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Topic:Infectious Disease

Infectious diseases in horses encompass a range of illnesses caused by bacteria, viruses, fungi, or parasites. These diseases can affect various systems within the equine body, leading to symptoms that range from mild discomfort to severe systemic illness. Common infectious diseases in horses include equine influenza, strangles, equine herpesvirus, and West Nile virus. These diseases can be transmitted through direct contact with infected animals, contaminated surfaces, or vectors such as insects. Understanding the mechanisms of transmission, pathogenesis, and immune response is essential for effective prevention and control. This page compiles peer-reviewed research studies and scholarly articles that explore the epidemiology, diagnosis, treatment, and management of infectious diseases in horses.
Isolation of the equine granulocytic ehrlichiosis agent, Ehrlichia equi, in tick cell culture.
Journal of clinical microbiology    March 1, 1996   Volume 34, Issue 3 664-670 doi: 10.1128/jcm.34.3.664-670.1996
Munderloh UG, Madigan JE, Dumler JS, Goodman JL, Hayes SF, Barlough JE, Nelson CM, Kurtti TJ.The equine granulocytic ehrlichiosis agent, Ehrlichia equi, is closely related or identical to the human granulocytic ehrlichiosis (HGE) agent. Both are suspected of being transmitted by ticks. We have successfully isolated E. equi in a cell line, IDE8, derived from a putative vector, the tick Ixodes scapularis. Peripheral blood leukocytes from an experimentally infected horse were inoculated onto IDE8 monolayers. Cultures were incubated in a candle jar at 34 degrees C in tick cell culture medium with NaHCO3 and an organic buffer [3-(N-morpholino)-propanesulfonic acid] (MOPS). Within 2 weeks, ...
Correlation between DNA restriction fragment length polymorphisms in Leptospira interrogans serovar pomona type kennewicki and host animal source.
Journal of clinical microbiology    February 1, 1996   Volume 34, Issue 2 424-425 doi: 10.1128/jcm.34.2.424-425.1996
Bolin CA, Zuerner RL.Isolates (n = 147) of Leptospira interrogans serovar pomona type kennewicki from cattle, swine, horses, and wildlife were analyzed by DNA restriction endonuclease analysis. Restriction fragment length polymorphisms were identified in DNA digested with HpaII, and the restriction fragment length polymorphisms were correlated with the host animal source of the isolates. These results will be useful in understanding the epidemiology of serovar pomona infections in livestock.
[Current concepts and implications for future research on Rhodococcus equi].
Nihon saikingaku zasshi. Japanese journal of bacteriology    February 1, 1996   Volume 51, Issue 2 485-496 doi: 10.3412/jsb.51.485
Takai S.No abstract available
Use of excretory/secretory antigens for the serodiagnosis of Anoplocephala perfoliata cestodosis.
Veterinary parasitology    February 1, 1996   Volume 61, Issue 3-4 239-247 doi: 10.1016/0304-4017(95)00837-3
Proudman CJ, Trees AJ.Whole worm extract (WWE) and excretory/secretory (E/S) antigens of Anoplocephala perfoliata were characterised by SDS-PAGE and their use in the serodiagnosis of equine cestodosis was evaluated. An enzyme-linked immunosorbent assay (ELISA) was used to compare WWE and E/S antigen as the capture layer in an antibody capture ELISA. E/S antigen gave the best differentiation between sera from tapeworm-positive and tapeworm-negative horses. The E/S-ELISA was optimised and validated against sera from horses of known tapeworm status. This assay gave a diagnostic sensitivity of 68% (n = 38) and a specif...
Serological evidence for the presence of A/equine-1 influenza virus in unvaccinated horses in Croatia.
The Veterinary record    January 20, 1996   Volume 138, Issue 3 68 doi: 10.1136/vr.138.3.68
Madić J, Martinović S, Naglić T, Hajsig D, Cvetnić S.No abstract available
A possible case of Lyme borreliosis in a horse in the UK.
Equine veterinary journal    January 1, 1996   Volume 28, Issue 1 84-88 doi: 10.1111/j.2042-3306.1996.tb01595.x
Hahn CN, Mayhew IG, Whitwell KE, Smith KC, Carey D, Carter SD, Read RA.No abstract available
Visceral neosporosis in a 10-year-old horse. Gray ML, Harmon BG, Sales L, Dubey JP.No abstract available
Nationwide serological survey of equine influenza in Nigeria.
