Seroepidemiological study of ovine toxoplasmosis in East and West Shewa Zones of Oromia Regional State, Central Ethiopia
© Gebremedhin et al.; licensee BioMed Central Ltd. 2013
Received: 13 July 2012
Accepted: 13 June 2013
Published: 15 June 2013
Toxoplasmosis is a globally distributed zoonosis. Consumption of raw or undercooked meat, which is among the main risk factors for acquiring human infection, is a popular tradition in Ethiopia. However, studies on toxoplasmosis in food animals used for human consumption in Ethiopia are very scarce. Thus, the objectives of the present study were to estimate the seroprevalence and the risk factors of T. gondii infection in sheep in Ambo, Ada’a-Liben and Fentale districts of Central Ethiopia. Sera from 1130 sheep were analyzed for Toxoplasma gondii specific IgG antibodies using an indirect enzyme linked immunosorbent assay (ELISA) with the P30 antigen. A questionnaire was administered to assess potential risk factors for T. gondii seropositivity. Association of seroprevalence with potential risk factors related to altitude, host and farm characteristics were analyzed by univariable and multivariable logistic regression.
Overall flock and animal level seroprevalences were 70.48% (160/227; 95% CI: 64.51, 76.46) and 31.59% (357/1130; 95% CI: 28.88, 34.31), respectively. The multivariable logistic regression model indicated that the probability of acquiring T. gondii was higher in sheep from highland (2300 – 3200 meters above sea level) [Odds ratio (OR) = 4.11, 95% confidence interval (CI): 2.65, 6.36; P < 0.001] and midland (OR = 4.54, 95% CI: 2.76, 7.49; P < 0.001) than from lowland (<1500 meters above sea level), in females than in males (OR = 1.60, 95% CI: 1.04, 2.43, P = 0.033), in adult than in young animals (OR = 2.93, 95% CI: 1.97, 4.35, P < 0.001), in small than in large flocks (OR = 3.34, 95% CI: 1.26, 8.86, P = 0.016), and in sheep that were given tap water (OR = 4.07, 95% CI: 1.07, 15.42, P = 0.039) and river water (OR = 4.18, 95% CI: 1.54, 11.35, P = 0.005) than in those that drunk water from mixed sources (i.e., river, well, lake and pond).
The high flock and animal level seroprevalence of toxoplasmosis in sheep is a good marker of the potential risk for human infections. Altitude, sex, age, flock size and source of water were identified as important risk factors to acquire the infection. Public education and awareness training are imperative in order to alleviate the danger posed to consumers. Further detailed studies to assess the impact of infections are warranted.
Sheep are important for mutton, wool and milk production throughout the world . There are approximately 26.1 million sheep in Ethiopia . Mutton is the most popular source of animal proteins in Ethiopia as well as in the importing countries (Arabian countries). It is estimated that 1,078,000 sheep are consumed in Ethiopia while 700,000 sheep are exported annually .
Toxoplasmosis is one of the most globally widespread zoonoses with considerable health and economic impacts. The disease is recognized as an emerging food-borne parasitic disease . In some countries T. gondii is among the highest ranking foodborne pathogens causing high disease burden both at individual and population levels .
Domestic cats and wild felids play a crucial role in the epidemiology of toxoplasmosis as the definitive hosts, through the shedding of millions of oocysts when infected [6, 7]. Human beings and other warm-blooded animals become infected primarily by ingesting food or water contaminated with sporulated oocysts or by ingesting meat that contain tissue cysts of T. gondii[6, 8–11]. Infection of pregnant women may result in abortion or congenital infection that may cause hydrocephalus, intracranial calcification and retinochoroiditis . In addition, recent studies have indicated that toxoplasmosis is a plausible risk factor for personality shifts and increased likelihood of reduced intelligence or schizophrenia . There is also a very high correlation between latent toxoplasmosis and car accidents [13, 14]. Recently, highly virulent genetically atypical strains of T. gondii have been incriminated with pneumonia, even in immunocompetent individuals .
