Kinetoplastibacterium

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. Some trypanosomatida are intracellular parasites, with the important exception of Trypanosoma brucei.

Medical importance

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 '' T. cruzi'' and transmitted by triatomine bugs), and leishmaniasis (a set of trypanosomal diseases caused by various species of ''Leishmania'' transmitted by sandflies).

Evolution

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 '' T. antiquus''.

Taxonomy

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 obligatory intracellular bacteria of the Kinetoplastibacterium genus.

* Family Trypanosomatidae Calkins 1926 rypanomorphidae Woodcock 1906; Trypanosomataceae Senn 1911** Genus '' Agamomonas'' Grassé 1952
** Genus '' Batracoleishmania'' Dasgupta 2011
** Genus ''Blastocrithidia'' Laird 1959
** Genus '' Cercoplasma'' Roubaud 1911
** Genus '' Cystotrypanosoma'' Roubaud 1911
** Genus '' Jaenimonas'' Votypka & Hamilton 2015
** Genus '' Lamellasoma'' Davis 1947
** Genus '' Leptowallaceina'' Podlipaev & Frolov 2000
** Genus '' Lewisonella'' Chalmers 1918 nomen dubium
** Genus '' Malacozoomonas'' Nicoli, Penaud & Timon-David 1972
** Genus '' Nematodomonas'' Nicoli, Penaud & Timon-David 1972
** Genus †''Paleoleishmania'' Poinar & Poinar, 2004
** Genus †'' Paleotrypanosoma'' Poinar 2008
** Genus '' Paramecioides'' Grassé 1882
** Genus '' Sauroleishmania'' Ranque 1973
** Genus '' Sergeia'' Svobodová et al. 2007 non Stimpson 1860 non Nasonov 1923 non Sergio Manning & Lemaitre 1994
** Genus '' Trypanomonas'' Danilewsky 1885
** Genus '' Trypanomorpha'' Woodcock 1906
** Genus '' Undulina'' Lankester 187
** Genus '' Wallaceina'' Bulat, Mokrousov & Podlipaev 1999 'Proteomonas''_Podlipaev,_Frolov_&_Kolesnikov_1990_non_Hill_&_Wetherbee_1986.html" ;"title="Proteomonas.html" ;"title="'Proteomonas">'Proteomonas'' Podlipaev, Frolov & Kolesnikov 1990 non Hill & Wetherbee 1986">Proteomonas.html" ;"title="'Proteomonas">'Proteomonas'' Podlipaev, Frolov & Kolesnikov 1990 non Hill & Wetherbee 1986** Genus ''Wallacemonas'' Kostygov & Yurchenko 2014
** Subfamily Paratrypanosomatinae Votýpka & Lukeš 2013
*** Genus '' Paratrypanosoma'' Votypka & Lukes 2013
** Subfamily Trypanosomatinae

::* Genus ''Trypanosoma'' Gruby 1843
:* Subfamily Blechomonadinae Votypka & Suková 2013
::* Genus '' Blechomonas'' Votypka & Suková 2013

:* Subfamily Leishmaniinae sensu Maslov & Lukeš 2012
::* Clade Crithidiatae Maslov & Lukeš 2012

:::* Genus ''Crithidia'' Léger 1902
:::* Genus ''Leptomonas'' Kent 1880
:::* Genus '' Lotmaria'' Schwarz 2015
::* Clade Leishmaniatae Maslov & Lukeš 2012
:::* 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
:* Subfamily Phytomonadinae Kostygov & Yurchenko 2015
::* Genus '' Herpetomonas'' Kent 1880 non Donovan 1909
:* Genus '' Lafontella'' Kostygov & Yurchenko 2015

::* Genus '' Phytomonas'' Donovan 1909
:* Subfamily Strigomonadinae Votypka et al. 2014

::* Genus '' Angomonas'' Souza & Corte-Real 1991
::* Genus '' Kentomonas'' Votypka et al. 2014
::* Genus '' Strigomonas'' Lwoff & Lwoff 1931

Life cycle

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, with most having 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.

Among commonly studied examples, '' T. brucei'', '' T. congolense'', and '' T. vivax'' are extracellular, while '' T. cruzi'' and ''Leishmania'' spp. are intracellular. Trypanosomatids with intracellular stages express proteins on their surfaces. de Paiva ''et al.'', 2015 illuminates δ-amastins' roles in intracellular success.

Morphologies

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'' amastigotes are particularly small and are among the smallest eukaryotic cells. The flagellum is very short, projecting only slightly beyond the flagellar pocket.
* (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.
* (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.
* (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.
* (herpetomonad). A rarer morphology where the flagellum posterior of nucleus, passing through a long groove in the cell.
* . A morphotype where the flagellum does not extend beyond the deep flagellar pocket.

Image:LeishmaniaMexicana Amastigote SEM.jpg, Amastigote: False colour SEM micrograph of amastigote form ''Leishmania mexicana''. The cell body is shown in orange and the flagellum is in red. 219 pixels/μm.
Image:LeishmaniaMexicana Promastigote SEM.jpg, Promastigote: False colour SEM micrograph of promastigote form ''Leishmania mexicana''. The cell body is shown in orange and the flagellum is in red. 119 pixels/μm.
Image:TrypanosomaBrucei_ProcyclicTrypomastigote_SEM.jpg, Trypomastigote: False colour SEM micrograph of procyclic form ''Trypanosoma brucei''. The cell body is shown in orange and the flagellum is in red. 84 pixels/μm.

Other features

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.

Bacterial endosymbioant

A grand total of six species of trypanosomatids carry an additional proteobacterial endosymbioant, termed TPE (trypanosomatid proteobacterial endosymbionts). These trypansomatids ('' Strigomonas oncopelti'', '' S. culicis'', '' S. galati'', '' Angomonas desouzai'', and '' A. deanei'') are in turn known as SHTs, for symbiont-harboring trypanosomatids. All such symbionts have a shared evolutionary origin and are classified in the Candidatus genus "Kinetoplastibacterium".

As with many symbionts, the bacteria have a much reduced genome compared to their free-living relatives of genera ''Taylorella'' and ''Achromobacter''. (GTDB finds the genus sister to '' Proftella'', a symbiont of ''Diaphorina citri''.) Reflecting their inability to live along, they have lost genes dedicated to essential biological functions, relying on the host instead. They have modified their devision to become synchronized with the host. In ''S. culicis'' at least, the TPE helps the host by synthesizing heme and producing essential enzymes, staying tethered to the kinetoplast.

References

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* (Archive: ) A comprehensive survey of the organisms' natural history.

External links

Trykipedia
Trypanosomatid specific ontologies

Tree of Life: TrypanosomatidaTaxonomya at BOLD SystemsTaxonomy at TaxonomiconOpen Tree TaxonomyZipcodeZoo

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Parasitic excavates
Extant Albian first appearances
Excavata orders