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Blastocladiomycota

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Abstract

The Blastocladiomycota are posteriorly uniflagellated zoosporic fungi found as saprotrophs and parasites primarily in freshwater and soil. Once considered Chytridiomycota, phylogenetically they are a monophyletic group divergent from other zoosporic fungi, clustering among the nonzoosporic fungi. Their thalli range from monocentric, polycentric, tubular, to hyphal and are unusual among fungi in exhibiting alternation of a haploid gametophytic generation with a diploid sporophytic generation. Thick-walled resistant sporangia are the sites of meiosis and aid in the survival of the organism when environmental conditions become adverse. The hallmark of the group is the ultrastructural architecture of their zoospores, which includes a single nucleus proximal to the kinetosome, an aggregated cluster of ribosomes capping the nucleus anteriorly, and a lateral microbody-lipid globule complex (MLC). In addition to being the center for utilization of stored energy, the MLC has been implicated in rhodopsin-based photoreception and signal transduction in response to blue-green light. Invertebrates, plants, algae, oomycetes, and other blastoclads serve as hosts of parasitic members. For example, Paraphysoderma is a highly destructive pathogen of algae grown in mass cultures for biofuels and pharmaceuticals. As a pathogen of mosquitoes, Coelomomyces has been explored as a biocontrol agent, but its life cycle requirement for alternation of hosts makes this a difficult system to maintain. The saprotrophs Allomyces and Blastocladiella are emerging as model organisms in developmental biology, genetics, physiology, and genomics.

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References

  • Aldrich, H. C., Barstow, W. E., & Lingle, W. L. (1984). Elemental analysis of particles in fungal zoospores. Archives für Mikrobiologie, 139, 102–104.

    Article  CAS  Google Scholar 

  • Aleshin, V. V., Konstantinova, A. V., Mikhailov, K. V., Nikitin, M. A., & Petrov, N. B. (2007). Do we need many genes for phylogenetic inference? Biochemistry (Moscow), 12, 1313–1323.

    Article  CAS  Google Scholar 

  • Aliaga, G. R., & Pommerville, J. C. (1990). Analysis of cytoplasmic microtubules and flagellar roots in the zoospores of Allomyces macrogynus. Protoplasma, 155, 221–232.

    Article  Google Scholar 

  • Avelar, G. M., Schumacher, R. I., Zaini, P. A., Leonard, G., Richards, T. A., & Gomes, S. L. (2014). A rhodopsin-guanylyl cyclase gene fusion functions in visual perception in a fungus. Current Biology, 24, 1234–1240.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Barr, D. J. S. (1981). The phylogenetic and taxonomic implications of flagellar rootlet morphology among zoosporic fungi. BioSystems, 14, 359–370.

    Article  CAS  PubMed  Google Scholar 

  • Barr, D. J. S. (1992). Evolution and kingdoms of organisms from the perspective of a mycologist. Mycologia, 84, 1–11.

    Article  Google Scholar 

  • Barr, D. J. S., & Babcock, C. E. (1994). Cryopreservation of unicellular, zoosporic fungi, a simple method. US Federation of Culture Collection Newsletter, 24, 6.

    Google Scholar 

  • Barr, D. J. S., & Hadland-Hartmann, V. E. (1978). The flagellar apparatus in the Chytridiales. Canadian Journal of Botany, 56, 887–900.

    Article  Google Scholar 

  • Barstow, W. E. (1979). Ultrastructure of the formation of gamma particles during zoosporogenesis in Allomyces macrogynus and Catenaria anguillulae. Experimental Mycology, 3, 28–41.

    Article  Google Scholar 

  • Berbee, M. L., & Taylor, J. W. (2007). Rhynie chert: A window into a lost world of complex plant-fungus interactions. New Phytologist, 174, 475–479.

    Article  PubMed  Google Scholar 

  • Bills, G. F., Christensen, M., Powell, M., & Thorn, G. (2004). Saprobic soil fungi. In G. M. Mueller, G. F. Bills, & M. S. Foster (Eds.), Biodiversity of fungi: Inventory and monitoring methods (pp. 271–302). Oxford: Elsevier.

