Open access peer-reviewed chapter

Prevalence of Trypanosomosis in Ruminants in Rivers State and Abia State, Nigeria and the Challenges of Trypanosomosis Control in Goat Production

Written By

Clara A.N. Akpan

Submitted: 02 December 2022 Reviewed: 31 December 2022 Published: 10 February 2023

DOI: 10.5772/intechopen.1001071

From the Edited Volume

Goat Science - From Keeping to Precision Production

Sándor Kukovics

Chapter metrics overview

80 Chapter Downloads

View Full Metrics

Abstract

Trypanosomosis is one of the major diseases hindering livestock production in tropical Africa. The disease negatively impacts food production and economic growth in sub-Saharan Africa. African animal trypanosomosis is a debilitating and often fatal disease of animals, caused by infection with pathogenic protozoan parasites of the genus ‘Trypanosoma’. A recent prevalence study for the infection in ruminants reared in two Southern states of Nigeria (Rivers and Abia) gave zero by the wet mount and buffy coat methods which only suggests low prevalence and may not mean that the infection has been eliminated in the country. More sensitive methods may detect low prevalence. It also suggests that common breeds of ruminants in the area may be genetically resistant to the infection or that they have acquired resistance. Relapse to susceptibility is still possible. So, prophylactic medications and other methods of control for the infection are still necessary for the area.

Keywords

  • prevalence
  • trypanosomosis
  • Nigeria
  • challenges
  • control

1. Introduction

Livestock diseases reduce agricultural output by about 30% in developing countries including Nigeria [1]. These diseases are endemic including fly-borne diseases like trypanosomosis, tick-borne diseases like babesiosis as well as helminthosis; all of which increase morbidity and mortality, reducing production and subsequently leading to hunger and poverty. Trypanosomosis is a debilitating and often fatal disease of man and animals, caused by infection with the pathogenic protozoan parasites of the genus Trypanosoma [2, 3, 4, 5]. It is an economically significant disease affecting livestock production in Nigeria and causing significant losses ranging from a decrease in production to death [6, 7]. The disease is characterized by anemia, parasitemia, fever, loss of condition, reduced productivity and frequently high mortality which among other factors limit the pace of development in tropical Africa. Trypanosomes are extracellular parasites that cause persistent infection of the blood (and/or body fluids) and induce immunosuppression [8]. Trypanosomes are widely distributed due to the abundant presence of its biological vector (tsetse, Glossina spp) [9] which covers about 80% of Nigeria's land mass; and mechanical transmission vectors, which are biting flies, like Tabanids (horse flies), Stomoxys (stable flies) and vampire bats [10]. The severity of disease caused by trypanosomes depends on the species and strain of the infecting trypanosomes [11], with T. congolense having a more severe impact than the other species, on ruminants’ health and production [12]. Infections with Trypanosoma brucei, Trypanosoma congolense, Typanosoma vivax and Trypanosoma evansi have been reported in goats [13, 14]. Concurrent infections can occur with more than one species of trypanosome [15].

Control of African Animal Trypanosomosis (AAT) includes the use of trypanotolerant breeds of livestock [16, 17], vector control [18], chemotherapeutic and chemoprophylactic agents [19] or a combination of the methods according to specific conditions of an area [20]. However, control of animal trypanosomoses relies primarily on the use of insecticides or traps to control the vector (especially in the case of tsetse-transmitted trypanosomes) and on the use of trypanocides to control the parasite [21]. The use of trypanocidal drugs for trypanosomes parasite control represents the main intervention tool in most poor rural endemic areas since vector control can be expensive when used on a large scale and is not always sustainable or effective [22, 23].

Drug resistance, relapse of infections and toxicity of trypanocidal drugs are major challenges encountered in parasite control (treatment) of trypanosomosis.

