Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Wheat American
striate mosaic nucleorhabdovirus
Index
Data collated by R.G. Timian, 1987.
Nomenclature
Synonyms
oat rhabdovirus, oat striate rhabdovirus, oat
striate mosaic virus, American wheat striate mosaic virus, wheat striate mosaic
virus.
Acronym
ICTV decimal code
Host range and symptoms
First reported
in Triticum vulgare; from South Dakota, U.S.A.; by Slykhuis (1953).
Natural host range and symptoms
Symptoms persist.
- Triticum dicoccum, T. vulgare, T. durum, Bromus inermis, Eragrostis
cilianensis, Panicum capillare - faint chlorotic streaks along the
veins, clearest on the abaxial surfaces of leaves, then necrosis. Brown necrotic
spots and streaks develop in some cultivars. Wheat plants die or become stunted
with sterile heads.
Transmission
Transmitted by a vector; an insect;
Elymana virescens and Endria inimica; Cicadellidae. Transmitted in
a persistent manner. Virus lost by the vector when it moults; multiplies in the
vector; not transmitted congenitally to the progeny of the vector; not
transmitted by mechanical inoculation; not transmitted by contact between
plants; not transmitted by seed; not transmitted by pollen.
Ecology
and control
Studies reported by Slykhuis (1953); Slykhuis (1963).
Geographical distribution
Spreads in the North American
region; Canada and the USA.
Experimental host range
Few (<3) families susceptible.
Experimentally infected plants mostly show severe striate mosaic.
Diagnostically susceptible host species and symptoms
- Avena sativa, Eragrostis cilianensis, Panicum capillare and
Triticum durum - severe chlorotic striping.
- Hordeum vulgare
and Zea mays - mild chlorotic striping.
Diagnostically
insusceptible host species
Maintenance and propagation hosts
Bromus inermis,
Triticum durum.
Assay hosts (Local lesions or
Whole plants)
Susceptible host species
Insusceptible host species
Families containing susceptible hosts
Families containing
insusceptible hosts
Comments on host-range
Few species
tested, none of them dicotyledons.
Sources of host-range data
Slykhuis
(1953); Slykhuis (1963).
Physical and
biochemical properties
Properties of particles in sap
TIP: 55
°C. LIV: 3 days (at 4ºC or -10ºC). DEP: log10 minus 5. Leaf sap
contains many virions. Electron microscopy: fix with gluteraldehyde before
mounting in PTA.
Purification method
Ahmed et
al. (1970), for infective virus; Thottappilly and Sinha (1973) for antigen.
Particle morphology
Virions rhabdo- or
bullet-shaped; enveloped; usually straight; with a clear modal length; of
200-250 nm; 75 nm wide. Axial canal obvious; 23 nm in diameter. Basic helix
obscure.
Physical properties
One sedimenting component in purified
preparations, or two sedimenting components in purified preparations;
sedimentation coefficient 875 S (major component).
Biochemical properties
Virions contain 5 % nucleic acid;
68 % protein; 25 % lipid. Also carbohydrate (probably) 2%.
Genome consists of RNA; single-stranded; linear. Total genome size 7 kb.
Genome unipartite; largest (or only) genome part 7 kb. Genomic nucleic acid
isolated by Sinha et al. (1976). Base composition 26.4 % G; 21.3 % A;
22.5 % C; 29.8 % U.
Features of proteins
Virion protein(s) four;
Mr of the largest 145000. Mr of 2nd largest 92000;
glycoprotein. Mr of 3rd largest 59000; N protein. Mr of 4th
largest 25000. Method of preparation: Trefzger et al. (1976). Amino acid
composition: Sinha et al. (1976).
Replication
Genome replicates in nuclei and in cytoplasm
(associated with the nuclear membrane and within cytoplasmic cisternae).
Replication does not depend on a helper virus.
Cytopathology
Virions found in leaves, roots, mesophyll,
epidermis, vascular parenchyma, companion cells and all parts of the host plant;
in cytoplasm, in nuclei, and in the perinuclear space. Other cellular changes:
the plasma membrane separating from the cell wall.
Taxonomy and
relationships
Best tests for diagnosis
Wheat
streak mosaic rymovirus is transmitted mechanically and by mites whereas wheat
striate mosaic cytorhabdovirus is transmitted by Endria inimica but not
mechanically.
Comments and
References
References
- Ahmed, M.E., Sinha, R.C.
and Hochster, R.M. (1970). Virology 41: 768.
- Sinha, R.C. and
Behki, R.M. (1972). CMI/AAB Descr. Pl. Viruses No. 99, 4 pp.
- Sinha,
R.C., Harwalkar, V.R. and Behki, R.M. (1976). Phytopath. Z. 87:
314.
- Slykhuis, J.T. (1953). Phytopathology 43: 537.
- Slykhuis, J.T. (1963). Can. J. Bot. 41: 1171.
- Thottappilly, G. and Sinha, R.C. (1973). Virology 33: 312.
- Trefzger-Stevens, J. and Lee, P. (1976). Virology 78: 144.
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.







Please send comments, corrections and suggestions to:
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