    Chapter  Google Scholar 

  • Bracker, C. E. (1967). Ultrastructure of fungi. Annual Review of Phytopathology, 5, 343–374.

    Article  Google Scholar 

  • Castillo, J. D., & Lawrence, K. S. (2011). First report of Catenaria auxiliaris parasitizing the reniform nematode Rotylenchulus reniformis on cotton in Alabama. Plant Disease, 95, 490.

    Article  Google Scholar 

  • Chong, J., & Barr, D. J. S. (1974). Ultrastructure of the zoospores of Entophlyctis confervae-glomeratae, Rhizophydium patellarium and Catenaria anguillulae. Canadian Journal of Botany, 52, 1197–1204.

    Article  Google Scholar 

  • Chukanhom, K., & Kishio, H. (2004). Freshwater fungi isolated from eggs of the common carp (Cyprinus carpio) in Thailand. Mycoscience, 45, 42–48.

    Article  Google Scholar 

  • Couch, J. N. (1945). Observations on the genus Catenaria. Mycologia, 37, 163–193.

    Article  Google Scholar 

  • Couch, J. N., & Bland, C. E. (1985). The genus Coelomomyces. Orlando: Academic.

    Google Scholar 

  • Couch, J. N., & Whiffen, A. J. (1942). Observations on the genus Blastocladiella. American Journal of Botany, 29, 582–591.

    Article  Google Scholar 

  • Czeczuga, B., & Muszynska, E. (1999). Aquatic fungi growing on the eggs of fishes representing 33 cyprinid taxa (Cyprinidae) in laboratory conditions. Acta Ichthyologica et Piscatoria, 29, 53–72.

    Article  Google Scholar 

  • Czeczuga, B., Godlewska, A., & Kiziewicz, B. (2004). Aquatic fungi growing on features of wild and domestic bird species in immunologically different water bodies. Polish Journal of Environmental Studies, 13, 21–31.

    CAS  Google Scholar 

  • Deacon, J. W., & Saxena, G. (1997). Orientated zoospore attachment and cyst germination in Catenaria anguillulae, a facultative endoparasite of nematodes. Mycological Research, 101, 513–522.

    Article  Google Scholar 

  • Dewel, R. A., & Dewel, W. C. (1990). The fine structure of the zoospore of Sorochytrium milnesiophthora. Canadian Journal of Botany, 68, 1968–1977.

    Article  Google Scholar 

  • Dewel, R. A., Joines, J. D., & Bond, J. J. (1985). A new chytridiomycete parasitizing the tardigrade Milnesium tardigradum. Canadian Journal of Botany, 63, 1525–1534.

    Article  Google Scholar 

  • Emerson, R. (1941). An experimental study of the life cycle and taxonomy of Allomyces. Lloydia, 4, 77–144.

    Google Scholar 

  • Emerson, R., & Natvig, D. O. (1981). Adaptation of fungi to stagnant waters. In D. T. Wicklow & G. C. Carroll (Eds.), The fungal community, its organization and role in the ecosystem (pp. 109–128). New York: Marcel Dekker.

    Google Scholar 

  • Emerson, R., & Robertson, J. A. (1974). Two new members of the Blastocladiaceae. I. Taxonomy, with an evaluation of genera and interrelationships in the family. American Journal of Botany, 61, 303–317.

    Article  Google Scholar 

  • Federici, B. A., & Lucarotti, C. J. (1986). Structure and behavior of the meiospore of Coelomomyces dodgei during encystment on the copepod host, Acanthocyclops vernalis. Journal of Invertebrate Pathology, 48, 259–268.

    Article  CAS  PubMed  Google Scholar 

  • Feeney, D. M., & Treimer, R. E. (1979). Cytochemical localization of Golgi marker enzymes in Allomyces. Experimental Mycology, 3, 151–163.

