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New hosts of Turnip mosaic virus in
Zimbabwe
S. Chivasa1*, E.J.A.Ekpo2 and R.G.T. Hicks3
1Department of Crop Science, University of Zimbabwe,
Harare (now at University of Durham, Biological Sciences Dept., Durham,
DH1 3LE, UK).
2Department of Crop Protection and Environmental Management,
University of Ibadan, Nigeria
3Department of Biology and Biochemistry, University of Bath, Bath,
BA2 7AY, UK
*stephen.chivasa@durham.ac.uk
Accepted for publication 10/08/01
Necrotic rings, lines and spots (Fig. 1) were observed on
approximately 90% of cabbage (Brassica oleracea var. capitata)
plants growing in a field in Harare. Inspection of cabbages in nearby
fields and in retail outlets, showed that these symptoms were
widespread. A virus isolated from an affected plant and established as a
single lesion culture, by serial passage in Chenopodium quinoa
(chlorotic/necrotic local lesions, no systemic infection), produced
symptoms typical of Turnip mosaic virus (TuMV) in a range of
indicator plants. TuMV was confirmed in cabbage and C. quinoa sap
by PAS-ELISA, using antiserum to a UK isolate of the virus. All
PAS-ELISAs included positive and negative (healthy) controls and test
samples were considered positive if their means (A405) exceeded negative
controls by more than 3 SD and were significantly different (P<0.05).

Fig. 1. Cabbage infected with Turnip mosaic virus in Zimbabwe
(scale bar divisions = cm)
Rothwell (1983) lists Brassica oleracea as the only
previously-known host for TuMV in Zimbabwe. In a survey of TuMV in crop
and wild hosts in the Harare region within 1-2 kilometres of the present
outbreak, sap samples from the following hosts tested positive in
PAS-ELISA and induced diagnostic symptoms in C. quinoa: the
dicotyledons Amaranthus hybridus, Brassica juncea, Conyza
sumatrensis, Galinsoga parviflora, Portulaca oleracea,
Sida alba, Sonchus oleraceus and Hibiscus esculentus;
the monocotyledons Commelina bengalensis and Musa sapientum
L. (banana). Bidens pilosa and Cyperus esculentus
(monocotyledons) also tested positive for TuMV in PAS-ELISAs, although
sap was not infectious. With the exception of B. juncea, and H.
esculentus, the above species are apparently new hosts of TuMV
(Broadbent, 1957; Stobbs & Stirling, 1990). Calanthe sp.
(Orchidaceae) is the only other monocotyledonous host reported for TuMV
(Brunt et al., 1990).
In tests, the aphids Myzus persicae, Brevicoryne brassicae
and Aphis fabae, transmitted the virus non-persistently, between
infected and healthy cabbage plants in Zimbabwe, and may have been
responsible for local spread of the virus. Further work is needed to
establish whether infection of Musa and other apparently new
hosts, is associated with disease.
References
Broadbent L, 1957. Investigation of Virus Diseases of Brassica
Crops. Cambridge, UK: Cambridge University Press.
Brunt A, Crabtree K, Gibbs A, eds, 1990. Viruses of Tropical
Plants. Descriptions and Lists from the VIDE Database. Wallingford,
UK: C.A.B. International.
Rothwell A, 1983. A revised list of plant diseases occurring in
Zimbabwe. Kirkia 12, 233-351.
Stobbs LW, Stirling A. 1990. Susceptibility of Ontario? weed species
to turnip mosaic virus. Canadian Journal of Plant Pathology 12,
255-262.
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