Most of trypanocides are expensive and/or toxic [24] and have the tendency to elicit drug resistance [25, 26]. Some of the trypanocidal drug-induced side effects can be serious and even life-threatening [27]. Relapse of infection, sometimes observed after treatment of trypanosomosis, has been attributed to the resurgence of parasites into blood and body fluids after the invasion of the brain tissue by the tissue-invasive Trypanosoma vivax and Trypanosoma brucei group parasites [28, 29, 30] which are inaccessible to trypanocidal drugs due to presence of a blood-brain barrier. Reports have shown that some strains of Trypanosoma brucei group of trypanosomes invade body tissues as early as four hours to four days post-infection [31, 32]. Apart from causing disease, trypanosomes are also responsible for producing a state of severe immunosuppression, which renders the infected host more susceptible to secondary infections and produces a poor immune response to bacterial and viral vaccines [8]. This is due to the reduction of their ability to mount protective immune responses against invading parasites [33]. Immunosuppression is a major obstacle to sustainable livestock production [34] and food security. The significance of immunosuppression is appreciated more in endemic areas where herd immunity against serious epizootic diseases depends on massive vaccination campaigns [35].

There is limited information on the prevalence of trypanosomosis in the southern part of Nigeria. A prevalence rate of 17.10% of ruminant trypanosomosis was recorded in a survey of livestock diseases from September 2002 to August 2003 in Enugu State, South-East Nigeria [36]. In a part of Abia State, a low prevalence rate of 1.9% was recorded in ruminants with goats having a prevalence rate of 1.2% for trypanosomosis [37]. The low prevalence rate of trypanosomosis in small ruminants compared to cattle, in Nigeria, has been attributed to trypanotolerant breeds being the majority among small ruminants [7, 38, 39]. The prevalence of trypanosomes in animals could be affected by several factors such as availability of reservoir hosts, seasonal factors, altitude, fly density and behavior, sensitivity of diagnostic techniques, stage of infection, method of sampling, conflict and other human activities [40, 41, 42].

A zero prevalence of trypanosomosis in goats was recorded recently in both Rivers and Abia States, Nigeria [43], agreeing with reports that goats are resistant to trypanosomosis [44]; however, several other studies on the prevalence of trypanosomosis in goats revealed that goats acquire natural infection resulting in economic losses [45, 46, 47]. These losses include a reduction in milk production, weight gain, reproduction and eventually death of the affected animals [48]. Goats that survive the infection become reservoirs of the parasite and endanger humans and other domestic animals [6].

The disease leads to a reduction of animal protein [49] thereby promoting food insecurity [50] and contributing greatly to underdevelopment through poverty and hunger [5, 51].

Goat production is a great source of income for commercial farmers. Goats also serve to improve the economy of peasant farmers who may not be able to keep large ruminants like cattle. They provide meat, milk, skin and manure. In Nigeria, goats can be used for important religious and social activities besides serving as cash reserves and a form of savings for rural populations or households. They serve as a source of income in times of stress, during drought and agricultural crop failure [52, 53, 54].

There is a paucity of information on the prevalence of trypanosomosis in the southern part of Nigeria, as the majority of studies on trypanosome prevalence were conducted in the northern and central parts of Nigeria. Hence, this study on the prevalence of trypanosomosis in Rivers and Abia States Nigeria, which are both in the southern part of the country, was aimed at investigating the current prevalence of trypanosomosis in cattle, sheep and goat in Rivers (South-South) and Abia (South-East) states, Nigeria.

Advertisement

2. Materials and methods

2.1 Study area

This study was conducted between July and October 2018 in Ahoada West LGA, Ahoada East LGA and Ikwere LGA of Rivers State as well as Umunneochi LGA and Ikwuano LGA of Abia State. Animals sampled belonged to individuals.

Geographically, Abia State occupies about 6320 square kilometers of land area, with a population of about 4,112,230 and a population density of 650/km2. It lies between latitude 5.251°N–5.417°N and longitude 7.30°E–7.500°E, altitude of 244–305 m above sea level. It is a low-lying tropical rainforest. The southern portion gets heavy rainfall of about 2400 mm per year which is especially, intense between the months of April through October [55].

