Analyze Diet

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.
Sporogony and experimental transmission of Babesia equi by Boophilus microplus.
Parasitology research    May 15, 1998   Volume 84, Issue 4 323-327 doi: 10.1007/s004360050404
Guimarães AM, Lima JD, Ribeiro MF.The development of Babesia equi in salivary glands of adult female Boophilus microplus was observed under a light microscope using semithin sections stained with toluidine blue. Engorged nymphs were obtained from splenectomized foals experimentally infected with B. equi. As adults, they were then fed on rabbits for 5 days and the salivary glands of manually collected individuals were removed at intervals of 24 h. Sporozoites were found in type III granular acini cells between the 2nd and 5th days following feeding on the rabbits. Sporoblasts and sporozoites were observed in the same or adjacen...
In vitro propagation of Theileria annulata infected schizonts in different media supplemented with heterologous sera.
Indian journal of experimental biology    May 6, 1998   Volume 35, Issue 11 1175-1181 
Nichani AK, Sharma RD, Sarup S.Efficacy of medium RPMI-1640 (supplied by Gibco USA, Centron and Hi-media) supplemented with horse, donkey, sheep and goat sera was evaluated for in vitro propagation of Theileria annulata (Hisar) infected bovine mononuclear cells. The results were compared with the growth rate in RPMI-1640 supplemented with foetal bovine serum (Gibco). RPMI-1640 (Gibco) proved to be the best medium for in vitro cultivation of the parasite infected cells. Foetal bovine serum could be easily, safely and reliably substituted with goat and sheep sera in the growth medium. Horse and donkey sera also gave comparabl...
Biotin-labeled DNA probe in a PCR-based assay increases detection sensitivity for the equine hemoparasite Babesia caballi.
Veterinary parasitology    February 27, 1998   Volume 73, Issue 1-2 53-63 doi: 10.1016/s0304-4017(97)00017-4
Sahagun-Ruiz A, Waghela SD, Holman PJ, Chieves LP, Wagner GG.A DNA probe from Babesia caballi (Bc1) was selected by antibody screening of a genomic library. The Bc1 probe hybridized specifically to B. caballi genomic DNA. A polymerase-chain-reaction-based assay for B. caballi DNA was developed from primers deduced from the probe nucleotide sequence. An amplified product of 1.6 kb was detected from as little as 500 fg B. caballi template DNA. Sensitivity increased 1000-fold when the biotin-labeled Bc1 probe was hybridized to the amplicons in a Southern blot.
Prevalence of equine piroplasmosis in Central Mongolia.
The Onderstepoort journal of veterinary research    June 1, 1997   Volume 64, Issue 2 141-145 
Avarzed A, De Waal DT, Igarashi I, Saito A, Oyamada T, Toyoda Y, Suzuki N.Antigen for the indirect fluorescent antibody test (IFAT) was routinely prepared from infected erythrocytes from horses experimentally infected with Babesia equi and Babesia caballi. With the successful establishment of in vitro cultures of B. equi and B. caballi, it is now possible to employ culture-derived antigens in this test. In this study, in vitro-propagated B. equi- and B. caballi-infected erythrocytes were used as antigen in the IFAT. Various modifications to an established protocol had to be implemented to allow repeatable results. Cultures with 3-4% parasitized erythrocytes were fou...
Serodiagnosis of Babesia equi infection–a comparison of Dot-ELISA, complement fixation test and capillary tube agglutination test.
Veterinary parasitology    May 1, 1997   Volume 69, Issue 3-4 171-176 doi: 10.1016/s0304-4017(96)01124-7
Kumar S, Malhotra DV, Dhar S.The present study aimed to develop Dot-ELISA, complement fixation test (CFT) and capillary tube agglutination test (CAT) for serodiagnosis of Babesia equi infection and to compare their sensitivity with each other. For this study, sequential serum samples were collected from four donkeys experimentally infected with B. equi up to 90 days post infection (P.I.). B. equi antigen was prepared from the blood of a donkey showing more than 80% parasitaemia. Dot-ELISA, CF and CA tests were standardized as per the standard method. While performing CFT, it was observed that CFT standardized for the donk...
Equine babesiosis associated with strenuous exercise: clinical and pathological studies in Jordan.