    Article  Google Scholar 

  • Forshay, K. J., Johnson, P. T. J., Stock, M., Peñalva, C., & Dodson, S. I. (2008). Festering food: Chytridiomycete pathogen reduces quality of Daphnia host as a food resource. Ecology, 89, 2692–2699.

    Article  PubMed  Google Scholar 

  • Fuller, M. S. (1977). The zoospore: Hallmark of the aquatic fungi. Mycologia, 69, 1–20.

    Article  Google Scholar 

  • Fuller, M. S., & Jaworski, A. (1987). Zoosporic fungi in teaching and research. Athens: Southeastern Publishing Corporation.

    Google Scholar 

  • Fuller, M. S., & Olson, L. W. (1971). The zoospore of Allomyces. Journal of General Microbiology, 66, 171–183.

    Article  Google Scholar 

  • Fultz, S. A., & Sussman, A. A. (1966). Antigenic differences in the surfaces of hyphae and of rhizoids in Allomyces. Science, 152, 785–787.

    Article  CAS  PubMed  Google Scholar 

  • Gleason, F. H., Fell, P., & Gordon, G. L. R. (2002). The ultrastructure of mitochondria in Blastocladia pringsheimii Reinsch. Australasian Mycologist, 21, 41–44.

    Google Scholar 

  • Gleason, F. H., Marano, A. V., Johnson, P., & Martin, W. W. (2010). Blastocladian parasites of invertebrates. Fungal Biology Reviews, 24, 56–67.

    Article  Google Scholar 

  • Gottschalk, W. K., & Sonneborn, D. R. (1985). Evidence that Blastocladiella emersonii zoospore maintenance factor is a sulfhydryl group-containing cyclic ribotide. The Journal of Biological Chemistry, 260, 6592–6599.

    CAS  PubMed  Google Scholar 

  • Guerin, M., Huntley, M. E., & Olaizola, M. (2003). Haematococcus astaxanthin: Applications for human health and nutrition. Trends in Biotechnology, 21, 210–216.

    Article  CAS  PubMed  Google Scholar 

  • Hibbett, D. S., Binder, M., Bischoff, J., Blackwell, M., Cannon, P., Eriksson, O., Huhndorf, S., James, T., Kirk, P., Lucking, R., Lumbsch, H., Lutzoni, F., Matheny, P., McLaughlin, D., Powell, M., Redhead, S., Schoch, C., Spatafora, J., Stalpers, J., Vilgalys, R., et al. (2007). A higher level phylogenetic classification of the fungi. Mycological Research, 111, 509–547.

    Article  PubMed  Google Scholar 

  • Hoffman, Y., Aflalo, C., Zarka, A., Gutman, J., James, T.Y., & Boussiba, S. (2008). Isolation and characterization of a novel chytrid species (phylum Blastocladiomycota), parasitic on the green alga Haematococcus. Mycological Research, 112, 70–81.

    Google Scholar 

  • Hohn, T. M., Lovett, J. S., & Bracker, C. E. (1984). Characterization of the major proteins in gamma particles, cytoplasmic organelles in Blastocladiella emersonii zoospores. Journal of Bacteriology, 158, 253–263.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Humber, R. A. (2012). Identification of entomopathogenic fungi. In L. A. Lacey (Ed.), Manual of techniques in invertebrate pathology (2nd ed., pp. 151–187). New York: Academic.

    Chapter  Google Scholar 

  • Idnurm, A., Verma, S., & Corrochano, L. M. (2010). A glimpse into the basis of vision in the kingdom Mycota. Fungal Genetics and Biology, 47, 881–892.