Rivers state occupies a total land area of 11,077 square kilometers with a population of about 5,198,716 and a population density of 635.89 per square kilometer. It lies between latitude 4°451N–4.750°N and longitude 6°501E–6.833°E. Its annual mean temperature ranges from 25°C to 28°C. Total annual rainfall decreases from about 4700 mm on the coast to about 1700 mm in the extreme north.

2.2 Sample size

The sample size was determined using the formula outlined by [56] and expected/anticipated prevalence of 3.7% for cattle; 1.1% for sheep and 1.2% for goat [17].

N=(Z2pq)/L2E1

Where:

p = anticipated/expected prevalence from similar study = [3.7% for cattle; 1.1% for sheep and 1.2% for goat, Z = 1.96; q = 1-p; N = sample size; L = allowable error (5%).

Fifty (50) cattle, twenty-five (25) sheep and twenty-five (25) goats were sampled in each of Rivers and Abia states, giving a total of 100 adult cattle (N’dama, Muturu, white Fulani and Red Bororo breeds), 50 adult sheep (WAD and Yankasa) and 50 adult goats (WAD and Sokoto red) of both sexes.

2.3 Study animals

The study was carried out on 100 cattle of breeds: 29 N’dama, 42 Muturu, 17 White Fulani and 12 Red Bororo; 50 sheep of breeds: 32 West African Dwarf (WAD) and 18 Yankasa; and 50 goats of breeds: 36 West African Dwarf (WAD) and 14 Sokoto Red selected by random sampling methods. Three herds of cattle, sheep and goats were sampled in three different locations in each of the states. The age of the animals was estimated, when not known by their owner, on the basis of the dentition, in which animals under 1 year were considered as young animals. Adult animals (above 1 year for sheep and goat; above 2 years for cattle), were sampled.

2.4 Sample collection

Blood samples were collected from the jugular vein of each sampled animal. Two (2) ml of blood was collected from each animal and put into a container with EDTA. The containers were gently rocked to homogeneously mix the blood with the anticoagulant (EDTA) in order to prevent clotting. The blood samples were either examined immediately or kept cool in a flask containing ice packs until examined microscopically within 4 hours, by wet mount and buffy coat methods.

2.5 Parasitological examination

The parasitological examination was done in the laboratory using the wet blood film [57] and microhematocrit buffy-coat methods [57].

2.5.1 Wet blood film examination

A blood film was made by placing a drop of blood on a clean glass slide which was then covered carefully with a clean cover slip so that the blood spreads evenly. The slide was placed on a microscope and the film was viewed systematically for movement of trypanosomes with x40 objective lens [58].

2.5.2 Micro-haematocrit buffy coat microscopy

A capillary tube was nearly filled (about ¾) with a blood sample and centrifuged at 2000 g for 5 min. The capillary tube was cut about 1 mm below (to include the uppermost layer of RBC) and 3 mm above (to include some plasma) the buffy coat layer. The content was gently expressed onto a slide using a micro-hematocrit capillary tube holder, mixed and covered with a cover slip. The preparation was then examined under a microscope with the ×40 objective lens [57].

Advertisement

3. Result

Out of the total of 100 cattle, 50 sheep and 50 goats sampled in the two states (Abia and Rivers), no positive sample was gotten. The species, number, sex and breed of animals sampled in the survey are shown in Table 1.

Animal speciesCattleSheepGoat
BreedN’damaMuturuWhite FulaniRed BororoWADYankasaWADSokoto Red
SexMFMFMFMFMFMFMFMF
Number22730121161022012117201686
Total No2942171232183614

Table 1.

Number, sex and breed of ruminants sampled for trypanosomes in Rivers and Abia states of Nigeria.

Advertisement

4. Discussion

The result of the survey seems to indicate the absence of trypanosome infection or zero prevalence of trypanosome infection in the studied areas. This is in agreement with the report of [59] in which N’dama and Muturu breeds among other breeds of cattle investigated in Keffi, Nassarawa State, were not infested with trypanosomes.

