Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
White clover
mosaic potexvirus
Index
Data collated by P.L. Guy, 1980. Revised 1983.
Nomenclature
Synonyms
clover mosaic virus, pea wilt virus (Bos et
al., 1959; Johnson, 1942).
Acronym
ICTV decimal code
Host range and symptoms
First reported
in Trifolium repens; from the U.S.A; by Pierce (1935).
Natural host range and symptoms
Symptoms vary seasonally.
- Trifolium spp. - chlorotic mottling, streaking and systemic
mosaic.
Transmission
Virus transmitted by mechanical inoculation;
transmitted by contact between plants; transmitted by seed (to 6% in
Trifolium pratense).
Geographical distribution
Probably distributed worldwide (in temperate regions).
Experimental host range
Several (3-9) families
susceptible.
Diagnostically susceptible host species and
symptoms
- Cucumis sativus - necrotic local lesions.
- Phaseolus vulgaris - necrotic and chlorotic local lesions,
systemic yellowing.
- Pisum sativum - chlorotic local lesions, leaf
shape malformation.
- Trifolium spp. - systemic mosaic.
- Vicia
faba - necrotic local lesions, systemic mosaic.
- Vigna
unguiculata - necrotic and chlorotic local lesions.
Diagnostically insusceptible host species
Maintenance and propagation hosts
Phaseolus
vulgaris, Pisum sativum.
Assay hosts (Local
lesions or Whole plants)
Susceptible host species
Insusceptible host species
Families containing susceptible hosts
Families containing
insusceptible hosts
Sources of host-range data
Bancroft
et al. (1960); Beczner and Vassanyi (1981).
Physical and
biochemical properties
Properties of particles in sap
TIP: 60
°C. LIV: 10-99 days. DEP: log10 minus 4-5. Infectivity of sap not changed by
treatment with di-ethyl ether. Leaf sap contains many virions (especially
that from French bean, although often fewer in sap of infected clover).
Purification method
Francki and
McLean (1968).
Particle morphology
Virions filamentous; not enveloped;
usually flexuous; with a clear modal length; of 480 nm; 13 nm wide. Axial canal
obscure; 3.5 nm in diameter. Basic helix obvious; pitch of basic helix 3.4 nm.
Physical properties
One sedimenting component in purified
preparations; sedimentation coefficient 119 S. Isoelectric point pH 4.5.
Biochemical properties
Virions contain 6 % nucleic acid;
94 % protein; 0 % lipid.
Genome consists of RNA; single-stranded; linear. Total genome size 5.845
kb. Genome unipartite; largest (or only) genome part 5.845 kb. Base composition
15.5 % G; 31.8 % A; 26.9 % C; 25.7 % U. 5´ terminus of RNA has an unusual
type; a nucleotide cap probably of the type m7GpppG. Infectivity retained
when deproteinised with phenol or detergent.
Sequence database accession code(s)
- M18920
Em(40)_vi:WCP3EA Gb(84)_vi:WCP3EA White clover mosaic potexvirus 3´-terminal
RNA region encoding ORFs of 17K, 5´ end; and of 13
- X06728
Em(40)_vi:POWC1MVX Gb(84)_vi:POWC1MVX Potexvirus white clover mosaic virus
(WC1MV) RNA genome. 9/93 5,845bp.
- X16636 Em(40)_vi:POWCLMV4
Gb(84)_vi:POWCLMV4 White clover mosaic virus total genomic mRNA. 9/93 5,846bp. 3
sequences.
Features of proteins
Virion protein(s) one;
Mr 14000-20000. Method of preparation: Miki et al. (1967);
Koenig et al. (1971).
Replication
Replication does not depend on a helper
virus.
Cytopathology
Virions found in all parts of the host
plant; in cytoplasm. Inclusions present in infected cells; are unusual in shape;
cytoplasmic banded bodies and few vesiculated aggregates; they contain virions.
Taxonomy and
relationships
Virus(es) with serologically related virions
Potato X, cactus X, hydrangea ringspot and clover yellow mosaic
viruses, but distantly.
Best tests for diagnosis
The banded
body inclusions induced by white clover mosaic virus are disrupted when
preparing epidermal strips for examination, but these inclusions distinguish
white clover mosaic virus from clover yellow mosaic virus.
Comments and
References
References
- Agrawal, H., Bos, L. and
Chessin, M. (1962). Phytopathology 62: 517.
- Bancroft, J.B.,
Tuite, J. and Hissong, G. (1960). Phytopathology 50: 711.
- Beczner, L. and Vassanyi, R. (1981). Acta Phytopath. Acad. Sci. Hung.
16: 109.
- Bos, L., Delvic, B. and van der Want, J.P.H. (1959).
Tijdschr. PlZiekt. 65: 89.
- Bucks, R. (1971). CMI/AAB Descr.
Pl. Viruses No. 41, 4 pp.
- Edwardson, J.R. and Christie, R.G. (1986).
Fla Agric. Exp. Stn Monog. No. 14, p. 350.
- Forster, R.L.S., Bevan,
M.V., Harrison, S.A. and Gardner, R.C. (1988). Nucl. Acids Res.
16: 291.
- Francki, R.I.B. and McLean, G.D. (1968). Aust. J. biol.
Sci. 21: 1311.
- Fry, P.R., Grogan, R.G. and Lyttleton, J.W.
(1960). Phytopathology 50: 175.
- Johnson, F. (1942).
Phytopathology 32: 103.
- Koenig, R. (1971). J. gen.
Virol. 10: 111.
- Miki, T. and Knight, C.A. (1967). Virology
31: 55.
- Pierce, W.H. (1935). J. Agric. Res. 51: 1017.
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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