Toxoplasmosis leads to great economic losses in sheep and goats by causing embryonic death and resorption, fetal death and mummification, abortion, stillbirth, neonatal death and reduced flock milk production and infertility [16–18]. Antibodies to T. gondii have been found in sheep worldwide . Seropositive small ruminants can be assumed to harbor tissue cysts in their meat [19, 20] thereby endangering the consumers of mutton.
Toxoplasma gondii infection of sheep and goats has been reported from various African countries [21–23]. Previous studies in Ethiopia have shown that seroprevalence of anti-T. gondii antibodies in sheep ranges from 11.9% to 56% [24–26]. However, the epidemiology of toxoplasmosis in food animals and humans is largely unknown in Ethiopia. The objectives of the present study were to estimate the seroprevalence and the risk factors of T. gondii infection in sheep in Ambo, Ada’a-Liben and Fentale districts of Central Ethiopia.
Description of the study districts and population
The study was conducted in three districts of Oromia regional state, Central Ethiopia. The study areas are separated from each other by 150 to 289 kms and represent the highland (≥2300 meters above sea level [mas]), midland (1500 – 2300 masl) and lowland (< 1500 masl) agro-ecologies of the region.
Ambo district (longitude 37° 32' to 38° 3′ E and latitude 8° 47′ to 9° 20′ N) is located in Western Shewa zone of the Oromia Regional State. The altitude within the district ranges from 1400 to 3045 masl. Majority of the places in Ambo district are high land. The annual rainfall and temperature range from 800 – 1000 mm and 15°C – 29°C, respectively. The mean temperature is 18.6°C.
Ada’a-Liben (longitude 38° 58′E to 39° 22′E and latitude 08° 22′N to 8° 56′ N) and Fentale Districts (longitude 39.93°E to 39° 56′0″E and latitude 8.975° N to 8.58′30″ N) are located in East Shewa zone at a distance of 45 kms and 190 kms from Addis Ababa, respectively. The altitude of Ada’a-Liben and Fentale districts range from 1500 to over 2000 and 955 to 2007 masl, respectively. The vast majority of Fentale is lowland (except at a place called mount Fentale where altitude reaches 2007 m) while that of Ada’a-Liben district is midland). The average rainfall and temperature of Ada’a-Liben and Fentale districts are about 839 mm and 553 mm and 7.9°C to 28°C and 29 to 38°C, respectively. Fentale district has an arid to semi-arid climate and the production system is predominantly pastoral and agro-pastoral. Sedentary farming dominated by extensive type of management system is a feature of the highlands and midlands of Ambo and Ada’a-Liben districts. However, semi-intensive farming is practiced in some urban and peri-urban areas.
Afar, Arsi-Bale and Horro breeds of sheep predominate in Central Ethiopia. Sheep are kept for mutton production in most parts of the country; however, pastoralists in Fentale district also use sheep for milk production. In this study, sheep of both sexes above six months old were included. Sheep aged ≤ 1 year are considered as young while those above 1 year are considered as adult.
Study design and sample size
Summary of peasant associations and flocks sampled from Ambo, Fentale and Ada’a-Liben districts
Blood collection and serum separation
Approximately 5 ml of whole blood samples were collected by venipuncture from the jugular vein using disposable plain vacutainer tubes and needles (BD Vacutainer Systems, Plymouth, UK). The blood samples were allowed to clot and then centrifuged at 4000 rpm for 5 minutes. Centrifugation took place in the field, i.e., during the evening in the town of each district. The serum was collected into 1.5 ml Eppendorf tubes (Eppendorf-AG, Hamburg, Germany) and transported to the School of Veterinary Medicine, Debre-Zeit, using an ice box and stored at −20°C until serologically tested.
A close-ended questionnaire was developed and filled in at flock or household level by interviewing flock owners or herders during sampling in order to assess potential risk factors for toxoplasmosis. Those included flock size, presence of cats in the households, presence of wild felids in the area, type of management (extensive: free ranging without supplementary feed; semi-intensive: supplementary feed provided), source of water and grazing/browsing place. Information about altitude and farming system of sampling sites was also collected. At animal level information about breed, sex and age was collected. Animal age determination was made based on dentition  and herders’ information.
