Tsetse fly

Tsetse without the "fly" has become more common in English, particularly in the scientific and development communities. The word is pronounced (tseh-tseh) in the Sotho languages and is easily rendered in other African languages. During World War II, a British de Havilland antisubmarine aircraft known as the Tsetse Mosquito helped establish the term in commonplace use among native English speakers. ==Biology==

The biology of tsetse flies is relatively well understood by entomologists. They have been extensively studied because of their medical, veterinary, and economic importance, because the flies can be raised in a laboratory, and because they are relatively large, facilitating their analysis. Morphology Tsetse flies can be seen as independent individuals in three forms: as third-instar larvae, pupae, and adults. Tsetse first become separate from their mothers during the third larval instar, during which they have the typical appearance of maggots. However, this life stage is short, lasting at most a few hours, and is almost never observed outside of the laboratory. Tsetse next develop a hard external case, the puparium, and become pupae – small, hard-shelled oblongs with two distinctively small, dark lobes at the tail (breathing) end. Tsetse pupae are under long. Within the puparial shell, tsetse complete the pupal stage. At the end of the pupal stage, tsetse emerges as adult flies. The adults are relatively large flies, with lengths of , Life cycle Tsetse flies have an unusual life cycle, which may be due to the richness of their blood food source. A female fertilizes only one egg at a time; she will retain each egg within her uterus, the offspring developing internally (during the first three larval stages), in an adaptation called adenotrophic viviparity. During this time, the female feeds the developing offspring with a milky substance (secreted by a modified gland) in the uterus. In the third larval stage, the tsetse larvae leave the uterus and begin an independent life. The newly-birthed larvae crawl into the ground and develop a hard outer shell (called the puparial case), within which they complete their morphological transformations into adult flies. The larval life stage has a variable duration, ranging from four to ten days, will require until it emerges as an adult. Technically, these insects undergo the standard development process of insects, beginning with oocyte formation, ovulation, fertilization, and development of the egg; following egg development and birth is the three larval stages, a pupal stage, and the emergence and maturation of the adult. Hosts Overall Suidae are the most important hosts. Waterbuck (Kobus ellipsiprymnus) are unmolested by Glossina because they produce volatiles which act as repellents. Waterbuck odor volatiles are under testing and development as repellents to protect livestock. By species, bloodmeals are derived from: Genetics The genome of Glossina morsitans was sequenced in 2014. Symbionts Tsetse flies have at least three bacterial symbionts. The primary symbiont is Wigglesworthia (Wigglesworthia glossinidia), which live within the fly's bacteriocytes. The second symbiont is Sodalis (Sodalis glossinidius) intercellularly or intracellularly, and the third is some kind of Wolbachia. Diseases The salivary gland hypertrophy virus causes abnormal bleeding in the lobes of the crop of G. m. centralis and G. m. morsitans. ==Systematics==

Tsetse flies are members of the order Diptera, the true flies. They belong to the superfamily Hippoboscoidea, in which the tsetse's family, the Glossinidae, is one of four families of blood-feeding obligate parasites. Up to 34 species and subspecies of tsetse flies are recognized, depending on the particular classification used. Current classifications place all species of tsetse fly in a single genus named Glossina, with most considering the genus as the sole member of the family Glossinidae. Species The tsetse genus is generally split into three groups of species based on a combination of distributional, ecological, behavioral, molecular and morphological characteristics. The genus includes; savannah flies, forest flies and riverine and lacustrine flies. Savannah flies The "savannah" flies: (Morsitans group, subgenus Glossina s.s.): • Glossina austeni (Newstead, 1912) patr. of Austen • Glossina longipalpis (Wiedemann, 1830) • Glossina morsitans (Westwood, 1851) • Glossina morsitans morsitans (Westwood, 1850) • Glossina morsitans submorsitans Forest flies The "forest" flies: (Fusca group, subgenus Austenina): (Newstead and Evans, 1921) [what is this - G.fusca austenia?] --> • Glossina brevipalpis (Newstead, 1910) • Glossina fusca (Walker, 1849) • Glossina fusca fusca (Walker, 1849) • Glossina fusca congolensis (Newstead and Evans, 1921) • Glossina fuscipleuris (Austen, 1911) • Glossina frezili (Gouteux, 1987) • Glossina haningtoni (Newstead and Evans, 1922) • Glossina longipennis (Corti, 1895) • Glossina medicorum (Austen, 1911) • Glossina nashi (Potts, 1955) • Glossina nigrofusca (Newstead, 1911) • Glossina nigrofusca nigrofusca (Newstead, 1911) • Glossina nigrofusca hopkinsi (van Emden, 1944) • Glossina schwetzi (Newstead and Evans, 1921) • Glossina severini (Newstead, 1913) • Glossina tabaniformis (Westwood, 1850) • Glossina vanhoofi (Henrard, 1952) Riverine and lacustrine flies The "riverine" and "lacustrine" flies: (Palpalis group, subgenus Nemorhina): • Glossina caliginea (Austen, 1911) • Glossina fuscipes (Newstead, 1911) • Glossina fuscipes fuscipes (Newstead, 1911) ==Range==

