Glossina morsitans

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Glossina morsitans
Glossina morsitans morsitans (white paper).jpeg
by [[es:User:Estefanía Alonso Gómez]]
Glossina-morsitans-adult-tsetse-fly-2.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Diptera
Family: Glossinidae
Genus: Glossina
Species:
G. morsitans
Binomial name
Glossina morsitans
Westwood, 1851

Glossina morsitans is a species of tsetse fly in the genus Glossina . It is one of the major vectors of Trypanosoma brucei rhodesiense [1] in African savannas. [2]

Contents

Taxonomy

Glossina morsitans is variously classified into the subgenus Glossina [2] or as the name species of a morsitans species group. Note that this includes both subspecies G. m. centralis and G. m. morsitans , and G. pallidipes . [2] [3]

G. m. submorsitans is a common substitute for G. m. morsitans , [4] [3] or rarely as a full species G. submorsitans .

G.m.s. is further subdivided into a G. m. s. ugandensis . [5]

Morphology

Egg

About 1.5–1.6 millimetres (15256116 in) long. [6] [7]

Pregnant female Glossina morsitans morsitans-pregnant female.jpg
Pregnant female

Larvae

First instar

1.8 millimetres (564 in) long. [6]

Second instar

4.5 millimetres (1164 in) long. [6]

Third instar

6–7 millimetres (1564932 in) long. [6]

Adult

Adults are 7.75 millimetres (516 in). G. morsitans is occasionally distinguishable from congeners by the unaided eye - there are differences in gross coloration - if it can be observed resting. It is more readily distinguishable by microscopic examination. [8]

Metabolism

Flight muscles are primarily powered by proline, which is synthesized from fatty acids mobilised out of the fat body. Proline is so efficiently used in muscle mitochondria because they are specialised towards proline oxidising enzymes, and away from enzymes using fatty acids and pyruvate. [9]

Distribution

by [[es:User:Estefania Alonso Gomez]] Mapa Distribucion Gossina morsitans morsitans.jpg
by [[es:User:Estefanía Alonso Gómez]]

G. morsitans is found heavily throughout East Africa and Equatorial Africa: Angola, [10] [3] Benin, [3] Botswana, [10] [3] Burkina Faso, [10] [3] Burundi, [10] [3] Cameroon, [10] [3] Central African Republic, [3] Chad, [10] [3] Democratic Republic of the Congo, [10] [3] Ethiopia, [10] [3] The Gambia, [10] [3] Ghana, [3] Guinea, [3] Guinea-Bissau, [3] Ivory Coast, [10] [3] Kenya, [10] [3] Malawi, [10] [3] Mali, [10] [3] Mozambique, [10] [3] Namibia, [10] [3] Niger, [10] [3] Nigeria, [10] [3] Rwanda, [3] Senegal, [10] [3] Sierra Leone, [3] South Africa, [10] Sudan, [10] [3] Tanzania, [10] [3] Togo, [10] [3] Uganda, [10] [3] Zambia, [10] [3] and Zimbabwe. [10] [3]

Hosts

G. morsitans feeds upon warthogs, oxen, buffaloes, kudus, and humans. [1] About 6% of G. m. s.'s bloodmeals come from birds (excluding ostriches). [3]

Genome

A sequence was made available in 2014. Among other results this reveals that G. morsitans's genome has incorporated some of its Wolbachia symbiont's genome (see also § Symbionts below). [11] The sense of taste of G. m. m. lacks the sense of sweetness - which may be due to its exclusively hematophagous diet. [12]

Genetics

G. morsitans carries 3 Ago2 s according to data compiled by Mongelli & Saleh 2016 [13] [14] and Dowling et al 2016 finds 2 Ago3 s [14] while Mongelli & Saleh's compilation shows 3. [13] [14]

