Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Physalis mosaic
tymovirus
Index
Data collated by A.J. Gibbs, 1991.
Nomenclature
Synonyms
belladonna mottle virus - US, belladonna mottle
virus - Iowa.
Acronym
ICTV decimal code
Host range and symptoms
First reported
in Physalis subglabrata; from U.S.A. (Urbana, Illinois); by Peters and
Derks (1974).
Natural host range and symptoms
Symptoms persist.
Symptoms mosaics and mottles.
- Physalis subglabrata, P. heterophylla - systemic mosaic or
mottle.
Geographical distribution
Experimental host range
Several (3-9) families
susceptible. Experimentally infected plants mostly show necrotic or chlorotic
local lesions, systemic mottle or mosaic.
Diagnostically
susceptible host species and symptoms
- Capsicum annuum -
chlorotic local lesions, systemic mottle.
- Datura metel, D. stramonium
- necrotic local lesions, systemic mosaic.
- Nicandra physalodes
- systemic mosaic.
- Nicotiana clevelandii, N. glutinosa, N. tabacum
cv. White Burley - necrotic local lesions.
- Chenopodium foetidum
- systemic chlorosis.
- Sonchus oleraceus - symptomless
infection.
Diagnostically insusceptible host species
Atropa belladonna, Brassica campestris ssp. pekinensis, Phaseolus
vulgaris, Pisum sativum, Solanum melongena.
Maintenance and
propagation hosts
Datura stramonium, Nicotiana clevelandii, N.
glutinosa.
Assay hosts (Local lesions or
Whole plants)
Datura stramonium (W),
Nicotiana clevelandii (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
LIV: 50
days. DEP: log10 minus 8. Infectivity of sap not changed by treatment with
di-ethyl ether. Leaf sap contains many virions.
Purification method
Particle morphology
Virions isometric; not enveloped;
27-29 nm in diameter; rounded in profile; with a conspicuous capsomere
arrangement.
Physical properties
Two sedimenting components in
purified preparations; sedimentation coefficient of the fastest 112-114
S; of the other(s) 50-54 S. Density 1.42 g cm-3 in CsCl (B),
or 1.27 g cm-3 in CsCl (T). A260/A280 ratio 1.63 (B), or 1.06 (T).
Biochemical properties
Virions contain 38 % nucleic acid;
62 % protein.
Genome consists of RNA; single-stranded; linear; unipartite. Base
composition 14.4 % G; 22.9 % A; 37.2 % C; 25.5 % U. Genome has
tRNA-like activity. Genome accepts valine.
Sequence database accession code(s)
- S97776
Em(40)_vi:S97776 Gb(84)_vi:S97776 replicase protein, coat protein (3´ region)
Physalis mottle virus PhMV.
Features of proteins
Virion protein(s) one;
Mr 20000; coat protein. Amino acid sequence: Jacob et al.
(1991).
Replication
Replication does not depend on a helper
virus.
Cytopathology
Virions found in all parts of the host
plant.
Taxonomy and
relationships
Virus(es) with serologically related virions
Belladonna mottle and dulcamara mottle viruses.
Differences between type strain and others
Most of the plant species inoculated with physalis mosaic virus or
with belladonna mottle virus (I) isolate reacted similarly however
Chenopodium quinoa and Solanum nigrum were infected by the latter
and not the former.
Additional comments on relationships
Slight cross protection with Andean potato latent and
dulcamara mottle viruses.
Comments and
References
References
- Jacob, A.N.K., Murthy,
M.R.N. and Savithri, H.S. (1991). J. gen. Virol. in press.
- Moline,
H.E. and Fries, R.E. (1974). Phytopathology 64: 44.
- Peters, D.
and Derks, A.F.L.M. (1974). Neth. J. Pl. Path. 80: 124.
- Peter,
R., Peter, C., Dupin, A. and Witz, J. (1989). C.r. Acad. Sci. Paris
309 Serie III, p. 599.
- Savithri, H.S., Monski, S.K., Suryanarayana,
S., Divikar, S. and Murthy, M.R.N. (1987). J. gen. Virol. 68:
1533.
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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