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Acta parasitologica2025; 70(4); 167; doi: 10.1007/s11686-025-01108-w

Seroprevalence of Toxoplasma gondii in Equids: A Global Systematic Review and Meta-analysis.

Abstract: Toxoplasmosis is a zoonotic infectious disease caused by T. gondii, a widely distributed obligate intracellular parasite. It has received widespread attention because it can infect a large number of domestic and wild animals, thereby posing a threat to public health and the economy on a global scale. Among them, equine animals are critical intermediate hosts. However, studies on T. gondii infection in equine animals are currently not systematic on a global scale. For this purpose, we conducted a systematic review and meta-analysis. Methods: This study searched for relevant studies in six significant databases (PubMed, Web of Science, ScienceDirect, Wanfang database, VIP database and CNKI database). From 1099 articles, we selected 30 articles from 17 countries published from the database creation to July 1, 2023, and used a random-effects model to estimate the T. gondii infection rate in equids. Results: The global infection rate of T. gondii in equids was estimated at 15.0% (2539/15,882, 95% CI 14.0-15.0%). The infection rate was highest in Africa (25.5%) and lowest in North America (8.4%). The infection rate after 2016 (24.0%) was higher than that before 2016 (14.6%). The infection rate was highest in equids aged 5-10 years (20.3%). Among equids, donkeys had the highest overall infection rate at 23.4%, which was higher than that of horses (15.8%) and mules (16.8%). The infection rate among female equine animals (17.5%) is higher than that among males (13.9%). These data indicate that T. gondii is widespread among equine animals globally, posing a potential infection risk to humans. Therefore, continuous monitoring of toxoplasmosis infection rates and control of T. gondii transmission are of great significance for both economic and public health.
Publication Date: 2025-08-07 PubMed ID: 40773076PubMed Central: 3346298DOI: 10.1007/s11686-025-01108-wGoogle Scholar: Lookup
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  • Journal Article
  • Systematic Review
  • Meta-Analysis
  • Review

Summary

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The article investigates the global prevalence of the infectious disease Toxoplasmosis, caused by T. gondii, in equine animals and its potential implications for public health and economy. The study’s key findings include varying infection rates based on geography, period, animal age and type, and gender.

Research Methodology

  • The article’s authors conducted a systematic review and meta-analysis to collectively analyze the available range of studies regarding T. gondii infection in equine animals.
  • Six significant databases – PubMed, Web of Science, ScienceDirect, WanFang, VIP, and CNKI – were scoured for pertinent studies.
  • From the 1099 identified articles, 30 were selected that spanned 17 different countries and were published up until July 1, 2023.
  • A random-effects model was applied to derive the rate of T. gondii infection in equids (horse family animals).

Results and Findings

  • The global infection rate of T. gondii in equids was calculated to be 15.0%.
  • Across continents, Africa had the highest infection rate at 25.5% while North America had the lowest at 8.4%.
  • Infection rates were notably higher after 2016 (24.0%) as compared to rates before 2016 (14.6%).
  • Among equids, animals in the 5 to 10-year-old age group were found to have the highest infection rate of 20.3%.
  • On comparing types of equids, donkeys had the highest infection rate at 23.4% which was higher than horses (15.8%) and mules (16.8%).
  • In terms of gender, female equids had a higher infection rate (17.5%) compared to males (13.9%).

Conclusion

  • The study reveals that T. gondii is widely prevalent among equine animals globally, thus posing a potential infection risk to humans and economic resources associated with these animals.
  • The authors stress the importance of continuous monitoring of toxoplasmosis infection rates and the control of T. gondii transmission for the sake of economy and public health.

Cite This Article

APA
Ye T, Li XM, Tan WX, Wang CL, Jiang J, Zhao Q. (2025). Seroprevalence of Toxoplasma gondii in Equids: A Global Systematic Review and Meta-analysis. Acta Parasitol, 70(4), 167. https://doi.org/10.1007/s11686-025-01108-w

Publication

ISSN: 1896-1851
NlmUniqueID: 9301947
Country: Switzerland
Language: English
Volume: 70
Issue: 4
Pages: 167

