Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Olive latent
ringspot nepovirus
Index
Data collated by D. Gallitelli, 1987.
Nomenclature
Acronym
ICTV decimal code
Host range and symptoms
First reported
in Olea europaea; from Lazio, Central Italy; by Savino et al.
(1983).
Natural host range and symptoms
Transmission
Virus transmitted by mechanical inoculation;
transmitted by grafting.
Geographical distribution
Spreads in
Italy (Lozio, central Italy).
Experimental host range
Several (3-9) families
susceptible.
Diagnostically susceptible host species and
symptoms
- Chenopodium quinoa, C. amaranticolor -
chlorotic or necrotic local lesions, systemic mosaic, apical necrosis.
- Gomphrena globosa - red-rimmed local lesions, tip leaves
malformed.
Diagnostically insusceptible host species
Nicotiana tabacum cvs Samsun, White Barley, N. glutinosa, Vigna
radiata.
Maintenance and propagation hosts
Chenopodium quinoa, Nicotiana clevelandii.
Assay hosts (Local lesions or Whole plants)
Chenopodium quinoa (W), Chenopodium amaranticolor (W), Cucumis
sativus cv. Markerer (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: 60
°C. LIV: 15 days. DEP: log10 minus 3.
Purification method
Gallitelli:
homogenise symptom bearing Chenopodium quinoa leaves in 0.1M neutral
phosphate buffer. Clarify the sap with Mg-activated bentonite. Purify by two
cycles of centrifugation.
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; sedimentation coefficient of the fastest 132 S
(B); of the other(s) 97 S (M), or 52 S (T). Density 1.52 g
cm-3 in CsCl (B2), or 1.51 g cm-3 in CsCl (B1), or 1.43 g
cm-3 in CsCl (M), or 1.29 g cm-3 in CsCl (T). A260/A280 ratio
1.8 (B), or 1.51 (M), or 1.03 (T).
Biochemical properties
Virions contain 45 % nucleic acid
(B2), or 43 % nucleic acid (B1), or 32 % nucleic acid (M), or 0 % nucleic
acid (T); 55 % protein (B2), or 57 % protein (B1), or 68 % protein (M), or
100 % protein (T).
Genome consists of RNA; single-stranded. Total genome size 11.4 kb.
Genome of two parts; largest (or only) genome part the larger 7.5 kb; the 2nd
largest 3.9 kb. Genomic nucleic acid isolated by Gallitelli; best means by
phenol - SDS. Infectivity retained when deproteinised with phenol or
detergent. Additional factor not required for infectivity.
Features of proteins
Virion protein(s) one;
Mr 58000; a polymer of a monomeric form of 16kDa. Method of
preparation: Gallitelli; boil for 3 minutes in 125mM Tris-Cl pH 6.8 containing
1% SDS, 2% beta-mercaptoethanol, 6M urea. Virion proteins not glycosylated.
Cytopathology
Virions found in leaves mesophyll and
epidermis; in cytoplasm and in cell vacuoles. Inclusions present in infected
cells; are crystals in the cytoplasm and membranous bodies; they contain
virions. Other cellular changes: clumping of chloroplasts and finger-like
outgrowths of the cell.
Taxonomy and
relationships
Virus(es) with serologically unrelated virions
Arabis mosaic, artichoke Italian latent, artichoke yellow ringspot,
artichoke vein banding, cherry leaf roll, cherry rasp leaf, chicory yellow
mottle, cacao necrosis, grapevine Bulgarian latent, grapevine fanleaf, grapevine
chrome mosaic, myrobalan latent ringspot raspberry ringspot, strawberry latent
ringspot, tobacco ringspot, tomato black ring and tomato ringspot viruses.
Comments and
References
References
- Gallitelli, D.,
Martelli, G.P. and Savino, V. (1985). AAB Descr. Pl. Viruses No. 301, 4
pp.
- Savino, V., Gallitelli, D. and Barba, M. (1983). Ann. appl. Biol.
103: 243.
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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