Glossina is almost entirely restricted to wooded grasslands and forested areas of the Afrotropics. As of 1990, tsetse flies were reported from a maximum latitude of approximately 15° north in Senegal (Niayes Region), to a minimum of 28.5° south in South Africa (KwaZulu-Natal Province). ==Trypanosomiasis==

in a blood smear Tsetse are biological vectors of trypanosomes, meaning that in the process of feeding, they acquire and then transmit small, single-celled trypanosomes from infected vertebrate hosts to uninfected animals. Some tsetse-transmitted trypanosome species cause trypanosomiasis, an infectious disease. In humans, tsetse transmitted trypanosomiasis is called sleeping sickness. In animals, tsetse-vectored trypanosomiases include nagana, souma (a French term which may not be a distinct condition), and surra according to the animal infected and the trypanosome species involved. The usage is not strict and while nagana generally refers to the disease in cattle and horses it is commonly used for any of the animal trypanosomiases. Trypanosomes are animal parasites, specifically protozoans of the genus Trypanosoma. These organisms are about the size of red blood cells. Different species of trypanosomes infect different hosts. They range widely in their effects on the vertebrate hosts. Some species, such as T. theileri, do not seem to cause any health problems except perhaps in animals that are already sick. Some strains are much more virulent. Infected flies have an altered salivary composition which lowers feeding efficiency and consequently increases the feeding time, promoting trypanosome transmission to the vertebrate host. These trypanosomes are highly evolved and have developed a life cycle that requires periods in both the vertebrate and tsetse hosts. Tsetse transmit trypanosomes in two ways, mechanical and biological transmission. • Mechanical transmission involves the direct transmission of the same individual trypanosomes taken from an infected host into an uninfected host. The name "mechanical" reflects the similarity of this mode of transmission to mechanical injection with a syringe. Mechanical transmission requires the tsetse to feed on an infected host and acquire trypanosomes in the blood meal, and then, within a relatively short period, to feed on an uninfected host and regurgitate some of the infected blood from the first blood meal into the tissue of the uninfected animal. This type of transmission occurs most frequently when tsetse are interrupted during a blood meal and attempt to satiate themselves with another meal. Other flies, such as horse-flies, can also cause mechanical transmission of trypanosomes. • Biological transmission requires a period of incubation of the trypanosomes within the tsetse host. The term 'biological' is used because trypanosomes must reproduce through several generations inside the tsetse host during the period of incubation (development within the fly is known as the extrinsic incubation period), which requires extreme adaptation of the trypanosomes to their tsetse host. In this mode of transmission, trypanosomes reproduce through several generations, changing in morphology at certain periods. This mode of transmission also includes the sexual phase of the trypanosomes. Tsetse are believed to be more likely to become infected by trypanosomes during their first few blood meals. Tsetse infected by trypanosomes are thought to remain infected for the remainder of their lives. Because of the adaptations required for biological transmission, trypanosomes that can be transmitted biologically by tsetse cannot be transmitted in this manner by other insects. The relative importance of these two modes of transmission for the propagation of tsetse-vectored trypanosomiases is not yet well understood. However, since the sexual phase of the trypanosome life cycle occurs within the tsetse host, biological transmission is a required step in the life cycle of the tsetse-vectored trypanosomes. The cycle of biological transmission of trypanosomiasis involves two phases, one inside the tsetse host and the other inside the vertebrate host. Trypanosomes are not passed between a pregnant tsetse and her offspring, so all newly emerged tsetse adults are free of infection. An uninfected fly that feeds on an infected vertebrate animal may acquire trypanosomes in its proboscis or gut. These trypanosomes, depending on the species, may remain in place, move to a different part of the digestive tract, or migrate through the tsetse body into the salivary glands. When an infected tsetse bites a susceptible host, the