Researcher Affiliations

Ye, Tong
  • College of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, Jilin, People's Republic of China.
  • College of Life Science, Changchun Sci-Tech University, Shuangyang, 130600, Jilin, People's Republic of China.
Li, Xue-Min
  • College of Veterinary Medicine, Qingdao Agricultural University, Qingdao, 266109, Shandong, People's Republic of China.
Tan, Wen-Xu
  • College of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, Jilin, People's Republic of China.
  • College of Veterinary Medicine, Qingdao Agricultural University, Qingdao, 266109, Shandong, People's Republic of China.
Wang, Chuan-Long
  • College of Veterinary Medicine, Qingdao Agricultural University, Qingdao, 266109, Shandong, People's Republic of China.
Jiang, Jing
  • College of Life Science, Changchun Sci-Tech University, Shuangyang, 130600, Jilin, People's Republic of China. jiangjingxiaoyao@163.com.
Zhao, Quan
  • College of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, Jilin, People's Republic of China. zhaoquan0825@163.com.

MeSH Terms

  • Animals
  • Toxoplasmosis, Animal / epidemiology
  • Toxoplasmosis, Animal / parasitology
  • Seroepidemiologic Studies
  • Toxoplasma / immunology
  • Equidae / parasitology
  • Horses / parasitology
  • Horse Diseases / epidemiology
  • Horse Diseases / parasitology
  • Antibodies, Protozoan / blood
  • Female
  • Male
  • Global Health

Conflict of Interest Statement

Declarations. Conflict of interest: The authors have no conflicts of interest to declare. Ethical approval and consent to participate: Not applicable. Consent for publication: Not applicable.

