Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Cycas necrotic
stunt nepovirus
Index
Data collated by M. Kusunoki, K. Hanada and M.
Kameya, 1987.
Nomenclature
Acronym
ICTV decimal code
Host range and symptoms
First reported
in Cycas revoluta; from Chiba Prefecture, Japan; by Kusunoki et
al. (1975).
Natural host range and symptoms
Symptoms persist and vary
seasonally.
- Cycas revoluta - twisted young leaves and chlorotic or
necrotic spots of mature leaves, stunting.
- Daphne odora - mild
mosaic.
- Aucuba japonica - vein clearing.
- Gladiolus spp.
- symptomless.
Transmission
Transmitted by possibly a vector; a
nematode. Virus transmitted by mechanical inoculation; transmitted by seed
(about 30% in Chenopodium amaranticolor and over 80% in C.
serotinum).
Geographical distribution
Experimental host range
Several (3-9) families
susceptible.
Diagnostically susceptible host species and
symptoms
- Tetragonia tetragonioides, Chenopodium amaranticolor,
C. quinoa, C. serotinum - chlorotic local lesions or ringspots, then
systemic mottling and necrosis.
- Celosia cristata - systemic
mottling.
- Gomphrena globosa, Beta vulgaris - latent infection.
- Spinacia oleracea - latent infection.
- Cycas revoluta
- chlorotic spotting, then systemic mottling and necrosis.
Diagnostically insusceptible host species
Cucumis
sativus, Cucurbita moschata, Glycine max, Nicotiana clevelandii, Lycopersicon
esculentum, Nicotiana tabacum, N. glutinosa, Phaseolus vulgaris, Pisum sativum,
Catharanthus roseus, Datura stramonium.
Maintenance and
propagation hosts
Chenopodium serotinum, C. quinoa, C.
amaranticolor, Celosia cristata.
Assay hosts (Local lesions or Whole plants)
Chenopodium quinoa (L and W), C. amaranticolor (L) and then (W),
C. murale (L) and then (W), C. serotinum (W), Tetragonia
tetragonioides (L).
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:
60-65 °C. LIV: 18-24 days. DEP: log10 minus 3. Leaf sap contains many
virions.
Purification method
Particle morphology
Virions isometric; not enveloped; 28
nm in diameter; angular in profile; with a conspicuous capsomere arrangement.
Physical properties
Three sedimenting components in
purified preparations; sedimentation coefficient of the fastest 112 S
(B); of the other(s) 85 S (M). Density 1.472 g cm-3 in CsCl (B), or
1.404 g cm-3 in CsCl (M). A260/A280 ratio 1.67 (B), or 1.41 (M), or
1 (T).
Biochemical properties
Virions contain 24 % nucleic acid
(B), or 12 % nucleic acid (M), or 0 % nucleic acid (T); 76 % protein (B), or 88
% protein (M), or 100 % protein (T).
Genome consists of RNA; single-stranded; linear. Total genome size 12.85
kb. Genome of two parts; largest (or only) genome part the larger 8.1 kb; the
2nd largest 4.75 kb. Genomic nucleic acid isolated by Hanada et al.
(1986). Infectivity retained when deproteinised with phenol or detergent.
Additional factor not required for infectivity.
Features of the genome
Non-genomic nucleic acid
not found in the virions.
Features of proteins
Virion protein(s) three;
Mr of the largest 71000. Mr of 2nd largest 65000.
Mr of 3rd largest 56000.
Replication
Genome replicates in cytoplasm. Replication
does not depend on a helper virus.
Cytopathology
Virions found in leaves; in cytoplasm, in
Golgi apparatus, and in cell vacuoles; in plasmodesmata. Inclusions present in
infected cells; are viroplasms (crystalline aggregates of virions and capsid
protein); they contain virions. Other cellular changes: vesicular structures
also occur in cytoplasm.
Taxonomy and
relationships
Virus(es) with serologically unrelated virions
Arabis mosaic, cacao necrosis, cherry leaf roll, crimson clover
latent, grapevine chrome mosaic, mulberry ringspot, myrobalan latent, tobacco
ringspot, tomato ringspot and tomato black ring viruses.
Best tests for diagnosis
Use gel
diffusion serology; species of Fabaceae and Solanaceae not
infected despite `nepovirus-like' symptoms in Chenopodium plants.
Comments and
References
References
- Hanada, K., Kusunoki, M.
and Iwaki, M. (1986). Ann. Phytopath. Soc. Japan 52: 422.
- Kusunoki, M., Nagai, Y., Yamashita, S., Doi, Y. and Yora, K. (1975). Ann.
Phytopath. Soc. Japan 41: 285.
- Kusunoki, M., Hanada, K., Iwaki,
M., Chang, M.U., Doi, Y. and Yora, K. (1986). Ann. Phytopath. Soc. Japan
52: 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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