Trypanosomatida is a group of kinetoplastid excavates distinguished by having only a single flagellum. The name is derived from the Greek trypano (borer) and soma (body) because of the corkscrew-like motion of some trypanosomatid species. All members are exclusively parasitic, found primarily in insects. A few genera have life-cycles involving a secondary host, which may be a vertebrate, invertebrate or plant. These include several species that cause major diseases in humans.
|Trypanosoma cruzi parasites|
The three major human diseases caused by trypanosomatids are; African trypanosomiasis (sleeping sickness, caused by Trypanosoma brucei and transmitted by tsetse flies), South American trypanosomiasis (Chagas disease, caused by Trypanosoma cruzi and transmitted by triatomine bugs), and leishmaniasis (a set of trypanosomal diseases caused by various species of Leishmania transmitted by sandflies).
The family is known from fossils of the extinct genus Paleoleishmania preserved in Burmese amber dating to the Albian (100 mya) and Dominican amber from the Burdigalian (20–15 mya) of Hispaniola. The genus Trypanosoma is also represented in Dominican amber in the extinct species Trypanosoma antiquus.
Three genera are dixenous (two hosts in the life cycle) – Leishmania, Phytomonas and Trypanosoma and the remainder are monoxenous (one host in the life cycle). Paratrypanosoma appears to be the first evolving branch in this order. Fifteen genera are recognised in the Trypanosomatidae and there are three subfamilies – Blechomonadinae, Leishmaniinae and Strigomonadinae. The genera in the subfamily Strigomonadinae are characterised by the presence of intracellular bacteria.
- Family Trypanosomatidae Calkins 1926 [Trypanomorphidae Woodcock 1906; Trypanosomataceae Senn 1911]
- Genus Blastocrithidia Laird 1959
- Genus Cercoplasma Roubaud 1911
- Genus Cystotrypanosoma Roubaud 1911
- Genus Jaenimonas Votypka & Hamilton 2015
- Genus Lafontella Kostygov & Yurchenko 2015
- Genus Lamellasoma Davis 1947
- Genus Leptowallaceina Podlipaev & Frolov 2000
- Genus Lewisonella Chalmers 1918 nomen dubium
- Genus †Paleoleishmania Poinar & Poinar, 2004
- Genus †Paleotrypanosoma Poinar 2008
- Genus Paramecioides Grassé 1882
- Genus Paratrypanosoma Votypka & Lukes 2013
- Genus Rhynchoidomonas Patton 1910
- Genus Sauroleishmania Ranque 1973
- Genus Trypanomonas Danilewsky 1885
- Genus Trypanomorpha Woodcock 1906
- Genus Undulina Lankester 187
- Genus Wallacemonas Kostygov & Yurchenko 2014
- Genus Wallaceina Bulat, Mokrousov & Podlipaev 1999 [Proteomonas Podlipaev, Frolov & Kolesnikov 1990 non Hill & Wetherbee 1986]
- Subfamily Trypanosomatinae
- Genus Trypanosoma Gruby 1843
- Subfamily Blechomonadinae Votypka & Suková 2013
- Genus Blechomonas Votypka & Suková 2013
- Subfamily Strigomonadinae
- Genus Agamomonas Grassé 1952
- Genus Angomonas Souza & Corte-Real 1991
- Genus Herpetomonas Kent 1880 non Donovan 1909
- Genus Kentomonas Votypka et al. 2014
- Genus Phytomonas Donovan 1909
- Genus Sergeia Svobodová et al. 2007 non Stimpson 1860 non Nasonov 1923 non Sergio Manning & Lemaitre 1994
- Genus Strigomonas Lwoff & Lwoff 1931
- Subfamily Leishmaniinae sensu Maslov & Lukeš 2012
- Genus Lotmaria Schwarz 2015
- Genus Crithidia Léger 1902
- Genus Leptomonas Kent 1880
- Genus Borovskyia Kostygov & Yurchenko 2017
- Genus Endotrypanum Mesnil & Brimont 1908
- Genus Leishmania Ross 1903
- Genus Novymonas Votýpka et al. 2015
- Genus Paraleishmania Cupolillo et al. 2000
- Genus Zelonia Shaw, Camargo et Teixeira 2016
Some trypanosomatids only occupy a single host, while many others are heteroxenous: they live in more than one host species over their life cycle. This heteroxenous life cycle typically includes the intestine of a bloodsucking insect and the blood and/or tissues of a vertebrate. Rarer hosts include other bloodsucking invertebrates, such as leeches, and other organisms such as plants. Different species go through a range of different morphologies at different stages of the life cycle, most have at least two different morphologies. Typically the promastigote and epimastigote forms are found in insect hosts, trypomastigote forms in the mammalian bloodstream and amastigotes in intracellular environments.
