D. and Pogany, J. 2012. Host factors with regulatory roles in tombusvirus replication. Curr. Opin. Virol. 2:691-698. https://doi.org/10.1016/j.coviro.2012.10.004
- Nagy, P. D. and Pogany, J. 2006. Yeast as a model host to dissect functions of viral and host factors in tombusvirus replication. Virology 344:211-220. https://doi.org/10.1016/j.virol.2005.09.017
- Nagy, P. D. and Pogany, J. 2008a. Host factors promoting viral RNA replication. Viral Genome Replication 1:267-295. https://doi.org/10.1007/b135974_14
- Nagy, P. D. and Pogany, J. 2008b. Multiple roles of viral replication proteins in plant RNA virus replication. Methods Mol. Biol. 451:55-68. https://doi.org/10.1007/978-1-59745-102-4_4
- Nambara, E. and Marion-Poll, A. 2005. Abscisic acid biosynthesis and catabolism. Annu. Rev. Plant Biol. 56:165-185. https://doi.org/10.1146/annurev.arplant.56.032604.144046
- Nishikiori, M., Dohi, K., Mori, M., Meshi, T., Naito, S. and Ishikawa, M. 2006. Membrane-bound tomato mosaic virus replication proteins participate in RNA synthesis and are associated with host proteins in a pattern distinct from those that are not membrane bound. J. Virol. 80:8459-8468. https://doi.org/10.1128/JVI.00545-06
- Nomura, H., Komori, T., Uemura, S., Kanda, Y., Shimotani, K., Nakai, K., Furuichi, T., Takebayashi, K., Sugimoto, T., Sano, S., Suwastika, I. N., Fukusaki, E., Yoshioka, H., Nakahira, Y. and Shiina, T. 2012. Chloroplast-mediated activation of plant immune signalling in Arabidopsis. Nat. Commun. 3:926.
- Noueiry, A. O. and Ahlquist, P. 2003. Brome mosaic virus RNA replication: revealing the role of the host in RNA virus replication. Annu. Rev. Phytopathol. 41:77-98. https://doi.org/10.1146/annurev.phyto.41.052002.095717
- Padmanabhan, M. S. and Dinesh-Kumar, S. P. 2010. All hands on deck: the role of chloroplasts, endoplasmic reticulum, and the nucleus in driving plant innate immunity. Mol. Plant-Microbe Interact. 23:1368-1380. https://doi.org/10.1094/MPMI-05-10-0113
- Panavas, T., Hawkins, C. M., Panaviene, Z. and Nagy, P. D. 2005. The role of the p33:p33/p92 interaction domain in RNA replication and intracellular localization of p33 and p92 proteins of cucumber necrosis tombusvirus. Virology 338:81-95. https://doi.org/10.1016/j.virol.2005.04.025
- Prod'homme, D., Jakubiec, A., Tournier, V., Drugeon, G. and Jupin, I. 2003. Targeting of the turnip yellow mosaic virus 66K replication protein to the chloroplast envelope is mediated by the 140K protein. J. Virol. 77:9124-9135. https://doi.org/10.1128/JVI.77.17.9124-9135.2003
- Prod'homme, D., Le Panse, S., Drugeon, G. and Jupin, I. 2001. Detection and subcellular localization of the turnip yellow mosaic virus 66K replication protein in infected cells. Virology 281:88-101. https://doi.org/10.1006/viro.2000.0769
- Qiao, Y., Li, H. F., Wong, S. M. and Fan, Z. F. 2009. Plastocyanin transit peptide interacts with potato virus X coat protein, while silencing of plastocyanin reduces coat protein accumulation in chloroplasts and symptom severity in host plants. Mol. Plant-Microbe Interact. 22:1523-1534. https://doi.org/10.1094/MPMI-22-12-1523
- Rubio, L., Galipienso, L. and Ferriol, I. 2020. Detection of plant viruses and disease management: relevance of genetic diversity and evolution. Front. Plant Sci. 11:1092.