fly may regurgitate part of a previous blood meal that contains trypanosomes, or may inject trypanosomes in its saliva. Inoculation must contain a minimum of 300 to 450 individual trypanosomes to be successful, and may contain up to 40,000 cells. The trypanosomes are injected into vertebrate muscle tissue, but make their way, first into the lymphatic system, then into the bloodstream, and eventually into the brain. The disease causes the swelling of the lymph glands, emaciation of the body, and eventually leads to death. Uninfected tsetse may bite the infected animal prior to its death and acquire the disease, thereby closing the transmission cycle. Disease hosts and vectors The tsetse-vectored trypanosomiases affect various vertebrate species including humans, antelopes, bovine cattle, camels, horses, sheep, goats, and pigs. These diseases are caused by several different trypanosome species that may also survive in wild animals such as crocodiles and monitor lizards. The diseases have different distributions across the African continent, so are transmitted by different species. This table summarizes this information: In humans Human African trypanosomiasis, also called sleeping sickness, is caused by trypanosomes of the species Trypanosoma brucei. This disease is invariably fatal if left untreated, but can almost always be cured with current medicines if the disease is diagnosed early enough. Sleeping sickness begins with a tsetse bite leading to an inoculation in the subcutaneous tissue. The infection moves into the lymphatic system, leading to a characteristic swelling of the lymph glands called ''Winterbottom's sign''. The infection progresses into the blood stream and eventually crosses into the central nervous system and invades the brain leading to extreme lethargy and eventually to death. The species Trypanosoma brucei, which causes the disease, has often been subdivided into three subspecies that were identified based either on the vertebrate hosts which the strain could infect or on the virulence of the disease in humans. The trypanosomes infectious to animals and not to humans were named Trypanosoma brucei brucei. Strains that infected humans were divided into two subspecies based on their different virulences: Trypanosoma brucei gambiense was thought to have a slower onset and Trypanosoma brucei rhodesiense refers to strains with a more rapid, virulent onset. This characterization has always been problematic but was the best that could be done given the knowledge of the time and the tools available for identification. A recent molecular study using restriction fragment length polymorphism analysis suggests that the three subspecies are polyphyletic, so the elucidation of the strains of T. brucei infective to humans requires a more complex explanation. Procyclins are proteins developed in the surface coating of trypanosomes whilst in their tsetse fly vector. Other forms of human trypanosomiasis also exist but are not transmitted by tsetse. The most notable is American trypanosomiasis, known as Chagas disease, which occurs in South America, caused by Trypanosoma cruzi, and transmitted by certain insects of the Reduviidae, members of the Hemiptera. In domestic animals Animal trypanosomiasis, also called nagana when it occurs in bovine cattle or horses or sura when it occurs in domestic pigs, is caused by several trypanosome species. These diseases reduce the growth rate, milk productivity, and strength of farm animals, generally leading to the eventual death of the infected animals. Certain species of cattle are called trypanotolerant because they can survive and grow even when infected with trypanosomes although they also have lower productivity rates when infected. The course of the disease in animals is similar to the course of sleeping sickness in humans. Trypanosoma congolense and Trypanosoma vivax are the two most important species infecting bovine cattle in sub-Saharan Africa. Trypanosoma simiae causes a virulent disease in swine. Other forms of animal trypanosomiasis are also known from other areas of the globe, caused by different species of trypanosomes and transmitted without the intervention of the tsetse fly. The tsetse fly vector ranges mostly in the central part of Africa. Trypanosomiasis poses a considerable constraint on livestock agricultural development in tsetse fly-infested areas of sub-Saharan Africa, especially in West and Central Africa. International research conducted by ILRI in Nigeria, the Democratic Republic of the Congo and Kenya has shown that the N'Dama is the most resistant breed. ==Control==