Veterinary parasitology    April 1, 1997   Volume 69, Issue 1-2 1-8 doi: 10.1016/s0304-4017(96)01100-4
Hailat NQ, Lafi SQ, al-Darraji AM, al-Ani FK.Clinical, haematological and pathological studies were undertaken in Jordan in a stud of 103 racing horses clinically suffering from babesiosis and apparently healthy animals. Out of 47 horses which participated in strenuous exercise, three mares showed sudden onset of immobility and reluctance to move and two mares died. Clinical examination revealed that these five horses (group 1) had fever, anorexia, weakness and severe icterus and, in two mares, haemoglobinuria. Haematological examination revealed that all five horses were heavily parasitized with Babesia equi. This was also found in four...
In vitro cultivation of Babesia equi: detection of carrier animals and isolation of parasites.
The Onderstepoort journal of veterinary research    March 1, 1997   Volume 64, Issue 1 51-56 
Zweygarth E, Just MC, De Waal DT.By means of an in vitro culture technique, 75 samples of horse blood were examined for Babesia equi, a causative agent of equine piroplasmosis. At the time of culture initiation, 15 samples were microscopically positive for B. equi, and this was subsequently confirmed by culture diagnosis. Sixty samples showed no parasites in Giemsa-stained thin blood smears. However, after the culturing process, parasites were found in blood smears of 36 of these samples. The sensitivity of the in vitro culture method was such that 2.5 microliters (1/40 of the usual volume used for the above-mentioned samples...
Case report: field-acquired subclinical Babesia equi infection confirmed by in vitro culture.
Journal of clinical microbiology    February 1, 1997   Volume 35, Issue 2 474-476 doi: 10.1128/jcm.35.2.474-476.1997
Holman PJ, Hietala SK, Kayashima LR, Olson D, Waghela SD, Wagner GG.A horse with no prior clinical history of equine piroplasmosis tested negative for Babesia caballi and Babesia equi in the complement fixation test before importation into the United States from France. After 5 years in residence in the United States, the animal tested serologically positive for B. equi by the complement fixation test, the immunofluorescent antibody test, and Western blot analysis. The carrier status of the horse was confirmed by culture of B. equi parasites. In vitro culture offers an efficient and comparatively inexpensive method to determine the carrier status of horses sus...
A sero-epidemiological survey of equine piroplasmosis in the northern and eastern Cape Provinces of South Africa.
Journal of the South African Veterinary Association    December 1, 1996   Volume 67, Issue 4 204-208 
Gummow B, de Wet CS, de Waal DT.Serum samples from yearling Thoroughbred horses (n = 176) in the magisterial districts of Colesberg, Venterstad, and Wodehouse in the Northern and Eastern Cape Provinces were collected between September and November 1995 to determine the prevalence of antibodies to Babesia equi and Babesia caballi in these regions. Samples were examined for specific antibodies using the indirect fluorescent antibody test. The 95% confidence intervals for the prevalence of serum antibodies in the 3 districts combined varied from 47% to 61% for B. equi and from 26% to 40% for B. caballi. Antibody prevalence did ...
Babesiosis in a foal.
The Veterinary record    October 26, 1996   Volume 139, Issue 17 428 
Silvey RE.No abstract available
An account on equine babesioses.
Revue scientifique et technique (International Office of Epizootics)    September 1, 1996   Volume 15, Issue 3 1191-1201 doi: 10.20506/rst.15.3.972
Friedhoff KT, Soulé C.A review of the distribution of Babesia equi and Babesia caballi, the transmission of these protozoa by ticks and the immune response of infected horses, in addition to a brief survey of diagnostic. tests and chemotherapy.
Control of Babesia equi parasitemia.
Parasitology today (Personal ed.)    May 1, 1996   Volume 12, Issue 5 195-198 doi: 10.1016/0169-4758(96)10007-7
Knowles DP.Infection of horses with the hemoprotozoan Babesia equi has been reported in southern Florida, US Virgin Islands, part of Asia, Russia, India, the Middle East, Europe, Africa, Australia, South America, Central America, Mexico, Philippine Islands and some Caribbean islands. The restrictions placed on the international movement of infected horses has refocused attention on potential methods to control or eliminate infection. Don Knowles here discusses the primary chemotherapeutic compounds that have been used; the current knowledge concerning immune responses that potentially contribute to contr...
