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First Report of Southern Blight of Ruellia brittoniana Caused by Sclerotium
rolfsii in Louisiana. G. E. Holcomb, Department of Plant Pathology and
Crop Physiology, Louisiana State University AgCenter, Baton Rouge 70803. Plant
Dis. 88:770, 2004; published on-line as D-2004-0430-01N, 2004. Accepted for
publication 14 April 2004.
Ruellia brittoniana, Mexican petunia, is an herbaceous flowering
perennial grown in hardiness zones 8 to 10 in the southern and western United
States. Popular dwarf forms with flower colors of white, pink, and blue are used
as ground covers and borders. In April of 2003, root and stem rot that caused
plant death was observed on cv. Katie (dwarf form, pink flowers) at a wholesale
nursery in southern Louisiana. Plants were growing in a vermiculite and sand
mix. The grower had purchased the plants from an out-of-state source, and
approximately one-half of 1,440 plants were dead or dying. Symptoms included
wilt, basal stem rot, and root rot. Peripheral roots were covered with a white
mycelial layer that contained white sclerotial initials and small, brown
sclerotia. Fungal isolates from infected roots grown on potato dextrose agar
(PDA) produced white mycelia and 1- to 2-mm-diameter dark brown sclerotia.
Sclerotia were nearly round with smooth surfaces and distributed over the entire
colony. Isolates were identified as Sclerotium rolfsii on the basis of
mycelial characteristics and color, size, and distribution of sclerotia.
Two-month-old seedlings (6 to 10 cm high) of R. brittoniana, from seed of
cv. Katie, were used in pathogenicity tests. Inoculum was grown in
10-cm-diameter plastic, culture dishes on PDA medium. Blended inoculum was
prepared from a single 1-week-old culture that was composed of mycelia and
sclerotia and blended 4 to 6 s at high speed in 100 ml of distilled water. In
test one, 5 ml of inoculum was placed at the base of each inoculated plant. In
test two, a single 5-mm-diameter agar plug with mycelium plus four sclerotia was
placed beside plant stems near soil line. In test three, 5 ml of blended
inoculum was dripped on exposed roots after plants were removed from pots. In
test four, exposed plant roots were dipped in the blended inoculum. Each test
contained 10 inoculated plants, and 10 noninoculated plants served as controls.
All plants were placed in a dew chamber maintained at 28°C for 2 days and then
returned to a greenhouse to observe development of symptoms and signs of
disease. In tests one and two, basal stem rot and wilt developed on inoculated
plants after 2 days and after 5 to 8 days all were dead. Inoculated plants from
tests three and four were alive 4 months after inoculation, but were showing
symptoms including leaf yellowing and drop, moderate to severe root rot, and
some plants had begun to show white mycelia and white sclerotial initials on
peripheral roots by January 2004. All noninoculated plants remained healthy and S.
rolfsii was reisolated from infected plants in each test. To my knowledge,
this is the first report of S. rolfsii causing disease on R.
brittoniana.
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