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Topic:Theileria equi

Theileria equi is a protozoan parasite that infects horses, causing a disease known as equine piroplasmosis. This parasite is transmitted primarily through tick bites, with species such as Rhipicephalus and Dermacentor acting as vectors. The infection can lead to a range of clinical signs in horses, including fever, anemia, jaundice, and lethargy. Infected horses may also exhibit decreased performance and, in severe cases, death. Diagnosis of Theileria equi involves blood tests, including polymerase chain reaction (PCR) assays and serological methods, to detect the presence of the parasite or antibodies. This page compiles peer-reviewed research studies and scholarly articles that explore the transmission, pathogenesis, diagnosis, and management of Theileria equi in equine populations.
Clotrimazole, ketoconazole, and clodinafop-propargyl as potent growth inhibitors of equine Babesia parasites during in vitro culture.
The Journal of parasitology    July 26, 2003   Volume 89, Issue 3 604-606 doi: 10.1645/0022-3395(2003)089[0604:CKACAP]2.0.CO;2
Bork S, Yokoyama N, Matsuo T, Claveria FG, Fujisaki K, Igarashi I.The antifungal agents clotrimazole (CLT) and ketoconazole (KC) and the herbicide clodinafop-propargyl (CP) inhibit growth of Plasmodium sp., Toxoplasma sp., and Trypanosoma sp. In the present study, we evaluated these drugs against the in vitro growth of the equine protozoan parasites Babesia equi and B. caballi. Clotrimazole (IC50: 2 and 17 microM), KC (IC50: 6 and 22 microM), and CP (IC50: 450 and 354 microM) were effective growth inhibitors. Interestingly, intraerythrocytic KC-treated Babesia sp. were observed to be in immediate contact with the plasma fraction of the blood in electron micr...
A field evaluation of PCR for the routine detection of Babesia equi in horses.
Veterinary parasitology    June 5, 2003   Volume 114, Issue 2 81-87 doi: 10.1016/s0304-4017(03)00129-8
Rampersad J, Cesar E, Campbell MD, Samlal M, Ammons D.We report on a study that evaluated the usefulness of PCR for the routine detection of Babesia equi in horses. The blood from a total of 105 horses comprising both sick and apparently healthy animals were examined for the presence of B. equi using both Wright-Giemsa-stained blood smears and PCR. Microscopic analysis of Giemsa-stained blood smears revealed 10/105 animals positive for Babesia, compared to 16/105 for the primary PCR and 36/105 for the nested PCR. Three of the 10 samples positive by Wright-Giemsa-stain were negative by PCR for B. equi. However, evidence is presented that these sam...
High-level expression and purification of a truncated merozoite antigen-2 of Babesia equi in Escherichia coli and its potential for immunodiagnosis.
Journal of clinical microbiology    March 8, 2003   Volume 41, Issue 3 1147-1151 doi: 10.1128/JCM.41.3.1147-1151.2003
Huang X, Xuan X, Yokoyama N, Xu L, Suzuki H, Sugimoto C, Nagasawa H, Fujisaki K, Igarashi I.The gene encoding a truncated merozoite antigen-2 (EMA-2t) of Babesia equi was cloned and highly expressed in Escherichia coli as a glutathione S-transferase fusion protein (G-rEMA-2t). Both G-rEMA-2t and rEMA-2t (after the removal of glutathione S-transferase) had good antigenicity. Either Western blot analysis with rEMA-2t or enzyme-linked immunosorbent assay (ELISA) with G-rEMA-2t clearly discriminated the sera of horses experimentally infected with B. equi from sera of horses infected with Babesia caballi and healthy horses, although rEMA-2t was not suitable for ELISA, probably owing to it...
Standardisation and comparison of serial dilution and single dilution enzyme linked immunosorbent assay (ELISA) using different antigenic preparations of the Babesia (Theileria) equi parasite.
