Rescue of Citrus sudden death-associated virus in Nicotiana benthamiana plants from cloned cDNA: insights into mechanisms of expression of the three capsid proteins.
Amino Acid Sequence
Capsid Proteins
/ chemistry
Citrus
/ virology
Cloning, Molecular
DNA, Complementary
/ genetics
Gene Expression Regulation, Viral
Mutation
/ genetics
Plant Diseases
/ virology
Plants, Genetically Modified
RNA, Guide, Kinetoplastida
/ genetics
RNA, Viral
/ genetics
Nicotiana
/ genetics
Transcription, Genetic
Tymoviridae
/ genetics
Virion
/ metabolism
Citrus sudden death-associated virus
Marafivirus
Tymoviridae
capsid protein expression
citrus disease
infectious clone
Journal
Molecular plant pathology
ISSN: 1364-3703
Titre abrégé: Mol Plant Pathol
Pays: England
ID NLM: 100954969
Informations de publication
Date de publication:
05 2019
05 2019
Historique:
pubmed:
24
12
2018
medline:
6
5
2020
entrez:
22
12
2018
Statut:
ppublish
Résumé
Citrus sudden death-associated virus (CSDaV) is a member of the genus Marafivirus in the family Tymoviridae, and has been associated with citrus sudden death (CSD) disease in Brazil. Difficulties in the purification of CSDaV from infected citrus plants have prevented progress in the investigation of the role of this virus in CSD and an understanding of its molecular biology. In this work, we have constructed a full-length cDNA clone of CSDaV driven by the 35S promoter (35SRbz-CSDaV). Agrobacterium tumefaciens-mediated inoculation of 35SRbz-CSDaV in Nicotiana benthamiana plants enabled a fast recovery of large amounts of virions from the agroinfiltrated leaves, which allowed a better molecular characterization of CSDaV. In vivo analyses of mutant versions of 35SRbz-CSDaV revealed the expression strategies used by CSDaV for production of the capsid proteins (CPs). We showed that CSDaV virions contain three forms of CP, each of which is generated from the same coding sequence, but by different mechanisms. The major CPp21 is a product of direct translation by leaky scanning from the second start codon in the subgenomic RNA (sgRNA), whereas the minor CPs, p25 and p23, are produced by direct translation from the first start codon in the sgRNA and by trans-proteolytic cleavage processing derived from the p25 precursor, respectively. Together, these findings contribute to advance our understanding of CSDaV genome expression strategies. In addition, the construction and characterization of the CSDaV infectious clone represent important steps towards the investigation of the role of this virus in CSD and of its use as a tool for citrus biotechnology.
Identifiants
pubmed: 30575252
doi: 10.1111/mpp.12780
pmc: PMC6637869
doi:
Substances chimiques
Capsid Proteins
0
DNA, Complementary
0
RNA, Guide
0
RNA, Viral
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
611-625Informations de copyright
© 2018 The Authors. Molecular Plant Pathology Published by British Society for Plant Pathology and John Wiley & Sons Ltd.
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