Literature DB >> 18434397

Citrus tristeza virus: survival at the edge of the movement continuum.

Svetlana Y Folimonova1, Alexey S Folimonov, Satyanarayana Tatineni, William O Dawson.   

Abstract

Systemic invasion of plants by viruses is thought to involve two processes: cell-to-cell movement between adjacent cells and long-distance movement that allows the virus to rapidly move through sieve elements and unload at the growing parts of the plant. There is a continuum of proportions of these processes that determines the degrees of systemic infection of different plants by different viruses. We examined the systemic distribution of Citrus tristeza virus (CTV) in citrus species with a range of susceptibilities. By using a "pure" culture of CTV from a cDNA clone and green fluorescent protein-labeled virus we show that both cell-to-cell and long-distance movement are unusually limited, and the degree of limitation varies depending on the citrus host. In the more-susceptible hosts CTV infected only a small portion of phloem-associated cells, and moreover, the number of infection sites in less-susceptible citrus species was substantially decreased further, indicating that long-distance movement was reduced in those hosts. Analysis of infection foci in the two most differential citrus species, Citrus macrophylla and sour orange, revealed that in the more-susceptible host the infection foci were composed of a cluster of multiple cells, while in the less-susceptible host infection foci were usually single cells, suggesting that essentially no cell-to-cell movement occurred in the latter host. Thus, CTV in sour orange represents a pattern of systemic infection in which the virus appears to function with only the long-distance movement mechanism, yet is able to survive in nature.

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Year:  2008        PMID: 18434397      PMCID: PMC2447058          DOI: 10.1128/JVI.00515-08

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  33 in total

1.  Genetic analysis of the cell-to-cell movement of beet yellows closterovirus.

Authors:  D V Alzhanova; Y Hagiwara; V V Peremyslov; V V Dolja
Journal:  Virology       Date:  2000-03-01       Impact factor: 3.616

2.  Genetic Diversity and Evolution of Closteroviruses.

Authors:  Alexander V Karasev
Journal:  Annu Rev Phytopathol       Date:  2000-09       Impact factor: 13.078

3.  THREAD-LIKE PARTICLES ASSOCIATED WITH TRISTEZA DISEASE OF CITRUS.

Authors:  E W KITAJIMA; D M SILVA; A R OLIVEIRA; G W MUELLER; A S COSTA
Journal:  Nature       Date:  1964-03-07       Impact factor: 49.962

Review 4.  Plant virus transport: motions of functional equivalence.

Authors:  Herman B Scholthof
Journal:  Trends Plant Sci       Date:  2005-08       Impact factor: 18.313

5.  Nucleotide sequence and organization of eight 3' open reading frames of the citrus tristeza closterovirus genome.

Authors:  H R Pappu; A V Karasev; E J Anderson; S S Pappu; M E Hilf; V J Febres; R M Eckloff; M McCaffery; V Boyko; S Gowda
Journal:  Virology       Date:  1994-02-15       Impact factor: 3.616

6.  Closterovirus encoded HSP70 homolog and p61 in addition to both coat proteins function in efficient virion assembly.

Authors:  T Satyanarayana; S Gowda; M Mawassi; M R Albiach-Martí; M A Ayllón; C Robertson; S M Garnsey; W O Dawson
Journal:  Virology       Date:  2000-12-05       Impact factor: 3.616

7.  Efficient infection of Nicotiana benthamiana by Tomato bushy stunt virus is facilitated by the coat protein and maintained by p19 through suppression of gene silencing.

Authors:  Feng Qu; T Jack Morris
Journal:  Mol Plant Microbe Interact       Date:  2002-03       Impact factor: 4.171

8.  Three genes of Citrus tristeza virus are dispensable for infection and movement throughout some varieties of citrus trees.