Veterinary research    February 18, 2003   Volume 34, Issue 1 71-83 doi: 10.1051/vetres:2002055
Kumar S, Kumar Y, Malhotra DV, Dhar S, Nichani AK.Serial dilution and single dilution enzyme linked immunosorbent assays (ELISA) were standardised and their sensitivity and specificity were compared for serodiagnosis of Babesia equi infection. The antibody titres of 24 donkey sera of known identity were determined separately by serial dilution ELISA using three different B. equi antigens namely whole merozoite (WM), cell membrane (CM) and high speed supernatant (HSS). The ratios of the optical density (OD) of known positive and known negative sera at different serum dilutions were calculated and termed as the positive/negative (P/N) ratio. Th...
Identification of a specific antigenic region of the P82 protein of Babesia equi and its potential use in serodiagnosis.
Journal of clinical microbiology    February 8, 2003   Volume 41, Issue 2 547-551 doi: 10.1128/JCM.41.2.547-551.2003
Hirata H, Xuan X, Yokoyama N, Nishikawa Y, Fujisaki K, Suzuki N, Igarashi I.The efficacy of the Be82 gene product fused with glutathione S-transferase (GST/Be82) in an enzyme-linked immunosorbent assay (ELISA) for the diagnosis of Babesia equi infection was reported previously (H. Hirata et al., J. Clin. Microbiol. 40:1470-1474, 2002). However, the ELISA with the GST/Be82 antigen cross-reacted with Babesia caballi-infected horse sera, despite the high rate of detection of B. equi. These results suggested that GST/Be82 has an antigen in common with B. caballi or antigenicity similar to that of B. caballi. In the present study, we constructed a series of five clones wit...
In vitro isolation of equine piroplasms derived from Cape Mountain zebra (Equus zebra zebra) in South Africa.
The Onderstepoort journal of veterinary research    October 3, 2002   Volume 69, Issue 3 197-200 
Zweygarth E, Lopez-Rebollar LM, Meyer P.Twenty blood samples of zebras (Equus zebra zebra) from the Karoo National Park and the Bontebok National Park in South Africa, all seropositive for Theileria equi, were subjected to in vitro culture to identify carrier animals and to isolate the parasites. Sixteen animals had a detectable parasitaemia in Giemsa-stained blood smears examined before culture initiation, the remaining four animals were identified as T. equi carriers by in vitro culture. Cultures were initiated either in an oxygen-reduced gas mixture or in a 5% CO2-in-air atmosphere. Out of the 20 blood samples, 12 cultures of T. ...
Diagnosis of equine piroplasmosis in Xinjiang province of China by the enzyme-linked immunosorbent assays using recombinant antigens.
Veterinary parasitology    September 5, 2002   Volume 108, Issue 2 179-182 doi: 10.1016/s0304-4017(02)00193-0
Xuan X, Chahan B, Huang X, Yokoyama N, Makala LH, Igarashi I, Fujisaki K, Maruyama S, Sakai T, Mikami T.The prevalence of equine piroplasmosis in Xinjiang province, China, was examined by enzyme-linked immunosorbent assays (ELISAs). A total of 70 serum samples were taken from horses pastured on three farms in western Xinjiang, and examined for diagnosis of equine Babesia equi (B. equi) infection and B. caballi infection by ELISAs using recombinant equi merozoite antigen 1 (EMA-1) and recombinant P48 antigen, respectively. Of the 70 samples, 28 (40.0%) and 17 (24.3%) samples were positive for B. equi infection and B. caballi infection, respectively. In addition, 11 (15.7%) samples were positive f...
Culture, isolation and propagation of Babesia caballi from naturally infected horses.
Parasitology research    June 7, 2002   Volume 88, Issue 5 460-462 doi: 10.1007/s00436-002-0609-4
Zweygarth E, Lopez-Rebollar LM, Nurton J, Guthrie AJ.Thirteen blood samples of horses from South Africa, five of which were seropositive for Babesia caballi and eight for both B. caballi and Theileria equi, were subjected to in vitro culture to identify carrier animals. None of the animals had a detectable parasitaemia on Giemsa-stained blood smears before culture initiation. Cultures were initiated in L-cysteine-enriched medium, either in an oxygen-reduced gas mixture or in a 5% CO2-in-air atmosphere. All five animals seropositive for B. caballi were identified as carrier animals using an oxygen-reduced atmosphere, whereas only four samples bec...
