Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Hibiscus
chlorotic ringspot carmovirus
Index
Data collated by C. Büchen-Osmond, 1987. Revised
by R. Bonfiglioli and K. Gibb, 1991.
Nomenclature
Acronym
ICTV decimal code
Host range and symptoms
First reported
in Hibiscus rosa-sinensis; from the U.S.A.; by Waterworth et al.
(1976).
Natural host range and symptoms
Symptoms persist.
- Hibiscus rosa-sinensis - mottling or chlorotic spots, rings
or vein-banding. Very variable.
- Abelmoschus manihot - mosaic.
Transmission
Transmitted by means not involving a vector;
is not transmitted by Myzus persicae, nor by Epilachna varivestis.
Virus transmitted by mechanical inoculation.
Ecology and
control
Studies reported by Waterworth (1980).
Geographical
distribution
Spreads in Australia, El Salvador, Fiji, the Solomon
Islands, Thailand, and the USA.
Experimental host range
Several (3-9) families
susceptible.
Diagnostically susceptible host species and
symptoms
- Chenopodium quinoa - chlorotic local lesions,
not systemic.
- Cyamopsis tetragonoloba, Gossypium hirsutum, Vigna
unguiculata ssp. cylindrica - necrotic local lesions, not
systemic.
- Hibiscus cannabinus (kenaf) - ringspots, local lesions,
then systemic mottle.
- Phaseolus vulgaris cv. Pinto - small local
lesions, not systemic.
Maintenance and propagation hosts
Hibiscus cannabinus - for purification. Althaea spp. and
Hibiscus rosa-sinensis - for maintaining cultures.
Assay
hosts (Local lesions or Whole plants)
Cyamopsis tetragonoloba (L); Vigna unguiculata ssp.
cylindrica (L). Hibiscus cannabinus (L) is the most sensitive
host.
Susceptible host species
Families containing susceptible hosts
Sources of host-range data
Waterworth et al. (1976).
Physical and
biochemical properties
Properties of particles in sap
TIP: 72
°C. LIV: 30 days (at 20ºC). DEP: log10 minus 8. Leaf sap contains many
virions.
Purification method
Waterworth
et al. (1976); Jones and Behncken (1980).
Particle morphology
Virions isometric; not enveloped; 28
nm in diameter; angular in profile; with a conspicuous capsomere arrangement
(negative stain apparently penetrates about one virion in five - Waterworth
et al., 1976; Jones and Behncken, 1980).
Physical properties
One sedimenting component in purified
preparations; sedimentation coefficient 118 S (Jones and Behncken, 1980;
Waterworth et al., 1976). Density 1.35 g cm-3 in CsCl.
Biochemical properties
Virions contain 14 % nucleic acid;
86 % protein; 0 % lipid.
Genome consists of RNA; single-stranded. Total genome size 4.4 kb. Genome
unipartite; largest (or only) genome part 4.4 kb. Base composition 23.8 % G;
25.5 % A; 26.4 % C; 24.3 % U.
Features of proteins
Virion protein(s) one;
Mr 44100; coat protein.
Replication
Replication does not depend on a helper
virus.
Cytopathology
Virions found in mesophyll; in cytoplasm
and in cell vacuoles (of broken cells). Inclusions absent from infected cells.
Taxonomy and
relationships
Virus(es) with serologically unrelated virions
45 viruses with isometric virions (Waterworth et al., 1976),
including okra mosaic virus (Givord and Hirth, 1973) and hibiscus latent
ringspot virus (Brunt et al., 1980). Isolates from the U.S.A. and El
Salvador (Waterworth et al., 1976), Australia (Jones and Behncken, 1980),
Fiji (Brunt, 1980) and Thailand (H.C. Phatak, unpublished data) are
serologically indistinguishable.
Additional comments on relationships
Hibiscus chlorotic ringspot virus may be related to, or the same, as
an agent that induces a mosaic disease of Hibiscus rosa-sinensis in
Hawaii (Hendrix and Murakishi, 1951).
Best tests for
diagnosis
Hibiscus chlorotic ringspot virus is
just one of several viruses that infect Malvaceae in nature. Others include
- (1) okra mosaic tymovirus which causes a mosaic in Abelmoschus
esculentus (Givord and Hirth, 1973).
- (2) hibiscus latent ringspot
nepovirus which sediments as 3 components and causes leaf chlorosis in
Hibiscus rosa-sinensis (Brunt et al., 1980).
- (3) malva yellows
luteovirus is an aphid-transmitted virus found in many species that hibiscus
chlorotic ringspot does not infect (Costa et al., 1959).
- (4)
chlorosis in Malvaceae is caused by abutilon mosaic bigeminivirus and is
transmitted by whitefly (Flores and Silberschmidt, 1967; Costa, 1954).
- (5)
yellow vein mosaic of Abelmoschus esculentus (bhendi) (Capoor and Varma,
1950), of A. esculentus (okra) and of Gossypium hirstutum (cotton)
(Santry and Singh, 1973).
- (6) hibiscus line pattern which is not
transmissible by sap inoculation (Wolfswinkel, 1966).
- (7) leaf curl virus
which induces different symptoms (Makherjie and Raychaudhuri, 1964).
Comments and
References
References
- Brunt, A.A. (1980).
UNDP/FAO Survey of Plant Virus Diseases in Fiji.
- Brunt, A.A., Barton,
R.J., Phillips, S. and Lana, A.O. (1980). Ann. appl. Biol. 96: 37.
- Capoor, S.P. and Varma, P.M. (1950). Ind. J. agric. Sci. 20:
217.
- Costa, A.S. (1954). Bragantia 13: 23.
- Costa, A.S.,
Duffus, J.E. and Bardin, R. (1959). J. Am. Soc. Sug. Beet Technol.
10: 371.
- Flores, E. and Silberschmidt, K. (1967). Phytopath.
Z. 60: 181.
- Givord, L. and Hirth, L. (1973). Ann. appl.
Biol. 74: 359.
- Hendrix, J.W. and Murakishi, H. (1951). Rep.
Hawaii Univ. agric. Exp. Stn 1948-1950, p. 123.
- Jones, D.R. and
Behncken, G.M. (1980). Aust. Plant Path. 9: 4.
- Lana, A.O.
(1974). Pl. Dis. Reptr 58: 1040.
- Mukherjee, A.K. and
Raychaudhuri, P. (1964). Indian J. Hort. 21: 176.
- Sastry,
K.S.M. and Singh, S.J. (1973). Indian Phytopath. 26: 136.
- Van
Velsen, R.J. (1967). Papua New Guin. agric. J. 19: 10.
- Waterworth, H.E. (1980). CMI/AAB Descr. Pl. Viruses No. 227, 4 pp.
- Waterworth, H.E., Lawson, R.H. and Monroe, R.L. (1976).
Phytopathology 66: 570.
- Wolfswinkel, L.D. (1966). S. Afr.
J. agric. Sci. 9: 483.
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.







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