Authors:  Satyanarayana Tatineni; Cecile J Robertson; Stephen M Garnsey; Moshe Bar-Joseph; Siddarame Gowda; William O Dawson
Journal:  Virology       Date:  2008-05-05       Impact factor: 3.616

9.  Characterization of citrus tristeza virus subgenomic RNAs in infected tissue.

Authors:  M E Hilf; A V Karasev; H R Pappu; D J Gumpf; C L Niblett; S M Garnsey
Journal:  Virology       Date:  1995-04-20       Impact factor: 3.616

10.  Brevipalpus-transmitted plant virus and virus-like diseases: cytopathology and some recent cases.

Authors:  E W Kitajima; C M Chagas; J C V Rodrigues
Journal:  Exp Appl Acarol       Date:  2003       Impact factor: 2.380

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  17 in total

1.  Enhancement or attenuation of disease by deletion of genes from Citrus tristeza virus.

Authors:  Satyanarayana Tatineni; William O Dawson
Journal:  J Virol       Date:  2012-05-16       Impact factor: 5.103

2.  A plant virus evolved by acquiring multiple nonconserved genes to extend its host range.

Authors:  Satyanarayana Tatineni; Cecile J Robertson; Stephen M Garnsey; William O Dawson
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-10       Impact factor: 11.205

3.  Superinfection exclusion is an active virus-controlled function that requires a specific viral protein.

Authors:  Svetlana Y Folimonova
Journal:  J Virol       Date:  2012-03-07       Impact factor: 5.103

4.  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.

Authors:  Susana Ruiz-Ruiz; Beatriz Navarro; Andreas Gisel; Leandro Peña; Luis Navarro; Pedro Moreno; Francesco Di Serio; Ricardo Flores
Journal:  Plant Mol Biol       Date:  2011-02-15       Impact factor: 4.076

5.  Genetic diversity and evidence for recent modular recombination in Hawaiian Citrus tristeza virus.

Authors:  Michael J Melzer; Wayne B Borth; Diane M Sether; Stephen Ferreira; Dennis Gonsalves; John S Hu
Journal:  Virus Genes       Date:  2009-10-16       Impact factor: 2.332

6.  The pathogenicity determinant of Citrus tristeza virus causing the seedling yellows syndrome maps at the 3'-terminal region of the viral genome.

Authors:  Maria R Albiach-Marti; Cecile Robertson; Siddarame Gowda; Satyanarayana Tatineni; Belén Belliure; Stephen M Garnsey; Svetlana Y Folimonova; Pedro Moreno; William O Dawson
Journal:  Mol Plant Pathol       Date:  2010-01       Impact factor: 5.663

7.  Infection with strains of Citrus tristeza virus does not exclude superinfection by other strains of the virus.

Authors:  Svetlana Y Folimonova; Cecile J Robertson; Turksen Shilts; Alexey S Folimonov; Mark E Hilf; Stephen M Garnsey; William O Dawson
Journal:  J Virol       Date:  2009-11-18       Impact factor: 5.103

8.  A viral protein mediates superinfection exclusion at the whole-organism level but is not required for exclusion at the cellular level.

Authors:  María Bergua; Mark P Zwart; Choaa El-Mohtar; Turksen Shilts; Santiago F Elena; Svetlana Y Folimonova
Journal:  J Virol       Date:  2014-07-16       Impact factor: 5.103

9.  Accumulation of transgene-derived siRNAs is not sufficient for RNAi-mediated protection against Citrus tristeza virus in transgenic Mexican lime.

Authors:  Carmelo López; Magdalena Cervera; Carmen Fagoaga; Pedro Moreno; Luis Navarro; Ricardo Flores; Leandro Peña
Journal:  Mol Plant Pathol       Date:  2010-01       Impact factor: 5.663

Review 10.  PAMPs, PRRs, effectors and R-genes associated with citrus-pathogen interactions.

Authors:  Ronaldo J D Dalio; Diogo M Magalhães; Carolina M Rodrigues; Gabriella D Arena; Tiago S Oliveira; Reinaldo R Souza-Neto; Simone C Picchi; Paula M M Martins; Paulo J C Santos; Heros J Maximo; Inaiara S Pacheco; Alessandra A De Souza; Marcos A Machado
Journal:  Ann Bot       Date:  2017-03-01       Impact factor: 4.357

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