Seroepidemiologic studies on Babesia caballi and Babesia equi infections in Japan.
The Journal of veterinary medical science    May 17, 2002   Volume 64, Issue 4 325-328 doi: 10.1292/jvms.64.325
Ikadai H, Nagai A, Xuan X, Igarashi I, Tsugihiko K, Tsuji N, Oyamada T, Suzuki N, Fujisaki K.Antibodies to Babesia caballi and Babesia equi were examined on a total of 2,019 horse serum samples that had been collected in 1971-1973 by the National Institute of Animal Health by enzyme-linked immunosorbent assay (ELISA) using recombinant proteins and by Western-blot analysis. Based on the criterion for positivity by ELISA, 5.4% (109/2,019) and 2.2% (44/2,019) had antibodies against B. caballi and B. equi, respectively. The ELISA-positive sera were further examined by Western blot; 30/109 for B. caballi and 2/ 44 for B. equi were positive for native B. caballi or B. equi, but none of them...
Detection of Babesia equi (Laveran, 1901) by nested polymerase chain reaction.
Veterinary parasitology    October 6, 2001   Volume 101, Issue 1 9-21 doi: 10.1016/s0304-4017(01)00471-x
Nicolaiewsky TB, Richter MF, Lunge VR, Cunha CW, Delagostin O, Ikuta N, Fonseca AS, da Silva SS, Ozaki LS.We describe a nested polymerase chain reaction (PCR) for the detection of Babesia equi in equine infected erythrocytes using oligonucleotides designed on the published sequence of a B. equi merozoite antigen gene (ema-1). A 102bp DNA fragment is specifically amplified from B. equi but not from Babesia caballi, Babesia bovis or Babesia bigemina DNA. In a mock infection we were able to detect down to six infected cells in 10(8) equine erythrocytes or to detect the parasite in blood with an equivalent parasitemia of 0.000006%. Furthermore, gene polymorphism was found by performing a PCR-RFLP (PCR...
Validation of a competitive enzyme-linked immunosorbent assay for diagnosing Babesia equi infections of Moroccan origin and its use in determining the seroprevalence of B. equi in Morocco. Rhalem A, Sahibi H, Lasri S, Johnson WC, Kappmeyer LS, Hamidouch A, Knowles DP, Goff WL.A highly specific and sensitive competitive enzyme-linked immunosorbent assay for detection of specific antibody to Babesia equi in serum from equids was validated for use in Morocco. The assay is based on the specific inhibition of binding of a monoclonal antibody to a conserved epitope within a recombinant parasite peptide by serum from infected animals. The assay was compared to an established indirect immunofluorescence assay, with a concordance of 91%. The assay was used to determine seroprevalence for B. equi infections in donkeys and horses throughout Morocco. A total of 578 sera (163 h...
Detection of antibodies to Babesia equi in horses by a latex agglutination test using recombinant EMA-1.
Clinical and diagnostic laboratory immunology    May 1, 2001   Volume 8, Issue 3 645-646 doi: 10.1128/CDLI.8.3.645-646.2001
Xuan X, Igarashi I, Tanaka T, Fukumoto S, Nagasawa H, Fujisaki K, Mikami T.A latex agglutination test (LAT) using recombinant equi merozoite antigen 1 (EMA-1) for the detection of antibodies to Babesia equi was developed. The LAT was able to differentiate very clearly between sera from B. equi-infected horses and sera from Babesia caballi-infected horses or from normal horses. The LAT results were identical to those of a previously developed enzyme-linked immunosorbent assay. These results indicate that LAT using recombinant EMA-1 might be very useful as a routine screening method for the diagnosis of B. equi infection.