References

This article includes 68 references
  1. Bigal E, Morick D, Scheinin AP, Salant H, Berkowitz A, King R, Levy Y, Melero M, Sánchez-Vizcaíno JM, Goffman O, Hadar N, Roditi-Elasar M, Tchernov D. Detection of Toxoplasma gondii in three common bottlenose dolphins (Tursiops truncatus); a first description from the Eastern Mediterranean Sea. Vet Parasitol 258:74–78.
    doi: 10.1016/j.vetpar.2018.06.009pubmed: 30105982google scholar: lookup
  2. Robert-Gangneux F, Dardé ML. Epidemiology of and diagnostic strategies for toxoplasmosis. Clin Microbiol Rev 25:264–296.
    doi: 10.1128/CMR.05013-11pubmed: 22491772pmc: 3346298google scholar: lookup
  3. Dubey JP. Toxoplasmosis of animals and humans. CRC Press, Boca Raton .
  4. Wang JL, Zhou DH, Chen J, Liu GX, Pu WB, Liu TY, Qin SY, Yin MY, Zhu XQ. The prevalence of antibodies to Toxoplasma gondii in horses in Changji Hui Autonomous Prefecture, Xinjiang, northwestern China. Rev Bras Parasitol Vet 24:298–302.
    doi: 10.1590/S1984-29612015050pubmed: 26331867google scholar: lookup
  5. Zhou P, Chen Z, Li HL, Zheng H, He S, Lin RQ, Zhu XQ. Toxoplasma gondii infection in humans in China. Parasites Vectors 4:165.
    doi: 10.1186/1756-3305-4-165pubmed: 21864327pmc: 3174123google scholar: lookup
  6. Ghazy AA, Shaapan RM, Abdel-Rahman EH. Comparative serological diagnosis of toxoplasmosis in horses using locally isolated Toxoplasma gondii. Vet Parasitol 145:31–36.
    doi: 10.1016/j.vetpar.2006.11.010pubmed: 17174034google scholar: lookup
  7. Pomares C, Ajzenberg D, Bornard L, Bernardin G, Hasseine L, Darde ML, Marty P. Toxoplasmosis and horse meat, France. Emerg Infect Dis 17:1327–1328.
    doi: 10.3201/eid1707.101642M.Jpubmed: 21762609pmc: 3381409google scholar: lookup
  8. Pomares C, Ajzenberg D, Bornard L, Bernardin G, Hasseine L, Darde ML, Marty P. Toxoplasmosis and horse meat, France. Emerg Infect Dis 17:1327–1328.
    doi: 10.3201/eid1707.101642pubmed: 21762609pmc: 3381409google scholar: lookup
  9. Munn Z, Moola S, Lisy K, Riitano D, Tufanaru C. Methodological guidance for systematic reviews of observational epidemiological studies reporting prevalence and cumulative incidence data. Jbi Evid Implement 13:147–153.
  10. Porritt K, Gomersall J, Lockwood C. JBI’s systematic reviews: study selection and critical appraisal. AJN Am J Nurs 114:47–52.
    pubmed: 24869584
  11. Viechtbauer W. Conducting meta-analyses in R with the metafor Package. J Stat Softw 36:1–48.
    doi: 10.18637/jss.v036.i03google scholar: lookup
  12. Balduzzi S, Rücker G, Schwarzer G. How to perform a meta-analysis with R: a practical tutorial. BMJ Ment Health 22:153–160.
  13. Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ 327:557–560.
    pubmed: 12958120pmc: 192859
  14. Egger M, Smith GD, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ 315:629–634.
    pubmed: 9310563pmc: 2127453
  15. Boughattas S, Bergaoui R, Essid R, Aoun K, Bouratbine A. Seroprevalence of Toxoplasma gondii infection among horses in Tunisia. Parasites Vectors 4:218.
    doi: 10.1186/1756-3305-4-218pubmed: 22107730pmc: 3253060google scholar: lookup
  16. Mohamed-Cherif A, Ait-Oudhia K, Khelef D. Detection of anti-Toxoplasma gondii antibodies among horses (Equus caballus) and donkeys (Equus asinus) in Tiaret province, northwestern Algeria. Rev Med Vet-Toulouse 166:271–274.
  17. Fereig RM, Mahmoud HYAH, Mohamed SGA, AbouLaila MR, Abdel-Wahab A, Osman SA, Zidan SA, El-Khodary SA, Mohamed AEA, Nishikawa Y. Seroprevalence and epidemiology of Toxoplasma gondii in farm animals in different regions of Egypt. Vet Parasitol Reg Stud Rep 3–4:1–6.
  18. Bártová E, Sedlák K, Kobédová K, Budíková M, Joel AY, Kamani J. Seroprevalence and risk factors of Neospora spp. and Toxoplasma gondii infections among horses and donkeys in Nigeria, West Africa. Acta Parasitol 62:606–609.
    doi: 10.1515/ap-2017-0073pubmed: 28682771google scholar: lookup
