Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Broad bean true
mosaic comovirus
Index
Data collated by A.J. Gibbs, 1981. Revised 1987.
Nomenclature
Synonyms
Vicia virus 1, Echtes
Ackerbohnenmosaikvirus.
Acronym
ICTV decimal code
Host range and symptoms
First reported
in Vicia faba; from Germany; by Quantz (1953).
Natural host range and symptoms
Symptoms vary cyclically
over a few weeks.
- Vicia faba - mild mosaic and malformation, necrosis.
Transmission
Transmitted by a vector; an insect; Apion
vorax, Sitonia spp. and other weevils; Coleoptera. Virus transmitted
by mechanical inoculation; transmitted by seed.
Geographical
distribution
Spreads in the African region and the Eurasian region;
China, Morocco, and the UK. Found, but with no evidence of spread, in Australia
in crops grown from imported seed.
Experimental host range
Few (<3) families susceptible.
Diagnostically susceptible host species and symptoms
- Pisum sativum - systemic chlorosis, shoot necrosis.
- Vicia faba - mottle, mosaic and shoot necrosis.
Diagnostically insusceptible host species
Chenopodium
amaranticolor, Nicotiana clevelandii.
Maintenance and propagation
hosts
Pisum sativum, Vicia faba.
Assay hosts (Local lesions or Whole plants)
Pisum sativum (W), Vicia faba (W).
Susceptible host
species
Insusceptible host
species
Families containing susceptible hosts
Families
containing insusceptible hosts
Sources of host-range data
Physical and
biochemical properties
Properties of particles in sap
TIP:
65-75 °C. LIV: 6-7 days. DEP: log10 minus 4. Infectivity of sap not changed
by treatment with di-ethyl ether. Leaf sap contains many virions.
Purification method
Blevings and
Stace-Smith (1976).
Particle morphology
Virions isometric; not enveloped; 28
nm in diameter; angular in profile; without a conspicuous capsomere arrangement.
Physical properties
Three sedimenting components in
purified preparations (in reducing buffer); sedimentation coefficient of the
fastest 116 S (B); of the other(s) 95 S (M), or 59 S (T).
A260/A280 ratio 1.81 (B), or 1.76 (M).
Biochemical properties
Virions contain 35 % nucleic acid
(B), or 26 % nucleic acid (M), or 0 % nucleic acid (T); 65 % protein (B), or 74
% protein (M), or 100 % protein (T).
Genome consists of RNA; single-stranded; linear. Base composition 22.8 %
G; 26.5 % A; 18.4 % C; 32.3 % U. Infectivity retained when deproteinised with
phenol or detergent.
Features of the genome
Non-genomic nucleic acid
not found in the virions.
Features of proteins
Virion protein(s) two;
Mr of the larger 37500. Mr of 2nd largest 24500. Method of
preparation: Blevings and Stace-Smith (1976).
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;
are tubules from plasmodesmata containing rows of virus virions, also
vesiculated bodies and virus aggregates (Russo et al., 1982).
Taxonomy and
relationships
Virus(es) with serologically related virions
Broad bean stain, glycine mosaic, radish mosaic and squash mosaic
viruses.
Comments and
References
References
- Blevings, S. and
Stace-Smith, R. (1976). J. gen. Virol. 31: 199.
- Cockbain,
A.J., Cook, S.M. and Bowen, R. (1975). Ann. appl. Biol. 81: 331.
- Cockbain, A.J., Bowen, R. and Vorra-Urai, S. (1976). Ann. appl. Biol.
84: 321.
- Gibbs, A.J. and Paul, H.L. (1970). CMI/AAB Descr. Pl.
Viruses No. 20, 4 pp.
- Gibbs, A.J., Giussani-Belli, G. and Smith, H.G.
(1968). Ann. appl. Biol. 61: 99.
- Jones, A.T. (1978). Ann.
appl. Biol. 88: 137.
- Quantz, L. (1953). Phytopath. Z.
20: 421.
- Randles, J.W. and Dube, A.J. (1977). Australas. Pl. Path.
Soc. Newsl. 6: 37.
- Russo, M., Castellano, M.A. and Martelli, G.P.
(1982). J. Submicrosc. Cytol. 14: 149.
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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