Ehrlichial diseases.
The Veterinary clinics of North America. Equine practice    February 24, 2001   Volume 16, Issue 3 487-ix doi: 10.1016/s0749-0739(17)30091-3
Madigan JE, Pusterla N.Equine granulocytic and monocytic ehrlichiosis caused by Ehrlichia equi and E. risticii, respectively, are seasonal diseases in horses that occur throughout the United States E. equi is transmitted by lxodes ticks and causes high fever, depression, anorexia, limb edema, petechiation, icterus, ataxia, and stiffness in gait. E. risticii, also known as the agent of Potomac horse fever, causes a febrile illness with a colitis of variable severity. Its occurrence is associated with aquatic habitats. The natural route of transmission is oral, through the ingestion of E. risticii infected trematode s...
Tick-borne diseases of livestock in Italy: general review and results of recent studies carried out in the Apulia region.
Parassitologia    November 9, 2000   Volume 41 Suppl 1 25-29 
Ceci L, Carelli G.This paper reviews basic information on the knowledge of tick-borne diseases, babesiosis, anaplasmosis and theileriosis, in horses, cattle, sheep and goats in Italy with particular reference to the southern part of the country. It is stressed that there is limited knowledge about the parasite species present, their vectors, distribution, prevalence and impact on livestock production and there is the need to assess their epidemiology. A study carried out in the Apulia region to assess the prevalence of Anaplasma marginale infection in 1,648 cattle showed a seroprevalence of 17% using the Card A...
The beta-tubulin gene of Babesia and Theileria parasites is an informative marker for species discrimination.
International journal for parasitology    October 12, 2000   Volume 30, Issue 11 1181-1185 doi: 10.1016/s0020-7519(00)00105-3
Cacciò S, Cammà C, Onuma M, Severini C.A fragment of the beta-tubulin gene was polymerase chain reaction (PCR) amplified from genomic DNAs of Babesia bovis, Babesia bigemina, Babesia divergens, Babesia major, Babesia caballi, Babesia equi, Babesia microti, Theileria annulata and Theileria sergenti. Single amplification products were obtained for each of these species, but the size of the amplicons varied from 310 to 460 bp. Sequence analysis revealed that this variation is due to the presence of a single intron, which ranged from 20 to 170 bp. The extensive genetic variability at the beta-tubulin locus has been exploited to develop...
Temporary importation of Babesia and Ehrlichia seropositive horses into Australia.
Australian veterinary journal    August 3, 2000   Volume 78, Issue 7 469 doi: 10.1111/j.1751-0813.2000.tb11861.x
Steel RJ.No abstract available
Equine piroplasmosis visits Australia in 2000.
Australian veterinary journal    August 2, 2000   Volume 78, Issue 6 380 doi: 10.1111/j.1751-0813.2000.tb11817.x
No abstract available
Procedurally similar competitive immunoassay systems for the serodiagnosis of Babesia equi, Babesia caballi, Trypanosoma equiperdum, and Burkholderia mallei infection in horses. Katz J, Dewald R, Nicholson J.Procedurally similar competitive enzyme-linked immunoassay (cELISA) methods were developed for the serodiagnosis of Babesia equi and Babesia caballi (piroplasmosis), Trypanosoma equiperdum (dourine), and Burkholderia mallei (glanders) infections in horses. Apparent test specificities for the B. equi, B. caballi, T. equiperdum, and B. mallei cELISAs were 99.2%, 99.5%, 98.9%, and 98.9%, respectively. Concordances and kappa values between the complement fixation (CF) and the cELISA procedures for the serodiagnosis of B. equi, B. caballi, T. equiperdum, and B. mallei infections in experimentally e...
Babesia and Ehrlichia seropositive horses temporarily imported into Australia.
Australian veterinary journal    February 24, 2000   Volume 77, Issue 11 726-727 doi: 10.1111/j.1751-0813.1999.tb12911.x
Steel RJ.No abstract available
AQIS to ease import restrictions on equestrian event horses which are piroplasmosis ‘positive’.