The result is also, in line with the report of [60] in which none of the Tsetse dissected in his work in Bassa, Plateau State was positive for trypanosomes thus suggesting a low prevalence of trypanosomes in ruminants in that area. A low prevalence rate of 1.9% in ruminants with goats having a prevalence rate of 1.2% in some parts of Abia State, has been reported [17].

There is a dearth of information on ruminant trypanosomosis in the areas studied (South-East and South-South, Nigeria), hence a lack of data for comparison.

The absence of infection or zero prevalence as observed in the study suggests a very low infection rate attributable to a decrease in the population of tsetse and other biting flies as a result of environmental, weather and anthropological changes. Since the survey was conducted on animals owned by individuals, it is also possible that farmers inject their animals with trypanocidal drugs and also use insecticide sprays to minimize the population of biting flies. The rise in human population and consequent increase in human activities causing significant changes in the availability of suitable habitats and hosts that potentially ensure tsetse survival and sustenance in a given location may also have occurred [61]. In addition, the expansion of veterinary services up to peasant associations and deforestation for crop cultivation and settlement might be a reason.

The zero prevalence observed in the area could also be due to the inadequacy of the parasite detection methods employed. The micro-hematocrit-buffy coat method used for diagnosis is still regarded as a good parasitological technique for quick detection of the parasite, allowing for quick and clear visualization [62], though it has been reported to be relatively insensitive as it fails to detect 66% of infected animals compared to molecular diagnostic techniques and serological diagnostic methods [63]. More so, trypanosome organisms are most likely to be found in the blood during the initial or early stages of the infection. They are less likely to be detected in chronically ill animals and may never be detected in healthy carriers [64].

Low prevalence or absence of infection may also relate to the reported resistance of indigenous ruminants to trypanosomes infections [65, 66, 67]. There are reports of trypanotolerance involving N’dama and Muturu breeds of cattle [68, 69], which form the majority of the sampled animals. The zero trypanosomes in Red Bororo observed in this study also agree with the report of [60] in Bassa LGA of Plateau State. This trypanotolerance could be largely due to innate resistance and natural genetic manipulation over time, to adapt to tsetse bites and partly due to their coat color that may serve as camouflage. Some trypanotolerant breeds tend to self-cure and eliminate the organism. Others may remain persistently infected but maintain productivity and show few or no signs of illness [64]. It might also be due to their hairy tail-end, used in warding off tsetse. More so, animals in the southern part of Nigeria are more or less intensively managed; extensive management of livestock has been reported to be a risk factor for trypanosomoses with higher prevalence rates compared with intensively managed animals [70].

Implications of the discovery include that Abia and Rivers States are good for sustainable livestock (ruminant) production since trypanosomosis identified as a serious constraint to livestock production and economic development in Nigeria appears to have become insignificant in the area. This, however, does not mean the infection has been eliminated. If more sensitive methods are used for purely epidemiologic studies low prevalence may be recorded. So, there is still a need to search for better and cheaper methods for prophylaxis and treatment of the disease.

Advertisement

5. Conclusions

Goat trypanosomosis, though of low prevalence in the southern part of Nigeria, could be of serious economic impact and public health importance, if neglected and uncontrolled.

Advertisement

Acknowledgments

I wish to acknowledge the efforts of the Late Prof. M.I. Ezeja, who also supervised this study but has been taken by the cold hands of death.

Advertisement

Conflict of interest

The author declares no conflicts of interest.