A case of Ehrlichia equi in an adult horse in British Columbia.
The Canadian veterinary journal = La revue veterinaire canadienne    March 1, 1996   Volume 37, Issue 3 174-175 
Berrington A, Moats R, Lester S.No abstract available
Equine babesiosis (piroplasmosis): a problem in the international movement of horses.
The British veterinary journal    March 1, 1996   Volume 152, Issue 2 123-126 doi: 10.1016/s0007-1935(96)80066-2
Knowles D.No abstract available
Equine piroplasmosis an update on diagnosis, treatment and prevention.
The British veterinary journal    March 1, 1996   Volume 152, Issue 2 139-151 doi: 10.1016/s0007-1935(96)80070-4
Brüning A.Two haemoprotozoan parasites, Babesia caballi and Babesia equi, can cause equine piroplasmosis. Due to the presence of potential tick vectors in areas so far unaffected by equine babesias, import and export regulations often require the serum testing of animals for evidence of infection. Although the complement fixation test (CFT) has been recommended for detecting the presence of antibodies to Babesia spp., it has been demonstrated to have several disadvantages, including false-positive results and low sensitivity for detecting latent infections. An enzyme-linked immunosorbent assay (ELISA) m...
Epidemiological aspects of equine babesioses in a herd of horses in Brazil.
Veterinary parasitology    May 1, 1995   Volume 58, Issue 1-2 1-8 doi: 10.1016/0304-4017(94)00704-g
Pfeifer Barbosa I, Böse R, Peymann B, Friedhoff KT.Epidemiological studies of Babesia equi and B. caballi were undertaken in a herd of 120 pastured horses in Rio de Janeiro, Brazil. The area where the horses were held was shown to be highly endemic for both Babesia spp., i.e. the prevalence of B. equi antibodies in horses aged 6 months or older ranged from 90.6% to 100% as determined by the immunofluorescence antibody (IFA) test, and the prevalence of B. caballi antibodies as determined by Western blot ranged from 59.4% to 65.5%. From the herd, 20 foals and their dams were selected to estimate the degree of tick infestation and the foals were ...
Recent developments in elucidating tick vector relationships for anaplasmosis and equine piroplasmosis.
Veterinary parasitology    March 1, 1995   Volume 57, Issue 1-3 97-108 doi: 10.1016/0304-4017(94)03114-c
Stiller D, Coan ME.This brief review focuses first on several epidemiologically relevant aspects of anaplasmosis, including: (1) the role of male ticks as intrastadial, biological vectors of Anaplasma through interhost transfer; (2) the application of molecular diagnostic assays in assessing tick vector competence and evaluating the role of chronically infected carrier cattle as sources of Anaplasma marginale infection in vector ticks; (3) opportunities provided by a recently developed in vitro tick feeding system in quantitating studies of tick-hemoparasite-host interactions. Lastly, current knowledge of the st...
Cloning and expression of two genes from Babesia equi merozoites and evaluation of their diagnostic potential.
Applied parasitology    February 1, 1995   Volume 36, Issue 1 1-10 
Schelp C, Böse R, Micha A, Hentrich B.High-titre equine immune sera were used to screen a lambda gt 11 expression library of Babesia equi cDNA fragments. Two cDNA clones which did not cross-hybridize to each other were studied. Both clones hybridized specifically to DNA from B. equi but not to DNA from B. caballi, B. divergens or B. ovis. Recombinant proteins were expressed as glutathione S-transferase (GST) fusion proteins with apparent molecular weights of 40 kDa and 75 kDa. Polyclonal antibodies directed against the 40 kDa and 75 kDa recombinant proteins detected native antigens of 55 kDa and 50 kDa respectively in crude lysate...
Continuous in vitro cultivation of erythrocytic stages of Babesia equi.
Parasitology research    January 1, 1995   Volume 81, Issue 4 355-358 doi: 10.1007/BF00931544
Zweygarth E, Just MC, de Waal DT.The protozoan parasite Babesia equi, a causative agent of equine piroplasmosis, was continuously cultivated in horse erythrocytes. The parasites were isolated from a carrier horse at a time when no parasite was detected in a thin blood smear. The culture medium consisted of modified medium 199 supplemented with 40% non-heat-inactivated horse serum in a humidified atmosphere containing 5% CO2, 2% O2, and 93% N2 at 37 degrees C. Parasites were detected after 2 days in culture. When the percentage of parasitized erythrocytes (PPE) reached 1%, the cultures were transferred into a humidified atmosp...