Australian veterinary journal    November 24, 1999   Volume 77, Issue 9 614-615 
No abstract available
Control of equine piroplasmosis in Brazil.
The Onderstepoort journal of veterinary research    November 24, 1999   Volume 66, Issue 2 123-127 
Kerber CE, Ferreira F, Pereira MC.The importance of equine piroplasmosis control in endemic countries has increased in recent years and plays an important role to maintain the international market open to the horse industry. The purpose of this study was to demonstrate the occurrence of equine piroplasmosis (Babesia equi or Theileria equi and Babesia caballi) in Brazil--a country where the disease occurs endemically--in different climatic conditions, and to evaluate the results of a strategy for tick control in order to decrease infection rates. Blood samples were taken from 720 horses on 28 farms from different regions and su...
Erythrocyte associated haemato-biochemical changes in Babesia equi infection experimentally produced in donkeys.
Veterinary parasitology    September 17, 1999   Volume 85, Issue 4 319-324 doi: 10.1016/s0304-4017(99)00110-7
Ambawat HK, Malhotra DV, Kumar S, Dhar S.Equine babesiosis, caused by Babesia equi and transmitted by ticks is of major economic importance in India. The adverse effects which B. equi organism and its metabolites inflict on red blood cells have not been reported. Erythrocytes were analysed for red cell membrane phospholipids, proteins and haemoglobin (Hb) concentration and plasma for malondialdehyde (MDA) in B. equi carrier donkeys before splenectomy (50% parasitaemia. Before splenectomy the mean values of membrane protein, phospholipids, plasma MDA and Hb were found to be 1.63 +/- 0.12 mg/ml PCV, 2.28 +/- 0.9 mg/ml PCV, 3.63 +/- 0.3...
Molecular detection of Babesia equi and Babesia caballi in horse blood by PCR amplification of part of the 16S rRNA gene.
Veterinary parasitology    August 6, 1999   Volume 84, Issue 1-2 75-83 doi: 10.1016/s0304-4017(99)00049-7
Bashiruddin JB, Cammà C, Rebêlo E.Babesia equi and Babesia caballi are tick-borne haemoparasites that may cause babesiosis of Equidae. In southern Europe B. equi is enzootic and infections may occur asymptomatically and more frequently than those due to B. caballi. Complement fixation test (CFT) is the official serological test for the diagnosis of equine babesiosis, but it has low sensitivity during early and latent stages of the disease. With the aim of developing more sensitive and rapid direct diagnostic alternatives, PCR systems that amplified DNA targets of 664 or 659 bp regions of the 16S rRNA genes were designed and de...
Equine piroplasmosis: the temporary importation of seropositive horses into Australia.
Australian veterinary journal    June 22, 1999   Volume 77, Issue 5 308-309 doi: 10.1111/j.1751-0813.1999.tb10269.x
Martin R.No abstract available
Tubular structures associated with Babesia caballi in equine erythrocytes in vitro.
Parasitology research    February 10, 1999   Volume 85, Issue 3 171-175 doi: 10.1007/s004360050530
Kawai S, Igarashi I, Abgaandorjiin A, Ikadai H, Omata Y, Saito A, Nagasawa H, Toyoda Y, Suzuki N, Matsuda H.In-vitro-propagated Babesia caballi parasites were examined by scanning and transmission electron microscopy. Many small pores were observed over the entire surface of infected erythrocytes on scanning electron microscopy, and on transmission electron microscopy these small pores were found to be openings of tubular structures. By the examination of a number of infected cells the tubular structures were found to be connected with the parasite, and this observation might indicate that the tubular structures arose the edge of the parasite and terminated at an Invagination on the surface of the e...
Pathogenesis of Babesia caballi infection in experimental horses.