- Rubino, L. and Russo, M. 1998. Membrane targeting sequences in tombusvirus infections. Virology 252:431-437. https://doi.org/10.1006/viro.1998.9490
- Salesse-Smith, C. E., Sharwood, R. E., Busch, F. A., Kromdijk, J., Bardal, V. and Stern, D. B. 2018. Overexpression of Rubisco subunits with RAF1 increases Rubisco content in maize. Nat. Plants 4:802-810. https://doi.org/10.1038/s41477-018-0252-4
- Salonen, A., Ahola, T. and Kaariainen, L. 2005. Viral RNA replication in association with cellular membranes. Curr. Top. Microbiol. Immunol. 285:139-173.
- Sanfacon, H. 2005. Replication of positive-strand RNA viruses in plants: contact points between plant and virus components. Can. J. Bot. 83:1529-1549. https://doi.org/10.1139/b05-121
- Serrano, I., Audran, C. and Rivas, S. 2016. Chloroplasts at work during plant innate immunity. J. Exp. Bot. 67:3845-3854. https://doi.org/10.1093/jxb/erw088
- Seyfferth, C. and Tsuda, K. 2014. Salicylic acid signal transduction: the initiation of biosynthesis, perception and transcriptional reprogramming. Front. Plant Sci. 5:697.
- Shi, Y., Chen, J., Hong, X., Chen, J. and Adams, M. J. 2007. A potyvirus P1 protein interacts with the Rieske Fe/S protein of its host. Mol Plant Pathol. 8:785-790. https://doi.org/10.1111/j.1364-3703.2007.00426.x
- Shimura, H., Pantaleo, V., Ishihara, T., Myojo, N., Inaba, J.-I., Sueda, K., Burgyan, J. and Masuta, C. 2011. A viral satellite RNA induces yellow symptoms on tobacco by targeting a gene involved in chlorophyll biosynthesis using the RNA silencing machinery. PLoS Pathog. 7:e1002021.
- Simon, A. E. and Miller, W. A. 2013. 3' cap-independent translation enhancers of plant viruses. Annu. Rev. Microbiol. 67:21-42. https://doi.org/10.1146/annurev-micro-092412-155609
- Stael, S., Kmiecik, P., Willems, P., Van der Kelen, K., Coll, N. S., Teige, M. and Van Breusegem, F. 2015. Plant innate immunity: sunny side up? Trends Plant Sci. 20:3-11. https://doi.org/10.1016/j.tplants.2014.10.002
- Thivierge, K., Cotton, S., Dufresne, P. J., Mathieu, I., Beauchemin, C., Ide, C., Fortin, M. G. and Laliberte, J.-F. 2008. Eukaryotic elongation factor 1A interacts with turnip mosaic virus RNA-dependent RNA polymerase and VPg-Pro in virusinduced vesicles. Virology 377:216-225. https://doi.org/10.1016/j.virol.2008.04.015
- Torres, M. A., Jones, J. D. G. and Dangl, J. L. 2006. Reactive oxygen species signaling in response to pathogens. Plant Physiol. 141:373-378. https://doi.org/10.1104/pp.106.079467
- Turner, J. G., Ellis, C. and Devoto, A. 2002. The jasmonate signal pathway. Plant Cell 14(Suppl):S153-S164. https://doi.org/10.1105/tpc.000679
- Wang, B., Li, Z., Ran, Q., Li, P., Peng, Z. and Zhang, J. 2018. ZmNF-YB16 overexpression improves drought resistance and yield by enhancing photosynthesis and the antioxidant capacity of maize plants. Front. Plant Sci. 9:709.
