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A coat-independent superinfection exclusion rapidly imposed in Nicotiana benthamiana cells by tobacco mosaic virus is not prevented by depletion of the movement protein.

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A coat-independent superinfection exclusion rapidly imposed in Nicotiana benthamiana cells by tobacco mosaic virus is not prevented by depletion of the movement protein.

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Julve Parreño, JM.; Gandia Fernàndez, A.; Fernandez Del Carmen, MA.; Sarrion-Perdigones, A.; Castelijns, B.; Granell Richart, A.; Orzáez Calatayud, DV. (2013). A coat-independent superinfection exclusion rapidly imposed in Nicotiana benthamiana cells by tobacco mosaic virus is not prevented by depletion of the movement protein. Plant Molecular Biology. 81(6):553-564. doi:10.1007/s11103-013-0028-1

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Title: A coat-independent superinfection exclusion rapidly imposed in Nicotiana benthamiana cells by tobacco mosaic virus is not prevented by depletion of the movement protein.
Author: Julve Parreño, Jose Manuel Gandia Fernàndez, Antoni Fernández Del Carmen, María Asunción Sarrion-Perdigones, Alejandro Castelijns, Bas Granell Richart, Antonio Orzáez Calatayud, Diego Vicente
UPV Unit: 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
Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia
Issued date:
Abstract:
[EN] New evidence is emerging which indicates that population variants in plant virus infections are not uniformly distributed along the plant, but structured in a mosaic-like pattern due to limitation to the superinfection ...[+]
Subjects: Superinfection exclusion , Tobacco mosaic virus , Agroinfiltration , Homologous interference
Copyrigths: Cerrado
Source:
Plant Molecular Biology. (issn: 0167-4412 )
DOI: 10.1007/s11103-013-0028-1
Publisher:
Springer Verlag (Germany)
Publisher version: http://doi.org/10.1007/s11103-013-0028-1
Thanks:
We wish to acknowledge Dr. Victor Klimyuk and Dr. Yuri Gleba from ICON-Genetics for kindly providing the MagnICON vectors. Thanks also to Dr. George Lomonossof for providing the pEAQ vectors. This work was supported by ...[+]
Type: Artículo

References

Abel PP, Nelson RS, De B, Hoffmann N, Rogers SG, Fraley RT, Beachy RN (1986) Delay of disease development in transgenic plants that express the tobacco mosaic virus coat protein gene. Science 232(4751):738–743

Abramoff MD, Magalhaes PJ, Ram SJ (2004) Image processing with imageJ. Biophotonics Int 11(7):36–42

Benbasat JA, Burck KB, Miller RC Jr (1978) Superinfection exclusion and lack of conservative transfer of bacteriophage T7 DNA. Virology 87(1):164–171 [+]
Abel PP, Nelson RS, De B, Hoffmann N, Rogers SG, Fraley RT, Beachy RN (1986) Delay of disease development in transgenic plants that express the tobacco mosaic virus coat protein gene. Science 232(4751):738–743

Abramoff MD, Magalhaes PJ, Ram SJ (2004) Image processing with imageJ. Biophotonics Int 11(7):36–42

Benbasat JA, Burck KB, Miller RC Jr (1978) Superinfection exclusion and lack of conservative transfer of bacteriophage T7 DNA. Virology 87(1):164–171

Bendahmane M, Beachy RN (1999) Control of tobamovirus infections via pathogen-derived resistance. Adv Virus Res 53:369–386

Bendahmane M, Fitchen JH, Zhang G, Beachy RN (1997) Studies of coat protein-mediated resistance to tobacco mosaic tobamovirus: correlation between assembly of mutant coat proteins and resistance. J Virol 71(10):7942–7950

Bendahmane M, Chen I, Asurmendi S, Bazzini AA, Szecsi J, Beachy RN (2007) Coat protein-mediated resistance to TMV infection of Nicotiana tabacum involves multiple modes of interference by coat protein. Virology 366(1):107–116

Dietrich C, Maiss E (2003) Fluorescent labelling reveals spatial separation of potyvirus populations in mixed infected Nicotiana benthamiana plants. J Gen Virol 84(10):2871–2876

