Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Cactus X
potexvirus
Index
Data collated by R. Koenig, 1987.
Nomenclature
Synonyms
barrel cactus virus (Attathom et al, 1978;
Milne, 1988).
Acronym
Strains
Chessin, Milicic, Braunschweig.
ICTV decimal code
Host range and symptoms
First reported
in Cacti; from Germany; by Amelunxen (1958).
Natural host range and symptoms
Symptoms none.
- Opuntia vulgaris, Austrocylindropuntia cylindrica, Pereskia
saccharosa, Schlumbergera bridgesii, Epiphyllum spp., Cereus spp.,
Echinopsis spp., Zygocactus spp., Ferocactus acanthodes,
Echinocereus procumbens - usually infected symptomlessly.
Transmission
Virus transmitted by mechanical inoculation;
transmitted by grafting; transmitted by contact between plants; not transmitted
by seed.
Geographical distribution
Probably distributed
worldwide (in cultivated cacti). Spreads in the North American region; the USA.
Experimental host range
Several (3-9) families
susceptible. Experimentally infected plants mostly show necrotic local lesions,
mottle.
Diagnostically susceptible host species and symptoms
- Amaranthus caudatus - necrotic local lesions; rarely
systemic.
- Gomphrena globosa, Chenopodium amaranticolor - necrotic
local lesions; not systemic.
- C. quinoa - systemic mottle.
Diagnostically insusceptible host species
Nicotiana
tabacum, Phaseolus spp., Cucumis sativus.
Maintenance and
propagation hosts
Assay hosts
(Local lesions or Whole plants)
Gomphrena globosa (L), Chenopodium quinoa (W).
Susceptible host species
Insusceptible host
species
Families containing susceptible hosts
Families containing
insusceptible hosts
Sources of host-range data
Plese
and Milicic (1966).
Physical and
biochemical properties
Properties of particles in sap
TIP: 82
°C. LIV: 28 days (or longer). DEP: log10 minus 5. Infectivity of sap not
changed by treatment with di-ethyl ether. Leaf sap contains many virions.
Purification method
Koenig and
Lesemann (1983).
Particle morphology
Virions filamentous; not enveloped;
usually flexuous; with a clear modal length; of 520 nm; 13 nm wide. Axial canal
obscure.
Physical properties
One sedimenting component in purified
preparations; sedimentation coefficient 120 S.
Biochemical properties
Virions contain 5 % nucleic acid;
95 % protein; 0 % lipid.
Genome consists of RNA; single-stranded; linear. Total genome size 6.5
kb. Genome unipartite; largest (or only) genome part 6.5 kb. Genomic nucleic
acid isolated by Attathom et al. (1978); Koenig (1971). Base composition
20.8 % G; 26.4 % A; 29.2 % C; 23.6 % U. Infectivity retained when deproteinised
with phenol or detergent.
Features of proteins
Virion protein(s) one;
Mr 20000. Method of preparation: Attathom et al. (1978). Amino
acid composition: Attathom et al. (1978).
Replication
Replication does not depend on a helper
virus.
Cytopathology
Virions found in all parts of the host
plant; usually in cytoplasm, or in cell vacuoles (occasionally). Inclusions
cytoplasmic present in infected cells; are unusual in shape; banded bodies or
paracrystalline structures; they contain virions.
Taxonomy and
relationships
Virus(es) with serologically unrelated virions
Comments and
References
References
- Amelunxen, F. (1958).
Protoplasma 49: 140.
- Attathom, S., Weathers, L.G. and Gumpf,
D.J. (1978). Pl. Dis. Reptr. 62: 228.
- Attathom, S., Weathers,
L.G. and Gumpf, D.J. (1978). Phytopathology 68: 1401.
- Bercks,
R. (1971). CMI/AAB Descr. Pl. Viruses No. 58, 3 pp.
- Koenig, R.
(1978). J. gen. Virol. 40: 309.
- Koenig, R. and Lesemann, D.-E.
(1983). CMI/AAB Descr. Pl. Viruses No. 265, 3 pp.
- Milne, R.G. (1988).
In: The Plant Viruses, Vol. 4; The Filamentous Viruses, p.6; ed
Milne, R.G., Plenum, New York.
- Plese, N. and Milicic, D. (1966).
Phytopath. Z. 55: 197
- Ready, K.F.M. and Bancroft, J.B. (1985).
Virology 141: 302.
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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