The eradication of sleeping sickness and nagana would be of immense benefit to rural development and contribute to poverty alleviation and improved food security in sub-Saharan Africa, although, with the current tools, the complete eradication of the disease is not considered feasible. Human African trypanosomosis (HAT) and animal African trypanosomosis (AAT) are sufficiently important to make virtually any intervention against these diseases beneficial. The disease can be managed by controlling the vector and thus reducing the incidence of the disease by disrupting the transmission cycle. Another tactic to manage the disease is to target the disease directly using surveillance and curative or prophylactic treatments to reduce the number of hosts that carry the disease. Economic analysis indicates that the cost of managing trypanosomiasis through the elimination of important populations of major tsetse vectors will be covered several times by the benefits of tsetse-free status. Land clearing Another early technique involved complete removal of brush and woody vegetation from an area. Preventing regrowth of woody vegetation requires continuous clearing efforts which is even more expensive, The use of chemicals as attractants to lure tsetse to the traps has been studied extensively in the late 20th century, but this has mostly been of interest to scientists rather than as an economically reasonable solution. Attractants studied have been those tsetse might use to find food, like carbon dioxide, octenol, and acetone—which are given off in animals' breath and distributed downwind in an odor plume. Synthetic versions of these chemicals can create artificial odor plumes. A cheaper approach is to place cattle urine in a half gourd near the trap. For large trapping efforts, additional traps are generally cheaper than expensive artificial attractants. A special trapping method is applied in Ethiopia, where the BioFarm Consortium (ICIPE, BioVision Foundation, BEA, Helvetas, DLCO-EA, Praxis Ethiopia) applies the traps in a sustainable agriculture and rural development context (SARD). The traps are just the entry point, followed by improved farming, human health and marketing inputs. This method is in the final stage of testing (as of 2006). Sterile insect technique The sterile insect technique (SIT) is a form of pest control that uses ionizing radiation (gamma ray or X-ray) to sterilize male flies that are mass-produced in special rearing facilities. The sterile males are released systematically from the ground or by air in tsetse-infested areas, where they mate with wild females, which do not produce offspring. As a result, this technique can eventually eradicate populations of wild flies. SIT is among the most environmentally friendly control tactics available, and is usually applied as the final component of an integrated campaign. It has been used to subdue the populations of many other fly species including the medfly, Ceratitis capitata. The sustainable removal of the tsetse fly is in many cases the most cost-effective way of dealing with the T&T problem resulting in major economic benefits for subsistence farmers in rural areas. Insecticide-based methods are normally very ineffective in removing the last remnants of tsetse populations, while, on the contrary, sterile males are very effective in finding and mating the last remaining females. Therefore, the integration of the SIT as the last component of an area-wide integrated approach is essential in many situations to achieve complete eradication of the different tsetse populations, particularly in areas of more dense vegetation. A project that was implemented from 1994 to 1997 on the Island of Unguja, Zanzibar (United Republic of Tanzania), demonstrated that, after suppression of the tsetse population with insecticides, SIT completely removed the Glossina austeni Newstead population from the Island. This was carried out without any understanding of the population genetics of G. a., but future SIT efforts can benefit from such preparation. Population genetics would help to select the Glossina population to be deployed for similarity to the target population. The eradication of the tsetse fly from Unguja Island in 1997 was followed by the disappearance of the AAT which enabled farmers to integrate livestock keeping with cropping in areas where this had been impossible before. The increased livestock and crop productivity and the possibility of using animals for transport and traction significantly contributed to an increase in the quality of people's lives. Surveys in 1999, 2002, 2014, and 2015 have confirmed this success - continued absence of tsetse and nagana on the island. In the Niayes region of Senegal, a coastal area close to Dakar, livestock keeping was difficult due to the presence of a population of Glossina palpalis gambiensis. Feasibility studies indicated that the fly population was confined to very fragmented habitats and a population genetics study indicated that the population was genetically isolated from the main tsetse belt in the south eastern part of Senegal. After completion of the feasibility studies (2006–2010), an area-wide integrated eradication campaign that included an SIT component was started in 2011, and by 2015, the Niayes region had become almost tsetse fly free. This has allowed a change of cattle breeds from lower producing trypanotolerant breeds to higher-producing foreign breeds. The entire target area (Block 1, 2 and 3) has a total surface of , and the first block (northern part) can be considered free of tsetse, as intensive monitoring has failed to detect since 2012 a single wild tsetse fly. The prevalence of AAT has decreased from 40 to 50% before the project started to less than 10% to date in blocks 1 and 2. Although insecticides are being used for fly suppression, they are applied for short periods on traps, nets and livestock, and are not spread into the environment. After the suppression activities are completed, no more insecticide is applied in the area. The removal of trypanosomosis will eliminate the need for constant prophylactic treatments of the cattle with trypanocidal drugs, therefore reducing residues of these drugs in the dung, meat and milk. The main beneficiaries of the project are the many small holder farmers, the larger commercial farms and the consumers of meat and milk. According to a socio-economic survey and benefit cost analysis, after eradication of the tsetse farmers will be able to replace their local breeds with improved breeds and increase their annual income by €2.8 million. In addition, it is expected that the number of cattle will be reduced by 45%, which will result in reduced environmental impacts. ==Societal impact==

