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The resistance of sour orange to Citrus tristeza virus is mediated by both the salicylic acid and RNA silencing defence pathways

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The resistance of sour orange to Citrus tristeza virus is mediated by both the salicylic acid and RNA silencing defence pathways

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Gomez-Muñoz, N.; Velazquez, K.; Vives, M.; Ruiz-Ruiz, S.; Pina, J.; Flores Pedauye, R.; Moreno, P.... (2017). The resistance of sour orange to Citrus tristeza virus is mediated by both the salicylic acid and RNA silencing defence pathways. Molecular Plant Pathology. 18(9):1253-1266. https://doi.org/10.1111/mpp.12488

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Título: The resistance of sour orange to Citrus tristeza virus is mediated by both the salicylic acid and RNA silencing defence pathways
Autor: Gomez-Muñoz, Neus Velazquez, K. Vives, M.C. Ruiz-Ruiz, Susana Pina, J.A. FLORES PEDAUYE, RICARDO Moreno, P. Guerri, J.
Entidad UPV: Universitat Politècnica de València. Instituto Universitario Mixto de Biología Molecular y Celular de Plantas - Institut Universitari Mixt de Biologia Molecular i Cel·lular de Plantes
Fecha difusión:
Resumen:
[EN] Citrus tristeza virus (CTV) induces in the field the decline and death of citrus varieties grafted on sour orange (SO) rootstock, which has forced the use of alternative decline-tolerant rootstocks in affected countries, ...[+]
Palabras clave: Citrus decline , CLBV , Reverse genetics , Salicylic acid signalling defence suppressor , Viral vector
Derechos de uso: Cerrado
Fuente:
Molecular Plant Pathology. (issn: 1464-6722 )
DOI: 10.1111/mpp.12488
Editorial:
Blackwell Publishing
Versión del editor: https://doi.org/10.1111/mpp.12488
Código del Proyecto:
info:eu-repo/grantAgreement/MINECO//AGL2012-32429/ES/DESARROLLO DE METODOS AVANZADOS PARA LA MEJORA SANITARIA Y GENETICA DE LOS CITRICOS/
Agradecimientos:
This work was supported by grant AGL2012-32429, co-financed by ERDF (European Regional Development Fund) and the Spanish Ministerio de Economia y Competitividad (MINECO). We thank Dr W. O. Dawson for providing the GFP-tagged ...[+]
Tipo: Artículo

References

Agüero, J., Ruiz-Ruiz, S., del Carmen Vives, M., Velázquez, K., Navarro, L., Peña, L., … Guerri, J. (2012). Development of Viral Vectors Based on Citrus leaf blotch virus to Express Foreign Proteins or Analyze Gene Function in Citrus Plants. Molecular Plant-Microbe Interactions®, 25(10), 1326-1337. doi:10.1094/mpmi-02-12-0048-r

Agüero, J., Vives, M. C., Velázquez, K., Ruiz-Ruiz, S., Juárez, J., Navarro, L., … Guerri, J. (2013). Citrus leaf blotch virusinvades meristematic regions inNicotiana benthamianaand citrus. Molecular Plant Pathology, 14(6), 610-616. doi:10.1111/mpp.12031

Agüero, J., Vives, M. del C., Velázquez, K., Pina, J. A., Navarro, L., Moreno, P., & Guerri, J. (2014). Effectiveness of gene silencing induced by viral vectors based on Citrus leaf blotch virus is different in Nicotiana benthamiana and citrus plants. Virology, 460-461, 154-164. doi:10.1016/j.virol.2014.04.017 [+]
Agüero, J., Ruiz-Ruiz, S., del Carmen Vives, M., Velázquez, K., Navarro, L., Peña, L., … Guerri, J. (2012). Development of Viral Vectors Based on Citrus leaf blotch virus to Express Foreign Proteins or Analyze Gene Function in Citrus Plants. Molecular Plant-Microbe Interactions®, 25(10), 1326-1337. doi:10.1094/mpmi-02-12-0048-r

Agüero, J., Vives, M. C., Velázquez, K., Ruiz-Ruiz, S., Juárez, J., Navarro, L., … Guerri, J. (2013). Citrus leaf blotch virusinvades meristematic regions inNicotiana benthamianaand citrus. Molecular Plant Pathology, 14(6), 610-616. doi:10.1111/mpp.12031

