Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Statistics
  • Help & Advice
University of Warwick

The Library

  • Login

Influence of cytoplasmic heat shock protein 70 on viral infection of Nicotiana benthamiana

Tools
- Tools
+ Tools

Chen, Zhaorong, Zhou, Tao, Wu, Xuehong, Hong, Yiguo , Fan, Zaifeng and Li, Huaifang. (2008) Influence of cytoplasmic heat shock protein 70 on viral infection of Nicotiana benthamiana. Molecular Plant Pathology, Volume 9 (Number 6). pp. 809-817. ISSN 1464-6722

Full text not available from this repository.
Official URL: http://dx.doi.org/10.1111/J.1364-3703.2008.00505.X

Abstract

The accumulation of heat shock protein 70 (Hsp70) generally occurs in plants infected with viruses. However, the effect of Hsp70 accumulation on plant viral infection and pathogenesis remains elusive. In this study, the expression of six Hsp70 genes was found to be induced by the four diverse RNA viruses, Tobacco mosaic virus, Potato virus X (PVX), Cucumber mosaic virus and Watermelon mosaic virus, in Nicotiana benthamiana. Heat treatment enhanced the accumulation and systemic infection of these viruses. Similar results were obtained for viral infection in plants heterologously expressing an Arabidopsis cytoplasmic Hsp70 through either a PVX vector or Agrobacterium infiltration. In contrast, viral infection was compromised in cytoplasmic NbHsp70c-1 gene-silenced plants. These data demonstrate that the cytoplasmic Hsp70s can enhance the infection of N. benthamiana by diverse viruses.

