Phloeosporella ceanothi causing leaf spot and
dieback on Ceanothus in the UK
J. Denton1, B. Henricot1*,
G. Denton1, A. V. Barnes2 and P. A. Beales2
1
Plant Pathology Department, Royal Horticultural Society Wisley (RHS), Wisley,
Woking, Surrey, GU23 6QB
2
Central Science Laboratory (CSL), Sand Hutton,
York, YO41 1LZ
*beatricehenricot@rhs.org.uk Accepted for publication 29/10/07
Ceanothus
is a genus of approximately 50-60 species native from North America but is now
widely planted as an ornamental garden plant in the United Kingdom. Recent cases
of leaf spotting followed by defoliation and dieback (Fig.1 A and B) on
Ceanothus shrubs have been observed in several counties in the UK through
the advisory services of the RHS and CSL. Since 2001, the disease has been
confirmed on Ceanothus thyrsiflorus var. repens,
C. arboreus
'Trewithen Blue',
‘Concha’ and ‘Blue Sapphire’ in Kent,
Hampshire, Herefordshire and Surrey.
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Figure 1:
Brown lesions caused by Phloeosporella ceanothi on Ceanothus (left)
on the leaves (right) on the stems |
Microscopic examination revealed conidiomata
producing thick, white tendrils of conidia (Fig. 2) that were hyaline, flexuous,
straight or slightly curved , fusiform, tapered at one end, each with two septa
(Fig.3 A and B) and measuring 54 µm x 2.4 µm (45.3 - 62.1 µm x 2 - 2.7 µm)
consistent with Phloeosporella ceanothi (Sutton, 1980).

Figure 2:
White tendrils of conidia produced on the abaxial leaf surface
Single spore cultures were
isolated on potato carrot agar supplemented with ampicillin and streptomycin.
The fungus was slow growing but produced discrete colonies of branched mycelium
with abundant sporulation when plated on potato dextrose agar (PDA). After 30
days growth on PDA, the colonies were removed and mixed with sterile distilled
water to a concentration of 1 x 105 spores/ml and used to perform
Koch’s postulates on healthy Ceanothus ‘Blue Mound’ plants.
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Figure 3:
Curved (left) and
straight (right) conidia of Phloeosporella ceanothi
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Inoculation was facilitated
by dipping whole branches into the spore suspension (3 repetitions). Sterile
distilled water was used for control plants. The plants were covered with a
polythene bag for 5 days, to maintain high humidity, and placed outside. After
23 days brown circular lesions on the leaves were observed. Phloeosporella
ceanothi was re-isolated from the leaf lesions fulfilling Koch’s postulates.
No symptoms were observed on the control plants. To our knowledge the disease
has only been recorded so far in the United States (Farr et al., 2007).
The records mentioned above are the first confirmed cases of Phloeosporella
ceanothi in the UK.
References
Farr DF, Rossman AY, Palm ME, McCray EB, 2007.
Fungal Databases, Systematic Botany & Mycology Laboratory, ARS, USDA. Retrieved
September 26, 2007, from http://nt.ars-grin.gov/fungaldatabases/
Sutton BC, 1980. The
Coelomycetes. Kew, UK: Commonwealth Mycological Institute.
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