- Wasternack, C. and Hause, B. 2013. Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development: an update to the 2007 review in Annals of Botany. Ann. Bot. 111:1021-1058. https://doi.org/10.1093/aob/mct067
- Wei, T., Zhang, C., Hou, X., Sanfacon, H. and Wang, A. 2013. The SNARE protein Syp71 is essential for turnip mosaic virus infection by mediating fusion of vrus-induced vesicles with chloroplasts. PLoS Pathog. 9:e1003378.
- Whitfield, A. E., Falk, B. W. and Rotenberg, D. 2015. Insect vector-mediated transmission of plant viruses. Virology 479- 480:278-289. https://doi.org/10.1016/j.virol.2015.03.026
- Widyasari, K., Alazem, M. and Kim, K.-H. 2020. Soybean resistance to soybean mosaic virus. Plants 9:219.
- Widyasari, K., Tran, P.-T., Shin, J., Son, H. and Kim, K.-H. 2022. Overexpression of purple acid phosphatase GmPAP2.1 confers resistance to soybean mosaic virus in a susceptible soybean cultivar. J. Exp. Bot. 73:1623-1642. https://doi.org/10.1093/jxb/erab496
- Wildermuth, M. C., Dewdney, J., Wu, G. and Ausubel, F. M. 2001. Isochorismate synthase is required to synthesize salicylic acid for plant defense. Nature 414:562-565. https://doi.org/10.1038/35107108
- Wu, J., Yang, R., Yang, Z., Yao, S., Zhao, S., Wang. Y. Li, P., Song, X., Jin, L., Zhou, T., Lan, Y., Xie, L., Zhou, X., Chu, C., Qi, Y., Cao, X. and Li, Y. 2017. ROS accumulation and antiviral defense control by microRNA528 in rice. Nat. Plants 3:16203.
- Xu, K. and Nagy, P. D. 2014. Expanding use of multi-origin subcellular membranes by positive-strand RNA viruses during replication. Curr. Opin. Virol. 9:119-126. https://doi.org/10.1016/j.coviro.2014.09.015
- Yang, F., Xiao, K., Pan, H. and Liu, J. 2021. Chloroplast: the emerging battlefield in plant-microbe interactions. Front. Plant Sci. 12:637853.
- Zhai, Y., Yuan, Q., Qiu, S., Li, S., Li, M., Zheng, H., Wu, G., Lu, Y., Peng, J., Rao, S., Chen, J. and Yan, F. 2021. Turnip mosaic virus impairs perinuclear chloroplast clustering to facilitate viral infection. Plant Cell Environ. 44:3681-3699. https://doi.org/10.1111/pce.14157
- Zhang, C., Grosic, S., Whitham, S. A. and Hill, J. H. 2012. The requirement of multiple defense genes in soybean Rsv1-mediated extreme resistance to soybean mosaic virus. Mol. Plant-Microbe Interact. 25:1307-1313. https://doi.org/10.1094/MPMI-02-12-0046-R
- Zhao, J., Liu, Q., Zhang, H., Jia, Q., Hong, Y. and Liu, Y. 2013. The RubisCO small subunit is involved in tobamovirus movement and Tm-22-mediated extreme resistance. Plant Physiol. 161:374-383.
- Zhao, J., Xu, J., Chen, B., Cui, W., Zhou, Z., Song, X, Chen, Z., Zheng, H., Lin, L., Peng, J., Lu, Y., Deng, Z., Chen, J. and Yan, F. 2019. Characterization of proteins involved in chloroplast targeting disturbed by rice stripe virus by novel protoplast-chloroplast proteomics. Int. J. Mol. Sci. 20:253.
- Zhao, J., Zhang, X., Hong, Y. and Liu, Y. 2016. Chloroplast in plant-virus interaction. Front. Microbiol. 7:1565.
- Zurbriggen, M. D., Carrillo, N. and Hajirezaei, M.-R. 2010. ROS signaling in the hypersensitive response: when, where and what for? Plant Signal. Behav. 5:393-396. https://doi.org/10.4161/psb.5.4.10793