Item Type: Journal Article
Subjects: Q Science > QK Botany
Q Science > QP Physiology
S Agriculture > SB Plant culture
Divisions: Faculty of Science > Life Sciences (2010- ) > Warwick HRI (2004-2010)
Library of Congress Subject Headings (LCSH): Nicotiana benthamiana -- Virus diseases, Heat shock proteins
Journal or Publication Title: Molecular Plant Pathology
Publisher: Wiley-Blackwell Publishing Ltd.
ISSN: 1464-6722
Date: November 2008
Volume: Volume 9
Number: Number 6
Number of Pages: 9
Page Range: pp. 809-817
Identification Number: 10.1111/j.1364-3703.2008.00505.x
Status: Not Peer Reviewed
Publication Status: Published
Access rights to Published version: Restricted or Subscription Access
Funder: Guo jia zi ran ke xue ji jin wei yuan hui (China) [National Natural Science Foundation of China] (NSFC), National Basic Research Program of China
Grant number: 2006CB101903 (NBRPC), 30340074 (NSFC)
References: Alzhanova, D.V., Napuli, A.J., Creamer, R. and Dolja, V.V. (2001) Cell-to-cell movement and assembly of a plant closterovirus: roles for the capsid proteins and Hsp70 homolog. EMBO J. 20, 6997–7007. Aoki, K., Kragler, F., Xoconostle-Cázares, B. and Lucas, W.J. (2002) A subclass of plant heat shock cognate 70 chaperones carries a motif that facilitates trafficking through plasmodesmata. Proc. Natl. Acad. Sci. USA, 99, 16 342–16 347. Aparicio, F., Thomas, C.L., Lederer, C., Niu, Y., Wang, D.W. and Maule, A.J. (2005) Virus induction of heat shock protein 70 reflects a general response to protein accumulation in the plant cytosol. Plant Physiol. 138, 529–536. Aranda, M. and Maule, A. (1998) Virus-induced host gene shut off in animals and plants. Virology, 243, 261–267. Aranda, M.A., Escaler, M., Wang, D. and Maule, A.J. (1996) Induction of HSP70 and polyubiquitin expression associated with plant virus replication. Proc. Natl. Acad. Sci. USA, 93, 15 289–15 293. von Bargen, S., Salchert, K., Paape, M., Piechulla, B. and Kellmann, J.W. (2001) Interactions between the tomato spotted wilt virus movement protein and plant proteins showing homologies to myosin, kinesin and DnaJ-like chaperones. Plant Physiol. Biochem. 39, 1083–1093. Boevink, P. and Oparka, K.J. (2005) Virus–host interactions during movement processes. Plant Physiol. 138, 1815–1821. Bradford, M.M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein–dye binding. Anal. Biochem. 72, 248–254. Broquet, A.H., Lenoir, C., Gardet, A., Sapin, C., Chwetzoff, S., Jouniaux, A-M., Lopez, S., Trugnan, G., Bachelet, M. and Thomas, G. (2007) Hsp70 negatively controls rotavirus protein bioavailability in Caco-2 cells infected by the rotavirus RF strain. J. Virol. 81, 1297–1304. Chapman, S., Kavanagh, T. and Baulcombe, D. (1992) Potato virus X as a vector for gene expression in plants. Plant J. 2, 549–557. Chromy, L.R., Pipas, J.M. and Garcea, R.L. (2003) Chaperone-mediated in vitro assembly of polyomavirus capsids. Proc. Natl. Acad. Sci. USA, 100, 10 477–10 482. Daugaard, M., Rohde, M. and Jäättelä, M. (2007) The heat shock protein 70 family: highly homologous proteins with overlapping and distinct functions. FEBS Lett. 581, 3702–3710. Dufresne, P.J., Thivierge, K., Cotton, S., Beauchemin, C., Ide, C., Ubalijoro, E., Laliberté, J-F. and Fortin, M.G. (2008) Heat shock 70 protein interaction with Turnip mosaic virus RNA-dependent RNA polymerase within virus-induced membrane vesicles. Virology, 374, 217–227. Escaler, M., Aranda, M.A., Thomas, C.L. and Maule, A.J. (2000) Pea embryonic tissues show common responses to the replication of a wide range of viruses. Virology, 267, 318–325. Glotzer, J.B., Saltik, M., Chiocca, S., Michou, A.I., Moseley, P. and Cotten, M. (2000) Activation of heat-shock response by an adenovirus is essential for virus replication. Nature, 407, 207–211. Hartl, F.U. (1996) Molecular chaperones in cellular protein folding. Nature, 381, 571–579. Hofius, D., Maier, A.T., Dietrich, C., Jungkunz, I., Börnke, F., Maiss, E. and Sonnewald, U. (2007) Capsid protein-mediated recruitment of host DnaJ-like proteins is required for Potato virus Y infection in tobacco plants. J. Virol. 81, 11 870–11 880. Jia, H.G., Pang, Y.Q. and Fang, R.X. (2003) Agroinoculation as a simple way to deliver a Tobacco mosaic virus-based expression vector. Acta Bot. Sin. 45, 770–773. Jockusch, H., Wiegand, C., Mersch, B. and Rajes, D. (2001) Mutants of Tobacco mosaic virus with temperature-sensitive coat proteins induce heat shock response in tobacco leaves. Mol. Plant–Microbe Interact. 14, 914–917. Kanzaki, H., Saitoh, H., Ito, A., Fujisawa, S., Kamoun, S., Katou, S., Yoshioka, H. and Terauchi, R. (2003) Cytosolic HSP90 and HSP70 are essential components of INF1-mediated hypersensitive response and non-host resistance to Pseudomonas cichorii in Nicotiana benthamiana. Mol. Plant Pathol. 