    Article  PubMed  PubMed Central  Google Scholar 

  • James, T. Y., Kauff, F., Schoch, C. L., Matheny, P. B., Hofstetter, V., Cox, C. J., Celio, G., Guiedan, C., Fraker, E., Miadlikowska, J., Lumbsh, H. T., Rauhut, A., Reeb, V., Arnold, A. E., Amtoft, A., Stajich, J. E., Hosaka, K., Sung, G.-H., Johnson, D., O’Rourke, B., Crockett, M., Binder, M., Curtis, J. M., Slot, J. C., Wang, Z., Wilson, A. W., Schüßler, A., Longcore, J. E., O’Donnell, K., Mozley-Standridge, S., Porter, D., Letcher, P. M., Powell, M. J., Taylor, J. W., White, M. M., Griffith, G. W., Davies, D. R., Humber, R. A., Morton, J. B., Sugiyama, J., Rossman, A. Y., Rogers, J. D., Pfister, D. H., Hewitt, D., Hansen, K., Hambleton, S., Shoemaker, R. A., Kohlmeyer, J., Volkmann-Kohlmeyer, B., Spotts, R. A., Serdani, M., Crous, P. W., Hughes, K. W., Matsuura, K., Langer, E., Langer, G., Untereiner, W. A., Lücking, R., Büdel, B., Geiser, D. M., Aptroot, A., Diederich, P., Schmitt, I., Schultz, M., Yahr, R., Hibbett, D. S., Lutzoni, F., McLaughlin, D. J., Spatafora, J. W., & Vilgalys, R. (2006a). Reconstructing the early evolution of the fungi using a six gene phylogeny. Nature, 443, 818–822.

    Article  CAS  PubMed  Google Scholar 

  • James, T. Y., Letcher, P. M., Longcore, J. E., Mozley-Standridge, S. E., Porter, D., Powell, M. J., Griffith, G. W., & Vilgalys, R. (2006b). A molecular phylogeny of the flagellated fungi (Chytridiomycota) and description of a new phylum (Blastocladiomycota). Mycologia, 98, 860–871.

    Article  PubMed  Google Scholar 

  • James, T. Y., Hoffman, Y., Zarka, A., & Boussiba, S. (2011). Paraphysoderma sedebokerense, gen. et sp. nov., an aplanosporic relative of Physoderma (Blastocladiomycota). Mycotaxon, 118, 177–180.

    Article  Google Scholar 

  • James, T. Y., Porter, T. M., & Martin, W. W. (2014). Blastocladiomycota. In D. J. McLaughlin & J. W. Spatafora (Eds.), The Mycota VII part A (pp. 177–207). New York: Springer.

    Google Scholar 

  • Jansson, H.-B., & Thiman, L. (1992). A preliminary study of chemotaxis of zoospores of the nematode-parasitic fungus Catenaria anguillulae. Mycologia, 84, 109–112.

    Article  Google Scholar 

  • Jaworski, A. (1987). Evidence for differential regulation of two classes of poly(A) RNA in Blastocladiella emersonii zoospores. Experimental Mycology, 11, 176–186.

    Article  CAS  Google Scholar 

  • Jaworski, A. J., & Stumhofer, P. (1981). Stage-specific synthesis of proteins complexed to ribonucleoprotein particles and ribosomes in zoospores of Blastocladiella emersonii. Molecular and Cellular Biology, 1, 310–320.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Johnson, P. T. J., Longcore, J. E., Stanton, D. E., Carnegie, R. B., Shields, J. D., & Preu, E. R. (2006a). Chytrid infections of Daphnia pulicaria: Development, ecology, pathology and phylogeny of Polycaryum laeve. Freshwater Biology, 51, 634–648.

    Article  Google Scholar 

  • Johnson, P. T. J., Stanton, D. E., Preu, E. R., Forshay, K. J., & Carpenter, S. R. (2006b). Dining on disease: How interactions between infection and environment affect predation risk. Ecology, 87, 1973–1980.

    Article  PubMed  Google Scholar 

  • Johnson, P. T. J., Ives, A. R., Lathrop, R. C., & Carpenter, S. R. (2009). Long-term disease dynamics in lakes: Causes and consequences of chytrid infections in Daphnia populations. Ecology, 90, 132–144.

    Article  PubMed  Google Scholar 

  • Karling, J. S. (1948). Chytridiosis of scale insects. American Journal of Botany, 35, 246–254.