  19. Ouslimani SF, Tennah S, Azzag N, Derdour SY, China B, Ghalmi F. Seroepidemiological study of the exposure to Toxoplasma gondii among horses in Algeria and analysis of risk factors. Vet World 12:2007–2016.
  20. Amairia S, Jbeli M, Mrabet S, Mahjoubi Jebabli L, Gharbi M. Molecular Prevalence of Sarcocystis spp. and Toxoplasma gondii in Slaughtered Equids in Northern Tunisia. J Equine Vet Sci 129:104894.
    doi: 10.1016/j.jevs.2023.104894pubmed: 37506984google scholar: lookup
  21. Yuan WY, Ma K, Yang HL. Surveys of Toxoplasma Ifections in animals in Hebei Province. CJSC 16:72 (in Chinese).
  22. Chen CY. Epidemiological survey of toxoplasmosis in domestic animals in Chase County. QJAVS 38:23.
  23. Ma GB, Ma LQ, Wang GP, Lu Y, Cai QG, Ye CY, Niu XY. Serolgical detection of toxoplasmosis in animals of Qinghai province. CJVS 41:25–26 (in Chinese).
  24. Miao Q, Wang X, She LN, Fan YT, Yuan FZ, Yang JF, Zhu XQ, Zou FC. Seroprevalence of Toxoplasma gondii in horses and donkeys in Yunnan Province, Southwestern China. Parasites Vectors 6:168.
    doi: 10.1186/1756-3305-6-168pubmed: 23742078pmc: 3679964google scholar: lookup
  25. Wang DW, Han XH, Mu MY, Yuan GM, Zhang GX, He JB, Na Y, Li HK. Epidemiological survey of toxoplasmasis in some animals from northeastern China. HASVM .
  26. Saqib M, Hussain MH, Sajid MS, Mansoor MK, Asi MN, Fadya AA, Zohaib A, Sial AUR, Muhammad G, Ullah I. Sero-epidemiology of equine toxoplasmosis using a latex agglutination test in the three metropolises of Punjab, Pakistan. Trop Biomed 32:276–285.
    pubmed: 26691256
  27. Tavalla M, Sabaghan M, Abdizadeh R, Khademvatan S, Rafiei A, Piranshahi AR. Seroprevalence of Toxoplasma gondii and Neospora spp. Infections in Arab Horses, Southwest of Iran. Jundishapur J Microbiol .
    doi: 10.5812/jjm.14939pubmed: 25861441pmc: 4386078google scholar: lookup
  28. Masatani T, Takashima Y, Takasu M, Matsuu A, Amaya T. Prevalence of anti-Toxoplasma gondii antibody in domestic horses in Japan. Parasitol Int 65:146–150.
    doi: 10.1016/j.parint.2015.11.006pubmed: 26593178google scholar: lookup
  29. Xing H, Xu L, Song X, Li X, Yan R. Seroprevalence of Toxoplasma gondii and Trichinella spiralis in Horses in Xinjiang, Northwestern China. J Equine Vet Sci 60:11–15.
  30. Meng QF, Li D, Yao GZ, Zou Y, Cong W, Shan XF. Seroprevalence of Toxoplasma gondii infection and variables associated with seropositivity in donkeys in eastern China. Parasite 25:66.
    doi: 10.1051/parasite/2018066pubmed: 30526821pmc: 6289070google scholar: lookup
  31. Zhao S, Wang N, Xie S, Wang H, Zhang S, Zhang X, Li H, Jia L. Molecular epidemiological survey of toxoplasmosis in horses from Jilin Province, China. CJVS 40:1791–1795.
  32. Chen L, Zhao Z, Meng Q. Detection of specific IgG-antibodies against Toxoplasma gondii in the serum and milk of domestic donkeys during lactation in China: a potential public health concern. Front Cell Infect Microbiol 11:760400.
    pubmed: 34746030pmc: 8566817
  33. Zhang YF, Duan BF, Guan SJ, Yang JF, Zou FC, Dong GD, Zhai GL. Serological investigation on toxoplasma infections of equus animals in some areas of Yunnan province. Prog Vet Med 43:135–137.
  34. Kouam MK, Diakou A, Kanzoura V, Papadopoulos E, Gajadhar AA, Theodoropoulos G. A seroepidemiological study of exposure to Toxoplasma, Leishmania, Echinococcus and Trichinella in equids in Greece and analysis of risk factors. Vet Parasitol 170:170–175.
    doi: 10.1016/j.vetpar.2010.02.004pubmed: 20197215google scholar: lookup
  35. Lopes AP, Sousa S, Dubey JP, Ribeiro AJ, Silvestre R, Cotovio M, Schallig HD, Cardoso L, Cordeiro-da-Silva A. Prevalence of antibodies to Leishmania infantum and Toxoplasma gondii in horses from the north of Portugal. Parasites Vectors 6:178.
    doi: 10.1186/1756-3305-6-178pubmed: 23773870pmc: 3686701google scholar: lookup
  36. Papini RA, Buzzone G, Nardoni S, Rocchigiani G, Mancianti F. Seroprevalence and genotyping of Toxoplasma gondii in horses slaughtered for human consumption in Italy. J Equine Vet Sci 35:657–661.