References

  1. 1. FAO. Cost-benefit Analysis for Animal Health Programmes in Developing Countries. Rome: FAO; 1990. p. 56
  2. 2. Barret MP, Burchmore RJS, Stich A, Lazzari JO, Frasch AC, Cazzilo JJ. The trypanosomiases. Lancet. 2003;362:1469-1480
  3. 3. Onditi S J, Silayo R S, Kimera S I, Kimbita E N and Mbilu T J N K. Preliminary studies on prevalence and importance of goat trypanosomosis in selected farms in Morogoro District, Tanzania. Livestock Research for Rural Development. 2007;19:65. Available from: http://www.lrrd.org/lrrd19/5/ondi19065.htm. [Accessed: October 5, 2022]
  4. 4. Rashid A, Rasheed K, Hussain A. Trypanosomiasis in dogs: A case report. Iranian Journal of Arthropod-Borne Diseases. 2008;2(2):48-51
  5. 5. Oyewusi JA, Saba AB, Oridupa OA. The course of trypanosomiasis in laboratory rabbits following experimental infection, treatment and re-infection: Haematological study. European Journal of Scientific Research. 2010;42:411-419
  6. 6. Swallow BM. Impact of Trypanosomosis on African Agriculture. Programme against African Trypanosomiasis Technical and scientific Series. Vol. 2. Rome: FAO; 2000
  7. 7. Odeniran and Ademola. A meta-analysis of the prevalence of African animal trypanosomiasis in Nigeria from 1960 to 2017. Parasites & Vectors. 2018;11:280. DOI: 10.1186/s13071-018-2801-0\
  8. 8. Tabel H, Wey G, Shi M. T-cells and immunopathogenesis of experimental African trypanosomiasis. Immunology Reviews. 2008;225:128-139
  9. 9. Kebede N, Animur A. trypanosomiais of cattle in selected districts of Awi zone, Northwestern Ethiopia. Tropical Animal Health and Production. 2009;41:1353-1356
  10. 10. Diall O, Cecchi G, Wanda G, Argilés-Herrero R, Vreysen MJB, Cattoli G, et al. Developing a progressive control pathway for African Animal Trypanosomosis. Trends in Parasitology. 2017;33(7):499-509. DOI: 10.1016/j.pt.2017.02.005
  11. 11. Taylor K, Authie E. Pathogenesis of animal trypanosomosis. In: Maudlin I, Holmes PH, Mills MA, editors. The Trypanosomiasis. UK: CAB International; 2004. pp. 331-353
  12. 12. Anene BM, Ogbuanya CE, Mbah ES, Ezeokonkwo RC. Preliminary efficacy trial of Cymelersan in dogs and mice artificially infected with Trypanosoma brucei isolated from dogs in Nigeria. Revue d’elevage et de Medicine Veterinaire des pays tropicaux. 1999;52:123-128
  13. 13. Gutierrez C, Corbera JA, Morales M, Büscher P. Trypanosomosis in goats: Current status. Annals of the New York Academy of Sciences. 2006;1081:300-310. DOI: 10.1196/annals.1373.040
  14. 14. Maser P, Luscher A, Kaminisky R. Drug transport and drug resistance in African Trypanosomes. Drug Resistance Updates. 2003;6(5):281-290
  15. 15. Institute for International Cooperation in Animal Biologics (IICAB). 2009. Available from: http://www.cfsph.iastate.edu/Factsheets/pdfs/trypanosomiasis_african.pdf. [Accessed: March 3, 2016]
  16. 16. Berthier D, Brenière SF, Bras-Gonçalves R, Lemesre JL, Jamonneau V, Solano P, et al. Tolerance to trypanosomatids: A threat, or a key for disease elimination? Trends in Parasitology. 2016;32(2):157-168. DOI: 10.1016/j.pt.2015.11.001
  17. 17. Yaro M, Munyard KA, Stear MJ, Groth DM. Combatting African animal trypanosomiasis (AAT) in livestock: The potential role of trypanotolerance. Veterinary Parasitology. 2016;225:43-52
  18. 18. Lehane M, Alfaroukh I, Bucheton B, Camara M, Harris A, Kaba D. Tsetse control and the elimination of Gambian sleeping sickness. PLoS Neglected Tropical Diseases. 2016;10(4):e0004437. DOI: 10.1371/journal.pntd.0004437
