Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Grapevine
fanleaf nepovirus
Index
Data collated by G.P. Martelli, 1987; S.A. Holland,
1986.
Nomenclature
Synonyms
grapevine arricciamento virus, grapevine court
noué virus, grapevine infectious degeneration virus, grapevine Reisigkrankheit
virus, grapevine roncet virus, grapevine urticado virus.
Acronym
Strains
Fanleaf strain (Hewitt,
1950b); yellow mosaic strain (Hewitt, 1950a) and Dias (1950);
veinbanding strain (Goheen and Hewitt, 1962) and Martelli and Hewitt
(1963a).
ICTV decimal code
Host range and symptoms
First reported
in Vitis vinifera; from Austria; by Rathay (1883).
Natural host range and symptoms
Symptoms persist and vary
seasonally.
Vitis vinifera, V. rupestris and many other Vitis spp. and
interspecific hybrids - systemic green or yellow mosaic, ring and line
patterns and flecks, leaf and nodal malformation.
Transmission
Transmitted by a vector; a nematode;
Xiphinema index (Hewitt et al., 1958) and X. italiae (Cohn
et al., 1970). Virus does not require a helper virus for vector
transmission; transmitted by mechanical inoculation; transmitted by grafting;
not transmitted by contact between plants; transmitted by seed (rarely if ever
transmitted to embryos of Vitis vinifera, virus abundant in endosperm of
infected viruses but not in embryo. Transmitted by seed in Chenopodium
amaranticolor (Dias, 1963), C. quinoa (Brückbauer and
Rüdel, 1961a), Glycine max (Cory and Hewitt, 1968); not
transmitted by pollen (although found in pollen of Vitis).
Ecology and control
Studies reported by Martelli (1978);
Raski et al. (1983); Esmenjavd (1983).
Geographical
distribution
Probably distributed worldwide (in all areas where
Vitis vinifera and American hybrid rootstocks are grown).
Experimental host range
Several (3-9) families
susceptible.
Diagnostically susceptible host species and
symptoms
- Vitis spp. - green or yellow systemic mosaic,
rings, line patterns and flecks.
- Chenopodium amaranticolor and C.
quinoa - systemic mottling and leaf malformation.
- Cucumis sativus,
Phaseolus vulgaris cv. Bountiful - systemic chlorotic or necrotic mosaic,
mottling, flecking or ringspots. Immune to some strains.
- Gomphrena
globosa - systemic chlorotic spots, leaves twisted.
- Nicotiana
benthamiana - systemic mottling, leaf malformation, stunting.
- Nicotiana clevelandii - systemic mottling and stunting.
Maintenance and propagation hosts
Chenopodium
amaranticolor; C. quinoa; Gomphrena globosa, Phaseolus vulgaris. Good
sources for virus purification are C. quinoa, Nicotiana clevelandii, N.
benthamiana. G. globosa is good for maintaining cultures.
Assay hosts (Local lesions or Whole plants)
Chenopodium amaranticolor (W);
Gomphrena globosa (W); Phaseolus vulgaris cv. Bountiful (W). No
satisfactory local lesion hosts are known.
Susceptible host species
Insusceptible host species
Families containing susceptible hosts
Families containing
insusceptible hosts
Sources of host-range data
Brückbauer and Rüdel (1961b); Cadman et al. (1960); Dias
(1963); Martelli and Hewitt (1963a); Taylor and Hewitt (1964); Vuittenez
(1963).
Physical and
biochemical properties
Properties of particles in sap
TIP:
60-65 °C. LIV: 15-30 days (at 20ºC). DEP: log10 minus 3-4
(Brückbauer and Rüdel, 1961b; Cadman et al., 1960; Dias,
1963; Taylor and Hewitt, 1964). Leaf sap contains few virions.
Purification method
Dias and
Harrison (1963); Martelli and Hewitt (1963b); Taylor and Hewitt (1964).
Particle morphology
Virions isometric; not enveloped; 30
nm in diameter; angular in profile; without a conspicuous capsomere arrangement.