Agüero, J., Vives, M. del C., Velázquez, K., Pina, J. A., Navarro, L., Moreno, P., & Guerri, J. (2014). Effectiveness of gene silencing induced by viral vectors based on Citrus leaf blotch virus is different in Nicotiana benthamiana and citrus plants. Virology, 460-461, 154-164. doi:10.1016/j.virol.2014.04.017

Alamillo, J. M., Saénz, P., & García, J. A. (2006). Salicylic acid-mediated and RNA-silencing defense mechanisms cooperate in the restriction of systemic spread of plum pox virus in tobacco. The Plant Journal, 48(2), 217-227. doi:10.1111/j.1365-313x.2006.02861.x

Albiach-Marti, M. R., Grosser, J. W., Gowda, S., Mawassi, M., Satyanarayana, T., Garnsey, S. M., & Dawson, W. O. (2004). Citrus tristeza virus replicates and forms infectious virions in protoplasts of resistant citrus relatives. Molecular Breeding, 14(2), 117-128. doi:10.1023/b:molb.0000038000.51218.a7

ALBIACH-MARTI, M. R., ROBERTSON, C., GOWDA, S., TATINENI, S., BELLIURE, B., GARNSEY, S. M., … DAWSON, W. O. (2010). The pathogenicity determinant ofCitrus tristeza viruscausing the seedling yellows syndrome maps at the 3â ²-terminal region of the viral genome. Molecular Plant Pathology, 11(1), 55-67. doi:10.1111/j.1364-3703.2009.00572.x

Ancillo, G., Gadea, J., Forment, J., Guerri, J., & Navarro, L. (2007). Class prediction of closely related plant varieties using gene expression profiling. Journal of Experimental Botany, 58(8), 1927-1933. doi:10.1093/jxb/erm054

Andika, I. B., Kondo, H., & Tamada, T. (2005). Evidence That RNA Silencing-Mediated Resistance to Beet necrotic yellow vein virus Is Less Effective in Roots Than in Leaves. Molecular Plant-Microbe Interactions®, 18(3), 194-204. doi:10.1094/mpmi-18-0194

Andika, I. B., Sun, L., Xiang, R., Li, J., & Chen, J. (2013). Root-Specific Role for Nicotiana benthamiana RDR6 in the Inhibition of Chinese wheat mosaic virus Accumulation at Higher Temperatures. Molecular Plant-Microbe Interactions®, 26(10), 1165-1175. doi:10.1094/mpmi-05-13-0137-r

Angel, C. A., & Schoelz, J. E. (2013). A Survey of Resistance to Tomato bushy stunt virus in the Genus Nicotiana Reveals That the Hypersensitive Response Is Triggered by One of Three Different Viral Proteins. Molecular Plant-Microbe Interactions®, 26(2), 240-248. doi:10.1094/mpmi-06-12-0157-r

Asins, M. J., Bernet, G. P., Ruiz, C., Cambra, M., Guerri, J., & Carbonell, E. A. (2003). QTL analysis of citrus tristeza virus-citradia interaction. Theoretical and Applied Genetics, 108(4), 603-611. doi:10.1007/s00122-003-1486-7

Baebler, Š., Witek, K., Petek, M., Stare, K., Tušek-Žnidarič, M., Pompe-Novak, M., … Hennig, J. (2014). Salicylic acid is an indispensable component of the Ny-1 resistance-gene-mediated response against Potato virus Y infection in potato. Journal of Experimental Botany, 65(4), 1095-1109. doi:10.1093/jxb/ert447

Baulcombe, D. (2004). RNA silencing in plants. Nature, 431(7006), 356-363. doi:10.1038/nature02874

Burch-Smith, T. M., Anderson, J. C., Martin, G. B., & Dinesh-Kumar, S. P. (2004). Applications and advantages of virus-induced gene silencing for gene function studies in plants. The Plant Journal, 39(5), 734-746. doi:10.1111/j.1365-313x.2004.02158.x

Campos, L., Granell, P., Tárraga, S., López-Gresa, P., Conejero, V., Bellés, J. M., … Lisón, P. (2014). Salicylic acid and gentisic acid induce RNA silencing-related genes and plant resistance to RNA pathogens. Plant Physiology and Biochemistry, 77, 35-43. doi:10.1016/j.plaphy.2014.01.016

