Analysis of local and systemic spread of the crucifer-infecting TMV-Cg virus in tobacco and several Arabidopsis thaliana ecotypes

2003 ◽  
Vol 30 (4) ◽  
pp. 401 ◽  
Author(s):  
Patricio Arce-Johnson ◽  
Consuelo Medina ◽  
Hal S. Padgett ◽  
Wilson Huanca ◽  
Carmen Espinoza
Keyword(s):  
Arabidopsis Thaliana ◽  
Tobacco Mosaic Virus ◽  
Mosaic Virus ◽  
Movement Protein ◽  
Host Interactions ◽  
Nicotiana Tabacum L ◽  
Systemic Spread ◽  
Movement Protein Gene ◽  
Local Movement

The crucifer-infecting tobacco mosaic virus, TMV-Cg, infects Arabidopsis thaliana (L.) Heynh. efficiently without causing severe symptoms. The systemic spread of TMV-Cg in Arabidopsis was evaluated in 14�ecotypes. Five days after inoculation, TMV-Cg was detected in apical leaves of 8 out of 14 ecotypes. As expected, the spread of TMV-Cg in the ecotypes tested was considerably faster than that of tobacco mosaic virus (TMV-U1). To study the participation of viral proteins in the TMV-Cg-induced infection, a complete genomic cDNA of TMV-Cg was cloned. The role of TMV-Cg movement protein in systemic spread was tested with a hybrid virus, constructed from the TMV-U1 genome and the TMV-Cg movement protein gene. Contrary to expectations, the systemic spread of this hybrid in Arabidopsis was similar to that of TMV-U1. The failure of the hybrid virus to spread at rates similar to those of TMV-Cg was not due to restrictions in local movement. In tobacco (Nicotiana tabacum L.), the hybrid virus spread efficiently and induced systemic mosaic symptoms characteristic of TMV-U1. The TMV-Cg cDNA clone provides an attractive tool to study virus–host interactions.

scholarly journals Challenging the Role of Microtubules in Tobacco Mosaic Virus Movement by Drug Treatments Is Disputable

2006 ◽  
Vol 80 (13) ◽  
pp. 6712-6715 ◽  
Author(s):  
Mark Seemanpillai ◽  
Rabab Elamawi ◽  
Christophe Ritzenthaler ◽  
Manfred Heinlein
Keyword(s):  
Tobacco Mosaic Virus ◽  
Mosaic Virus ◽  
Movement Protein ◽  
Viral Rna ◽  
Virus Movement ◽  
Direct Role ◽  
Microtubule Inhibitors ◽  
Microtubule Polymerization ◽  
Drug Treatments

ABSTRACT The movement protein (MP) of Tobacco mosaic virus interacts with microtubules during infection. Although this interaction is correlated with the function of MP in the cell-to-cell transport of viral RNA, a direct role of microtubules in the movement process was recently challenged by studies involving the treatment of plants with inhibitors of microtubule polymerization. Here, we report evidence suggesting that such treatments may not efficiently disrupt all microtubules. Thus, results obtained from studies using microtubule inhibitors may have to remain open to interpretation with regard to the involvement of microtubules in viral RNA trafficking.

scholarly journals Dysfunctionality of a tobacco mosaic virus movement protein mutant mimicking threonine 104 phosphorylation

2003 ◽  
Vol 84 (3) ◽  
pp. 727-732 ◽  
Author(s):  
E. M. Karger ◽  
O. Yu. Frolova ◽  
N. V. Fedorova ◽  
L. A. Baratova ◽  
T. V. Ovchinnikova ◽  
...  
Keyword(s):  
Endoplasmic Reticulum ◽  
Tobacco Mosaic Virus ◽  
Mosaic Virus ◽  
Movement Protein ◽  
Cell Movement ◽  
Specific Protein ◽  
Virus Movement ◽  
Wild Type ◽  
Molecular Masses

Replication of tobacco mosaic virus (TMV) is connected with endoplasmic reticulum (ER)-associated membranes at early stages of infection. This study reports that TMV movement protein (MP)-specific protein kinases (PKs) associated with the ER of tobacco were capable of phosphorylating Thr104 in TMV MP. The MP-specific PKs with apparent molecular masses of about 45–50 kDa and 38 kDa were revealed by gel PK assays. Two types of mutations were introduced in TMV MP gene of wild-type TMV U1 genome to substitute Thr104 by neutral Ala or by negatively charged Asp. Mutation of Thr104 to Ala did not affect the size of necrotic lesions induced by the mutant virus in Nicotiana tabacum Xanthi nc. plants. Conversely, mutation of Thr to Asp mimicking Thr104 phosphorylation strongly inhibited cell-to-cell movement. The possible role of Thr104 phosphorylation in TMV MP function is discussed.

scholarly journals Host Suppressors in Arabidopsis thaliana of Mutations in the Movement Protein Gene of Cauliflower mosaic virus

2000 ◽  
Vol 13 (5) ◽  
pp. 512-519 ◽  
Author(s):  
Anton S. Callaway ◽  
Zhong Huang ◽  
Stephen H. Howell
Keyword(s):  
Arabidopsis Thaliana ◽  
Mosaic Virus ◽  
Protein Gene ◽  
Movement Protein ◽  
Cauliflower Mosaic Virus ◽  
Host Factors ◽  
Chromosome 1 ◽  
Movement Protein Gene ◽  
Trait Locus ◽  
Made In