Revue d'elevage et de medecine veterinaire des pays tropicaux    January 1, 1996   Volume 49, Issue 1 24-27 
Adeyefa CA, Hamblin C, Cullinane AA, McCauley JW.The objective of this work was to examine the incidence of equine influenza viruses in the equine population of an area of tropical Africa where equine influenza virus activity has recently been reported for the first time. A serological survey of sera from horses and donkeys from regions of Nigeria taken from 1990 to 1993 was carried out and the results obtained were com-pared with equine sera from Western Europe (Ireland). The sera were assayed for presence of antibodies by both haemagglutination inhibition (HI) and ELISA using a monoclonal antibody to the prototype H3 equine influenza virus...
Rapid diagnosis of African horse sickness.
Revue d\'elevage et de medecine veterinaire des pays tropicaux    January 1, 1996   Volume 49, Issue 4 295-298 
Adeyefa CA.The rapid diagnosis of African horse sickness (AHS) during the incubation period using virus antigens in peripheral blood mononuclear cells (PBMC) and red blood cells (RBC) in a sandwich indirect enzyme-linked immunosorbent assay (ELISA) is reported. PMBC consistently gave higher positive ELISA results than RBC from blood collected during viraemia from clinically affected horses. The potential of the method described for wider application in rapid diagnosis and virus surveillance in susceptible equine populations, particularly in AHS-free and in enzootic areas, for effective control strategies...
Control of Karoo paralysis ticks through vegetation management.
Medical and veterinary entomology    January 1, 1996   Volume 10, Issue 1 39-43 doi: 10.1111/j.1365-2915.1996.tb00080.x
Fourie LJ, Kok DJ, Krugel L, Snyman A, Van Der Lingen F.Karoo paralysis, caused by feeding Ixodes rubicundus females, is a major disease of small stock in South Africa. Control methods currently practised are almost exclusively chemical based. To limit overdependance on chemicals, vegetation management was investigated as a possible method for control, to be incorporated in an integrated tick management system. Laboratory and field experiments were conducted to determine, firstly, the extent of vertical migration and survival of ticks on long and short copper rods which simulated grasses as questing substrates; secondly, the infestation burdens of ...
Differences between Taylorella equigenitalis strains in their invasion of and replication in cultured cells.
Clinical and diagnostic laboratory immunology    January 1, 1996   Volume 3, Issue 1 47-50 doi: 10.1128/cdli.3.1.47-50.1996
Bleumink-Pluym NM, ter Laak EA, Houwers DJ, van der Zeijst BA.The ability of Taylorella equigenitalis, the causative agent of contagious equine metritis, to invade and replicate in equine derm cells was studied. The kinetics of invasion and replication were determined for four T. equigenitalis strains. On the basis of these experiments, a simpler assay in which the invasive as well as the replicative properties of a particular strain could be determined was developed. This assay was used to characterize 32 strains, which had previously been typed by field inversion gel electrophoresis of genomic restriction fragments. The invasiveness of T. equigenitalis...
[Identification and diagnosis of Taylorella equigenitalis by a DNA amplification method (PCR)].
Schweizer Archiv fur Tierheilkunde    January 1, 1996   Volume 138, Issue 3 115-120 
Miserez R, Frey J, Krawinkler M, Nicolet J.A polymerase chain reaction (PCR) for identification of Taylorella equigenitalis was developed. The oligonucleotide primers are based on the DNA sequence of the rrs gene of T. equigenitalis, encoding for the 16S ribosomal RNA. Analysis of 21 strains of T. equigenitalis from England, USA and Switzerland showed an amplification product of 410 bp with identical Sau3A restriction profile. The sensitivity of the PCR-Assay was estimated to detect 50 to 500 bacteria of T. equigenitalis in a mixture with frequently found contaminants. Further analysis of culture from 60 genital swabs, taken in the cou...
Ixodes pacificus (Acari: Ixodidae) as a vector of Ehrlichia equi (Rickettsiales: Ehrlichieae).
Journal of medical entomology    January 1, 1996   Volume 33, Issue 1 1-5 doi: 10.1093/jmedent/33.1.1
Richter PJ, Kimsey RB, Madigan JE, Barlough JE, Dumler JS, Brooks DL.Ehrlichia equi, a rickettsia described from horses in California 30 yr ago, causes equine granulocytic ehrlichiosis throughout the Americas and possibly Europe. Here, we report experimental transmission of E. equi from infected to susceptible horses through bites of western blacklegged ticks, Ixodes pacificus (Cooley & Kohls). In preliminary field studies, only I. pacificus consistently infested horses and vegetation at 3 locations with contemporary cases of equine ehrlichosis, and in particular, I. pacificus was the only species found attached to all of the infected horses. Exposure to bites ...