A variety of different morphological forms appear in the life cycles of trypanosomatids, distinguished mainly by the position, length and the cell body attachment of the flagellum. The kinetoplast is found closely associated with the basal body at the base of the flagellum and all species of trypanosomatid have a single nucleus. Most of these morphologies can be found as a life cycle stage in all trypanosomatid genera however certain morphologies are particularly common in a particular genus. The various morphologies were originally named from the genus where the morphology was commonly found, although this terminology is now rarely used because of potential confusion between morphologies and genus. Modern terminology is derived from the Greek; "mastig", meaning whip (referring to the flagellum), and a prefix which indicates the location of the flagellum on the cell. For example, the amastigote (prefix "a-", meaning no flagellum) form is also known as the leishmanial form as all Leishmania have an amastigote life cycle stage.
- Amastigote (leishmanial). Amastigotes are a common morphology during an intracellular lifecycle stage in a mammalian host. All Leishmania have an amastigote stage of the lifecycle. Leishmania amastigoes are particularly small and are among the smallest eukaryotic cells. The flagellum is very short, projecting only slightly beyond the flagellar pocket.
- Promastigote (leptomonad). The promastigote form is a common morphology in the insect host. The flagellum is found anterior of nucleus and flagellum not attached to the cell body. The kinetoplast is located in front of the nucleus, near the anterior end of the body.
- Epimastigote (crithidial). Epimastigotes are a common form in the insect host and Crithidia and Blastocrithidia, both parasites of insects, exhibit this form during their life cycles. The flagellum exits the cell anterior of nucleus and is connected to the cell body for part of its length by an undulating membrane. The kinetoplast is located between the nucleus and the anterior end.
- Trypomastigote (trypanosomal). This stage is characteristic of the genus Trypanosoma in the mammalian host bloodstream as well as infective metacyclic stages in the fly vector. In trypomastigotes the kinetoplast is near the posterior end of the body, and the flagellum lies attached to the cell body for most of its length by an undulating membrane.
- Opisthomastigote (herpetomonad). A rarer morphology where the flagellum posterior of nucleus, passing through a long groove in the cell.
Notable characteristics of trypanosomatids are the ability to perform trans-splicing of RNA and possession of glycosomes, where much of their glycolysis is confined to. The acidocalcisome, another organelle, was first identified in trypanosomes.
- Podlipaev S (May 2001). "The more insect trypanosomatids under study-the more diverse Trypanosomatidae appears". Int. J. Parasitol. 31 (5–6): 648–52. doi:10.1016/S0020-7519(01)00139-4. PMID 11334958.
- Simpson AG, Stevens JR, Lukes J; Stevens; Lukes (April 2006). "The evolution and diversity of kinetoplastid flagellates". Trends Parasitol. 22 (4): 168–74. doi:10.1016/j.pt.2006.02.006. PMID 16504583.CS1 maint: Multiple names: authors list (link)
- Poinar, G. (2008). "Lutzomyia adiketis sp. n. (Diptera: Phlebotomidae), a vector of Paleoleishmania neotropicum sp. n. (Kinetoplastida: Trypanosomatidae) in Dominican amber". Parasites & Vectors. 1 (1): 22. doi:10.1186/1756-3305-1-22. PMC 2491605. PMID 18627624.
- Poinar, G. (2005). "Triatoma dominicana sp. n. (Hemiptera: Reduviidae: Triatominae), and Trypanosoma antiquus sp. n. (Stercoraria: Trypanosomatidae), the First Fossil Evidence of a Triatomine-Trypanosomatid Vector Association". Vector-Borne and Zoonotic Diseases. 5 (1): 72–81. doi:10.1089/vbz.2005.5.72. PMID 15815152.
