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First Report of Ergot of Bermudagrass Caused by Claviceps cynodontis
in Oklahoma. S. M. Marek, R. A. Muller, and N. R. Walker, Department of
Entomology and Plant Pathology, Oklahoma State University, Stillwater 74078.
Plant Dis. 90:376, 2006; published on-line as DOI: 10.1094/PD-90-0376C. Accepted
for publication 14 December 2005.
During late June and early July of 2005, signs of bermudagrass ergot were
reported from numerous northern and eastern counties in Oklahoma. Signs were
observed primarily on forage-type bermudagrass (Cynodon dactylon (L.)
Pers.), as well as bermudagrass turf. During the “honeydew” stage, honeydew was
frequently observed exuding from most of the ovaries of infected
inflorescences. These signs of ergot have been observed previously on
bermudagrass in Oklahoma and Texas (1). Sphacelia-type conidia were
abundantly produced during the honeydew stage and were single-celled, hyaline,
averaged 14 × 5 µm in size, and were reniform to allantoid in shape. When
streaked on water agar, conidia produced terminal holoblastic secondary
conidia. Single-spore cultures were isolated from the honeydew of bermudagrasses
from Logan and Muskogee counties in Oklahoma and grew slowly as white mycelium
on potato dextrose agar (PDA). Koch’s postulates were fulfilled for these two
isolates by spray inoculating four bermudagrass inflorescences at anthesis with
mycelium scraped from a PDA plate and homogenized in water. Control plants’
inflorescences were sprayed with a water suspension of a similar amount of
sterile PDA as inoculated plants. Plants were placed inside plastic bags to
maintain humidity and incubated in a growth chamber at 22°C (14-h photoperiod)
and 20°C (10 h of darkness). After 9 days, honeydew exuded from the inoculated
inflorescences, but not from the controls. Single-spore cultures were reisolated
from the honeydew, and conidia streaked on water agar formed identical secondary
conidia. The complete nuclear ribosomal internal transcribed spacer (ITS) region
was amplified from DNA extracted from honeydew and single-spore cultures using
the ITS4 and ITS5 primers (4) and sequenced. All sequences were identical and a
search of GenBank at NCBI found these sequences were most similar to the ITS
regions of Claviceps cynodontis Langdon (100%, Accession No. AJ557074)
and C. maximensis Theis (99%, Accession No. AJ133396). The ITS sequence
from the Logan County isolate was deposited at GenBank (Accession DQ187312).
The morphology, secondary conidiation, and ITS sequences identify the causal
fungus as C. cynodontis (2) and differentiate it from C. purpurea
(Fr.) Tul., the previously identified cause of bermudagrass ergot (1). To our
knowledge, this is the first report of C. cynodontis on bermudagrass in
Oklahoma and may represent a recent introduction to the United States (2; S.
Pažoutová and M. Flieger, personal communication). A Claviceps sp.
isolated from bermudagrass has been shown to produce ergot alkaloids possibly
causing “bermudagrass tremors” in cattle (3). In regions where bermudagrass is
the predominant forage for livestock, the toxicological significance of
bermudagrass ergot caused by C. cynodontis is unclear and requires
further research.
References: (1) K. E. Conway et al. Plant Dis. 76:1077, 1992. (2) S.
Pažoutová et al. Can J. Plant Pathol. 27:541, 2005. (3) J. K. Porter et al. J.
Agric. Food Chem. 22:838, 1974. (4) T. J. White et al. Pages 315-322 in: PCR
Protocols: A Guide to Methods and Applications. Academic Press Inc., New York,
1990.
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