Plant Viruses
Online
Descriptions and Lists from
the VIDE Database
Araujia mosaic
potyvirus
Index
Data collated by A.A. Brunt, and E. Hiebert, 1987.
Nomenclature
Acronym
ICTV decimal code
Host range and symptoms
First reported
in Araujia angustifolia and Morrenia odorata; from Argentina; by
Charudattan et al. (1976).
Natural host range and symptoms
Symptoms persist.
- Araujia angustifolia, Morrenia odorata - mosaics.
Transmission
Transmitted by a vector; an insect; Aphis
nerii, Aphis spiraecola, Myzus persicae; Aphididae. Transmitted in a
non-persistent manner. Virus transmitted by mechanical inoculation; not
transmitted by contact between plants.
Ecology and control
Studies reported by Charudattan et al. (1980).
Geographical
distribution
Spreads in the South and Central American region;
Argentina.
Experimental host range
Few (<3) families susceptible.
Experimentally infected plants mostly show mosaics, malformation.
Diagnostically susceptible host species and symptoms
- Araujia angustifolia, A. hortorum, A. sericofera, Matelea floridana,
Morrenia brachystephana, Sarcostemma clausum - systemic mosaic and
malformation.
- Hoya carnosa, H. coronaria - symptomless.
Diagnostically insusceptible host species
Chenopodium
amaranticolor, Cucumis sativus, Phaseolus vulgaris, Nicotiana benthamiana,
Nicotiana tabacum.
Maintenance and propagation hosts
Morrenia odorata, Araujia angustifolia, Araujia sericofera.
Assay hosts (Local lesions or Whole plants)
Susceptible host species
Insusceptible host
species
Families containing susceptible hosts
Families containing
insusceptible hosts
Sources of host-range data
Charudattan et al. (1980).
Physical and
biochemical properties
Properties of particles in sap
TIP:
56-58 °C. LIV: 2-2.5 days. DEP: log10 minus 2-3. Leaf sap contains few
virions.
Purification method
Hiebert and
Charudattan (1984).
Particle morphology
Virions filamentous; not enveloped;
usually flexuous; with a clear modal length; of 741 nm. Axial canal obscure.
Basic helix obscure.
Biochemical properties
Genome consists of RNA;
single-stranded.
Features of proteins
Virion protein(s) one;
Mr 32000; coat protein.
Virus-coded non-virion proteins identified by genomic sequence
analysis (Hiebert and Charudattan (1984)); five proteins found. Mr of
the largest 81000; helper component related. Mr of 2nd largest 70000;
cylindrical inclusion. Mr of 3rd 53000; nuclear inclusion.
Mr of 4th 49000; nuclear inclusion. Mr of 5th and smaller
40000; function unknown.
Cytopathology
Virions found in mesophyll and epidermis.
Inclusions present in infected cells; are pinwheels; they do not contain
virions.
Taxonomy and
relationships
Virus(es) with serologically unrelated virions
Bean common mosaic, bidens mottle, blackeye cowpea mosaic, dasheen
mosaic, lettuce mosaic, papaya ringspot, pepper mottle, potato Y, soybean
mosaic, tobacco etch, tobacco veinal mottle, tobacco etch and turnip mosaic
viruses.
Additional comments on relationships
The 49kDa and 53kDa proteins produced by in vitro translation
react with antisera to tobacco etch (TEV) nuclear proteins and the 32kDaprotein
with antiserum to TEV capsid protein; the cylindrical inclusion protein of
araujia mosaic is serologically related to that of dasheen mosaic virus but not
TEV; and the 81kDaprotein of araujia mosaic virus reacted with antiserum to the
helper component of tobacco vein mottling virus.
Comments and
References
General comments
Charudattan et
al. (1980) suggest that the virus might be used to control Morrenia
weeds in citrus orchards in Florida, U.S.A.
References
- Charudattan, R., Zettler, F.W., Cordo,
H.A. and Christie, R.G. (1976). Proc. Am. Phytopath. Soc. 3: 272.
- Charudattan, R., Zettler, F.W., Cordo, H.A. and Christie, R.G. (1980).
Phytopathology 70: 909.
- Hiebert, E. and Charudattan, R.
(1984). Phytopathology 74: 642.
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