  19. 19. Field MC, Horn D, Fairlamb AH, Ferguson MAJ, Gray DW, Read KD. Anti trypanosomatid drug discovery: An ongoing challenge and a continuing need. Nature Reviews. Microbiology. 2017;15:217-231. DOI: 10.1038/nrmicro.2016.193
  20. 20. Gutiérrez C, González-Martín M, Corbera JA, Tejedor-Junco MT. Chemotherapeutic agents against pathogenic animal Trypanosomes. In: Méndez-Vilas A, editor. Microbial Pathogens and Strategies for Combating Them: Science, Technology and Education. Spain: Formatex Research Center; 2013. pp. 1564-1573
  21. 21. Holmes P. Tsetse-transmitted trypanosomes – their biology, disease impact and control. Journal of Invertebrate Pathology. 2013;112:S11-S14
  22. 22. Grace D, Randolph T, Affognon H, Dramane D, Diall O, Clausen PH. Characterisation and validation of farmers' knowledge and practice of cattle trypanosomosis management in the cotton zone of West Africa. Acta Tropica. 2009;111:137-143
  23. 23. Van den Bossche P, Delespaux V. Options for the control of tsetse-transmitted livestock trypanosomosis. An epidemiological perspective. Veterinary Parasitology. 2011;181(1):37-42
  24. 24. Deterding A, Dungey FA, Thompson K-A, Steverding D. Anti-trypanosomal activities of DNA topoisomerase inhibitors. Acta Tropica. 2005;93:311-316
  25. 25. Legros D, Ollivier G, Gastelluetchegorry M, Paquet C, Burri C, Jannin J, et al. Treatment of Human African trypanosomiasis – present situation and needs for research and development. The Lancet, Infectious Diseases. 2002;2(7):437-440
  26. 26. Wurochekke AU, Chechet G, Nok AJ. In vitro and in vivo antitrypanosomal activity of the leaf of Lawsonia inermis against Trypanosoma brucei brucei infection in mice. Journal of Medical Sciences. 2004;4:236-239
  27. 27. Hoet S, Pieters L, Muccioli GG, Habib-Jiwan J, Opperdoes FR, Quentin-Leclercq J. Antitrypanosomal activity of triterpenoids and sterols from the leaves of Strychnos spinosa and related compounds. Journal of Natural Products. 2007;70:1360-1363
  28. 28. Soulsby EJI. Helminthes, Arthropods and Protozoa of Domesticated Animals. 7th ed. London: Balliere Tindall; 1982. pp. 203-206
  29. 29. Anene BM, Ezeokonkwo RC, Mmesirionye TI, et al. A Diminazene-Resistant strain of Trypanosoma brucei isolated from a dog in cross resistant to Pentamidium in experimentally infected albino rats. Parasitology. 2006;132:127-133
  30. 30. Ezeokonkwo RC, Ezeh IO, Onunkwo JI, Obi PO, Onyenwe IW, Agu WE. Comparative haematological study of single and mixed infections of mongrel dogs with Trypanosoma congolense and Trypanosoma brucei. Journal of Veterinary Parasitology. 2010;173:48-54
  31. 31. Frevert U, Movila A, Nikolskaia OV, Raper J, Mackey ZB, et al. Early invasion of brain parenchyma by African trypanosomes. PLoS One. 2012;7:e43913
  32. 32. Sanderson L, Dogruel M, Rodgers J, Bradley B, Thomas SA. The blood-brain barrier significantly limits eflornithine entry into Trypanosoma brucei brucei infected mouse brain. Journal of Neurochemistry. 2008;107:1136-1146
  33. 33. Taylor KA, Mertens B. Immune response of cattle infected with African trypanosome. International Livestock Institute, Nairobi, Kenya. 1999;94(2):239-232
  34. 34. Abebe G. Trypanosomosis in Ethiopia. Ethiopia Journal of Biological Science. 2005;4(1):75-121
  35. 35. Murray M, Trail JCM, Davis CE, Black SJ. Genetic resistance to African trypanosomosis. The Journal of Infectious Diseases. 1984;149:311-319