Cervera, M., Navarro, A., Navarro, L., & Pena, L. (2008). Production of transgenic adult plants from clementine mandarin by enhancing cell competence for transformation and regeneration. Tree Physiology, 28(1), 55-66. doi:10.1093/treephys/28.1.55

Comellas , M. 2009

Csorba, T., Kontra, L., & Burgyán, J. (2015). viral silencing suppressors: Tools forged to fine-tune host-pathogen coexistence. Virology, 479-480, 85-103. doi:10.1016/j.virol.2015.02.028

Dawson, W. O., Bar-Joseph, M., Garnsey, S. M., & Moreno, P. (2015). Citrus Tristeza Virus: Making an Ally from an Enemy. Annual Review of Phytopathology, 53(1), 137-155. doi:10.1146/annurev-phyto-080614-120012

Dean, J. D., Goodwin, P. H., & Hsiang, T. (2005). Induction of glutathione S-transferase genes of Nicotiana benthamiana following infection by Colletotrichum destructivum and C. orbiculare and involvement of one in resistance. Journal of Experimental Botany, 56(416), 1525-1533. doi:10.1093/jxb/eri145

Deleris, A., Gallego-Bartolome, J., Bao, J., Kasschau, K. D., Carrington, J. C., & Voinnet, O. (2006). Hierarchical Action and Inhibition of Plant Dicer-Like Proteins in Antiviral Defense. Science, 313(5783), 68-71. doi:10.1126/science.1128214

Dong, X. (2004). NPR1, all things considered. Current Opinion in Plant Biology, 7(5), 547-552. doi:10.1016/j.pbi.2004.07.005

FAGOAGA, C., PENSABENE-BELLAVIA, G., MORENO, P., NAVARRO, L., FLORES, R., & PEÑA, L. (2011). Ectopic expression of the p23 silencing suppressor of Citrus tristeza virus differentially modifies viral accumulation and tropism in two transgenic woody hosts. Molecular Plant Pathology, 12(9), 898-910. doi:10.1111/j.1364-3703.2011.00722.x

Folimonova, S. Y., Folimonov, A. S., Tatineni, S., & Dawson, W. O. (2008). Citrus Tristeza Virus: Survival at the Edge of the Movement Continuum. Journal of Virology, 82(13), 6546-6556. doi:10.1128/jvi.00515-08

Fu, Z. Q., & Dong, X. (2013). Systemic Acquired Resistance: Turning Local Infection into Global Defense. Annual Review of Plant Biology, 64(1), 839-863. doi:10.1146/annurev-arplant-042811-105606

Fu, Z. Q., Yan, S., Saleh, A., Wang, W., Ruble, J., Oka, N., … Dong, X. (2012). NPR3 and NPR4 are receptors for the immune signal salicylic acid in plants. Nature, 486(7402), 228-232. doi:10.1038/nature11162

Galipienso, L., Navarro, L., Ballester-Olmos, J. F., Pina, J. A., Moreno, P., & Guerri, J. (2000). Host range and symptomatology of a graft-transmissible pathogen causing bud union crease of citrus on trifoliate rootstocks. Plant Pathology, 49(2), 308-314. doi:10.1046/j.1365-3059.2000.00449.x

Gandía, M., Conesa, A., Ancillo, G., Gadea, J., Forment, J., Pallás, V., … Guerri, J. (2007). Transcriptional response of Citrus aurantifolia to infection by Citrus tristeza virus. Virology, 367(2), 298-306. doi:10.1016/j.virol.2007.05.025

Garcia-Ruiz, H., Takeda, A., Chapman, E. J., Sullivan, C. M., Fahlgren, N., Brempelis, K. J., & Carrington, J. C. (2010). Arabidopsis RNA-Dependent RNA Polymerases and Dicer-Like Proteins in Antiviral Defense and Small Interfering RNA Biogenesis during Turnip Mosaic Virus Infection. The Plant Cell, 22(2), 481-496. doi:10.1105/tpc.109.073056

Garnsey, S. M. (1977). Mechanical Transmission of Citrus Tristeza Virus. Phytopathology, 77(8), 965. doi:10.1094/phyto-67-965

Harper, S. J., Cowell, S. J., Robertson, C. J., & Dawson, W. O. (2014). Differential tropism in roots and shoots infected by Citrus tristeza virus. Virology, 460-461, 91-99. doi:10.1016/j.virol.2014.04.035