Symbionts

G. m. m. is in obligate symbiosis with Wigglesworthia glossinidia and Wolbachia . Without Wigglesworthia, G. m. m. is sterile, and without Wolbachia they are reproductively incompatible with normal flies. [15]

Economic impact

Trypanosomiasis transmitted by G. morsitans and other tsetse species is one of the largest economic problems Africa faces. It has radically altered the cattle agroeconomy across the middle of Africa, severely shrinking the cattle pastoral lifestyle by shrinking the extent of safe grazing lands. This has left about 10,400,000 square kilometres (4,000,000 sq mi) of otherwise usable land devoid of cattle. Raising cattle in the manner common in 1963, this would have allowed for another 125,000,000 head - more than doubling the 114,000,000 being raised at the time. [16]

Related Research Articles

<span class="mw-page-title-main">Endosymbiont</span> Organism that lives within the body or cells of another organism

An endosymbiont or endobiont is any organism that lives within the body or cells of another organism most often, though not always, in a mutualistic relationship. This phenomenon is known as endosymbiosis. Examples are nitrogen-fixing bacteria, which live in the root nodules of legumes, single-cell algae inside reef-building corals and bacterial endosymbionts that provide essential nutrients to insects.

<span class="mw-page-title-main">African trypanosomiasis</span> Parasitic disease also known as sleeping sickness

African trypanosomiasis, also known as African sleeping sickness or simply sleeping sickness, is an insect-borne parasitic infection of humans and other animals. It is caused by the species Trypanosoma brucei. Humans are infected by two types, Trypanosoma brucei gambiense (TbG) and Trypanosoma brucei rhodesiense (TbR). TbG causes over 92% of reported cases. Both are usually transmitted by the bite of an infected tsetse fly and are most common in rural areas.

<span class="mw-page-title-main">Tsetse fly</span> Genus of disease-spreading insects

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.

<span class="mw-page-title-main">Trypanosomiasis</span> Medical condition

Trypanosomiasis or trypanosomosis is the name of several diseases in vertebrates caused by parasitic protozoan trypanosomes of the genus Trypanosoma. In humans this includes African trypanosomiasis and Chagas disease. A number of other diseases occur in other animals.

<i>Wolbachia</i> Genus of bacteria in the Alphaproteobacteria class

Wolbachia is a genus of gram-negative bacteria that can either infect many species of arthropod as an intracellular parasite, or act as a mutualistic microbe in filarial nematodes. It is one of the most common parasitic microbes of arthropods, and is possibly the most common reproductive parasite in the biosphere. Its interactions with its hosts are often complex. Some host species cannot reproduce, or even survive, without Wolbachia colonisation. One study concluded that more than 16% of neotropical insect species carry bacteria of this genus, and as many as 25 to 70% of all insect species are estimated to be potential hosts.

<i>Trypanosoma</i> Genus of parasitic flagellate protist in the Kinetoplastea class

Trypanosoma is a genus of kinetoplastids, a monophyletic group of unicellular parasitic flagellate protozoa. Trypanosoma is part of the phylum Sarcomastigophora. 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.

<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.

<span class="mw-page-title-main">David Bruce (microbiologist)</span> Scottish pathologist (1855–1931)

Major-General Sir David Bruce was a Scottish pathologist and microbiologist who made some of the key contributions in tropical medicine. In 1887, he discovered a bacterium, now called Brucella, that caused what was known as Malta fever. In 1894, he discovered a protozoan parasite, named Trypanosoma brucei, as the causative pathogen of nagana.

Trypanosoma suis is a species of excavate trypanosome in the genus Trypanosoma that causes one form of the surra disease in animals. It infects pigs. It does not infect humans.

<span class="mw-page-title-main">Animal trypanosomiasis</span> Parasitic disease of vertebrates

Animal trypanosomiasis, also known as nagana and nagana pest, or sleeping sickness, is a disease of vertebrates. The disease is caused by trypanosomes of several species in the genus Trypanosoma such as T. brucei. T. vivax causes nagana mainly in West Africa, although it has spread to South America. The trypanosomes infect the blood of the vertebrate host, causing fever, weakness, and lethargy, which lead to weight loss and anemia; in some animals the disease is fatal unless treated. The trypanosomes are transmitted by tsetse flies.