  36. 36. Paul-Abiade CU, Onunkwo JI, Aka L. A Questionnaire Survey of Reports of Livestock Disease Outbreaks in Enugu North, South East Nigeria. Nigerian Veterinary Journal. 2008;27(3):1-5. DOI: 10.4314/nvj.v27i3.3521
  37. 37. Ohaeri CC. Prevalence of trypanosomiasis in ruminants in parts of Abia State, Nigeria. Journal of Animal and Veterinary Advances. 2010;9(18):2422-2426
  38. 38. Adu IF, Ngere LO. The indigenous sheep of Nigeria. W Review Animal Production. 1979;15:51-62
  39. 39. Ngere LO, Adu IF, Okubanjo IO. The indigenous goats of Nigeria. Ağrı. 1984;3:1-9
  40. 40. Majekodunmi AO, Fajinmi A, Dongkum C, Picozzi K, Thrusfield MV, Welburn SC. A longitudinal survey of African animal trypanosomiasis in domestic cattle on the Jos Plateau, Nigeria: Prevalence, distribution and risk factors. Parasites & Vectors. 2013;6(1):239. DOI: 10.1186/1756-3305-6-239
  41. 41. Albert M, Wardrop NA, Atkinson PM, Torr SJ, Welburn SC. Tsetse fly (G. f. fuscipes) distribution in the Lake Victoria Basin of Uganda. PLoS Neglected Tropical Diseases. 2015;9:e00R03705
  42. 42. Karshima SN, Lawal IA, Bata SI, Barde IJ, Adamu PV, Salihu A. Animal reservoirs of Trypanosoma brucei gambiense around the old Gboko sleeping sickness focus in Nigeria. Journal of Parasitology and Vector Biology. 2016;8:47-54
  43. 43. Akpan CAN, Ezeja MI, Ezeibe MCO. Prevalence of trypanosomosis in large and small ruminants in Abia State and Rivers State, Nigeria. Journal of Sustainable Veterinary and Allied Sciences. 2021;1(2):173-177
  44. 44. Oladele OI, Adenegan KO. Implications of small ruminant farmer's socio-economic characteristics for extension services in South Western Nigeria. In: Ologhobo AD, Iyayi EA, editors. The Nigeria Livestock Industry in the 21st Century. Lagos, Nigeria: Publication of Animal Science Association of Nigeria; 1998. pp. 243-246
  45. 45. Griffin L. African trypanosomosis in sheep and goats: A review. The Veterinary Bulletin. 1978;48:819-825
  46. 46. Katunguka-Rwakishaya E. The prevalence of trypanosomosis in small ruminants and pigs in a sleeping sickness endemic area. Revue d'Elevage et de Médecine Vétérinaire des Pays Tropicaux. 1996;49:56-58
  47. 47. Irungu P, Nyamwaro SO, Masiga DK. Financial Implication of rearing sheep and goats under natural trypanosomosis challenge at Galana ranch Kenya. Tropical Animal Health and Production. 2002;34:503-513
  48. 48. Hoet S, Opperdoes F, Brun R, Quetin-Leclercq J. Natural products active against African trypanosomes: A step towards new drugs. Natural Product Reports. 2004;21:353-364
  49. 49. Guilherme M, Andre T. Nutritional status driving infection by Trypanosoma cruzi: Lessons from experimental animals. Journal of Tropical Medicine. 2011;98(1):87-89
  50. 50. Abimbola AM, Baba IA, Yenusa EZ, Omanibe SJ, Oladimeji IH. Anti–trypanosomal effect of Peristrophe bicalyculata extract on Trypanosoma brucei brucei–infected rats. Asian Pacific Journal of Tropical Biomedicine. 2021;3(7):523-531. DOI: 10.1016/S2221-1691(13)60107-0
  51. 51. Onyiah JA. African animal trypanosomosis: An overview of the current status in Nigeria. Tropical Veterinary. 1997;15:111-116
  52. 52. Osaer S, Goossens B, Kora S, Gaye M, Darboe L. Health and productivity of traditionally managed Djallonke sheep and West African dwarf goats under high and moderate trypanosomosis. Veterinary Parasitology. 1999;82(2):109-119
  53. 53. Pannin A, Mahbile M. Profitability and household income contribution of small ruminant to small scale farmers in Botswana. Small Ruminant Research. 1997;25:9-15