Equine infectious anemia virus replication is upregulated during differentiation of blood monocytes from acutely infected horses.
Journal of virology    January 1, 1996   Volume 70, Issue 1 590-594 doi: 10.1128/JVI.70.1.590-594.1996
Sellon DC, Walker KM, Russell KE, Perry ST, Covington P, Fuller FJ.Equine infectious anemia virus is a lentivirus that replicates in mature tissue macrophages of horses. Ponies were infected with equine infectious anemia virus. During febrile episodes, proviral DNA was detectable, but viral mRNA was not detectable. As cultured blood monocytes from these ponies differentiated into macrophages, viral expression was upregulated. In situ hybridization confirmed that viral transcription occurred in mature macrophages.
Transmission patterns of St. Louis encephalitis and eastern equine encephalitis viruses in Florida: 1978-1993.
Journal of medical entomology    January 1, 1996   Volume 33, Issue 1 132-139 doi: 10.1093/jmedent/33.1.132
Day JF, Stark LM.Sentinel chickens were maintained at field sites in 40 Florida counties for varying periods between 1978 and 1993. For each county, the total number of St. Louis encephalitis virus (SLE) or eastern equine encephalitis (EEE) virus seroconversions were divided by the number of chickens exposed to calculate a mean annual seroconversion rate. These rates were used to evaluate the annual and geographical distributions of these viruses within Florida. For SLE, the rates in counties that reported human SLE cases during a widespread epidemic in 1990 were compared with adjusted mean annual seroconversi...
Survey of equine rotaviruses shows conservation of one P genotype in background of two G genotypes.
Archives of virology    January 1, 1996   Volume 141, Issue 9 1601-1612 doi: 10.1007/BF01718285
Isa P, Wood AR, Netherwood T, Ciarlet M, Imagawa H, Snodgrass DR.DIG-labelled ssRNA probes were prepared from variable regions of VP4 and VP7 cognate genes, and used in hybridization assays for P and G genotyping of group A cell culture-adapted equine rotaviruses and fecal samples collected from foals with and without diarrhea. The probes confirmed known P and G serotypes of sixteen cell culture-adapted strains. From one-hundred and twenty-one rotavirus-positive samples, 83 reacted when tested for their P and G genotype specific probes. From these, 71 were found to contain G3 P12 genotypes, and 11 G14 P12 genotypes. No sample reacted with H1 or L338 P and G...
Species-specific and interspecies relatedness of NSP1 sequences in human, porcine, bovine, feline, and equine rotavirus strains.
Archives of virology    January 1, 1996   Volume 141, Issue 1 1-12 doi: 10.1007/BF01718584
Kojima K, Taniguchi K, Kobayashi N.We have sequenced gene 5 encoding NSP1 for three human, two porcine, two bovine, one feline, and five equine rotavirus strains, and compared the nucleotide and deduced amino acid sequences with the published sequences for other various strains. Subgroup I human strains L26, 69M, and DS-1 were found to have a similar NSP1 sequence despite their different G serotypes, VP4 genotypes, and RNA patterns. The NSP1 sequence of the human strain K8 showed a high degree of homology to those of porcine strains OSU and YM. A high degree of homology was found among three equine strains (H2, FI-14, and FI23)...
Comparison of nucleic and amino acid sequences and phylogenetic analysis of the Gs protein of various equine arteritis virus isolates.
Virus genes    January 1, 1996   Volume 13, Issue 1 87-91 doi: 10.1007/BF00576983
Lepage N, St-Laurent G, Carman S, Archambault D.The genetic variation in equine arteritis virus (EAV) Gs protein encoding gene was investigated. Nucleic and deduced amino acid sequences from eight different EAV isolates (one European, two American and five Canadian isolates) were compared with those of the Bucyrus reference strain. Nucleotide and amino acid identities between these isolates and the Bucyrus reference strain ranged from 92.3 to 96.4%, and 93.2 to 95.5%, respectively. However, phylogenetic tree analysis and estimation of genetic distances based on the Gs protein encoding gene sequences showed that the European prototype Vienna...
Sequence variability of Borna disease virus open reading frame II found in human peripheral blood mononuclear cells.