All the collected serum samples were tested for the presence of IgG antibodies against T. gondii following the protocol of the manufacturer of the indirect enzyme linked immunosorbent assay (P-30 ELISA) kit (ID VET Innovative Diagnostic, ID Screen®, Montpellier, France), which is coated with the P30 surface antigen of the organism.
Data management and analysis
The data generated were stored in Microsoft excel spreadsheet (Microsoft Corporation) and analyzed using STATA version 11.0 for MA Windows (Stata Corp. College Station, USA). Univariable logistic regression analysis was performed, and odds ratios (OR) and 95% confidence intervals (CI 95%) were used to quantify the association between risk factors and T. gondii infection. Continuous data were collected from the field for age and flock size. These variables were categorized during data analysis. The categories of the variables were as follows. Altitude (lowland, mid land, high land), sex (male vs. female), age (young vs. adult), flock size (large vs. small taking 50 as a cut-off), management type (extensive vs. semi-extensive), residential place (urban vs. rural), source of drinking water (stagnant, river, tap, mixed), grazing land (plain, mountainous, mixed), presence of cats (present vs. absent) and presence of wild felids (yes vs. no). Hence, all variables were handled as categorical variables. Collinear variables with lpl >0.5 were identified using a collinearity matrix. One of the recommended methods of handling collinear variables is to eliminate less plausible ones. Hence, elimination of one of the collinear variable was decided based on biological ground to explain the disease better. Non-collinear variables that presented P-value of < 0.15 in univariable analysis were entered in the multivariable regression model. During the analysis the clustering nature of the outcome within flock was considered by including flock as a clustering variable. This enabled us to use clustered sandwich estimator i.e., robust standard error rather than the standard error of the parameters estimated using maximum likelihood method. Variables with more than two categories were transformed into indicator (dummy) variables. Potential risk factors included in the model were selected based on the existing literature. Flocks containing at least one seropositive animal were considered positive. After obtaining final model interaction of pre-specified factors (i.e. age and sex, flock size and cat ownership, source of water and cat ownership, flock size and source of water, flock size and management, source of water and management) was assessed. The model was constructed by backward stepwise exclusion method. The variable ‘presence of cat’ was purposively allowed to join the variables used for fitting best model due to its biological importance, while the variables ‘grazing land, presence of wild felids and residential place’ were excluded due to a high p-value. Finally, the model fitness was assessed by Hosmer–Lemeshow goodness-of-fit test . The reliability of the fitted model was further evaluated using receiver operating characteristic curve (ROC). The 95% confidence level was used and results were considered significant at P ≤ 0.05.
This research project was reviewed and approved by the ethical committee for animal experimentation of the College of Veterinary Medicine and Agriculture, Addis Ababa University, Ethiopia.
Animal and flock level seroprevalence of T. gondii infection in Ambo, Fentale and Ada’a-Liben districts
Animal level seroprevalence
Flock level seroprevalence
95% CI [Lower–upper]
95% CI [Lower–upper]
Risk factor analysis
Univariable logistic regression analysis of potential risk factors for T. gondii seropositivity in study districts
Risk factors category
Crude OR (95% CI)
5.58 (3.79, 8.22)
5.73 (3.72, 8.82)
5.23 (3.42, 8.00)
5.77 (3.89, 8.56)
2.17 (1.49, 3.16)
2.67 (1.86, 3.85)
Large (n ≥ 50)
Small (n < 50)
2.02 (1.35, 3.01)
1.34 (0.92, 1.95)
Source of water
7.26 (2.42, 21.84)
7.6 (2.81, 20.57)
10.28 (2.96, 35.71)
1.64 (1.06, 2.54)
3.06 (1.82, 5.15)
Presence of cats
1.42 (1.00, 2.02)
Presence of wild felids
1.75 (1.23, 2.48)
2.73 (1.40, 5.33)
11.12 (5.99, 20.64)
Multivariable logistic regression analysis of predictors of T. gondii infection in sheep of study districts
Risk factors category
Adjusted OR (95% CI)
4.54 (2.76, 7.49)
4.11 (2.65, 6.36)
1.60 (1.04, 2.43)
2.93 (1.97, 4.35)
Large (n ≥ 50)
Small (n < 50)
3.34 (1.26, 8.86)
2.88 (0.96, 8.69)
Source of water
2.34 (0.69, 7.94)
4.18 (1.54, 11.35)
4.07 (1.07, 15.42)
Presence of cats
1.11 (0.77, 1.60)
Management type*source of water
1.23 (0.30, 5.09)
3.64 (1.16, 11.43)
2.12 (0.33, 13.42)
Although no population estimates of Ethiopian cats are available, the present study demonstrated that cats are favorite animals kept by 118 of 227 studied households (52.0%), mainly to control rodents around the home and in the grain stores.
