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Occurrence and distribution of citrus leprosis virus (CiLV-C) in Honduras, Central America
First report of Phomopsis viticola
causing bunch rot of grapes in Australia
S. Savocchia*, L.A. Greer
and C.C. Steel
National Wine and Grape Industry
Centre, Charles Sturt University, Locked Bag 588,
Wagga Wagga, NSW, 2678,
Australia.
*ssavocchia@csu.edu.au Accepted for publication
25/10/06
From 2004 to
2006, grapevines (Vitis vinifera cv. Cabernet Sauvignon) in a commercial
vineyard in the Hastings Valley (north eastern Australia) were surveyed for
bunch rot diseases at dormancy, flowering, berries pea-sized, veraison and
harvest. During the growing season black lesions were observed on green shoots
and leaves. At harvest, abundant black pycnidia were consistently observed on
the surface of bunches with berries becoming desiccated and rachis necrotic
(Fig. 1).

Figure 1:
Bunch rot of Vitis vinifera
(cv. Cabernet Sauvignon) caused by Phomopsis viticola.
Necrotic rachis
and desiccated berries with black pycnidia developing on the surface are
observed. Buds, canes, leaves, flowers and bunches were surface sterilized in
1% sodium hypochlorite for 1 min, followed by three successive washings in
sterile distilled water. Isolations were initially made on Dichloran Rose
Bengal Chloramphenicol agar and incubated at 25°C for 7 days. Any resulting
fungal growth was sub-cultured onto potato dextrose agar. The plates were
incubated at 25°C for 7 days. Phomopsis viticola was isolated
from canes, leaves, flowers, rachis and bunches and identified based on
morphological characteristics of the conidia. Koch’s postulates were satisfied
by inoculation of Cabernet Sauvignon berries from excised bunches taken at
harvest. Whole bunches were surface
sterilized
by dipping in 1% sodium hypochlorite for 2 min, followed by three successive
washings in sterile distilled water. Berries were inoculated with a 10 µl drop
of 1 × 106 conidia per ml suspension. Control bunches were
inoculated with 10 µl drops of sterile distilled water. Bunches were placed in
plastic containers lined with sterile paper towel, moistened with sterile
distilled water to maintain humidity and incubated at 23ºC for 14 days. Black
pycnidia developed on the surface that eventually sporulated to produce yellow
oozing of spores. Phomopsis viticola was re-isolated from the pycnidia
that had formed on the berries.
Phomopsis viticola
was first described as a rot of Niagara grapes in New York vineyards in 1911 by
Gregory (1913), but is primarily recognised as a pathogen of the vegetative
tissues. In Australia, Phomopsis viticola is a recognised
pathogen of grapevine buds, canes, shoots and leaves (Merrin et al.,
1995; Emmett et al., 1994). This is the first report of Phomopsis
viticola causing bunch rot on grape in sub-tropical regions of Australia.
Currently there are no fungicides registered for the control of Phomopsis fruit
rot of grape in Australia.
References
Emmett RW, Nair NG,
Wicks TJ, 1994. Phomopsis. In: Nicholas P, Magarey PA, Wachtel M, eds.
Diseases and Pests. Grape Production Series. Adelaide, Australia:
Winetitles, 22-24.
Gregory CT, 1913. A rot of grapes
caused by Cryptosporella viticola. Phytopathology 3, 20-23.
Merrin SJ, Nair NG, Tarran J, 1995.
Variation in Phomopsis recorded on grapevine in Australia and its
taxonomic and biological implications. Australasian Plant Pathology 24,
44–56.
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