Theileria

Theileria
Kinete stage of Theileria parva in the transmitting tick Rhipicephalus appendiculatus
Scientific classification
Domain: Eukaryota
Clade: Sar
Clade: Alveolata
Phylum: Apicomplexa
Class: Aconoidasida
Order: Piroplasmida
Family: Theileriidae
Genus: Theileria
Bettencourt, França & Borges, 1907
Species

Theileria annulata
Theileria electrophori
Theileria equi
Theileria microti
Theileria orientalis
Theileria parva

Synonyms[1]
  • Haematoxenus Uilenberg, 1964
  • Cytauxzoon Neitz & Thomas, 1948
  • Gonderia Toit, 1918

Theileria is a genus of parasites that belongs to the phylum Apicomplexa, and is closely related to Plasmodium. Two Theileria species, T. annulata and T. parva, are important cattle parasites.[2] T. annulata causes tropical theileriosis and T. parva causes East Coast fever. Theileria species are transmitted by ticks.[3] The genomes of T. orientalis Shintoku[4], Theileria equi WA,[5] Theileria annulata Ankara[6] and Theileria parva Muguga[7] have been sequenced and published.

Theileria equi infects equid blood cells causing equine piroplasmosis.[8] The disease presents with a variety of clinical conditions, such as fever, depression, jaundice, cramps, haemolytic anaemia, hemoglobinuria and even death, but asymptomatic infections are frequently observed.[9] The most common vectors are the ticks Dermacentor nitens and Rhipicephalus microplus[10] but Amblyomma cajennense was also implicated in the disease transmission.[11]

Vaccines against Theileria are in development.[2][12] In May 2010, a vaccine that was reported to protect cattle against East Coast fever had been approved and registered by the governments of Kenya, Malawi, and Tanzania.[13]

Description

Species in this genus undergo exoerythrocytic merogony in the lymphocytes, histiocytes, erythroblasts, and other cells of the internal organs. This is followed by invasion of the erythrocytes by the merozoites, which may or may not reproduce. When merogony does occur, no more than four daughter cells are produced. The frequent occurrence of elongated bacillary or "bayonet" forms within the erythrocyte is considered as characteristic of this genus.

The organism is transmitted by various tick species, including Rhipicephalus, Dermacentor, and Haemaphysalis. The organism reproduces in the tick as it progresses through its life stages.[14] Both T. annulata and T. parva induce transformation of infected cells of lymphocyte or macrophage/monocyte lineages. T. orientalis does not induce uncontrolled proliferation of infected leukocytes and instead multiplies predominantly within infected erythrocytes.

Following infection with Theileria equi, horses may develop detectable antibodies, with seroprevalence varying widely across regions. Serological surveys have revealed a high prevalence of T. equi antibodies in horses and other equids, including 39.8% in Central-Southern Italy[15] and 33.4% in Northern Brazil.[16]

Genomics

The genomes of T. orientalis Shintoku[4], Theileria equi WA,[5] Theileria annulata Ankara[6] and Theileria parva Muguga[7] have been sequenced. Genomic data can be accessed though PiroplasmaDB which is part of the Eukaryotic Pathogen Database).[17]

Evolution

The genus is thought to have first appeared in ruminants during the Miocene. It is named for parasitologist Gertrud Theiler, daughter of Arnold Theiler.

Transmission

Theileria spp. can be transmitted to cattle through tick bites, including the brown ear tick, a Rhipicephalus sp.

Important species

Treatment

  • Buparvaquone is a promising compound for the therapy and prophylaxis of all forms of theileriosis.


One Health and emerging significance in North America

In North America, Theileria orientalis (specifically the virulent Ikeda genotype) has emerged as a significant One Health challenge, representing a complex intersection of invasive species biology, agricultural stability, and wildlife livestock interfaces. Since its first detection in a Virginia cow-calf herd in 2017, the parasite has undergone a rapid geographical expansion across the United States. As of early 2026, the Ikeda genotype has been confirmed in at least 25 states, including recent expansions into Missouri, where it is considered endemic in over half of the state's counties, as well as first-time detections in Ontario, Canada in late 2025. [19][20]

Invasive vector and wildlife interface

The primary driver of this emergence is the invasive Asian longhorned tick (Haemaphysalis longicornis). This vector is uniquely suited for rapid dispersal due to its parthenogenetic nature, allowing a single asexual female to establish a massive localized population without a mate. [21] While the disease primarily impacts cattle, the "Animal" pillar of the One Health triad extends to wildlife; 2026 studies have detected T. orientalis Ikeda DNA in ticks collected from various non-bovine hosts, including raccoons, opossums, and domestic cats. [22] Although clinical disease has not been documented in these wildlife species, they facilitate the spread of the vector across fragmented landscapes.

