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Occurrence and distribution of citrus leprosis virus (CiLV-C) in Honduras, Central America
First report of powdery mildew (Oidium sp.) on
greater celandine (Chelidonium majus) T. Jankovics
Plant Protection Institute of the Hungarian Academy of Sciences, H-1525
Budapest, PO Box 102, Hungary
*tjan@nki.hu Accepted for publication 08/08/06
Since 2004, symptoms of powdery mildew infection were observed on greater
celandine (Chelidonium majus), a common weed of shaded habitats, in
several places in Hungary. Sporulating mildew mycelia covered large areas
of the upper, and rarely the lower, leaf surfaces (Fig. 1), in addition to
the petioles and unripe capsular fruits.

Figure 1: Chelidonium majus infected with powdery mildew
The pathogen was identified as a powdery mildew anamorph belonging to the
genus Oidium subgenus Pseudoidium. Conidia were cylindrical
to doliiform, measured 25-48 x 10-20 µm and were produced singly on 80-150
µm long conidiophores consisting of a foot-cell measuring 20-40 x 7-10 µm,
followed by two or three shorter cells (Fig. 2). During conidial germination,
short germ tubes were produced apically terminating in lobed appressoria.
Hyphal appressoria were lobed or multi-lobed (Fig. 3). The teleomorph stage
was not found. Specimens were deposited in the herbarium of Martin Luther
University, Halle, Germany (HAL 1842 F).
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| Figure 2: A conidiophore of the
powdery mildew anamorph infecting greater celandine (bar represents
30 µm) |
Figure 3: Hyphal appressoria of
the pathogen found on greater celandine (bar represents 10 µm) |
No well-founded report of powdery mildew on C. majus is known worldwide
(Braun, 1987; 1995). To contribute to a more precise identification of the
novel powdery mildew anamorph, DNA was extracted from its mycelium, the internal
transcribed spacer (ITS) region of the ribosomal DNA was PCR-amplified, cloned
and sequenced as described in Landwehr et al. (2002) for Glomus.
The ITS sequence (GenBank accession number DQ665673) was 99% similar to those
determined in O. neolycopersici infecting tomato in Europe and North
America (Kiss et al., 2005). However, our cross-inoculation tests
using conidia of O. neolycopersici and those of the C. majus
mildew showed that these pathogens could infect their host plants only. The
tests were repeated three times in two greenhouses using healthy potted
C. majus and tomato plants kept in isolation after artificial inoculations.
Non-inoculated plants served as controls. These results confirmed the pathogenicity
of the Oidium sp. on C. majus. Acknowledgements
The author would like to thank Dr Levente Kiss for his helpful
comments on the manuscript and Dr Gábor M. Kovács for his help in DNA sequencing.
References Braun U, 1987. A Monograph of the Erysiphales
(Powdery Mildews). Beihefte zur Nova Hedwigia 89, 1-700.
Braun U, 1995. The Powdery Mildews (Erysiphales) of Europe. Jena,
Germany: Gustav Fischer Verlag. Kiss L, Takamatsu S, Cunnington JH,
2005. Molecular identification of Oidium neolycopersici as the
casual agent of the recent tomato powdery mildew epidemics in North
America. Plant Disease 89, 491-496. Landwehr M, Hildebrandt U, Wilde P,
Nawrath K, Tóth T, Biró B, Bothe H, 2002. The arbuscular mycorrhizal fungus
Glomus geosporum in European saline, sodic and gypsum soils. Mycorrhiza
12, 199-211.
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