The present study reported an overall seroprevalence of 70.48% (160/227) at flock and 31.59% (357/1130) at animal level. Our results are within the range of the prevalence estimated in previous studies in Ethiopia, which ranged from 11.9% in Central Ethiopia  and 52.6% in Nazareth . The great variation in the seroprevalence of T. gondii infection is likely to be the result of the geographic area, the farm management and the general hygienic conditions of the farms, and of technical issues such as, the serological method used, the cut off values and the sample size . ELISA that uses P30 antigen, expressed exclusively by tachyzoites (fast multiplying form of the parasite) was used in the present study. Similar commercial ELISA has been previously used for diagnosis of T. gondii infection in sheep and goats with reliable results [31–33].
This study showed that sheep from the highlands and midland areas of Central Ethiopia are at significantly higher risk of T. gondii infection than those from the lowland (P < 0.001). This variation can be explained by the difference of environmental temperature and moisture in these areas. The Ethiopian tropical climate is subjected to wide topographic-induced variations . The influence of the environment on the epidemiology of toxoplasmosis has been well documented [11, 35]. The lowest prevalence (13.36%) was recorded in lowland area, which is characterized by a hot and arid climate compared to the tepid to cool sub moist agro-ecology in the midland and the moist agro climate in the highlands of the study area. Highland and midland areas receive more rainfall; evaporation is relatively less and those areas have more forest canopies or vegetation. The resulting humidity is favorable to a higher chance of oocyst survival in the environment and infectivity to sheep, thereby contributing to the higher seroprevalence. It is well known that a dry climate has an adverse effect on the persistence and dissemination of oocysts of T. gondii[6, 36]. Furthermore, it is worth mentioning, that as compared to lowland, human settlements and cat ownership are higher in mid and highland. Many farmers in the mid and the highlands practice mixed crop-livestock farming. Grazing land is limited and some farmers’ supplement sheep with grains or commercial concentrate feeds that is often protected from rodent attack by keeping cats around. Similar to our findings, Kamani et al.  also reported in Nigeria that a milder climate with higher rainfall and relative humidity favors a higher seroprevalence as compared to arid Sahel northern zones. However, a study from Mexico found that prevalence was higher at low altitudes .
Significantly higher seroprevalence in adult (35.42%) compared to young sheep (17.02%) is consistent with earlier studies [6, 19, 38–42] and is the result of higher likelihood of ingestion of oocysts with increasing age.
The higher seroprevalence in female sheep (34.39%) as compared to males (19.43%) is significant and might be attributed to the management system in that ewes are retained in the farm for longer periods for breeding purpose than males. Few rams are retained for mating while the majority are culled and sold for cash purpose. The hormonal difference in relation to stress of lactation and pregnancy leading to immunosuppression may also increase susceptibility to toxoplasmosis in females . Teshale et al.  and Negash et al.  also reported higher seroprevalence in female sheep in Ethiopia.
Toxoplasma gondii seropositivity in small flocks (34.17%) was significantly higher than in large flocks (4.0%). This result could be ascribed to the fact that small flocks are often repeatedly tethered or allowed to graze on a small area close to the farm and households where domestic cats have an easy access and may contaminate the pasture and feed reserves (roughage and concentrate) around the homestead. On the other hand, large flocks are commonly found in pastoral areas where animals spend more time grazing over a wide area away from the farm and the home. We cannot exclude other sources of infection and there could also be risk factors independent of flock size that might have been distributed over fewer animals .
