Rhizophydiales

Rhizophydiales
Scientific classification
Kingdom: Fungi
Division: Chytridiomycota
Class: Chytridiomycetes
Order: Rhizophydiales
Letcher 2006[1]
Type species
Rhizophydium globosum
Schenk 1858

Rhizophydiales are an important group of chytrid fungi. They are found in soil as well as marine and fresh water habitats where they function as parasites and decomposers.

Role in the environment

Rhizophydiales are parasites of a range of organisms, including invertebrates, other chytrids and algae, and they may have a role in natural control of aquatic populations, especially phytoplankton.[2][3] One member, Rhizophydium graminis, is a parasite of wheat roots, but causes no extensive damage to the plant. The only documented cases of a chytrid parasitizing vertebrates are Batrachochytrium dendrobatidis and Batrachochytrium salamandrivorans, members of this order. They are highly destructive pathogens of frogs and salamanders respectively.[4]

The majority of the described saprotrophic species of this order are biodegraders of pollen, with only a few growing on keratin, chitin, and cellulose. The transformational role of the Rhizophydiales in aquatic food webs is little studied but recently more recognized.[5]

Life history

Their thalli (=bodies) consist of two parts: an absorptive branching rhizoidal system that contains no nuclei and a multinucleate sporangium that ranges in shape from spherical, to oval, to pear-shaped, and to multi-lobbed. The rhizoids attach the thallus to a substrate (food source) and absorbs nutrients. When the thallus is fully grown, the sporangium releases numerous, unwalled, uninucleate-zoospores, each bearing a single posteriorly directed flagellum.

The zoospore has to use its own stored food reserves (lipids and glycogen) as it swims until it attaches to a suitable host or substrate, absorbs its flagellum, produces a wall around itself, grows a germ tube that penetrates the substrate, and develops into a new thallus.[6] Zoospores of parasitic chytrids use light and chemical cues to locate hosts. Zoospores of Rhizophydium littoreum, a parasite of marine green algae, are positively phototactic toward blue light, a mechanism that might assure that zoospores swim to the photic zone where its host resides.[7] Zoospores of both R. littoreum and B. dendrobatidis exhibit chemotaxis to specific sugars, proteins and amino acids, also a mechanism by which zoospores might detect signals to potential hosts.[8][9]

Sexual reproduction is more rarely reported and occurs when two adjacent sporangia function as gametangia with one transferring all of its cytoplasmic contents into the other, resulting in the development of a thick-walled, lipid-laden resting spore.[10]

Taxonomic classification

The Rhizophydiales is an order of fungi that includes the following genera:

The following families have been established:

Biodiversity

New species and genera are still being discovered in this order. A member of this order, Kappamyces, was the first phylogenetic genus of a chytrid circumscribed based primarily on monophly demonstrated in molecular sequence analysis and confirmed with unique zoospore structure [11] Coralloidiomyces digitatus defied the original view held that the thallus of members of the Rhizophydiales was conservative. Collected from submersed mud at the edge of an oligotrophic lake in southern Argentina near the Andes in Patagonia, C. digitatus has a thallus with a sporangium shaped like a coral.[16]