  37. Rodrigues FT, Pereira C, Dubey JP, Nóvoa M, Quaresma M, Schallig H, Cardoso L, Lopes AP. Seroprevalence of Toxoplasma gondii and Leishmania spp. in domestic donkeys from Portugal. Rev Bras Parasitol Vet 28:172–176.
    doi: 10.1590/S1984-296120180091pubmed: 30892383google scholar: lookup
  38. Cano-Terriza D, Franco JJ, Jose-Cunilleras E, Buono F, Almeria S, Veneziano V, Alguacil E, Garcia J, Villena I, Dubey JP, Jimenez-Martin D, Garcia-Bocanegra I. Seroepidemiological study of Toxoplasma gondii in equids in different European countries. Zoonoses Public Health 70:276–283.
    doi: 10.1111/zph.13026pubmed: 36688475google scholar: lookup
  39. Dubey JP, Ness SL, Kwok OC, Choudhary S, Mittel LD, Divers TJ. Seropositivity of Toxoplasma gondii in domestic donkeys (Equus asinus) and isolation of T. gondii from farm cats. Vet Parasitol 199:18–23.
    doi: 10.1016/j.vetpar.2013.09.027pubmed: 24140163google scholar: lookup
  40. Alvarado-Esquivel C, Alvarado-Esquivel D, Dubey JP. Prevalence of Toxoplasma gondii antibodies in domestic donkeys (Equus asinus) in Durango, Mexico slaughtered for human consumption. BMC Vet Res 11:6.
    doi: 10.1186/s12917-015-0325-9pubmed: 25595816pmc: 4301930google scholar: lookup
  41. Cazarotto CJ, Balzan A, Grosskopf RK, Boito JP, Portella LP, Vogel FF, Fávero JF, de Cucco D, Biazus AH, Machado G, Da Silva AS. Horses seropositive for Toxoplasma gondii, Sarcocystis spp. and Neospora spp.: Possible risk factors for infection in Brazil. Microb Pathog 99:30–35.
    doi: 10.1016/j.micpath.2016.07.016pubmed: 27475033google scholar: lookup
  42. Venturi SS, Da Silva AF, Frazão-Teixeira E, de Oliveira FCR, Consalter A, Padilha FGF, Fonseca ABM, Ferreira AMR. Characterization of the zoonotic potential of Toxoplasma gondii in horses from Rio de Janeiro State. Acta Trop 171:159–162.
  43. Moreira TR, Sarturi C, Stelmachtchuk FN, Andersson E, Norlander E, de Oliveira F, Machado PJ, Marcili A, Emanuelson U, Gennari SM, Minervino A. Prevalence of antibodies against Toxoplasma gondii and Neospora spp. in equids of Western Pará, Brazil. Acta Trop 189:39–45.
  44. Dubey JP. Toxoplasma gondii oocyst survival under defined temperatures. J Parasitol 862–865.
  45. Alvarado-Esquivel C, Rodriguez-Pena S, Villena I, Dubey JP. Seroepidemiological survey of toxoplasmosis in domestic horses in Durango State, Mexico. J Parasitol 98:944–945.
    doi: 10.1645/GE-3174.1pubmed: 22559329google scholar: lookup
  46. Du F, Feng HL, Nie H, Tu P, Zhang QL, Hu M, Zhou YQ, Zhao JL. Survey on the contamination of Toxoplasma gondii oocysts in the soil of public parks of Wuhan, China. Vet Parasitol 184:141–146.
    pubmed: 21906882
  47. Wang YB, Yang XD, Yang GR. Progress in research of toxoplasmosis. China Tropical Medicine .
  48. Dubey JP. Strategies to reduce transmission of Toxoplasma gondii to animals and humans. Vet Parasitol 64:65–70.
    doi: 10.1016/0304-4017(96)00961-2pubmed: 8893464google scholar: lookup
  49. Lélu M, Villena I, Dardé M, Aubert D, Geers R, Dupuis E, Marnef F, Poulle M, Gotteland C, Dumètre A. Quantitative estimation of the viability of Toxoplasma gondii oocysts in soil. Appl Environ Microbiol 78:5127–5132.
    pubmed: 22582074pmc: 3416395
  50. Shapiro K, Bahia-Oliveira L, Dixon B, Dumètre A, de Wit LA, VanWormer E, Villena I. Environmental transmission of Toxoplasma gondii: Oocysts in water, soil and food. Food Waterborne Parasitol 15:e49.
  51. Liu Q, Ma R, Zhao Q, Shang L, Cai J, Wang X, Li J, Hu G, Jin H, Gao H. Seroprevalence of Toxoplasma gondii infection in Tibetan sheep in northwestern China. J Parasitol 96:1222–1223.
    pubmed: 21158639
  52. Munhoz AD, Souza MA, Costa S, Freitas JS, Silva A, Lacerda LC, Cruz R, Albuquerque GR, Pereira M. Factors associated with the distribution of natural Toxoplasma gondii infection among equids in Northeastern Brazil. Rev Bras Parasitol Vet 28:283–290.