Ji, L.-H., & Ding, S.-W. (2001). The Suppressor of Transgene RNA Silencing Encoded by Cucumber mosaic virus Interferes with Salicylic Acid-Mediated Virus Resistance. Molecular Plant-Microbe Interactions®, 14(6), 715-724. doi:10.1094/mpmi.2001.14.6.715

Hunter, L. J. R., Westwood, J. H., Heath, G., Macaulay, K., Smith, A. G., MacFarlane, S. A., … Carr, J. P. (2013). Regulation of RNA-Dependent RNA Polymerase 1 and Isochorismate Synthase Gene Expression in Arabidopsis. PLoS ONE, 8(6), e66530. doi:10.1371/journal.pone.0066530

Jovel, J., Walker, M., & Sanfaçon, H. (2011). Salicylic Acid-Dependent Restriction of Tomato ringspot virus Spread in Tobacco Is Accompanied by a Hypersensitive Response, Local RNA Silencing, and Moderate Systemic Resistance. Molecular Plant-Microbe Interactions®, 24(6), 706-718. doi:10.1094/mpmi-09-10-0224

Laino, P., Russo, M. P., Guardo, M., Reforgiato-Recupero, G., Valè, G., Cattivelli, L., & Moliterni, V. M. C. (2015). Rootstock-scion interaction affecting citrus response to CTV infection: a proteomic view. Physiologia Plantarum, 156(4), 444-467. doi:10.1111/ppl.12395

Laird, J., McInally, C., Carr, C., Doddiah, S., Yates, G., Chrysanthou, E., … Milner, J. J. (2013). Identification of the domains of cauliflower mosaic virus protein P6 responsible for suppression of RNA silencing and salicylic acid signalling. Journal of General Virology, 94(12), 2777-2789. doi:10.1099/vir.0.057729-0

Lee, R. F., & Keremane, M. L. (2013). Mild strain cross protection of tristeza: a review of research to protect against decline on sour orange in Florida. Frontiers in Microbiology, 4. doi:10.3389/fmicb.2013.00259

Lee, W.-S., Fu, S.-F., Verchot-Lubicz, J., & Carr, J. P. (2011). Genetic modification of alternative respiration in Nicotiana benthamiana affects basal and salicylic acid-induced resistance to potato virus X. BMC Plant Biology, 11(1), 41. doi:10.1186/1471-2229-11-41

Livak, K. J., & Schmittgen, T. D. (2001). Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method. Methods, 25(4), 402-408. doi:10.1006/meth.2001.1262

Love, A. J., Geri, C., Laird, J., Carr, C., Yun, B.-W., Loake, G. J., … Milner, J. J. (2012). Cauliflower mosaic virus Protein P6 Inhibits Signaling Responses to Salicylic Acid and Regulates Innate Immunity. PLoS ONE, 7(10), e47535. doi:10.1371/journal.pone.0047535

Lu, R., Folimonov, A., Shintaku, M., Li, W.-X., Falk, B. W., Dawson, W. O., & Ding, S.-W. (2004). Three distinct suppressors of RNA silencing encoded by a 20-kb viral RNA genome. Proceedings of the National Academy of Sciences, 101(44), 15742-15747. doi:10.1073/pnas.0404940101

Mandadi, K. K., & Scholthof, K.-B. G. (2013). Plant Immune Responses Against Viruses: How Does a Virus Cause Disease? The Plant Cell, 25(5), 1489-1505. doi:10.1105/tpc.113.111658

Meister, G. (2013). Argonaute proteins: functional insights and emerging roles. Nature Reviews Genetics, 14(7), 447-459. doi:10.1038/nrg3462

Molnár, A., Csorba, T., Lakatos, L., Várallyay, E., Lacomme, C., & Burgyán, J. (2005). Plant Virus-Derived Small Interfering RNAs Originate Predominantly from Highly Structured Single-Stranded Viral RNAs. Journal of Virology, 79(12), 7812-7818. doi:10.1128/jvi.79.12.7812-7818.2005

Moreno , P. Guerri , J. Ballester-Olmos , J.F. Martínez , M.E. 1991 Proceedings of the 11th Conference of the International Organization of Citrus Virologists

MORENO, P., GUERRI, J., BALLESTER-OLMOS, J. F., ALBIACH, R., & MARTÍNEZ, M. E. (1993). Separation and interference of strains from a citrus tristeza virus isolate evidenced by biological activity and double-stranded RNA (dsRNA) analysis. Plant Pathology, 42(1), 35-41. doi:10.1111/j.1365-3059.1993.tb01469.x

