© 2008 Plant Management Network.
Phytophthora ramorum Infects Hazelnut, Vine Maple, Blue Blossom, and Manzanita Species in California
Matthew V. DiLeo, Department of Plant Pathology, University of California, Davis 95616; John C. Bienapfl, Department of Plant Pathology, University of Minnesota, St. Paul 55108; and David M. Rizzo, Department of Plant Pathology, University of California, Davis 95616
Corresponding author: Matthew V. DiLeo. email@example.com
DiLeo, M. V., Bienapfl, J. C., and Rizzo, D. M. 2008. Phytophthora ramorum infects hazelnut, vine maple, blue blossom, and manzanita species in California. Online. Plant Health Progress doi:10.1094/PHP-2008-0118-02-BR.
Phytophthora ramorum was isolated from symptomatic tissue of California hazelnut (Corylus cornuta var. californica), vine maple (Acer circinatum), blue blossom (Ceanothus thyrsiflorus), and two species of manzanita (Arctostaphylos columbiana and A. manzanita) in the spring of 2006. This is the first report of these plant species as natural hosts of P. ramorum. Symptomatic C. cornuta var. californica plants were found in Marin, Mendocino, and Sonoma Counties. Symptomatic A. circinatum plants were found among infected Lithocarpus densiflorus and Umbellularia californica trees in Humboldt Co. Symptomatic C. thyrsiflorus plants were found in Humboldt Co. within an infected forest of Sequoia sempervirens, Pseudotsuga menziesii, L. densiflorus, and Arbutus menziesii trees. Both Arctostaphylos species were found in Humboldt Co. Symptomatic hairy manzanita (A. columbiana) was found in Humboldt Redwoods State Park, near the Avenue of the Giants, within a forest of P. menziesii, L. densiflorus, and A. menziesii trees displaying unconfirmed symptoms of P. ramorum. Cultures of P. ramorum had not previously been obtained from Arctostaphylos species; however the pathogen had been associated with A. manzanita through PCR analysis of symptomatic tissue (1).
Field symptoms of ramorum blight on C. cornuta var. californica included leaf water-soaking and marginal necrosis. The infection apparently spread into young stems, causing shoot dieback (Fig. 1). A. circinatum exhibited petiole necrosis similar to symptoms observed on bigleaf maple (Acer macrophyllum). Leaf lesions, often appearing as marginal scorching, have also been observed on bigleaf maple but were not apparent on naturally infected A. circinatum (Fig. 2). C. thyrsiflorus and both Arctostaphylos species displayed leaf spots and stem lesions. Shoot dieback was observed in naturally infected C. thyrsiflorus plants (Fig. 3).
Association of symptomatic tissues with P. ramorum was confirmed by plating on PARP agar as described in Davidson et al. (1). Each isolate was tested for pathogenicity on its corresponding host by dipping five asymptomatic detached shoots for 1 min in suspensions of 10,000 zoospores/ml, which were produced as described in Davidson et al. (1). Control plants were dipped in distilled water. Treated shoots were placed in water-filled flasks in moist chambers for 5 to 11 days at room temperature in front of a south-facing window.
P. ramorum was re-isolated from symptomatic tissues of all inoculated shoots but not from control shoots. Symptoms on inoculated C. cornuta var. californica leaves included diffuse, light brown, water-soaked patches and discrete, dark, necrotic spots. Stem lesions were present but dieback was not observed, possibly due to the lack of actively growing shoots on inoculated material. Foliar symptoms on inoculated A. circinatum consisted of dark necrotic lesions and water-soaked patches, frequently along leaf margins. Petiole lesions were also present. Dark lesions formed on inoculated C. thyrsiflorus stems and leaves, resulting in dieback as lesions spread from stems into asymptomatic leaves. Extensive dieback was observed on both inoculated Arctostaphylos species, with lesions found on leaves, stems, and buds.
The native ranges of these new host species overlap considerably with regions that are considered to be highly favorable to P. ramorum epidemics (2,3). It is unknown how these newly-identified hosts affect the epidemiology of sudden oak death in California ecosystems or the spread of P. ramorum into un-infested areas. Finally, species that are very closely related to many of these are common elsewhere in North America where the climate has been estimated to be favorable to P. ramorum (3). Although deciduous trees such as C. cornuta var. californica and A. circinatum are leafless, and therefore presumably limited in their ability to support pathogen sporulation during the epidemic season in California, year-round rains in temperate climates could increase the importance that related species would play in epidemics.
1. Davidson, J. M., Werres, S., Garbelotto, M., Hansen, E. M., and Rizzo, D. M. 2003. Sudden oak death and associated diseases caused by Phytophthora ramorum. Online. Plant Health Progress doi:10.1094/PHP-2003-0707-01-DG.
2. Hickman, J. C., ed. 1993. The Jepson Manual Higher Plants of California. University of California Press, Berkeley, CA.
3. Venette, R. C., and Cohen, S. D. 2006. Potential climatic suitability for establishment of Phytophthora ramorum within the contiguous United States. For Ecol Manage. 231:18-26.