Physical properties
Three sedimenting components in
purified preparations; sedimentation coefficient of the fastest 120 S
(B); of the other(s) 86 S (M), or 50 S (T). Density 1.49 g
cm-3 in CsCl (B), or 1.41 g cm-3 in CsCl (M), or 1.31 g cm-3
in CsCl (T). Isoelectric point pH 4. A260/A280 ratio 1.67 (B), or 1.58
(M), or 0.73 (T; Quacquarelli et al., 1976).
Biochemical properties
Virions contain 42 % nucleic acid
(B), or 30 % nucleic acid (M), or 0 % nucleic acid (T); 58 % protein (B), or 70
% protein (M), or 100 % protein (T).
Genome consists of RNA; single-stranded; linear. Total genome size 11.116
kb. Genome of two parts; largest (or only) genome part the larger 7.342 kb; the
2nd largest 3.774 kb (Quacquarelli et al., 1976). Genomic nucleic acid
isolated by Diener and Schneider (1968); Quacquarelli et al. (1972;
1976): single-phase phenol/SDS; freezing and thawing or heating for 90 secs at
66ºC. Infectivity retained when deproteinised with phenol or detergent.
Sequence database accession code(s)
- D00915
Em(40)_vi:GFLRNA1 Gb(84)_vi:GFLRNA1 Grapevine fanleaf virus (GFLV) RNA1 for
polyprotein. 4/94 7,342bp.
- S38553 Em(40)_vi:S38553 Gb(84)_vi:S38553 RNA1=VPg
(253K polyprotein) grapevine fanleaf nepovirus, Genomic RNA, 84 nt. 1/94 84bp.
- X16907 Em(40)_vi:NEGFLVR2 Gb(84)_vi:NEGFLVR2 Grapevine Fanleaf virus
(GFLV-F13) RNA2 encoding capsid protein. 9/93 3,774bp.
- X60775
Em(40)_vi:GVFVCP Gb(84)_vi:GVFVCP Grapevine fanleaf virus genomic RNA for capsid
protein. 10/91 2,305bp.
- U11768 Em(43)_vi:Gf11768 Gb(89)_vi:U11768 Grapevine
fanleaf virus coat protein gene, partial cds. 10/94 1,515bp.
- U11770
Em(43)_vi:Gf770 Gb(89)_vi:Gfu11770 Grapevine fanleaf virus RNA2, deletion
mutant. 10/94 501bp.
Features of proteins
Virion protein(s) one;
Mr 54000 (Quacquarelli et al., 1976). Method of preparation:
Agrawal and Tremaine (1972): boil in presence of 1% SDS, 1% 2-mercaptoethanol
and 4 M urea.
Replication
Replication does not depend on a helper virus
(Morris-Krsinich et al., 1983).
Cytopathology
Virions found in roots, mesophyll and
vascular parenchyma in herbaceous hosts or grapevines (Gerola et al.,
1969; Saric and Wrischer, 1975; Kalasjan et al., 1979); in cytoplasm, or
in nuclei (where empty capsids may accumulate (Savina et al., 1985)).
Inclusions present in infected cells; are membranous bodies and unusual in shape
(crystalline aggregates in the cytoplasm and tubules); they contain virions.
Other cellular changes: leaf deformations that are open marginal, petiolar
sinuses and prominent marginal teeth. Canes have unevenly spaced or double nodes
and are flat. Cell walls have outgrowths (Saric and Wrischer, 1975; Kalasjan
et al., 1979) and trabeculae in phloem and xylem tissues (Gifford et
al., 1956).
Taxonomy and
relationships
Virus(es) with serologically related virions
Different strains of grapevine fanleaf virus are antigenically close
(Cadman et al., 1960; Barabino, 1963; Dias and Harrison, 1963; Martelli
and Hewitt, 1963b; Taylor and Hewitt, 1964), and all are distantly
related to arabis mosaic virus.
Virus(es) with serologically unrelated
virions
Tomato ringspot and tobacco ringspot
viruses.
Best tests for diagnosis
Serology
must be used to identify fanleaf virus. Seedlings or rooted cuttings of V.
vinifera and V. rupestris are good bait plants in studies with
nematode vectors.
