Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Zucchini yellow
mosaic potyvirus
Index
Data collated by C. Büchen-Osmond and D.
Purcifull, 1987.
Nomenclature
Synonyms
muskmelon yellow stunt virus (Lecoq et al.,
1981; 1983).
Acronym
Strains
22
isolates of the virus have been grouped into three pathotypes by their effect on
muskmelon line PI 414723 (Pitrat and Lecoq, 1984; Risser et al., 1981;
Lecoq and Pitrat, 1985 and unpublished data). ZYMV isolates differ in the
symptoms they cause (Lecoq et al., 1981; Provvidenti et al.,
1984), aphid transmissibility (Lecoq, 1986) or virulence towards a resistance
gene (Lecoq and Pitrat, 1985).
ICTV decimal code
Host range and symptoms
First reported
in Cucurbita pepo; from Italy; by Lisa et al. (1981).
Natural host range and symptoms
Symptoms persist.
- Cucurbita pepo (zucchini squash), Cucumis melo
(muskmelon), Cucumis sativus (cucumber) and Citrullus lanatus
(watermelon) - mosaic, yellowing, shoestring leaves, stunting, and fruit and
seed deformation.
- Melothria pendula - mosaic, yellowing.
Transmission
Transmitted by a vector; an insect; Aphis
citricola (Purcifull et al., 1984), Aphis gossypii; Myzus
persicae (Lecoq et al., 1981; Lisa et al., 1981) and
Macrosiphum euphorbiae (Lecoq, unpublished data) and Aphis
middletonii, Aphis craccivora, Acrythosiphon pisum, Lipaphis erysimi,
Uroleucon sp. (Adlerz, 1987); Aphididae. Transmitted in a non-persistent
manner. Virus transmitted by mechanical inoculation; not transmitted by seed
(Lecoq et al., 1981; Dodds et al., 1984).
Geographical
distribution
Spreads in Algeria, Australia, Egypt, France, Germany,
Israel, Italy, Japan, Jordan, Lebanon, Mauritius, Morocco, Spain, Taiwan,
Turkey, the UK, and the USA (Zucchini yellow mosaic virus has been isolated from
the wild perennial cucurbit Melothria pendula in Florida (Adlerz et
al., 1983b)).
Experimental host range
Several (3-9) families
susceptible.
Diagnostically susceptible host species and
symptoms
- Chenopodium amaranticolor, C. quinoa -
chlorotic local lesions; not systemic.
- Cucumis melo - chlorotic
local lesions; systemic vein clearing, yellowing, mosaic, leaf deformation,
stunting and occasional necrosis.
- Cucurbita okeechobeensis -
systemic mosaic (N.B. this species is not susceptible to most cucumber mosaic
virus isolates).
- Cucurbita pepo - chlorotic local lesions;
systemic vein netting, yellowing, mosaic and leaf deformation, often lethal.
- Gomphrena globosa - local lesions; not systemic (N.B. this species
is not infected by squash mosaic virus).
- Luffa acutangula -
systemic mosaic or latent.
- Ranunculus sardous - symptomless
systemic infection with most isolates (N.B. this species is not infected by
papaya ringspot virus-W or watermelon mosaic virus 2).
Diagnostically
insusceptible host species
Lavatera trimestris - but
watermelon virus 2 induces necrotic local lesions.
Maintenance and
propagation hosts
Assay hosts (Local lesions or Whole plants)
Chenopodium amaranticolor (L), Cucurbita pepo (W).
Susceptible host species
Insusceptible host species
Families containing susceptible hosts
Families containing
insusceptible hosts
Sources of host-range data
Lecoq
et al. (1983); Lesemann et al. (1983); Provvidenti et al.
(1984); Lecoq et al. (1981); Lisa et al. (1981); Purcifull et
al. (1984).
Physical and
biochemical properties
Properties of particles in sap
TIP:
55-60 °C. LIV: 3-5 days (at room temperature). DEP: log10 minus 4-5. Leaf sap
contains few virions.
Purification method
Lisa et
al. (1981); Lisa and Lecoq (1984); Lesemann et al. (1983); Purcifull
et al. (1984).