Wigglesworthia glossinidia is a species of gram-negative bacteria which was isolated from the gut of the tsetse fly. W. glossinidia is a bacterial endosymbiont of the tsetse fly. Because of this relationship, Wigglesworthia has lost a large part of its genome and has one of the smallest known genomes of any living organism, consisting of a single chromosome of 700,000 bp and a plasmid of 5,200. Together with Buchnera aphidicola, Wigglesworthia has been the subject of genetic research into the minimal genome necessary for any living organism. Wigglesworthia also synthesizes key B-complex vitamins which the tsetse fly does not get from its diet of blood. Without the vitamins Wigglesworthia produces, the tsetse fly has greatly reduced growth and reproduction. Since the tsetse fly is the primary vector of Trypanosoma brucei, the pathogen that causes African trypanosomiasis, it has been suggested that W. glossinidia may one day be used to help control the spread of this disease.

Paratransgenesis is a technique that attempts to eliminate a pathogen from vector populations through transgenesis of a symbiont of the vector. The goal of this technique is to control vector-borne diseases. The first step is to identify proteins that prevent the vector species from transmitting the pathogen. The genes coding for these proteins are then introduced into the symbiont, so that they can be expressed in the vector. The final step in the strategy is to introduce these transgenic symbionts into vector populations in the wild. One use of this technique is to prevent mortality for humans from insect-borne diseases. Preventive methods and current controls against vector-borne diseases depend on insecticides, even though some mosquito breeds may be resistant to them. There are other ways to fully eliminate them. “Paratransgenesis focuses on utilizing genetically modified insect symbionts to express molecules within the vector that are deleterious to pathogens they transmit.” The acidic bacteria Asaia symbionts are beneficial in the normal development of mosquito larvae; however, it is unknown what Asais symbionts do to adult mosquitoes.

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Scolopendra morsitans, also known as the Tanzanian blue ringleg or red-headed centipede, is a species of centipede in the family Scolopendridae. S. morsitans is the type species for the genus Scolopendra.

Sodalis glossinidius is a species of bacteria, the type and only species of its genus. It is a microaerophilic secondary endosymbiont of the tsetse fly. Strain M1T is the type strain. Sodalis glossinidius is the only gammaproteobacterial insect symbiont to be cultured and thus amenable to genetic modification, suggesting that it could be used as part of a control strategy by vectoring antitrypanosome genes. The organism may increase the susceptibility of tsetse flies to trypanosomes.

Sodalis is a genus of bacteria within the family Pectobacteriaceae. This genus contains several insect endosymbionts and also a free-living group. It is studied due to its potential use in the biological control of the tsetse fly. Sodalis is an important model for evolutionary biologists because of its nascent endosymbiosis with insects.

Glossina fuscipes is a riverine fly species in the genus Glossina, which are commonly known as tsetse flies. Typically found in sub-Saharan Africa but with a small Arabian range, G. fuscipes is a regional vector of African trypanosomiasis, commonly known as sleeping sickness, that causes significant rates of morbidity and mortality among humans and livestock. Consequently, the species is among several being targeted by researchers for population control as a method for controlling the disease.

A trypanotolerant organism is one which is relatively less affected by trypanosome infestation.

Alan Christoffels is a bioinformatics scientist, academic, and an author. He is Professor of Bioinformatics, and the director of the South African National Bioinformatics Institute at the University of the Western Cape. He has been serving as a senior advisor to the Africa Centres for Disease Control and Prevention Pathogen genomics & Partnerships and DSI/NRF Research Chair in Bioinformatics and Public Health Genomics.

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Further reading