A severe dieback of box elder ( Acer negundo ) caused by Fusarium solani (Mart.) Sacc. in Turkey

Abstract

A severe dieback has recently been observed on box elder (Acer negundo) grown on roadsides and in gardens in Ankara, the capital of Turkey. Fusarium solani was isolated from diseased box elder branches and was identified as the causal agent of dieback on this host. Pathogenicity tests were carried out on young box elder shoots. Symptoms of the pathogen are illustrated. Fusarium solani (Mart.) Sacc. has been isolated from an extremely wide range of both plant and animal tissue including ulcerated human tissue. It can cause root rot and stem cankers on many host plants. However, it is frequently found associated with damage or stress events caused by other biotic or abiotic agents (Booth 1971). Strains of F. solani have been associated with cankers of hardwood trees like teak (Tectona grandis) in Tanzania (Hocking 1968), mulberry (Broussonetia papyrifera) (Schreiber and Docinger 1967), yellow poplar (Liriodendron tulipifera L.) (Dochinger and Seliskar 1962), cottonwood (Populus deltoides) (Boyer 1961), musizi (Maesopsis emini) (Brown 1964), aspen (Populus tremuloides) (Maini and Dance 1965), tupelo (Nyssa sylvatica var. biflora) (Toole 1962), English walnut (Juglans regia L.) (Chen and Stewart 2000), spineless cactus (Opuntia ficus-indica) (Moura et al. 1998), tapiscia (Tapiscia sinensis) (Mei et al. 1999), red oak (Quercus rubra), (Toole 1966), citrus species (Citrus spp.) (Fawcett 1936) and black poplar (Populus nigra subs. betulifolia) (Barbee 1962). F. solani is considered to be the primary organism responsible for Fusarium canker of sugar maple (Acer saccharum) (Wood and Skelly 1964; Weidensaul and Wood 1973). Another fungus, the basidiomycete Inonotus rickii, was also reported to be the causal agent of canker and decay on Acer negundo L. in Italy (Annesi et al. 2003). Severe dieback symptoms have been observed on many box elders (Acer negundo), a common tree in Ankara, Turkey. The diseased trees showed partial chlorosis and wilting on the infected branches. Infected branches had brown and red discoloration in their sapwood. The bark of the old infected branches peeled off and deep cracks were seen on them. Box elder branches 5 cm in diameter showing dieback symptoms and red stain in the sapwood (Fig. 1) were removed from 2.5 to 3.0 m up the stems of different 20-25-year-old trees. A piece of wood was cut from the junction between diseased and healthy tissue showing the red stain and surface sterilised with 1% NaOCl for 3 min and then plated onto PDA + streptomycin medium. After a week, similar fungal cultures were obtained from 90% of all isolations. Mycelial tips from these colonies were removed and inoculated on PDA. The Petri plates were incubated at 24 • C for 10 days under fluorescent and black-light lamps with a 12 h L : 12 h D photoperiod. Each culture was observed under a stereoscopic microscope and a small part of the mycelial mass containing spores was taken by a sterile needle and introduced into a drop of sterile water on a sterile microscope slide. The spore suspension was observed microscopically and a loop of the suspension was taken up and streaked onto plates containing water agar (1%). These Petri plates were observed under a stereoscopic microscope after 24 h incubation. A mycelial tip which had been initiated from a single spore was taken up by a sterile needle tip and inoculated on PDA (Booth 1971). The fungus was identified as F. solani, based on the descriptions given by Booth (1971). The single spore cultures were preserved as spore suspensions in 10% glycerin at −20 • C. The fungus was grown on PDA for 10 days. One-year-old shoots of young box elder plants, which had been obtained from the ornamental plant nursery of the Faculty of Agriculture, University of Ankara, were surface disinfected with 70% ethanol and pieces of bark were split longitudinally with a sterile blade and inoculated with an agar piece (3 × 3 mm) cut from the edge of the fungus culture. The control shoots were prepared in the same way but inoculated with sterile agar pieces. All the inoculated areas were covered with sterile wet cotton and completely encased