The higher seroprevalence (33.33%) in sheep that drunk river water is expected and suggest higher chance of contamination by oocysts while the higher seroprevalence (40.35%) in sheep that were given water from the tap than those drinking from both river and stagnant water bodies (6.17%) is puzzling. This may suggest that surrounding felid populations are contaminating the source of tap water with oocysts, and water purification and chlorination processes are either ineffective against oocysts or non-existent [11, 45]. It could also be possible that some unknown confounding factors such as the poor sanitation of watering troughs can influence the probability of T. gondii seropositivity.
The presence of cats is crucial in the life cycle of T. gondii and is significantly associated with increased seroprevalence in many reports [6, 7]. In our study the presence of cats was not an independent predictor of toxoplasmosis in the final model. We expect that in those households reporting absence of cats at their home, stray and wild cats from neighboring areas might visit their area and access sheep grazing land. We didn’t isolate oocysts or study seroprevalence in cats. Probably cats in some households are not infected at all and in this case presence of cats and their numbers is not directly related to seroprevalence. Similarly, the presences of wild felids viz. Leopard (Panthera pardus, Linnaeus, 1758), Serval (Leptailurus serval, Schreber, 1776), Cheetah (Acinonyx jubatus, Schreber, 1776) and African Lion (Panthera leo, Linnaeus, 1758), in the study areas did not affect the seroprevalence of toxoplasmosis.
The high seroprevalence in this study illustrates the probability of T. gondii transmission to consumers through mutton and lamb. A strong correlation between the seroprevalence of T. gondii in sheep and the risk of human infection has been reported [6, 9, 10, 19, 46]. The inadequate culinary hygiene, the inadequate meat freezing facility, “tasting” of the raw meat during the cooking process, and the widespread consumption of raw and undercooked meat in the study areas increases pressure of infection by T. gondii to humans.
We conclude that T. gondii infection of sheep at flock and animal levels in the study districts is high and that altitude, sex, age, flock size and source of water are independent predictors of T. gondii seropositivity. Enforcing hygienic measures, the education of people and provision of rendering facilities to kill the bradyzoites in meat whenever possible are recommended. Further detailed studies to assess the impact of infections are warranted.
The financial support of Oromia Regional State Rural Capacity Building, Addis Ababa University, VLIR-UOS project no. “ZEIN 2010 PR 372” “promotion of the PhD program in veterinary public health at the Faculty of Veterinary Medicine”, Belgium and the Italian National Reference Centre for Toxoplasmosis at the Istituto Zooprofilattico Sperimentale Della Sicilia A. Mirri, Italy, are highly acknowledged. We are extremely indebted to Professor Dr. Bruno Goddeeris, from the Catholic University of Leuven who is leading the VLIR-UOS project, for facilitation of the overall research grant, continuous support and follow up. We thank the National Animal Health and Disease Investigation Center at Sebeta for availing their laboratory facility and equipment. The authors also would like to extend their gratitude to the district assistant veterinary technicians and the farmers for their collaboration in the sampling and supplying information.