A novel genetic screen was used to identify host factors in Arabidopsis thaliana that suppress mutations in the Cauliflower mosaic virus (CaMV) movement protein gene (gene I). A series of small mutations was made in gene I and the mutations were tested for their suitability in a suppressor screen. The first round of screening yielded only revertants or second-site mutations in gene I. A derivative of one of the second-site mutant viruses (N7) that was delayed in symptom production was used in a second round of screening for suppressor plants that accelerated symptom production. Two candidate suppressor plants were found that accelerated by 1 to 4 days the first appearance of symptoms caused by the mutant viruses. One of the suppressors (5-2), called asc1 (acceleration of symptoms by CaMV N7), was mapped to chromosome 1. Two additional loci that differentially affect N7 virus susceptibility in the parental Columbia and Ler ecotypes were mapped to chromosomes 3 and 4 by quantitative trait locus (QTL) analysis.

scholarly journals Requirement of the Movement Protein for Long Distance Spread of Tobacco Mosaic Virus in Grafted Plants

1997 ◽  
Vol 10 (6) ◽  
pp. 691-699 ◽  
Author(s):  
Patricio Arce-Johnson ◽  
Ulrich Reimann-Philipp ◽  
Hal S. Padgett ◽  
Rafael Rivera-Bustamante ◽  
Roger N. Beachy
Keyword(s):  
Tobacco Mosaic Virus ◽  
Mosaic Virus ◽  
Movement Protein ◽  
Systemic Infection ◽  
Cauliflower Mosaic Virus ◽  
35S Promoter ◽  
Long Distance ◽  
Gene Encoding ◽  
Systemic Spread ◽  
Root Stock

Systemic spread of tobacco mosaic virus (TMV) that lacks a functional movement protein (TMVΔMP) was investigated in grafted tobacco (Nicotiana tabacum) plants. Transgenic plants that express the 30-kDa movement protein (MP) gene (MP) under the control of the rolC (phloem-specific) or pal2 (xylem-specific) promoters were unable to support systemic infection by the mutant virus, while plants that express the MP gene from the cauliflower mosaic virus 35S promoter (35S:MP) led to systemic infection. Doubly grafted plants were constructed in which plants containing the 35S:MP gene were used as root stock and plants carrying various MP constructs constituted the middle scion. The upper scion contained the 35S:MP gene in plants that produce a hypersensitive response when systemically infected by TMV. TMVΔMP moved systemically and produced complete necrosis in the upper scion when expression of MP in the middle scion was under the control of the rolC or 35S promoter, but not when the pal2 promoter was used. When plants expressing a gene encoding a defective MP were used as the middle scion, there was no systemic infection by TMVΔMP, and a delay in systemic infection by wild-type TMV. In grafted plants with middle scions that expressed the TMV 54 kDa gene sequence there was no apparent systemic infection by TMVΔMP in the upper scion. The results obtained indicate that the MP has a role in long distance movement, and support the suggestion that replication is necessary for systemic infection of these grafted plants.

scholarly journals The Absence of Eukaryotic Initiation Factor eIF(iso)4E Affects the Systemic Spread of a Tobacco etch virus Isolate in Arabidopsis thaliana

2013 ◽  
Vol 26 (4) ◽  
pp. 461-470 ◽  
Author(s):  
Carlos A. Contreras-Paredes ◽  
Laura Silva-Rosales ◽  
José-Antonio Daròs ◽  
Naholi D. Alejandri-Ramírez ◽  
Tzvetanka D. Dinkova
Keyword(s):  
Arabidopsis Thaliana ◽  
Mosaic Virus ◽  
Resistance Mechanism ◽  
Tobacco Etch Virus ◽  
Translation Initiation Factor ◽  
Initiation Factor ◽  
Viral Translation ◽  
Systemic Spread ◽  
Viral Coat

Translation initiation factor eIF4E exerts an important role during infection of viral species in the family Potyviridae. Particularly, a eIF(iso)4E family member is required for Arabidopsis thaliana susceptibility to Turnip mosaic virus, Lettuce mosaic virus, and Tobacco etch virus (TEV). In addition, a resistance mechanism named restriction of TEV movement (RTM) in A. thaliana controls the systemic spread of TEV in Col-0 ecotype. Here, we describe that TEV-TAMPS, a Mexican isolate, overcomes the RTM resistance mechanism reported for TEV-7DA infection of the Col-0 ecotype but depends on eIF(iso)4E for its systemic spread. To understand at which level eIF(iso)4E participates in A. thaliana TEV-TAMPS infection, the viral RNA replication and translation were measured. The absence or overexpression of eIF(iso)4E did not affect viral translation, and replication was still observed in the absence of eIF(iso)4E. However, the TEV-TAMPS systemic spread was completely abolished in the null mutant. The viral protein genome-linked (VPg) precursor NIa was found in coimmunoprecipitated complexes with both, eIF(iso)4E and eIF4E. However, the viral coat protein (CP) was only present in the eIF(iso)4E complexes. Since both the VPg and the CP proteins are needed for systemic spread, we propose a role of A. thaliana eIF(iso)4E in the movement of TEV-TAMPS within this host.

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