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Cladus: Eukaryota
Supergroup: Opisthokonta
Regnum: Fungi
Phylum: Oomycota
Class: Oomycetes
Ordines: Albuginales - Lagenismatales - Leptomitales - Myzocytiopsidales - Olpidiopsidales - PeronosporalesPythiales - Rhipidiales - Salilagenidiales - Saprolegniales - Ordines incertae sedis


Bisby FA, Roskov YR, Orrell TM, Nicolson D, Paglinawan LE, Bailly N, Kirk PM, Bourgoin T, Baillargeon G., eds (2009). Species 2000 & ITIS Catalogue of Life: 2009 Annual Checklist. Digital resource at www.catalogueoflife.org/annual-checklist/2009/. Species 2000: Reading, UK.

Harpellales is an order of fungus classified under Kickxellomycotina. Thalli are either unbranched or branched, producing basipetal series of trichospores. Zygospores biconical. Attached to the gut lining of aquatic larvae of Insecta or (rarely) Isopoda. Harpellales are divided into two other families; Harpellaceae and Legeriomycetaceae.[1]

Species include Allantomyces zopilotei, Bojamyces olmecensis, Gauthier-omyces viviparus and Graminella ophiuroidea.[2]


^ "Zygomycota". Retrieved 2009-03-07.
^ Valle LG, White MM, Cafaro MJ (2008). "Harpellales in the digestive tracts of Ephemeroptera and Plecoptera nymphs from Veracruz, Mexico". Mycologia 100 (1): 149–62. doi:10.3852/mycologia.100.1.149. PMID 18488361.Oömycota or oömycetes form a distinct phylogenetic lineage of fungus-like eukaryotic microorganisms (Protists). They are filamentous, microscopic, absorptive organisms that reproduce both sexually and asexually. Oomycetes occupy both saprophytic and pathogenic lifestyles – and include some of the most notorious pathogens of plants, causing devastating diseases such as late blight of potato and sudden oak death. They are also often referred to as water molds (or water moulds), although the water-loving nature which led to that name is not true of most species, which are terrestrial pathogens.


The oomycetes rarely have septa, and if they do, they are scarce,[1] appearing at the bases of sporangia, and sometimes in older parts of the filaments.[2] Some are unicellular, but others are filamentous and branching.[2]

The group is arranged into six orders. Briefly:[2]

The Lagenidiales are the most primitive; some are filamentous, others unicellular; they are generally parasitic.
The Leptomitales have wall thickenings that give their continuous cell body the appearance of septation. They bear chitin and often reproduce asexually.
The Rhipidiales use rhizoids to attach their thallus to the bed of stagnant or polluted water bodies.
The Saprolegniales are the most widespread, lack cell walls, and branch a lot. Many break down decaying matter; others are parasites.
The Peronosporales too are mainly saprophytic or parasitic on plants, and have an aseptate, branching form. Many of the most damaging agricultural parasites belong to this order.
The Albuginales are considered by some authors to be a family (Albuginaceae) within the Paronosporales.

(The above after [2]).

Most of the oomycetes produce two distinct types of spores. The main dispersive spores are asexual, self-motile spores called zoospores, which are capable of chemotaxis (movement toward or away from a chemical signal, such as those released by potential food sources) in surface water (including precipitation on plant surfaces). A few oomycetes produce aerial asexual spores that are distributed by wind. They also produce sexual spores, called oospores, that are translucent, double-walled, spherical structures used to survive adverse environmental conditions.

Many oomycetes are economically important because they are aggressive plant pathogens. Some species can cause disease in fish. The majority of the plant pathogenic species can be classified into four groups, although more exist.

The Phytophthora group is a paraphyletic genus that causes diseases such as dieback, late blight in potatoes (the cause of the Great Hunger or Potato Famine of the 1840s in Ireland and other parts of Europe),[3] sudden oak death, rhododendron root rot, and ink disease in the American chestnut.

The paraphyletic Pythium group is even more prevalent than Phytophthora and individual species have larger host ranges, usually causing less damage. Pythium damping off is a very common problem in greenhouses, where the organism kills newly emerged seedlings. Mycoparasitic members of this group (e.g. P. oligandrum) parasitize other oomycetes and fungi, and have been employed as biocontrol agents. One Pythium species, Pythium insidiosum, is also known to infect mammals.

The third group are the downy mildews, which are easily identifiable by the appearance of white, brownish or olive "mildew" on the lower leaf surfaces (although this group can be confused with the unrelated fungal powdery mildews).

The fourth group are the white blister rusts (Albuginales, which cause white blister disease on a variety of flowering plants. White blister rusts sporulate beneath the epidermis of their hosts, causing spore-filled blisters on stems, leaves and the inflorescence. The Albuginales are currently divided into three genera, Albugo parastic predominantly to Brassicales, Pustula, parasitic predominantly to Asterales, and Wilsoniana, predominantly parasitic to Caryophyllales. Like the downy mildews, the white blister rusts are obligate biotrophs, which means that they are unable to survive without the presence of a living host.

Phylogenetic relationships and classification

Although, based on their general morphology and lifestyles, this group was traditionally classified as fungi,[4] a cladistic classification based on modern insights, supports a relatively close relationship with the photosynthetic organisms such as brown algae and diatoms, within the eukaryotic group - the heterokonts.

This relationship is supported by a number of observed differences in the characteristics of oomycetes and fungi. For instance, the cell walls of oomycetes are composed of cellulose rather than chitin[5] and generally do not have septations. Also, in the vegetative state they have diploid nuclei, whereas fungi have haploid nuclei. Most oomycetes produce self-motile zoospores with two flagella. One flagellum has a "whiplash" morphology, and the other a branched "tinsel" morphology. Spores of the few fungal groups which retain flagella (such as the Chytridiomycetes) have only one whiplash flagellum.[5] Oomycota and fungi have different metabolic pathways for synthesizing lysine and have a number of enzymes which differ.[5] The ultrastructure is also different, with oomycota having tubular mitochondrial cristae and fungi having flattened cristae.[5] In spite of this, many species of oomycetes are still described or listed as types of fungi and may sometimes be referred to as pseudofungi, or lower fungi.

"Oomycota" means "egg fungi", referring to the large round oogonia, structures containing the female gametes, that are characteristic of the oomycetes.

The name "water mold" refers to their earlier classification as fungi and their preference for conditions of high humidity and running surface water, which is characteristic for the basal taxa of the oomycetes.

^ Kortekamp, A. (2005). "Growth, occurrence and development of septa in Plasmopara viticola and other members of the Peronosporaceae using light- and epifluorescence-microscopy". Mycological research 109 (Pt 5): 640–648. PMID 16018320. edit
^ a b c d .
^ Haas, BJ; Kamoun, S; Zody, MC; Jiang, RH; Handsaker, RE; Cano, LM; Grabherr, M; Kodira, CD et al. (2009). "Genome sequence and analysis of the Irish potato famine pathogen Phytophthora infestans.". Nature 461 (7262): 393–8. doi:10.1038/nature08358. PMID 19741609.
^ "Introduction to the Oomycota". Retrieved 2009-05-26.
^ a b c d Van der Auwera G, De Baere R, Van de Peer Y, De Rijk P, Van den Broeck I, De Wachter R (July 1995). "The phylogeny of the Hyphochytriomycota as deduced from ribosomal RNA sequences of Hyphochytrium catenoides". Mol. Biol. Evol. 12 (4): 671–8. PMID 7659021.

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