    Article  Google Scholar 

  • Karling, J. S. (1950). The genus Physoderma (Chytridiales). Lloydia, 13, 29–71.

    Google Scholar 

  • Karling, J. S. (1965). Catenophlyctis, a new genus of the Catenariaceae. American Journal of Botany, 52, 133–138.

    Article  Google Scholar 

  • Karling, J. S. (1973). A note on Blastocladiella (Blastocladiaceae). Mycopathologia et Mycologia Applicata, 49, 169–172.

    Article  Google Scholar 

  • Karling, J. S. (1977). Chytridiomycetarum Iconographia. Monticello: Lubrecht and Cramer.

    Google Scholar 

  • Khandjian, E. W., Turian, G., & Eisen, H. (1977). Characterization of the RNA mycovirus infecting Allomyces arbuscula. Journal of General Virology, 35, 415–424.

    Article  Google Scholar 

  • Krishnan, A., Almén, M. S., Fredriksson, R., & Schiöth, H. B. (2012). The origin of GPCRs: Identification of mammalian like rhodopsin, adhesion, glutamate and frizzled GPCRs in fungi. PLoS One, 7, e29817. doi:10.1371/journal.pone.0029817.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lange, L., & Olson, L. W. (1979). The uniflagellate phycomycete zoospore. Dansk Botanisk Arkiv, 33, 7–95.

    Google Scholar 

  • Lange, L., & Olson, L. W. (1980a). Germination of the resting sporangia of Physoderma maydis, the causal agent of Physoderma disease of maize. Protoplasma, 102, 323–342.

    Article  Google Scholar 

  • Lange, L., & Olson, L. W. (1980b). Transfer of the Physodermataceae from the Chytridiales to the Blastocladiales. Transactions of the British Mycological Society, 74, 449–457.

    Article  Google Scholar 

  • Letcher, P. M., Lee, P. A., Lopez, S., Burnett, M., McBride, R. C., & Powell, M. J. (2016). An ultrastructural study of Paraphysoderma sedebokerense (Blastocladiomycota), an epibiotic parasite of microalgae. Fungal Biology, 120, 324–337.

    Article  PubMed  Google Scholar 

  • Lingle, W. L., & Barstow, W. E. (1983). Ultrastructure of the zoospore of Blastocladia ramosa (Blastocladiales). Canadian Journal of Botany, 61, 3502–3513.

    Article  Google Scholar 

  • Liu, Y. J., Hodson, M. C., & Hall, B. D. (2006). Loss of the flagellum happened only once in the fungal lineage: Phylogenetic structure of Kingdom Fungi inferred from RNA polymerase II subunit genes. BMC Evolutionary Biology, 6, 74–86.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lorelli, J. P., & Held, A. A. (1983). Screening of Blastocladialean fungi for antibiotic production by a modified “cross-streak” test. Mycologia, 75, 909–913.

    Article  Google Scholar 

  • Loubès, C., & Manier, J. F. (1974). Étude ultrastructurale de Coelomycidium simulii Debaisieux, 1920 sa position systématique parmi les Chyridiomycètes. Protistologica, 1, 47–57.

    Google Scholar 

  • Lucarotti, C. J., & Federici, B. A. (1984). Ultrastructure of the gametes of Coelomomyces dodgei Couch (Blastocladiales, Chytridiomycetes). Protoplasma, 121, 77–86.

    Article  Google Scholar 

  • Lucarotti, C. J., & Shoulkamy, M. A. (2000). Coelomomyces stegomyiae infection in adult female Aedes aegypti following the first, second, and third host blood meals. Journal of Invertebrate Pathology, 75, 292–295.

    Article  CAS  PubMed  Google Scholar 

  • Manier, J. F., & Loubès, C. (1978). Callimastix cyclopsis Weissenberg, 1912 (Phycomycéte, Blastocladiale) parasite d’un Microcyclops Claus, 1893 (Copépode, Cyclopoide) récolté au Tchad: Particularités ultrastructurales. Protistologica, 14, 493–501.