- Hoare, Cecil A.; Wallace, Franklin G. (1966). "Developmental Stages of Trypanosomatid Flagellates: a New Terminology". Nature. 212 (5068): 1385–6. doi:10.1038/2121385a0.
- Docampo R, de Souza W, Miranda K, Rohloff P, Moreno SN; De Souza; Miranda; Rohloff; Moreno (March 2005). "Acidocalcisomes — conserved from bacteria to man". Nature Reviews Microbiology. 3 (3): 251–61. doi:10.1038/nrmicro1097. PMID 15738951.CS1 maint: Multiple names: authors list (link)
- Bütikofer P, Ruepp S, Boschung M, Roditi I; Ruepp; Boschung; Roditi (September 1997). "'GPEET' procyclin is the major surface protein of procyclic culture forms of Trypanosoma brucei brucei strain 427". Biochem. J. 326 (Pt 2): 415–23. doi:10.1042/bj3260415. PMC 1218686. PMID 9291113.CS1 maint: Multiple names: authors list (link)
- Dean S, Marchetti R, Kirk K, Matthews KR; Marchetti; Kirk; Matthews (May 2009). "A surface transporter family conveys the trypanosome differentiation signal". Nature. 459 (7244): 213–7. doi:10.1038/nature07997. PMC 2685892. PMID 19444208.CS1 maint: Multiple names: authors list (link)
- Engstler M, Boshart M; Boshart (November 2004). "Cold shock and regulation of surface protein trafficking convey sensitization to inducers of stage differentiation in Trypanosoma brucei". Genes Dev. 18 (22): 2798–811. doi:10.1101/gad.323404. PMC 528899. PMID 15545633.
- Hofer A, Steverding D, Chabes A, Brun R, Thelander L; Steverding; Chabes; Brun; Thelander (May 2001). "Trypanosoma brucei CTP synthetase: a target for the treatment of African sleeping sickness". Proc. Natl. Acad. Sci. U.S.A. 98 (11): 6412–6. doi:10.1073/pnas.111139498. PMC 33482. PMID 11353848.CS1 maint: Multiple names: authors list (link)
- Janovy, J; Roberts, L.S. (2005). Foundations of Parasitology (7th ed.). New York NY: McGraw Hill. pp. 61–69.
- Legros D, Ollivier G, Gastellu-Etchegorry M, et al. (July 2002). "Treatment of human African trypanosomiasis--present situation and needs for research and development". Lancet Infect Dis. 2 (7): 437–40. doi:10.1016/S1473-3099(02)00321-3. hdl:10144/18268. PMID 12127356.
- Matthews KR (January 2005). "The developmental cell biology of Trypanosoma brucei". J. Cell Sci. 118 (Pt 2): 283–90. doi:10.1242/jcs.01649. PMC 2686837. PMID 15654017.
- Matthews KR, Gull K; Gull (June 1994). "Evidence for an interplay between cell cycle progression and the initiation of differentiation between life cycle forms of African trypanosomes". J. Cell Biol. 125 (5): 1147–56. doi:10.1083/jcb.125.5.1147. PMC 2120053. PMID 8195296.
- Morrison LJ, Marcello L, McCulloch R; Marcello; McCulloch (December 2009). "Antigenic variation in the African trypanosome: molecular mechanisms and phenotypic complexity" (PDF). Cell. Microbiol. 11 (12): 1724–34. doi:10.1111/j.1462-5822.2009.01383.x. PMID 19751359.CS1 maint: Multiple names: authors list (link)
- Seed JR, Wenck MA; Wenck (June 2003). "Role of the long slender to short stumpy transition in the life cycle of the African trypanosomes". Kinetoplastid Biol Dis. 2 (1): 3. doi:10.1186/1475-9292-2-3. PMC 165594. PMID 12844365.
- Shadan S (May 2009). "Microbiology: Signals for change". Nature. 459 (7244): 175. doi:10.1038/459175a. PMID 19444199.
- Sherwin T, Gull K; Gull (June 1989). "The cell division cycle of Trypanosoma brucei brucei: timing of event markers and cytoskeletal modulations". Philosophical Transactions of the Royal Society B. 323 (1218): 573–88. doi:10.1098/rstb.1989.0037. PMID 2568647.
- "African trypanosomiasis". World Health Organization. August 2006.