    doi: 10.1590/S1984-29612019035pubmed: 31215612google scholar: lookup
  53. Fernando P, Starkey P. Donkeys and development: socio-economic issues in the use and management of donkeys. Donkeys, People and Development: A Resource Book of the Animal Traction Network for Eastern and Southern Africa (ATNESA). Proceedings of the ATNESA Workshop, Debre Zeit, Ethiopia pp 5–9.
  54. García-Bocanegra I, Cabezón O, Arenas-Montes A, Carbonero A, Dubey JP, Perea A, Almería S. Seroprevalence of Toxoplasma gondii in equids from Southern Spain. Parasitol Int 61:421–424.
    pubmed: 22366344
  55. Belluco S, Simonato G, Mancin M, Pietrobelli M, Ricci A. Toxoplasma gondii infection and food consumption: a systematic review and meta-analysis of case-controlled studies. Crit Rev Food Sci 58:3085–3096.
  56. Kapperud G, Jenum PA, Stray-Pedersen B, Melby KK, Eskild A, Eng J. Risk factors for Toxoplasma gondii infection in pregnancy: results of a prospective case-control study in Norway. Am J Epidemiol 144:405–412.
    pubmed: 8712198
  57. Tao Q, Wang Z, Feng H, Fang R, Nie H, Hu M, Zhou Y, Zhao J. Seroprevalence and risk factors for Toxoplasma gondii infection on pig farms in central China. J Parasitol 97:262–264.
    pubmed: 21506784
  58. Tonouhewa AB, Akpo Y, Sessou P, Adoligbe C, Yessinou E, Hounmanou YG, Assogba MN, Youssao I, Farougou S. Toxoplasma gondii infection in meat animals from Africa: systematic review and meta-analysis of sero-epidemiological studies. Vet World 10:194–208.
    doi: 10.14202/vetworld.2017.194-208pubmed: 28344403pmc: 5352845google scholar: lookup
  59. Chen L, Zhao ZJ, Meng QF. Detection of specific IgG-antibodies against Toxoplasma gondii in the serum and milk of domestic donkeys during lactation in China: a potential public health concern. Front Cell Infect Microbiol 11:760400.
    doi: 10.3389/fcimb.2021.760400pubmed: 34746030pmc: 8566817google scholar: lookup
  60. Fanelli A, Battisti E, Zanet S, Trisciuoglio A, Ferroglio E. A systematic review and meta-analysis of Toxoplasma gondii in roe deer (Capreolus capreolus ) and red deer (Cervus elaphus ) in Europe. Zoonoses Public Health 68:182–193.
    doi: 10.1111/zph.12780pubmed: 33164352google scholar: lookup
  61. Lopes AP, Dubey JP, Dardé ML, Cardoso L. Epidemiological review of Toxoplasma gondii infection in humans and animals in Portugal. Parasitology 141:1699–1708.
    doi: 10.1017/S0031182014001413pubmed: 25215422google scholar: lookup
  62. Montoya JG, Liesenfeld O. Toxoplasmosis. Lancet 363:1965–1976.
    doi: 10.1016/S0140-6736(04)16412-Xpubmed: 15194258google scholar: lookup
  63. Machacova T, Bartova E, Di Loria A, Sedlak K, Mariani U, Fusco G, Fulgione D, Veneziano V, Dubey JP. Seroprevalence of Toxoplasma gondii in donkeys (Equus asinus) in Italy. J Vet Med Sci 76:265–267.
    pubmed: 24107428
  64. Ribeiro MJ, Rosa MH, Bruhn FR, Garcia AM, Rocha CM, Guimarães AM. Seroepidemiology of Sarcocystis neurona, Toxoplasma gondii and Neospora spp. among horses in the south of the state of Minas Gerais, Brazil. Rev Bras Parasitol Vet 25:142–150.
    doi: 10.1590/S1984-29612016029pubmed: 27334814google scholar: lookup
  65. Liu Q, Jin HT. Toxoplasma gondii infection and its control in pets. Chin J Comp Med .
  66. Dubey JP, Cerqueira-Cézar CK, Murata FHA, Kwok OCH, Yang YR, Su C. All about toxoplasmosis in cats: the last decade. Vet Parasitol 283:109145.
    doi: 10.1016/j.vetpar.2020.109145pubmed: 32645556google scholar: lookup
  67. Ahmed SM, Ibrahim AM, Alshafie NK, Mohammed RH, Ismail AA, Angara TEE. The first report on sero-prevalence of Toxoplasma gondii in working horses and donkeys in the Sudan. J Life Sci 7:1284–1287.
  68. Li X, Ni H, Ren W, Jiang J, Gong Q, Zhang X. Seroprevalence of Toxoplasma gondii in horses: a global systematic review and meta-analysis. Acta Trop 201:105222.
    pubmed: 31639325

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