  54. 54. Itty PP, Ankers J, Zinnsta S, Trawally PK. Productivity and profitability of sheep production in Gambia: Implication for livestock development in West Africa. Journal of International Agriculture. 1997;36:153-172
  55. 55. Chiegeonu AS. Nigeria: State by State: A Road Tour Profile. 2009. Available from: www.nigeriabookofrecord.com
  56. 56. Mahajian BK. Methods of Biostatistics for Medical Students and Research Workers. 6th ed. India: Jaypee Brothers Medical Publishers Ltd; 1997. pp. 88-94
  57. 57. Murray M, Murray PK, McIntyre WIM. An improved parasitological technique for the diagnosis of African trypanosomiasis. Transactions of the Royal Society for Tropical Medicine and Hygiene. 1977;71:235-236
  58. 58. Woo PTK. The hematocrit centrifugation technique for the diagnosis of Africa trypanosomiasis. Acta Tropica. 1970;27:384-386
  59. 59. Idahor KO, Adua MM, Saleh DF. Serological examination of trypanosomes infestation in cattle reared in Keffi, Nasarawa State, Nigeria. Journal of Vector Borne Diseases. 2019;56:154-158
  60. 60. Idehen CO, Ishola OO, Adeyemi IG, Abongaby G, Olaleye OO, Aluma AL, et al. Prevalence of African trypanosomosis in cattle and sheep in Bassa local government area of Plateau State, Nigeria. Sokoto journal of Veterinary Sciences. 2018;16(3):11-17. DOI: 10.4314/sokjvs.v16i3.2
  61. 61. Dede P, Pizzeria L, Lawani F. Situation actualle et nouvelle strategie de lutte contre les tsetse et la trypanosomiase au Nigeria basee sur I’nitiatiave PATTEC. ISCTRC. 2007;2007:162-176
  62. 62. Chappuis F, Loutan L, Simarro P, Lejon V, Büscher P. Options for field diagnosis of human African trypanosomiasis. Clinical Microbiology Reviews. 2005;18(1):133-146
  63. 63. Marcotty T, Simukoko H, Berkvens D, Vercruysse J, Praet N, Van den Bossche P. Evaluating the use of packed cell volume as an indicator of trypanosomal infections in cattle in eastern Zambia. Preventive Veterinary Medicine. 2008;87(3-4):288-300
  64. 64. Spickler AR. African Animal Trypanosomiasis. 2018. Available from: http://www.cfsph.iastate.edu/diseaseInfo/factsheets.php
  65. 65. Murray M, Trail JC, D'Ieteren GD. Trypanotolerance in cattle and prospects for the control of trypanosomiasis by selective breeding. Revue Scientifique et Technique. 1990;9:369-386
  66. 66. Kalu AU. Acute trypanosomosis in a sedentary herd on the tsetse-free Jos Plateau, Nigeria. British Veterinary Journal. 1996;152(4):477-479
  67. 67. Takeet MI, Fagbemi BO, De Donato M, Yakubu A, Rodulfo HE, Peters SO, et al. Molecular survey of pathogenic trypanosomes innaturally infected Nigerian cattle. Research in Veterinary Science. 2013;94:555-556
  68. 68. Ogunsanmi AO, Ikede BO, Akpavie SO. Effects of management, season, vegetation zone and breed on the prevalence of bovine trypanosomiasis in southwestern Nigeria. Israel Journal of Veterinary Medicine. 2000;55(2):1-6
  69. 69. Usman SB, Babatunde OO, Oladipo KJ, Felix LAG, Gutt BG, Dongkum C. Epidemiological survey of animal trypanosomiasis in Kaltungo Local Government Area, Gombe State, Nigeria. Journal of Protozoological Research. 2008;18(96):105
  70. 70. Kalu AU, Uzoukwu M, Ikeme MM. Prevalence of tsetse fly and ruminant trypanosomosis in Katsina – Ala Local Government Area, Benue State, Nigeria. Romanian Archives of Microbiology and Immunology. 1996;55(4):341-352

Written By

Clara A.N. Akpan

Submitted: 02 December 2022 Reviewed: 31 December 2022 Published: 10 February 2023