Journal of virology    January 1, 1996   Volume 70, Issue 1 635-640 doi: 10.1128/JVI.70.1.635-640.1996
Kishi M, Arimura Y, Ikuta K, Shoya Y, Lai PK, Kakinuma M.A cDNA fragment of the Borna disease virus (BDV) open reading frame II (ORF-II), which encodes a 24-kDa phosphoprotein (p24 [P protein]), was amplified from total RNA of peripheral blood mononuclear cells (PBMC) from three psychiatric inpatients. The amplified cDNA fragments were cloned, sequenced, and analyzed. A total of 15 clones, 5 from each patient, were studied. Intrapatient divergencies of the BDV ORF-II nucleotide sequence were 4.2 to 7.3%, 4.8 to 7.3%, and 2.8 to 7.1% for the three patients, leading to differences of 7.7 to 14.5%, 10.3 to 17.1%, and 6.0 to 16.2%, respectively, in the ...
Lymphoid leukosis viruses, their recognition as ‘persistent’ viruses and comparisons with certain other retroviruses of veterinary importance.
Veterinary research communications    January 1, 1996   Volume 20, Issue 1 83-108 doi: 10.1007/BF00346580
Darcel C.Diseases caused by lymphoid leukosis virus (LLV), a retrovirus, take a long time after infection to develop and have a wide variety of pathological manifestations. This long latent period is characteristic of 'persistent virus infections'. Disease produced by LLV infection and its underlying mechanisms is compared with 'persistent' infections caused by other retroviruses in birds and mammals of veterinary importance. The diseases considered for comparison are those caused by reticuloendotheliosis, feline leukaemia, bovine leukosis and equine infectious anaemia viruses. There are significant ch...
Equine gammaherpesvirus 2 (EHV2) is latent in B lymphocytes.
Archives of virology    January 1, 1996   Volume 141, Issue 3-4 495-504 doi: 10.1007/BF01718313
Drummer HE, Reubel GH, Studdert MJ.Peripheral blood leukocytes were collected from 5 Thoroughbred horses and examined for the presence of EHV2 in sub-populations of mononuclear cells. Peripheral blood mononuclear cells were separated on Percoll gradients and then enriched for plastic adherent cells (predominantly monocytes), surface immunoglobulin positive (sIg+) B lymphocytes and T lymphocytes, using panning techniques. The purity of each cell population was assessed by fluorescence activated cell scanning. In an infectious centre assay, each cell population was inoculated onto equine foetal kidney monolayer cell cultures whic...
Phylogenetic analysis of open reading frame 5 of field isolates of equine arteritis virus and identification of conserved and nonconserved regions in the GL envelope glycoprotein.
Virology    December 20, 1995   Volume 214, Issue 2 690-697 doi: 10.1006/viro.1995.0087
Balasuriya UB, Timoney PJ, McCollum WH, MacLachlan NJ.The variation and phylogenetic relationship of open reading frame 5 (ORF5) of 3 different laboratory strains of the original prototype Bucyrus strain of equine arteritis virus (EAV), the modified live virus vaccine (ARVAC, Fort Dodge Laboratories), and 18 field isolates of EAV from North America and Europe were determined by comparison of their gene sequences. The viruses differed from the published sequence by between 3 (99.6% homology) and 94 (87.8%) nucleotides and by between 3 (98.8%) and 24 (90.6%) amino acids. The field isolates differed from each other by between 2 (99.7%) and 110 (85.7...
Outbreak of Severe Respiratory Disease in Humans and Horses Due to a Previously Unrecognized Paramyxovirus.
Journal of travel medicine    December 1, 1995   Volume 2, Issue 4 275 doi: 10.1111/j.1708-8305.1995.tb00679.x
Selvey L, Sheridan J.No abstract available
Recent advances in the laboratory diagnosis of equine parasitic diseases.
The Veterinary clinics of North America. Equine practice    December 1, 1995   Volume 11, Issue 3 437-442 doi: 10.1016/s0749-0739(17)30309-7
Granstrom DE.This article reviews recent advances in laboratory diagnosis of equine parasitic diseases. Laboratory diagnosis of most equine parasitic diseases continues to rely on standard methods. Only laboratory diagnostic tests for EPM, cryptosporidiosis, and giardiasis were included. The criteria for testing and interpretation of results for each new diagnostic method were explained. Western blot and PCR testing for EPM and immunofluorescent staining with monoclonal antibodies for cryptosporidiosis and giardiasis were reviewed.