Diagnosis of Babesia caballi infections in horses by enzyme-linked immunosorbent assay (ELISA) and western blot.
International journal for parasitology    May 1, 1994   Volume 24, Issue 3 347 
Böse R, Peymann B.From Babesia caballi in vitro cultures a preparation of 100% infected erythrocytes was obtained. From this, B. caballi antigens were extracted with the detergent 3-[(3-Cholamidopropyl)-dimethylammonio]-1-propane-sulfonate (CHAPS) and used as ELISA antigens. A control antigen of normal erythrocytes from the same donor horse was prepared in an identical manner. The ELISA and Western blot were validated by testing of sera from horses experimentally infected with B. caballi or B. equi or not infected with Babesia spp. ELISA and Western blot results were compared with those obtained by the immunofl...
Specific immune responses are required to control parasitemia in Babesia equi infection.
Infection and immunity    May 1, 1994   Volume 62, Issue 5 1909-1913 doi: 10.1128/iai.62.5.1909-1913.1994
Knowles DP, Kappmeyer LS, Perryman LE.Horses possessing a normal immune system and spleen often control infection caused by Babesia equi. However, splenectomized horses are unable to control B. equi infection and usually succumb to the infection. To investigate the role of the spleen in the control of B. equi infection in the absence of specific immune responses, two 1-month-old foals with severe combined immunodeficiency (SCID) and two age-matched normal foals were inoculated with B. equi. The SCID foals became febrile seven days postinoculation and developed terminal parasitemias of 41 and 29%. The SCID foals had greater than 50...
Babesia equi erythrocytic stage continuously cultured in an enriched medium.
The Journal of parasitology    April 1, 1994   Volume 80, Issue 2 232-236 
Holman PJ, Chieves L, Frerichs WM, Olson D, Wagner GG.Babesia equi was continuously cultured through 90 passages in an enriched chemically defined basal medium (HL-1) supplemented with 20% fetal bovine serum and serum replacement factors, including lipid-rich bovine serum albumin, bovine insulin, and human transferrin. Cryopreservation and subsequent recovery of B. equi were easily achieved. Inoculation of a splenectomized and an intact horse with cultured infected erythrocytes resulted in parasitemias and B. equi in vitro reisolation from both animals. In vitro forms of the parasite resembled in vivo forms. After establishment, parasitemias of 1...
The development of Babesia (Theileria) equi (Laveran, 1901) in the gut and the haemolymph of the vector ticks, Hyalomma species.
Parasitology research    January 1, 1994   Volume 80, Issue 4 297-302 doi: 10.1007/BF02351869
Zapf F, Schein E.The development of the piroplasm Babesia equi was studied by light microscopy in the gut and the haemolymph of three different Hyalomma species during and after the nymphs had engorged on parasitaemic horses. The stock of B. equi used was isolated from a horse imported from Turkmenistan (CIS) in 1991. The existence of gamogony was identified by the occurrence of gamonts and gametes in the gut contents of the nymphs at between 3 and 4 days after infestation of the nymphs, before the ticks dropped off the experimentally infected horses. Zygotes and kinetes were observed in the intestinal cells f...
New findings in the development of Babesia (Theileria) equi (Laveran, 1901) in the salivary glands of the vector ticks, Hyalomma species.
Parasitology research    January 1, 1994   Volume 80, Issue 7 543-548 doi: 10.1007/BF00933000
Zapf F, Schein E.The development of the piroplasm Babesia equi was studied by light microscopy in the salivary glands of three different Hyalomma species during and after the engorgement of nymphs on experimentally infected horses and after adults had fed on a vertebrate host following ecdysis. The stock of B. equi used was isolated from a horse imported from Turkmenistan (CIS) in 1991. The findings, being identical in all three Hyalomma species, differ with regard to the chronological order of the development stages in several respects from the results of previous studies based upon light or electron microsco...
Culture confirmation of the carrier status of Babesia caballi-infected horses.
