Literature DB >> 18705856

Citrus tristeza virus: a pathogen that changed the course of the citrus industry.

Pedro Moreno1, Silvia Ambrós, Maria R Albiach-Martí, José Guerri, Leandro Peña.   

Abstract

Citrus tristeza virus (CTV) (genus Closterovirus, family Closteroviridae) is the causal agent of devastating epidemics that changed the course of the citrus industry. Adapted to replicate in phloem cells of a few species within the family Rutaceae and to transmission by a few aphid species, CTV and citrus probably coevolved for centuries at the site of origin of citrus plants. CTV dispersal to other regions and its interaction with new scion varieties and rootstock combinations resulted in three distinct syndromes named tristeza, stem pitting and seedling yellows. The first, inciting decline of varieties propagated on sour orange, has forced the rebuilding of many citrus industries using tristeza-tolerant rootstocks. The second, inducing stunting, stem pitting and low bearing of some varieties, causes economic losses in an increasing number of countries. The third is usually observed by biological indexing, but rarely in the field. CTV polar virions are composed of two capsid proteins and a single-stranded, positive-sense genomic RNA (gRNA) of approximately 20 kb, containing 12 open reading frames (ORFs) and two untranslated regions (UTRs). ORFs 1a and 1b, encoding proteins of the replicase complex, are directly translated from the gRNA, and together with the 5' and 3'UTRs are the only regions required for RNA replication. The remaining ORFs, expressed via 3'-coterminal subgenomic RNAs, encode proteins required for virion assembly and movement (p6, p65, p61, p27 and p25), asymmetrical accumulation of positive and negative strands during RNA replication (p23), or suppression of post-transcriptional gene silencing (p25, p20 and p23), with the role of proteins p33, p18 and p13 as yet unknown. Analysis of genetic variation in CTV isolates revealed (1) conservation of genomes in distant geographical regions, with a limited repertoire of genotypes, (2) uneven distribution of variation along the gRNA, (3) frequent recombination events and (4) different selection pressures shaping CTV populations. Measures to control CTV damage include quarantine and budwood certification programmes, elimination of infected trees, use of tristeza-tolerant rootstocks, or cross protection with mild isolates, depending on CTV incidence and on the virus strains and host varieties predominant in each region. Incorporating resistance genes into commercial varieties by conventional breeding is presently unfeasible, whereas incorporation of pathogen-derived resistance by plant transformation has yielded variable results, indicating that the CTV-citrus interaction may be more specific and complex than initially thought. A deep understanding of the interactions between viral proteins and host and vector factors will be necessary to develop reliable and sound control measures.

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Year:  2008        PMID: 18705856      PMCID: PMC6640355          DOI: 10.1111/j.1364-3703.2007.00455.x

Source DB:  PubMed          Journal:  Mol Plant Pathol        ISSN: 1364-3703            Impact factor:   5.663


  76 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.  Monoclonal antibody-based serological methods for detecting Citrus tristeza virus in citrus groves.

Authors:  Zhen Liu; Zhe Chen; Jian Hong; Xuefeng Wang; Changyong Zhou; Xueping Zhou; Jianxiang Wu
Journal:  Virol Sin       Date:  2016-07-11       Impact factor: 4.327

3.  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

4.  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

5.  Analyses of 3' half genome of citrus tristeza virus reveal existence of distinct virus genotypes in citrus growing regions of India.

Authors:  Kajal K Biswas; Supratik Palchoudhury; Susheel K Sharma; Bikram Saha; Shruti Godara; Dilip K Ghosh; Manjunath L Keremane
Journal:  Virusdisease       Date:  2018-07-02

6.  Characterization of a new bunyavirus and its derived small RNAs in the brown citrus aphid, Aphis citricidus.

Authors:  Wei Zhang; Tengfei Wu; Mengmeng Guo; Tengyu Chang; Li Yang; Yang Tan; Chao Ye; Jinzhi Niu; Jin-Jun Wang
Journal:  Virus Genes       Date:  2019-05-11       Impact factor: 2.332

7.  Minor Coat and Heat Shock Proteins Are Involved in the Binding of Citrus Tristeza Virus to the Foregut of Its Aphid Vector, Toxoptera citricida.

Authors:  N Killiny; S J Harper; S Alfaress; C El Mohtar; W O Dawson
Journal:  Appl Environ Microbiol       Date:  2016-10-14       Impact factor: 4.792

8.  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

9.  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

10.  Evidence of Recombinant Citrus tristeza virus Isolate Occurring in Acid Lime cv. Pant Lemon Orchard in Uttarakhand Terai Region of Northern Himalaya in India.

Authors:  Jaywant Kumar Singh; Avijit Tarafdar; Susheel Kumar Sharma; Kajal Kumar Biswas
Journal:  Indian J Virol       Date:  2012-12-18
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