Sero-positivity of domestic animals against Japanese encephalitis in Bareilly area, U.P.
The Journal of communicable diseases    December 1, 1995   Volume 27, Issue 4 242-246 
Mall MP, Kumar A, Malik SV.A study on seroprevalence of Japanese Encephalitis (JE), West Nile (WN) and Dengue-2 (DN-2) was undertaken in and around Bareilly, Uttar Pradesh to explore the role of non-human hosts in the natural cycle of these infections. A total of 1449 animal sera samples collected from 104 dogs, 170 pigs, 170 horses, 333 buffaloes, 252 cattle, 168 sheep and 252 goats were screened for antibodies against JE, WN and DN-2 by Micro-haemagglutination inhibition (HI) test employing 4 to 16 HA units of JE, WN and DN-2 antigens. The HI positivity against JE was found in dogs (55.77%) followed by pigs (40%), hor...
Reactions to strangles vaccination.
Australian veterinary journal    December 1, 1995   Volume 72, Issue 12 480 doi: 10.1111/j.1751-0813.1995.tb03502.x
Sezun GS.No abstract available
Evidence for a high rate of false-positive results with the indirect fluorescent antibody test for Ehrlichia risticii antibody in horses.
Journal of the American Veterinary Medical Association    December 1, 1995   Volume 207, Issue 11 1448-1453 
Madigan JE, Rikihisa Y, Palmer JE, DeRock E, Mott J.The original objective was to determine seroprevalence of Ehrlichia risticii antibody among horses in California. On the basis of the unexpected results of the survey, an investigation into the accuracy and reproducibility of results of the indirect fluorescent antibody (IFA) test for E risticii was carried out. Methods: Prospective, seroprevalence study. Methods: Healthy horses (n = 655) and horses with clinical signs of equine monocytic ehrlichiosis (EME; n = 514) from various regions of California. Methods: The IFA test was performed. Results were compared with results of an ELISA and with ...
Protection against Ehrlichia equi is conferred by prior infection with the human granulocytotropic Ehrlichia (HGE agent).
Journal of clinical microbiology    December 1, 1995   Volume 33, Issue 12 3333-3334 doi: 10.1128/jcm.33.12.3333-3334.1995
Barlough JE, Madigan JE, DeRock E, Dumler JS, Bakken JS.A Thoroughbred filly that developed clinical signs of equine granulocytic ehrlichiosis following inoculation with the human granulocytotropic ehrlichia was shown to be resistant to challenge with Ehrlichia equi, a closely related agent. This result further substantiates the close and potentially conspecific relationship between these two granulocytotropic ehrlichiae.
Identification of opossums (Didelphis virginiana) as the putative definitive host of Sarcocystis neurona.
The Journal of parasitology    December 1, 1995   Volume 81, Issue 6 916-919 
Fenger CK, Granstrom DE, Langemeier JL, Stamper S, Donahue JM, Patterson JS, Gajadhar AA, Marteniuk JV, Xiaomin Z, Dubey JP.Sarcocystis neurona is an apicomplexan that causes equine protozoal myeloencephalitis (EPM) in North and South America. Horses appear to be an aberrant host, because the merozoites continually divide in the central nervous system, without encysting. The natural host species has not previously been identified. The small subunit ribosomal RNA (SSURNA) gene of S. neurona was compared to those of Sarcocystis muris, Sarcocystis cruzi, Toxoplasma gondii, and Cryptosporidium parvum to identify a unique region suitable for a species-specific amplification primer. The S. neurona SSURNA primer was used ...
Sarcocystis falcatula from passerine and psittacine birds: synonymy with Sarcocystis neurona, agent of equine protozoal myeloencephalitis.
The Journal of parasitology    December 1, 1995   Volume 81, Issue 6 930-935 
Dame JB, MacKay RJ, Yowell CA, Cutler TJ, Marsh A, Greiner EC.Equine protozoal myeloencephalitis (EPM) is a neurologic disease of horses caused by Sarcocystis neurona. The horse is a dead-end host for S. neurona and the definitive and intermediate hosts have not previously been identified. We hypothesized that S. neurona is actually Sarcocystis falcatula, a parasite that cycles in nature between Virginia opossums (Didelphis virginiana) and any of a variety of avian intermediate hosts. We extracted DNA from S. falcatula sarcocysts in the muscle of a brown-headed cowbird (Molothrus ater) and from schizonts in a fixed specimen of lung from a Moluccan cockat...