Elena SF, Bedhomme S, Carrasco P, Cuevas JM, de la Iglesia F, Lafforgue G, Lalic J, Prosper A, Tromas N, Zwart MP (2011) The evolutionary genetics of emerging plant RNA viruses. Mol Plant Microbe Interact 24(3):287–293

Ellenberg P, Linero FN, Scolaro LA (2007) Superinfection exclusion in BHK-21 cells persistently infected with Junín virus. J Gen Virol 88(10):2730–2739

Folimonova SY (2012) Superinfection exclusion is an active virus-controlled function that requires a specific viral protein. J Virol 86(10):5554–5561

Folimonova SY, Robertson CJ, Shilts T, Folimonov AS, Hilf ME, Garnsey SM, Dawson WO (2010) Infection with strains of Citrus tristeza virus does not exclude superinfection by other strains of the virus. J Virol 84(3):1314–1325

Fulton RW (1986) Practices and precautions in the use of cross protection for plant-virus disease-control. Annu Rev Phytopathol 24:67–81

Genovés A, Pallás V, Navarro JA (2011) Contribution of topology determinants of a viral movement protein to its membrane association, intracellular traffic, and viral cell-to-cell movement. J Virol 85(15):7797–7809

Giritch A, Marillonnet S, Engler C, van Eldik G, Botterman J, Klimyuk V, Gleba Y (2006) Rapid high-yield expression of full-size IgG antibodies in plants coinfected with noncompeting viral vectors. Proc Natl Acad Sci U S A 103(40):14701–14706

Gleba Y, Marillonnet S, Klimyuk V (2004) Engineering viral expression vectors for plants: the ‘full virus’ and the ‘deconstructed virus’ strategies. Curr Opin Plant Biol 7(2):182–188

Gleba Y, Klimyuk V, Marillonnet S (2005) Magnifection—a new platform for expressing recombinant vaccines in plants. Vaccine 23(17–18):2042–2048

Gleba Y, Marillonnet S, Klimyuk V (2006) High throughput gene assembly and expression using viral RNA replicons delivered by agrobacterium. In Vitro Cell Dev Biol Anim 42:10A–10A

Gonzalez-Jara P, Fraile A, Canto T, Garcia-Arenal F (2009) The multiplicity of infection of a plant virus varies during colonization of its eukaryotic host. J Virol 83(15):7487–7494

Gopinath K, Wellink J, Porta C, Taylor KM, Lomonossoff GP, van Kammen A (2000) Engineering cowpea mosaic virus RNA-2 into a vector to express heterologous proteins in plants. Virology 267(2):159–173

Kawakami S, Watanabe Y, Beachy RN (2004) Tobacco mosaic virus infection spreads cell to cell as intact replication complexes. Proc Natl Acad Sci U S A 101(16):6291–6296

Kliem M, Dreiseikelmann B (1989) The superimmunity gene sim of bacteriophage P1 causes superinfection exclusion. Virology 171(2):350–355

Koo JC, Asurmendi S, Bick J, Woodford-Thomas T, Beachy RN (2004) Ecdysone agonist-inducible expression of a coat protein gene from tobacco mosaic virus confers viral resistance in transgenic Arabidopsis. Plant J 37(3):439–448

Lee Y-M, Tscherne DM, Yun S-I, Frolov I, Rice CM (2005) Dual mechanisms of pestiviral superinfection exclusion at entry and RNA replication. J Virol 79(6):3231–3242

Lu B, Stubbs G, Culver JN (1998) Coat protein interactions involved in tobacco mosaic tobamovirus cross-protection. Virology 248(2):188–198

Marillonnet S, Giritch A, Gils M, Kandzia R, Klimyuk V, Gleba Y (2004) In planta engineering of viral RNA replicons: efficient assembly by recombination of DNA modules delivered by Agrobacterium. Proc Natl Acad Sci USA 101(18):6852–6857