4, 383–391. Koenig, R. (1981) Indirect ELISA methods for the broad specificity detection of plant viruses. J. Gen. Virol. 55, 53–62. Lee, J.H. and Schöffl, F. (1996) An Hsp70 antisense gene affects the expression of HSP70/HSC70, the regulation of HSF, and the acquisition of thermotolerance in transgenic Arabidopsis thaliana. Mol. Gen. Genet. 252, 11–19. Maule, A.J., Escaler, M. and Aranda, M.A. (2000) Programmed responses to virus replication in plants. Mol. Plant Pathol. 1, 9–15. Mayer, M.P. and Bukau, B. (2005) Hsp70 chaperones: cellular functions and molecular mechanism. Cell. Mol. Life Sci. 62, 670–684. Medina, V., Peremyslov, V.V., Hagiwara, Y. and Dolja, V.V. (1999) Subcellular localization of the HSP70-homolog encoded by Beet yellows closterovirus. Virology, 260, 173–181. Noël, L.D., Cagna, G., Stuttmann, J., Wirthmüller, L., Betsuyaku, S., Witte, C.-P., Bhat, R., Pochon, N., Colby, T. and Parker, J.E. (2007) Interaction between SGT1 and cytosolic/nuclear HSC70 chaperones regulates Arabidopsis immune responses. Plant Cell, 19, 4061–4076. Oglesbee, M.J., Liu, Z., Kenney, H. and Brooks, C.L. (1996) The highly inducible member of the 70 kDa family of heat shock proteins increases canine distemper virus polymerase activity. J. Gen. Virol. 77, 2125–2135. Peremyslov, V.V., Hagiwara, Y. and Dolja, V.V. (1999) HSP70 homolog functions in cell-to-cell movement of a plant virus. Proc. Natl. Acad. Sci. USA, 96, 14 771–14 776. Prokhnevsky, A.I., Peremyslov, V.V., Napuli, A.J. and Dolja, V.V. (2002) Interaction between long-distance transport factor and Hsp70-related movement protein of Beet yellows virus. J. Virol. 76, 11 003–11 011. Reyes-del Valle, J., Chávez-Salinas, S., Medina, F. and del Angel, R.M. (2005) Heat shock protein 90 and heat shock protein 70 are components of Dengue virus receptor complex in human cells. J. Virol. 79, 4557–4567. Senthil, G., Liu, H., Puram, V.G., Clark, A., Stromberg, A. and Goodin, M.M. (2005) Specific and common changes in Nicotiana benthamiana gene expression in response to infection by enveloped viruses. J. Gen. Virol. 86, 2615–2625. Senthil-Kumar, M., Govind, G., Kang, L., Mysore, K.S. and Udayakumar, M. (2007) Functional characterization of Nicotiana benthamiana homologs of peanut water deficit-induced genes by virus-induced gene silencing. Planta, 225, 523–539. Serva, S. and Nagy, P.D. (2006) Proteomics analysis of the tombusvirus replicase: Hsp70 molecular chaperone is associated with the replicase and enhances viral RNA replication. J. Virol. 80, 2162–2169. Su, P.H. and Li, H.M. (2008) Arabidopsis stromal 70-kD heat shock proteins are essential for plant development and important for thermotolerance of germinating seeds. Plant Physiol. 146, 1231–1241. Sung, D.Y. and Guy, C.L. (2003) Physiological and molecular assessment of altered expression of Hsc70-1 in Arabidopsis. Evidence for pleiotropic consequences. Plant Physiol. 132, 979–987. Sung, D.Y., Vierling, E. and Guy, C.L. (2001) Comprehensive expression profile analysis of the Arabidopsis Hsp70 gene family. Plant Physiol. 126, 789–800. Tomita, Y., Mizuno, T., Díez, J., Naito, S., Ahlquist, P. and Ishikawa, M. (2003) Mutation of host dnaJ homolog inhibits Brome mosaic virus negative-strand RNA synthesis. J. Virol. 77, 2990–2997. Walter, M., Chaban, C., Schütze, K., Batistic, O., Weckermann, K., Näke, C., Blazevic, D., Grefen, C., Schumacher, K., Oecking, C., Harter, K. and Kudla, J. (2004) Visualization of protein interactions in living plant cells using bimolecular fluorescence complementation. Plant J. 40, 428–438. Wang, W., Vinocur, B., Shoseyov, O. and Altman, A. (2004) Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci. 9, 244–252. van Wezel, R., Liu, H., Tien, P., Stanley, J. and Hong, Y. (2001) Gene C2 of the monopartite geminivirus Tomato yellow leaf curl virus-China encodes a pathogenicity determinant that is localized in the nucleus. Mol. Plant–Microbe Interact. 14, 1125–1128. Whitham, S.A. and Wang, Y.Z. (2004) Roles for host factors in plant viral pathogenicity. Curr. Opin. Plant Biol. 7, 365–371. Whitham, S.A., Quan, S., Chang, H.S., Cooper, B., Estes, B., Zhu, T., Wang, X. and Hou, Y.M. (2003) Diverse RNA viruses elicit the expression of common sets of genes in susceptible Arabidopsis thaliana plants. Plant J. 33, 271–283. Wroblewski, T., Tomczak, A. and Michelmore, R. (2005) Optimization of Agrobacterium-mediated transient assays of gene expression in lettuce, tomato and Arabidopsis. Plant Biotechnol. J. 3, 259–273.
URI: http://wrap.warwick.ac.uk/id/eprint/29174

Data sourced from Thomson Reuters' Web of Knowledge

Request changes to a record

Actions (login required)

View Item View Item
twitter

Email us: publications@warwick.ac.uk
Contact Details
About Us