Trypanosoma vivax

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Trypanosoma vivax
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Phylum: Euglenozoa
Class: Kinetoplastea
Order: Trypanosomatida
Family: Trypanosomatidae
Genus: Trypanosoma
Species:
T. vivax
Binomial name
Trypanosoma vivax
Ziemann, 1905
Synonyms
  • Trypanosoma caprae
  • Trypanosoma angolense
  • Trypanosoma (subg. Duttonella) vivax [1] [2]

Trypanosoma vivax is a parasite species in the genus Trypanosoma . It causes the disease nagana, affecting cattle or wild mammals. It is mainly occurs in West Africa, although it has spread to South America. [3] [1]

Contents

Range

Historically restricted to sub-Saharan Africa especially West Africa, it has spread to 13 countries of South America. This has been made easier by its mechanical transmission route, see § Life cycle below. [1]

Hosts

Hosts include, cattle, horses, sheep, and camels. [2] [1] As of 2016 in South America it is an emerging pathogen of cattle, and sometimes horses and other ruminants. [1]

The vector host is Glossina .

Life cycle

Unusual for a trypanosome, T. vivax does not infect the Glossina vector midgut. Instead it infects and completes an abbreviated life cycle only in the vector's proboscis. Thus it is entirely mechanically transmitted. For this reason it has had a relatively easy time jumping vectors, and thereby even jumping geographic ranges which do not have its customary vector. [1]

Symptoms

Symptoms of T. vivax include "rapid weight loss, lethargy, weakness, clumsiness, pale mucosa, swelling of superficial lymph nodes, anemia, and fluctuating pyrexia, causing[...]a drop in animal productivity." [4]

Enzymes

A novel proline racemase of medical and veterinary importance has been described in T. vivax ( B8LFE4 ). [5]

It also produces vivapain, a cysteine peptidase. [6]

Host immunity

The smallest variable surface glycoprotein (40 kDa in size) to date has been found in T. vivax, which bears little carbohydrate. [7]

Economic impact

Trypanosoma vivax is a significant drag on Africa's cattle production every year, and increasingly is a concern in South America: One outbreak in 1995 in the Pantanal in Brazil and Bolivia cost the industry over US$160 million. [1]

Trypanocide resistance

Some resistance to trypanocides has been observed: Some African countries have isometamidium-resistant populations, with some of these also being resistant to diminazene. (This has been ascribed variously to cross-resistance or to two separate events of acquisition of separate resistance genetics. Isometamidium and diminazene are not thought to be in the same trypanocide class.) Resistance to both is widespread in both West and East Africa. Diminazene resistance has been observed in South America. [1]

Mechanisms of resistance are not necessarily shared across the genus, and this is especially true for this, the most genetically divergent species. [1]

Related Research Articles

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Tsetse are large, biting flies that inhabit much of tropical Africa. Tsetse flies include all the species in the genus Glossina, which are placed in their own family, Glossinidae. The tsetse is an obligate parasite, which lives by feeding on the blood of vertebrate animals. Tsetse has been extensively studied because of their role in transmitting disease. They have a pronounced economic impact in sub-Saharan Africa as the biological vectors of trypanosomes, causing human and animal trypanosomiasis.

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Trypanosoma is a genus of kinetoplastids, a monophyletic group of unicellular parasitic flagellate protozoa. Trypanosoma is part of the phylum Euglenozoa. The name is derived from the Greek trypano- (borer) and soma (body) because of their corkscrew-like motion. Most trypanosomes are heteroxenous and most are transmitted via a vector. The majority of species are transmitted by blood-feeding invertebrates, but there are different mechanisms among the varying species. Trypanosoma equiperdum is spread between horses and other equine species by sexual contact. They are generally found in the intestine of their invertebrate host, but normally occupy the bloodstream or an intracellular environment in the vertebrate host.

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<i>Trypanosoma brucei</i> Species of protozoan parasite

Trypanosoma brucei is a species of parasitic kinetoplastid belonging to the genus Trypanosoma that is present in sub-Saharan Africa. Unlike other protozoan parasites that normally infect blood and tissue cells, it is exclusively extracellular and inhabits the blood plasma and body fluids. It causes deadly vector-borne diseases: African trypanosomiasis or sleeping sickness in humans, and animal trypanosomiasis or nagana in cattle and horses. It is a species complex grouped into three subspecies: T. b. brucei, T. b. gambiense and T. b. rhodesiense. The first is a parasite of non-human mammals and causes nagana, while the latter two are zoonotic infecting both humans and animals and cause African trypanosomiasis.

<i>Trypanosoma evansi</i> Contagious protist

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<span class="mw-page-title-main">Variant surface glycoprotein</span>

Variant surface glycoprotein (VSG) is a ~60kDa protein which densely packs the cell surface of protozoan parasites belonging to the genus Trypanosoma. This genus is notable for their cell surface proteins. They were first isolated from Trypanosoma brucei in 1975 by George Cross. VSG allows the trypanosomatid parasites to evade the mammalian host's immune system by extensive antigenic variation. They form a 12–15 nm surface coat. VSG dimers make up ~90% of all cell surface protein and ~10% of total cell protein. For this reason, these proteins are highly immunogenic and an immune response raised against a specific VSG coat will rapidly kill trypanosomes expressing this variant. However, with each cell division there is a possibility that the progeny will switch expression to change the VSG that is being expressed. VSG has no prescribed biochemical activity.

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References

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"Trypanosoma vivax". National Center for Biotechnology Information (NCBI).