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RNA1-Independent Replication and GFP Expression from Tomato marchitez virus Isolate M Cloned cDNA.
Ferriol, I; Turina, M; Zamora-Macorra, E J; Falk, B W.
Afiliação
  • Ferriol I; First and fourth authors: Plant Pathology Department, University of California Davis, 95616, Davis; second author: Istituto per la Protezione Sostenibile delle Piante, Sez. di Torino, CNR, Turin, Italy; and third author: Colegio de Postgraduados-Campus Montecillo, 56230, Texcoco, Mexico.
  • Turina M; First and fourth authors: Plant Pathology Department, University of California Davis, 95616, Davis; second author: Istituto per la Protezione Sostenibile delle Piante, Sez. di Torino, CNR, Turin, Italy; and third author: Colegio de Postgraduados-Campus Montecillo, 56230, Texcoco, Mexico.
  • Zamora-Macorra EJ; First and fourth authors: Plant Pathology Department, University of California Davis, 95616, Davis; second author: Istituto per la Protezione Sostenibile delle Piante, Sez. di Torino, CNR, Turin, Italy; and third author: Colegio de Postgraduados-Campus Montecillo, 56230, Texcoco, Mexico.
  • Falk BW; First and fourth authors: Plant Pathology Department, University of California Davis, 95616, Davis; second author: Istituto per la Protezione Sostenibile delle Piante, Sez. di Torino, CNR, Turin, Italy; and third author: Colegio de Postgraduados-Campus Montecillo, 56230, Texcoco, Mexico.
Phytopathology ; 106(5): 500-9, 2016 May.
Article em En | MEDLINE | ID: mdl-26756828
Tomato marchitez virus (ToMarV; synonymous with Tomato apex necrosis virus) is a positive-strand RNA virus in the genus Torradovirus within the family Secoviridae. ToMarV is an emergent whitefly-transmitted virus that causes important diseases in tomato (Solanum lycopersicum) in Mexico. Here, the genome sequence of the ToMarV isolate M (ToMarV-M) was determined. We engineered full-length cDNA clones of the ToMarV-M genomic RNA (RNA1 and RNA2), separately, into a binary vector. Coinfiltration of both triggered systemic infections in Nicotiana benthamiana, tomato, and tomatillo (Physalis philadelphica) plants and recapitulated the biological activity of the wild-type virus. The viral progeny generated from tomato and tomatillo plants were transmissible by the whitefly Bemisia tabaci biotype B. Also, we assessed whether these infectious clones could be used for screening tomato cultivars for resistance to ToMarV and our results allowed us to differentiate resistant and susceptible tomato lines. We demonstrated that RNA1 of ToMarV-M is required for the replication of RNA2, and it can replicate independently of RNA2. From this, ToMarV-M RNA2 was used to express the green fluorescent protein in N. benthamiana plants, which allowed us to track cell-to-cell movement. The construction of full-length infectious cDNA clones of ToMarV-M provides an excellent tool to investigate virus-host-vector interactions and elucidate the functions of torradovirus-encoded proteins or the mechanisms of replication of torradovirus genomic RNA.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus de RNA / Genoma Viral / Solanum lycopersicum Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus de RNA / Genoma Viral / Solanum lycopersicum Idioma: En Ano de publicação: 2016 Tipo de documento: Article