In the literature of environmental determinism, the tsetse has been linked to difficulties during early state formation for areas where the fly is prevalent. A 2012 study used population growth models, physiological data, and ethnographic data to examine pre-colonial agricultural practices and isolate the effects of the fly. A "tsetse suitability index" was developed from insect population growth, climate and geospatial data to simulate the fly's population steady state. An increase in the tsetse suitability index was associated with a statistically significant weakening of the agriculture, levels of urbanization, institutions and subsistence strategies. Results suggest that the tsetse decimated livestock populations, forcing early states to rely on slave labor to clear land for farming, and preventing farmers from taking advantage of natural animal fertilizers to increase crop production. These long-term effects may have kept population density low and discouraged cooperation between small-scale communities, thus preventing stronger nations from forming. The authors also suggest that under a lower burden of tsetse, Africa would have developed differently. Agriculture (measured by the usage of large domesticated animals, intensive agriculture, plow use and female participation rate in agriculture) as well as institutions (measured by the appearance of indigenous slavery and levels of centralization) would have been more like those found in Eurasia. Qualitative support for this claim comes from archaeological findings; e.g., Great Zimbabwe is located in the African highlands where the fly does not occur, and represented the largest and technically most advanced precolonial structure in Southern sub-Sahara Africa. Other authors are more skeptical that the tsetse fly had such an immense influence on African development. One conventional argument is that the tsetse fly made it difficult to use draught animals. Hence, wheeled forms of transportations were not used as well. While this is certainly true for areas with high densities of the fly, similar cases outside tsetse-suitable areas exist. While the fly definitely had a relevant influence on the adoption of new technologies in Africa, it has been contended that it does not represent the single root cause. History According to an article in the New Scientist, the depopulated and apparently primevally wild Africa seen in wildlife documentary films was formed in the 19th century by disease, a combination of rinderpest and the tsetse fly. Rinderpest is believed to have originated in Asia, later spreading through the transport of cattle. In 1887, the rinderpest virus was accidentally imported in livestock brought by an Italian expeditionary force to Eritrea. It spread rapidly, reaching Ethiopia by 1888, the Atlantic coast by 1892 and South Africa by 1897. Rinderpest, a cattle plague from central Asia, killed over 90% of the cattle of the pastoral peoples such as the Masai of east Africa. In South Africa, with no native immunity, most of the livestock – some 5.5 million domestic cattle – died. Pastoralists and farmers were left with no animals – their source of income – and farmers were deprived of their working animals for ploughing and irrigation. The pandemic coincided with a period of drought, causing widespread famine. The starving human populations died of smallpox, cholera, and typhoid, as well as African Sleeping Sickness and other endemic diseases. It is estimated that two-thirds of the Masai died in 1891. The land was left emptied of its cattle and its people, enabling the colonial powers Germany and Britain to take over Tanzania and Kenya with little effort. With greatly reduced grazing, grassland turned rapidly to bush. The closely cropped grass sward was replaced in a few years by woody grassland and thornbush, ideal habitat for tsetse flies. Wild mammal populations increased rapidly, accompanied by the tsetse fly. Highland regions of east Africa which had been free of tsetse fly were colonised by the pest, accompanied by sleeping sickness, until then unknown in the area. Millions of people died of the disease in the early 20th century. Current situation Tsetse flies are regarded as a major cause of rural poverty in sub-Saharan Africa-US$4.75b. million people in 20 countries are at different levels of risk and only 3-4 million people are covered by active surveillance. ==History of study==

In East Africa, C. F. M. Swynnerton played a large role in the first half of the 20th century. Swynnerton did much of the earliest tsetse ecology research. For this E. E. Austen named a patronymic taxon for him, G. swynnertoni, in 1922. ==Resistance to trypanosomes==

Tsetse flies have an arsenal of immune defenses to resist each stage of the trypanosome infectious cycle, and thus are relatively refractory to trypanosome infection. Among the host flies' defenses is the production of hydrogen peroxide, a reactive oxygen species that damages DNA. These defenses limit the population of infected flies. ==See also==