Marillonnet S, Thoeringer C, Kandzia R, Klimyuk V, Gleba Y (2005) Systemic Agrobacterium tumefaciens-mediated transfection of viral replicons for efficient transient expression in plants. Nat Biotechnol 23(6):718–723

Michel N, Allespach I, Venzke S, Fackler OT, Keppler OT (2005) The Nef protein of human immunodeficiency virus establishes superinfection immunity by a dual strategy to downregulate cell-surface CCR5 and CD4. Curr Biol 15(8):714–723

Nakazono-Nagaoka E, Takahashi T, Shimizu T, Kosaka Y, Natsuaki T, Omura T, Sasaya T (2009) Cross-protection against bean yellow mosaic virus (BYMV) and clover yellow vein virus by attenuated BYMV isolate M11. Phytopathology 99(3):251–257

Nejidat A, Beachy RN (1989) Decreased levels of TMV coat protein in transgenic tobacco plants at elevated temperatures reduce resistance to TMV infection. Virology 173(2):531–538

Orzaez D, Mirabel S, Wieland WH, Granell A (2006) Agroinjection of tomato fruits. A tool for rapid functional analysis of transgenes directly in fruit. Plant Physiology 140(1):3–11

Powell PA, Sanders PR, Tumer N, Fraley RT, Beachy RN (1990) Protection against tobacco mosaic virus infection in transgenic plants requires accumulation of coat protein rather than coat protein RNA sequences. Virology 175(1):124–130

Ramirez S, Perez-del-Pulgar S, Carrion JA, Coto-Llerena M, Mensa L, Dragun J, Garcia-Valdecasas JC, Navasa M, Forns X (2010) Hepatitis C virus superinfection of liver grafts: a detailed analysis of early exclusion of non-dominant virus strains. J Gen Virol 91(Pt 5):1183–1188

Ranade K, Poteete AR (1993) Superinfection exclusion (sieB) genes of bacteriophages P22 and lambda. J Bacteriol 175(15):4712–4718

Roossinck MJ (2005) Symbiosis versus competition in plant virus evolution. Nat Rev Microbiol 3(12):917–924

Sainsbury F, Thuenemann EC, Lomonossoff GP (2009) pEAQ: versatile expression vectors for easy and quick transient expression of heterologous proteins in plants. Plant Biotechnol J 7(7):682–693

Sarkar S, Smitamana P (1981) A proteinless mutant of tobacco mosaic virus: evidence against the role of a viral coat protein for interference. Mol Gen Genet 184(1):158–159

Syller J (2012) Facilitative and antagonistic interactions between plant viruses in mixed infections. Mol Plant Pathol 13(2):204–216

Takahashi T, Sugawara T, Yamatsuta T, Isogai M, Natsuaki T, Yoshikawa N (2007) Analysis of the spatial distribution of identical and two distinct virus populations differently labeled with cyan and yellow fluorescent proteins in coinfected plants. Phytopathology 97(10):1200–1206

Tscherne DM, Evans MJ, von Hahn T, Jones CT, Stamataki Z, McKeating JA, Lindenbach BD, Rice CM (2007) Superinfection exclusion in cells infected with hepatitis C virus. J Virol 81(8):3693–3703

Voinnet O, Rivas S, Mestre P, Baulcombe D (2003) An enhanced transient expression system in plants based on suppression of gene silencing by the p19 protein of tomato bushy stunt virus. Plant J 33(5):949–956

Walkey DGA, Lecoq H, Collier R, Dobson S (1992) Studies on the control of zucchini yellow mosaic-virus in courgettes by mild strain protection. Plant Pathol 41(6):762–771

Zaitlin M, Palukaitis P (2000) Advances in understanding plant viruses and virus diseases. Annu Rev Phytopathol 38:117–143

Ziebell H, Carr JP (2010) Chapter 6—Cross-protection: a century of mystery. In: John PC, Gad L (eds) Advances in virus research, vol 76. Academic Press, London, pp 211–264

Zou G, Zhang B, Lim P-Y, Yuan Z, Bernard KA, Shi P-Y (2009) Exclusion of West Nile virus superinfection through RNA replication. J Virol 83(22):11765–11776

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