Comments and
References
References
- Agrawal, H.D. and
Tremaine, J.H. (1972). Virology 47: 8.
- Barabino, G. (1963).
Hort. Res. 3: 27.
- Bercks, R. (1968). Weinb. Kell.
14: 151.
- Bovey, R., Brugger, J.J. and Gugerli, P. (1982). Proc.
7th Meeting ICVG, Niagara Falls 1980, p. 251.
- Brückbauer, H. and
Rüdel, M. (1961a). Wein-Wiss. 16: 177.
- Brückbauer, H. and Rüdel, M. (1961b). Wein-Wiss.
16: 197.
- Cadman, C.H., Dias, H.F. and Harrison, B.D. (1960).
Nature, Lond. 187: 577.
- Cohn, E., Tanne, E. and Nitzany, F.E.
(1970). Phytopathology 60: 181.
- Cory, L. and Hewitt, W.B.
(1968). Phytopathology 58: 1316.
- Dias, H.F. (1963). Ann.
appl. Biol. 51: 85.
- Dias, H.F. and Harrison, B.D. (1963). Ann.
appl. Biol. 51: 97.
- Diener, T.O. and Schneider, I.R. (1968).
Arch. Biochim. Biophys. 124: 401.
- Esmenjavd, D. (1983).
Prog. Agric. Viticole 100: 514.
- Gerola, F.M., Bassi, M. and
Belli, G. (1971). G. Bot. Ital. 103: 271.
- Gifford, E.M.,
Hewitt, W.B., Graham, A.D. and Lamoureux, C.H. (1956). Bull. Calif. Dep.
Agric. 45: 268.
- Goheen, A.C. and Hewitt, W.B. (1962). Am. J.
Enol. Vitic. 13: 73.
- Hewitt, W.B. (1950a). Bull. Calif.
Dep. Agric. 39: 6.
- Hewitt, W.B. (1950b). Bull. Calif.
Dep. Agric. 39: 62.
- Hewitt, W.B., Martelli, G., Dias, H.F. and
Taylor, R.H. (1970). CMI/AAB Descr. Pl. Viruses No. 28, 4 pp.
- Kalasjan, J.A., Litvak, L.A. and Marinesku, V. (1979). Arch. Phytopath.
Pflschutz 6: 373.
- Martelli, G.P. (1978). Nematol. Medit.
6: 1.
- Martelli, G.P. and Hewitt, W.B. (1963a). Phytopathol.
Medit. 2: 275.
- Martelli, G.P. and Hewitt, W.B. (1963b).
Phytopathol. Medit. 2: 285.
- Morris-Krsinich, B.A.M., Foster,
R.L.S. and Mossop, D.W. (1983). Virology 130: 523.
- Quacquarelli, A., Piazzolla, P. and Vovlas, C. (1972). J. gen. Virol.
17: 147.
- Quacquarelli, A., Gallitelli, D., Savino, V., and Martelli,
G.P. (1976). J. gen. Virol. 32: 349.
- Raski, D.J., Goheen,
A.C., Lider, L.A. and Meredith, C.P. (1983). Plant Dis. 67: 335.
- Rathay, E. (1883). Önol. Lehranstalt Klosterneuburg, 3.
- Ritzenhaler, C., Viry, M., Pinck, M., Margis, R., Fuchs, M. and Pinck, L.
(1991). J. gen. Virol. 172: 2357.
- Russo, M. (1985).
Phytopathol. Medit. 24: 144.
- Russo, M., Martelli, G.P. and
Savino, V. (1982). Proc. 7th Meeting ICVG, Niagara Falls 1980, p. 251.
- Saric, A. and Wrischer, M. (1975). Phytopath. Z. 84: 97.
- Savino, V., Cherif, C. and Martelli, G.P. (1985). Phytopathol. Medit.
24: 29.
- Taylor, R.H. and Hewitt, W.B. (1964). Aust. J. agric.
Res. 15: 571.
- Vuittenez, A. (1963). C. r. hebd. Seanc. Acad.
Agric. Fr. 49: 795.
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:
vide-manager@biology.anu.edu.au