Phytophthora

Sudden oak death caused by Phytophthora ramorum

Phytophthora spp. are mostly pathogens of dicotyledons, and many are relatively host-specific parasites. Phytophthora cinnamomi, though, infects thousands of species ranging from club mosses, ferns, cycads, conifers, grasses, lilies, to members of many dicotyledonous families. Many species of Phytophthora are plant pathogens of considerable economic importance. Phytophthora infestans was the infective agent of the potato blight that caused the Great Famine of Ireland, and still remains the most destructive pathogen of solanaceous crops, including tomato and potato.[3] The soya bean root and stem rot agent, Phytophthora sojae, has also caused longstanding problems for the agricultural industry. In general, plant diseases caused by this genus are difficult to control chemically, thus the growth of resistant cultivars is the main management strategy. Other important Phytophthora diseases are:

• Phytophthora agathidicida—causes collar-rot on New Zealand kauri (Agathis australis), New Zealand's most voluminous tree, an otherwise successful survivor of the Jurassic
• Phytophthora cactorum—causes rhododendron root rot affecting rhododendrons, azaleas, and orchids, and causes bleeding canker in hardwood trees
• Phytophthora capsici—infects Cucurbitaceae fruits, such as cucumbers and squash
• Phytophthora cinnamomi—causes cinnamon root rot affecting forest and fruit trees, and woody ornamentals including arborvitaee, azalea, Chamaecyparis, dogwood, forsythia, Fraser fir, hemlock, Japanese holly, juniper, Pieris, rhododendron, Taxus, white pine, American chestnut and Australian woody plants, especially eucalypt and banksia.
• Phytophthora citricola—causes root rot and stem cankers in citrus trees
• Phytophthora fragariae—causes red root rot affecting strawberries
• Phytophthora infestans causes the serious disease known as potato (late) blight: responsible for the Great Famine of Ireland.
• Phytophthora kernoviae—pathogen of beech and rhododendron, also occurring on other trees and shrubs including oak, and holm oak. First seen in Cornwall, UK, in 2003.[4]
• Phytophthora lateralis—causes cedar root disease in Port Orford cedar trees
• Phytophthora megakarya—one of the cocoa black pod disease species, is invasive and probably responsible for the greatest cocoa crop loss in Africa
• Phytophthora multivora—discovered in analysis of isolates with P. cinnamomi dieback infections of tuart forests of Southwest Australia, which were previously diagnosed as P. citricola. The species was found occurring on many other taxa, so named multivora.[5]
• Phytophthora nicotianae—infects tobacco and onions
• Phytophthora palmivora—causes fruit rot in coconuts and betel nuts
• Phytophthora ramorum—infects over 60 plant genera and over 100 host species; causes sudden oak death[6]
• Phytophthora quercina—causes oak death
• Phytophthora sojae—causes soybean root rot

Research beginning in the 1990s has placed some of the responsibility for European forest die-back on the activity of imported Asian Phytophthoras.[7]

In 2019, scientists in Connecticut were conducting experiments testing various methods to grow healthier Fraser trees when they accidentally discovered a new species of Phytophthora, which they called Phytophthora abietivora. The fact that these scientists so readily discovered a new species further suggests that there could be many more species waiting to be discovered.[8]

Phytophthora species may reproduce sexually or asexually. In many species, sexual structures have never been observed, or have only been observed in laboratory matings. In homothallic species, sexual structures occur in single culture. Heterothallic species have mating strains, designated as A1 and A2. When mated, antheridia introduce gametes into oogonia, either by the oogonium passing through the antheridium (amphigyny) or by the antheridium attaching to the proximal (lower) half of the oogonium (paragyny), and the union producing oospores. Like animals, but not like most true fungi, meiosis is gametic, and somatic nuclei are diploid. Asexual (mitotic) spore types are chlamydospores, and sporangia which produce zoospores. Chlamydospores are usually spherical and pigmented, and may have a thickened cell wall to aid in their role as a survival structure. Sporangia may be retained by the subtending hyphae (noncaducous) or be shed readily by wind or water tension (caducous) acting as dispersal structures. Also, sporangia may release zoospores, which have two unlike flagella which they use to swim towards a host plant.

Zoospores (and zoospores of Pythium, also in the Peronosporales) recognize not only hosts but particular locations on hosts.[9] Phytophthora zoospores recognize and attach to specific root surface regions.[9] This is a high degree of specificity at an early stage of cell development.[9]

Phytophthora forms: A: Sporangia. B: Zoospore. C: Chlamydospore. D: Oospore

Phytophthora is sometimes referred to as a fungus-like organism, but it is classified under a different clade altogether: SAR supergroup (Harosa) (also under Stramenopila and previously under Chromista). This is a good example of convergent evolution: Phytophthora is morphologically very similar to true fungi yet its evolutionary history is completely distinct. In contrast to fungi, SAR supergroup is more closely related to plants than to animals. Whereas fungal cell walls are made primarily of chitin, Phytophthora cell walls are constructed mostly of cellulose. Ploidy levels are different between these two groups; Phytophthora species have diploid (paired) chromosomes in the vegetative (growing, nonreproductive) stage of life, whereas fungi are almost always haploid in this stage. Biochemical pathways also differ, notably the highly conserved lysine synthesis path.

The NCBI lists:[10]

Sanna GP, Bottos A, Maddau L, Montecchio L, Linaldeddu BT. 2020.Diversity and pathogenicity of Phytophthora species associated with declining alder trees in Italy and description of Phytophthora alpina sp. nov. Forests 11 (8): 848

• Lucas, J.A. et al. (eds.) (1991) Phytophthora based on a symposium held at Trinity College, Dublin, Ireland September 1989. British Mycological Society, Cambridge University Press, Cambridge, UK, ISBN 0-521-40080-5;
• Erwin, Donald C. and Ribeiro, Olaf K. (1996) Phytophthora Diseases Worldwide American Phytopathological Society Press, St. Paul, Minnesota, ISBN 0-89054-212-0
• Erwin, Donald C. (1983) Phytophthora: its biology, taxonomy, ecology, and pathology American Phytopathological Society Press, St. Paul, Minnesota, ISBN 0-89054-050-0
• "APHIS List of Regulated Hosts and Plants Associated with Phytophthora ramorum" U.S. Animal and Plant Health Inspection Services
• "Dieback" Department of Environment and Conservation, Western Australia
• Lamour, Kurt (2013). Lamour, K. (ed.). Phytophthora: A Global Perspective. CABI Plant Protection Series. CABI (Centre for Agriculture and Bioscience International). pp. xi+244. doi:10.1079/9781780640938.0000. ISBN 9781780640938. LCCN 2012042152. 978-1-78064-093-8.

Wikispecies has information related to Phytophthora.

Wikimedia Commons has media related to Phytophthora.

• Goodwin, Stephen B. (January 2001) "Phytophthora Bibliography" Purdue University
• Abbey, Tim (2005) "Phytophthora Dieback and Root Rot" College of Agriculture and Natural Resources, University of Connecticut
• "Phytophthora Canker – Identification, Biology and Management" Bartlett Tree Experts Online Resource Library
• "Phytophthora Root Rot – Identification, Biology and Management" Bartlett Tree Experts Online Resource Library
• Dieback Working Group – Western Australia