The Journal of veterinary medical science    November 20, 1998   Volume 60, Issue 10 1127-1132 doi: 10.1292/jvms.60.1127
Hanafusa Y, Cho KO, Kanemaru T, Wada R, Sugimoto C, Onuma M.The present study was designed to investigate the role of cytokines in the pathogenesis of Babesia caballi in experimentally infected horses. The expression of cytokine mRNA was determined by using reverse transcription-polymerase chain reaction in two B. caballi-infected horses for 2 weeks after the infection. In one horse, there was up-regulation of interferon-gamma, tumor necrosis factor-alpha (TNF-alpha) and interleukin-2 mRNAs, while in the second horse, expression of only TNF-alpha mRNA was up-regulated. No change was observed in interleukin-4 mRNA in both of the horses. To know the rela...
Babesia equi field isolates cultured from horse blood using a microcentrifuge method.
The Journal of parasitology    August 26, 1998   Volume 84, Issue 4 696-699 
Holman PJ, Becu T, Bakos E, Polledo G, Cruz D, Wagner GG.Babesia equi, a causative agent of equine piroplasmosis, was isolated from horses in the Chaco Province of Argentina, a known piroplasmosis endemic region. Fifteen B. equi field isolates were acquired by culture from 23 actively working horses from 2 ranches. The horses appeared healthy with no clinical signs or histories indicative of equine piroplasmosis. All 23 horses had B. equi-specific antibody activity by the indirect fluorescent antibody test and 18 were also complement fixation test positive for B. equi. Equine erythrocytes were prepared for parasite culture using a microcentrifuge tu...
Redescription of Babesia equi Laveran, 1901 as Theileria equi Mehlhorn, Schein 1998.
Parasitology research    July 11, 1998   Volume 84, Issue 6 467-475 doi: 10.1007/s004360050431
Mehlhorn H, Schein E.The horse-parasitizing species Babesia equi Laveran, 1901 was redescribed as Theileria equi Mehlhorn, Schein 1998 and, thus, transferred from one valid genus to another. This transfer was needed since it turned out that this horse parasite showed the relevant characteristics of theilerians with regard to biological data, morphological features, biochemical properties, and molecular biological relationships.
Monoclonal antibody against Babesia equi: characterization and potential application of antigen for serodiagnosis.
Journal of clinical microbiology    July 3, 1998   Volume 36, Issue 7 1835-1839 doi: 10.1128/JCM.36.7.1835-1839.1998
Avarzed A, Igarashi I, De Waal DT, Kawai S, Oomori Y, Inoue N, Maki Y, Omata Y, Saito A, Nagasawa H, Toyoda Y, Suzuki N.Monoclonal antibody (MAb) BEG3 was produced against Babesia equi parasites to define a species-specific antigen for diagnostic use. The MAb reacted with single, paired, and Maltese cross forms of B. equi, and no reaction was observed with this MAb on acetone-fixed Babesia caballi, Babesia ovata, or Babesia microti parasites in the indirect immunofluorescent antibody test. Confocal laser and immunoelectron microscopic studies showed that the antigen which was recognized by this MAb was located on the surface of B. equi parasites. This MAb recognized a 19-kDa protein of B. equi antigen and did n...
Seroprevalence of Babesia equi among horses in Israel using competitive inhibition ELISA and IFA assays.
Veterinary parasitology    July 3, 1998   Volume 76, Issue 4 251-259 doi: 10.1016/s0304-4017(97)00228-8
Shkap V, Cohen I, Leibovitz B, Savitsky , Pipano E, Avni G, Shofer S, Giger U, Kappmeyer L, Knowles D.Sera from 361 horses were tested by indirect immunofluorescence antibody test (IFA) and by competitive inhibition ELISA (cELISA), to detect antibodies to Babesia equi. The concordance between the assays was 95.7%. Application of a cutoff based on a calculated percent inhibition of 20% inhibition was used. Approximately one-third of all the horses tested were found serologically positive to B. equi, with more horses testing positive from northern Israel. Among horses raised with access to pasture there was a significant difference in the percentage of seropositive reactors (76.6% in the north ...