References

  1. 1 2 Letcher, P.M.; Powell, MJ; Churchill, PF; Chambers, JG (2006). "Ultrastructural and molecular phylogenetic delineation of a new order, the Rhizophydiales (Chytridiomycota)". Mycol. Res. 110 (Pt 8): 898–915. doi:10.1016/j.mycres.2006.06.011. PMID 16919432.
  2. ↑ Powell, M.J. (1993). "Looking at mycology with a Janus face. A glimpse at Chytridiomycetes active in the environment". Mycologia. 85 (1): 1–20. doi:10.2307/3760471.
  3. ↑ Ibelings, B.W.; et al. (2004). "Host parasite interactions between freshwater phytoplankton and chytrid fungi (Chytridiomycota)". J. Phycol. 40 (3): 437–453. doi:10.1111/j.1529-8817.2004.03117.x.
  4. 1 2 Longcore, J.E..; Pessier, A.P.; Nichols, D.K (1999). "Batrachochytrium dendrobatidis gen. et sp. nov., a chytrid pathogenic to amphibians". Mycologia. 91 (2): 219–227. doi:10.2307/3761366.
  5. ↑ Kagami, M.; de Bruin, A; Ibelings, B.W.; Van Donk, E. (2007). "Parasitic chytrids: their effects on phytoplankton communities and food-web dynamics". Hydrobiologia. 578: 113–129. doi:10.1007/s10750-006-0438-z.
  6. ↑ Powell, M.J. (1976). "Ultrastructure and isolation of glyoxysomes (microbodies) in zoospores of the fungus Entophlyctis sp". Protoplasma. 89: 1–27. doi:10.1007/BF01279325.
  7. ↑ Muehlstein, L.K.; Amon, J.P.; Leffler, D.L. (1987). "Phototaxis in the marine fungus Rhizopohydium littoreum". Appl. Environ. Microbiol. 53 (8): 1819–1821. PMC 204006Freely accessible. PMID 16347407.
  8. ↑ Muehlstein, L.K.; Amon, J.P.; Leffler, D.L. (1988). "Chemotaxis in the marine fungus Rhizophydium littoreum". Appl. Environ. Microbiol. 54 (7): 1668–1672. PMC 202725Freely accessible. PMID 16347677.
  9. ↑ Moss, A.S.; et al. (2008). "Chemotaxis of the amphibian pathogen Batrachochytrium dendrobatidis and its response to a variety of attractants". Mycologia. 100 (1): 1–5. doi:10.3852/mycologia.100.1.1. PMID 18488347.
  10. ↑ Sparrow, F.K. (1935). "Recent contributions to our knowledge of the aquatic phycomycetes". Biol. Rev. Cambridge Phil. Soc. 10 (2): 152–186. doi:10.1111/j.1469-185X.1935.tb00480.x.
  11. 1 2 Letcher, P.M.; Powell, M.J. (2005). "Kappamyces, a new genus in the Chytridiales (Chytridiomycota)". Nova Hedwigia. 80: 113–133.
  12. ↑ Letcher, P.M.; Vélez, CG; Barrantes, M.E.; Powell, M.J.; Churchill, P.F.; Wakefield, W.S. (2008). "Ultrastructural and molecular analyses of Rhizophydiales (Chytridiomycota) isolates from North America and Argentina". Mycol. Res. 112 (Pt 7): 759–782. doi:10.1016/j.mycres.2008.01.025. PMID 18501579.
  13. ↑ Letcher, P.M.; Vélez, CG; Schultz, S; Powell, MJ (2012). "New taxa are delineated in Alphamycetaceae (Rhizophydiales, Chytridiomycota)". Nova Hedwigia. 94 (Pt 1-2): 9–29. doi:10.1127/0029-5035/2012/0094-0009.
  14. ↑ Lepelletier, F.; Karpov, S. A.; Alacid, E.; LePanse, S.; Bigeard, E.; Garces, E.; Jeanthon, C.; Guillou, L. (2014). "Dinomyces arenysensis gen. et sp. nov. (Rhizophydiales, Dinomycetaceae fam. nov.), a chytrid infecting marine dinoflagellates". Protist. 165: 230–244. doi:10.1016/j.protis.2014.02.004. PMID 24709472.
  15. ↑ Powell, M.J.; Letcher, P.M.; Chambers, J.G.; Roychoudhury, S. (2015). "A new genus and family for the misclassified chytrid, Rhizophlyctis harderi". Mycologia. 107 (2): 419–431. doi:10.3852/14-223. PMID 25572098.
  16. 1 2 Letcher, P.M.; Powell, M.J.; Viusent, M.C. (2008). "Rediscovery of an unusual chytridiaceous fungus new to the order Rhizophydiales". Mycologia. 100 (2): 325–334. doi:10.3852/mycologia.100.2.325. PMID 18592907.
  17. ↑ Powell, M.J.; Letcher, P.M.; Longcore, J.E. (2011). "Operculomyces is a new genus in the order Rhizophydiales". Mycologia. 103 (4): 854–862. doi:10.3852/10-293. PMID 21262983.
  18. 1 2 3 4 Letcher, P.M.; Powell, M.J.; Davis, W.J. (2015). "A new family and four new genera in Rhizophydiales (Chytridiomycota)". Mycologia. 107 (4): 808–830. doi:10.3852/14-280. PMID 25911694.
  19. ↑ Hibbett, D.S.; et al. (March 2007). "A higher level phylogenetic classification of the Fungi". Mycological Research. 111 (5): 509–547. doi:10.1016/j.mycres.2007.03.004. PMID 17572334.
  20. ↑ Longcore, J.E.; Letcher, P.M.; James, T.Y. (2011). "Homolaphlyctis polyrhiza gen. et sp. nov., a species in the Rhizophydiales (Chytridiomycetes) with multiple rhizoidal axes". Mycotaxon. 118: 433–440.


Wikimedia Commons has media related to Chytridiomycota.
This article is issued from Wikipedia - version of the 11/17/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.