Journal of clinical microbiology    March 1, 1993   Volume 31, Issue 3 698-701 doi: 10.1128/jcm.31.3.698-701.1993
Holman PJ, Frerichs WM, Chieves L, Wagner GG.Culture of horse blood for Babesia caballi identified four carrier horses among nine previously infected horses. Three of the carriers had no detectable parasitemias on stained blood smears, and sera from two carrier horses were complement fixation test negative. Three cultures were continuously cultivated. Cryopreserved fourth-passage B. caballi was successfully reestablished in vitro. Blood from a 10th horse previously subinoculated with blood from a suspected carrier was cultured, with negative results.
Detection of humoral antigen and antibody by enzyme-linked immunosorbent assay in horses with experimentally induced Ehrlichia equi infection. Corstvet RE, Gaunt SD, Karns PA, McBride JW, Battistini RA, Mauterer LA, Austin FW.An enzyme-linked immunosorbent assay (ELISA) was used to detect antigen in plasma and antibody in serum of 3 horses inoculated with Ehrlichia equi. Clinical signs, including rectal temperature, were correlated with the antigen and antibody detection. ELISA was very efficient in detection of serum antibody. Antigen detection using monoclonal antibodies to E. equi and ELISA should be considered as a diagnostic method.
Antibody to a recombinant merozoite protein epitope identifies horses infected with Babesia equi.
Journal of clinical microbiology    December 11, 1992   Volume 30, Issue 12 3122-3126 doi: 10.1128/jcm.30.12.3122-3126.1992
Knowles DP, Kappmeyer LS, Stiller D, Hennager SG, Perryman LE.Horses infected with Babesia equi were previously identified by the presence of antibodies reactive with a merozoite surface protein epitope (D. P. Knowles, Jr., L. E. Perryman, L. S. Kappmeyer, and S. G. Hennager. J. Clin. Microbiol. 29:2056-2058, 1991). The antibodies were detected in a competitive inhibition enzyme-linked immunosorbent assay (CI ELISA) by using monoclonal antibody 36/133.97, which defines a protein epitope on the merozoite surface. The gene encoding this B. equi merozoite epitope was cloned and expressed in Escherichia coli. The recombinant merozoite protein, designated equ...
Efficacy of buparvaquone as a therapeutic and clearing agent of Babesia equi of European origin in horses.
American journal of veterinary research    August 1, 1992   Volume 53, Issue 8 1396-1399 
Zaugg JL, Lane VM.We evaluated the efficacy of buparvaquone in eliminating infection with Babesia equi of European origin in carrier horses and in splenectomized horses with experimentally induced acute infection. When administered at the rate of 5 mg/kg of body weight, IV, 4 times at 48-hour intervals, buparvaquone prompted rapid abatement of parasitemia. However, secondary and tertiary recrudescent parasitemias invariably returned with establishment of the carrier state. Buparvaquone, at the dosage evaluated, had transitory therapeutic efficacy against acute B equi infection in splenectomized horses, but was ...
Equine piroplasmosis: a review.
The British veterinary journal    January 1, 1992   Volume 148, Issue 1 6-14 doi: 10.1016/0007-1935(92)90061-5
de Waal DT.This review focuses on equine piroplasmosis with specific reference to its distribution, diagnosis and clinical and pathological signs. The more common used drugs are discussed both with reference to treatment and chemosterilization. Areas requiring further research are also briefly mentioned.
A monoclonal antibody defines a geographically conserved surface protein epitope of Babesia equi merozoites.
Infection and immunity    July 11, 1991   Volume 59, Issue 7 2412-2417 doi: 10.1128/iai.59.7.2412-2417.1991
Knowles DP, Perryman LE, Goff WL, Miller CD, Harrington RD, Gorham JR.Babesiosis is a tick-borne hemoparasitic disease affecting horses worldwide. To investigate mechanisms of immunity to this parasite, the antibody response of infected horses to Babesia equi merozoite proteins was evaluated. Immunoprecipitation of B. equi merozoite antigens with sera from infected horses revealed 11 major proteins of 210, 144, 108, 88, 70, 56, 44, 36, 34, 28, and 25 kDa. Monoclonal antibody (MAb) 36/133.97, which binds to live merozoites, immunoprecipitated proteins of 44, 36, 34, and 28 kDa. When immunoprecipitations were performed with in vitro translation products of merozoi...