- Cenci-Goga BT, Rossitto PV, Sechi P, Cheryl ME, McCrindle CME, Cullo JS: Toxoplasma in animals, food, and humans: an old parasite of new concern. Foodborne Pathog Dis. 2011, 8 (7): 1-12.View ArticleGoogle Scholar
- Central Statistical Authority (CSA): Federal democratic republic of Ethiopia central statistical agency agricultural sample survey 2007/08. Volume II, report on livestock and livestock characteristics. Addis Ababa: Statistical Bulletin No. 417; 2008.Google Scholar
- Hirpa A, Abebe G: Economic significance of sheep and goats. In Sheep and goat production handbook for Ethiopia. Edited by Yami A, Merkel RC.Addis Ababa: Ethiopian sheep and goat productivity improvement program;2008:1–4.Google Scholar
- Dorny P, Praet N, Deckers N, Gabriel S: Emerging food-borne parasites. Vet Parasitol. 2009, 163: 196-206. 10.1016/j.vetpar.2009.05.026.PubMedView ArticleGoogle Scholar
- Havelaar AH, Haagsma JA, Mangen MJ, Kemmeren JM, Verhoef LPB, Vijgen SMC, Wilson M, Friesema IHM, Kortbeek LM, van Duynhoven YTHP, van Pelt W: Disease burden of foodborne pathogens in the Netherlands, 2009. Int J Food Microbiol. 2012, 156: 231-238. 10.1016/j.ijfoodmicro.2012.03.029.PubMedView ArticleGoogle Scholar
- Dubey JP: Toxoplasmosis of animals and humans. 2nd edition. Boca Raton,Florida, U.S.A: CRC Press; 2010.Google Scholar
- Dubey JP, Beattie CP: Toxoplasmosis of animals and man. Florida: CRC Press Boca Raton; 1988.Google Scholar
- Munoz M, Liesenfeld O, Heimesaat MM: Immunology of Toxoplasma gondii. Immuno Rev. 2011, 240: 269-285. 10.1111/j.1600-065X.2010.00992.x.View ArticleGoogle Scholar
- Opsteegh M, Langelaar M, Sprong H, den Hartog L, De Craeye S, Bokken G, Ajzenberg D, Kijlstra A, van der Giessen J: Direct detection and genotyping of Toxoplasma gondii in meat samples using magnetic capture and PCR. Int J Food Microbiol. 2010, 139: 193-201. 10.1016/j.ijfoodmicro.2010.02.027.PubMedView ArticleGoogle Scholar
- Radostits OM, Gay CC, Hinchcliff KW, Constable PD: Veterinary medicine: a textbook of the diseases of cattle, horses, sheep, pigs and goats. 10th edition.London: Saunders; 2006.Google Scholar
- Dubey JP: Toxoplasmosis - a waterborne zoonosis. Vet Parasitol. 2004, 126 (1–2): 57-72.PubMedView ArticleGoogle Scholar
- Dogruman-Al F, Aslan S, Yalcin S, Kustimur S, Turk S: A possible relationship between toxoplasma gondii and schizophrenia: a seroprevalence study. Int J Psychiat Clin Prac. 2009, 13 (1): 82-87. 10.1080/13651500802624738.View ArticleGoogle Scholar
- Yereli K, Balcioglu IC, Ozbilgin A: Is Toxoplasma gondii a potential risk for traffic accidents in Turkey?. Forensic Sci Int. 2006, 163: 34-37. 10.1016/j.forsciint.2005.11.002.PubMedView ArticleGoogle Scholar
- Flegr J, Havlícek J, Kodym P, Malý M, Smahel Z: Increased risk of traffic accidents in subjects with latent toxoplasmosis: a retrospective case–control study. BMC Infect Dis. 2002, 2: 11-10.1186/1471-2334-2-11.PubMedPubMed CentralView ArticleGoogle Scholar
- Leal FE, Cavazzana CL, de Andrade HF, Galisteo AJ, de Mendonc JS, Kallas EG: Toxoplasma gondii pneumonia in immunocompetent subjects: case report and review. Clin Infect Dis. 2007, 44: e62-e66. 10.1086/511871.PubMedView ArticleGoogle Scholar
- Buxton D, Lesson B: Toxoplasmosis: general considerations. Protozoal abortion in farm ruminants: guideline for diagnosis and control. Edited by: Ortega-Mora LM, Gottstein B, Conraths FJ, Buxton D. 2007, Reading, UK: CAB International, 122-171.Google Scholar
