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Gummy stem blight was first reported in 1891 in France, Italy, and the
United States. It affects the leaves, stems, and fruits of all cucurbits. On
fruit the disease is known as black rot. The disease has become increasingly
severe as fungicide usage and genetic resistance have resulted in the
effective control of other cucurbit diseases. The pathogen is most common in
the southern United States and in subtropical and tropical areas of the world.
It is also found in temperate regions, especially on winter squash and
pumpkin, and on greenhouse-grown cucumber.
Symptoms
Circular, tan to dark brown spots appear on the leaves, often first at the
margins, and enlarge rapidly until the entire leaf is blighted (Fig. 1).
Circular, black or tan spots appear on the cotyledons and stems of young
plants. Water-soaking may occur on hypocotyls and leaves. Stem cankers develop
in the cortical tissue, and a brown, gummy exudate is commonly produced on the
surface (Fig. 2). Small fruiting bodies (pycnidia or perithecia) may appear
as black specks on the cankers (Fig. 3). (See Compendium of Cucurbit
Diseases, Table 7 and Part V, Fig. 14.)
Stems may be girdled and seedlings killed.
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| Fig 2. Stem canker. Courtesy B.
D. Bruton. (Click image for larger
view). |
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Fig. 3. Pycnidia of P.
cucurbitacearum. Courtesy T. A. Zitter. (Click image for larger
view). |
If infection occurs in older plants, lesions develop more slowly on stems
near the center of a hill. Cankered vines usually wilt after mid-season.
Small, water-soaked spots develop on infected fruit, enlarge to indefinite
size, and exude gummy material. The spots contain conspicuous black fruiting
bodies.
In the tropics infection can occur through fresh blossom scars and is
manifested as a rapid decay of inner fruit tissue, which proceeds from the
blossom end to the stem end and then moves to the fruit surface.
Causal Organism
Gummy stem blight is caused by Didymella bryoniae
(Auersw.) Rehm (syn.
Mycosphaerella melonis (Pass.) Chiu & J. C. Walker). Dark pycnidia
of the anamorph, Phoma cucurbitacearum (Fr.:Fr.) Sacc. (syn. Ascochyta
cucumis Fautrey & Roum.), 120–180 µm in diameter, form on the
surface of leaves, stems, and fruits. The conidia are hyaline, cylindrical
with rounded ends, non- or monoseptate, and 6–13 µm long. Dark pseudothecia,
125–213 µm in diameter, may also form, especially on stems. The numerous
bitunicate asci usually produce eight ascospores per ascus. The ascospores are
14–18 × 4–6 µm, hyaline, monoseptate with a constriction at the septum,
and rounded on the ends. The upper cell is usually wider than the lower cell.
No physiological specialization has been reported. The fungus grows in culture
between 12 and 32°C, with an optimum temperature of 24°C.
Disease Cycle
The pathogen survives between seasons on diseased vines and crop debris and
may be seedborne. The optimum temperature for infection is 20°C in melon and
24–25°C in watermelon and cucumber. Moisture is more important for disease
development than temperature. Peak ascospore dispersal occurs after rain and
during dew periods at night. Free moisture on leaves for at least 1 hr is
necessary for infection, and further continuous leaf wetness is required for
lesion expansion. Leaves are penetrated either directly through the cuticle or
through intercellular spaces around the bases of trichomes. Stems are
penetrated through wounds or by the extension of leaf lesions. Fruits are
penetrated either through wounds or through flower scars at the time of
pollination. Fruit rot begins to develop about 3 days after infection.
Cotyledons and young leaves of watermelon and melon are very susceptible, but
those of cucumber and certain squash are resistant and become susceptible only
as they mature.
Control
The use of treated seed should be a standard procedure, and a 2-year
rotation cycle is essential. Although plant breeders have identified
resistance genes in several cucurbits, no commercially acceptable resistant
cultivars of watermelon, melon, or cucumber have been developed.
Satisfactory chemical control may be obtained by regular applications of
protectant fungicides. Isolates of D. bryoniae resistant to
benzimidazole fungicides have been detected in greenhouse cucumber culture in
Greece and the Netherlands and recently in cucurbit fields in the eastern
United States.
In addition to fungicide sprays, greenhouse ventilation and irrigation
should be managed to minimize free moisture on leaf surfaces.
Selected References
Chiu, W. F., and Walker, J. C. 1949. Physiology and pathogenicity of the
cucurbit black rot fungus. J. Agric. Res. 78:589-615.
Keinath, A. P.,
Farnham, M. W., and Zitter, T. A. 1995. Morphological,
pathological, and genetic differentiation of Didymella bryoniae and Phoma
spp. isolated from cucurbits. Phytopathology 85:364-369.
Keinath, A. P., and
Zitter, T. A. 1995. First report of benomyl-insensitive
Didymella bryoniae in the United States. (Abstr.) Phytopathology
85:1126.
Malathrakis, N. E., and
Vakalounakis, D. J. 1983. Resistance to
benzimidazole fungicides in the gummy stem blight pathogen Didymella
bryoniae in cucurbits. Plant Pathol. 32:395-399.
Schenck, N. C. 1968. Incidence of airborne fungus spores over watermelon
fields in Florida. Phytopathology 58:91-94.
Van
Steekelenburg, N. A. M. 1985. Influence of humidity on incidence of Didymella
bryoniae on cucumber leaves and growing tips under controlled
environmental conditions. Neth. J. Plant Pathol. 91:277-283.
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