Particle morphology
Virions filamentous; not enveloped;
usually flexuous; with a clear modal length; of 750 nm; 11 nm wide. Axial canal
obscure. Basic helix obscure.
Physical properties
One sedimenting component in purified
preparations. Density 1.323 g cm-3 in CsCl (at 10ºC).
Biochemical properties
Virions contain 4.5-7 % nucleic
acid; 93-95.5 % protein.
Genome consists of RNA; single-stranded; linear. Total genome size 9 kb.
Genome unipartite; largest (or only) genome part 9 kb.
Sequence database accession code(s)
- D00593
Em(40)_vi:ZYMCP Zucchini yellow mosaic virus, nuclear inclusion protein and coat
protein genes. 2/92 1,963bp.
- D00692 Em(40)_vi:ZYMV Gb(84)_vi:ZYMV Zucchini
yellow mosaic virus gene, 3´ terminal region, coat protein and RNA
polymerase. 6/91
- D13914 Em(40)_vi:ZYMCP1 Gb(84)_vi:ZYMCP Zucchini yellow
mosaic virus, nuclear inclusion protein and coat protein genes. 1/94 1,944bp.
- L29569 Em(40)_vi:ZYMP13PRE Gb(84)_vi:ZYMP13PREP Zucchini yellow mosaic virus
polyprotein; P1 protease; helper component-protease; P3 protein;
- L31350
Em(40)_vi:ZYMPROPOL Gb(84)_vi:ZYMPROPOLR Zucchini yellow mosaic virus
polyprotein, complete cds; P1 protease; P2 HC-protease
- L35588
Gb(84)n:ZYMP1PROTA Zucchini yellow mosaic virus P1 protease, 5´ end. 8/94
918bp.
- L35589 Gb(84)n:ZYMP1PROTB Zucchini yellow mosaic virus P1 protease,
5´ end. 8/94 897bp.
- L35590 Gb(84)n:ZYMP13PROT Zucchini yellow mosaic
virus P1 protease, helper component, and P3 protease; 5´ end. 8/94 3,5
- M35095 Em(40)_vi:ZYMCPA Gb(84)_vi:ZYMCPA Zucchini yellow mosaic virus coat
protein (cp) mRNA, 3´ end. 7/90 1,374bp
- S46009 Em(40)_un:S46009
Gb(84)_vi:S46009 coat protein zucchini yellow mosaic virus ZYMV,
aphid-transmissible isolate, Genomic RNA, 12
- X62662 Em(40)_vi:ZYMVCP
Gb(84)_vi:ZYMVCP Zucchini yellow mosaic virus (ZYMV-S) mRNA for coat protein.
4/94 1,250bp.
- X68509 Em(40)_vi:ZYMVSR Gb(84)_vi:ZYMVSR Zucchini Yellow
Mosaic Virus-S RNA. 3/93 3,048bp.
- X77756 Em(40)_vi:ZYMVHCPRO
Gb(84)_vi:ZYMVHCPRO Zucchini Yellow Mosaic Virus (ZYMV) HC-PRO gene. 6/94
1,368bp.
- Z22759 Em(40)_vi:ZCHELCOMA Gb(84)_vi:ZCHELCOMA Zucchini yellow
mosaic virus helper component RNA. 3/94 1,368bp.
Features of proteins
Virion protein(s) one;
Mr 36000; coat protein. Method of preparation: Lisa et al.
(1981).
Virus-coded non-virion proteins identified by genomic sequence
analysis; seven proteins found. Mr of the largest 39000. Mr
of 2nd largest 51000; helper component. Mr of 3rd 50000. Mr
of 4th 70000; cylindrical inclusion. Mr of 5th and smaller 49000, or
58000, or 34000; protease, polymerase, coat protein.
Replication
Replication does not depend on a helper
virus.
Cytopathology
Virions found in all parts of the host
plant; in cytoplasm. Inclusions present in infected cells; are pinwheels (but
not laminated aggregates (Lisa et al., 1981)); they do not contain
virions (endoplasmic reticulum and vesicles containing fibrillar material
accumulate (Lesemann et al., 1983)).