- Williams RH, Morley EK, Hughes JM, Duncanson P, Terry RS, Smith JE, Hide G: High levels of congenital transmission of Toxoplasma gondii in longitudinal and cross-sectional studies on sheep farms provides evidence of vertical transmission in ovine hosts. Parasitol. 2005, 130: 301-307. 10.1017/S0031182004006614.View ArticleGoogle Scholar
- West DM: Ovine abortion in New Zealand. N Z Vet J. 2002, 50: S93-S95.View ArticleGoogle Scholar
- Halos L, Thébault A, Aubert D, Thomas M, Perret C, Geers R, Alliot A, Escotte-Binet S, Ajzenberg D, Dardé ML, Durand B, Boireau P, Villena I: An innovative survey underlining the significant level of contamination by Toxoplasma gondii of ovine meat consumed in France. Int J Parasitol. 2010, 40: 193-200. 10.1016/j.ijpara.2009.06.009.PubMedView ArticleGoogle Scholar
- Jones DJP, Jones JL: Toxoplasma gondii infection in humans and animals in the United States. Inter J Parasitol. 2008, 38: 1257-1278. 10.1016/j.ijpara.2008.03.007.View ArticleGoogle Scholar
- Kamani J, Mani AU, Godwin O, Egwu GO: Seroprevalence of Toxoplasma gondii infection in domestic sheep and goats in Borno state, Nigeria. Trop Anim Health Prod. 2010, 42: 793-797. 10.1007/s11250-009-9488-3.PubMedView ArticleGoogle Scholar
- Sharma SP, Baipoledi EK, Nyange JFC, Tlagae L: Isolation of Toxoplasma gondii from goats with a history of reproductive disorders and the prevalence of Toxoplasma and chlamydial antibodies. Onderstepoort J Vet Res. 2003, 70: 65-68.PubMedGoogle Scholar
- Van der Puije WNA, Bosompem KM, Canacoo EA, Wastling JM, Akanmori BD: The prevalence of anti-Toxoplasma gondii antibodies in Ghanaian sheep and goats. Acta Trop. 2000, 76: 21-26. 10.1016/S0001-706X(00)00084-X.PubMedView ArticleGoogle Scholar
- Negash T, Tilahun G, Patton S, Prevot F, Dorchies PH: Serological survey of toxoplasmosis in sheep and goats in Nazareth, Ethiopia. Revue Med Vet. 2004, 155: 486-487.Google Scholar
- Tilaye D, Getachew T: Study on toxoplasmosis in sheep and goats in Debre Birhan and surrounding areas in Ethiopia. Bull Anim Hlth Prod Afr. 2002, 50: 138-147.Google Scholar
- Bekele T, Kassali OB: Toxoplasmosis in sheep, goats and cattle in central Ethiopia. Vet Res Commun. 1989, 13: 371-375. 10.1007/BF00346069.PubMedView ArticleGoogle Scholar
- Thrusfield M: Veterinary Epidemiology. 3rd edition. Blackwell Science Ltd:Oxford, UK; 2007.Google Scholar
- Dohoo I, Martin W, Stryhn H: Veterinary epidemiologic research. Canada:AVS Inc; 2003.Google Scholar
- Shively MJ: Veterinary anatomy: basic comparative and clinical. Texas USA:A and M Press; 1987.Google Scholar
- Opsteegh M, Teunis P, Mensink M, Zuchner L, Titilincu A, Langelaar M, van der Giessen J: Evaluation of ELISA test characteristics and estimation of Toxoplasma gondii seroprevalence in Dutch sheep using mixture models. Prev Vet Med. 2010, 96: 232-240. 10.1016/j.prevetmed.2010.06.009.PubMedView ArticleGoogle Scholar
- Khezri M, Mohammadian B, Esmailnia K, Khezri O: Toxoplasmosis in sheep from Kurdistan province. Iran Asian J Anim Sci. 2012, 6 (4): 182-188. 10.3923/ajas.2012.182.188.View ArticleGoogle Scholar
- Berger-Schoch AE, Bernet D, Doherr MG, Gottstein B, Frey CF: Toxoplasma gondii in Switzerland: a serosurvey based on meat juice analysis of slaughtered pigs, wild boar, sheep and cattle. Zoonoses Public Health. 2011, 58 (7): 472-478. 10.1111/j.1863-2378.2011.01395.x.PubMedView ArticleGoogle Scholar