Economic and Public Health impact

Although T. orientalis Ikeda does not currently pose a direct infection risk to humans, it significantly impacts human well-being through threats to food security and agricultural economics. In newly affected regions, naive cattle herds can experience mortality rates of up to 5%, while surviving animals often suffer from chronic anemia, reduced weight gain, and late-term abortions. [23] The lack of an FDA-approved treatment or vaccine in the United States as of 2026 has forced a management shift toward aggressive tick suppression and biosecurity, with annual industry losses estimated in the millions of dollars. [24]

References

  1. ^ "Theileria Bettencourt, França & Borges, 1907". Catalogue of Life. Species 2000: Leiden, the Netherlands. Retrieved 12 February 2026.
  2. ^ a b Morrison W, McKeever D (2006). "Current status of vaccine development against Theileria parasites". Parasitology. 133: S169–87. doi:10.1017/S0031182006001867. PMID 17274845. S2CID 928055.
  3. ^ Florin-Christensen, M.; Schnittger, L. (Jan 2009). "Piroplasmids and ticks: a long-lasting intimate relationship". Frontiers in Bioscience. 14 (14): 3064–3073. doi:10.2741/3435. ISSN 1093-9946. PMID 19273257.
  4. ^ a b Hayashida K, Hara Y, Abe T, Yamasaki C, Toyoda A, Kosuge T, Suzuki Y, Sato Y, Kawashima S, Katayama T, Wakaguri H, Inoue N, Homma K, Tada-Umezaki M, Yagi Y, Fujii Y, Habara T, Kanehisa M, Watanabe H, Ito K, Gojobori T, Sugawara H, Imanishi T, Weir W, Gardner M, Pain A, Shiels B, Hattori M, Nene V, Sugimoto C (2012). "Comparative genome analysis of three eukaryotic parasites with differing abilities to transform leukocytes reveals key mediators of Theileria-induced leukocyte transformation". mBio. 3 (5): e00204–12. doi:10.1128/mBio.00204-12. PMC 3445966. PMID 22951932.
  5. ^ a b Kappmeyer, Lowell S.; Thiagarajan, Mathangi; Herndon, David R.; Ramsay, Joshua D.; Caler, Elisabet; Djikeng, Appolinaire; Gillespie, Joseph J.; Lau, Audrey OT; Roalson, Eric H. (2012-01-01). "Comparative genomic analysis and phylogenetic position of Theileria equi". BMC Genomics. 13 603. doi:10.1186/1471-2164-13-603. PMC 3505731. PMID 23137308.
  6. ^ a b Pain, Arnab; Renauld, Hubert; Berriman, Matthew; Murphy, Lee; Yeats, Corin A.; Weir, William; Kerhornou, Arnaud; Aslett, Martin; Bishop, Richard (2005-07-01). "Genome of the host-cell transforming parasite Theileria annulata compared with T. parva". Science. 309 (5731): 131–3. doi:10.1126/science.1110418. hdl:10568/33166. PMID 15994557. S2CID 34556923.
  7. ^ a b Gardner, Malcolm J.; Bishop, Richard; Shah, Trushar; de Villiers, Etienne P.; Carlton, Jane M.; Hall, Neil; Ren, Qinghu; Paulsen, Ian T.; Pain, Arnab (2005-07-01). "Genome sequence of Theileria parva, a bovine pathogen that transforms lymphocytes". Science. 309 (5731): 134–7. doi:10.1126/science.1110439. hdl:10568/33167. PMID 15994558. S2CID 37769438.
  8. ^ Mehlhorn, H.; Schein, E. (1998-05-01). "Redescription of Babesia equi Laveran, 1901 as Theileria equi Mehlhorn, Schein 1998". Parasitology Research. 84 (6): 467–475. doi:10.1007/s004360050431. ISSN 1432-1955.
  9. ^ Rothschild, Chantal M. (2013-07-01). "Equine Piroplasmosis". Journal of Equine Veterinary Science. 33 (7): 497–508. doi:10.1016/j.jevs.2013.03.189. ISSN 0737-0806.