Taxonomy and
relationships
Virus(es) with serologically related virions
Watermelon mosaic virus II, bean yellow mosaic virus (Lecoq et
al., 1981; Lisa et al., 1981; Adlerz et al., 1983a;
Lesemann, 1983; Lesemann et al., 1983; Makkouk and Abbasher, 1983;
Purcifull et al., 1984) and amaranthus leaf mottle viruses (Lovisolo and
Lisa, 1976; V. Lisa and G. D'Agostino, unpublished data), but distantly.
Differences between type strain and others
No serological differences have been detected between Italian and
other isolates of the virus (Lecoq et al., 1983; Lesemann et al.,
1983; Purcifull et al., 1984; Provvidenti et al., 1984). Different
isolates cross-protect in muskmelon (Lecoq et al., 1981).
Best
tests for diagnosis
Some isolates of ZYMV cause
symptoms similar to those attributed to other cucurbit viruses (cucumber mosaic
virus, watermelon mosaic virus 1, strain W of papaya ringspot virus, watermelon
mosaic virus 2 and squash mosaic virus), thus a diagnosis based on symptoms is
uncertain, and serological tests must be used. ZYMV frequently occurs with other
viruses in cucurbits, but can be isolated alone by inoculating, for example,
Cucurbita okeechobeensis and Ranunculus sardous. ZYMV can be
separated from squash mosaic by aphid transmission or by inoculation to
Gomphrena globosa. Zucchini yellow fleck potyvirus, found in the the
Mediterranean region (Vovlas et al., 1981), is not serologically related
to ZYMV (M. Russo, unpublished data).
Comments and
References
References
- Adlerz, W.C. (1987).
Econ. Ent. 71: 531.
- Adlerz, W.C., Purcifull, D.E., Simone,
G.W. and Hiebert, E. (1983a). Abstr. 4th Int. Congr. Pl. Path.,
Melbourne, 1983, No. 440:
- Adlerz, W.C., Purcifull, D.E., Simone,
G.W. and Hiebert, E. (1983b). Proc. Fla Stn hort. Soc. 96:
72.
- Dodds, J.A., Lee, J.G., Nameth, S.T. and Laemmlen, F.F. (1984).
Phytopathology 74: 221.
- Hiebert, E., Thornbury, H.H. and
Pirone, T.P. (1984). Virology 135: 1.
- Lecoq, H. (1986).
Phytopathology 76: 1063.
- Lecoq, H. and Pitrat, M. (1985).
Phytopathology 75: 890.
- Lecoq, H., Pitrat, M. and Clement, M.
(1981). Agronomie 1: 827.
- Lecoq, H., Lisa, V. and Dellavalle,
G. (1983). Plant Dis. 67: 824.
- Lesemann, D.-E. (1983). Acta
Hort. 127: 159.
- Lesemann, D.-E., Makkouk, K.M., Koenig, R. and
Samman, E.N. (1983). Phytopath. Z. 108: 304.
- Lisa, V. and
Lecoq, H. (1984). CMI/AAB Descr. Pl. Viruses No. 282, 4 pp.
- Lisa, V.,
Boccardo, G., D'Agostino, G., Dellavalle, G. and d'Aquilio, M. (1981).
Phytopathology 71: 667.
- Lovisolo, O. and Lisa, V. (1976).
Poljopr. znanst. Smotra 39(49): 553.
- Makkouk, K.M. and
Abbasher, A. (1983). Abstr. 4th Int. Congr. Pl. Path., Melbourne, 1983,
No. 472:
- Pitrat, M. and Lecoq, H. (1984). Euphytica 33:
57.
- Provvidenti, R., Gonsalves, D. and Humaydan, H. (1984). Plant
Dis. 68: 443.
- Purcifull, D.E., Adlerz, W.C., Simone, G.W.,
Hiebert, E. and Christie, R.G. (1984). Plant Dis. 68: 230.
- Risser, G., Pitrat, M., Lecoq, H. and Rode, J.-C. (1981). Agronomie
1: 835.
- Vovlas, C., Hiebert, E. and Russo, M. (1981). Phytopathol.
Medit. 20: 123.
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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