    Google Scholar 

  • Martin, W. W. (1971). The ultrastructure of Coelomomyces punctatus zoospores. Journal of the Elisha Mitchell Scientific Society, 87, 209–221.

    Google Scholar 

  • Martin, W. W. (1991). Egg parasitism by zoosporic fungi in a littoral chironomid community. Journal of the North American Benthological Society, 10, 455–462.

    Article  Google Scholar 

  • Medina, M., Collins, A. G., Taylor, J. W., Valentine, J. W., Lipps, J. H., Amaral-Zettler, L., & Sogin, M. L. (2003). Phylogeny of Opisthokonta and the evolution of multicellularity and complexity in Fungi and Metazoa. International Journal of Astrobiology, 2, 203–211.

    Article  Google Scholar 

  • Nishida, H., & Nishiyama, M. (2000). What is characteristic of fungal lysine synthesis through the alpha-aminoadipate pathway? Journal of Molecular Evolution, 51, 299–302.

    Article  CAS  PubMed  Google Scholar 

  • Ojha, M., & Barja, F. (2002). Spatial and cellular localization of calcium-dependent protease (CDP II) in Allomyces arbuscula. Journal of Cell Science, 116, 1095–1105.

    Article  CAS  Google Scholar 

  • Olson, L. W. (1973). The meiospore of Allomyces. Protoplasma, 78, 113–127.

    Article  CAS  PubMed  Google Scholar 

  • Olson, L. W. (1984). Allomyces – A different fungus. Opera Botanica, 73, 1–96.

    Google Scholar 

  • Olson, L. W., & Lange, L. (1978). The meiospore of Physoderma maydis. The causal agent of Physoderma disease of maize. Protoplasma, 97, 275–290.

    Article  Google Scholar 

  • Olson, L. W., & Reichle, R. (1978a). Meiosis and diploidization in the aquatic Phycomycete Catenaria anguillulae. Transactions of the British Mycological Society, 70, 423–437.

    Article  Google Scholar 

  • Olson, L. W., & Reichle, R. (1978b). Synaptonemal complex formation and meiosis in resting sporangium of Blastocladiella emersonii. Protoplasma, 97, 261–273.

    Article  Google Scholar 

  • Olson, L. W., Lange, L., & Reichle, R. E. (1978). The zoospore of the aquatic phycomycete Catenaria anguillulae. Protoplasma, 94, 53–71.

    Article  Google Scholar 

  • Paquin, B., & Lang, B. F. (1996). The mitochondrial DNA of Allomyces macrogynus: The complete genomic sequence from an ancestral fungus. Journal of Molecular Biology, 255, 688–701.

    Article  CAS  PubMed  Google Scholar 

  • Petersen, H. E. (1909). Studier over Ferskvands-Phycomyceter. Botanisk Tidsskrift, 29, 345–440.

    Google Scholar 

  • Pommerville, J. C. (1977). Chemotaxis of Allomyces gametes. Experimental Cell Research, 109, 43–51.

    Article  CAS  PubMed  Google Scholar 

  • Pommerville, J. C. (1978). Analysis of gamete and zygote motility in Allomyces. Experimental Cell Research, 113, 161–172.

    Article  CAS  PubMed  Google Scholar 

  • Pommerville, J. C., & Olson, L. W. (1987). Evidence for a male-produced pheromone in Allomyces macrogynus. Experimental Mycology, 11, 245–248.

    Article  CAS  Google Scholar 

  • Porter, T. M., Martin, W., James, T. Y., Longcore, J. E., Gleason, F. H., Adler, P. H., Letcher, P. M., & Vilgalys, R. (2011). Molecular phylogeny of the Blastocladiomycota (Fungi) based on nuclear ribosomal DNA. Fungal Biology, 115, 381–392.