- O’Donovan J, Proctor A, Gutierrez J, Worrell S, Nally J, Marques P, Brady C, McElroy M, Sammin D, Buxton D, Maley S, Bassett H, Markey B: Distribution of lesions in fetal brains following experimental infection of pregnant sheep with Toxoplasma gondii. Vet Pathol. 2011, 49: 462-469.PubMedView ArticleGoogle Scholar
- Hurni H: Agroecological belts of Ethiopia: explanatory notes on three maps.Soil conservation research program, centre for development and environment.Switzerland: University of Bern; 1998:1–32.Google Scholar
- Tenter AM, Heckerotha AR, Weiss LM: Toxoplasma gondii: from animals to humans. Int J Parasitol. 2000, 3: 1217-1258.View ArticleGoogle Scholar
- Jones JL, Moran KD, Wilson M, McQuillan G, Navin T, James B, McAuley JB: Toxoplasma gondii infection in the United States: seroprevalence and risk factors. Am J Epidemiol. 2001, 154: 357-365. 10.1093/aje/154.4.357.PubMedView ArticleGoogle Scholar
- Caballero-Ortega H, Palma M, Garcia-Marquez J, Gildo-Cardenas A, Correa D: Frequency and risk factors for toxoplasmosis in ovines of various regions of the State of Colima, Mexico. Parasitol. 2008, 135: 1385-1389. 10.1017/S0031182008004873.View ArticleGoogle Scholar
- Ramzan M, Akhtar M, Muhammad F, Hussain I, Hiszczyńska-Sawicka E, Haq AU, Mahmood MS, Hafeez MA: Seroprevalence of Toxoplasma gondii in sheep and goats in Rahim Yar Khan (Punjab), Pakistan. Trop Anim Health Prod. 2009, 41: 1225-1229. 10.1007/s11250-009-9304-0.PubMedView ArticleGoogle Scholar
- Carneiro ACAV, Carneiro M, Gouveia AMG, Guimaraes AS, Marques APR, Vilas-Boas LS, Vitor RWA: Seroprevalence and risk factors of caprine toxoplasmosis in Minas Gerais, Brazil. Vet Parasitol. 2009, 160: 225-229. 10.1016/j.vetpar.2008.10.092.PubMedView ArticleGoogle Scholar
- Teshale S, Dumetre A, Darde ML, Merga B, Dorchies PH: Serological survey of toxoplasmosis in Ethiopia: prevalence and risk factors. Parasite. 2007, 14: 155-159. 10.1051/parasite/2007142155.PubMedView ArticleGoogle Scholar
- Hall S, Ryan M, Buxton D: The epidemiology of toxoplasma infection. Toxoplasmosis. A comprehensive clinical guide.1st edition Edited by: Joynson DHM, Wreghitt TG.New York: Cambridge University Press; 2001: 58-124.View ArticleGoogle Scholar
- Dorny P, Casman C, Sani N, Vercruysse J: Toxoplasmosis in goats: a seroepidemiological study in Peninsular Malaysia. Ann Trop Med Parasitol. 1993, 87: 407-410.PubMedGoogle Scholar
- Dubey JP, Lappin MR: Toxoplasmosis and Neosporosis. In Infectious diseases of the dog and cat. Edited by Greene CE. Philadelphia: WB Saunders;1998:493–509.Google Scholar
- Weigel RM, Dubey JP, Siegel AM, Kitron UD, Mannelli A, Mitchell MA, Mateus-Pinilla NE, Thulliez P, Shen SK, Kwok OC: Risk factors for transmission of Toxoplasma gondii on swine farms in Illinois. J Parasitol. 1995, 81: 736-741. 10.2307/3283964.PubMedView ArticleGoogle Scholar
- Bowie WR, King AS, Werker DH, Isaac-Renton JL, Bell A, Eng SB, Marion SA: Outbreak of toxoplasmosis associated with municipal drinking water. Lancet. 1997, 350: 173-177. 10.1016/S0140-6736(96)11105-3.PubMedView ArticleGoogle Scholar
- Dubey JP, Sundar N, Hill D, Velmurugan GV, Bandini LA, Kwok OC, Majumdar D, Su C: High prevalence and abundant atypical genotypes of Toxoplasma gondii isolated from lambs destined for human consumption in the USA. Int J Parasitol. 2008, 38: 999-1006. 10.1016/j.ijpara.2007.11.012.PubMedView ArticleGoogle Scholar
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