Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Beet western
yellows ST9-associated RNA virus
Index
Data collated by M.J. Gibbs (1995).
Nomenclature
ICTV decimal code
Host range and symptoms
First reported
in Brassica oleracea var. botrytis (broccoli); from California,
U.S.A.; by Falk and Duffus (1984).
Transmission
Transmitted by a vector; an insect; Myzus
persicae; Aphididae. Transmitted in a persistent manner (probably). Virus
requires, for vector transmission, a helper virus (beet western yellows
luteovirus). The virus genome is probably transcapsidated in the virions of the
helper virus (Falk and Duffus, 1984). Virus transmitted by mechanical
inoculation (when transcripts from a DNA encoding the genome of the virus were
inoculated to young plants of shepherd's purse (Capsella bursa-pastoris).
Geographical distribution
Found, but with no evidence of
spread, in California, U.S.A.
Experimental host range
Few (<3) families susceptible.
Experimentally infected plants mostly show stunting, yellowing and twisting.
Diagnostically susceptible host species and symptoms
- Capsella bursa-pastoris - lethal yellowing and
necrosis, but causes milder yellowing, twisting and stunting when with beet
western yellows luteovirus.
Diagnostically insusceptible host species
Cichorium endiva, C. intybus, Lactuca sativa, Nicotiana
clevelandii and Solanum nigrum.
Maintenance and propagation
hosts
Assay hosts (Local lesions or Whole plants)
Capsella bursa-pastoris (W).
Susceptible host species
Insusceptible host species
Families containing susceptible hosts
Families containing
insusceptible hosts
Physical and biochemical properties
Biochemical properties
Genome consists of RNA;
single-stranded; linear. Total genome size 2.843 kb (Chin et al.,
1993). Genome unipartite; largest (or only) genome part 2.843 kb. Infectivity
retained when deproteinised with phenol or detergent (Passmore et al.,
1993). Poly A region absent. Additional factor not required for infectivity.
Nucleotide sequence references: Chin et al., 1993.
Sequence database accession code(s)
Features of the genome
Features of the genome: Four
ORFs. Only ORF3 encodes a protein with recognizable function, the polymerase.
ORF2 may be translated after tRNA suppression of the amber stop codon of
ORF1, but sequence analysis suggests that the reported sequence may be in error
and that ORFs 2 and 3 may be a single ORF (Gibbs, 1995). ORF4 is probably
translated from a subgenomic RNA.
Sub-genomic mRNA found in infected cells; c. 400 bp long
and co-terminal with the 3´ end. 2 virus specified dsRNA species found in
infected cells (one from the helper virus and of c. 2.9 kb pairs).
Replication
Replication does not depend on a helper
virus; ST9 a-virus does not produce its own virion proteins or virions, however
plants co-infected with it and its helper produce 10 times more virions than the
helper does alone (Sanger et al., 1994).
Taxonomy and
relationships
Additional comments on relationships
This virus is not sufficiently similar to viruses in any of the
currently recognized groups to be comfortably placed with them. Its polymerase
protein shows affinities with those of the carmoviruses, dianthoviruses, type 1
and 2 luteoviruses, machlomoviruses, necroviruses, tombusviruses, umbraviruses
and pea enation mosaic virus RNA-2.
Comments and
References
General comments
This organism has
features of a satellite RNA, but can replicate independently, and therefore is
included as a virus.
References
- Chin, L.-S., Forster, J.L., Falk, B.W.
and Bruening, G. (1993). Proc. Natl. Acad. Sci. USA 90: 10168.
- Falk, B.W. and Duffus, J.E. (1984). Phytopathology 74: 1224.
- Gibbs, M.J. (1995). D. Phil. thesis, Oxford University.
- Sanger,
M. Passmore, B., Falk, B.W., Bruening, G., Ding, B. and Lucas, W.J. (1994).
Virology 200: 48.
Cite this publication as:
Brunt, A.A., Crabtree, K., Dallwitz, M.J., Gibbs, A.J., Watson, L. and Zurcher, E.J. (eds.)
(1996 onwards).
`Plant Viruses Online: Descriptions and Lists from the VIDE Database.
Version: 20th August 1996.' URL
http://biology.anu.edu.au/Groups/MES/vide/
Dallwitz (1980)
and
Dallwitz, Paine and Zurcher (1993)
should also be cited.







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