    Article  CAS  PubMed  Google Scholar 

  • Powell, M. J. (1976). Ultrastructural changes in the cell surface of Coelomomyces punctatus infecting mosquito larvae. Canadian Journal of Botany, 54, 1419–1437.

    Article  Google Scholar 

  • Powell, M. J. (1978a). Phylogenetic implications of the microbody-lipid-globule complex in zoosporic fungi. BioSystems, 10, 167–180.

    Article  CAS  PubMed  Google Scholar 

  • Powell, M. J. (1978b). Ultrastructure of the host-parasite interface between Allomyces javanicus and its endoparasite Catenaria allomycis. Botanical Gazette, 143, 176–187.

    Article  Google Scholar 

  • Powell, M. J. (1993). Looking at mycology with a Janus face: A glimpse at Chytridiomycetes active in the environment. Mycology, 85, 1–20.

    Article  Google Scholar 

  • Powell, M. J. (1994). Production and modifications of extracellular structures during development of Chytridiomycetes. Protoplasma, 181, 123–141.

    Article  Google Scholar 

  • Reichle, R. E., & Fuller, M. S. (1967). The fine structure of Blastocladiella emersonii zoospores. American Journal of Botany, 54, 81–92.

    Article  Google Scholar 

  • Reinsch, P. F. (1877–1878). Beobachtungen über einige neue Saprolegnieae, über die Parasiten in Desmidienzellen und über die Stachelkugeln in Achlyaschläuchen. Pringsheim’s Jahrbucher fur Wissenschaftliche Botanik, 11, 283–311.

    Google Scholar 

  • Remy, W., Taylor, T. N., & Hass, H. (1994). Early Devonian fungi: A blastocladialean fungus with sexual reproduction. American Journal of Botany, 81, 690–702.

    Article  Google Scholar 

  • Renaud, F. L., & Swift, H. (1964). The development of basal bodies and flagella in Allomyces arbusculus. Journal of Cell Biology, 23, 339–354.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Robertson, F. A. (1972). Phototaxis in a new Allomyces. Archives für Mikrobiologie, 85, 259–266.

    Article  CAS  Google Scholar 

  • Saranak, J., & Foster, K. W. (1997). Rhodopsin guides fungal phototaxis. Nature, 387, 465–466.

    Article  CAS  PubMed  Google Scholar 

  • Scholte, E.-J., Knols, B. G. J., Samson, R. A., & Takken, W. (2004). Entomopathogenic fungi for mosquito control: A review. Journal of Insect Science, 4, 19–42, Available online: insectscience.org/4.19.

    Article  PubMed  PubMed Central  Google Scholar 

  • Sewall, T., Roberson, R., & Pommerville, J. (1989). Identification and characterization of Golgi equivalents from Allomyces macrogynus. Experimental Mycology, 13, 239–252.

    Article  Google Scholar 

  • Shearer, C. A., Langsam, E. M., & Longcore, J. E. (2004). Fungi in freshwater habitats. In G. M. Mueller, G. F. Bills, & M. S. Foster (Eds.), Biodiversity of fungi: Inventory and monitoring methods (pp. 513–531). Oxford: Elsevier.

    Chapter  Google Scholar 

  • Silva, A. M., Maia, J. C. C., & Juliani, M. H. (1987). Changes in the pattern of protein synthesis during zoospore germination in Blastocladiella emersonii. Journal of Bacteriology, 169, 2069–2078.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Singh, K. P., Jaiswal, R. K., & Kumar, N. (2007). Catenaria anguillulae Sorokin: A natural biocontrol agent of Meloidogyne graminicola causing root knot disease of rice (Oryza sativa L.). World Journal of Microbiology and Biotechnology, 23, 291–294.

    Article  Google Scholar 

  • Sparrow, F. K. (1939). The entomogenous chytrid Myrophagus Thaxter. Mycologia, 31, 439–444.

    Article  Google Scholar 

  • Sparrow, F. K. (1960). Aquatic Phycomycetes (2nd ed. Rev.). Ann Arbor: University of Michigan Press.