MORENO, P., AMBRÓS, S., ALBIACH-MARTÍ, M. R., GUERRI, J., & PEÑA, L. (2008). Citrus tristeza virus: a pathogen that changed the course of the citrus industry. Molecular Plant Pathology, 9(2), 251-268. doi:10.1111/j.1364-3703.2007.00455.x

Pina , J.A. Moreno , P. Juárez , J. Guerri , J. Cambra , M. Gorris , M.T. Navarro , L. 2005 Proceedings of the 16th Conference of the International Organization of Citrus Virologists

Renovell, Á., Gago, S., Ruiz-Ruiz, S., Velázquez, K., Navarro, L., Moreno, P., … Guerri, J. (2010). Mapping the subgenomic RNA promoter of the Citrus leaf blotch virus coat protein gene by Agrobacterium-mediated inoculation. Virology, 406(2), 360-369. doi:10.1016/j.virol.2010.07.034

Ruiz-Ruiz, S., Moreno, P., Guerri, J., & Ambrós, S. (2005). The complete nucleotide sequence of a severe stem pitting isolate of Citrus tristeza virus from Spain: comparison with isolates from different origins. Archives of Virology, 151(2), 387-398. doi:10.1007/s00705-005-0618-6

Ruiz-Ruiz, S., Moreno, P., Guerri, J., & Ambrós, S. (2007). A real-time RT-PCR assay for detection and absolute quantitation of Citrus tristeza virus in different plant tissues. Journal of Virological Methods, 145(2), 96-105. doi:10.1016/j.jviromet.2007.05.011

Ruiz-Ruiz, S., Navarro, B., Gisel, A., Peña, L., Navarro, L., Moreno, P., … Flores, R. (2011). Citrus tristeza virus infection induces the accumulation of viral small RNAs (21–24-nt) mapping preferentially at the 3′-terminal region of the genomic RNA and affects the host small RNA profile. Plant Molecular Biology, 75(6), 607-619. doi:10.1007/s11103-011-9754-4

Ruiz-Ruiz, S., Soler, N., Sánchez-Navarro, J., Fagoaga, C., López, C., Navarro, L., … Flores, R. (2013). Citrus tristeza virus p23: Determinants for Nucleolar Localization and Their Influence on Suppression of RNA Silencing and Pathogenesis. Molecular Plant-Microbe Interactions®, 26(3), 306-318. doi:10.1094/mpmi-08-12-0201-r

Sambade, A., Ambrós, S., López, C., Ruiz-Ruiz, S., Hermoso de Mendoza, A., Flores, R., … Moreno, P. (2007). Preferential accumulation of severe variants of Citrus tristeza virus in plants co-inoculated with mild and severe variants. Archives of Virology, 152(6), 1115-1126. doi:10.1007/s00705-006-0932-7

Satyanarayana, T., Bar-Joseph, M., Mawassi, M., Albiach-Martí, M. R., Ayllón, M. A., Gowda, S., … Dawson, W. O. (2001). Amplification of Citrus Tristeza Virus from a cDNA Clone and Infection of Citrus Trees. Virology, 280(1), 87-96. doi:10.1006/viro.2000.0759

Senthil-Kumar, M., & Mysore, K. S. (2011). New dimensions for VIGS in plant functional genomics. Trends in Plant Science, 16(12), 656-665. doi:10.1016/j.tplants.2011.08.006

Shi, B.-J., Palukaitis, P., & Symons, R. H. (2002). Differential Virulence by Strains of Cucumber mosaic virus is Mediated by the 2b Gene. Molecular Plant-Microbe Interactions®, 15(9), 947-955. doi:10.1094/mpmi.2002.15.9.947

Soler, N., Fagoaga, C., López, C., Moreno, P., Navarro, L., Flores, R., & Peña, L. (2014). Symptoms induced by transgenic expression of p23 fromCitrus tristeza virusin phloem-associated cells of Mexican lime mimic virus infection without the aberrations accompanying constitutive expression. Molecular Plant Pathology, 16(4), 388-399. doi:10.1111/mpp.12188