  10. ^ de Waal, D. T. (1992-01-01). "Equine piroplasmosis: A review". British Veterinary Journal. 148 (1): 6–14. doi:10.1016/0007-1935(92)90061-5. ISSN 0007-1935.
  11. ^ Scoles, Glen A.; Hutcheson, H. Joel; Schlater, Jack L.; Hennager, Steven G.; Pelzel, Angela M.; Knowles, Don P. (October 2011). "Equine piroplasmosis associated with Amblyomma cajennense Ticks, Texas, USA". Emerging Infectious Diseases. 17 (10): 1903–1905. doi:10.3201/eid1710.101182. ISSN 1080-6059. PMC 3310643. PMID 22000367.
  12. ^ Darghouth, A. (Dec 2008). "Review on the experience with live attenuated vaccines against tropical theileriosis in Tunisia: considerations for the present and implications for the future". Vaccine. 26. Suppl 6: G4–G10. doi:10.1016/j.vaccine.2008.09.065. ISSN 0264-410X. PMID 19178892.
  13. ^ "Cattle disease vaccine launched 30 years after invention". 2010-05-07. SciDev.net (7 May 2010).
  14. ^ a b c d *Theileria reviewed and published by WikiVet, accessed 11 October 2011.
  15. ^ Bartolomé Del Pino, Leticia Elisa; Roberto, Nardini; Vincenzo, Veneziano; Francesca, Iacoponi; Antonella, Cersini; Luca, Autorino Gian; Francesco, Buono; Teresa, Scicluna Maria (2016-04-01). "Babesia caballi and Theileria equi infections in horses in Central-Southern Italy: Sero-molecular survey and associated risk factors". Ticks and Tick-borne Diseases. 7 (3): 462–469. doi:10.1016/j.ttbdis.2016.01.011. ISSN 1877-959X.
  16. ^ Minervino, Antonio Humberto Hamad; Torres, Allana Cavalcante; Moreira, Thiago Rocha; Vinholte, Brena Peleja; Sampaio, Bruna Matarucco; Bianchi, Daniela; Portela, Juliana Machado; Sarturi, Cristiane; Marcili, Arlei; Barrêto Júnior, Raimundo Alvês; Gennari, Solange Maria; Machado, Rosangela Zacarias (2020). "Factors associated with the prevalence of antibodies against Theileria equi in equids of Western Pará, Brazil". Transboundary and Emerging Diseases. 67 (S2): 100–105. doi:10.1111/tbed.13268. ISSN 1865-1682.
  17. ^ Harb, Omar S.; Roos, David S. (2015-01-01). "The Eukaryotic Pathogen Databases: A Functional Genomic Resource Integrating Data from Human and Veterinary Parasites". Parasite Genomics Protocols. Methods in Molecular Biology. Vol. 1201. pp. 1–18. doi:10.1007/978-1-4939-1438-8_1. ISBN 978-1-4939-1437-1. PMC 6157018. PMID 25388105.
  18. ^ Mehlhorn, Heinz; Schein, Eberhard (1998). "Redescription of Babesia equi Laveran, 1901 as Theileria equi Mehlhorn, Schein 1998". Parasitology Research. 84 (6): 467–475. doi:10.1007/s004360050431. PMID 9660136. S2CID 27992280. Retrieved June 19, 2020.
  19. ^ Carrico, J. (2026-03-01). "New Tick Borne Cattle Disease Spreads in the US". DTN Progressive Farmer.
  20. ^ "Canada confirms its first case of Theileria orientalis Ikeda in dairy cattle in Ontario". BEACON. 2025-10-24.
  21. ^ Loftin, K. (2026-02-17). "Bovine Theileriosis Update – February 2026" (PDF). University of Arkansas System Division of Agriculture.
  22. ^ Butler, R.A.; Muller, L.I. (2026). "Retrospective discovery of Theileria orientalis Ikeda in Haemaphysalis longicornis Neumann ticks on a cow-calf farm in Tennessee (US)". Frontiers in Veterinary Science. 13. doi:10.3389/fvets.2026.1770304.
  23. ^ "K-State experts monitoring Asian longhorned tick presence in Kansas". Kansas State University. 2025-10-13.
  24. ^ Payne, C. (2025). "Active surveillance for Theileria orientalis and the invasive Asian longhorned tick in Missouri". PMC. 11960879.