    Google Scholar 

  • Sparrow, F. K. (1962). Urophlyctis and Physoderma. Transactions of the Mycological Society of Japan, 3, 16–18.

    Google Scholar 

  • Steenkamp, E. T., Wright, J., & Baldauf, S. L. (2006). The protistan origins of animals and fungi. Molecular Biology and Evolution, 23, 93–106.

    Article  CAS  PubMed  Google Scholar 

  • Strittmatter, M., Guerra, T., Silva, J., & Gachon, C. M. M. (2016). A new flagellated dispersion stage in Paraphysoderma sedebokerense, a pathogen of Haematoccous pluvialis. Journal of Applied Phycology, 28, 1553–1558.

    Article  CAS  PubMed  Google Scholar 

  • Tambor, J. H. M., Ribichich, K. F., & Gomes, S. L. (2008). The mitochondrial view of Blastocladiella emersonii. Gene, 424, 33–39.

    Article  CAS  PubMed  Google Scholar 

  • Travland, L. B. (1979). Structures of the motile cells of Coelomomyces psorophorae and function of the zygote in encystment on a host. Canadian Journal of Botany, 57, 1021–1035.

    Article  Google Scholar 

  • Tribe, H. T. (1977). A parasite of white cysts of Heterodera: Catenaria auxiliaris. Transactions of the British Mycological Society, 69, 367–376.

    Article  Google Scholar 

  • Vargas, M. M., Aronson, J. M., & Roberson, R. W. (1993). The cytoplasmic organization of hyphal tip cells in the fungus Allomyces macrogynus. Protoplasma, 176, 43–52.

    Article  Google Scholar 

  • Vogel, J. J. (1964). Distribution of lysine pathways among fungi: Evolutionary implications. The American Naturalist, 68, 435–446.

    Article  Google Scholar 

  • Wallroth, F. G. (1833). Physoderma. Flora Crytogamica Germaniae, 2, 1–928.

    Google Scholar 

  • Weete, J. D., Fuller, M. S., Huang, M. Q., & Gandhi, S. (1989). Fatty acids and sterols of selected Hyphochytridomycetes and Chytridiomycetes. Experimental Mycology, 13, 183–195.

    Article  CAS  Google Scholar 

  • Weiser, J., & Zizka, Z. (1975). The ultrastructure of the chytrid Coelomycidium simulii Deb. II Division of the thallus and structures of zoospores. Ceská Mykologie, 28, 227–232.

    Google Scholar 

  • Whisler, H. C. (1987). On the isolation and culture of water molds: The Blastocladiales and Monoblepharidales. In M. S. Fuller & A. Jaworski (Eds.), Zoosporic fungi in teaching and research (pp. 121–124). Athens: Southeastern Publishing Corp.

    Google Scholar 

  • Whisler, H. C., Shemanchuk, J. A., & Traviand, L. B. (1972). Germination of the resistant sporangia of coelomomyces psorophorae. Journal of Invertebrate pathology, 19, 139–147.

    Google Scholar 

  • Whisler, H. C., Zebold, S. L., & Shemanchuk, J. A. (1975). Life history of Coelomomyces psorophorae. Proceedings of the National Academy of Sciences, 72, 693–696.

    Article  CAS  Google Scholar 

  • Willoughby, L. G. (1984). Viability of Allomyces in a dry soil, investigated by Polycell-gel analysis. Transaction of the British Mycological Society, 82, 581–587.

    Article  Google Scholar 

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Acknowledgments

The author is grateful to Dr. Peter Letcher for assistance in assembling illustrations. This work was supported in part by All Fungal Tree of Life (AFTOL) DEB-0732599 and Partnerships for Enhancing Expertise in Taxonomy (PEET) DEB-0529694 grants from the National Science Foundation.

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Correspondence to Martha J. Powell .

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Powell, M.J. (2016). Blastocladiomycota. In: Archibald, J., et al. Handbook of the Protists. Springer, Cham. https://doi.org/10.1007/978-3-319-32669-6_17-1

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