Spoel, S. H., Mou, Z., Tada, Y., Spivey, N. W., Genschik, P., & Dong, X. (2009). Proteasome-Mediated Turnover of the Transcription Coactivator NPR1 Plays Dual Roles in Regulating Plant Immunity. Cell, 137(5), 860-872. doi:10.1016/j.cell.2009.03.038

Tatineni, S., Robertson, C. J., Garnsey, S. M., & Dawson, W. O. (2011). A plant virus evolved by acquiring multiple nonconserved genes to extend its host range. Proceedings of the National Academy of Sciences, 108(42), 17366-17371. doi:10.1073/pnas.1113227108

Velázquez, K., Agüero, J., Vives, M. C., Aleza, P., Pina, J. A., Moreno, P., … Guerri, J. (2016). Precocious flowering of juvenile citrus induced by a viral vector based onCitrus leaf blotch virus: a new tool for genetics and breeding. Plant Biotechnology Journal, 14(10), 1976-1985. doi:10.1111/pbi.12555

Vives, M. C., Rubio, L., L√≥pez, C., Navas-Castillo, J., Albiach-Mart√≠, M. R., Dawson, W. O., … Moreno, P. (1999). The complete genome sequence of the major component of a mild citrus tristeza virus isolate. Journal of General Virology, 80(3), 811-816. doi:10.1099/0022-1317-80-3-811

Vives, M. C., Galipienso, L., Navarro, L., Moreno, P., & Guerri, J. (2001). The Nucleotide Sequence and Genomic Organization of Citrus Leaf Blotch Virus: Candidate Type Species for a New Virus Genus. Virology, 287(1), 225-233. doi:10.1006/viro.2001.1040

Vives, M. C., Galipienso, L., Navarro, L., Moreno, P., & Guerri, J. (2002). Characterization of Two Kinds of Subgenomic RNAs Produced by Citrus Leaf Blotch Virus. Virology, 295(2), 328-336. doi:10.1006/viro.2001.1349

VIVES, M. C., MARTÍN, S., AMBRÓS, S., RENOVELL, Á., NAVARRO, L., PINA, J. A., … GUERRI, J. (2008). Development of a full-genome cDNA clone ofCitrus leaf blotch virusand infection of citrus plants. Molecular Plant Pathology, 9(6), 787-797. doi:10.1111/j.1364-3703.2008.00501.x

Voinnet, O., Pinto, Y. M., & Baulcombe, D. C. (1999). Suppression of gene silencing: A general strategy used by diverse DNA and RNA viruses of plants. Proceedings of the National Academy of Sciences, 96(24), 14147-14152. doi:10.1073/pnas.96.24.14147

White, R. F. (1979). Acetylsalicylic acid (aspirin) induces resistance to tobacco mosaic virus in tobacco. Virology, 99(2), 410-412. doi:10.1016/0042-6822(79)90019-9

Wu, Y., Zhang, D., Chu, J. Y., Boyle, P., Wang, Y., Brindle, I. D., … Després, C. (2012). The Arabidopsis NPR1 Protein Is a Receptor for the Plant Defense Hormone Salicylic Acid. Cell Reports, 1(6), 639-647. doi:10.1016/j.celrep.2012.05.008

Xie, Z., Fan, B., Chen, C., & Chen, Z. (2001). An important role of an inducible RNA-dependent RNA polymerase in plant antiviral defense. Proceedings of the National Academy of Sciences, 98(11), 6516-6521. doi:10.1073/pnas.111440998

Yang, S.-J., Carter, S. A., Cole, A. B., Cheng, N.-H., & Nelson, R. S. (2004). A natural variant of a host RNA-dependent RNA polymerase is associated with increased susceptibility to viruses by Nicotiana benthamiana. Proceedings of the National Academy of Sciences, 101(16), 6297-6302. doi:10.1073/pnas.0304346101

Yu, D., Fan, B., MacFarlane, S. A., & Chen, Z. (2003). Analysis of the Involvement of an Inducible Arabidopsis RNA-Dependent RNA Polymerase in Antiviral Defense. Molecular Plant-Microbe Interactions®, 16(3), 206-216. doi:10.1094/mpmi.2003.16.3.206

Zhang, Y., Cheng, Y. T., Qu, N., Zhao, Q., Bi, D., & Li, X. (2006). Negative regulation of defense responses in Arabidopsis by twoNPR1paralogs. The Plant Journal, 48(5), 647-656. doi:10.1111/j.1365-313x.2006.02903.x

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